US20150165176A1 - Methods and apparatus for treating disorders of the ear, nose and throat - Google Patents

Abstract

Methods and apparatus for treating disorders of the ear, nose, throat or paranasal sinuses, including methods and apparatus for dilating ostia, passageways and other anatomical structures, endoscopic methods and apparatus for endoscopic visualization of structures within the ear, nose, throat or paranasal sinuses, navigation devices for use in conjunction with image guidance or navigation system and hand held devices having pistol type grips and other handpieces.

Description

RELATED APPLICATIONS
• This application is a continuation-in-part of copending U.S. patent application Ser. No. 10/829,917 entitled Devices, Systems and Methods for Diagnosing and Treating Sinusitis and Other Disorders of the Ears, Nose and/or Throat filed on Apr. 21, 2004; Ser. No. 10/944,270 entitled Apparatus and Methods for Dilating and Modifying Ostia of Paranasal Sinuses and Other Intranasal or Paranasal Structures filed on Sep. 17, 2004; Ser. No. 11/116,118 entitled Methods and Devices for Performing Procedures Within the Ear, Nose, Throat and Paranasal Sinuses filed Apr. 26, 2005 and [Serial No. to be determined] entitled Devices, Systems And Methods Useable For Treating Sinusitus filed on Jun. 10, 2005, each such application being expressly incorporated herein by reference.
FIELD OF THE INVENTION
• The present invention relates generally to medical apparatus and methods and more particularly to devices and methods that are useable to treat disorders of the paranasal sinuses as well as other ear, nose & throat disorders.
BACKGROUND OF THE INVENTION
• Functional endoscopic sinus surgery (FESS) is currently the most common type of surgery used to treat chronic sinusitis. In a typical FESS procedure, an endoscope is inserted into the nostril along with one or more surgical instruments. The surgical instruments are then used to cut tissue and/or bone, cauterize, suction, etc. In most FESS procedures, the natural ostium (e.g., opening) of at least one paranasal sinus is surgically enlarged to improve drainage from the sinus cavity. The endoscope provides a direct line-of-sight view whereby the surgeon is typically able to visualize some but not all anatomical structures within the surgical field. Under visualization through the endoscope, the surgeon may remove diseased or hypertrophic tissue or bone and may enlarge the ostia of the sinuses to restore normal drainage of the sinuses. FESS procedures can be effective in the treatment of sinusitis and for the removal of tumors, polyps and other aberrant growths from the nose.
• The surgical instruments used in the prior art FESS procedures have included; applicators, chisels, curettes, elevators, forceps, gouges, hooks, knives, saws, mallets, morselizers, needle holders, osteotomes, ostium seekers, probes, punches, backbiters, rasps, retractors, rongeurs, scissors, snares, specula, suction canulae and trocars. The majority of such instruments are of substantially rigid design.
• In order to adequately view the operative field through the endoscope and/or to allow insertion and use of rigid instruments, many FESS procedures of the prior art have included the surgical removal or modification of normal anatomical structures. For example, in many prior art FESS procedures, a total uncinectomy (e.g., removal of the uncinate process) is performed at the beginning of the procedure to allow visualization and access of the maxilary sinus ostium and/or ethmoid bulla and to permit the subsequent insertion of the regid surgical instruments. Indeed, in most traditional FESS procedures, if the uncinate process is allowed to remain, such can interfere with endoscopic visualization of the maxillary sinus ostium and ethmoid bulla, as well as subsequent dissection of deep structures using the available rigid instrumentation.
• More recently, new devices, systems and methods have been devised to enable the performance of FESS procedures and other ENT surgeries with minimal or no removal or modification of normal anatomical structures. Such new methods include, but are not limited to, uncinate-sparing Baloon Sinuplasty™ procedures and uncinate-sparing ethmoidectomy procedures using catheters, non-rigid instruments and advanced imaging techniques (Acclarent, Inc., Menlo Park, Calif.). Examples of these new devices, systems and methods are described in incorporated U.S. patent application Ser. No. 10/829,917 entitled Devices, Systems and Methods for Diagnosing and Treating Sinusitis and Other Disorders of the Ears, Nose and/or Throat; Ser. No. 10/944,270 entitled Apparatus and Methods for Dilating and Modifying Ostia of Paranasal Sinuses and Other Intranasal or Paranasal Structures; Ser. No. 11/116,118 entitled Methods and Devices for Performing Procedures Within the Ear, Nose, Throat and Paranasal Sinuses filed Apr. 26, 2005 and [Serial No. to be determined] entitled Devices, Systems And Methods Useable For Treating Sinusitus filed on Jun. 10, 2005, of which this application is a continuation-in-part.
• There remains a need for further development of new and different devices and methodology for surgical treatment of sinusitis and other ear, nose and throat disorders.
SUMMARY OF THE INVENTION
• The present invention provides apparatus and disorders for treating sinusitis and other disorders of the ear, nose, throat and paranasal sinuses. The various devices and methods of the present invention may be used separately or in any possible and desirable combinations with each other.
• In accordance with the invention, there is provided endoscopic guide systems that generally comprise tubular guides (e.g., rigid, flexible and/or malleable guide catheters) that incorporate or are attachable to endoscopic apparatus. The endoscopic apparatus is useable to enable endoscopically view areas ahead of or adjacent to the distal end of the tubular guide. In some embodiments, such endoscopic guide systems are useable to facilitate trans-nasal advancement of a guidewire, catheter, instrument or other device to a position within or near an opening or a paranasal sinus (e.g., any transnasally accessible opening in a paranasal sinus or air cell including but not limited to; natural ostia, surgically altered natural ostia, surgically created openings, antrostomy openings, ostiotomy openings, burr holes, drilled holes, ethmoidectomy openings, natural or man made passageways, etc.). To facilitate this, the endoscopic guide system may comprise a) a tubular guide having a proximal end, a distal end and a lumen that extends longitudinally therethrough, said tubular guide having a distal portion that is more flexible than the remainder of the guide and said tubular guide being configured such that it may be i) inserted, distal end first, through a nostril of the subject's nose and ii) advanced, without requiring substantial modification or removal of any normal anatomical structure, to a position where the distal end of the guide is within or adjacent to the ostium of the paranasal sinus; and b) an endoscopic device incorporated in or attached to the tubular guide, said endoscopic device being useable to view a visual field that includes an area beyond the distal end of the tubular guide. In some embodiments, a portion (e.g., a distal portion) of the tubular guide may be curved and the endoscopic apparatus may allow to user to essentially see around the curve. The endoscopic apparatus may comprise a rigid, flexible, deflectable or steerable endoscopes that is incorporated into, inserted into or through, or attached to the tubular guide. Or, the endoscopic apparatus may comprise a waveguide, periscope or other device that serves as an extension of a separate endoscope such that the endoscope may be connected (e.g., attached, inserted, coupled or otherwise associated) to the proximal end of the endoscopic apparatus and will receive an image from the distal end of the endoscopic apparatus.
• Further in accordance with the invention, there are provided seeker devices that are useable to locate or access structures within the ear, nose and throat. In some embodiments, these seeker devices have lumens extending therethrough. In such embodiments having lumens, guidewires may be inserted or advanced through the lumen, thereby providing seeker/guidewire systems that are useable for placing guidewires into various anatomical structures (e.g., into a paranasal sinus). In embodiments having lumens, the proximal end of the seeker device may be attachable to a source of fluid for irrigation or substance delivery through the lumen and/or to a source of negative pressure to permit suction through the lumen. Also, in some embodiments that have lumens, a slot opening may extend along all or a portion of the lumen to allow a guidewire or other elongate device to be extracted laterally from all or a portion of the lumen. Additionally or alternatively, in some embodiments, the seeker device may have an expandable member (e.g., a balloon) that is useable to dilate anatomical structures, anchor the seeker and/or for other purposes. Structurally, a seeker device of the present invention may comprise an elongate substantially rigid (e.g., straight, pre-shaped, bent, curved, malleable) shaft, optionally having a bulbous (e.g., enlarged) distal tip on one or both ends. Various curves may be formed or formable in the seeker shaft.
• Still further in accordance with the invention, there are provided dilator devices (e.g., balloon dilators) that may be used to dilate anatomical structures within the ear, nose or throat of a human or animal subject (e.g., opening of paranasal sinuses as defined hereabove, metal passageways, other openings or passages). Such dilator devices may comprise a) a handpiece, b) an elongate shaft that extends from the handpiece, such elongate shaft having a distal portion that is insertable through a nostril of the subject's nose, c) a dilator having a non-expanded configuration and an expanded configuration and a dilator expansion control or trigger apparatus on or associated with the handpiece, such dilator expansion control or trigger apparatus being useable to move the dilator between its non-expanded configuration and its expanded configuration. In some embodiments, the dilator may be advanceable (or advanceable/retractable) from the elongate shaft. In such embodiments having an advanceable or advanceable/retractable dilator, the handpiece may additionally have a dilator advancement control or trigger. In some designs of these devices, the handpiece, dilator expansion control or trigger and/or dilator advancement control or trigger may be operable by one hand, thereby leaving the operators other hand free for handling other instruments or performing other tasks. In embodiments where the dilator comprises a balloon, the expansion of the dilator may result for the provision of a flow of infusion fluid into the balloon. Accordingly, such devices may incorporate pumps and/or sources of pressurized inflation fluid to facilitate inflation of the balloon. The balloon may be compliant or non-compliant. In embodiments having non-compliant balloons, the device may additionally comprise apparatus for applying negative pressure to the balloon thereby evacuating and collapsing the non-compliant balloon.
• Further still in accordance with the invention, there are provided devices for deterring unwanted movement of catheter(s) or other device(s) (e.g., guidewires, endoscopes, dilators, etc.) that have been inserted into the nose of a human or animal subject. Such support device may generally comprise a support member (e.g., an elongate body) that is positionable adjacent to the subject's nose and an attachment substance or apparatus (e.g., adhesive, resilient or pliable projections, fingers, members, hook and loop connector material, other apparatus for frictional engagement, etc.). The attachment substance or apparatus is useable for releasably holding the catheter(s) or other device(s) in substantially fixed position relative to the support member. Additionally, these devices may comprise positioning apparatus (e.g., legs, brackets, holders, adhesive) for holding the support member in position adjacent to the subject's nose.
• Still further in accordance with the invention, there are provided balloon catheters that are constructed in new ways. Such balloon catheters have guidewire lumens that extend though some or all of the length of the catheter. In some embodiments, an optional slot opening may be formed along some or all of the length of the guidewire lumen to allow a guidewire or other device to be extracted laterally from all or part of that lumen.
• Further still in accordance with the invention, there are provided balloon folding tools that are useable to facilitate folding of catheter-mounted balloons, such as non-compliant balloons. A balloon folding tool of this invention may comprise a) a rigid body having a central bore formed therein, the central bore having a diameter that is less than the fully inflated balloon diameter, b) a plurality of side channels located adjacent to and substantially parallel with the central bore, each of such side channels being connected to the bore through a slot. The balloon is insertable into the central bore while in a less than fully inflated state. Thereafter the balloon is inflatable to a fully or partially inflated state causing a separate portion of the balloon to pass through the each slot and into each side channel. Thereafter the balloon is deflatable such that each separate portion of the balloon that has passed into each side channel will form a separate wing of the deflated balloon. Those wings are, thereafter, foldable to a collapsed shape.
• Even further in accordance with the invention, there are provided apparats for compressing balloons to a low profile to facilitate subsequent insertion or reinsertion of the balloon into the body of a human or animal subject. Such a balloon compression apparatus may comprise a plurality of compression members disposed radially about a central cavity, such compression members being spaced apart from each other such that gaps exist between adjacent compression members, such compression members being moveable from non-compressing positions to compressing positions. The balloon is insertable into the central cavity of the compression device while the compression members are in their non-compressing positions. The compression members are then moveable to their compressing positions, thereby compressing portions of the balloon causing any inflation fluid to be forced out of the balloon and causing portions of the balloon to protrude outwardly into the gaps between the compression members. This results in the formation of a plurality of wings on the deflated balloon, such wings being thereafter foldable into a collapsed shape.
• Still further in accordance with the invention, there are provided inflator handpiece devices that are attachable to balloon catheters or other balloon equipped devices (e.g., balloon equipped tubular guides, seekers, guidewires, etc, as described herein and elsewhere) and useable to inflate the balloon. An inflator handpiece of the present invention may comprise a) a handpiece body configured to be grasped by a human hand, such handpiece body being attachable to the proximal end of a balloon catheter or other balloon equipped device, b) an inflator (e.g., a pump or source of compressed inflation fluid) and an inflation trigger useable to cause the inflator to inflate the balloon. These handpieces may facilitate precise handling and positioning of balloon catheters and other balloon equipped devices. In some embodiments, the handpiece may comprise and elongate body having a grip member that extends at an angle from the elongate body (e.g., generally similar to a pistol grip type of arrangement). In some embodiments, the handpiece and inflation trigger may be configured to be useable by a single hand, thereby freeing the operators other hand for handling of other instruments or performing other tasks. In embodiments where the catheter or other balloon equipped device has a lumen useable for passage of a guidewire or other device or substance, the inflator handpiece device may incorporate a port or passage to permit a guidewire or other device to be advanced through that lumen and/or to permit fluids to be infused or suction applied through that lumen. Various valves, grippers, etc. may be associated with such passageway or port to provide hemostasis, prevent fluid leakage, deter unwanted movement of guidewires or devices, etc.
• Further yet in accordance with the present invention, there are provided devices for breaking nasal turbinates or other bony anatomical structures in a human or animal subject. Such a breaking device may comprise a) first and second members positionable at spaced apart positions on one side of the turbinate or bony structure and a third member positionable on the other side of the turbinate or bony structure, between the first and second members. The third member and/or said first and second members are then moveable to exert pressure on the nasal turbinate or bony structure to cause the bone of the nasal turbinate or bony structure to break.
• Still further in accordance with the invention, there are provided navigation adapters that are attachable to cannulae, catheters or elongate devices to facilitate their use in conjunction with navigation systems (e.g., optical, electromagnetic, etc.) of the type used in performing image guided surgery. Such navigation adapter may comprise a) an elongate adapter body that is attachable to the substantially rigid cannula, catheter or elongate device and b) apparatus useable by the image guidance system to determine the position of the substantially rigid cannula, catheter or elongate device within the body of a human it animal subject. The apparatus useable by the image guidance system may comprise various sensors, emitters, reflectors, transponders, reflective passive elements, light emitting diodes, transmitters or receivers of energy (e.g. optical energy, radiofrequency energy, etc.) or combinations thereof that are useable to enable a navigation system to track the position of catheter, cannula or other device within the body. Examples of commercially available navigation systems that may be useable in conjunction with these navigation adapters include but are not limited to (insert list from navigation application).
• Still further in accordance with the invention, there are provided methods for using the above summarized devices.
• Further yet in accordance with the present invention, there are provided methods where one or more anatomical structures (e.g. uncinate process, wall of ethmoid air cell, turbinate) and/or pathological structures (e.g., polyps, etc) are removed or modified in combination with a procedure where a dilator is inserted transnasally and used to dilate an opening of a paranasal sinus (as defined hereabove) or other anatomical structure within the ear, nose, throat or paranasal sinus of a human or animal subject. Such removal or modification of normal or pathological anatomical structures may facilitate visualization and/or access to various anatomical locations during and after the procedure.
• Still further in accordance with the invention, there is provided a nasal introducer that comprises an introducer body (e.g., a plug) that insets into the nostril of a human or animal subject. One or more lumen(s) (e.g., passageway(s) or bore(s)) extend through the introducer body to allow one or more catheters or other devices (e.g., endoscopes, dilators, seekers, tubular guides, etc.) to be advanced through the introducer and into the nasal cavity or beyond. Various valves, grippers, etc. may be associated with such lumen(s) to provide hemostasis, prevent fluid leakage and/or deter unwanted movement of catheters or other devices that have been inserted through the lumen(s).
• Further aspect, elements and advantages of the present invention will be understood by those of skill in the art upon reading of the detailed description set forth herebelow.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a perspective view of a human subject undergoing a procedure for treating sinusitis in accordance with the present invention.
• FIG. 2A shows a perspective view of an embodiment of a support device having finger members in the nature of bristles.
• FIG. 2B shows a perspective view of an embodiment of a support device having finger members in the nature of pliable or resilient projections.
• FIG. 2C shows a perspective view of an embodiment of a support device comprising an adhesive surface.
• FIGS. 2D through 2G show perspective views of various embodiments of a support device being used to support a working device.
• FIGS. 3-3A show an embodiment of a nasal introducer that is insertable in to nares of a human or animal subject and useable to facilitate subsequent insertion and handling of catheters and other devices.
• FIG. 4A shows a perspective view of an embodiment of a guidewire comprising an enlarged distal end.
• FIG. 4B shows a longitudinal sectional view of an embodiment of a guidewire comprising an anchoring balloon.
• FIG. 5A shows a cross sectional view of a first embodiment of a seeker device having a lumen.
• FIG. 5B shows a perspective view of a second embodiment of a seeker device having a lumen.
• FIG. 5C shows a cross section of the seeker inFIG. 5B through theplane5C-5C.
• FIG. 5D shows a cross sectional view of a third embodiment of a seeker device comprising a lumen.
• FIG. 5E shows a longitudinal section of an embodiment of a seeker device comprising a deflectable or bendable distal tip.
• FIG. 5F shows a cross sectional view throughplane5F-5F inFIG. 5E.
• FIG. 6A is a perspective, partially section view of a tubular guide having a balloon.
• FIG. 6B is a cross sectional view throughline6B-6B ofFIG. 6A.
• FIG. 6C shows a perspective view of a tubular guide having a separate lumen useable for insertion of an endoscope.
• FIG. 6D shows a perspective view of a tubular guide having clip(s) useable for attachment of an endoscope or other apparatus.
• FIG. 6E shows an embodiment of a combination endoscope and tubular guide.
• FIG. 6F shows another embodiment of a combination endoscope and tubular guide.
• FIG. 6G shows another embodiment of a combination endoscope and tubular guide.
• FIGS. 6H and 6I show apparatus useable to hold a tubular guide and an endoscope in substantially fixed side-by-side positions.
• FIG. 6J shows a perspective view of a removable clip device useable for attaching a second device (e.g., an endoscope) to a tubular guide or other elongate device.
• FIGS. 6K and 6L show steps in a method wherein the removable clip device ofFIG. 6J is used to attach an endoscope to a tubular guide.
• FIGS. 6M through 6O show steps of a method of introducing one or more diagnostic or therapeutic devices through a tubular guide having an associated endoscope.
• FIG. 6P shows a method for introducing a dilator through a tubular guide that has an associated endoscope.
• FIG. 6Q shows a perspective view of a combination endoscope/tubular guide that is bendable or deflectable.
• FIG. 6R shows the distal end of the device ofFIG. 6Q in a bent or deflected state.
• FIGS. 7A-7C show a method for advancing a guidewire or other device through the working lumen of an endoscope into an anatomical opening viewed by the endoscope.
• FIG. 8A shows a perspective view of a tubular guide equipped for optional suctioning.
• FIG. 8B shows a perspective view of a guide having a handpiece that is configured to receive a detachable navigational modality to facilitate use of the device in an image guided surgical or interventional procedure.
• FIG. 9 shows a perspective view of a tubular guide having a tapered connector on its proximal end to facilitate attachment of a suction tube to the tubular guide.
• FIG. 10A is an exploded view showing the components of a tubular guide device formed of a straight proximal segment and a curved distal segment.
• FIG. 10B is an assembled view of the device shown inFIG. 10A.
• FIG. 10C shows a distal portion of a tubular guide comprising a polymeric inner tube and an outer tube having apertures, wherein the polymeric material of the inner tube is caused to flow or protrude through the apertures thereby holding the inner tube in substantially fixed position within the outer tube.
• FIG. 11 shows a side-deflecting distal tip that may be formed on or attached to a tubular cannula or catheter.
• FIG. 12 shows the distal portion of a guide catheter having a plurality of lumens through which guidewires or other devices may be introduced on different trajectories.
• FIG. 12A is a cross sectional view throughline12A-12A ofFIG. 12.
• FIG. 13A shows a distal portion of a tubular guide having a curved endoscopic apparatus attached thereto.
• FIG. 13B is a longitudinal sectional view of an endoscopic apparatus in the nature of a periscope.
• FIG. 13C is a longitudinal sectional view of an endoscopic apparatus in the nature of a curved wave guide.
• FIGS. 13D-E show steps in a method wherein the device ofFIG. 13A is used in combination with a straight endoscope to accomplish position of the distal tip of the tubular guide at an obscured anatomical location within the body of a human or animal subject.
• FIG. 14A is a perspective view of a straight tubular guide of the present invention having an endoscopic device attached thereto or integrated therewith and an optional balloon.
• FIG. 14B is a perspective view of a curved tubular guide of the present invention having an endoscopic device attached thereto or integrated therewith and an optional balloon.
• FIG.14B′ is a view of the distal portion of the tubular guide device ofFIG. 14B showing details of the curve formed therein.
• FIG. 14C is a perspective view of another curved tubular guide of the present invention having an endoscopic device attached thereto or integrated therewith and an optional balloon.
• FIG.14C′ is a view of the distal portion of the tubular guide device ofFIG. 14C showing details of the curve formed therein.
• FIG. 14D is a perspective view of another curved tubular guide of the present invention having an endoscopic device attached thereto or integrated therewith and an optional balloon.
• FIG.14D′ is a view of the distal portion of the tubular guide device ofFIG. 14D showing details of the curve formed therein.
• FIG. 14E is a perspective view of another curved tubular guide of the present invention having an endoscopic device attached thereto or integrated therewith and an optional balloon.
• FIG.14E′ is a view of the distal portion of the tubular guide device ofFIG. 14E showing details of the curve formed therein.
• FIG. 15 is a perspective view of a balloon catheter constructed of first and second tubes such that a short lumen (e.g., a rapid exchange guidewire lumen) extends through the balloon.
• FIG. 15A is a cross sectional view through line15A-15A ofFIG. 15.
• FIG. 16 is a perspective view of a balloon catheter constructed of first, second and third tubes such that a short lumen (e.g., a rapid exchange guidewire lumen) extends through the balloon.
• FIG. 16A is a cross sectional view throughline16A-16A ofFIG. 16.
• FIG. 16B is a cross sectional view throughline16B-16B ofFIG. 16.
• FIG. 16C is a cross sectional view throughline16C-16C ofFIG. 16.
• FIG. 17 is a broken, partially sectional view of a balloon catheter having a stylet permanently positioned therein and a guidewire tip protruding from its distal end.
• FIG. 17A is a cross sectional view throughline17A-17A ofFIG. 17.
• FIG. 17B is a partial perspective view of the stylet of the balloon catheter shown inFIG. 17.
• FIG. 18 is a broken, partially sectional view of a balloon catheter having a side slit.
• FIG. 18A is a cross sectional view throughline18A-18A ofFIG. 18.
• FIG. 18B is a cross sectional view throughline18B-18B ofFIG. 18.
• FIG. 19 shows a partial perspective view of the distal region of another balloon catheter that has capacitance measuring means for real time determination of balloon diameter.
• FIG. 19A shows a side view of the distal region of the balloon catheter ofFIG. 21.
• FIG. 19B is a cross sectional view throughline19B-19B of FIG.19A.
• FIG. 19C is a cross sectional view throughline19C-19C ofFIG. 19A.
• FIG. 20 shows a partial perspective view of the distal region of another balloon catheter that has capacitance measuring means for real time determination of balloon diameter.
• FIG. 20A shows a side view of the distal region of the balloon catheter ofFIG. 20.
• FIG. 20B is a cross sectional view throughline20B-20B ofFIG. 20A.
• FIG. 20C is a cross sectional view throughline20C-20C ofFIG. 20A.
• FIG. 21 shows a partial perspective view of a distal portion of balloon catheter having a malleable distal shaft.
• FIG. 22 shows a partial perspective view of a distal portion of balloon catheter having a flexible distal shaft.
• FIG. 23 shows a partial perspective view of a balloon folding tool of the present invention.
• FIG. 23A shows a balloon catheter being inserted into the balloon folding tool ofFIG. 23.
• FIG. 23B shows a cross sectional view of the balloon folding tool ofFIG. 23 with a fully deflated/collapsed balloon positioned therein.
• FIG. 23C shows a cross sectional view of the balloon folding tool ofFIG. 23 with a balloon partially inflated therein such that positions of the balloon protrude into side channels.
• FIG. 23 D shows a deflated/collapsed balloon after removal from the balloon folding tool ofFIG. 23.
• FIG. 24 is a front perspective view of a balloon compressing apparatus of the present invention.
• FIG. 24A is an exploded view of the balloon compressing apparatus ofFIG. 24.
• FIG. 25 shows a longitudinal sectional view of an embodiment of a catheter for simultaneous aspiration and irrigation of an anatomical region.
• FIG. 26 is a perspective view of a navigation adapter device that is attachable to a variety of other devices to facilitate use of those other devices in image guided surgical or interventional procedures.
• FIG. 26A is a perspective view of the navigation adaptor device ofFIG. 26 attached to the proximal end of a guide tube of the present invention and having an optical navigation assembly mounted on the navigation adapter device.
• FIG. 26B is a perspective view of the navigation adaptor device ofFIG. 26 attached to the proximal end of a guide tube of the present invention and having an electromagnetic navigation assembly mounted on the navigation adapter device.
• FIG. 27A is a top view of a dilation device useable to dilate the ostia of paranasal sinuses and other anatomical passages within the ear, nose and throat.
• FIG. 27B is a side view of the device ofFIG. 27A.
• FIGS. 27C-27D show steps in a method for using the dilation device ofFIGS. 27A-27B.
• FIG. 27E is a side view of another dilation device useable to dilate openings of paranasal sinuses and other anatomical passages within the ear, nose and throat.
• FIG. 27F is a side view of another dilation device which uses compressed inflation fluid to inflate a dilator balloon to dilate openings of paranasal sinuses and other anatomical passages within the ear, nose and throat.
• FIG. 27G is a schematic diagram of the valving arrangement of the device shown inFIG. 27F.
• FIG. 27H is a partial sectional view through a portion of the device ofFIG. 27A-B.
• FIG. 28A is a perspective view of a hand grip inflator device attached to a balloon catheter.
• FIG. 28B is a perspective view of a balloon dilation device having a hand grip inflator.
• FIG. 29 shows a perspective view of a hand-held squeezing device useable to break or deform anatomical structures such a nasal turbinates.
• FIG. 29A shows a distal portion of the device ofFIG. 29 in an open position.
• FIG. 29B shows a distal portion of the device ofFIG. 29 in a closed position.
• FIGS. 29C-D show steps in a method for temporarily or permanently breaking or deforming a nasal turbinate using the squeezing device ofFIG. 29.
• FIG. 29E shows a broken perspective view of a twistable device that is useable to break or deform anatomical structures such a nasal turbinates.
• FIGS. 29F-G show steps in a method for temporarily or permanently breaking or deforming a nasal turbinate using the twisting device ofFIG. 29E.
• FIG. 30 is a flow diagram of a method useable for treating sinus disorders by removal or modification of an anatomical or pathological structure in combination with dilation of an opening of a paranasal sinus.
• FIG. 31 is a flow diagram of a method useable for treating sinus disorders by dilation of an opening of a paranasal sinus in combination with suction and/or irrigation of a sinus cavity.
• FIG. 32 is a flow diagram of a method useable for treating conditions where unwanted scar or adhesion tissue has formed by forming a puncture tract in the scar or adhesion tissue, inserting a dilator into the puncture tract and dilating the puncture tract.
• FIG. 33 a flow diagram of a method useable for treating sinus disorders by dilation of a natural opening of a paranasal sinus in combination with the creation of a new opening in the paranasal sinus.
DETAILED DESCRIPTION
• The following detailed description, the accompanying drawings and the above-set-forth Brief Description of the Drawings are intended to describe some, but not necessarily all, examples or embodiments of the invention. The contents of this detailed description do not limit the scope of the invention in any way.
• A number of the drawings in this patent application may show anatomical structures of the ear, nose and throat. In general, these anatomical structures are labeled with the following reference letters:
• • Nasal Cavity NC
  • Nasopharynx NP
  • Nasal Turbinate NT
  • Frontal Sinus FS
  • Frontal Sinus Ostium FSO
  • Ethmoid Sinus ES
  • Ethmoid Air Cells EAC
  • Sphenoid Sinus SS
  • Sphenoid Sinus Ostium SSO
  • Maxillary Sinus MS
  • Maxillary sinus ostium MSO
  • Mucocyst MC
  • Middle turbinate MT
  • Inferior turbinate IT
  • Uncinate UN
  • Suprabullar ostium/recess SO
  • Retro-bullar ostium/recess RO
• The devices disclosed herein may be used alone or in various combinations to perform various procedures including, but not limited to, various transnasal procedures within paranasal sinuses and/or within openings of paranasal sinuses. As used herein, unless specified otherwise, the term “opening(s) of paranasal sinus(es)” shall include any transnasally accessible opening in a paranasal sinus or air cell including but not limited to; natural ostia, natural canals, surgically altered natural ostia, surgically created openings, antrostomy openings, ostiotomy openings, burr holes, drilled holes, puncture tracts, ethmoidectomy openings, fenestrations and other natural or man made passageways.
• FIG. 1 shows a human subject undergoing a procedure for treating sinusitis in accordance with one particular example of the present invention. The human subject is subjected to one or more diagnostic, therapeutic or access devices introduced through asupport device100. One example of a therapeutic device is a balloon catheter used to dilate openings of paranasal sinuses or other endonasal anatomical structures. One example of an access device is a guidewire used to access dilate natural ostia of paranasal sinuses or a natural or artificial passageway or tract leading to paranasal sinuses. In the embodiment shown inFIG. 1,support device100 comprises a support member that is stabilized by three or more legs that rest on the operating table. The one or more diagnostic, therapeutic or access devices may be tracked or navigated through the anatomy using one or more tracking or navigation modalities. In the embodiment shown inFIG. 1, a C-arm fluoroscope102 provides fluoroscopic visualization of anatomical regions during the procedure. Aninstrument console104 comprising one or more functional modules may also be provided.Instrument console104 can be controlled by console control means e.g. a foot pedal controller, a remote controller etc.Instrument console104 may be fitted with wheels to enable an operator to change the position of the instrument console in an operating area.Instrument console104 may comprise functional modules including, but not limited to:
• 1. Suction pump for delivering a controlled amount of vacuum to a suction device,
  2. Irrigation pump to deliver saline or other suitable irrigation medium,
  3. Power module to supply power to drills or other electrical devices,
  4. Storage modules for storing instruments, medications etc.,
  5. Energy delivery module to provide radiofrequency, laser, ultrasound or other therapeutic energy to a surgical device,
  6. Fluoroscope, MRI, CT, Video,Endoscope106 or Camera or other imaging modules to connect or interact with devices used during various diagnostic or therapeutic procedures,
  7. Display module e.g. a LCD, CRT or Holographic screen to display data from various modules such as an endoscope, fluoroscope or other data or imaging module,
  8. Remote control module to enable an operator to control one or more parameters of one or more functional modules, and
  9. Programmable Microprocessor that can store one or more operation settings for one or more functional modules etc.
  In the embodiment shown inFIG. 1,instrument console104 is connected toendoscope106.Endoscope106 may be introduced in the anatomy through one or more introducingdevices108 such as guide catheters. A physician may use a hand heldintroducer110 comprising a surgical navigation modality to introduce one or more diagnostic, therapeutic or access devices into the anatomy. Examples of surgical navigation modalities that may be located onintroducer110 include, but are not limited to navigation modalities comprising reflective passive elements, light emitting diodes, transmitters or receivers of energy (e.g. optical energy, radiofrequency energy, etc.), a combination of tow or more of the abovementioned navigation modalities, etc.
• One or more devices disclosed herein may be supported by one or more support devices while performing diagnostic, therapeutic or access procedures on a patient. For example,FIG. 2A shows a perspective view of one embodiment of asupport device200 comprising an elongate, generallycylindrical body202 having a plurality of projections204 (e.g., strands, wires, bristles, pliable or resilient members, etc.) extending therefrom.Projections204 are located sufficiently close to each other and are made of a suitable material to frictionally grip a device that has been inserted betweenadjacent projections204. For example,projections204 may be made of polymers, rubber materials including, but not limited to neoprene, silicone rubber, ABS, Nylon, PVC, Pebax, etc.Projections204 can be used to reversibly support one or more devices while performing diagnostic, therapeutic or access procedures on a patient. In some embodiments, one or more attachment substances or apparatus may be used to attach thebody202 to a region of the patient's body such as face, head, etc; a table; a flexible, rigid or repositionable arm mounted on a support; etc. In the embodiment shown inFIG. 2A,body202 is attached to fourarms206 that enablesupport device200 to be placed on a suitable surface.
• FIG. 2B shows a perspective view of another embodiment of a support device. In this example, thesupport device210 comprises a andelongate body212 having having an adhesive material disposed on one or more regions of its outer surface to reversibly adhere thesupport device216 to a surface, such as the patient's body, a table or a flexible arm, etc. Thebody212 of thissupport device210 further comprises two ormore fingers214 constructed and spaced in relation to each other to frictionally grip and substantially hold device(s) (e.g., catheter, cannula, endoscope, guidewire, etc.) that has been inserted betweenadjacent fingers214. Thefingers214 may be formed of any suitable material, typically a pliable or resilient material such as certain polymer foams, elastomers, rubber materials including, but not limited to neoprene, silicone rubber, ABS, Nylon, PVC, Pebax, etc.Fingers214 can be used to frictionally hold one or more device(s) (e.g., catheter, cannula, endoscope, guidewire, etc.) in substantially fixed position while performing diagnostic, therapeutic or access procedures on a patient.Body212 is connected to one or more attachment mechanisms to attachbody212 to a region such as the patient's body, a table or a flexible arm, etc.
• FIG. 2C shows a perspective view of another embodiment of asupport device216 comprising an elongate body having one or more regions of its outer surface coated with an adhesive material to which one or more device(s) (e.g., catheter, cannula, endoscope, guidewire, etc.) may releasably adhere. The body of thissupport device216 may be made of any suitable biocompatible materials including, but not limited to silicone, nylon, DELRIN®, polycarbonate, stainless steel, ABS, etc. Typical examples of adhesives that may be disposed on the outer surface of the body to include, but are not limited to medical grade rubber pressure sensitive adhesives, acrylic adhesives such as 3M Emtech adhesive P1500™, 3M Emtech adhesive P1510™, etc. The adhesive coated regions may also be used to reversibly adhere the body of thissupport device216 to another surface such as the patient's body, a table or a flexible arm, etc.
• FIGS. 2D through 2G show perspective views of various embodiments of support devices being used to support working devices. InFIG. 2D,support device210 is reversibly attached to a the patient's face.FIG. 2D also shows aguide catheter226 introduced through the nose and supported betweenadjacent fingers214 of thesupport device210 with the elongate body of the support device being disposed transversely (e.g., from side to side) inferior to the subject's nose (e.g., below the nares).
• In the example ofFIG. 2E, asupport device230 comprises abody232 and two or more thin strands, wires, or bristles234 that are connected tobody232.Bristles234 are designed to frictionally grip a device located betweenadjacent bristles234.Body232 is connected to one or more attachment mechanisms such asarms236 that enablesupport device230 to be placed on a patient's face. In the embodiment shown inFIG. 2E, aguide catheter238 is supported bysupport device230.
• InFIG. 2F, asupport device240 comprises abody242 and two or more thin strands, wires, or bristles244 that are connected tobody242. One region ofbody242 is in contact with a facial region of a patient.Bristles244 are designed to frictionally grip a device located betweenadjacent bristles244.Body242 is connected to one or more attachment mechanisms such asarms246 that enablesupport device240 to be supported on a patient's face. In the embodiment shown inFIG. 2F, aguide catheter248 is supported bysupport device240.
• InFIG. 2G, asupport device250 comprises abody252 and two or more thin strands, wires, or bristles254 that are connected tobody252.Bristles254 are designed to frictionally grip a device located betweenadjacent bristles254.Body252 is connected to one or more attachment mechanisms such asarms256 that enablesupport device250 to be placed on a mount table. In the embodiment shown inFIG. 2G, aguide catheter258 is supported bysupport device250.
• Similar support devices may also be designed using hook and loop fasteners such as Velcro™.
• One or more devices disclosed herein may be introduced through one or more nasal introducers. Such nasal introducers may also be used for keeping catheters or devices separate from each other and/or for anchoring for deterring unwanted movement or slippage of one or more catheter or other devices that have been inserted into the nose. Such nasal introducers may also be used for plugging the nostrils to prevent leakage of fluids through the nostril. For example,FIGS. 3-3A show an embodiment of a nasal introducer that is insertable in to nares of a human or animal subject and useable to facilitate subsequent insertion and handling of catheters and other devices.FIG. 3 shows a perspective view of an embodiment of thenasal introducer300 comprising a body having a proximal region, a distal region and one or more lumens or bores extending therethrough to permit insertion of the desired device(s). The outer diameter of proximal region is larger than the outer diameter of the distal region. The outer diameter ofnasal introducer300 gradually reduces or tapers in the distal direction, as shown inFIG. 3. Thisnasal introducer300 is placed in a nostril and one or more diagnostic, therapeutic or access devices may be introduced throughnasal introducer300. Examples of such diagnostic, therapeutic or access devices include, but are not limited to guide catheters, guidewires, endoscopes, etc. In the example shown inFIGS. 3 and 3A, thenasal introducer300 has two lumens, a firstdevice introducing lumen302 and a seconddevice introducing lumen304. The proximal end of firstdevice introducing lumen302 emerges out of the proximal end ofnasal introducer300 through afirst opening306. The distal end of firstdevice introducing lumen302 emerges out of the distal end ofnasal introducer300 through asecond opening307. Similarly, the proximal end of seconddevice introducing lumen304 emerges out of the proximal end ofnasal introducer300 through athird opening308. The distal end of seconddevice introducing lumen304 emerges out of the distal end ofnasal introducer300 through afourth opening309. In one embodiment,first opening306 andthird opening308 are provided with a locking mechanism such as a rotating hemostasis valve. The locking mechanism can be used to anchor one or more devices being introduced throughnasal introducer300 to the nose.Nasal introducer300 may be made of suitable biocompatible materials including, but not limited to rubber, polymers, metals, etc.
• FIG. 4A shows a side view of an embodiment of a guidewire comprising an enlarged distal end.Guidewire400 comprises anelongate body402.Elongate body402 may be made of a variety of biocompatible materials including, but not limited to stainless steel, Nickel-titanium alloy (e.g., Nitinol), etc.Elongate body402 may be coated with a variety of guidewire coatings including, but not limited to lubricious coatings such as PTFE coatings, etc. The distal end ofelongate body402 comprises anenlarged region404. In one embodiment,enlarged region404 is substantially spherical in shape. The length ofelongate body402 may range from 65 to 75 cm. The distal region ofguidewire400 may comprise a curved, bent or angled region. In one embodiment, the distal region ofguidewire400 comprises a J-tip.
• In some method embodiments of the invention disclosed herein, a guidewire may be inserted into a paranasal sinus or into/near the opening of a paranasal sinus and, thereafter, one or more diagnostic or therapeutic devices may be introduced over the guidewire. In some instances, forces generated during introduction of devices over the guidewire may tend to cause the position of the guidewire to change. The forces may also cause the guidewire to get dislodged from a desired position in a paranasal sinus or opening of a paranasal sinus. To prevent such unwanted movement of the guidewire, one or more anchoring or occlusion apparatus may be present on the guidewire. For example,FIG. 4B shows a longitudinal sectional view of aguidewire410 having anelongate body412, alumen414 and aballoon416 or other inflatable member that may be used to anchor the distal end of theguidewire410 or for other purposes (e.g., dilation).Elongate body412 may be made of a variety of biocompatible materials including, but not limited to stainless steel, Nickel-titanium alloy (e.g., Nitinol), etc. In one embodiment,elongate body412 is made of a suitable hypotube.Elongate body412 may be coated with a variety of guidewire coatings including, but not limited to lubricious coatings such as PTFE coatings, etc. The outer diameter ofelongate body412 may range from 0.014 inches to 0.040 inches. In a preferred embodiment, the outer diameter ofelongate body412 is 0.035 inches.Elongate body412 comprises alumen414. The distal end oflumen414 is in fluid communication with an anchoringballoon416. Anchoringballoon416 may be made of a compliant, semi-compliant or non-compliant material. Anchoringballoon416 may be present on the distal end ofelongate body412 or on the distal region ofelongate body412. The proximal region ofelongate body412 may comprise a microvalve located inlumen414. The microvalve allows a user to inflate or deflate anchoringballoon416 and also provide a fluid seal to lumen414 whenguidewire410 is used to perform a diagnostic or therapeutic procedure. The distal region ofguidewire400 may comprise a curved, bent or angled region. In one embodiment, the distal region ofguidewire400 comprises a J-tip. In one embodiment of a method of usingguidewire400, distal end ofguidewire400 is introduced into an anatomical region such as a paranasal sinus with anchoringballoon416 deflated. Thereafter, anchoringballoon416 is inflated.Guidewire400 is then pulled in the proximal direction to anchor anchoringballoon416 in the ostium of the paranasal sinus. Thereafter, guidewire400 is used to perform a diagnostic or therapeutic procedure. It will be appreciated that, as an alternative to aballoon416, other anchoring apparatus such as deployable projections or expandable polymer or metal mesh structures may be incorporated into or on theguidewire410.
• Various diagnostic, therapeutic or access devices disclosed herein may be introduced in the anatomy through a seeker.FIG. 5A shows aseeker device500 that comprises anelongate body502 having alumen506 extending therethrough. Theelongate body502 can be made of suitable biocompatible material(s) including, but not limited to metals e.g. stainless steel, titanium, nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Pebax, PEEK, Nylon, polyethylene, etc. Some or all of theelongate body502 may be bent, angled, curved or malleable. The distal end ofelongate body502 may comprise atip structure504.Such tip member504 may be constructed to be substantially atraumatic so as to prevent or reduce damage to adjacent anatomy while usingseeker500. In the embodiment shown inFIG. 5A,tip structure504 comprises an enlarged, substantially spherical or bulbous region.Lumen506 extends from the proximal end ofelongate body502 and to the distal end of the device. Thelumen506 can be used for introducing one or more elongate devices, suctioning, introducing one or more fluids, etc. The proximal end ofelongate body502 may comprise a suitable hub such as a luer lock.Seeker500 may be introduced through an opening in the human body to determine the location of a cavity, sinus or other anatomical regions. Thereafter, one or more elongate devices such a guidewires may be inserted throughlumen506 and into the cavity, sinus or other anatomical regions. In one method embodiment,seeker500 is inserted through the nose into the nasal cavity. Thereafter,seeker500 is advanced such thatoptional tip structure504 is located near a target anatomy e.g. an opening of a paranasal sinus.Seeker500 is then moved by the user such thatatraumatic tip504 engages with the target anatomy. This provided the user information about the location and orientation of the target anatomy such as an ostium or passageway leading to a paranasal sinus.Seeker500 is then used to introduce a guidewire throughlumen506 into the paranasal sinus. Thereafter,seeker500 is removed leaving the guidewire in place. The guidewire is then used to introduce one or more diagnostic or therapeutic devices into the paranasal sinus. In another method embodiment, an endoscope may be incorporated within or introduced throughlumen506 and used to visualize anatomical structures and/or to guide the navigation ofseeker500. Optionally, a dilator (e.g., a balloon) may be mounted on theseeker500 at or near the distal end of the device and may be used to dilate structures into which theseeker device500 has been inserted. In instances where a balloon or other inflatable dilator is used, a second lumen may extend through theshaft502 terminating distally in an opening within the balloon to permit inflation/deflation of the balloon.
• FIGS. 5B-C show a second embodiment of aseeker device510 comprising anelongate body512 having alumen518 extending therethrough from end to end.Elongate body512 can be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Pebax, PEEK, Nylon, polyethylene, etc. The distal region ofelongate body512 may comprise a bent, angled or curved region. In some embodiments, some (e.g., a distal region) or all of theelongate body512 may be substantially curved or malleable. The distal end ofelongate body512 may, in some cases, comprise anatraumatic tip514 to prevent or reduce damage to adjacent anatomy while usingseeker510. In the embodiment shown inFIG. 5B,atraumatic tip514 comprises an enlarged, substantially spherical region. The proximal region ofelongate body512 may comprise ahandle516 to enable a user to advance and/ortwist seeker510. In the particular example ofFIG. 5B, thelumen518 extends from the proximal end ofelongate body512 to through distal end of theatraumatic tip514. Also, in this particular example, theelongate body512 further comprises alongitudinal slit520 that extends intolumen518. The proximal end ofelongate body512 may comprise a suitable hub such as a luer lock. In one method of use, thisseeker510 may be inserted through the nose into the nasal cavity. Thereafter,seeker510 is advanced such thatatraumatic tip514 becomes positioned near a target anatomy e.g. an ostium of a paranasal sinus.Seeker510 is then moved by the user such that itsatraumatic tip514 touches adjacent anatomical structures. This provides the user with information about the location and orientation of the target anatomy and/or surrounding anatomical structures. In some applications, after theatraumatic tip514 of theseeker510 has been inserted into or through an ostium of a paranasal sinus, a guidewire may be advanced throughlumen518 into the paranasal sinus. Thereafter, theseeker510 may be removed leaving the guidewire in place. To facilitate removal of theseeker510 while leaving the guidewire in place, the proximal portion of the guidewire may be extracted laterally throughslit520. After theseeker510 has been removed, the guidewire may be used to introduce one or more working devices (e.g., diagnostic or therapeutic devices) into the paranasal sinus. In some applications, an endoscope is introduced throughlumen518 to guide the navigation ofseeker510.FIG. 5D shows Anotherseeker530 comprising anelongate body532 having alumen534 extending therethrough. Thebody532 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Pebax, PEEK, Nylon, polyethylene, etc. The distal region ofelongate body532 may comprise a bent, angled or curved region. In one embodiment,elongate body532 is substantially malleable.Lumen534 is an end-to-end lumen extending from the proximal end ofelongate body532 through an opening in the distal end ofelongate body532. Aguidewire536, which may optionally have anatraumatic tip538, is loaded inlumen534 as shown. The distal region ofguidewire536 may be curved, bent or angled such that it forms an internal angle, for example an angle of about 30 degrees, about 60 degrees, about 90 degrees, about 110 degrees, etc. The proximal end ofelongate body532 may comprise a suitable hub such as a rotating hemostasis valve to reversiblysecure guidewire536 toseeker530. In one method embodiment,seeker530 along withguidewire536 is inserted through the nose into the nasal cavity. Thereafter,seeker530 is advanced such thatatraumatic tip538 is located near a target anatomy e.g. an ostium of a paranasal sinus.Seeker530 is then moved by the user such thatatraumatic tip538 engages with the target anatomy. This provided the user information about the location and orientation of the target anatomy.Seeker530 is then used to advanceguidewire536 throughlumen534 into the paranasal sinus. Thereafter,seeker530 is removed leavingguidewire536 in place. This step is performed by slidingseeker530 in the proximal direction overguidewire536.Guidewire536 is then used to introduce one or more diagnostic or therapeutic devices into the paranasal sinus.
• Any of the seeker devices disclosed herein may comprise a deflectable or bendable distal tip. For example,FIG. 5E shows aseeker device540 having a deflectable or bendable distal tip.Seeker540 comprises anelongate body542 having afirst lumen544 and asecond lumen546 extending therethrough. Theelongate body542 may be made from suitable biocompatible material(s) including, but not limited to Pebax, PEEK, Nylon, polyethylene, etc. The distal end ofelongate body542 may optionally comprise an atraumatic tip. In one embodiment, the distal end ofelongate body542 comprises an enlarged, spherical region. In the embodiment shown inFIG. 5E, the inner diameter of thefirst lumen544 is larger than the inner diameter of thesecond lumen546. The proximal end ofelongate body542 may be connected to asuitable hub548, such as a female luer lock.Hub548 may comprise one ormore wings550 to enable a user to twist ortorque seeker540.Seeker540 further comprises a deflecting or bending mechanism. In this embodiment, the deflecting or bending mechanism comprises a deflectinghandle552 attached to apivot554. One end of deflectinghandle552 is connected to apull wire556. The distal end ofpull wire556 is attached to the distal region ofelongate body542 by an attachment means558. In one embodiment, attachment means558 is glue. To cause deflecting or bending of the distal tip ofelongate body542, a user pulls deflectinghandle552. Deflectinghandle552 in turn pullspull wire556. This causes deflecting or bending of the distal tip ofelongate body542.FIG. 5F shows a cross sectional view throughplane5F-5F inFIG. 5E.FIG. 5F showselongate body542 comprisingfirst lumen544 andsecond lumen546. Pullwire556 passes throughsecond lumen546. Similar deflecting mechanisms may also be used for constructing one or more guide catheters disclosed herein. Such guide catheters may be used for introducing one or more diagnostic, therapeutic or access devices into the anatomy.
• Any of the seeker devices disclosed herein may be used to open or puncture scar tissue or adhesions of paranasal sinus ostia or passageways leading to paranasal sinuses. Such scar tissue or adhesions may be caused for example due to infection, prior surgery, etc.
• FIG. 6A shows a tubular guide or guidecatheter600 having anelongate guide shaft602, alumen603 extending therethrough and an expandable dilator such as aballoon606.Guide shaft602 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, nickel-titanium alloy (e.g., Nickel-titanium alloy (e.g., Nitinol)), etc.; polymers e.g. Pebax, PEEK, Nylon, polyethylene, etc. The distal region ofguide shaft602 may comprise an angled, curved or bent region. In one embodiment, the distal tip ofguide catheter600 comprises a soft, atraumatic tip to reduce or prevent damage to surrounding anatomy. The distal region ofguide shaft602 may comprise anavigational marker604 such as a radiopaque marker band or a sensor/emitter usable with an electromagnetic or other type of navigation or image guidance system.Balloon606 may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, polyurethane, silicone, etc.Balloon606 can be inflated by a hollowballoon inflation tube608.Balloon inflation tube608 is attached to guideshaft602 and is substantially collinear to guideshaft602. The proximal end ofballoon inflation tube608 is in fluid connection to aballoon inflation port610. The proximal end ofguide shaft602 may comprise a suitable hub such as afemale luer lock612.Guide catheter600 can be used for introducing one or more devices or fluids throughlumen603.Lumen603 can also be used for suctioning fluids.Balloon606 may be used for dilating anatomical regions including, but not limited to anatomical passageways, ostia of paranasal sinuses, etc.FIG. 6B shows a cross sectional view through theplane6B-6B ofFIG. 6A.FIG. 6B showsballoon inflation tube608 is attached to guideshaft602.
• FIG. 6C shows aguide catheter620 that has anelongate body622 comprising a lumen and a side channel, such as aside tube626.Elongate body622 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, etc. or polymers e.g. Pebax, PEEK, etc. The distal end ofelongate body622 may comprise a curved, angled or bent region. The distal end ofelongate body622 may comprise a malleable region or may be actively deflectable by a user. The proximal end ofelongate body622 comprises ahub624. In one embodiment,hub624 is a female luer lock. Theside lumen626 may be aligned substantially parallel to the lumen ofelongate body622 and may extend distally to be flush with the distal end of theelongate body622 or, in some cases, may terminate proximal to the distal end of the elongate body. In the particular example shown in the drawings,side lumen626 extends from a proximal region ofguide catheter620 to a location that is substantially flush with the distal end of theelongate body622.Side lumen626 may be permanently or detachably attached to elongatebody622. Asuitable endoscope628 or other imaging device or imaging probe can be introduced throughelongate side lumen626 such that the distal end ofendoscope628 emerges out of the distal end ofelongate side lumen626. Examples ofsuitable endoscopes628 that can be used withguide catheter620 include Karl Storz Flexible Rhino-Laryngoscope (11101RP), made by Karl Storz Endoscopy—America, Culver City, Calif. The proximal end ofendoscope628 is connected to avideo camera630 to enable a user to view the anatomy around the distal region ofguide catheter620. This combination ofguide catheter620 andendoscope628 is introduced in a target anatomy. Thereafter, one or more diagnostic, therapeutic or access devices are introduced through the lumen ofelongate body622 under endoscopic guidance. The curved, angled or bent region in the distal end ofelongate body622 is especially useful to navigateendoscope628 around a tight bend in the anatomy.
• FIG. 6D shows aguide catheter650 having anelongate body652, a lumen that extends through the elongate body and one or more attachment apparatus such as side clip(s)656.Elongate body652 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, etc. or polymers e.g. Pebax, PEEK, etc. The distal end ofelongate body652 may comprise a curved, angled or bent region. The proximal end ofelongate body652 may comprise ahub654. In one embodiment,hub654 is a female luer lock. Side clips656 may be permanently or removably attached to the outer surface ofelongate body652 as shown inFIG. 6C. The one or more side clips656 may form a channel through which an endoscope may be introduced or may otherwise hold an endoscope in a position beside theelongate body652 such that the endoscope may view a field ahead of or adjacent to the distal end of thedevice650. Thus, one or more diagnostic, therapeutic or access devices may be introduced through the lumen ofelongate body652 under endoscopic guidance using an endoscope (or other imaging device or probe) that has been inserted or as other wise positioned within or supported by side clips656. In one embodiment, side clips656 may be cylindrical. In another embodiment, side clips656 may be ring shaped.
• FIG. 6E shows anendoscope660 or other imaging device or imaging probe is combined with aguide catheter662.Guide catheter662 has a lumen.Guide catheter662 may comprise a bent, angled or curveddistal tip664. In this particular example amagnet666 causes theendoscope660 to be attached by magnetic force to theguide catheter662, as shown inFIG. 6D. This combination ofendoscope660 and guidecatheter662 is then introduced in the anatomy. Thereafter, one or more diagnostic, therapeutic or access devices may be introduced through the lumen ofguide catheter662 under endoscopic guidance or other image guidance using anendoscope660 or other imaging device or imaging probe attached by magnetic force to theguide catheter662.
• FIG. 6F shows an endoscope670-guide catheter672 combination device or system. In this example, theguide catheter672 has a lumen.Guide catheter672 may comprise a bent, angled or curveddistal tip674. In this embodiment,endoscope670 is combined withguide catheter672 by an attachment apparatus that comprises a collar, such as arubber collar676.Rubber collar676 comprises two parallel lumens.Endoscope670 fits in the first lumen ofrubber collar676.Rubber collar676 may be made of suitable biocompatible rubber materials including, but not limited to silicone, Pebax, PVC, etc. Similarly, guidecatheter672 fits in the second lumen ofrubber collar676. Thus,endoscope670 is combined withguide catheter672 to enable simultaneous introduction ofendoscope670 and guidecatheter672 into a target anatomy. Thereafter, one or more diagnostic, therapeutic or access devices are introduced through the lumen ofguide catheter672 under endoscopic guidance.
• FIG. 6G shows an endoscope680-guide catheter682 combination device or system.Guide catheter682 has a lumen and may comprise a bent, angled or curveddistal tip684. In this embodiment,endoscope680 is combined withguide catheter682 by aremovable band686 that tiesendoscope680 withguide catheter682. In one embodiment,removable band686 comprises a hook and loop type of attaching mechanism such as Velcro.Removable band686 may be made of suitable biocompatible materials including, but not limited to silicone, Pebax, nylon, stainless steel, Nickel-titanium alloy (e.g., Nitinol)™), etc. Thus,endoscope680 is combined withguide catheter682 to enable simultaneous introduction ofendoscope680 and guidecatheter682 into a target anatomy. Thereafter, one or more diagnostic, therapeutic or access devices are introduced through the lumen ofguide catheter682 under endoscopic guidance.
• FIGS. 6H and 6I show another endoscope-guide catheter combination device orsystem698. As seen inFIG. 6H, the guide catheter comprises anelongate shaft690. In some cases, a distal region ofelongate shaft690 may further comprise a curved, bent orangled region692. The guide catheter further comprises ahub694 located on the proximal end ofelongate shaft690. In one embodiment,hub694 is a female luer lock. The guide catheter is attached to anendoscope696 such as a fiber-optic endoscope by anadjustable connector698 comprising ahollow body699.Hollow body699 comprises two channels: a first channel comprising a firstproximal orifice6000 and a firstdistal orifice6002 and a second channel comprising a secondproximal orifice6004 and a seconddistal orifice6006. The first channel allows the guide catheter to pass throughadjustable connector698. The second channel allowsendoscope696 to pass throughadjustable connector698. Adjustable connector comprises a firstgripping mechanism6008 and a secondgripping mechanism6010. Firstgripping mechanism6008 enablesadjustable connector698 to grip the guide catheter. Similarly, secondgripping mechanism6010 enablesadjustable connector698 to gripendoscope696. In the embodiment shown inFIG. 6H, firstgripping mechanism6008 comprises anelongate lever6012 pivoted on apivot6014 located onadjustable connector698. One end ofelongate lever6012 is attached by aspring mechanism6016 toadjustable connector698.Spring mechanism6016 causes the distal end ofelongate lever6012 to press on the guide catheter. This in turn causes the guide catheter to press on an edge of firstproximal orifice6000 and firstdistal orifice6002. This in turn causesadjustable connector698 to grip the guide catheter. Similarly, secondgripping mechanism6010 comprises anelongate lever6018 pivoted on apivot6020 and aspring mechanism6022 to causeadjustable connector698 to gripendoscope696. To adjust the relative positions of the guide catheter and/or theendoscope696, a user presses the proximal regions ofelongate lever6012 and/orelongate lever6018 as shown inFIG. 6I. Pressing the proximal region ofelongate lever6012 causes the distal region ofelongate lever6012 to move away from the guide catheter. This in turn releases the guide catheter fromadjustable connector698. Similarly, pressing the proximal region ofelongate lever6018 releases endoscope696 fromadjustable connector698. Thus,adjustable connector698 can be used to maintain the relative position of the guide catheter andendoscope696 during introduction or removal of the guide catheter in the anatomy and/or while performing a diagnostic, therapeutic or access procedure. If needed, the relative position of the guide catheter andendoscope696 can be adjusted before during or after a procedure. Various regions of adjustable connector may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, Nickel-titanium alloy (e.g., Nitinol), titanium, etc.; suitable polymers, etc. Similarly, other embodiments of adjustable connectors can be used to maintain the relative position of the guide catheter andendoscope696 during introduction or removal of the guide catheter in the anatomy and/or while performing a diagnostic, therapeutic or access procedure.
• FIG. 6J shows a perspective view of an embodiment of a removable attachment apparatus comprising aclipping device6030 useable to introduce or support an endoscope, image apparatus or various other devices along side aguide catheter6020. In the example shown,guide catheter6020 comprises anelongate hypotube6022 enclosing anelongate tubular member6024. Elongatetubular member6024 encloses a lumen to allow for insertion of one or more devices throughguide catheter6020. The distal end oftubular member6024 may be angled, bent or curved. The distal end oftubular member6024 may comprise anatraumatic tip6026. The proximal end oftubular member6024 comprises a hub. In one embodiment, the hub is a female luer lock. Aremovable clipping device6030 can clip on to guidecatheter6020.Clipping device6030 can be made of suitable biocompatible materials such as metals, rubbers, polymers, etc.Clipping device6030 comprises afirst clip6032 and asecond clip6034.First clip6032 is adapted to attach to the outer surface ofguide catheter6020.Second clip6034 is adapted to attach to the outer surface of an endoscope. Such a combination of an endoscope and a device such as a guide catheter can be introduced by a physician using a single hand.
• FIGS. 6K and 6L show the steps of a method of accessing an anatomical region using the removable clipping device shown inFIG. 6J. InFIG. 6K,clipping device6030 is attached to guidecatheter6020. Thereafter, guidecatheter6020 is introduced in an anatomical region such as the nasal cavity. Anendoscope6036 is introduced in the anatomy along withguide catheter6020.Endoscope6036 helps to visualize the anatomy to facilitate the introduction and/or the navigation ofguide catheter6020 in the anatomy. If desired,endoscope6036 may be attached to guidecatheter6020 usingclipping device6030 as shown inFIG. 6L. This enables the relative position ofendoscope6036 and guidecatheter6020 to be relatively fixed during a procedure.Endoscope6036 and guidecatheter6020 can thus be co-introduced in an anatomical region. In one embodiment,clipping device6030 is made of a flexible material such as a suitable rubber to allow for angular displacement of the axis ofendoscope6036 relative to the axis ofguide catheter6020. In another embodiment, the contact surface betweenclipping device6030 and one or both ofendoscope6036 and guidecatheter6020 is smooth. This allowsendoscope6036 to slide relative to guidecatheter6020. In another embodiment,endoscope6036 and/or guidecatheter6020 can be rotated around their axes even when attached toclipping device6030. In another embodiment,clipping device6030 allows minimal motion ofendoscope6036 relative to guidecatheter6020.
• FIGS. 6M through 6O shows various steps of a method of introducing one or more diagnostic or therapeutic devices along or beside another device such as an endoscope or other imaging device or imaging probe. In the example ofFIG. 6M, the introducingdevice6040 comprises anendoscope6042 and an attachment or receiving apparatus comprising aside lumen6044. Introducingdevice6040 is introduced in a desired region of the anatomy. This introduction may be performed usingendoscope6042, using a separate endoscope or using fluoroscopy or other imaging/guidance techniques. Thereafter, aguidewire6046 is introduced throughside lumen6044.Guidewire6046 is navigated through the anatomy under endoscopic visualization byendoscope6042. Thereafter,guidewire6046 is placed in a desired target region. In one method embodiment,guidewire6046 is placed across an ostium of a paranasal sinus. Thereafter, inFIG. 6N, a working device such as aballoon catheter6048 comprising a dilatingballoon6050 is introduced overguidewire6046 into the target anatomy. Thereafter, inFIG. 6O,balloon6050 is inflated to dilate a region of the target anatomy. In one method embodiment,balloon6050 is inflated to dilate an ostium of a paranasal sinus. Thereafter,balloon6050 is deflated andballoon catheter6048 and introducingdevice6040 are removed form the anatomy. Similarly, other diagnostic or therapeutic devices may be introduced throughside lumen6044 to perform one or more diagnostic or therapeutic procedures.
• FIG. 6P shows an embodiment of a method of introducing a dilator through the introducing device ofFIG. 6M. In this embodiment,dilator6052 comprises a flexible shaft and a rounded distal end to dilate or displace tissue.
• FIG. 6Q shows a deflectable introducingdevice6054 that generally comprises an endoscope and an introducing lumen. Introducingdevice6054 comprises aproximal handle6056.Proximal handle6056 encloses an elongatetubular element6058. In one embodiment, the proximal region oftubular element6058 is substantially rigid. In another embodiment, the distal region oftubular element6058 comprises a bent region. In another embodiment, the distal region oftubular element6058 is malleable or plastically deformable. InFIG. 6Q, the distal region oftubular element6058 is removed to show structures enclosed by the distal region oftubular element6058.Tubular element6058 encloses anendoscope6060 and an introducinglumen6062.Endoscope6060 is used to visualize the anatomy or one or more diagnostic or therapeutic devices while performing a diagnostic or therapeutic procedure. The proximal end of introducinglumen6062 may comprise asuitable hub6064. In one embodiment,hub6064 is a female luer hub. Introducinglumen6062 can be used to introduce one or more diagnostic, therapeutic or access devices into the anatomy. In one embodiment, introducingdevice6054 comprises a steering or deflecting mechanism to allow a user to controllably bend or deflect the distal region oftubular element6058. In the embodiment shown inFIG. 6Q, introducingdevice6054 comprises a slidingbutton6066 that is attached to a pull wire. The pull wire in turn is attached to one or moredistal rings6068 located on the distal region oftubular element6058. A user can move slidingbutton6066 to cause a distal region oftubular element6058 to controllably bend or deflect. In another embodiment of a steering or deflecting mechanism, the distal region ofendoscope6060 is attached to a distal region oftubular element6058. The distal region ofendoscope6060 may be attached to a distal region oftubular element6058 by one or moredistal rings6068. In this embodiment, pullingendoscope6060 causes a distal region oftubular element6058 to controllably bend or deflect.FIG. 6R shows a perspective view of the distal region of the introducing device ofFIG. 6Q in a bent or deflected state. A distal region oftubular element6058 has been removed to show structures enclosed by the distal region oftubular element6058. Introducingdevice6054 may be used to introduce one or more diagnostic, therapeutic or access devices into the anatomy. In one embodiment, introducingdevice6054 is used to introduce a balloon catheter. In another embodiment, introducingdevice6054 is used to introduce a guidewire into the anatomy. The guidewire is thereafter used to introduce one or more diagnostic, therapeutic or access devices into the anatomy.
• FIGS. 7A through 7C show various steps of a method of accessing an anatomical opening using an introducingdevice700 that generally comprises anendoscope702 and an introducinglumen704. The introducingdevice700 may be inserted into the body through an orifice or opening such as a nostril. Thereafter, introducingdevice700 is positioned, possibly under endoscopic visualization or other image guidance, such that the distal end of introducingdevice700 is positioned near a target of interest such as an opening of a paranasal sinus. Thereafter, inFIG. 6S, a diagnostic, therapeutic or access device is inserted through introducinglumen704 into the target of interest. In the example shown inFIG. 7B, the target of interest is an opening of a paranasal sinus and a guidewire706 is being inserted through introducinglumen704 into a retro-bullar ostium or recess. Guidewire706 may then be used to introduce one or more diagnostic, therapeutic or access into the retro-bullar ostium or recess, as shown.FIG. 7C shows a perspective view of a region of the human face showing the manner in which the introducingdevice700 may be transnasally inserted in the method shown inFIGS. 7A and 7B. After the introducingdevice700 has been inserted and positioned, various guidewires or other diagnostic, therapeutic or access devices may be inserted through introducinglumen704.
• Any of the guide catheters or other luminal devices disclosed herein may comprise an arrangement for suctioning an anatomical region through the distal end of the guide catheter or device unless to do so would render the device unusable for its intended purpose. For example,FIG. 8A shows aguide catheter800 comprising anelongate tube802 that may be made of suitable biocompatible materials including, but not limited to metals such as stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; plastics such as Pebax, PEEK, Nylon, polyethylene, etc. The distal region ofelongate tube802 may comprise a curved, bent or angled region. In some embodiments, the distal end ofelongate tube802 may comprise anatraumatic tip804. Although various modes of construction may be used, in the example shown, anelongate hypotube806 is disposed on the outer surface ofelongate tube802 and the proximal end ofguide catheter800 comprises a branched or Y-connector808. The proximal region of Y-connector808 comprises astraight arm810 and aside arm812. The proximal end ofstraight arm810 comprises asuitable hub814. In one embodiment,hub814 is a female luer hub. In another embodiment,hub814 comprises a rotating hemostasis valve such as a Touhy-Borst adapter. The proximal end ofside arm812 comprises asuitable hub816. In one embodiment,hub816 comprises a rotating hemostasis valve such as a Touhy-Borst adapter to adjust the amount of suction.Hub816 is connected to asuction tube818 that provides suction to guidecatheter800. Thus, guidecatheter800 can be used to provide suction as well as introduce one or more diagnostic, therapeutic or access devices into the anatomy.
• Various devices being introduced in the anatomy may comprise a detachable navigation apparatus (e.g., a navigation module or localizer) useable in conjunction with a navigation or image guidance system to track and/or navigate the devices through the anatomy. For example,FIG. 8B shows a perspective view of aguide catheter820 having anavigation adapter830 that is designed to receive detachable navigation apparatus such as a navigation module or localizer containing sensor(s), emitter(s), transmitter(s), reflector(s), etc. that are useable in conjunction with a navigation system. The navigation apparatus may be selected from the various navigation apparatus disclosed herein or in one of the patent applications incorporated herein by reference. In the embodiment shown inFIG. 8B, guidecatheter820 comprises anelongate body822 having a lumen.Elongate body822 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Pebax, PEEK, Nylon, polyethylene, etc. The distal end ofelongate body822 may comprise a bent, curved or angled region. The proximal region ofelongate body822 may comprise ahypotube824 located on the external surface ofelongate body822. The distal end ofelongate body822 may comprise anatraumatic tip826. The proximal end ofguide catheter820 comprises afirst attachment mechanism828. In one embodiment,first attachment mechanism828 is a female luer lock.First attachment mechanism828 is used to attachguide catheter820 to anavigational adaptor830.Navigational adaptor830 comprises asecond attachment mechanism832 that attached tofirst attachment mechanism828 on the proximal end ofguide catheter820. In one embodiment,second attachment mechanism832 is a male luer lock.Navigational adaptor830 further comprises aproximal hub834 that is in fluid communication withsecond attachment mechanism832.Navigational adaptor830 further comprises ahandle836 to enable a user to hold and navigateguide catheter820. The outer surface ofhandle836 may be roughened to increase the grip of a user onhandle836. In one embodiment, outer surface ofhandle836 is roughened by knurling. Handle836 comprises a bay to attach a suitablenavigational localizer838 tonavigational adaptor830. Examples ofnavigational localizer838 are encoded passive manipulator, active manipulator, ultrasound localizer, electromagnetic localizer, active optical localizer, passive optical localizer, etc.Navigation adaptor830 may further comprise anidentification module840.Identification module840 enablesnavigational localizer838 to identify the type ofnavigational adaptor830 that is being connected tonavigational localizer838. This enables the registration of the location and orientation of the distal tip ofnavigational adaptor830 bynavigational localizer838. In the embodiment shown inFIG. 8B,identification module840 comprises a pair of magnets. The unique magnetic field generated by the pair of magnets is measured bynavigational localizer838. This enablesnavigational localizer838 to identify the type ofnavigational adaptor830 being attached tonavigational localizer838. Other examples ofidentification module840 include, but are not limited to electrical modules e.g. a ROM that provides electrical information tonavigational localizer838; mechanical modules e.g. connector-pin arrangements that provide mechanical information tonavigational localizer838; other magnetic modules that provides magnetic information tonavigational localizer838; etc. In a particular embodiment, the distal end ofelongate body822 comprises a malleable or shapeable region. In this embodiment, the position and orientation of the distal tip ofguide catheter820 is re-calibrated tonavigational localizer838 after performing a step of bending or shaping the distal end ofelongate body822.
• In an alternate embodiment ofnavigational adaptor830 ofFIG. 8B, handle836 may comprise a non-detachablenavigational localizer838.
• The devices disclosed herein, especially the guide catheters, may comprise a proximal region adapted to fit to a suction tube. For example,FIG. 9 shows a perspective view of a tubular guide having a tapered connector on its proximal end to facilitate attachment of a suction tube to the tubular guide.FIG. 9 shows atubular guide900 comprising anelongate shaft902. The proximal end ofelongate shaft902 may comprise asuitable hub904 to attach one or more devices to the proximal end ofguide catheter900. In one embodiment,hub904 is a female luer lock.Tubular guide900 further comprises a taperedregion906 on the proximal region ofelongate shaft902.Tapered region906 comprises a wider proximal region and a narrower distal region to allow a suction tube to be fitted on the proximal end oftubular guide900. One or more grooves or ridges of the external surface of taperedregion906 may be provided to increase the grip of the suction tube on taperedregion906.Tapered region906 may also be used to attach a tube on the proximal end oftubular guide900 to deliver a suitable flushing fluid. The distal region oftubular guide900 may comprise a bent, curved or angleddistal region908.
• Bent, curved or angled regions of one or more devices disclosed herein may be made by bending a portion of the device and, in some instances, the devices will me formed of malleable material or may incorporate a malleable region to permit the user to bend, curve, angle or otherwise configure the device as desired. Some of the devices disclosed herein may be made by joining two elements, one of which comprises a bent, curved or angled region. For example,FIG. 10A is an exploded view showing the components of a tubular guide device ofFIG. 9 formed of a straightproximal segment902 and a curveddistal segment908. In this example, the bent, curved or angleddistal segment908 is attached to theproximal segment902 as shown in the assembled view ofFIG. 10B. The distal end ofproximal region902 may be joined to the proximal end ofdistal region908 at any desired angle. This may be done, for example, by cutting the distal end ofproximal segment902 at and angle and/or cutting the proximal end ofdistal segment908 at an angle and then joining the segments in an end-to-end butt joint fashion. Optionally, a sleeve or covering may surround the joint between the proximal end of thedistal segment902 and the distal end of theproximal segment908. Embodiments where thedistal segment908 is joined to theproximal segment902 at an angle may be used to make one or more of the devices disclosed herein that comprise a bent, curved or angled region.
• In an alternate method of manufacture, bent, curved or angled regions of one or more devices disclosed herein are made by joining two molded parts. The two molded parts are made such that each molded part comprises a bent, curved or angled region. The two molded parts are then joined to each other to produce a tubular element enclosing a lumen.
• FIG. 10C shows a tubular guide or guidecatheter1000 that comprises a afirst tube1004 and asecond tube1002 that is formed of polymeric or other material that melts or softens so as to be flowable throughopenings1006 formed in thefirst tube1004. Thesecond tube1002 protrudes out of and beyond the distal end of thefirst tube1004.Second tube1002 may be made of suitable biocompatible materials including, but not limited to Pebax, PEEK, Nylon, polyethylene, etc. Thefirst tube1004 may also be formed of any suitable material such as hypotube made of a biocompatible metals including, but not limited to stainless steel, Nickel-titanium alloy (e.g., Nitinol), etc. During manufacture, thesecond tube1002 is positioned such that a proximal portion of thesecond tube1002 extends into of through the lumen of thefirst tube1004 and thesecond tube1002 is caused to melt or soften (e.g., by heating) in the area of theopenings1006. The melted or softened material ofsecond tube1002 thereafter enters the one or more openings (e.g., holes or notches)1006 offirst tube1004 and is allowed to resolidify, thereby forming a bond or lock between thefirst tube1004 and thesecond tube1002. Such a method of manufacture may be used for manufacturing one or more devices comprising hypotubes disclosed herein or in the patent applications incorporated herein by reference.
• FIG. 11 shows a perspective view of an embodiment of a guide catheter comprising a curved, bent or angled distal flap.Guide catheter1100 comprises anelongate body1102 comprising a lumen.Elongate body1102 may be made from suitable biocompatible materials including, but not limited to metals such as stainless steel or Nickel-titanium alloy (e.g., Nitinol), or polymers such as Nylon, Pebax, PEEK, polyethylene, etc. The lumen ofelongate body1102 may be used to introduce one or more elongate devices throughguide catheter1100. The distal region ofelongate body1102 comprises a curved, bent or angleddistal flap1104.Flap1104 is oriented at an angle to the axis ofguide catheter1100 as shown inFIG. 11. In one embodiment,flap1104 is created by removing material from the distal end ofelongate body1102 and bending the distal end ofelongate body1102. In another embodiment,flap1104 is created by attaching anelement comprising flap1104 to the distal region ofelongate body1102. Such guide catheters may be used for introducing one or more elongate devices such as aguidewire1106 at a desired angle to the guide catheter.
• Similar flap regions may also be attached to the distal end of endoscopes comprising one or more endoscope lumens. This enables a user to introduce one or more devices through the one or more endoscope lumens at an angle to the axis of the distal region of the endoscope.
• FIG. 12 shows a perspective view of a guide catheter comprising anelongate body1202,lumens1206,1210 terminating inopenings1208,1212 and an optional atraumaticdistal tip1204. Atraumaticdistal tip1204 prevents or reduces damage to the anatomy while introducingguide catheter1200 into the anatomy. Elongate body6172 may be made from suitable biocompatible materials including, but not limited to Nylon, Pebax, PEEK, polyethylene, etc.Guide catheter1200 further comprises alumen1206 that extends from the proximal region ofguide catheter1200. The distal end oflumen1206 emerges out of the distal region ofguide catheter1200 through alumen opening1208. The distal end oflumen1206 comprises a bent, curved or angled region such that an elongate device introduced throughlumen1206 emerges out oflumen opening1208 at an angle to the axis ofguide catheter1200.Guide catheter1200 may comprise one or more lumens. In the example shown inFIG. 12,guide catheter1200 further comprises asecond lumen1210 that extends from the proximal region ofguide catheter1200. The distal end ofsecond lumen1210 emerges out of the distal region ofguide catheter1200 through asecond lumen opening1212.FIG. 12A shows a cross section through the guide catheter shown inFIG. 12 through theplane12A-12A.Guide catheter1200 comprises anelongate body1202 comprisinglumen1206 andsecond lumen1210. Such guide catheters may be used for introducing one or more elongate devices such as guidewires at a desired angle to the guide catheter. Such guide catheters may also comprise an endoscope lumen. In one embodiment, the endoscope lumen has a side opening to enable a user to introduce one or more elongate devices such as guidewires under endoscopic guidance.
• FIG. 13A shows a tubular guide or guidecatheter1300 comprises an elongatetubular body1302 that may be substantially rigid and anendoscopic apparatus1306 attached to thebody1302 and useable to facilitate endoscopic viewing of a field ahead or or adjacent to the distal end of thetubular guide body1302.Elongate body1302 may be made of suitable biocompatible materials including, but not limited to metals such as stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; plastics such as Nylon, Pebax, PEEK, polyethylene, etc. The distal region ofelongate body1302 comprises a curved, bent or angled region to enable the user to introduce one or more devices into the target region around the anatomical obstruction. The curved, bent or angled region ofelongate body1302 may be bent by an angle ranging from 25 degrees to 130 degrees. The distal end ofelongate guide1302 may comprise anatraumatic tip1304 to reduce or eliminate trauma to surrounding tissues while usingdevice guide1300. In this example, theendoscopic apparatus1306 comprises a periscope or waveguide that is attached to the side of thetubular body1302. The proximal end of thisperiscope1306 comprises asocket1308.Socket1308 enables the distal end of an endoscope to attach toperiscope1306. Distal end ofperiscope1306 comprises a curved, bent or angled region to enable the user to visualize the target region around the anatomical obstruction. The curved, bent or angled region ofperiscope1306 may be bent by an angle ranging from 25 degrees to 130 degrees. In one embodiment of a method of usingdevice guide1300, the target region around the anatomical obstruction is visualized by an endoscope attached toperiscope1306. Thereafter, one or more diagnostic, therapeutic or introducing devices are introduced into the target region throughelongate body1302.FIG. 13B shows a longitudinal sectional view of the device guide shown inFIG. 13A.FIG. 13B showsdevice guide1300 comprising anelongate body1302 with anatraumatic tip1304. The proximal end ofperiscope1306 comprises asocket1308.Socket1308 comprises agasket1312 to substantially seal the interface between an endoscope andsocket1308. The distal end ofperiscope1306 compriseslens1310.Light entering lens1310 is reflected by amirror1314 and is directed towardssocket1308. Thereafter, the light enters the endoscope to provide the user an image of the target anatomy to be visualized. In one alternate embodiment, the mirror may be polarized to improve image quality and reduce glare.
• FIG. 13C shows a longitudinal sectional view of a second embodiment of a device guide comprising a periscope to enable a user to endoscopically visualize a target region around an anatomical obstruction.Device guide1320 comprises anelongate body1322 comprising a lumen.Elongate body1322 may be made of suitable biocompatible materials including, but not limited to metals such as stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; plastics such as Nylon, Pebax, PEEK, polyethylene, etc. The distal region ofelongate body1322 comprises a curved, bent or angled region to enable the user to introduce one or more devices into the target region around the anatomical obstruction. The curved, bent or angled region ofelongate body1322 may be bent by an angle ranging from 25 degrees to 130 degrees. The distal end ofelongate guide1322 may comprise anatraumatic tip1324 to reduce or eliminate trauma to surrounding tissues while usingdevice guide1320. Aperiscope1326 is attached lengthwise to elongatebody1320. Distal end ofperiscope1326 comprises a curved, bent or angled region to enable the user to visualize the target region around the anatomical obstruction. The curved, bent or angled region ofperiscope1326 may be bent by an angle ranging from 25 degrees to 130 degrees. The proximal end ofperiscope1326 comprises asocket1328.Socket1328 enables the distal end of an endoscope to attach toperiscope1326.Socket1328 comprises agasket1330 to substantially seal the interface between an endoscope andsocket1328. The distal end ofperiscope1326 comprises alens1332.Periscope1326 further comprisesfiber optic fibers1334 located proximal tolens1332. Light passing throughlens1332 passes throughfiber optic fibers1334. Thus, light emitted by the endoscope is transmitted byfiber optic fibers1334 throughlens1332 to illuminate a field of view. The light is reflected from anatomical regions and enters lend1332.Light entering lens1332 is transmitted byfiber optic fibers1334 tosocket1328. Thereafter, the light enters the endoscope attached tosocket1328 to provide the user an image of the target anatomy to be visualized.Fiber optic fibers1334 ofperiscope1326 are arranged such that they are substantially aligned with the fiber optic fibers of the endoscope attached tosocket1328. In one embodiment, a part offiber optic fibers1334 ofperiscope1326 are designed to transmit light emitted from the endoscope to illuminate the field of view. Another part offiber optic fibers1334 ofperiscope1326 are designed to transmit light reflected from anatomical structures to the endoscope. In one embodiment,periscope1326 further comprises one or moreintermediate lenses1336 located between the ends of adjacent bundles offiber optic fibers1334 as shown inFIG. 13C. In one embodiment of a method of usingdevice guide1320, the target region around the anatomical obstruction is visualized by an endoscope that is attached toperiscope1326. Thereafter, one or more diagnostic, therapeutic or introducing devices are introduced into the target region throughelongate body1322.
• FIGS. 13D and 13E show the various steps of an embodiment of a method to endoscopically visualize a target region around an anatomical obstruction using a device guide comprising a periscope. In this method embodiment,device guide1320 shown inFIG. 13A is used as an example of a device guide comprising a periscope. InFIG. 13D, a user attempts to visualize a target anatomical region around an anatomical obstruction using anendoscope1340. In one embodiment, the target anatomical region is the ostium of a maxillary sinus and the anatomical obstruction is a nasal turbinate. If the attempt is unsuccessful, the method proceeds to the step shown inFIG. 13E. InFIG. 13E, the user fits the distal tip ofendoscope1340 into the proximal end ofperiscope1306. This enables the user to visualize the anatomy around the anatomical obstruction. Thereafter, one or more devices may be introduced throughdevice guide1320 into the anatomy.
• The various devices described or incorporated herein may include one or more optical marker(s). Such optical marker(s) may be used for example for optically determining the relative location of the balloon of the balloon catheter with respect to the distal end of a guide catheter through which the balloon catheter is introduced. Such optical marker(s) may enable a user to determine the location of the balloon of the balloon catheter with respect to the distal end of a guide catheter without using methods like fluoroscopy that used ionizing radiation. If the balloon is too close to the distal end of the guide catheter, there is a risk that the balloon may be inflated by a user while it is inside the guide catheter. If the balloon is too far from the distal end of the guide catheter, the guide catheter may not provide adequate support to the balloon catheter. Thus, the balloon of the balloon catheter should be located at an optimal distance with respect to the distal end of the guide catheter. In one embodiment, the optimal distance is ensured by providing an optical marker on the proximal region of the balloon catheter. The balloon catheter is inserted through a guide catheter such that the distal region of the balloon catheter emerges out of the distal end of the guide catheter. The location of the optical marker relative to the proximal region of the guide catheter is used to determine the relative location of the balloon of the balloon catheter with respect to the distal end of the guide catheter. In another embodiment, the optimal distance is ensured by providing an optical marker on the distal region of the balloon catheter. The balloon catheter is inserted through a guide catheter such that the distal region of the balloon catheter emerges out of the distal end of the guide catheter. The location of each optical marker may be tracked by an endoscope inserted in the anatomy. The location of the optical marker relative to the distal end of the guide catheter is used to determine the relative location of the balloon of the balloon catheter with respect to the distal end of the guide catheter.
• Similar optical markers may be located on other balloon catheters disclosed herein. For example, an optical marker may be located on a balloon catheter proximal to a balloon on the balloon catheter. Such an optical marker is especially useful to determine the location of the balloon with respect to a paranasal sinus ostium after the balloon has been introduced in a paranasal sinus. After the balloon is inserted inside the paranasal sinus, the balloon can no longer be visually seen by an endoscope. The user can then note the location of the optical marker proximal to the balloon. This information enables the user to determine the length of the balloon that is present inside the opening. This information in turn can be used by the user to accurately position the balloon with respect to the paranasal sinus ostium to achieve optimal dilation of the paranasal sinus ostium.
• The optical markers disclosed herein may be combined optical-radiopaque markers. In one embodiment, the combined optical-radiopaque marker comprises a platinum coil or marker. Preferably, the combined optical-radiopaque marker comprises a coating of a colored polymer including, but not limited to colored heat shrink polyethylene terephthalate. The length of the combined optical-radiopaque marker ranges preferably from 0.5 mm-10 mm.
• While removing a balloon catheter from the anatomy, the balloon of the balloon catheter might accidentally pull anatomical structures like the uncinate and damage the anatomical structures. To prevent such damage, in the method embodiments where a balloon catheter is introduced through a guide device, the balloon catheter may be removed from the anatomy along with the guide device. This step may be performed after ensuring that an undesirably long distal region of the balloon catheter is not protruding from the distal end of the guide device. The guide device may have a suitable attachment mechanism such as a rotating hemostasis valve, a clip, etc. to temporarily attach the balloon catheter to the guide device. The attachment mechanism enables a user to remove the balloon catheter from the anatomy along with the guide device.
• The flexible endoscopes disclosed herein may comprise one or more endoscope lumens. In one embodiment, the endoscope lumen is a side lumen. The side lumen is designed such that one or more diagnostic, therapeutic or access devices can be inserted in the anatomy through the side lumen under endoscopic guidance.
• The guide catheters disclosed herein may comprise a bent, curved or angled distal region to allow easier access to a paranasal sinus ostium. Such guide catheters may further comprise mechanisms to introduce an endoscope along the guide catheters. For example, FIGS.14A through14E′ show side views of embodiments of guide devices comprising bent, curved or angled distal regions and mechanisms to introduce an endoscope along the guide catheters. One or more of these guide devices may be provided as a part of the system for diagnosing or treating paranasal sinus pathologies.FIG. 14A shows a side view of a first embodiment of a guide device comprising a substantially straight distal portion.Guide device1400 comprises anelongate tube1402.Elongate tube1402 may be made of suitable biocompatible materials such polymers e.g. Nylon, Pebax, etc. In a preferred embodiment, the material ofelongate tube1402 has Rockwell hardness in the range of about 70 R to about 110 R. In this preferred embodiment, the distal portion is flexible enough to prevent or reduce damage to the anatomy. Yet, the distal portion is rigid enough to retain its shape as one or more devices are passed throughguide device1400. Furthermore, the distal portion is rigid enough to enable a user to use the distal portion to displace anatomical structures. The distal portion ofelongate tube1402 comprises a curved, bent or angled region curved at an angle of less then 5 degrees. In one embodiment, distal portion ofelongate tube1402 is substantially straight. The inner surface ofelongate tube1402 may be lined by a lubricious coating or a tubular lubricious liner made of a suitable biocompatible material such as PTFE. In one embodiment, the outer diameter ofelongate tube1402 is around 0.134+/−0.005 inches. Anoptional dilating balloon1403 may be located on the distal region ofguide device1400. Dilating balloon may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, etc. The distal portion ofelongate tube1402 comprises anatraumatic tip1404.Atraumatic tip1404 may be made of suitable biocompatible materials including, but not limited to Pebax, etc.Atraumatic tip1404 prevents or reduces damage to the anatomy caused by the distal end ofguide device1400. In one embodiment, length ofatraumatic tip1404 is 0.08+/−0.04 inches and the material oftip1404 has Shore Durometer hardness in the range of about 35 D to about 72D. Guide device1400 further comprises ahypotube1406.Hypotube1406 may be made of suitable biocompatible materials such asstainless steel 304, titanium, Nickel-titanium alloy (e.g., Nitinol), polymers such as Nylon etc. In one embodiment, the outer diameter ofhypotube1406 is 0.154+/−0.005 inches. In one embodiment of a method of constructingguide device1400, astainless steel hypotube1406 is bonded to anelongate tube1402 such as a Nylonelongate tube1402 to increase the strength ofelongate tube1402. In one embodiment, hypotube1406 is heat bonded to elongatetube1402. One or more openings, perforations or holes may be located onhypotube1406 to enable material ofelongate tube1402 to melt into the one or more openings, perforations or holes. When the melted material ofelongate tube1402 solidifies, an additional mechanical bonding is created betweenhypotube1406 andelongate tube1402.Guide device1400 further comprises an endoscope introducing mechanism for introducing an endoscope EN. In the embodiment shown inFIG. 14A, the endoscope introducing mechanism comprises aside lumen1407 through which a suitable flexible endoscope EN can be introduced in the anatomy. The proximal end ofguide device1400 comprises ahub1408. In one embodiment,hub1408 is a female luer hub.Hub1408 may havewings1409 to enable a user to turnguide device1400. In one embodiment, the axial length ofguide device1400 is 5+/−0.25 inches. In one embodiment, the inner diameter ofguide device1400 is around 0.1 inches. The distal portion ofguide device1400 may comprise a radiopaque marker. In one embodiment, the radiopaque marker is a platinum/iridium marker band. The guide device design shown inFIG. 14A is especially suited for trans-nasal access of the sphenoid sinuses.
• FIG. 14B shows a side view of a first embodiment of a guide device comprising a bent, angled or curved distal portion.Guide device1410 comprises anelongate tube1412.Elongate tube1412 may be made of suitable biocompatible materials such polymers e.g. Nylon, Pebax, etc.Elongate tube1412 comprises a substantially straight proximal portion enclosed by a hypotube and a distal portion comprising a curved, bent or angled region. The angle of the curved, bent or angled region of the distal portion can range from 5 degrees to 45 degrees. In this embodiment, distal portion ofelongate tube1412 is bent by an angle of around 30 degrees. The inner surface ofelongate tube1412 may be lined by a lubricious coating or a tubular lubricious liner made of a suitable biocompatible material such as PTFE. In one embodiment, the outer diameter ofelongate tube1412 is around 0.134+/−0.005 inches. Anoptional dilating balloon1413 may be located on the distal region ofguide device1410. Dilating balloon may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, etc. The distal portion ofelongate tube1412 comprises anatraumatic tip1414.Atraumatic tip1414 may be made of suitable biocompatible materials including, but not limited to Pebax, etc.Atraumatic tip1414 prevents or reduces damage to the anatomy caused by the distal end ofguide device1410. In one embodiment, length ofatraumatic tip1414 is 0.08+/−0.04 inches.Guide device1410 further comprises ahypotube1416 covering the proximal portion ofelongate tube1412.Hypotube1416 may be made of suitable biocompatible materials such asstainless steel 304, titanium, Nickel-titanium alloy (e.g., Nitinol), polymers such as Nylon etc. In one embodiment, the outer diameter ofhypotube1416 is 0.154+/−0.005 inches. In one embodiment of a method of constructingguide device1410, astainless steel hypotube1416 is bonded to a Nylonelongate tube1412.Guide device1410 further comprises an endoscope introducing mechanism for introducing an endoscope EN. In the embodiment shown inFIG. 14B, the endoscope introducing mechanism comprises aside lumen1417 through which a suitable flexible endoscope EN can be introduced in the anatomy. The proximal end ofguide device1410 comprises ahub1418. In one embodiment,hub1418 is a female luer hub.Hub1418 may havewings1419 to enable a user to turnguide device1410.Wings1419 may be aligned in the plane of the curve of the distal tip as an indicator of the position and orientation of the distal tip in the anatomy. In one embodiment, the axial length ofguide device1410 is 5+/−0.25 inches. In one embodiment, the inner diameter ofguide device1410 is around 0.1 inches. The distal portion ofguide device1410 may comprise a radiopaque marker. In one embodiment, the radiopaque marker is a platinum/iridium marker band. FIG.14B′ shows an enlarged view of the distal portion of the guide device inFIG. 14B. FIG.14B′ shows elongatedtube1412 enclosed byhypotube1416. Distal end ofelongated tube1412 comprisesatraumatic tip1414. Several parameters defined hereafter characterize the design of the distal portion ofguide device1410. The width of the distal end ofguide device1410 is called W as shown. The length measured from the proximal-most point on the distal curved portion ofelongate tube1412 to the distal-most part of the distal tip is called L1. L1 is measured along the linear direction of the straight proximal portion ofguide device1410 as shown in FIG.14B′. The length of the straight region ofelongate tube1412 from the distal end of t hypotube1416 till the proximal most point on the curved region of the distal portion is called L2. In one particular embodiment, W is 0.34+/−0.08 inches, L1 is 0.46+/−0.08 inches, L2 is 0 to 2 inches and the radius of curvature of the distal curved region ofelongate tube1412 is 0.180 inches. The guide device design shown in FIGS.14B and14B′ is especially suited for trans-nasal access of the sphenoid sinuses.
• FIG. 14C shows a side view of a second embodiment of a guide device comprising a bent, angled or curved distal portion. The design ofguide device1420 is similar to the design ofguide device1410.Guide device1420 comprises anelongate tube1422. The distal portion ofelongate tube1422 comprises a curved, bent or angled region curved at an angle ranging from 30 degrees to 140 degrees. In this embodiment, distal portion ofelongate tube1422 is bent by an angle of around 70 degrees. Anoptional dilating balloon1423 may be located on the distal region ofguide device1420. Dilating balloon may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, etc. The distal portion ofelongate tube1422 comprises anatraumatic tip1424.Guide device1420 further comprises ahypotube1426.Guide device1420 further comprises an endoscope introducing mechanism for introducing an endoscope EN. In the embodiment shown inFIG. 14C, the endoscope introducing mechanism comprises aside lumen1427 through which a suitable flexible endoscope EN can be introduced in the anatomy. The proximal end ofguide device1420 comprises ahub1428. In one embodiment,hub1428 is a female luer hub.Hub1428 may havewings1429 to enable a user to turnguide device1420. FIG.14C′ shows an enlarged view of the distal portion of the guide device inFIG. 14C. FIG.14C′ showselongated tube1422 enclosed byhypotube1426. Distal end ofelongated tube1422 comprisesatraumatic tip1424. In one particular embodiment, W is 0.45+/−0.08 inches, L1 is 0.32+/−0.08 inches, L2 is 0 to 2 inches and the radius of curvature of the distal curved region ofelongate tube1422 is 0.180 inches. The guide device design shown in FIGS.14C and14C′ is especially suited for trans-nasal access of the frontal sinuses.
• FIG. 14D shows a side view of a second embodiment of a guide device comprising a bent, angled or curved distal portion. The design ofguide device1430 is similar to the design ofguide device1410.Guide device1430 comprises anelongate tube1432. The distal portion ofelongate tube1432 comprises a curved, bent or angled region curved at an angle ranging from 70 degrees to 135 degrees. In this embodiment, distal portion ofelongate tube1432 is bent by an angle of around 90 degrees. Anoptional dilating balloon1433 may be located on the distal region ofguide device1430. Dilating balloon may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, etc. The distal portion ofelongate tube1432 comprises anatraumatic tip1434.Guide device1430 further comprises ahypotube1436.Guide device1430 further comprises an endoscope introducing mechanism for introducing an endoscope EN. In the embodiment shown inFIG. 14D, the endoscope introducing mechanism comprises aside lumen1437 through which a suitable flexible endoscope EN can be introduced in the anatomy. The proximal end ofguide device1430 comprises ahub1438. In one embodiment,hub1438 is a female luer hub.Hub1438 may havewings1439 to enable a user to turnguide device1430. FIG.14D′ shows an enlarged view of the distal portion of the guide device inFIG. 14D. FIG.14D′ showselongated tube1432 enclosed byhypotube1436. Distal end ofelongated tube1432 comprisesatraumatic tip1434. In one particular embodiment, W is 0.39+/−0.080 inches, L1 is 0.25+/−0.08 inches, L2 is 0 to 2 inches and the radius of curvature of the distal curved region ofelongate tube1432 is 0.180 inches. W may be as small as 5 mm with a corresponding reduction in the radius of curvature of the distal curved region ofelongate tube1432. The guide device design shown in FIGS.14D and14D′ is especially suited for trans-nasal access of the maxillary sinuses.
• FIG. 14E shows a side view of a third embodiment of a guide device comprising a bent, angled or curved distal portion. The design ofguide device1440 is similar to the design ofguide device1410.Guide device1440 comprises anelongate tube1442. The distal portion ofelongate tube1442 comprises a curved, bent or angled region curved at an angle ranging from 140 degrees to 120 degrees. In this embodiment, distal portion ofelongate tube1442 is bent by an angle of around 110 degrees. Anoptional dilating balloon1443 may be located on the distal region ofguide device1440. Dilating balloon may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, etc. The distal portion ofelongate tube1442 comprises anatraumatic tip1444.Guide device1440 further comprises ahypotube1446.Guide device1440 further comprises an endoscope introducing mechanism for introducing an endoscope EN. In the embodiment shown inFIG. 14E, the endoscope introducing mechanism comprises a side lumen1447 through which a suitable flexible endoscope EN can be introduced in the anatomy. The proximal end ofguide device1440 comprises ahub1448. In one embodiment,hub1448 is a female luer hub.Hub1448 may havewings1449 to enable a user to turnguide device1440. FIG.14E′ shows an enlarged view of the distal portion of the guide device inFIG. 14E. FIG.14E′ showselongated tube1442 enclosed byhypotube1446. Distal end ofelongated tube1442 comprisesatraumatic tip1444. In one particular embodiment, W is 0.46+/−0.08 inches, L1 is 0.25+/−0.08 inches, L2 is 0 to 0.5 inches and the radius of curvature of the distal curved region ofelongate tube1442 is 0.180 inches. L1 and W may be smaller than 0.25+/−0.08 inches and 0.46+/−0.08 inches respectively. The guide device design shown in FIGS.14E and14E′ is especially suited for trans-nasal access of the maxillary sinuses.
• FIG. 15A shows a cross sectional view of a first embodiment of a balloon catheter comprising a short guidewire lumen.Balloon catheter1500 comprises a hollow,elongate shaft1502.Elongate shaft1502 can be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Nylon, Pebax, PEEK, polyethylene, etc. The proximal end ofelongate shaft1502 is connected to asuitable inflation port1504 such as a female luer lock. In one embodiment,balloon catheter1500 further comprises anelongate hypotube1506 located betweenelongate shaft1502 andinflation port1504. The distal end ofelongate shaft1504 is attached to the proximal end of aballoon1508 such thatinflation port1504 is in fluid communication withballoon1508.Balloon1508 can be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, polyethylene, polyurethane, Pebax, etc.Balloon1508 also encloses aguidewire shaft1510 enclosing aguidewire lumen1512. The length ofguidewire shaft1510 is less then the length ofelongate shaft1502. In one embodiment, the length ofguidewire shaft1510 ranges from 5-12 cm. The proximal region ofguidewire shaft1512 is connected sideways to elongateshaft1502 such thatguidewire shaft1512 is substantially parallel to elongateshaft1502. The proximal end ofguidewire shaft1512 is located in a region proximal toballoon1508. The distal end ofguidewire lumen1512 is located in a region distal toballoon1508.Guidewire shaft1512 enablesballoon catheter1500 to be introduced over a suitable guidewire into an anatomical region. In one embodiment, the length ofballoon catheter1500 from the distal end ofinflation port1504 till the distal end ofguidewire shaft1510 is around 30 cm. In one embodiment,guidewire shaft1512 comprises a navigational marker such as aradiopaque marker band1514. Similar navigational markers may be present on other embodiments of balloon catheters disclosed herein and in the patent applications incorporated herein by reference. In one embodiment, two navigational markers are present on the balloon catheter shaft corresponding to the proximal and distal end respectively of the working length of the balloon. In another embodiment, a navigational marker is present on the balloon shaft corresponding to the proximal end of the balloon. Such a navigational marker is especially useful to determine the position of the proximal end of the balloon relative to the distal end of an introducing catheter when the balloon catheter is introduced through the introducing catheter. The user tracks the position of the navigational marker relative to the distal end of the introducing catheter to ensure that the balloon is not inflated within the introducing catheter. Examples of such a navigational marker include, but are not limited to a radiopaque marker band for fluoroscopic visualization, a colored ring for endoscopic visualization, etc.
• FIGS. 16-16C show aballoon catheter1600 constructed of afirst shaft1602 having afirst lumen1604, asecond shaft1612 and third shafts such that a short lumen (e.g., a rapid exchange guidewire lumen) extends through the balloon.Balloon catheter1600 comprises a hollow, firstelongate shaft1602. Firstelongate shaft1602 can be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Nylon, Pebax, PEEK, polyethylene, etc. Firstelongate shaft1602 comprises afirst lumen1604. The proximal end ofelongate shaft1602 is connected to a suitable hub such as afemale luer lock1606 which is in fluid communication withfirst lumen1604. Ahypotube1608 may be provided betweenfemale luer lock1606 and firstelongate shaft1602. The distal end offirst lumen1604 is in fluid communication with aballoon1610 located on the distal region of firstelongate shaft1602. Thus,first lumen1604 can be used to inflateballoon1610.Balloon1610 can be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, polyethylene, polyurethane, Pebax, etc. The distal region of firstelongate shaft1602 is enclosed by a secondelongate shaft1612. Secondelongate shaft1612 further encloses a region of a thirdelongate shaft1614 comprising a lumen. The proximal end of the lumen of thirdelongate shaft1614 is located proximal toballoon1610. The distal end of the lumen of thirdelongate shaft1614 is located distal toballoon1610. In one embodiment, the length of thirdelongate shaft1614 may range from 5-12 cm. Thirdelongate shaft1614 enablesballoon catheter1600 to be introduced over a suitable guidewire GW into an anatomical region. Thirdelongate shaft1614 may further comprise a navigational marker such as aradiopaque marker band1616 made of suitable radiopaque materials such as platinum-iridium alloys, etc. In one embodiment, the length ofballoon catheter1600 from the proximal end offemale luer lock1606 till the distal end of thirdelongate shaft1614 is around 30 cm.
• FIG. 16A is a cross sectional view throughline16A-16A ofFIG. 16.FIG. 16A shows a cross sectional view ofelongate shaft1602 comprisingfirst lumen1604.FIG. 16B is a cross sectional view throughline16B-16B ofFIG. 16.FIG. 16B shows secondelongate shaft1612 enclosing firstelongate shaft1602 and thirdelongate shaft1614.FIG. 16C is a cross sectional view throughline16C-16C ofFIG. 16.FIG. 16C shows secondelongate shaft1612 enclosing thirdelongate shaft1614.
• FIG. 17 shows aballoon catheter1700 that comprises anelongate shaft1702 having amandrel1712 positioned therein. Theelongate shaft1702 may be made of suitable biocompatible materials including, but not limited to polyethylene, Pebax, Nylon, etc.Elongate shaft1702 encloses a lumen. The proximal end ofelongate shaft1702 comprises asuitable hub1704. In one embodiment,hub1704 is a female luer lock. Astrain relief tubing1706 may be present betweenhub1704 andelongate shaft1702. The distal region ofelongate shaft1702 comprises aballoon1708.Balloon1708 may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, polyethylene, polyurethane, Pebax, etc. The region ofelongate shaft1702 enclosed byballoon1708 comprises anopening1710 that provides fluid communication between the lumen ofelongate shaft1702 andballoon1708. The lumen ofelongate shaft1702 can thus be used to inflateballoon1708.Elongate shaft1702 may further comprise a navigational marker such as aradiopaque marker band1711 located on the distal region ofelongate shaft1702. Amandrel1712 is located in lumen1703 such that a distal region ofmandrel1712 emerges out of the distal end ofelongate shaft1702. The distal end ofelongate shaft1702 is connected tomandrel1712 by a fluid-tight seal.FIG. 17A shows a cross sectional view ofballoon catheter1700 ofFIG. 17 throughplane17A-17A.FIG. 17A showselongate shaft1702 enclosing a lumen andmandrel1712 located in the lumen.
• FIG. 17B shows an enlarged perspective view of the mandrel inFIG. 8F.Mandrel1712 comprises aproximal region1714, atapering region1716, adistal region1718 and adistal tip1720.Proximal region1714 may have an outer diameter ranging from 0.005 inches to 0.12 inches.Distal tip1720 emerges out of the distal end ofelongate shaft1702 and can be used to navigateballoon catheter1700 through the anatomy or to insertballoon catheter1700 through an anatomical opening or passageway.Distal tip1720 further comprises acoil1722 coiled around a region of or around the entire length ofdistal tip1720.Coil1722 can be made of suitable materials including, but not limited to platinum, stainless steel, nickel-titanium alloys such as Nitinol, etc. In a particular embodiment, the distance from the proximal end of taperingregion1716 to the distal end ofdistal region1718 ranges from 2 to 6 cm and the length of distal tip ranges from 1 to 3 cm.Mandrel1712 may be made of suitable biocompatible materials including, but not limited to stainless steel, Nickel-titanium alloy (e.g., Nitinol), etc.
• FIG. 18 shows aballoon catheter1800 comprising ashaft1802 having alumen1804 with aside slit1809 and a balloon1810 or other expandable dilator.Elongate shaft1802 can be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Nylon, Pebax, PEEK, polyethylene, etc. In the particular example shown, theelongate shaft1802 comprises afirst lumen1804 useable as a guidewire lumen and and asecond lumen1806 useable to inflate the balloon1810. The proximal end offirst lumen1804 may be occluded proximal to aslit1809. The proximal region ofelongate shaft1802 may be connected to ahub1808 which is in fluid communication withsecond lumen1806. In this example,hub1808 is a female luer lock. Theslit1809 extends along one side of theshaft1802 proximal to the balloon1810 and allows a guidewire to be pulled laterally out of thefirst lumen1804 and through theslit1809. This enablesballoon catheter1800 to be advanced or withdrawn over a suitable elongate devices such as a guidewire such that the a portion of the suitable elongate device entersballoon catheter1800 from the distal end offirst lumen1804 and exits out ofballoon catheter1800 through slit1807. A balloon1810 is located on the distal region ofelongate shaft1802. Balloon1810 may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, polyethylene, polyurethane, Pebax, etc. A navigational marker1812 such as a radiopaque marker band may be located on the region ofelongate shaft1802 enclosed by balloon1810. The distal end offirst lumen1804 terminates in a region distal to balloon1810. The distal end ofsecond lumen1806 is in fluid communication with balloon1810 such thatsecond lumen1806 can be used to inflate or deflate balloon1810.FIG. 18A shows a cross sectional view of the balloon catheter inFIG. 18 through theplane18A-18A.FIG. 18A shows a cross section ofelongate sheath1802 showingfirst lumen1804,second lumen1806 and slit1807.FIG. 18B shows a cross sectional view of the balloon catheter inFIG. 18 through theplane18B-18B.FIG. 18B shows a cross section ofelongate sheath1802 showingfirst lumen1804.
• FIGS. 19-19C show acatheter device1900 comprising anelongate catheter shaft1902, aballoon1906 or other expandable dilator mounted onelongate shaft1902 and apparatus such ascapacitance plates1908,1910 located on opposite sides of the balloon or other dilator for determining its diameter. In the example shown, theelongate shaft1902 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Nylon, Pebax, PEEK, polyethylene, etc.Elongate shaft1902 may comprise aguidewire lumen1904 to enableballoon catheter1900 to be advanced or withdrawn over a suitable guidewire. The distal region ofballoon catheter1900 comprises aballoon1906 made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, polyurethane, etc.Balloon1906 may be inflated or deflated by introducing or withdrawing fluid through a balloon inflation lumen present inelongate shaft1902.Balloon1906 further comprises afirst capacitance plate1908 and asecond capacitance plate1910.First capacitance plate1908 andsecond capacitance plate1910 may be made of suitable biocompatible metals sheets.First capacitance plate1908 andsecond capacitance plate1910 are electrically insulated fromballoon1906 and the fluid used to inflateballoon1906.First capacitance plate1908 is connected by a firstinsulated wire1912 to a source of electrical supply.Second capacitance plate1910 is connected by a secondinsulated wire1914 to the source of electrical supply such that an electric field is generated betweenfirst capacitance plate1908 andsecond capacitance plate1910. This causesballoon1906 to behave like a capacitor with a capacitance depending on various properties such as distance betweenfirst capacitance plate1908 andsecond capacitance plate1910, type of inflation fluid, size offirst capacitance plate1908 andsecond capacitance plate1910, etc. Asballoon1906 is inflated or deflated, the distance betweenfirst capacitance plate1908 andsecond capacitance plate1910 changes. This in turn changes the capacitance. The change in capacitance can be measured through firstinsulated wire1912 and secondinsulated wire1914 to non-invasively measure the degree of inflation ofballoon1906. Using this method, the degree of inflation ofballoon1906 may be measured without the use of ionizing radiation. Firstinsulated wire1912 and secondinsulated wire1914 may be further insulated from the surroundings by a layer of insulatingcovering1916. Insulating covering1916 covers first insulatedwire1912, secondinsulated wire1914 andelongate shaft1902.FIG. 19A shows a side view of the balloon catheter inFIG. 19.FIG. 19A showsballoon catheter1900 comprisingelongate shaft1902,balloon1906,first capacitance plate1908 and firstinsulated wire1912 connected tofirst capacitance plate1908.FIGS. 19B and 19C show cross sectional views of the balloon catheter inFIG. 19 throughplanes19B-19B and19C-19C respectively.FIG. 19B shows a cross section ofshaft1902 comprisingguidewire lumen1904 and aballoon inflation lumen1918. In this embodiment,balloon inflation lumen1918 is annular and is coaxial toguidewire lumen1904.Shaft1902 further comprises first insulatedwire1912 and secondinsulated wire1914 covered by insulatingcovering1916.FIG. 19C shows a cross section throughballoon1906showing shaft1902enclosing guidewire lumen1904. Also shows arefirst capacitance plate1908 andsecond capacitance plate1910 located onballoon1906.
• FIGS. 20-20C show aballoon catheter2000 comprising anelongate catheter shaft2002, aballoon2006 or other expandable dilator mounted on thecatheter shaft2002 and apparatus for determining the diameter of theballoon2006, such ascapacitance plates2008,2010, one of which is located on the wall of theballoon2006 and the other of which is located on a portion of thecatheter shaft2016 that extends through theballoon2006. Theelongate shaft2002 can be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Nylon, Pebax, PEEK, polyethylene, etc.Elongate shaft2002 may comprise aguidewire lumen2004 to enableballoon catheter2000 to be advanced or withdrawn over a suitable guidewire.Balloon2006 made of suitable biocompatible materials including, but not limited to PET, Nylon, PVC, polyethylene, polyurethane, Pebax, etc.Balloon2006 may be inflated or deflated by introducing or withdrawing fluid through a balloon inflation lumen present inelongate shaft2002.First capacitance plate2008 andsecond capacitance plate2010 are electrically insulated fromballoon2006 and the fluid used to inflateballoon2006.First capacitance plate2008 is connected by a firstinsulated wire2012 to a source of electrical supply.Second capacitance plate2010 connected by a secondinsulated wire2014 to the source of electrical supply such that an electric field is generated betweenfirst capacitance plate2008 andsecond capacitance plate2010. This causesballoon2006 to behave like a capacitor with a capacitance depending on various properties such as distance betweenfirst capacitance plate2008 andsecond capacitance plate2010, type of inflation fluid, size offirst capacitance plate2008 andsecond capacitance plate2010, etc. Asballoon2006 is inflated or deflated, the distance betweenfirst capacitance plate2008 andsecond capacitance plate2010 changes. This in turn changes the capacitance. The change in capacitance can be measured through firstinsulated wire2012 and secondinsulated wire2014 to non-invasively measure the degree of inflation ofballoon2006. Using this method, the degree of inflation ofballoon2006 may be measured without the use of ionizing radiation. Firstinsulated wire2012 and secondinsulated wire2014 may be further insulated from the surroundings by a layer of insulatingcovering2016. Insulating covering2016 covers first insulatedwire2012, secondinsulated wire2014 andelongate shaft2002.FIG. 20A shows a side view of the balloon catheter inFIG. 20.FIG. 20A showsballoon catheter2000 comprisingelongate shaft2002,balloon2006,first capacitance plate2008 and firstinsulated wire2012 connected tofirst capacitance plate2008.FIGS. 20B and 20C show cross sectional views of the balloon catheter inFIG. 20A throughplanes20B-20B and20C-20C respectively.FIG. 20B shows a cross section ofshaft2002 comprisingguidewire lumen2004 and aballoon inflation lumen2018. In this embodiment,balloon inflation lumen2018 is annular and is coaxial toguidewire lumen2004.Shaft2002 further comprises first insulatedwire2012 and secondinsulated wire2014 covered by insulatingcovering2016.FIG. 20C shows a cross section throughballoon2006showing shaft2002enclosing guidewire lumen2004. Also shows arefirst capacitance plate2008 andsecond capacitance plate2010 located onballoon2006.
• In an alternate embodiment, a balloon catheter comprises a first capacitance plate located on or within the balloon material; a second capacitance plate located on or within the balloon material and one or more shaft plates located on or within the balloon shaft. A user measures a first capacitance between the first capacitance plate and the one or more shaft plates. Also, the user measures a second capacitance between the second capacitance plate and the one or more shaft plates. The first capacitance and the second capacitance may be used to measure the degree of balloon inflation and also to measure the evenness of balloon inflation.
• Any of the balloon catheters comprising capacitance measuring means disclosed herein may comprise a temperature sensor to measure the temperature of the inflation fluid. This is useful in cases where the dielectric constant of the inflation fluid varies significantly with temperature.
• FIG. 21 shows aballoon catheter2100 having aproximal shaft2104, a malleabledistal shaft2102, an expandable dilator such as aballoon2106 and, optionally, a distal guide projection such as awire2108. This balloon catheter device is useable for a variety of applications including, but not limited to the diagnosis and treatment of certain Ethmoid sinus pathologies. The malleabledistal region2102 may be made of suitable biocompatible materials including, but not limited to stainless steel, Nickel-titanium alloy (e.g., Nitinol), polymer/metal composites, etc. Malleabledistal region2102 may be deformed or shaped by a user during a procedure to allow for easier access and navigation through a target anatomy. The proximal region of the catheter shaft may comprise a substantially non-malleableproximal region2104. Malleabledistal region2102 comprises aballoon2106.Balloon2106 may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PE etc. The length ofballoon2106 ranges from 3 to 40 mm and the inflated diameter ofballoon2106 ranges from 3 to 10 mm. In one embodiment adapted to treat Ethmoid sinuses, the length ofballoon2106 ranges from 3 to 10 mm and the inflated diameter ofballoon2106 ranges from 3 to 6 mm.Balloon catheter2100 further comprises a navigation mechanism. In one embodiment, the navigation mechanism comprises a length ofwire2108 fixed to the distal end ofballoon catheter2100. The length ofwire2108 may range from 1 to 3 cm. In an alternate embodiment, the navigation mechanism is a rapid exchange lumen through the catheter shaft. In one embodiment, the length of rapid exchange lumen is more then half the total catheter length. For example, in a balloon catheter of total length around 20 cm, the length of the rapid exchange lumen may be about 10 cm. In a balloon catheter of total length around 15 cm, the length of the rapid exchange lumen may be about 13.5 to 10 cm. In an alternate embodiment, the navigation mechanism is an end-to-end lumen through the catheter shaft to allowballoon catheter2100 to be introduced over a guidewire.
• FIG. 22 showsballoon catheter2200 having aproximal shaft2202, a flexibledistal shaft2204, an expandable dilator such as aballoon2206 and, optionally, a distal guide projection such as awire2208. Thisballoon catheter device2200 is useable to perform a variety of diagnostic or therapeutic procedures, some of which are disclosed herein. Such a balloon catheter design comprising a flexible distal shaft is especially suitable for diagnosing or treating pathologies including, but not limited to Ethmoid sinus pathologies. Theproximal region2202 of this catheter is substantially stiff and thedistal region2204 is more flexible than theproximal region2202. Flexibledistal region2204 may be made of suitable biocompatible materials including, but not limited to Nylon, Pebax, HDPE, LDPE, Polyimide, polymer/metal composites, braided materials, etc. Flexibledistal region2204 is deformed during a procedure to allow for easier access and navigation through a target anatomy. Flexibledistal region2204 comprises aballoon2206.Balloon2206 may be made of suitable biocompatible materials including, but not limited to PET, Nylon, PE etc. The length ofballoon2206 ranges from 3 to 40 mm and the inflated diameter ofballoon2206 ranges from 3 to 10 mm. In one embodiment adapted to treat Ethmoid sinuses, the length ofballoon2206 ranges from 3 to 10 mm and the inflated diameter ofballoon2206 ranges from 3 to 6 mm.Balloon catheter2200 further comprises a navigation mechanism. In one embodiment, the navigation mechanism comprises a length ofwire2208 fixed to the distal end ofballoon catheter2200. The length ofwire2208 may range from 1 to 3 cm. In an alternate embodiment, the navigation mechanism is a rapid exchange lumen through the catheter shaft. The length of the rapid exchange lumen may range from 1 cm to 15 cm. In one embodiment, the length of rapid exchange lumen is more then half the total catheter length. For example, in a balloon catheter of total length around 20 cm, the length of the rapid exchange lumen may be about 10 cm. In a balloon catheter of total length around 15 cm, the length of the rapid exchange lumen may be about 13.5 to 10 cm. In an alternate embodiment, the navigation mechanism is an end-to-end lumen through the catheter shaft to allowballoon catheter2200 to be introduced over a guidewire.
• The balloon catheters disclosed herein and in the patent applications incorporated herein by reference may comprise a balloon of a working length adapted for dilating a particular region of the anatomy. For example, a balloon catheter comprising a balloon of working length ranging from 10-40 mm may be used for treating a disease of the frontal sinuses. Ideally, the balloon comprises a working length ranging from 20-30 mm. The inflated diameter of such balloons may range from 4-10 mm. In another example, a balloon catheter comprising a balloon of working length ranging from 6-10 mm may be used for treating a disease of the maxillary sinuses. In another example, a balloon catheter comprising a balloon of working length ranging from 3-10 mm may be used for dilating the Ethmoid sinuses.
• The shafts of the balloon catheters disclosed herein and in the patent applications incorporated herein by reference may comprise one or more angled regions. Such balloon catheters may for example comprise an angled balloon located on an angled region of the shaft. Such balloon catheters are especially suited for treating diseases of the maxillary sinuses.
• The balloon catheters disclosed herein and in the patent applications incorporated herein by reference may comprise a substantially compliant balloon. Such a substantially compliant balloon may be inflated at an inflation pressure preferably less than 4 atmospheres. Such balloon catheter may be used for example to dilate the mucosa of anatomical regions such as passageways leading to paranasal sinuses. The step of dilation of the mucosa may or may not include dilation of the underlying bony structures. Such balloon catheters may also be used for sizing anatomical regions such as passageways leading to paranasal sinuses. This is performed by inflating the substantially compliant balloon by a fluid comprising radiopaque contrast and observing the radiographic image of the balloon. The step of sizing an anatomical region may be performed before and/or after the step of dilating the anatomical region.
• The balloon catheters disclosed herein and in the patent applications incorporated herein by reference may be introduced in the anatomy by a variety of manual introducing tools. Examples of such manual introducing tools include, but are not limited to forceps (e.g. giraffe forceps), pincers, tweezers, tongs, etc. Such manual introducing tools may have curved, bent, angled or substantially straight distal regions. For example, a balloon catheter may be grasped in a region proximal to the balloon by a forceps and then introduced in the target anatomy.
• The balloon catheters disclosed herein and in the patent applications incorporated herein by reference may be used to deliver heat or cold, a gas, electromagnetic energy in the visible spectrum, etc.
• If a balloon catheter is used for performing multiple procedures, it may be useful to refold the balloon of the balloon catheter after each procedure to lower the profile of the balloon before the next procedure.
• FIGS. 23-23D show aballoon folding tool2300 useable to facilitate folding of aballoon2308 mounted on aballoon catheter2306. Theballoon folding tool2300 comprises a rigid body having a central bore orfolding channel2302 formed therein,such folding channel2306 having a diameter that is less than the fully inflated balloon diameter. A plurality of side channels orparallel channels2304 are located adjacent to and substantially parallel with the central bore orfolding channel2302 and are connected to the central bore orfolding channel2302 through slots or elongate openings. Theballoon2308 is insertable into the central bore orfolding channel2302 while in a less than fully inflated state and, thereafter, may be fully or partially inflated to cause separate portions of theballoon2308 to pass through the each slot and into eachside channel2304 as seen inFIG. 23C. Thereafter, the balloon may be deflated such that each separate portion of the balloon that has passed into each side channel will form a separate wing of the deflatedballoon2308, as seen inFIG. 23D. The wings are thereafter foldable (e.g., to a creased, wrapped or furled state) to provide a collapsed balloon shape. The number of side orparallel channels2304 and the resultant number of wings formed in the deflatedballoon2308 may vary depending of the size of theballoon2308 and the manner in which it is intended to fold or furl the balloon. In some embodiments, about 2-6side channels2304 will be used, providing about 2-6 wings on the deflatedballoon2308.
• The elongate body of thefolding tool2300 may be made of suitable biocompatible materials including, but not limited to metals e.g. titanium, stainless steel, etc.; polymers e.g. PVC, Nylon, DELRIN®, Polycarbonate, ABS, etc.Folding tool2300 further comprises aballoon folding channel2302. In one embodiment, the cross section ofballoon folding channel2302 is substantially uniform along the length offolding tool2300. In another embodiment, the cross sectional size ofballoon folding channel2302 is larger at the proximal end offolding tool2300. In this embodiment, the cross sectional size ofballoon folding channel2302 gradually reduces towards the distal end offolding tool2300 to facilitate loading a balloon catheter inballoon folding channel2302. In one embodiment,balloon folding channel2302 extends through the entire length of the elongate body. In another embodiment,balloon folding channel2302 extends through a part of the length of the elongate body.Folding tool2300 further comprises one or moreparallel channels2304.Parallel channels2304 are aligned substantially parallel toballoon folding channel2302 and overlap lengthwise toballoon folding channel2302 as shown inFIG. 23.FIG. 23A shows a perspective view of aballoon catheter2306 comprising aballoon2308 being introduced intofolding tool2300.
• FIGS. 23B and 23C show an end view of the folding tool ofFIG. 23 showing the steps of an embodiment of a method of folding the balloon of a balloon catheter.FIG. 23D shows a cross sectional view through a foldedballoon2308. InFIG. 23B,balloon catheter2306 is introduced intoballoon folding channel2302. Thereafter, inFIG. 23C,balloon2308 is partially inflated such that regions ofballoon2308 extend inparallel channels2304. Thereafter,balloon2308 is deflated and a vacuum is created inballoon2308. This creates one or more ridges inballoon2308. Thereafter,folding tool2308 is turned to obtain one or more folds inballoon2308. Thereafter,balloon2308 is pulled out offolding tool2300 to obtain a folded balloon as shown inFIG. 23D. Such a folded balloon may thereafter be introduced in a small diameter tube to further reduce the profile of the balloon.
• In an alternate method offolding balloon2308,balloon catheter2306 is introduced intoballoon folding channel2302. Thereafter,balloon2308 is partially inflated such that regions ofballoon2308 extend inparallel channels2304. Thereafter,balloon2308 is deflated and a vacuum is created inballoon2308. This causes one or more ridges to be created inballoon2308. Thereafter,balloon2308 is pulled out offolding tool2300.Balloon2308 is then folded manually to obtain a folded balloon with a low profile.
• Similarly, other folding tools comprising one or more folding channels, folding grooves, folding cavities, folding slits, etc. may be used for folding one or more balloons of the balloon catheters disclosed herein.
• FIG. 24 shows aballoon compressing apparatus2400 that is useable to facilitate folding of aballoon2308 mounted on a catheter. Thisballoon compressing apparatus2400 generally comprises aclamping element2404 having a plurality ofcompression members2416 disposed radially about acentral cavity2417. Thecompression members2416 are spaced apart from each other such that gaps exist betweenadjacent compression members2416. Thecompression members2416 are moveable from non-compressing positions where the central cavity had a first diameter to compressing positions where the central cavity has a second diameter that is smaller than the first diameter. Theballoon2308 is insertable into thecentral cavity2417 while the compression members are in their non-compressing positions and, thereafter, the compression members are moveable to their compressing positions, thereby compressing portions of theballoon2308 and causing any inflation fluid to be forced out of the balloon and causing portions of the balloon to protrude outwardly into the gaps between the compression members. Such protrusion into the gaps betweencompression members2416 forms a plurality of wings on the deflatedballoon2308. The wings are thereafter foldable (e.g., to a creased, wrapped or furled state) to provide a collapsed balloon shape. The number of gaps and the resultant number of wings formed in the deflatedballoon2306 may vary depending of the size of theballoon2308 and the manner in which it is intended to fold or furl the balloon. In some embodiments, about 2-6 side gaps will be used, providing about 2-6 wings on the deflatedballoon2308.
• In the particular example shown in the figures,folding tool2400 comprises ascrew cap2402 that encloses aclamping element2404. The distal end of clampingelement2404 and the distal end ofscrew cap2402 are in contact with adistal handle2406. Clampingelement2404,screw cap2402 anddistal handle2406 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, etc.; polymers e.g. PVC, Polycarbonate, Delrin®, Nylon, ABS, etc.FIG. 24A shows an exploded view of the various components of the balloon folding tool ofFIG. 24.Distal handle2406 comprises an elongate body comprisingscrew threads2408 located on the proximal end of the elongate body.Distal handle2406 may comprise alumen2410. The outer surface ofdistal handle2406 may be roughened to increase the grip of a user ondistal handle2406. In one embodiment, outer surface ofdistal handle2406 is roughened by knurling.Screw cap2402 comprises alumen2412. The inner surface ofscrew cap2402 comprises screw threads that screw overscrew threads2408 ofdistal handle2406. The outer surface ofscrew cap2402 may be roughened to increase the grip of a user onscrew cap2402. In one embodiment, outer surface ofscrew cap2402 is roughened by knurling. Clampingelement2404 is enclosed byscrew cap2402 anddistal handle2406. Clampingelement2404 comprises adistal body2414. The proximal end of distal body is connected to two ormore clamping arms2416. One or more gaps are located between two ormore clamping arms2416. Clampingarms2416 enclose acentral cavity2417 that is substantially collinear withlumen2412 ofscrew cap2402. The proximal ends of clampingarms2416 comprise a taperedregion2418. Tighteningscrew cap2402 overdistal handle2406 causes a region ofscrew cap2402 to slide over taperedregion2418. This in turn displaces the proximal regions of clampingarms2416 in a radially inward direction. Thus, clampingarms2416 can clamp on a device located in the hollow region that is enclosed by clampingarms2416. Similarly, looseningscrew cap2402 overdistal handle2406causes clamping arms2416 to release a device located in the hollow region that is enclosed by clampingarms2416. In one embodiment of a method of folding a balloon of a balloon catheter, an uninflated balloon is inserted in the hollow region that is enclosed by clampingarms2416. Thereafter, the balloon is partially inflated such that portions of the balloon enter one or more gaps located between two ormore clamping arms2416. Thereafter,screw cap2402 is tightened overdistal handle2406. Thereafter, the balloon is deflated. Simultaneously,folding tool2400 is rotated to create one or more folds in the balloon.
• Folding tool2300 andfolding tool2400 may comprise a centering element to align the shaft of a balloon catheter with the central axis of the folding tools. In one embodiment, the centering element comprises a centering wire attached to the folding tool. The shaft of the balloon catheter slides over the centering wire. This aligns the shaft of the balloon catheter with the central axis of the folding tool.
• FIG. 25 shows acatheter2500 that is useable for simultaneous irrigation and aspiration. Thiscatheter2500 comprises aninner tube2502 enclosing aninner lumen2504.Inner tube2502 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Nylon, Pebax, PEEK, polyethylene, etc. The proximal end ofinner tube2502 comprises a suitable hub such as afemale luer lock2505.Inner tube2502 is surrounded by anouter tube2506.Outer tube2506 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, Nickel-titanium alloy (e.g., Nitinol), etc.; polymers e.g. Nylon, Pebax, PEEK, polyethylene, etc. In one embodiment,inner tube2502 has an inner diameter of 0.040 inches and an outer diameter of 0.050 inches andouter tube2506 has an inner diameter of 0.080 inches and an outer diameter of 0.092 inches. The distal end ofouter tube2506 is attached toinner tube2502 to create a fluid-tightdistal seal2508. The region betweenouter tube2506 andinner tube2502 encloses anouter lumen2510. The distal region ofouter tube2506 comprises one or more openings orperforations2512 that are in fluid communication withouter lumen2510. The proximal end ofouter tube2506 is enclosed by a Y-connector2514 as shown inFIG. 25. A side arm of Y-connector2514 is in fluid communication withouter lumen2510. The proximal end of the side arm comprises ahub2516 such as a luer lock. Y-connector2514 is attached tofemale luer lock2505 to create a fluid-tightproximal seal2518. In one embodiment,catheter2500 further comprises a hypotube surroundingouter tube2506.Catheter2500 may be used to simultaneously introduce fluids into and suction fluids out of a target anatomy such as a paranasal sinus, openings or passageways leading to a paranasal sinus, etc. In one method embodiment,outer lumen2510 is used to introduce one or more fluids into the target anatomy.Inner lumen2504 is used to suction out one or more fluids from the target anatomy. In another embodiment,inner lumen2504 is used to introduce one or more fluids into the target anatomy.Outer lumen2510 is used to suction out one or more fluids from the target anatomy. In this embodiment, one or more openings orperforations2512 may be made larger to prevent blockage by materials being suctioned intoouter lumen2510.
• Image guided surgery (IGS) procedures (sometimes referred to as “computer assisted surgery”) were first developed for use in neurosurgery and have now been adapted for use in certain ENT surgeries, including sinus surgeries. See, Kingdom T. T., Orlandi R. R.,Image-Guided Surgery of the Sinuses: Current Technology and Applications, Otolaryngol. Clin. North Am. 37(2):381-400 (April 2004). Generally speaking, in a typical IGS procedure, a digital tomographic scan (e.g., a CT or MRI scan) of the operative field (e.g., the nasal cavities and paranasal sinuses) is obtained prior to surgery. A specially programmed computer is then used to convert the digital tomographic scan data into a digital map. During surgery, sensors mounted on the surgical instruments send data to the computer indicating the position of each surgical instrument. The computer correlates the data received from the instrument-mounted sensors with the digital map that was created from the preoperative tomographic scan. One or more image(s) is/are then displayed on a monitor showing the tomographic scan along with an indicator (e.g., cross hairs or an illuminated dot) of the real time position of each surgical instrument. In this manner, the surgeon is able to view the precise position of each sensor-equipped instrument relative to the surrounding anatomical structures shown on the tomographic scan. Various embodiments of adapter devices comprising image guidance sensors are disclosed herein. Such adapter devices are adapted to be fitted to one or more devices that are being introduced in the anatomy. This enables a user to view the real time position of the one or more devices that are being introduced in the anatomy. For example,FIGS. 26-26B show a navigation adapter adapter that may be attached to the proximal end of a catheter, seeker, cannula, or any other device to facilitate mounting of navigation unit (e.g., a navigation module, localizer or other apparatus such as sensor(s), emitter(s), transmitter(s), reflector(s), etc. that are useable in conjunction with a navigation system. The particular navigation apparatus may be selected from the various navigation apparatus disclosed herein or in one of the patent applications incorporated herein by reference. In the example ofFIG. 26, thenavigation adapter2600 comprises anelongate body2602 comprising a lumen.Elongate body2602 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, etc.; polymers e.g. Nylon, Pebax, PEEK, polyethylene, etc. The outer surface ofelongate body2602 may be roughened. The distal end ofelongate body2602 comprises afirst hub2604. In one embodiment,first hub2604 is a male luer lock. The proximal end ofelongate body2602 comprises asecond hub2606. In one embodiment,second hub2606 is a female luer lock.Navigation adapter2600 further comprises a tracking system for image guided surgery.Navigation adapter2600 is adapted to be fixed to a device being introduced in the anatomy. The position of the device can then be tracked using the tracking system located onnavigation adapter2600. Thus, suitable rigid catheters or guide devices may be tracked using existing tracking systems. Similarly, suitable devices with malleable regions may also be tracked using existing tracking systems. The outer surface ofelongate body2602 may be roughened to increase the grip of a user onnavigation adapter2600. In one embodiment, outer surface ofelongate body2602 is roughened by knurling.
• FIG. 26A shows a perspective view of an embodiment of a navigation adapter comprising an optical navigation unit.Navigation adapter2610 comprises anelongate body2612 comprising a lumen.Elongate body2612 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, nickel-titanium alloys such as Nitinol, etc.; polymers e.g. Pebax, PEEK polyimide, etc.; composites, etc. The distal end ofelongate body2612 comprises afirst hub2614. In one embodiment,first hub2614 is a male luer lock. The proximal end ofelongate body2612 comprises asecond hub2616. In one embodiment,second hub2616 is a female luer lock.Navigation adapter2610 further comprises anavigation unit2618 for image guided surgery. In one embodiment,navigation unit2618 is an optical navigation unit. One example of such an optical navigation unit is a BrainLAB surgical instrument adapter.Navigation unit2618 comprises anattachment region2620. One end ofattachment region2620 is connected to a series ofarms2622 that extend radially outward from the axis ofattachment region2620. The outer ends ofarms2622 comprise one or moreoptical energy emitters2624 that emit optical energy. In one embodiment,optical energy emitters2624 comprise infrared light emitting LEDs. In another embodiment,optical energy emitters2624 comprise a reflecting surface that reflects externally generated optical energy reaching the surface ofoptical energy emitters2624. A camera is positioned such that it receives the optical energy emitted fromoptical energy emitters2624. The camera is then used to track the position and orientation ofnavigation adapter2610. Other examples ofnavigation unit2618 include, but are not limited to navigation units comprising reflective passive elements, light emitting diodes, transmitters or receivers of energy (e.g. optical energy, radiofrequency energy, etc.), a combination of tow or more of the abovementioned navigation technologies, etc.Navigation adapter2610 is adapted to be fixed to a diagnostic, therapeutic oraccess device2626 being introduced in the anatomy.Device2626 may comprise a curved, angled or bentdistal end2628. The position of the device can then be tracked using thenavigation unit2618 located onnavigation adapter2610. Thus, suitable rigid catheters or guide devices may be tracked using existing image guidance systems. One example of an optical image guidance system that is useable in ENT and sinus surgery is the LandmarX Evolution® ENT II Image Guidance System available from Medtronic Xomed Surgical Products, Inc., Jacksonville, Fla. The outer surface ofelongate body2612 may be roughened to increase the grip of a user onnavigation adapter2610. In one embodiment, outer surface ofelongate body2612 is roughened by knurling. In one method embodiment, a surgical navigation modality is attached to a rigid device disclosed herein, and the position and orientation of the distal tip of the rigid device is calibrated to the position and orientation of the imaging modality. Thereafter, the rigid device is used to perform a diagnostic, therapeutic or access procedure. If the position or orientation of the rigid device changes with respect to the position or orientation of the surgical navigation modality, the position and orientation of the distal tip of the rigid device may be re-calibrated to the position and orientation of the imaging modality. Such a re-calibration may be necessary for example when a user bends or shapes the distal tip of a rigid device comprising a malleable or shapeable distal tip.
• FIG. 26B shows a perspective view of an embodiment of a navigation adapter comprising an electromagnetic navigation unit. In image guidance systems that employ electromagnetic sensors/tracking systems, radiofrequency electromagnetic sensors (e.g., electromagnetic coils) are placed on the surgical instruments and on a localizer frame worn by the patient. A transmitter is positioned near the operative field. The transmitter transmits signals that are received by the instrument-mounted sensors. The tracking system detects variations in the electromagnetic field caused by the movement of the instrument-mounted sensors relative to the transmitter. Examples of commercially available electromagnetic IGS systems that have been used in ENT and sinus surgery include the ENTrak Plus™ and InstaTrak ENT™ systems available from GE Medical Systems, Salt Lake City, Utah. Other examples of electromagnetic image guidance systems that may be modified for use in accordance with the present invention include but are not limited to those available from Surgical Navigation Technologies, Inc., Louiville, Colo., Biosense-Webster, Inc., Diamond Bar, Calif. and Calypso Medical Technologies, Inc., Seattle, Wash.Navigation adapter2630 comprises anelongate body2632 comprising a lumen.Elongate body2632 may be made of suitable biocompatible materials including, but not limited to metals e.g. stainless steel, titanium, etc.; polymers e.g. Nylon, Pebax, PEEK, polyethylene, etc. The distal end ofelongate body2632 comprises afirst hub2634. In one embodiment,first hub2634 is a male luer lock. The proximal end ofelongate body2632 comprises asecond hub2636. In one embodiment,second hub2636 is a female luer lock.Navigation adapter2630 further comprises a radiofrequencyelectromagnetic sensor2638 for image guided surgery. Radiofrequencyelectromagnetic sensor2638 is attached to elongatebody2632 by anattachment region2640. In one embodiment, radiofrequencyelectromagnetic sensor2638 is attached to anelectrical cord2642 to transmit data from radiofrequencyelectromagnetic sensor2638 to an electromagnetic image guidance system.Navigation adapter2630 is adapted to be fixed to a diagnostic, therapeutic oraccess device2644 being introduced in the anatomy.Device2644 may comprise a shapeable or malleabledistal tip2646. The position of the device can then be tracked using radiofrequencyelectromagnetic sensor2638 located onnavigation adapter2630. Thus, suitable rigid catheters or guide devices may be tracked using existing image guidance systems. The outer surface ofelongate body2632 may be roughened to increase the grip of a user onnavigation adapter2630. In one embodiment, outer surface ofelongate body2632 is roughened by knurling.
• Similar navigation adapters can be designed whereinelectromagnetic sensor2638 is replaced by other surgical navigation units. Examples of such surgical navigation units include, but are not limited to navigation units comprising reflective passive elements, light emitting diodes, transmitters or receivers of energy (e.g. optical energy, radiofrequency energy, etc.), a combination of tow or more of the abovementioned navigation technologies, etc.
• One or more of the devices disclosed herein may comprise a magnetic navigation element located at the distal region of the devices. Such a magnetic navigation element may comprise a permanent magnet or an electromagnet. The distal region of the devices can then be navigated through the anatomy by providing a magnetic field of specified direction and magnitude, positioned externally to the patient.
• FIGS. 27A and 27B show top and side views respectively of a surgical hand tool comprising a balloon catheter.FIG. 27A shows asurgical hand tool2700 comprising a hollowproximal body2702 made of biocompatible materials including, but not limited to ABS, nylon, polyurethane, polyethylene, etc.Proximal body2702 encloses aballoon catheter2704.Balloon catheter2704 comprises aballoon inflation port2706 to inflate a balloon onballoon catheter2704.Balloon inflation port2706 emerges out ofproximal body2702 through alongitudinal slit2708 throughproximal body2702 such thatballoon catheter2704 can slide along the axis ofproximal body2702.Balloon inflation port2706 is connected to a suitable inflating device to inflate the balloon ofballoon catheter2704. In this embodiment,balloon catheter2704 is introduced into a desired region of the anatomy over aguidewire2710. The proximal region ofguidewire2710 may comprise atorquing device2712. A user can usetorquing device2712 to rotate, advance, retract, ortorque guidewire2710. The distal region ofproximal body2702 comprises a suitable hub that allows aguide catheter2714 to attach toproximal body2702. In an alternate embodiment,guide catheter2714 is permanently attached toproximal body2702. In this embodiment,guide catheter2714 comprises an elongatetubular element2716 made of suitable biocompatible materials including, but not limited to PEEK, Pebax, Nylon, Polyimide, ABS, PVC, polyethylene, etc. The proximal region oftubular element2716 may be covered by ahypotube2718 made of suitable biocompatible metals or polymers. The proximal end oftubular element2716 is attached to asuitable hub2720.Hub2720 allows the reversible attachment ofguide catheter2714 toproximal body2702. In one embodiment,hub2720 is a female luer lock that attached to a suitable hub onproximal body2702. Thus, various guide catheters can be attached to the distal region ofproximal body2702 to provide access to various anatomical regions. The distal end oftubular element2716 may comprise anatraumatic tip2722. The distal end oftubular element2716 may comprise a curved, bent or angled region.FIG. 27B shows the side view ofsurgical hand tool2700 showing ahandle2724 attached toproximal body2702.
• FIGS. 27C through 27D show various steps of a method of dilating an anatomical region using the surgical hand tool shown inFIGS. 27A and 27B. InFIG. 27C,surgical hand tool2700 is introduced in the anatomy.Surgical hand tool2700 is positioned such that the distal tip ofsurgical hand tool2700 is located near an anatomical region to be accessed. Thereafter, aguidewire2710 is introduced throughsurgical hand tool2700 such that the distal tip ofguidewire2710 is located near an anatomical region to be accessed. During this step,guidewire2710 may be navigated through the anatomy usingtorquing device2712. In one embodiment,guidewire2710 is positioned across a paranasal sinus ostium to be dilated. Thereafter, inFIG. 27D,balloon catheter2704 is advanced over guidewire2710 into the anatomy. This is done by pushingballoon inflation port2706 in the distal direction. Thereafter,balloon catheter2704 is used to perform a diagnostic or therapeutic procedure. In one embodiment,balloon catheter2704 is used to dilate an opening leading to a paranasal sinus such as a paranasal sinus ostium.
• FIG. 27E shows a side view of a first alternate embodiment of a surgical hand tool comprising a balloon catheter. The design ofsurgical hand tool2726 is similar to the design ofsurgical hand tool2700.Surgical hand tool2726 comprises a hollowelongate body2727 made of biocompatible materials including, but not limited to ABS, nylon, polyurethane, polyethylene, etc.Elongate body2727 is attached to ahandle2728 to allow a user to graspsurgical hand tool2726.Elongate body2727 comprises alongitudinal slit2729.Elongate body2727 encloses aballoon catheter2730.Balloon catheter2730 comprises aballoon inflation port2731 to inflate a balloon onballoon catheter2730.Balloon inflation port2731 emerges out ofelongate body2727 throughlongitudinal slit2729 such thatballoon catheter2730 can slide along the axis ofelongate body2727.Balloon catheter2730 is further connected to atrigger2732.Trigger2732 is pivoted onelongate body2727 such that pullingtrigger2732 in the proximal direction causesballoon catheter2730 to move in the distal direction. Similarly, pushingtrigger2732 in the distal direction causesballoon catheter2730 to move in the proximal direction Thusballoon catheter2730 can be moved by movingtrigger2732. The distal region ofelongate body2727 comprises a suitable hub that allows aguide catheter2733 to attach to elongatebody2727. In this embodiment,guide catheter2733 comprises an elongatetubular element2734 made of suitable biocompatible materials including, but not limited to PEEK, Pebax, Nylon, polyethylene, etc. The proximal region oftubular element2734 may be covered by ahypotube2735 made of suitable biocompatible metals or polymers. The proximal end oftubular element2734 is attached to asuitable hub2736.Hub2736 allows the reversible attachment ofguide catheter2733 to elongatebody2727. In one embodiment,hub2736 is a female luer lock that attached to a suitable hub onelongate body2727. Thus, various guide catheters can be attached to the distal region ofelongate body2727 to provide access to various anatomical regions. The distal end oftubular element2734 may comprise anatraumatic tip2737. The distal end oftubular element2734 may comprise a curved, bent or angled region. In this embodiment,balloon catheter2730 is introduced into a desired region of the anatomy over aguidewire2738. The proximal region ofguidewire2738 may comprise atorquing device2739. A user can usetorquing device2739 to rotate, advance, retract, ortorque guidewire2738.Surgical hand tool2726 can be used to introduceballoon catheter2730 into a desired anatomical region to perform a diagnostic or therapeutic procedure in the anatomical region.
• FIG. 27F shows a side view of a second alternate embodiment of a surgical hand tool comprising a balloon catheter. The design ofsurgical hand tool2740 is similar to the design ofsurgical hand tool2726.Surgical hand tool2740 further comprises a fluid delivery mechanism to deliver inflating fluid for inflating the balloon ofballoon catheter2730. The fluid delivery mechanism comprises anelongate tube2741 connected to ballooninflation port2731.Elongate tube2741 is further connected to afluid reservoir2742. In one embodiment,fluid reservoir2742 comprises a pressurized gas such as air, nitrogen, carbon dioxide, etc. The delivery of fluid fromfluid reservoir2742 toballoon catheter2730 is controlled by avalve2743.
• FIG. 27H shows partial sectional view of the surgical hand tool shown inFIG. 27F. The proximal region ofelongate body2727 compriseslongitudinal slit2729.Elongate body2727 enclosesballoon catheter2730. The proximal end ofballoon catheter2730 comprises a Y shaped hub. The Y-shaped hub comprisesballoon inflation port2731.Balloon inflation port2731 in turn is connected to elongatetube2741.Guidewire2738 enterselongate body2727 through an opening in the proximal end ofelongate body2727.
• FIG. 27G shows a perspective view of an embodiment of the valve arrangement of the device shown inFIG. 27F. The valve arrangement comprises a threeway valve2743. In one embodiment, threeway valve2743 is a three way luer valve. Afirst arm2744 of threeway valve2743 is connected byelongate tube2741 tofluid reservoir2742. Asecond arm2745 of threeway valve2743 is in fluid communication with the balloon ofballoon catheter2730. Athird arm2746 of threeway valve2743 is connected to a drain or is open to the atmosphere.Third arm2746 may be connected to a syringe or a source of vacuum to deflate balloon ofballoon catheter2730. Such an arrangement comprising a syringe or a source of vacuum connected tothird arm2746 is especially useful to deflate a non-compliant balloon. Threeway valve2743 further comprises acontrol knob2747. In a first position ofcontrol knob2747, a fluid communication is created betweenfirst arm2744 andsecond arm2745. In a second position ofcontrol knob2747, a fluid communication is created betweensecond arm2745 andthird arm2746. A user can turncontrol knob2747 in the first position to inflate the balloon ofballoon catheter2730. The user can then turncontrol knob2747 in the second position to deflate the balloon ofballoon catheter2730. Other suitable valve arrangements may also be used instead of a three way valve for controllably inflating or deflating the balloon ofballoon catheter2730.
• FIG. 28A shows a perspective view of an embodiment of a handheld balloon catheter tool.Balloon catheter tool2750 comprises aproximal region2751.Proximal region2751 comprises ahandle2752 to enable a user to holdballoon catheter tool2750.Balloon catheter tool2750 further comprises aballoon catheter shaft2753. In one embodiment,balloon catheter shaft2753 extends distally from the distal region ofproximal region2751. In another embodiment,balloon catheter shaft2753 extends till the proximal end ofproximal region2751.Balloon catheter shaft2753 may further comprise ahypotube2754 surrounding a region ofballoon catheter shaft2753. The distal region ofballoon catheter shaft2753 comprises aninflatable balloon2755 that can be used to dilate one or more regions of the anatomy.Balloon2755 is inflated by atrigger2756 located adjacent to handle2752.Trigger2756 is connected to a plunger that is further connected to an inflating fluid reservoir. Pullingtrigger2756 causes the inflating fluid stored in an inflating fluid reservoir to be delivered toballoon2755 under pressure.Balloon catheter tool2750 may further comprise aflushing port2757 to flush a lumen ofballoon catheter shaft2753. During a procedure, a user inflatesballoon2755 to a desired pressure using the inflating fluid stored in the inflating fluid reservoir. The pressure inballoon2755 can be measured by a pressure sensor orgauge2758 that is in fluid communication with the inflating fluid withinballoon2755.Balloon catheter tool2750 may further comprise aratcheting mechanism2759 to allow a user to pulltrigger2756 in incremental steps. This allows the user to inflateballoon2755 in incremental steps. Similarly,balloon catheter tool2750 may comprise a ratcheting mechanism to allow a user to releasetrigger2756 in incremental steps after inflatingballoon2755. This allows the user to deflateballoon2755 in incremental steps. In one embodiment,balloon catheter tool2750 can be advanced over a guidewire to a desired target location in the anatomy. In this embodiment,balloon catheter tool2750 may further comprise aproximal guidewire port2760 that is in fluid communication with a guidewire lumen inballoon catheter shaft2753. This enablesballoon catheter tool2750 to be introduced over a guidewire into the anatomy. In another embodiment,balloon catheter tool2750 comprises a fixedguidewire2761 at the distal tip ofballoon catheter tool2750 to navigateballoon catheter tool2750 through the anatomy. In one embodiment,balloon catheter tool2750 comprises a rotation knob2662.Rotation knob2762 allows a user to rotateballoon catheter shaft2753.Balloon catheter tool2750 may further comprise one or more navigational modalities including, but not limited to radio opaque markers, electromagnetic navigational sensors, etc. The distal region ofballoon catheter tool2750 may be introduced in the anatomy through a variety of introducing devices disclosed herein including, but not limited to guidecatheter620 ofFIG. 6C.
• FIG. 28B shows a perspective view of an embodiment of a detachable handheld balloon catheter inflation tool.Detachable inflation tool2770 comprises abody2771 comprising ahandle2772 to enable a user to holdinflation tool2770.Detachable inflation tool2770 attaches to aballoon catheter2773. In one embodiment, a user is provided with a kit comprising adetachable inflation tool2770 and multiple balloon catheters. In the embodiment shown inFIG. 28B,balloon catheter2773 comprises an elongateballoon catheter shaft2774. The distal region ofballoon catheter shaft2774 comprises aninflatable balloon2775 that can be used to dilate one or more regions of the anatomy. The proximal region ofballoon catheter shaft2774 is connected to asuitable hub2776 comprising a side port for inflatingballoon2775. In one embodiment,balloon catheter shaft2774 comprises ahypotube2777 surrounding a region ofballoon catheter shaft2775.Balloon2775 is inflated by atrigger2778 located adjacent to handle2772.Trigger2778 is connected to a plunger that is further connected to an inflating fluid reservoir. Pullingtrigger2778 causes an inflating fluid stored in the inflating fluid reservoir to be delivered toballoon2755 under pressure. The inflating fluid is delivered through afluid delivery port2779 that attaches to the side port ofhub2776. During a procedure, a user inflatesballoon2775 to a desired pressure using the inflating fluid stored in the inflating fluid reservoir. The pressure inballoon2775 can be measured by a pressure sensor orgauge2780 that is in fluid communication with the inflating fluid withinballoon2775.Detachable inflation tool2770 may further comprise aratcheting mechanism2781 to allow a user to pulltrigger2778 in incremental steps. This allows the user to inflateballoon2775 in incremental steps. Similarly,detachable inflation tool2770 may comprise a ratcheting mechanism to allow a user to releasetrigger2778 in incremental steps after inflatingballoon2775. This allows the user to deflateballoon2775 in incremental steps. In one embodiment, the combination ofballoon catheter2773 andballoon catheter tool2770 can be advanced over a guidewire to a desired target location in the anatomy. In this embodiment,balloon catheter tool2770 may further comprise aproximal guidewire port2782 that is in fluid communication with a guidewire lumen inballoon catheter shaft2774. This enablesballoon catheter tool2770 to be introduced over aguidewire2783 into the anatomy. In another embodiment,balloon catheter2773 comprises a fixed guidewire at the distal tip ofballoon catheter2773 to navigateballoon catheter2773 through the anatomy. In another embodiment,balloon catheter2773 comprises a rapid exchange lumen. The rapid exchange lumen enablesballoon catheter2773 to be introduced over a suitable guidewire.Balloon catheter tool2770 may further comprise aflushing port2784 to flush a lumen ofballoon catheter2773.Balloon catheter tool2770 may further comprises one or more navigational modalities including, but not limited to radio opaque markers, electromagnetic navigational sensors, etc. The distal region ofballoon catheter2773 may be introduced in the anatomy through a variety of introducing devices disclosed herein including, but not limited to guidecatheter620 ofFIG. 6C.
• The balloon catheter tool ofFIG. 28A or the detachable handheld balloon catheter inflation tool ofFIG. 28B may be designed to inflate a balloon to a fixed pressure. Alternatively, they may be designed to deliver a fixed volume of inflating fluid to inflate a balloon.
• Any of the handle assemblies of the tools described herein and in the patent applications incorporated herein by reference may comprise a rotatable handle. Such a rotatable handle may be designed to convert a part of a rotational force exerted by a user to a rectilinear force to draw components of the handle assembly towards each other. One embodiment of a rotatable handle is disclosed in U.S. Pat. No. 5,697,159 (Linden) titled ‘Pivoted hand tool’, the entire disclosure of which is expressly incorporated herein by reference. Such designs of rotatable handles may be used for handle assemblies including, but not limited to a)handle2752 andtrigger2756 inFIG. 28A, b) handle2772 andtrigger2778 inFIG. 28B, etc.
• FIG. 29 shows a perspective view of a hand-held squeezing device to break or deform one or more anatomical structures such a nasal turbinates. Squeezingdevice2800 comprises a two or more of distal squeezing elements that are used by a user to squeeze tissue located between the distal squeezing elements. Squeezingdevice2800 can be used to temporarily or permanently deform tissue, break tissue, etc. In the embodiment shown inFIG. 29, squeezingdevice2800 comprises aproximal handle element2802 and adistal handle element2804.Distal handle element2804 may comprise anopening2806 to enable a user to insert one or more fingers throughopening2806 to pulldistal handle element2804.Proximal handle element2802 anddistal handle element2804 are hinged together by afirst hinge2808. Aspring device2810 is used to biasproximal handle element2802 anddistal handle element2804 such that the proximal regions ofproximal handle element2802 anddistal handle element2804 are spaced apart. In this embodiment,spring device2810 comprises a bent, elastic metal strip as shown. One end of the strip is fixed toproximal handle element2802 and the other end of the strip slides over a surface ofdistal handle element2804. The distal region ofproximal handle element2802 is connected by asecond hinge2812 to the proximal region of an elongate firstdistal element2814. The distal region of firstdistal element2814 may comprise one ormore compression arms2816 to compress tissue.Compression arms2816 may be substantially straight or may comprise one or more bent, curved or angled regions. In this embodiment, the distal region of firstdistal element2814 comprises asingle compression arm2816. The distal region ofdistal handle element2804 is connected by athird hinge2818 to the proximal region of an elongate seconddistal element2820. The distal region of seconddistal element2820 may comprise one ormore compression arms2822 to compress tissue.Compression arms2822 may be substantially straight or may comprise one or more bent, curved or angled regions. In this embodiment, the distal region of seconddistal element2820 comprises a twocompression arm2822. The curved middle regions of firstdistal element2814 and seconddistal element2820 are connected to each other by afourth hinge2824. In one embodiment of a method of using squeezingdevice2800, a user squeezesproximal handle element2802 anddistal handle element2804 towards each other. This causes the distal ends ofproximal handle element2802 anddistal handle element2804 move away from each other. This in turn causes the proximal ends of firstdistal element2814 and seconddistal element2820 to move apart from each other. This in turn causescompression arm2816 andcompression arms2822 to move closer to each other. This squeezes tissue located betweencompression arm2816 andcompression arms2822. In one method embodiment, squeezingdevice2800 is used to crush or break a region of a nasal turbinate to gain access to a paranasal sinus ostium. The various components of squeezingdevice2800 may be made using suitable biocompatible materials including, but not limited to stainless steel, titanium, etc.FIGS. 29A and 29B show enlarged views of the distal region of the squeezing device ofFIG. 29.FIG. 29A shows the orientation ofcompression arm2816 andcompression arms2822 when squeezingdevice2800 is in an undeployed configuration.FIG. 29B shows the orientation ofcompression arm2816 andcompression arms2822 when squeezingdevice2800 is being used to squeeze tissue.
• FIGS. 29C and 29D show a coronal section through a region of a human head showing the steps of temporarily or permanently breaking or deforming a nasal turbinate NT using the squeezing device ofFIG. 29. InFIG. 29C, squeezingdevice2800 is introduced in the nasal cavity. Thereafter, squeezingdevices2800 is positioned such thatcompression arm2816 is located on one side of the nasal turbinate NT andcompression arms2822 are located on the other side of the nasal turbinate. InFIG. 29D, a user deploys squeezingdevice2800. This causescompression arm2816 andcompression arms2822 to squeeze the region of the nasal turbinate NT located betweencompression arm2816 andcompression arms2822.
• FIG. 29E shows a perspective view of a hand-held device to twist one or more anatomical structures such a nasal turbinates.Twisting device2830 comprises two or more distal arms that are placed around an anatomical structure. Thereafter, the two or more arms are twisted to temporarily or permanently deform or break the anatomical structure. In the embodiment shown inFIG. 29E,twisting device2830 comprises aproximal handle2832, amiddle region2834 and twodistal arms2836.Proximal handle2832 may have a substantially larger outer diameter than the maximum width of the distal region of twistingdevice2830 to enable a user to easily twist the anatomical structure. The various components of squeezingdevice2800 may be made using suitable biocompatible materials including, but not limited to stainless steel, titanium, etc. In one method embodiment, twistingdevice2830 is used to deform or break a region of a nasal turbinate to gain access to a paranasal sinus ostium.
• FIGS. 29G and 29G show a coronal section through a region of a human head showing the steps of temporarily or permanently breaking or deforming a nasal turbinate NT using the squeezing device ofFIG. 29. InFIG. 29G, twistingdevice2830 is introduced in the nasal cavity. Thereafter, twistingdevice2830 is positioned such that one ofarms2836 is located on one side of the nasal turbinate NT and the other ofarms2836 is located on the other side of the nasal turbinate. InFIG. 29G, a usertwists twisting device2830. This causesarms2836 to twist the region of the nasal turbinate NT located betweenarms2836 to temporarily or permanently break or deform the nasal turbinate NT.
• The devices disclosed inFIGS. 298 through 29G are especially useful to treat patients with narrow noses to controllably fracture a nasal turbinate to allow access to a paranasal sinus ostium.
• The rigid or flexible endoscopes disclosed herein may have a range of view ranging from 0 degrees to 145 degrees. The embodiments of endoscopes comprising a curved, bent or angled region may be manufactured by curving or bending the optical fibers before fusing the optical fibers. The optical fibers may be fused for example by heating them to a temperature ranging from 500 to 700 degrees Celsius or by using suitable epoxy adhesives to attach the optical fibers to each other. The endoscopes may be made using reduced cladding thickness optical fibers to allow curved, bent or angled regions with a large angle or curvature but a small radius of curvature. The endoscopes may also be made using glass/glass/polymer (GGP) multimode fiber such as the ones made by 3M to allow curved, bent or angled regions with a large angle or curvature but a small radius of curvature. For example, in embodiments of endoscopes that have a bent, curved or angled region enclosing an angle of 90 degrees or more, the radius of curvature of the bent, curved or angled region may preferably be less than or equal to 1.5 cm. Such endoscopes comprising curved, bent or angled regions with a large angle or curvature but a small radius of curvature are especially useful to enable a user to access the maxillary sinuses.
• The embodiments herein have been described primarily in conjunction with minimally invasive procedures, but they can also be used advantageously with existing open surgery or laparoscopic surgery techniques. For example, the methods and devices disclosed herein may be combined with one or more techniques of Functional Endoscopic Sinus Surgery (FESS). In FESS, a surgeon may remove diseased or hypertrophic tissue or bone and may enlarge the ostia of paranasal sinuses to restore normal drainage of the sinuses. It is typically performed with the patient under general anesthesia using endoscopic visualization.
• Although FESS continues to be the gold standard therapy for severe sinuses, it has several shortfalls such as post-operative pain and bleeding associated with the procedure, failure to relieve symptoms in a significant subset of patients, risk of orbital, intracranial and sinonasal injuries, etc. Replacing one or more steps of FESS may reduce the shortfalls associated with the traditional FESS. The following are some examples of procedures involving a combination of FESS and the procedures disclosed in this patent application and the patent applications incorporated herein by reference.
• 1. In one combination procedure, a maxillary sinus is treated by balloon dilation with or without total or partial removal of the uncinate. Total or partial removal of the uncinate may make it easier or faster for some physicians to visualize and access the maxillary sinus.
• 2. In another combination procedure, a maxillary sinus is treated by balloon dilation in conjunction with removal of a nasal turbinate. During this combination procedure, a part or the entire nasal turbinate e.g. the middle turbinate may be removed. Removing a part or the entire middle turbinate provides additional working space in the region medial to the uncinate for instruments. This may potentially make the combination procedure easier or faster.
• 3. In another combination procedure, a sphenoid sinus ostium is treated by balloon dilation in conjunction with ethmoidectomy. The step of ethmoidectomy may enable a physician to introduce a guide catheter through the middle meatus to the sphenoid sinus ostium. This may potentially enable easy access to the sphenoid sinus ostium.
• 4. In another combination procedure, a frontal sinus is treated by balloon dilation in conjunction with middle turbinate resection and/or ethmoidectomy. This combination procedure may make easier for a physician to find, visualize or access the frontal sinus once anatomical structures like Ethmoid bulla, turbinate, etc. are removed or reduced.
• 5. In another type of combination procedures, multiple sinuses are treated by balloon dilation with no or minimal tissue or bone removal. This is then followed by standard techniques to treat sinus disease. Examples of such combination procedures include:
• 5A. Frontal, maxillary, or sphenoid sinuses are treated by balloon dilation. Also, ethmoidectomy is performed while preserving the uncinate. The presence of the uncinate may preserve the natural function of the uncinate. This in turn may lead to lower incidence of complications like infection, etc. in the sinuses.
• 5B. Any paranasal sinus may be treated by balloon dilation combined with a second procedure including, but not limited to ethmoidectomy, septoplasty, reduction of a turbinate (e.g. inferior turbinate, middle turbinate, etc.), etc.
• 6. Any of the procedures disclosed herein may be performed in conjunction with irrigation and suction of one or more paranasal sinuses with a flexible catheter or rigid instrument. A flexible catheter is particularly useful to reach regions that are difficult to access by rigid instruments. Such regions may be located in lateral aspects of the frontal sinuses, the inferior or medial aspects of the maxillary sinuses, etc.
• 7. Any of the procedures disclosed herein may further include removal of one or more polyps. Polyp removal by standard techniques such as using shavers can be combined with balloon dilation of various paranasal sinus ostia. Once one or more polyps are removed, one or more ostia of paranasal sinuses may be dilated by balloon dilation.
• 8. In another type of combination procedures, balloon dilation of one or more paranasal sinus ostia may be performed to revise a previously performed surgery or in conjunction with standard endoscopic sinus surgery techniques. Examples of such procedures include:
• 8A. Treating scar formation over frontal recess: In this combination procedure, an attempt is made to access frontal recess with a guidewire. A balloon catheter is then passed over the guidewire. If the guidewire is unable to access the frontal sinus ostia because of scarring or because the frontal sinus ostia are too small, a surgical instrument e.g. curette or seeker may be used to open or puncture scar tissue or adhesions or the frontal sinus ostia. Such scar tissue or adhesions may be caused for example due to infection, prior surgery, etc. Thereafter, the frontal sinus ostia may be dilated by balloon dilation.
• 8B. Combination procedures similar to the abovementioned combination procedure may be performed to treat scarring near sphenoid sinuses and maxillary sinuses.
• 9. In another type of combination procedures, one or more paranasal sinuses e.g. a maxillary sinus may be accessed by an artificially created opening leading to the sinuses. Thereafter, a diagnostic or therapeutic procedure disclosed herein or in the patent documents incorporated herein by reference may be performed. The artificially created opening may be used to endoscopically visualize the placement of devices such as balloon catheters, guidewires, or other devices through a natural ostium of the paranasal sinus. The artificially created opening may also be used to introduce one or more diagnostic, therapeutic or access devices. The artificially created opening may be used to introduce liquids including, but not limited to solutions of antibiotics, solutions of anti-inflammatory agents, etc. The artificially created opening may be made by using suitable devices including, but not limited to drilling devices, chopping devices, puncturing devices, etc.
• Some specific examples of hybrid procedures of the present invention are shown in the flow diagrams ofFIGS. 30-33.
• FIG. 30 shows steps in a method wherein an anatomical or pathological structure, such as the uncinate process, a turbinate, the wall of an ethmoid air cell, a polyp, etc. is removed or substantially modified and a dilator (e.g., the balloon of a balloon catheter) is positioned within an opening of a paranasal sinus and used to dilate that opening. Removal or modification of the anatomical or pathological structure may provide clearer access to and/or visibility of certain anatomical structures during the procedure or during post-operative examinations and follow-up.
• FIG. 31 shows steps in a method where a dilator such as the balloon of a balloon catheter is positioned in the opening of a paranasal sinus and used to dilate that opening and, either before or after such dilation, the cavity of the paranasal sinus is suctioned or irrigated. In cases where a balloon catheter or other dilator device having a through lumen is used to accomplish the dilation step, the irrigation and/or suction step may be carried out by passing fluid or negative pressure through the through lumen of the dilation catheter. Or, a guidewire may be advanced into or near the sinus cavity during the dilation step and, thereafter, a suction and/or irrigation device may be advanced over such guidewire and used to carry out the suction and/or irrigation step.
• FIG. 32 shows steps in a method where scar or adhesion tissue has formed in a location that obstructs a lumen, orifice, or passageway (e.g., scar tissue obstruction the opening of a paranasal sinus) and a puncture tract is initially formed in the scar or adhesion tissue. This may be accomplished by pushing a needle, seeker, probe, guidewire or other penetrator through the tissue. Thereafter, a dilator (e.g., a balloon catheter) is advanced into the puncture tract and is used to dilate the puncture tract, thereby relieving the obstruction caused by the aberrant scar or adhesion tissue.
• FIG. 33 shows steps in a method wherein a dilator (e.g., the balloon of a balloon catheter) is placed in a pre-existing opening of a paranasal sinus, such as the natural ostium of the sinus (or a previously surgically altered ostium) and is used to dilate that opening. Also, a separate opening is created in that paranasal sinus, either from the nasal cavity or through the exterior of the face (e.g., a bore hole, antrostomy or trephination). This may provide improved ventilation and/or drainage of the sinus cavity. Optionally, the two openings may then be used to perform other procedures. For example, a “flow through” lavage may be carried out by passing lavage solution through one of the openings and out of the other. Or, a device may be inserted through one of the openings, leaving the other opening unobstructed. Or, the physician may visualize (e.g., through an endoscope) through the newly created opening while treated the pre-existing opening or performing other diagnosis or treatment of the sinus cavity.
• It is to be appreciated that the devices and methods of the present invention relate to the accessing and dilation or modification of sinus ostia or other passageways within the ear nose and throat. These devices and methods may be used alone or may be used in conjunction with other surgical or non-surgical treatments, including but not limited to the delivery or implantation of devices and drugs or other substances as described in copending U.S. patent application Ser. No. 10/912,578 entitled Implantable Devices and Methods for Delivering Drugs and Other Substances to Treat Sinusitis and Other Disorders filed on Aug. 4, 2004, the entire disclosure of which is expressly incorporated herein by reference.
• It is to be appreciated that the invention has been described hereabove with reference to certain examples or embodiments of the invention but that various additions, deletions, alterations and modifications may be made to these examples and embodiments without departing from the intended spirit and scope of the invention. For example, any element or attribute of one embodiment or example may be incorporated into or used with another embodiment or example, unless to do so would render the embodiment or example unsuitable for its intended use. All reasonable additions, deletions, modifications and alterations are to be considered equivalents of the described examples and embodiments and are to be included within the scope of the following claims.

Claims (21)

1-151. (canceled)

152. An apparatus comprising:

(a) an elongate shaft assembly having:

(i) a proximal end,

(ii) a distal end,

(iii) a first lumen, wherein the first lumen distally terminates at a first distal end, and

(iv) a second lumen, wherein the second lumen distally terminates at a second distal end;

(b) a first port located at the proximal end of the elongate shaft assembly, wherein the first port is in fluid communication with the first lumen;

(c) a second port located at the proximal end of the elongate shaft assembly, wherein the second port is in fluid communication with the second lumen; and

(d) an inflatable member positioned proximal to the first distal end, wherein the inflatable member is in fluid communication with the second lumen such that the inflatable member is in fluid communication with the second port via the second lumen,

wherein the inflatable member is sized and configured to transition between a first state and a second state, wherein the inflatable member is sized to fit in an anatomical passageway associated with a paranasal sinus in the first state,

wherein the inflatable member is configured to dilate an anatomical passageway associated with a paranasal sinus in which the inflatable member is position in the second state.

153. The apparatus ofclaim 152, wherein the second distal end is located within the inflatable member.

154. The apparatus ofclaim 152, wherein the shaft assembly further comprises a first tubular member and a second tubular member.

155. The apparatus ofclaim 154, wherein the first and second tubular members are laterally offset from each other such that the first and second tubular members extend along offset parallel axes.

156. The apparatus ofclaim 152, wherein the first distal end is open.

157. The apparatus ofclaim 152, wherein the distal end of the shaft assembly includes a navigational marker configured to provide visibility through an electromagnetic image guidance system.

158. The apparatus ofclaim 152, wherein the shaft assembly includes a bent region.

159. The apparatus ofclaim 152, wherein the shaft assembly defines a longitudinal axis, wherein the longitudinal axis passes through the first port, wherein the second port is positioned distal to the first port, wherein at least a portion of the second port is oriented transversely relative to the longitudinal axis.

160. An apparatus comprising:

(a) a handle assembly, wherein the handle assembly comprises:

(i) a body, and

(ii) an actuator, wherein the actuator is movable relative to the body;

(b) a guide member extending distally from the handle assembly, wherein the guide member has a distal end; and

(c) a dilation catheter coaxially disposed with respect to the guide member, wherein the dilation catheter comprises a dilator, wherein the dilator is sized and configured to transition between a non-expanded state and an expanded state, wherein the dilator is sized to fit in an anatomical passageway associated with a paranasal sinus in the non-expanded state, wherein the dilator is configured to dilate an anatomical passageway associated with a paranasal sinus in which the dilator is position in the expanded state;

wherein the dilation catheter is coupled with the actuator such that the actuator is operable to drive the dilation catheter relative to the guide member from a proximal position to a distal position, wherein the dilation catheter is configured such that the dilator is positioned distal to the distal end of the guide member when the dilation catheter is in the distal position.

161. The apparatus ofclaim 160, wherein the guide member comprises a guide catheter.

162. The apparatus ofclaim 161, wherein the dilation catheter is slidably disposed within the guide catheter.

163. The apparatus ofclaim 160, further comprising a guidewire, wherein the guidewire is slidably disposed through the dilation catheter.

164. The apparatus ofclaim 163, further comprising a guidewire actuator secured to the guidewire, wherein the guidewire actuator is operable to translate and rotate the guidewire relative to the dilation catheter.

165. The apparatus ofclaim 164, wherein the guidewire actuator is positioned proximal to the body of the handle assembly.

166. The apparatus ofclaim 160, further comprising an inflation port in fluid communication with the dilator, wherein a portion of the inflation port protrudes from the body of the handle assembly, wherein the portion of the inflation port protruding from the body of the handle assembly is slidable relative to the handle assembly.

167. The apparatus ofclaim 160, wherein the actuator comprises a trigger, wherein the trigger is pivotable relative to the body of the handle assembly.

168. The apparatus ofclaim 160, further comprising a hub secured to the proximal end of the guide member, wherein the hub is removably coupled with the body of the handle assembly.

169. A method of using an apparatus to dilate an anatomical passageway associated with a paranasal sinus in a patient, the method comprising:

(a) grasping a handle assembly of the apparatus, wherein the handle assembly comprises a body and an actuator;

(b) inserting a guide member of the apparatus through a nostril of the patient, wherein the guide member extends distally from the handle assembly;

(c) moving the actuator in a first direction relative to the body of the handle assembly, thereby advancing a dilation catheter distally relative to the guide member, wherein the act of advancing the dilation catheter distally results in a dilator of the dilation catheter being positioned in an anatomical passageway associated with a paranasal sinus in the patient; and

(d) expanding the dilator in the anatomical passageway, thereby dilating the anatomical passageway.

170. The method ofclaim 169, further comprising moving the actuator in a second direction relative to the body of the handle assembly, thereby retracting the dilation catheter proximally relative to the guide member.

171. The method ofclaim 169, further comprising advancing a guidewire into a paranasal sinus associated with the anatomical passageway, wherein the act of advancing the dilation catheter distally comprises advancing the dilation catheter distally along the guidewire.

Images