US20140012309A1 - Device and method for treatment of sinusitis - Google Patents

Abstract

A method of treating a constricted sinus passageway of a patient includes traversing the canine fossa region of the patient so as to form a passageway in the sinus cavity. An elongate member is inserted through the passageway, the elongate member having an inflation member such as a balloon disposed thereon. The inflation member is positioned within the constricted passageway. The inflation member is expanded so as to expand at least a portion of the constricted sinus passageway.

Description

FIELD OF THE INVENTION
• The field of the invention generally relates to devices and methods for the treatment or amelioration of sinusitis.
BACKGROUND OF THE INVENTION
• Sinusitis is a condition affecting over 35 million Americans, and similarly large populations in the rest of the developed world. Sinusitis occurs when one or more of the four paired sinus cavities (i.e., maxillary, ethmoid, frontal, sphenoid) becomes obstructed. These paired cavities are located in the skull behind the face, as is depicted inFIGS. 1,2, and3A. Normally the sinus cavities, each of which are lined by mucosa, produce mucous which is then moved by beating cilia from the sinus cavity out to the nasal cavity and down the throat. The combined sinuses produce approximately one liter of mucous daily, so the effective transport of this mucous is important to sinus health.
• Each sinus cavity has an opening into the nasal passage called an ostium. When the mucosa of one or more of the ostia or regions near the ostia become inflamed, the egress of mucous is interrupted, setting the stage for an infection of the sinus cavity, i.e., sinusitis. Infections of the maxillary and/or ethmoid sinuses make up the vast majority of cases of sinusitis, with far fewer cases involving the sphenoids and frontals.
• Though many instances of sinusitis may be treatable with antibiotics, in some cases sinusitis persists for months, a condition called chronic sinusitis. Some patients are also prone to multiple episodes of sinusitis in a given period of time, a condition called recurrent sinusitis.
• Currently, patients experiencing chronic sinusitis are eligible to have a surgical procedure called functional endoscopic sinus surgery (FESS). In this procedure, which almost always done in an operating room setting with the patient under general anesthesia, surgical cutting instruments are guided with an endoscopic visualization tool to the various sinus ostia and adjacent regions. Inflamed mucosa and underlying bony tissue are cut away in an effort to widen the outlet of the sinuses of interest. Once opened, the infected sinuses are able to drain and return to a relatively normal state.
• While this procedure is generally effective, it is a relatively invasive procedure to the nasal cavity and sinuses. There can be significant post-operative pain for the patient, and sometimes there are bleeding complications that require packing to be placed in the nasal cavity. Subsequent removal of this packing can be quite painful. Also, since the nasal and sinus tissue are significantly traumatized, it may take several days to weeks to know whether the surgery was successful. This is especially true if various healing agents such as MeroGel® (Medtronic/Xomed) were placed at the surgical site, as these often block the sinus drainage until they are flushed away or degrade away after several days.
• Additionally, in certain patients, the ostial regions of the surgically-treated sinuses can become re-obstructed with excess growth of scar tissue as a result of the tissue trauma. When the advantages and disadvantages of the surgery are considered for a patient with sinusitis, there are many patients in whom the surgery may not be appropriate. For example, their condition may not be considered “chronic enough” or extensive enough to warrant FESS surgery. In other situations, the patient may be fearful of the pain or other aspects of having FESS performed. Alternatively, the FESS procedure may be too costly for a particular patient.
• For these and other reasons, there is a clear need for better methods and devices for the treatment of sinusitis.
SUMMARY OF THE INVENTION
• In a first aspect of the invention, a method of treating a constricted sinus passageway of a patient includes traversing the canine fossa region of the patient so as to form a passageway to a sinus cavity. An elongate member having an inflation member thereon (e.g., a balloon) is inserted through the passageway. The inflation member is positioned within the constricted sinus passageway. The inflation member is then expanded so as to expand at least a portion of the constricted sinus passageway.
• In a second aspect of the invention, a method of accessing a constricted sinus passageway of a patient includes traversing the canine fossa region of the patient to as to form a passageway to a sinus cavity. A visualization tool is inserted through the passageway. A wire guide is also inserted through the passageway. The constricted sinus passageway is viewed with the visualization tool. The wire guide is positioned adjacent to or within the constricted sinus passageway.
• In another aspect of the invention, a method of accessing a constricted sinus passageway of a patient includes traversing the canine fossa region of the patient so as to form a first passageway to a sinus cavity. A visualization tool is inserted through the first passageway. The canine fossa region is traversed again to form a second passageway. This traversal may be performed at the same time that the first passageway is formed. A wire guide is then inserted through the second passageway. The constricted sinus passageway is then viewed with a visualization tool. The wire guide is then placed adjacent to or within the constricted sinus passageway. A balloon catheter may be advanced over the wire guide to expand or open the constricted sinus passageway.
• In yet another embodiment, a method of accessing a constricted sinus passageway of a patient includes traversing the canine fossa region of the patient so as to form a passageway to a sinus cavity. An illumination member is inserted into the sinus cavity. The sinus cavity is illuminated via the illumination member. A guide catheter is inserted through the nasal passageway, the guide catheter including a wire guide slidably disposed within a lumen contained therein. A visualization tool is inserted through the nasal passageway. A distal tip of the wire guide is placed across or adjacent to the constricted sinus passageway.
• In still another aspect of the invention, a method of confirming the location of a wire guide intended to be positioned within a patient's sinus cavity includes introducing a wire guide through a nasal passageway to place a distal tip of the wire guide in a test position. The elongate member is advanced over the wire guide to place a distal end at or adjacent to the distal tip of the wire guide. The elongate member emits illuminating light via the distal end of the elongate member. The location of the light (e.g., the source) is viewed through the patient's skin to confirm the positioning (or confirm incorrect positioning) of the wire guide.
• In another embodiment of the invention, a method of confirming the location of the wire guide intended to be positioned within a patient's sinus cavity includes introducing a wire guide through a nasal passageway to place a distal tip of the wire guide in a test position, the wire guide including a detection element positioned at or adjacent to the distal tip of the wire guide. A detector device is then placed external to the patient's skin adjacent to the intended sinus cavity so as to detect the presence or absence of the detection element.
• In still another aspect of the invention, a system for accessing a sinus cavity of a patient includes a trocar having an outer cannula and a piercing member slidably disposed within a lumen of the cannula. The system includes an elongate member having an inflation member disposed thereon, the elongate member being slidably disposed within the lumen of the cannula.
• In yet another aspect of the invention, a device for accessing the sinus cavity of a patient includes an outer cannula having a lumen and a piercing member slidably disposed within the lumen of the cannula. An adjustable stop is secured to a distal portion of the piercing member.
• In still another aspect of the invention, a device for accessing the sinus cavity of a patient includes an outer cannula having a lumen and a piercing member slidably disposed within the lumen of the cannula. A stop is secured to one of the outer cannula and the piercing member.
• In another aspect of the invention, a device for accessing the sinus cavity of a patient includes an outer cannula having a lumen, a piercing member slidably disposed within the lumen of the cannula, the piercing member including a threaded portion on a proximal section of the piercing member. The device further includes a threaded hub configured to rotationally engage the threaded portion of the piercing member.
• In still another aspect of the invention, a device for accessing the sinus cavity of a patient includes an outer cannula having a lumen, a piercing member slidably disposed within the lumen of the cannula, the piercing member including a proximal section. The device further includes an advancement member frictionally engaged with the proximal section of the piercing member, wherein the advancement member controls the displacement of the piercing member relative to the outer cannula.
• In yet another embodiment of the invention, a balloon catheter for treating a constricted sinus passageway of a patient includes a flexible elongate member having a proximal end and a distal end and including first and second lumens passing therethrough. A hub is secured to a proximal end of the flexible elongate member, the hub including a first port in communication with the first lumen of the flexible elongate member and a second port in communication with the second lumen of the flexible elongate member. An inflation member is disposed on or adjacent to the distal end of the flexible elongate member, an interior of the inflation member being in communication with the first lumen of the flexible elongate member. An outer membrane surrounds the inflation member, an interior of the outer membrane being in communication with the second lumen of the flexible elongate member, the outer membrane including a plurality of perforations.
• In still another embodiment of the invention, a stabilizing device for securing one or more tools passing into a nasal or sinus cavity of a patient includes a base member fixedly secured to the face of the patient, an adjustable support arm secured at a first end to the base member, and a securing member fixed to a second end of the adjustable support arm, the securing member configured to releasable hold at least one tool passing into the nasal or sinus cavity of a patient.
• In another embodiment of the invention, a method of stabilizing one or more tools passing into a nasal passage of a patient includes inserting a tool into the nasal passage of the patient. A stabilizing element is then inserted into the nasal passage of the patient adjacent to the tool, the stabilizing element being inserted in a non expanded state. The stabilizing element is expanded to an expanded state to frictionally engage the tool within the nasal passage of the patient.
• In another embodiment of the invention, a stabilizing device for securing one or more tools passing into a sinus cavity of a patient includes a mouth piece fixedly secured to the mouth of the patient, an adjustable support arm secured at a first end to the mouth piece, and a securing member fixed to a second end of the adjustable support art, the securing member configured to releasably hold at least one tool passing into the sinus cavity of a patient.
• In still another aspect of the invention, a system for manipulating a guide catheter within a patient's nasal passages or sinus cavities is provided. The system includes a guide catheter formed from an elongate flexible member having a lumen passing therethrough and a wire guide slidably disposed within the lumen of the guide catheter. The system includes a steering member fixedly secured to a proximal end of the wire guide and a proximal hub secured to a proximal end of the guide catheter. The system further includes a recessed handle having a first recess for fixedly receiving the proximal hub of the guide catheter and a second recess for receiving the steering member, the second recess being dimensioned to permit axial and rotational movement of the steering member while disposed in the second recess.
• In yet another aspect of the invention, a system for manipulating a guide catheter within a patient's nasal passages or sinus cavities is provided. The system includes a guide catheter formed from an elongate flexible member having a lumen passing therethrough, the guide catheter including a proximal handle including a recess therein. A wire guide is slidably disposed within the lumen of the guide catheter. The system includes a steering member fixedly secured to a proximal end of the wire guide and disposed in the recess of the handle, the recess being dimensioned to permit axial and rotational movement of the steering member while disposed in the recess.
• In another embodiment of the invention, a guide catheter for accessing a sinus cavity of a patient includes an elongate member having a proximal end and distal end and at least one lumen passing therethrough, the distal end including a flexible tip portion, the elongate member being formed from a polymeric material containing a wire braid. The guide catheter further includes a hub connected to the proximal end of the elongate member.
• In still another aspect of the invention, a balloon catheter for treating a constricted sinus passageway of a patient includes an elongate flexible shaft comprising an inner tube and an outer tube, the elongate flexible shaft having a proximal end and distal region, wherein at least one of the inner tube and outer tube is formed with a kink-resistant coil in the distal region. A hub is affixed to a proximal end of the elongate flexible shaft, the hub including a port in communication with a lumen formed between the inner tube and the outer tube. An expandable member is disposed on a distal region of the elongate flexible shaft, an interior of the expandable member being in communication with the lumen formed between the inner tube and the outer tube.
• In another embodiment of the invention, a guide catheter for guiding one or more devices into an ostium of a paranasal sinus includes an elongate shaft defining a proximal region and a distal region, the elongate shaft including a lumen passing from the proximal region to the distal region. The elongate shaft includes a curved portion in the distal region, the curved portion having a radius of curvature of between about 1 mm and about 5 mm and an angle of between about 120° and about 180°.
• In still another aspect of the invention, a method of placing a wire guide into the ostium of a paranasal sinus includes introducing a directable endoscope into the nasal cavity. A guide catheter is inserted into the nasal cavity to position a distal tip near the sinus ostium. The endoscope is manipulated to move the viewing field toward the sinus ostium. A wire guide is inserted through a lumen in the guide catheter and the wire guide is manipulated to place the same at least partially within or adjacent to the sinus ostium.
• In another embodiment of the invention, a method of placing a wire guide into the ostium of a paranasal sinus includes introducing a retrograde rigid endoscope into the nasal cavity and introducing a guide catheter into the nasal cavity to position a distal tip near the sinus ostium. The endoscope is oriented to move the viewing field toward the sinus ostium. A wire guide is inserted through a lumen in the guide catheter and the wire guide is manipulated to place the wire guide at least partially within or adjacent to the sinus ostium.
• In yet another embodiment of the invention, a method of placing a wire guide into the ostium of a paranasal sinus includes introducing a guide catheter into the nasal cavity to position a distal tip near the sinus ostium. A wire guide is inserted through a lumen in the guide catheter and the wire guide is manipulated to place the wire guide at least partially beyond a distal tip of the guide catheter. A flexible visualization scope is introduced over the wire guide to position a viewing field toward the sinus ostium. The wire guide is manipulated to place the wire guide at least partially within the sinus ostium.
• In still another aspect of the invention, a method of placing a wire guide into the ostium of a paranasal sinus includes introducing a directable endoscope sheath into the nasal cavity, the endoscope sheath including at least one working lumen therein. The endoscope is manipulated to move the viewing field toward the sinus ostium. A wire guide is inserted through the lumen in the endoscope sheath. The wire guide is manipulated to place the wire guide at least partially within or adjacent to the sinus ostium.
• In yet another aspect of the invention, a method of remodeling the uncinate process associated with a paranasal sinus includes positioning at least one shim member in the infundibulum, the shim member deforming the uncinate process and widening at least a portion of the infundibulum. The shim member may be permanent or biodegradable. In addition, multiple shims may be positioned within the infundibulum. The at least one shim members may be delivered using a delivery tool. For example, the at least one shim member may be inserted into the infundibulum in a first orientation and then rotated into position. The at least one shim member may include a gripping member (e.g., teeth) on an exterior surface thereof.
• In another aspect of the invention, a device for remodeling the uncinate process associated with a paranasal sinus includes an elongate delivery tool and at least one shim member detachably mounted to a distal end of the elongate delivery tool. The elongate delivery tool may include a torque driver to transmit rotational movement of a proximal end to rotational movement of a distal end. In one aspect, the at least one shim member and the elongate delivery tool are slidably disposed within a guide catheter.
• In another embodiment of the invention, a method of treating a constricted sinus passageway of a patient includes traversing the external skull wall of the patient so as to form a passageway to the frontal sinus cavity and inserting an elongate member through the passageway, the elongate member having an inflation member disposed thereon. The inflation member is positioned within the constricted sinus passageway and the inflation member is expanded so as to expand at least a portion of the constricted sinus passageway.
• In still another embodiment of the invention, a device for accessing the sinus cavity of a patient includes an outer cannula having a lumen, the outer cannula having a flexible curved tip. The device further includes a piercing member slidably disposed within the lumen of the cannula, the piercing member including a proximal section. An advancement member is frictionally engaged with the proximal section of the piercing member.
• Further features and advantages will become apparent upon review of the following drawings and description of the preferred embodiments.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 illustrates is a schematic view illustrating the paranasal sinuses in relation to the face.
• FIG. 2 is a coronal section of the human skull, showing the paranasal sinuses.
• FIGS. 3A-3C are of a sagittal view of the lateral nasal wall, illustrating various anatomical features thereof.
• FIG. 4 illustrates one embodiment of the current invention showing a balloon dilation catheter in the ostial region of a paranasal sinus.
• FIG. 5A illustrates one embodiment of a guide catheter according to the invention.
• FIG. 5B is a cross-sectional view of the embodiment shown inFIG. 5A.
• FIG. 5C is a cross-sectional view of an alternative embodiment of a guide catheter.
• FIG. 5D is an alternative embodiment of a guide catheter.
• FIG. 5E shows the guide catheter of the embodiment illustrated inFIG. 5D being positioned within the nasal cavity.
• FIG. 5F is a cross-sectional view of an alternative embodiment of a guide catheter.
• FIG. 6A illustrates an embodiment of a balloon dilation catheter according to one embodiment of the invention.
• FIG. 6B is a longitudinal sectional view of a portion of the distal shaft of the embodiment ofFIG. 6A.
• FIG. 6C is a cross-section of the distal shaft of the embodiment ofFIG. 6A.
• FIG. 7A illustrates an alternative embodiment of a balloon dilation catheter according to one embodiment.
• FIG. 7B is a longitudinal sectional view of a portion of the distal shaft of the embodiment ofFIG. 7A.
• FIG. 7C is a cross-sectional view of the distal shaft of the embodiment ofFIG. 7A.
• FIG. 8 illustrates an embodiment of a stabilization device according to one aspect of the invention.
• FIG. 9 illustrates an alternative embodiment of a stabilization device according to another aspect of the invention.
• FIG. 10A illustrates a further alternative embodiment of a stabilization device according to another aspect of the invention.
• FIG. 10B is a partially exploded top view of the stabilization device ofFIG. 10A.
• FIG. 100 is a partially exploded front view of the stabilization device ofFIG. 10A.
• FIG. 10D is an assembled front view of the stabilization device ofFIG. 10A.
• FIG. 11A illustrates an embodiment of a wire movement guide according to one aspect of the invention.
• FIG. 11B is a cross-sectional view of the wire movement guide ofFIG. 11A.
• FIG. 11C is an assembly drawing of the wire movement guide ofFIG. 11A attached to a guide catheter.
• FIG. 11D illustrates a method for placement of a wire guide in a sinus ostium according to one aspect of the invention.
• FIG. 12 illustrates a method and device for confirming the placement of a wire guide in a sinus according to one aspect of the invention.
• FIG. 13 illustrates an alternative method and device for confirming the placement of a wire guide, according to another aspect of the invention.
• FIG. 14 illustrates methods and devices for accessing a sinus according to one aspect of the invention.
• FIG. 15 shows additional methods and devices for accessing a sinus, according to another aspect of the invention.
• FIG. 16A shows additional methods and devices for accessing a sinus according to another aspect of the invention.
• FIG. 16B shows a flexible visualization scope as used in connection withFIG. 16A.
• FIG. 16C is a cross-sectional view of the flexible visualization scope ofFIG. 16B.
• FIG. 17A shows additional methods and devices for accessing a sinus according to one of the invention.
• FIG. 17B shows an embodiment of a directable endoscope sheath as used in connection withFIG. 17A.
• FIG. 17C is a cross-sectional view of the directable endoscope sheath ofFIG. 17B.
• FIG. 18A illustrates methods and devices for accessing a sinus from an external location according to one aspect of the invention.
• FIG. 18B illustrates additional methods and devices for accessing a sinus ostium from an external location according to one aspect of the invention.
• FIG. 18C illustrates further additional methods and devices for accessing a sinus ostium from an external location according to another aspect of the invention.
• FIGS. 19A-19C are cross-sectional images depicting various arrangements of devices used in accessing a sinus ostium in connection withFIG. 18B.
• FIG. 20 illustrates methods and devices for treating a sinus ostium in one aspect of the invention.
• FIG. 21 shows an embodiment of a trocar in accordance with one aspect of the invention.
• FIG. 22 shows another embodiment of a trocar according to another aspect of the invention.
• FIGS. 23A and 23B show additional methods and devices for accessing a sinus ostium from an external location according to one aspect of the invention.
• FIG. 24 shows additional methods and devices for accessing a sinus ostium from an external location according to another aspect of the invention.
• FIG. 25A is a coronal view showing anatomical features of the maxillary sinus.
• FIG. 25B is a sagittal view showing the anatomical features ofFIG. 25A.
• FIG. 26A is a coronal view illustrating methods and devices for the treatment of the uncinate process in accordance with one aspect of the invention.
• FIG. 26B is a sagittal view illustrating methods and devices for the treatment of the uncinate process in accordance with one aspect of the invention.
• FIG. 27A is a top view of an embodiment of a shim member in accordance with one aspect of the invention.
• FIG. 27B is an isometric view of the shim member ofFIG. 27A.
• FIG. 28 is an embodiment of a shim member delivery device in accordance with one aspect of the invention.
• FIG. 29 illustrates a method and device for widening the infundibulum in accordance with another aspect of the invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
• FIG. 1 illustrates a frontal anatomical representation (parallel to the coronal plane) showing the sinuses FS, ES, MS located within a patient's head H. Above and behind the eyebrows are the frontal sinuses FS. Between the eyes are the ethmoid sinuses ES. Note that unlike the other sinuses, the ethmoids are typically formed as a “honeycombed” structure consisting of several individual air cells. Located behind the cheeks are the maxillary sinuses MS. The sphenoid sinuses are not shown inFIG. 1, but are located further posterior to the ethmoid sinuses.
• FIG. 2 is another frontal view of the sinuses located within the skull bone SK showing additional features. The nasal septum NS divides the nasal cavity into left and right sides. Because the following described structures are generally symmetrical bilaterally, only one of the paired structures is illustrated for sake of convenience. Within the nasal cavity are the middle turbinate MT and the inferior turbinate IT. The middle turbinate MT is connected to the base of the skull SK, while the inferior turbinate IT is connected to the lateral wall of the sinus cavity. The turbinates MT, IT have an underlying bony structure, but are covered with a thick mucosa lining. When this lining swells (rhinitis), it can inhibit breathing through the nose, particularly the inferior turbinate IT. The ethmoid sinuses ES are depicted by a single air cell inFIG. 2. The uncinate process UP is a complex three-dimensional structure, projecting off of the lateral wall like a crescent shaped leaf (better seen inFIGS. 3B and 25B) The curved aspect of the medial bone defining the ethmoid sinuses ES is called the ethmoid bulla EB. The passageway between the ethmoid bulla EB and the uncinate process UP is referred to as the infundibulum I. The drainage path of the maxillary MS, frontal FS, and some of the ethmoid ES air cells runs into the infundibulum I. At the most inferior part of the maxillary sinus is a thin portion of skull bone referred to as the canine fossa CF. Though this is not a true opening, it is a relatively thin bone region, just above the root of the outer aspect of the canine teeth, inside the mouth. The relationship of the sinuses to the orbit O of the eye can also be seen. Note also that all of the sinus cavities have a mucosa lining (ML) disposed over the bone.
• FIG. 3A is a side view parallel to the sagittal plane, looking at the right lateral nasal wall. The right nostril N is seen. The sphenoid sinus SS and frontal sinus FS may also be seen in this view. The flap-like structures illustrated inFIG. 3A are the inferior turbinate IT and middle turbinate MT. Other structures of the nasal cavity have been left out for clarification, e.g., the superior turbinate. Located underneath the middle turbinate MT (shown in a “lifted” state inFIG. 3B and removed inFIG. 25B) are the structures of the lateral nasal wall. As seen inFIG. 3A, the ethmoid bulla EB is a rounded projection of the bony wall of the nasal cavity. Behind the wall of the ethmoid bulla EB are one or more of the individual air cells of the ethmoid sinus ES (not shown inFIGS. 3B and 25B). Anterior and inferior of the ethmoid bulla is the uncinate process UP. The uncinate process UP has essentially two edges to it including a free edge FE and a connected edge CE. The free edge FE stands out from the nasal wall, while the connected edge CE connects the structure to the nasal wall. The narrow space between the ethmoid bulla EB and the uncinate process UP is the infundibulum I. Thus, it can be appreciated the complexity of the anatomy involving the maxillary and ethmoid sinus structures MS, ES.
• FIG. 3C illustrates the structure beneath or underneath the uncinate process UP. InFIG. 3C, the uncinate process UP has been removed for clarity purposes, leaving only the connected edge CE. Two ostia can be seen including the maxillary sinus ostium MO, and the frontal sinus ostium FO. Drainage from the frontal sinuses FS and maxillary sinuses MS emerges into the infundibulum I through the maxillary sinus ostium MO and the frontal sinus ostium FO. Also, some of the ethmoid air cells ES drain into the infundibulum I, but they are not shown as they are substantially smaller than the frontal and maxillary ostia FO, MO. Drainage problems can arise and/or extend from the ostia of one or more of these sinuses to the infundibulum I or vise versa. Consequently, conventional FESS surgical treatment of sinusitis typically involves widening one or more of the ostia FO, MO, as well as complete removal of the uncinate process UP. Incidentally, removal of the uncinate process UP is usually required even to just allow visualization of these sinus ostia FO, MO for the proper placement of the various surgical cutting instruments. Ethmoids are often treated with the FESS procedure by removing some of the wall of the ethmoid bulla EB and some of the “honeycomb” structure between the individual air cells.
• FIG. 4 illustrates a generic therapeutic approach contemplated by one embodiment of the invention. Rather than remove obstructing tissue associated with the sinus ostia FO, MO, adilation balloon10 is positioned in the narrowed region to dilate open the structure. Generally, the dilation balloon is carried on a distal end or region ofelongate member12 such as a balloon catheter. Theballoon catheter12 may include aproximal hub14 that includes aninflation port16 that is used inflate (and deflate) thedilation balloon10. For example, theinflation port16 may connect to a syringe or the like (not shown) using, for instance, a Leur lock connection. Theballoon catheter12 may be disposed within a central lumen of aguide catheter18. Theguide catheter18 may include aflexible tip portion18bas well as acurved portion20 that is used to navigate the tortuous pathway around the uncinate process UP. The proximal end of theguide catheter18 may include ahub22.
• Still referring toFIG. 4, awire guide24 is located within a central lumen in theballoon catheter12. Thewire guide24 inFIG. 4 is introduced into the maxillary sinus MS with the aid of theguide catheter18 and asteering device26. Thewire guide24 preferably has a curved tip24bsuch as a “J” bend located at or adjacent to adistal tip24aof thewire guide24. Thesteering device26 connects to a proximal end of thewire guide24 to allow rotation of thewire guide24, and subsequent rotation of the curved tip24bto steer and direct thewire guide24. As can be seen inFIG. 4, there is a relatively sharp bend that thewire guide24 andballoon catheter12 must traverse to enter into the maxillary ostial MO region. It is contemplated that aguide catheter18 may not be utilized at the time that theballoon catheter12 is positioned in the ostium of interest, but rather theguide catheter18 would be utilized just for placement of thewire guide24. In this case, theballoon catheter12 would be advanced over thewire guide24. This helps to minimize the size of the “hardware” that is present in the nasal cavity at any one time by allowing use of a smallerdiameter guide catheter18, and minimizes the amount of distortion required on various structures in the nasal cavity, such as the middle turbinate MT.
• Still referring toFIG. 4, dilation of the maxillary ostial MO region is accomplished by inflation of the balloon19 via theinflation port16 with an inflation apparatus (not shown) which may included, for example, a syringe. It is contemplated that a combination of remodeling the soft tissues as well as fracturing/crushing bony tissues will result in a more open drainage path for the sinus(es) being treated. WhileFIG. 4 shows aballoon catheter12 positioned in the maxillary sinus ostium (MO), it is contemplated that theballoon10 could be positioned in any of the sinus ostia, either naturally occurring ostia, or ostia created intra-procedurally. In particular, treatment of the ethmoid air cells ES may be accomplished by creating one or more small passageways in the walls surrounding the air cells, for example with a needle, followed up by a dilation process using thedilation balloon catheter12. Moreover, reference to a particular ostium does not necessarily mean an opening or passageway per se. Rather, reference to ostium may include the general region or anatomical area surrounding or adjacent to the ostium of interest and is not limited to a single, discrete structure or location.
• Access to the maxillary sinus ostium MO from within the nasal cavity is particularly challenging due in part to the anatomy of the uncinate process UP and infundibulum I.FIGS. 5A and 5B illustrate various embodiments of aguide catheter18 used to facilitate access to the maxillary sinus from the nasal cavity. InFIG. 5A, theguide catheter18 has a relatively tightcurved portion20 near thetip18b, with a preferred inside radius of curvature between about 0.5 mm and about 10 mm, and more preferably between about 1 mm and about 5 mm. Such a radius of curvature will assist in thetip18bof the guide catheter “hooking” around the uncinate process UP, to help direct thewire guide24 and subsequently theballoon catheter12 into the maxillary sinus ostium MO. The degree of bend of the curved portion of theguide catheter18 is preferably between 90 degrees and 180 degrees from the longitudinal axis of thehub22, and more preferably between 120 and 160 degrees.
• In one preferred aspect of the invention, theguide catheter18 includes ashaft portion18aand aflexible tip portion18b. Thetip portion18bis preferably of a softer material than theshaft portion18a.Tip portion18bmay formed of a polymer such as PEBAX (Arkema), polyurethane, NYLON (DuPont), HYTREL (DuPont), or silicone.FIG. 5B illustrates a cross-sectional view of one preferred embodiment of theshaft portion18b. As seen inFIG. 5B, aliner34 of a lubricious material such as PTFE defines acentral lumen36. Theliner34 is surrounded by awire braid32. Thewire braid32 is encased in a polymeric material such as PEBAX (Arkema), polyurethane (DuPont), NYLON (DuPont), HYTREL (DuPont), or silicone. Thewire braid32 adds torsional strength to theshaft18, allowing thecurved tip portion18bto be controlled and directed by manipulations near thehub22. Thetip portion18bmay be pre-formed by a suitable process such as heat forming.
• Alternatively, as shown in5C, theguide catheter18shaft portion18aand/ortip portion18bmay incorporate a shapingelement38, such as a removable wire. Thewire38 is preferably axially slidable within alumen40 formed in theguide catheter18. For example, differentpre-shaped wires38 may be axially slid within thelumen40 to impart the desired shape or bend in theguide catheter18. Alternatively, shapingelement38 could be a ductile non-removable wire that could be shaped and re-shaped to fit to a particular patient's anatomy. This feature advantageously allows the tip curvature or the curvature of any portion of theguide catheter18 to be customized by the user prior to or during a procedure.
• Alternatively, theshaft portion18bof theguide catheter18 can be formed of a metallic tube rather than the braid and jacket construction. This embodiment is illustrated inFIG. 5F. Preferably aliner34 is inside the metallic tube. Such a construction would allow theshaft portion18bto be shaped and reshaped to suit any particular anatomy.
• The diameter of theguide catheter18 is determined by the size of the devices that might pass through it. For example, if theguide catheter18 is used only for the placement of awire guide24 of 0.014 inch diameter, then theguide catheter18 may have an inner diameter of between 0.016 and 0.025 inches, and a total wall thickness of between 0.004 and 0.020 inches. However if theguide catheter18 is used to assist in placement of adilation balloon catheter12, the inner diameter is preferably between 0.040 and 0.100 inches, with a total wall thickness of between 0.005 and 0.030 inches. The outer diameter of theguide catheter shaft18aandtip18bis preferably uniform in diameter. The length of theguide catheter18 is preferably between about 8 and about 25 cm, and more preferably between about 10 and about 20 cm.
• FIG. 5D illustrates another embodiment of aguide catheter18 that is particularly useful for cannulating the maxillary sinus ostium MO. In this embodiment, thecurved portion42 is of a substantially larger radius of curvature compared to the embodiment shown inFIG. 5A. Rather than take a “direct” path up to and around the uncinate process UP, the embodiment shown inFIG. 5D makes use of the significant anterior-posterior space in the nasal passage NP. Thecurvature42 of theguide catheter18 may be formed using ashaping element38 of the type disclosed inFIG. 5C.
• FIG. 5E illustrates how theguide catheter18 shown inFIG. 5D makes a more gradual sweeping turn in the nasal cavity to reach towards the maxillary sinus ostium MO. By possessing a larger radius of curvature, any devices used inside thisguide catheter18 are not forced to negotiate such a tight bend. In a preferred embodiment, the inside radius of curvature is preferably between about 1 cm and about 3 cm, and more preferably between about 1.5 and about 2.5 cm.
• FIGS. 6A,6B, and6C show a preferred embodiment of adilation balloon catheter12 for dilation of a sinus ostium, particularly a maxillary sinus ostium MO. Theballoon catheter12 includes aballoon10,distal shaft portion12a,proximal shaft portion12b, and ahub14 with aninflation port16 for inflation of theballoon10. Theballoon catheter12 is formed using aninner tube50 coaxially arranged within an outer tube52 (described in more detail below). Aninflation lumen56 is formed between theinner tube50 and theouter tube52. Theballoon catheter12 terminates at adistal tip12cthat projects distally from theballoon10. Theballoon catheter12 may be formed as an “over the wire” design (as shown inFIGS. 6A-6C), but it is contemplated that it could be a “fixed wire” design or a “monorail” design, as is known in the balloon catheter art, particularly the coronary angioplasty art. However, the length of theballoon catheter12 shown is relatively short in comparison, preferably from about 10 to about 30 cm, and more preferably between about 15 and about 25 cm. The expanded diameter of theballoon10 would depend on the initial and final desired size of the sinus ostium to be dilated. Preferred diameters would be from about 2 mm to about 10 mm, and most preferably from about 3 to about 7 mm. A preferred “set” ofballoon catheters12 would include a series of catheters having inflated balloon diameters of 2, 4, 6, and 8 mm. Alternatively, a series ofcatheters12 having 3, 5, and, 7 mm expanded balloon diameters could be provided. Theballoon10 is preferably from about 5 mm to 40 mm in length (not including the conical portions), and more preferably from about 10 mm to about 20 mm in length.
• With particular reference toFIG. 6B, thedistal shaft portion12aof theballoon catheter12 is preferably of a coaxial construction, with aninner tube50 located inside of anouter tube52. The inner tube defines thewire guide lumen54 for passage of the wire guide24 (not shown inFIG. 6B). The annular space formed between the inner andouter tubes50,52 defines aninflation lumen56. Theinflation lumen56 may hold a fluid which is used to inflate theballoon10. In the embodiment ofFIG. 6B,lumens54,56 are coaxially arranged. However it is contemplated that a single tube with two side-by-side lumens54,46 could be utilized as well.
• Because of the anatomic challenge of accessing the maxillary sinus ostium MO, a preferred embodiment of theballoon catheter12 includes a kink-resisting structure in the shaft, particularly in thedistal shaft portion12a, as this is the portion of thecatheter12 that may be exposed to a particularly tight bend as it is advanced around the uncinate process UP. The kink resisting structure is preferably acoil58,60 or braid (not shown) that is incorporated into theinner tube50 and/or theouter tube52.FIG. 6B illustratescoils58,60 incorporated in both the inner andouter tubes50,52, respectively. If acoil58 is incorporated in theinner tube50, it is preferably included in the entiredistal portion12a, including that portion that traverses theballoon10. It is contemplated that for other constructions such as “fixed wire” or “rapid exchange” that the kink resisting structure could also be incorporated.
• Inner andouter tubes50,52 are preferably formed of a suitable material such as polyethylene, PEBAX (Arkema), PTFE, NYLON (DuPont), HYTREL (DuPont), or a combination thereof.Proximal shaft portion12bmay be more rigid thandistal portion12b, and may further incorporate a metallic tube (not shown) for either theinner tube50 or theouter tube52 of the proximal shaft region.
• To assist in positioning of theballoon catheter12 to a target site, one ormore shaft markers62 may be provided at one or more locations along the shaft of the balloon catheter. Preferably, themarkers62 are positioned in uniform increments (e.g., 1 cm increments) along the full length of the shaft (proximal region12banddistal region12a). Additionally, one ormore markers64 on theballoon10 may be provided. Both theshaft markers62 and theballoon markers64 are useful in positioning theballoon10 relative to thewire guide24 and/or guidecatheter18, together with prior or continuous optical visualization using a visualization tool such as an endoscope. Although not shown, thewire guide24 could also include markers spaced at predefined increments.Balloon markers64,shaft markers62, and/or wire guide markers (not shown) could make use of a color-coding system or some other recognizable pattern to facilitate endoscopic imaging. For instance, a certain color of marker could pertain to a certain distance from a particular location, such as the tip of thewire guide24 or the center of thedilation balloon10. Alternatively, one or more radiopaque markers (not shown) could be provided on the shaft underneath theballoon10 if fluoroscopic imaging is utilized.
• FIGS. 7A,7B, and7C show an alternative embodiment for a sinus ostiumdilation balloon catheter12. In addition to the structures associated with the catheter shown inFIGS. 6A and 6B, this embodiment further incorporates structure to facilitate the infusion and delivery of one or more therapeutic and/or diagnostic agents at the site of thedilation balloon10. In a preferred embodiment, a portion of theballoon catheter12 that extends proximally and distally with respect to theballoon10 includes anouter membrane70 with one ormore perforations72 in the membrane wall. The space between theballoon10 and themembrane70 is in fluid communication with an infusion lumen74 (shown inFIG. 7B) formed in the shaft of theballoon catheter12. Theinfusion lumen74 could be formed by the addition of aninfusion tube76 located on the outside of theouter tube52. Aninfusion port76 located in theproximal hub14 is in fluid communication with theinfusion lumen74.
• Theballoon catheter12 illustrated inFIGS. 7A-7C may be particularly useful for the delivery of an adhesion preventing substance such as MeroGel (Medtronic/Xomed) or Sepragel® (Genzyme Biosurgical/Gyrus ENT) prior to, during, or following the dilation process. This would result in a coating or “sleeve” of the agent being disposed on the contacted tissue region. The fact that the coating or “sleeve” would have an open passageway would provide for immediate ventilation and drainage of the treated sinus.
• FIGS. 8,9, and10 shows various embodiments of a stabilizingdevice80 for use with the device and methods disclosed herein. The stabilizingdevice80 is used to assist in holding and stabilizing one or more of the various tools used in the treatment of a sinus ostium. Since at times many devices may be in use, it may be difficult for the physician to manage all such devices. Use of a stabilizing device can free the hands to manage fewer devices at any given time. For example, the stabilizingdevice80 may be used to stabilize a guide catheter18 (as shown inFIG. 8), aballoon catheter12, and/or anendoscope82.
• The embodiment shown inFIG. 8 utilizes abase member84 which secures to various portions of the head H, such as the ears and/or top of the nose. Preferably, two ear hooks86 wrap around the ear in a similar way as eyeglasses. Thebase member84 also rests on the nose with anose bridge88. Asupport arm90 is secured to thebase member84. In one aspect of the invention, thesupport arm90, can preferably be manipulated or formed into any desired shape. For example, thesupport arm90 may be formed from a flexible material. A securingmember92 such as a clamp is located on the free end of thesupport arm90. The securingmember92 may be removable and/or interchangeable via a tightening member.Support arm90 and securingmember92 are held fast by a tighteningmember94 such as a tightening nut. In this figure, aclamp92 is shown stabilizing aguide catheter18, which allows the physician to use his or her hands on theendoscope82 and thewire guide24, while the position of theguide catheter18 is maintained. This may be helpful while the physician tries to advance thewire guide24 into the desired sinus. It is contemplated that more than one securingmember92 and/or more than onesupport arm90 could be mounted to thebase member84 to stabilize more than one device.
• The embodiment illustrated inFIG. 9, a stabilizingelement100 stabilizes a device against an interior surface of the nostril. As shown inFIG. 9, the stabilizing element is stabilizing aguide catheter18. In one preferred embodiment, the stabilizingelement100 is formed as an expandable tubular structure, such as a self-expanding tubular braid. In the expanded state, the tubular structure includes a lumen or passageway through which one or more devices may be placed. Theexpandable tube100 is positioned in the nostril next to the device(s) to be stabilized. Friction holds the device(s) in place, while maintaining a passageway for additional devices such as an endoscope (not shown inFIG. 9) to be introduced into the nasal cavity. More than oneexpandable tube100 could be used, either next to another, or in a nesting relationship.
• With reference now toFIGS. 10A,10B,100, and10D, a stabilizingdevice110 makes use of the patient's mouth M.A mouth piece112 is connected coupled to asupport arm114, which is connected to a securingmember116 such as a clamp to stabilize the position of a device such as aguide catheter18. Thesupport arm114 and clamp116 can be positioned, e.g. by rotating around pivot points, to bring theclamp116 to any desired position.FIG. 10B shows a top view of the stabilizingdevice110 in a partially exploded view. Themouth piece112 is configured to engage the upper and/or lower jaw of the patient. Thesupport arm114 is connected to themouth piece112, preferably by alockable pivot point118. Theclamp116 is likewise connected to thesupport arm114. A series of securingmembers120 such as locking screws or nuts locks theclamp116 position relative to the mouth M.
• FIG. 100 is a partially exploded frontal view of the stabilizingdevice110 ofFIG. 10B.FIG. 10D shows the stabilizing110 device in the fully assembled state. Again, one or more support arms and/or one ormore clamps116 could be used to stabilize multiple devices such asguide catheters18, wire guides24,endoscopes82, or other instruments used by the physician.
• FIGS. 11A,11B, and11C illustrate awire movement guide130 that is used to facilitate one-handed movement of both thewire guide24 and guidecatheter18. Thewire movement guide130 may be formed as a recessed handle or the like. As seen inFIG. 11C, during operation of theguide catheter18, asteering device26 is secured to thewire guide24. Thesteering device26 is able to slide axially and rotate in the movement path (as shown by arrows A and B inFIG. 11C). In a preferred embodiment, the recessedhandle130 includes ahub recess132 that is sized to receive thehub22 of theguide catheter18. For example, thehub recess132 may be sized to frictionally secure thehub22 within the same. Alternatively, one or more detents, tabs, or the like may be positioned on thehub recess132 and/orhub22 to releasably secure wire movement guide to thehub22 of theguide catheter18. Thewire movement guide130 also includes arecess134 for receiving thesteering device26. Therecess134 is dimensioned to permit axial and rotational movement of thesteering device26 as is shown inFIG. 11C. Thewire movement guide130 may also include awire recess136 for receiving thewire guide24. Thewire recess136 may be interposed between the tworecesses132,134. In addition, awire recess136 may be located at a proximal end of thewire movement guide130 to permit thewire guide24 to exit the proximal end of thewire movement guide130.FIG. 11B illustrates a cross-sectional view of thewire movement guide130.
• In an alternative aspect of the invention, thewire movement guide130 could be formed integrally with thehub22 or simply formed integrally on the proximal end of theguide catheter18.
• With the use of awire movement guide130, the physician can move theguide catheter18 into a desired position (preferably with the use of endoscopic imaging, as depicted inFIG. 11D), while simultaneously advancing and/or rotating thewire guide24 with a single hand. For example, the fingers could be manipulating thewire movement guide130 and therefore theguide catheter18, while the thumb is able to manipulate thewire guide24 to a desired position in the nasal cavity or sinus. A portion of the exterior surface of thesteering device26 may be scored, roughened, or otherwise textured to aid the physician in manipulating thesteering device26. Thewire movement guide130 advantageously permits the physician to use his or her other hand to independently manipulate another tool such as, for example, anendoscope82.
• One preferred embodiment for positioning awire guide24 into the maxillary sinus ostium MO is depicted inFIG. 11D. In this embodiment, theguide catheter18,wire movement guide130, and wire guide24 are manipulated under endoscopic visualization. Here, theendoscope82 is a “rigid” endoscope, a standard tool in nasal surgery. The rigid endoscope generally has a forward looking viewing field a which may or may not be offset, alight port82a, and aviewing port82bthrough which an image is obtained (indicated with an eyeball symbol). Theendoscope82 is used to help identify the uncinate process UP, and theguide catheter18 is “hooked” around the uncinate process UP. Additional tools such as a sinus “seeker” (not shown) can be utilized to help pull the uncinate process UP away from the opposite wall and make room for thetip18bof theguide catheter18. Once theguide catheter tip18bis positioned, thewire guide24 is manipulated by tactile feedback until it is felt to have passed into the maxillary sinus ostium MO and into the maxillary sinus MS.FIG. 11D illustrates asimplified obstruction138 located adjacent the uncinate process UP and maxillary sinus ostium MO. Thisobstruction138 may include mucous, inflamed mucosa, scar tissue, abnormal bony structure, or other substances. In this manner, only conventional endoscopic imaging is utilized—without the need for fluoroscopic imaging and/or other specialized “image guidance” technology. This same technique could be utilized for the other sinuses and their ostia as well. In addition, one or more of thestabilization devices80,100,110 previously described could be utilized as would be useful in this or any of the subsequently described methods.
• During operation of the device, it may be desirable to have a way to independently confirm that thedistal tip24aof thewire guide24 has been positioned in the desired sinus, and not inadvertently passed through some other structure, such as the orbital wall. Since the sinuses are difficult if not impossible to image with the standard rigid endoscopes, endoscopic imaging is not readily amenable for this confirmation. One such confirmation approach is illustrated inFIG. 12. As seen inFIG. 12, after thewire guide24 has been positioned in what is believed to be the desired location (maxillary sinus MS), afiber optic catheter140 is positioned over thewire guide24 and advanced distally towards the tip of thewire guide24. Thefiber optic catheter140 may be positioned using aguide catheter18 of the type illustrated inFIG. 12. Thedistal tip140aof thefiber optic catheter140 emits light142 that is input into thefiber optic catheter140 via alight port144. In one aspect of the invention, the emittedlight142 is bright enough such that it lights up or illuminates the sinus cavity and can be visualized externally. In this regard, the surrounding environment (e.g., physicians office) may need to have the level of ambient light reduced or turned off completely to aid in the visualization process.
• If a structure other than the desired sinus is illuminated, the physician or other operator knows that thewire guide24 has been improperly positioned and can subsequently be repositioned into the proper location. Once the position of thewire guide24 has been confirmed to be in the desired position, aballoon catheter12 can then be confidently placed into the sinus ostium (e.g., MO) and dilated.
• FIG. 13 illustrates an alternative embodiment for confirming the position of awire guide24. In this embodiment, thewire guide24 is fitted with adetection element150 at or near thedistal tip24a. In one aspect, thedetection element150 can be made of a magnetic material. A magnetic detection device (not shown) which could be as simple as a floating magnetic needle such as a compass needle may then be positioned outside the patient's face near the sinus to confirm the position of thewire tip24a. For example, in this case, the deflection of the magnetic needle would indicate the presence of the detection element150 (and thus thedistal tip24aof the wire guide24) within the desired sinus cavity.
• Alternatively, thedetection element150 could be formed from a dense metallic material that can be detected with a metal detector device (not shown). For example, the metal detector device may include a probe or the like that can be manipulated near to patient's face near the sinus cavity of interest to detect the presence (or absence) of themetallic detection element150. In yet another aspect, thedetection element150 may emit a signal (e.g., radiofrequency pulse or the like) that can then be detected externally to confirm the presence or absence of thedistal tip24aof thewire guide24 within the sinus cavity of interest.
• Independent confirmation methods and devices as described above may not be necessary if more versatile optical imaging techniques and devices are utilized in the placement of the various devices such as wire guides24,guide catheters18, and/orballoon catheters12. For instance,FIG. 14 illustrates a method for placing awire guide24 across a sinus ostium (e.g., maxillary ostium MO) with the aid of a directable orsteerable endoscope152.Directable endoscopes152 make use of flexible fiber optic bundles which can be bent or curved to alter the direction of theviewing field154. A typical construction of adirectable endoscope152 includes multiple control wires (not shown) connected near thedistal tip152aand to adeflection knob155. In this method, thedirectable endoscope152 is positioned superior to the uncinate process UP and then directed retrograde to allow direct viewing of theviewing field154 where theguide catheter18 and wire guide24 are being manipulated. To further aid in the identification of the maxillary sinus ostium MO, particularly in the case ofocclusion156 associated with sinusitis, the maxillary sinus MO is illuminated with the placement of asmall illumination member158 into the sinus. Theillumination member158 may be formed as an elongate member having a light-emittingdistal end158aand aproximal end158bthat is typically connected or otherwise coupled to alight source160. In one aspect, theillumination member158 is formed as a fiber optic light based device.
• Theillumination member158 can be placed into the sinus cavity of interest (e.g., maxillary sinus MS) by using a piercingmember162 such as, for example, anintroducer needle162 that is introduced through the canine fossa CF region. It should be understood that reference to the canine fossa CF refers to the general region or anatomical area surrounding or adjacent to the canine fossa CF and is not limited to a single, discrete structure or location. Theintroducer needle162 may include a hollow lumen or the like to permit the passage of theillumination member158. The canine fossa CF is a thin portion of the maxillary sinus wall located adjacent the root of the canine teeth. The canine fossa CF has been utilized for other intrasinus procedures. After the formation of apassageway164 through the canine fossa CF, theillumination member158 is advanced distally such that thedistal tip158aof theillumination member158 is disposed inside the sinus cavity. The emitted light162 in the maxillary sinus MS (or other sinus cavity) will be visible through theblockage156 of the ostium MO using thedirectable endoscope152. This aids the physician or other user to direct thewire guide24.
• FIG. 15 illustrates a similar method toFIG. 14, the difference being the use of a rigidretrograde endoscope170. A rigidretrograde endoscope170 is similar to a normal rigid endoscope, but the direction ofviewing field172 is in a retrograde direction. The rigidretrograde endoscope170 has a substantiallyrigid shaft portion173 and aretrograde viewing window174 located at or near thedistal tip170a. Retrograde visualization is accomplished through the use of one or more mirrors and/or lenses located at or adjacent to theviewing window174 to deflect theviewing field172. Since theviewing field172 is retrograde, thisendoscope170 can assist in accessing the sinus ostium in a similar manner as described with respect to the method shown inFIG. 14. One difficulty with a rigidretrograde endoscope170 is that it can be awkward to initially position it, since it cannot be used to see straight ahead. However, this difficulty is overcome by utilizing a normal rigid endoscope (not shown) alongside the retrograderigid endoscope170 to get it positioned initially in the nasal cavity. Again, anillumination member158 in the sinus, placed via the canine fossa CF, can be further utilized to aid in accessing the sinus ostium.
• Still other alternative methods for accessing the sinus ostium are illustrated inFIGS. 16A,16B, and16C. In these embodiments, aflexible visualization scope180 is utilized. Theflexible visualization scope180 includes an elongateflexible body182 that contains a flexible fiber optic bundle183 (as shown inFIG. 16C) for viewing around bends. Although not shown in the figures, thefiber optic bundle183 includes both “imaging” fibers and “illumination” fibers for lighting up theviewing field184. Theflexible visualization scope180 is not directable like theendoscope152 ofFIG. 14. Rather, theflexible visualization scope180 includes a lumen orpassageway185 for thewire guide24 and follows thewire guide24 around bends as illustrated inFIG. 16A.
• Consequently, in this method, particularly for a maxillary sinus ostium MO, aguide catheter18 having a curveddistal portion20 is positioned near or around the uncinate process UP. A conventional rigid endoscope (not shown) may be used to assist in this positioning. Next, thewire guide24 is positioned near thetip18bof theguide catheter18. Then theflexible visualization scope180 is advanced over thewire guide24, curving back in a retrograde fashion, allowing theviewing field184 to be directed towards the sinus ostium (MO in this case). A blockage is shown186 positioned within the maxillary ostium MO. Thewire guide24 and guidecatheter18 may then be manipulated under visual observation to access the ostium MO. Again, as has been mentioned previously, additional tools or the use of a “seeker” can be used in addition to thevisualization scope180, guidecatheter18 andwire guide24. In addition, the sinus cavity of interest may be illuminated using the canine fossa CF access method described above with respect toFIGS. 14 and 15.
• Another alternative device and method for accessing a sinus ostium is illustrated inFIGS. 17A,17B, and17C. In this embodiment, adirectable endoscope sheath190 is provided that has adeflectable tip190a. Thedirectable endoscope sheath190 is similar to thedirectable endoscope152 ofFIG. 14, but further includes a working channel orlumen192, as best seen inFIG. 16C, together with thedeflection wires194 and optical fibers196 (which contain both imaging and illuminating fibers). In use, thedirectable endoscope sheath190 can be introduced into the nasal cavity relatively straight, so as to see straight ahead. When thedirectable endoscope sheath192 is near the uncinate process UP, thetip190ais deflected retrograde using, for instance, adeflection knob197, so that theviewing field198 is directed towards the sinus ostium MO which contains anobstruction200. At this point, awire guide24 is positioned in the workinglumen192 and the ostium MO is accessed under visual observation.
• In one preferred embodiment, thedirectable endoscope sheath190 has a large enough workingchannel192 that aballoon catheter12 can be advanced into thesheath190 over thewire24. In this manner, aseparate guide catheter18 is not necessary. In yet another preferred embodiment, the workingchannel192 is only large enough to accommodate thewire guide24. This allows for thesheath190 to have a reasonably small outer diameter. Once thewire24 is positioned in the sinus, thedirectable endoscope sheath190 is removed from thewire24, leaving thewire24 in position. Thereafter, aballoon catheter12 can be installed over thewire24 and into the sinus ostium MO for dilation.
• FIGS. 18A and 18B illustrate adevice210 and method for accessing and dilating a sinus ostium (e.g., maxillary sinus ostium MO) via a direct sinus puncture technique, in contrast to a transnasal technique. This approach can generally be done with the frontal sinus FS and the maxillary sinus MS. While a description of thedevice210 and process is provided for the maxillary sinus MS, it should be understood thatsimilar access devices210 can be used with the frontal sinus FS.
• InFIG. 18A, atrocar212 is shown being advanced into the maxillary sinus MS via the canine fossa CF approach. Thetrocar212 includes ahollow cannula214 and aneedle216 contained within thelumen218 of thecannula214. Theneedle216 has asharp tip220 for penetrating the thin bone surrounding the sinus. Theneedle216 may be a solid piece or having one or more lumens therein. Once thecannula214 is inside the sinus, theneedle216 is then removed and thecannula214 serves as a guide catheter for subsequent devices. As an alternative to a needle-cannula type oftrocar212, a hollow sharpened needle could be used as well.
• Referring now toFIG. 18B, once thecannula214 is in place, awire guide24 and anendoscope222 can be introduced into the sinus. Thecannula214 is pointed towards the ostium MO, which points theviewing field224 to the ostium MO. Manipulation of thewire guide24 through use of asteering device26 then delivers thewire guide24 across the ostium MO which may contain ablockage200 as is shown inFIG. 18B. Optionally, anillumination member226 can be placed in the nasal cavity to “back-light” the ostium MO and enhance the ability for the ostium MO to be seen, further aiding the ability to direct thewire guide24 across the ostium MO. Alternatively, a bright light placed at the nostril may be adequate to perform this back-lighting.
• With the above-described “direct sinus puncture” technique such as through the canine fossa CF, various stabilization devices can be utilized to stabilize one or more of the various tools used for accessing and/or treating the ostium. For example, as shown inFIG. 18C, astabilization device110 is shown stabilizing thecannula214. Thestabilization device110 could also be used to stabilize thewire guide24, theendoscope222,trocar212, and/or theballoon catheter12. Similarly, any of the previously described stabilization devices can be utilized with the direct sinus puncture techniques.
• FIGS. 19A,19B, and19C illustrate various arrangements and types ofendoscopes222a,222b,222cthat can be used with this canine fossa CF approach. InFIG. 19A, the endoscope222ais a flexible visualization scope having a bundle ofoptical fibers228. The endoscope222afurther includes alumen230 through which thewire guide24 is fed.FIG. 19B shows arigid endoscope222bused next to thewire guide24, insidecannula214.FIG. 19C illustrates a similar arrangement to that shown inFIG. 19B, but with an additionaldual lumen catheter232 to better manage the positioning of thewire guide24 relative to therigid endoscope222c. In all these approaches, the diameter of theendoscope222a,222b,222cused is preferably small, about 0.5 mm to about 4 mm, and most preferably about 1 mm to about 2 mm. This allows for the use of a relatively small trocar and relatively small puncture size. Preferred trocar diameters are from 0.7 mm to 4.2 mm (depending on the size of the devices used with them), and more preferably from about 1 mm to 2.5 mm, and most preferably 1.2 to 2.0 mm.
• FIG. 20 illustrates the introduction of aballoon dilation catheter12 into thecannula214 and into the sinus ostium MO, dilating the ostium MO, and deforming and/or remodeling the uncinate process UP. To aid in the positioning of theballoon10, anoptional endoscope240 is placed in the nasal cavity may be used to visualize thecatheter tip12crelative to the uncinate process UP.
• Alternatively, the position of theballoon10 may not require “real time” visualization with an endoscope, if various markers on the wire guide and/or balloon catheter shaft as described earlier are utilized. For example, if thewire guide24 includes markers, the marker that is seen at or near the ostium can be noted. Markers on the proximal portion of thewire guide24 can then be used to determine the “depth” that thewire guide24 has been advanced to reach the ostium. Theballoon catheter12 can then be advanced a distance over thewire guide24 a predetermined distance on thewire guide24, such that theballoon10 is positioned at a desired position relative to the noted marker on thewire guide24.Markers62 on the shaft of theballoon catheter12 can aid in this positioning. With this use ofmarkers62, theballoon10 can be confidently positioned in the desired region of the sinus ostium. The desired length of the balloon can be selected by viewing the computed tomography (CT) scans of the patient, which are part of a standard diagnostic workup of the patient prior to any intervention.
• Though not shown, once the maxillary ostium MO has been treated, the ethmoids and/or frontal sinuses ES, FS can also be treated by this same canine fossa access. Thewire guide24 can be manipulated into the ethmoids and/or frontals, with subsequent dilation of the ostia of these sinuses. Similar endoscopic visualization techniques as described above can also be utilized to assist in placement of the various devices such as thewire guide24 to these locations. In the case of the ethmoids, it may be desirable to use a sharpened wire in lieu of awire guide24 to puncture into the wall of the ethmoid sinus air cells, followed by balloon dilation of the puncture.
• As mentioned above, the frontal sinus FS can also be accessed directly from outside the skull, through the wall of the frontal sinus FS to facilitate treatment of the frontal sinus ostium FO. Rather than a trocar, the frontal sinus FS can be directly accessed through a mini trephination through the skin and the sinus wall, as is known in the art. With a mini-trephination, the access is performed with a drill tool. Once accessed, the frontal sinus ostium FO may be directly accessed with awire guide24. A preferred location for accessing the frontal sinus FS is through the floor of the frontal sinus FS. Since the frontal sinus FS is relatively small, and there is only one outflow tract and its position can be approximated relative to the nose, visualization may not be required to pass thewire guide24 through the frontal sinus ostium FO and into the nasal cavity. Standard endoscopic visualization could be performed in the nasal cavity via the nostrils to observe thewire guide24 after it passes into the nasal cavity. Subsequent to passing thewire guide24 into the frontal ostium FO, aballoon dilation catheter12 can be positioned in the ostium FO to dilate it.
• Although the maxillary sinus MS is easily accessible via the canine fossa CF, it is important to control the depth of the initial puncture so as to not inadvertently advance theneedle216 too far and potentially into the orbit O or elsewhere.FIG. 21 illustrates atrocar212 with astop250 secured to a portion of thetrocar212. Thestop250 prevents theneedle216 from advancing too far into the sinus cavity. In one aspect, thestop250 is clamped on to either theneedle216 or thecannula214 at a predetermined position. In a preferred embodiment of the invention, thestop250 is adjustable and/or removable with respect to the fixation point (e.g.,needle216 or cannula214). For example, thestop250 may include one ormore tightening members252 such as screws or the like that can be selectively tightened or loosen thestop250. Once thetrocar212 is inserted up to thestop250, thestop250 is removed. Thecannula214 can then be advanced with little force, as the puncture site has already been made.
• FIG. 22 shows analternative trocar212 arrangement for improving the control of the puncturing into the canine fossa CF. Here, theneedle216 includesneedle threads216alocated on an exterior surface thereof. Thethreads216aof theneedle216 engage with a threadedhub254 in a threaded interface. The threadedhub254 may be in the form of a “clamshell” of two treaded pieces orhalves254a,254bthat surround and engage theneedle threads216a. The position of the threadedhub254 may be held fast by attachment to a stabilizing device such as the stabilizingdevices80,110 shown inFIGS. 8 and 10. Theneedle216 is then advanced into the canine fossa CF by controlled rotation of theneedle216. Once theneedle216 has penetrated or traveled the desired amount, the threadedhub254 is removed, and thecannula214 is advanced to a desired position within the sinus. Alternatively, the threadedhub254 could be attached to a stabilizingdevice80,110 in a manner that allows rotation of the threadedhub254 about theneedle threads216a, by utilizing a bearing surface (not shown) with the stabilizingdevice80,110. The threadedhub254 when rotated would controllably advance theneedle216 into the sinus. In this manner, theneedle216 is not rotated.
• Sometimes the desired direction and positioning for placing thetrocar212 in the canine fossa CF does not provide good alignment with the location of the sinus ostium. In this case, atrocar212 having aflexible tip260 can be used, as shown inFIGS. 23A and 23B. InFIG. 23A, thecannula214 has a somewhat flexiblecurved tip260, that, inFIG. 23A, is maintained straight by the presence of theneedle216. Thistrocar212 is advanced into the sinus. Upon removal of theneedle216, theflexible tip260 takes on its curved shape, more oriented to the ostium MO. Thereafter awire guide24 is advanced across the ostium MO, preferably under the visual guidance of aflexible visualization scope262 as shown inFIG. 23B. Thevisualization scope262 is preferably dimensioned such that it can be slidably passed through thecannula214. Theflexible visualization scope262 includes a lumen orpassageway264 for thewire guide24. Theflexible visualization scope262 is able to be oriented to place thevisualization field266 within the vicinity of the ostium MO. Manipulation of thecurved tip260 of thecannula214 can assist in directing thewire guide24 to and through the ostium MO. Also as shown, the nasal cavity can be back-lit using anillumination member268 to aid in seeing the ostium. Also, other tools and methods may be used as desired, such as, for example, thetrocar212 modifications illustrated inFIGS. 21 and 22.
• FIG. 24 illustrates another device and method for accessing the maxillary sinus ostium MO via the canine fossa CF. In this embodiment, twosmall punctures270,272 are made, side-by-side in the canine fossa CF region. Apuncture device210 like that disclosed inFIG. 18A may be used. For example, arigid endoscope274 is positioned in thecannula214 of thefirst puncture site270. Awire guide24 is then positioned in thecannula214 of thesecond puncture site272. One or more of thecannulas212 may have acurved tip260 to better access the maxillary sinus ostium MO. Thewire guide24 may then be positioned across the ostium MO under the visualization of therigid endoscope274. A balloon dilation catheter (not shown in FIG.24) may then be advanced over thewire24 to dilate the sinus. The ostial region may be back-lit using anillumination member276.
• FIGS. 25A and 25B illustrate a common anatomical characteristic present in patients with sinusitis associated with the maxillaries, ethmoids, and frontals. The uncinate process UP is shown in close association with the opposite wall, typically on the ethmoid bulla EB. This condition creates a narrow slit-like space called the infundibulum I. The maxillary sinus ostium MO is actually located below (i.e., inferior to) the infundibulum I.FIG. 25B more clearly shows the “topography” of the structures of the uncinate process UP and ethmoid bulla EB. It is believed that a narrowed infundibulum I may be part of the condition leading to the patient's sinusitis, as well as one or more narrowed ostia. In some patents, a narrowed infundibulum I may be the sole anatomical cause leading to sinusitis.
• The previously described approaches to dilating the maxillary sinus ostium MO may result in a widening of the infundibulum I by deforming or remodeling the uncinate process UP, as well as the widening of the ostium MO itself. However, in some patients, the uncinate process UP may not stay permanently deformed following removal of thedilation catheter12.
• An alternative approach to widening the infundibulum I is illustrated inFIGS. 26A and 26B. One ormore shim members280 are placed in the gap of the infundibulum I to forcibly spread it away from the ethmoid bulla EB and improve drainage for the maxillary, frontal and portions of the ethmoid sinus. In one preferred aspect of the invention, the one ormore shim members280 are left in place after implantation. Theshim members280 may remain in place for a temporary period of time or permanently. The sinus ostium may still be dilated with the use of aballoon dilation catheter12.FIG. 26B illustrates threesuch shim members280 secured in the infundibulum I. As seen inFIG. 26B, the gap is widened to expose the maxillary sinus ostium MO.
• FIGS. 27A and 27B illustrate one preferred embodiment of ashim member280. Theshim members280 may be dimensioned such that one or more sides are longer than the remaining sides. For example, theshim member280 may be longer than it is wide, with a length dimension preferably about 1 mm to about 6 mm in length, and more preferably about 2 mm to about 4 mm in length. Theshim members280 may include one or moregripping members282 on all or a portion of an exterior surface. The grippingmembers282 may be formed as a serrated surface or even a plurality of teeth or similar projections. As seen inFIGS. 27A and 27B, the grippingmembers282 are located on opposing sides of theshim member280 to allow for theshim member280 to be rotated into position and held in place.
• Theshim member280 may include one ormore engagement holes284 that are used for the delivery of theshim member280. For example, the engagement holes284 may be dimensioned to fit on the distal end of a tool as shown inFIG. 28. Theshim member280 may be a permanent implant, or more preferably a degradable bioabsorbable implant. Suitable materials for adegradable shim member280 include poly-lactic acid, poly-glycolic acid, poly-L-lactic acid or other materials such as those used in degradable sutures. It is believed that after theshim members280 are implanted in the infundibulum I, the uncinate process UP will remodel over time to maintain a widened infundibulum.
• FIG. 28 illustrates adelivery tool290 for use in the delivery of the shim member(s)280. Thedelivery tool290 includes anelongate torque driver292 constructed of a multi-layer, multi-filar drive shaft similar to that used in speedometer cables. Thetorque driver292 is dimensioned to be positionable within aguide catheter18 or the like. Theshim member280 is connected to thetorque driver292 at itsdistal end292a. Theproximal end292bof thetorque driver292 is coupled to ahandle294 or the like that is used to rotate the torque driver292 (and attached shim member280) in the direction of the arrows shown inFIG. 28.
• Theguide catheter18 is used to place theshim member280 over the uncinate process UP and in the narrowed infundibulum I, initially in a narrow or “sideways” orientation. Thetorque driver292 is then rotated by rotation of thehandle294. Rotation of about 60 to about 90 degrees will widen the infundibulum I as shown inFIG. 26B. The connection between thetorque driver292 and theshim member280 is disconnected. This could be done, for example, by reversing the rotational direction of thetorque handle294 and causing a weakened portion of the connection to break. Alternatively, thetorque driver292 may be frictionally engaged with theholes284 of theshim member280. Retraction of thetorque driver292 in the proximal direction may disengage thetorque driver292 from theshim member280. Once place, the one ormore shim members280 will maintain the infundibulum I in a widened condition, while minimizing the interruption of the mucosa by the presence of the shim member(s)280.
• Alternatively, as shown inFIG. 29, the infundibulum I can be widened by delivery of anexpandable stent300, oriented more or less in the infundibulum I. Thisstent300 can be similar to that used in coronary stenting procedures, and can be either “self-expanding” or “balloon expandable.” The geometry of thestent300 may be tubular as is shown inFIG. 29. Thestent300 can be placed in the infundibulum I using aballoon catheter12 and awire guide24. As one example, thestent300 may be positioned via a transnasal approach wherein thewire guide24 is directed along the infundibulum1 up towards the frontal sinus ostium FO (as shown inFIG. 3C) and then deployed between the uncinate process UP and the ethmoid bulla EB.
• While embodiments of the present invention have been shown and described, various modifications may be made without departing from the scope of the present invention. The invention, therefore, should not be limited, except to the following claims, and their equivalents.

Claims (12)

1.-107. (canceled)

108. A system for dilating tissue of a drainage pathway of a sinus cavity of a patient comprising:

a guide catheter secured to a distal end of a handle, the handle defining a recess that opens along a longitudinal length of a side surface of the handle;

a steering device disposed in the recess and configured to slide along the recess in a direction parallel to a major longitudinal axis of the handle and further configured to rotate;

a wire guide extending through the guide catheter and the steering device, wherein rotation of the steering device effectuates rotation of the wire guide through complete revolutions while the steering device is positioned within the steering device recess; and

a balloon catheter having a central lumen, wherein the wire guide extends through the central lumen, the balloon catheter further comprising an inflatable balloon.

109. The system ofclaim 108, wherein the proximal end of the guide catheter includes a hub.

110. The system ofclaim 109, wherein the distal end of the handle comprises a hub recess configured to receive the hub.

111. The system ofclaim 110, wherein the guide catheter is releasably secured to the hub recess by at least one of detents or tabs.

112. The system ofclaim 110, wherein the guide catheter is releasably secured to the hub recess by a frictional fit.

113. The system ofclaim 108, wherein the steering device is textured.

114. The system ofclaim 108 further comprising a light emitting elongate member configured to emit light within a sinus cavity.

115. The system ofclaim 114, wherein the light emitting elongate member is a fiber optic catheter disposed over the wire guide.

116. The system ofclaim 114, wherein the emitted light has a brightness sufficient to be viewed external to the patient to confirm the location of the wire guide within the sinus cavity.

117. The system ofclaim 108, further comprising a directable endoscope.

118. The system ofclaim 117, wherein the directable endoscope comprises a knob disposed thereon and configured to direct a viewing field of the endoscope.

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