US20100121337A1 - Device for drilling angled osteal tunnels - Google Patents

Abstract

A surgical drill guide device for drilling an angled osteal tunnel having an support rack having a first end and a second end; a drill guide sleeve having a passage for receiving a drill therethrough, the drill guide sleeve being adjustably securable and positionable on the rack between the first end and the second end of the rack; and a guide component secured on the first end of said rack, the guide component having a suture seizing mechanism for seizing a suture.

Description

BACKGROUND OF THE INVENTION
• 1. Technical Field
• The present invention generally is related to the field of osteal guides, surgical drilling systems and methods and devices for drilling osteal tunnels, and more particularly is related to osteal guides capable of being used for drilling angled osteal tunnels.
• 2. Related Art
• The anterior and posterior cruciate ligaments in the knee assist in providing stability to the function of the knee. The cruciate ligaments control gliding, sliding, and rotation of the knee. To accomplish this, the anterior and posterior cruciate ligaments function according to the principles of a crossed four bar linkage, which is closely related to and dependent upon the bony constraints of the surrounding bones. Thus, the anatomic origin and insertion of both of the ligaments is crucial. Often the anterior cruciate ligament (ACL) becomes ruptured or torn, requiring replacement and reconstruction of the ligament in order to restore normal usage of the knee. When the ACL is restored or replaced, the ACL or a substitute synthetic or harvested graft must be reattached to the bone. The ACL graft is anchored in place either inside or outside of osteal tunnels or passages formed in the tibia or femur. It is preferential to locate and drill the tunnels at precise locations so the ACL will be reattached at the natural location or so the graft will be implanted in the optimum position. If a ligament reconstruction is performed in the appropriate location, then normal motion and stability can be restored. Otherwise, the ligament will eventually be too loose or too tight for normal function.
• Similarly, tissue repair to the shoulder area, such as reattaching torn rotator cuff tendons to bone, also can be accomplished through open surgery or arthroscopic surgery. Because open surgery introduces potential problems with the trauma associated with the large area of skin, muscle and tissue that must be incised to perform such surgery, arthroscopic surgery is preferred because it has the advantages of requiring only a small incision, thus reducing the risk of infection, blood loss and the like sometimes caused by open surgery. The rotator cuff can be reattached to the humerus by suturing the tendon to the bone by passing the suture through a transosteal tunnel drilled through the proximal portion of the humerus. The location at which the tunnel is to be drilled is paramount because the axillary nerve, a major nerve which innervates the deltoid muscle, lies close to the preferred reattachment site. Movement of the shoulder may be impaired if the axillary nerve is damaged. Often, this results in a tunnel being close to the surface of the bone, which tunnel may have a thin wall and therefore be relatively weak and subject to breaking.
• The repair of torn ligaments by anchoring them into an osteal tunnel created within the affected bone is dependent upon complex interdependencies between the ligaments of a human body. Not only must an osteal tunnel be created so as to provide optimal positioning and tension, but avoidance of major nerves, blood vessels, and other anatomical obstructions also dictate the positioning of the tunnels. Further, while it may be desirable for surgeons to employ their discretion in selecting the entrance site of the osteal tunnel, limitations in visibility and accuracy considerations dictate that surgical positioning instruments are needed to ensure that an osteal tunnel has a precise drill exit point. Often, surgeons are required to work in an area that is “boxed in” by nerves, which gives rise to a need for surgeons to forego the use of conventional surgical positioning instruments that might interfere with these delicate areas.
• There are several limitations to current techniques of fixing soft tissue to bone. The primary methods can be divided into two categories, the implementation of bone tunnels or the use of fixation devices such as suture anchors. The latter carries the risk of implant complications including infection and bony osteolysis in addition to failure of fixation. Transosseous tunnels are a more attractive option. Current transosseous tunnel techniques can be divided into two types. The first involves the creation of a straight tunnel using guides placed on the surface of the bone and drilling from one point to the other. The second involves the creation of curved tunnels using drilling or awling devices that begin at both entry point of the tunnel and meet in the middle. However, these techniques are limited by technical constraints including the size of the bony bridge, surgical exposure required to allow for access to the bone, and anatomical constraints such as nerve and vessel proximity. As such, these limitations further limit the use of transosseous techniques in the setting of arthroscopic surgery, especially in the shoulder. This is because such this type of surgery is performed through limited exposure and is technically constrained by anatomic landmarks.
• Surgical drill guides for use in drilling precision transosteal tunnels through bone are known in the art. For example, U.S. Pat. Nos. 5,163,940, 5,330,468 and 6,120,511 all disclose surgical drill guides. Drill guide devices, such as those taught in the above-referenced patents, generally comprise a housing having an axial opening, a probe connected to the housing and having a tip that is adapted to be disposed within the interior of the joint at the distal point where one end of the tunnel is to exit the target bone, and a guide wire sleeve for directing a guide wire into position on the surface of one of the bones of the joint. The housing is connected to the probe by an adjustable rack that is generally of a circular arc configuration. The housing is arranged so that its axial opening is more or less aligned to intersect with the aforementioned probe tip, and the guide wire sleeve is generally slidable or variable in position within the housing's axial opening. The relative angular position of the probe and the guide wire sleeve contained within the housing is slidably adjustable on the rack in order to accommodate differently sized human bones and joints. All of the aforementioned parts are held in relation to one another by releasable locking means known in the art.
• The guide wire sleeve is positioned such that a guide wire can be inserted into the bone in order to properly position a drill. Once the guide wire is inserted, the sleeve is removed from the guide wire, leaving the guide wire embedded in the bone. A cannulated drill bit is then positioned about the guide wire and a straight hole is drilled to the exit point initially marked by the tip of the probe. A suture is then affixed to, through, or around the torn ligament, and the suture or both are drawn into the osteal tunnel by a needle eye or alligator clamp that is run through either the sleeve, the osteal tunnel, or both. The suture is then tied in a knot, stapled to the bone, or the instrument used to pull the suture through the osteal tunnel remains in the tunnel as an anchor which must later be removed from the bone.
• In use, the drill guide device tip is placed at the desired exit point of the tunnel and the guide wire sleeve is positioned at the desired entry point of the tunnel. A drill bit is inserted through the guide wire sleeve and a tunnel is drilled through the bone from the guide wire sleeve (entry point) to the tip (exit point). Generally, the tunnel is a straight bore in the form of a hypotenuse across the corner of the bone. With smaller bones, this tunnel can be very close to the surface of the bone, and therefore the tunnel wall closest to the surface of the bone can be thin and weak.
• Each of the disclosed prior art guides are for performing straight transosteal tunneling, which can result in a weakening of the bone, especially when the tunnel created is close to the bone surface, or the guides require entry or exit points for the tunnel which are difficult to access. Further, prior art guides do not allow for flexibility in the positioning on the entrance point of the osteal tunnel, which is desirable when a surgeon meets with biological obstacles such as nerves or blood vessels. Also, many different and complex instruments are required to perform the completed surgery, which makes the surgery more difficult and susceptible to error. Finally, prior art methods of attaching the suture to or within the bone often require either a complex procedure to secure the suture, or a second surgery to remove an embedded anchoring device.
• Accordingly, there is a need for an improved osteal guide, more particularly an osteal guide with improved stability and performance, resulting in improved tunnel strength. There is also a need for an improved method for drilling osteal tunnels, more particularly angled osteal tunnels, which allows a surgeon to be both flexible and accurate in the placement of the osteal tunnels. Further, there is a need for improved osteal guide components that simplify surgery while maintaining accuracy. Finally, there is a need for an improved device for securing or anchoring sutures used in ligament reconstruction. It is to these and other needs that the present invention is directed.
BRIEF SUMMARY OF THE INVENTION
• Briefly, the present invention comprises:
• (a) Osteal guides capable of facilitating the accurate drilling of an angled osteal tunnel, namely, an osteal tunnel having an angle or turn within the bone, which guides also can allow for the preparation or creation of an angled osteal tunnel having an intraosseous angle;
• (b) Methods for drilling an angled osteal tunnel in which a first tunnel portion can be drilled free-hand into the bone, a second tunnel portion can be drilled into the bone using a guide component to guide the drill bit to the interior end (the end of the tunnel within the bone, the exterior being at the surface of the bone), such that the two portions of the tunnel intersect and connect at an angle, which methods also can include the intraosseous (that is, blind or without direct visualization) retrieval of sutures from within the osteal tunnel;
• (c) Guide components that can be inserted into the first tunnel portion and can function as a guide into which the drill bit is aimed for drilling the second tunnel portion and for receiving and seizing a suture or another feeding device, such as a wire, inserted through the second tunnel portion (or alternatively if the suture is inserted through the first tunnel portion, the guide component can be inserted into the second tunnel portion for receiving and seizing a suture inserted through the first tunnel portion);
• (d) Retrieving systems to grab or seize a suture or another suture-feeding device, which retrieving systems also can allow for the intraosseous (that is, blind or without direct visualization) retrieval of sutures from within a bone; and
• (e) Suture anchoring methods and components that can secure or anchor a suture from within or outside of an osteal tunnel when a suture is positioned within an anchor and the anchor is compressed and deformed tightly about the suture.
• For the purposes of this specification, the term “drilling” includes all forms of tunnel creation performed by physicians, such as, but not limited to, drilling with bits or wires, tamping, punching, and using awls.
• As shown inFIG. 1, a typical prior art surgical drill guide comprises three primary components: a guide sleeve through which a drill bit is passed for drilling the osteal tunnels through a bone, a guide tip for guiding the drilling direction of the drill bit, and a rack onto which the guide sleeve and the guide tip are mounted. The guide sleeve and/or guide tip are typically slidably mounted on the rack, which may be arcuate, such that different angles of osteal tunnels can be drilled through the bone. The guide sleeve also can be displaceably mounted on the rack such that different sized bones can be accommodated and different lengths of osteal tunnels can be drilled.
• In the device of the present invention, the typical guide tip is replaced with a novel guide component that facilitates the drilling of an angled osteal tunnel, namely an osteal tunnel having a first portion drilled from one surface of the bone, a second portion drilled from a second surface of the bone, wherein the first portion and the second portion intersect and connect at an angle in the interior of the bone. This guide component is structured to be insertable into the first tunnel portion so as to guide the drilling of the second tunnel portion at the appropriate angle and depth to connect and intersect with the first tunnel portion within the interior of the bone. The resulting tunnel generally will have straight or approximately straight first and second portions intersecting at an angle such that the tunnel as a whole will be more within the interior of the bone and farther away from the surface of the bone than a typical transosteal tunnel, resulting in a stronger tunnel. An angled osteal tunnel created in this manner gives a surgeon the ability to allow small distances between the entry sites into the bone and at the same time have a sufficiently strong bony bridge to maintain the integrity of the surgical site.
• In the method of the present invention, the first tunnel portion can be and preferably is drilled or punched free-hand at a predetermined distance into any bone in a human body located a suitable distance from a torn tendon or ligament, such as those in the hand, elbow, shoulder, ankle, and knee. Various devices can be used in conjunction with the free-hand drilling or punching such that the first tunnel is drilled in a proper direction, at a proper angle and for a proper distance. For example, drill stops known in the art can be attached to the drill bit or the drill guide to set or limit the depth of the drilling.
• After the first tunnel portion is drilled or punched into the bone, the guide component is inserted into the first tunnel portion a certain distance, usually a distance equal or approximately equal to (but not necessarily) the length of the first tunnel portion. The guide sleeve then is adjusted on the rack to allow for a drilling angle and distance desired for the second tunnel portion. The second tunnel portion then is drilled or punched using the guide sleeve, guide component, and rack configuration (that is, not free-hand) whereby the second tunnel portion is drilled or punched at a specific angle and length so as to intersect and connect with the first tunnel portion. The configuration of the guide sleeve and guide component on the rack provides that the guide sleeve is angled directly at the interior (inserted) end of the guide component such that the second tunnel is drilled directly at the interior end of the guide component. The guide component can include a target at the interior end, specifically, a hole or open area, such that the drill bit passes through the target and does not contact the guide component. The devices and methods of this invention thus can allow the surgeon to drill an angled osteal tunnel without direct visualization of the intersection of the first tunnel portion and the second tunnel portion.
• After the second tunnel is drilled, the guide component can be left in place in the first tunnel portion such that a suture or wire inserted into the length of the second tunnel portion can reach the guide component. The guide component also can have a suture seizing mechanism, so that the suture or wire can be seized by this suture seizing mechanism, and the suture or wire can be pulled through the first tunnel portion. Thus, the present guide component can allow for the retrieval of a suture from within a bone without direct visualization of the interior of the osteal tunnel or the osteal tunnel end points. Alternatively, a wire having a loop at one end can be pulled through the osteal tunnels so that a suture can be inserted into the loop and pulled back through the osteal tunnels. One end of the suture or wire can be attached to the ligament or muscle in known manners, and another end of the suture can be attached to the bone in known manners, or tied together to the ends of other sutures emanating from other tunnels, or anchored together with sutures emanating from other tunnels using the novel anchor and anchoring method of the present invention. A suture also can be tied off in a “mattress” tying method, by looping a suture around a torn ligament or tendon in a mattress suture pattern, and then pulling the suture, and often with it, a portion of the tendon, into the tunnel. In another illustrative embodiment, one or more ends of a suture that have been drawn through an angled osteal tunnel can be wrapped around both the torn ligament or tendon and the bony bridge between the tunnel entrances and tied or stapled off.
• In the guide component of the present invention, the interior end (the end that is inserted into the osteal tunnel) comprises a target and a suture seizing ring. For example, the guide component can be a cylinder having a grip and trigger mechanism on the exterior end and a target ring and piston or pestle on the interior end. Alternatively, hinged scissor handles can be used on the exterior end. The target ring can be structured to accommodate the drill bit exiting the second tunnel portion as the drill bit causes the second tunnel portion to intersect and connect with the first tunnel portion. The trigger mechanism or scissor handles can be squeezed or engaged to force the piston or pestle axially in the cylinder and into the target ring so as to pin a suture or wire against the inner surface of the target ring, thus seizing the suture. Thus, the suture can inserted into the second tunnel portion, or can be gripped by a suture inserter and inserted into the second tunnel portion, a distance where the suture interacts with the guide component such that the suture can be seized by the guide component. As the guide component is removed from the first tunnel portion, the captured suture or wire is pulled through the tunnel. Suture inserters are known and can have a mechanism for gripping and releasing the suture, such as a claw grip.
• An illustrative alternative of the method for creating osteal tunnels includes drilling or punching multiple second tunnel portions all intersecting and connecting with a single first tunnel portion. For example, a single first tunnel portion can be drilled as disclosed previously. After the first tunnel portion is drilled, the guide component is inserted into the first portion a certain distance as disclosed previously. The guide sleeve is then moved to a first location on the surface of the bone and is adjusted on the rack to allow for a drilling angle and distance desired for a first second tunnel portion. This first second tunnel portion then is drilled using the guide sleeve, guide component, and rack configuration as disclosed previously so as to intersect and connect with the first tunnel portion. The guide sleeve then is moved to a second location on the surface of the bone and is adjusted on the rack to allow for a drilling angle and distance desired for a second second tunnel portion. This second second tunnel portion then is drilled using the guide sleeve, guide component, and rack configuration in the same manner as the first second tunnel portion so as to intersect and connect with the first tunnel portion. The guide sleeve then can be moved to drill third and additional second tunnel portions, all of which intersect with the first tunnel portion.
• A suture or wire is inserted into each of the second tunnel portions so as to reach the guide component. The sutures are seized by the suture seizing mechanism of the guide component, preferably all at once but potentially individually, and are pulled through the first tunnel portion. One end of each of the sutures can be attached to the ligament or muscle in known manners, and other ends of the sutures can be attached to the bone in known manners, or tied together to ends of other sutures emanating from other tunnels, or anchored together with sutures emanating from other tunnels using the novel anchor and anchoring method of the present invention. Sutures also can be tied off in the “mattress” tying method, or by wrapping the suture around both the torn ligament or tendon and the bony bridge between the tunnel entrance and tied or stapled off, as disclosed earlier. The second tunnel portions can be in a fan-shaped configuration or in a linear configuration, or any geometric configuration, relative to the first tunnel portion.
• Another illustrative alternative of the method for drilling osteal tunnels includes drilling a number of second tunnel portions for intersecting with a smaller number of first tunnel portions such that at least one first tunnel portion intersects and connects with at least two second tunnel portions. This alternative is similar to the alternative disclosed above, but at least two first tunnel portions are drilled, and at least three second tunnel portions are drilled, with at least two of the second tunnel portions intersecting and connecting with one of the first tunnel portions.
• In the anchor component of the present invention, at least one suture extending through the tunnel can be secured using an anchor, thus avoiding the use of knots or a staple into the bone. An illustrative anchor is an oval device through which one or more sutures can extend. The anchor is then compressed or deformed to anchor the suture, thus preventing the suture from being pulled back through the tunnel. In the multi-tunnel embodiments, the multiple sutures all can be passed through a single anchor. Alternatively, knots can be used to secure a suture in accordance with the present invention.
• The present invention, including both the devices and the methods, can be performed during open surgery and during arthroscopic surgery. The present invention also can be used or performed generally anywhere on a human body affected by a torn muscle, ligament or tendon.
• The present invention involves both methodology and tools necessary to allow for the creation of angled tunnels, including the blind creation of angled osteal tunnels, and the intraosseous retrieval of sutures from osteal tunnels. This entails the use of an intraosseous guide, a feeder and retrieval system. The resultant tunnels provide robust bony bridges even with minimal distance between the surface points of entry and exit on the bone, can be created through limited exposure, and the technique may be performed arthroscopically, especially in the shoulder. Arthroscopic surgery of the shoulder to repair a torn rotator cuff involves fixation of the torn tendon to bone. Straight tunnels are precluded because the closer the point of entry and exit, the more shallow the tunnel and the weaker the bony bridge. The setting of arthroscopic rotator cuff repair allows for an excellent example of the utility of the present invention.
• These features, and other features and advantages of the present invention will become more apparent to those of ordinary skill in the art when the following detailed description of the preferred embodiments is read in conjunction with the appended figures.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a prior art surgical drill guide device.
• FIG. 2A is an elevational view of an embodiment of the present invention having a movable drill guide.
• FIG. 2B is a top plan view of the present invention shown inFIG. 2A, further showing the attachment of the drill guide.
• FIG. 2C is bottom plan view of an embodiment of the guide component with suture seizing mechanism of the present invention.
• FIG. 3 is a perspective view of a human bone showing an angled osteal tunnel drilled using the method and device of present invention and having a single entrance and exit point.
• FIG. 4 is a perspective view of a human bone with an angled osteal tunnel similar to that shown inFIG. 3, showing the typical positional relationships of both the drill guide and guide component with suture seizing mechanism ofFIG. 2A and showing scissor handles on the suture seizing mechanism.
• FIG. 4A is a top cross-sectional view of a human bone as shown inFIG. 4 showing the typical positional relationship of the guide component with suture seizing mechanism within the angled osteal tunnel.
• FIG. 5 is a schematic cross-sectional view of a human bone showing an embodiment of the suture seizing mechanism and method of the present invention in use prior to the seizing of a suture.
• FIG. 6 is a schematic cross-sectional view of a human bone showing an embodiment of the suture seizing mechanism and method of the present invention in use subsequent to the seizing of a suture.
• FIG. 7 is a schematic cross-sectional view of a human bone showing osteal tunnels having one entrance point and multiple exit points formed by an alternate embodiment of the method of the present invention.
• FIG. 8 is a perspective view of a human bone showing osteal tunnels having multiple entrance points and one exit point formed by an alternate embodiment of the method of the present invention.
• FIG. 9 is a perspective view of a human bone showing osteal tunnels having one entrance point and multiple exit points formed by an embodiment of the method of the present invention.
• FIG. 10 is a perspective view of an embodiment of the anchor of the present invention showing the typical positioning of a suture to be anchored.
• FIG. 11 is a perspective view of an embodiment of the anchor of the present invention showing an alternate method for anchoring multiple sutures within the same anchor.
• FIG. 12 is a perspective view of the anchor ofFIG. 10 in a deformed and anchored position about a suture.
• FIG. 13 is a perspective view of a human bone showing the anchor and alternate method for anchoring multiple sutures within the same anchor ofFIG. 11 in use, with multiple sutures emerging from multiple osteal tunnel exit points.
• FIG. 14 is a perspective view of a human bone, anchor, and sutures ofFIG. 13, showing the anchor in a deformed and anchored position about the multiple sutures.
• FIG. 15A is a cross-sectional side view of an embodiment of a guide component showing an illustrative suture seizing mechanism.
• FIG. 15B is a top plan view of an illustrative insertion end of an embodiment of a guide component with the seizing pestle in the retracted position.
• FIG. 15C is a top plan view of an illustrative insertion end of an embodiment of a guide component with the seizing pestle in the extended or seizing position.
• FIG. 16 is an alternate embodiment of the invention shown inFIG. 2A having a movable guide component and showing a straight rod and plunger suture seizing mechanism.
• FIG. 17 is an alternate embodiment of the invention shown inFIG. 2A having a movable drill guide and a movable guide component.
• FIG. 18A is a perspective view of a clamp and tightening screw that can be used with the movable drill guide and/or movable guide component.
• FIG. 18B is a cross-sectional side view of a clamp and tightening screw shown inFIG. 18A.
• FIG. 19 is a perspective view of a human bone showing an alternate method for tying and anchoring a ligament with a suture between osteal tunnels.
• FIG. 20 is a perspective view of a suture feeding sleeve as part of the present invention.
• FIG. 21 is a cross-sectional side view of the suture feeding sleeve ofFIG. 20 in use.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
• The following detailed description of preferred embodiments is presented only for illustrative and descriptive purposes and is not intended to be exhaustive or to limit the scope and spirit of the invention. The embodiments were selected and described to best explain the principles of the invention and its practical applications. One of ordinary skill in the art will recognize that many variations can be made to the invention disclosed in this specification without departing from the scope and spirit of the invention.
• Illustrative embodiments of a device and method for drilling angled osteal tunnels and anchoring sutures therein according to the present invention are shown inFIGS. 2A through 9.FIG. 2A is an elevation view of an embodiment of the present invention having a movable drill guide.FIG. 2B is a top plan view of the present invention shown inFIG. 2A, further showing the attachment of the drill guide.FIG. 2C is bottom plan view of an embodiment of the guide component with suture seizing mechanism of the present invention.
• FIG. 3 is a perspective view of a human bone showing an angled osteal tunnel drilled using the method and device of present invention and having a single entrance and exit point.FIG. 4 is a perspective view of a human bone with an angled osteal tunnel similar to that shown inFIG. 3, showing the typical positional relationships of both the drill guide and guide component with suture seizing mechanism ofFIG. 2A and showing scissor handles on the suture seizing mechanism.FIG. 4A is a top cross-sectional view of a human bone as shown inFIG. 4 showing the typical positional relationship of the guide component with suture seizing mechanism within the angled osteal tunnel.
• FIG. 5 is a schematic cross-sectional view of a human bone showing an embodiment of the suture seizing mechanism and method of the present invention in use prior to the seizing of a suture.FIG. 6 is a schematic cross-sectional view of a human bone showing an embodiment of the suture seizing mechanism and method of the present invention in use subsequent to the seizing of a suture.FIG. 7 is a schematic cross-sectional view of a human bone showing osteal tunnels having one entrance point and multiple exit points formed by an alternate embodiment of the method of the present invention.FIG. 8 is a perspective view of a human bone showing osteal tunnels having multiple entrance points and one exit point formed by an alternate embodiment of the method of the present invention.FIG. 9 is a perspective view of a human bone showing osteal tunnels having one entrance point and multiple exit points formed by an embodiment of the method of the present invention.
• FIG. 10 is a perspective view of an embodiment of the anchor of the present invention showing the typical positioning of a suture to be anchored.FIG. 11 is a perspective view of an embodiment of the anchor of the present invention showing an alternate method for anchoring multiple sutures within the same anchor.FIG. 12 is a perspective view of the anchor ofFIG. 10 in a deformed and anchored position about a suture.FIG. 13 is a perspective view of a human bone showing the anchor and alternate method for anchoring multiple sutures within the same anchor ofFIG. 11 in use, with multiple sutures emerging from multiple osteal tunnel exit points.FIG. 14 is a perspective view of a human bone, anchor, and sutures ofFIG. 13, showing the anchor in a deformed and anchored position about the multiple sutures.
• FIG. 15A is a cross-sectional side view of an embodiment of a guide component showing an illustrative suture seizing mechanism.FIG. 15B is a top plan view of an illustrative insertion end of an embodiment of a guide component with the seizing pestle in the retracted position.FIG. 15C is a top plan view of an illustrative insertion end of an embodiment of a guide component with the seizing pestle in the extended or seizing position.
• FIG. 16 is an alternate embodiment of the invention shown inFIG. 2A having a movable guide component and showing a straight rod and plunger suture seizing mechanism.FIG. 17 is an alternate embodiment of the invention shown inFIG. 2A having a movable drill guide and a movable guide component.
• FIG. 18A is a perspective view of a clamp and tightening screw that can be used with the movable drill guide and/or movable guide component.FIG. 18B is a cross-sectional side view of a clamp and tightening screw shown inFIG. 18A.
• FIG. 19 is a perspective view of a human bone showing an alternate method for tying and anchoring a ligament with a suture between osteal tunnels.
• FIG. 20 is a perspective view of a suture feeding sleeve as part of the present invention.FIG. 21 is a cross-sectional side view of the suture feeding sleeve ofFIG. 20 in use.
• The present invention is an improved drill guide device for drilling osteal tunnels and methods for using the same, and components to be used therewith. The present invention is suitable for use in conjunction with ACL and rotator cuff ligament repair surgery in humans, as well as other human ligament, muscle and tendon repairs. Currently, there is a need for devices and methods for creating angled osteal tunnels in conjunction with human ligament, muscle and tendon repair that allows users to be both accurate and flexible, as wells as devices to simplify surgery, improve surgical results, and minimize errors. There is a further need for intraosseous devices and methods for creating osteal tunnels and retrieving sutures from within osteal tunnels without having to see or visualize within the bone or osteal tunnels.
• FIG. 1, shows is an illustrative example of a knownsurgical drill guide201 comprising three primary components: adrill guide sleeve202 through which a guide wire and/ordrill bit203 is passed for drilling theosteal tunnel204 through thebone205; aguide tip206 for guiding the drilling direction of thedrill bit203 or guide wire; and arack207 onto which thedrill guide sleeve202 and theguide tip206 are mounted, which may be arcuate in shape. Thedrill guide sleeve202 and/orguide tip206 are typically slidably mounted on therack207 such that different angles ofosteal tunnels204 can be drilled through thebone205. Thedrill guide sleeve202 also can be displaceably mounted on therack207 such that differentsized bones205 can be accommodated and different lengths ofosteal tunnels204 can be drilled.
• Referring now toFIGS. 2A,2B and2C, an illustrative example of thesurgical tool8 of the present invention comprises aguide component10 mounted to an end of rack7 which may be arcuate in shape, and adrill guide sleeve2 slidably or removably mounted to the rack7, which is capable of being securely positioned about the rack7, toward either end. Theguide component10 facilitates the drilling of an angled osteal tunnel11 (FIG. 3), namely anosteal tunnel11 having afirst tunnel portion12 drilled from afirst surface12aof thebone5, asecond tunnel portion13 drilled from asecond surface13aof thebone5, wherein thefirst tunnel portion12 and thesecond tunnel portion13 meet at anintersection14 and connect at anangle15 in the interior of thebone5. Theguide component10 is structured to be insertable into the first tunnel portion12 (FIG. 4) so as to guide the drilling of thesecond tunnel portion13 at theappropriate angle15 and depth to connect with thefirst tunnel portion12 at theintersection14 within the interior of thebone5. The resultingosteal tunnel11 generally will have straight or approximately straight first andsecond portions12,13 intersecting at anangle15 such that theosteal tunnel11 as a whole tends to be situated deeper within the interior of thebone5 and farther away from the surface of thebone5 than a typical transosteal tunnel, resulting in astronger osteal tunnel11.
• Theguide component10 of one embodiment of thesurgical tool8 comprises aninterior end16, which is inserted into anosteal tunnel11 within abone5 during a surgical procedure. Theinterior end16 comprises atarget ring17 and asuture seizing pestle18. Theguide component10 further comprises anexterior end19, which is mounted on an end of rack7. Agrip20 and atrigger mechanism21 facilitate the operation of thetarget ring17 andsuture seizing pestle18, such that a suture22 (seeFIG. 5) or wire can be seized within anosteal tunnel11 and pulled from an entrance point at the surface of thebone5 to an exit point at another location at the surface of thebone5. For example, theguide component10 can be a hollow cylinder attached to the rack7 at theexterior end19 and having a blunt or rounded tip. Theguide component10 also has an opening near the tip of theinterior end16 that forms thetarget ring17. The opening within thetarget ring17 may be round, oval, or otherwise shaped so as to accommodate a suture.
• Theguide component10 of another embodiment of thesurgical tool8 comprises aninterior end16 having anawl tip16aand anexterior end19 having a tampingplate19a. Depending on the conditions and quality of thebone5 in which the osteal tunnel is formed, it may be preferable to tamp or punch any portion of the angled osteal tunnel4 using a punching device with a sharp tip, such as an awl. A surgeon can punch an osteal tunnel4 by either pushing theawl tip16ainto thebone5, or using a hammer or other suitable object to tap the tampingplate19a, thus driving theawl tip16aof theguide component10 into thebone5. Theguide component10 can remain in a tamped or punchedfirst tunnel portion12, and thedrill guide sleeve2 can be coupled with a drill to create asecond tunnel portion13. Alternatively, asecond tunnel portion13 is tamped or punched in a similar manner using a punching device, such as anawl tip16awith a tampingplate19a.
• In a preferred embodiment, thedrill guide sleeve2 is a hollow tube through which an osteo drill can be operated, and is of a structure generally known in the art. In an embodiment in which thedrill guide sleeve2 is movable on the rack7, thedrill guide sleeve2 is slidably mounted on the rack7 by aclamp23 and tighteningscrew24 so that the positioning of thedrill guide sleeve2 is adjustable about the length of the rack7. Alternatively, thedrill guide sleeve2 can be fastened to the rack7 by a clip, a bolt, or any other means known in the art to securely fix thedrill guide sleeve2 in the desired position on the rack7. In the present invention, and as is disclosed in more detail below, it is preferable that thedrill guide sleeve2 is movable on the rack7 and that theguide component10 is fixed on the rack7 because, as theguide component10 is placed into afirst tunnel portion12 that has been drilled free-hand without the use of adrill guide sleeve2, theguide component10 supports the rack7 so that thedrill guide sleeve2 can be moved to any convenient position about the rack7 for drilling thesecond tunnel portion13. The preferably rigid attachment of theguide component10 to the rack7 assists in ensuring that thesecond tunnel portion13, when drilled, will accurately intersect thefirst tunnel portion12 without regard to the position of thefirst tunnel portion12, forming a functional angled osteal tunnel4. However, as disclosed in conjunction withFIGS. 16 and 17, in alternate embodiments either or both of thedrill guide sleeve2 and guidecomponent10 can be slidably mounted on the rack7.
• Referring now toFIG. 3, in a preferred embodiment of the method of the present invention, thefirst tunnel portion12 is drilled from a preferredfirst surface12aof thebone5 to a predetermined depth into thebone5. Drilling can be performed free-hand or with a drill guide. Free-hand drilling is performed without the aid of a drill guide, where afirst tunnel portion12 is created by any means known in the art, but preferably using a surgical drill and drill bit3 or by punching or tamping a tamping plate19ato create a hole with anawl tip16a. After a preferredfirst surface12aof thebone5 is chosen, a first tunnel portion can be created by positioning the drill bit3 over thefirst surface12aand engaging the drill. Thefirst tunnel portion12 is drilled to a predetermined depth, which may be gauged by indicia on the drill or the drill bit3. The depth of thefirst tunnel portion12 is limited to avoid drilling from one surface to an opposing surface of thebone5.
• Referring now toFIG. 4, which shows thesurgical tool8 of the present invention in use, after thefirst tunnel portion12 is drilled, theguide component10 is positioned in thefirst tunnel portion12, and thedrill guide sleeve2 is placed at the desired position at thesecond surface13aof thebone5. A drill bit3, sometimes referred to as an osteo drill bit, is aimed by thedrill guide sleeve2 and can be used to drill a measured distance into thebone5 to create thesecond tunnel portion13, which intersects within the interior of thebone5 at anangle15 withfirst tunnel portion12. Thetarget ring17 on theinterior end16 of theguide component10 can be structured to accommodate a drill bit3 drilling thesecond tunnel portion13 through to thefirst tunnel portion12. More specifically, and as disclosed in more detail in conjunction withFIG. 15, when the drill bit3 exits thesecond tunnel portion13 and enters thefirst tunnel portion12, the drill bit3 can pass into and through the center of thetarget ring17 without touching theguide component10.
• After thefirst tunnel portion12 is drilled, theguide component10 is inserted into thefirst tunnel portion12 a certain distance, usually a distance equal or approximately equal to (but not necessarily) the length of the first tunnel portion12 (see alsoFIG. 4A). The interior end ofguide component10 is within the bone and generally cannot be seen with the naked eye. Thedrill guide sleeve2 then is adjusted on the rack7 so that thedrill guide2 is located proximal to the position on thesecond surface13aof thebone5 where it is desired to drill thesecond tunnel portion13. The positioning of thesurgical tool8 with theguide component10 within thefirst tunnel portion10 and thedrill guide sleeve2 proximal to the surface of thebone5 where thesecond tunnel portion13 is to be drilled allows for a proper drilling location and angle for thesecond tunnel portion13. This feature is advantageous because regardless of the relative position or length of thefirst tunnel portion12, a user is able to use thesurgical tool8 to achieve any desired entrance or exit point into or out of thebone5 for thesecond tunnel portion13 such that asuture22 can be threaded and to avoid encountering impediments such as nerves or blood vessels. In other words, the location of thesecond surface13ais not dependent upon the location of thefirst surface12aand provides a user a great amount of freedom in selecting the entrance and exit points of the angled osteal tunnels4.
• After thedrill guide sleeve2 is positioned at the chosensecond surface13aand clamped into place on the rack7, thesecond tunnel portion13 then is drilled using a drill bit3 inserted through thedrill guide sleeve2. The rack7 is structured, and thedrill guide sleeve2 and guidecomponent10 attached to rack7, such that theguide sleeve2 points towards thetarget ring17. Thus, the positioning of thedrill guide sleeve2, theguide component10, and the rack7 provides for a drilling configuration (that is, not free-hand) whereby thesecond tunnel portion13 is drilled at aspecific angle15 and length so as to intersect and connect with thefirst tunnel portion12 at apoint14. The drill bit3 then is removed from thedrill guide sleeve2. Thedrill guide sleeve2 also can be removed from thesecond tunnel portion13. Thetarget ring17 now is generally aligned with the axis of thesecond tunnel portion13. Alternatively, use of an awl or an awl-tippedguide component10 or other drilling or tunneling devices and methods can be used.
• Theguide component10 and thedrill guide sleeve2 preferably are selectively positionable relative to each other on the rack7 between the first end and the second end of the rack7 such that when the interior end of theguide component10 is located within afirst tunnel portion12 drilled into thebone5, thedrill guide sleeve2 directs the drill towards thetarget ring17, whereby asecond tunnel portion13 drilled into thebone5 intersects at anangle15 to thefirst tunnel portion12. Preferably, theangle15 is greater than 0° and less than 180°. More preferably, theangle15 is between approximately 10° and approximately 170°. Theangle15 also can be between approximately 45° and approximately 135°.
• In one embodiment of the method of the present invention, once thesecond tunnel portion13 of the angled osteal tunnel4 has been completed, the drill bit3 is removed, and theguide component10 and thedrill guide sleeve2 can be left in place. Referring now toFIGS. 5 and 6, asuture22, which may or may not be attached to a torn or synthetic ligament, is fed into thedrill guide sleeve2 and through thesecond tunnel portion13. Alternatively, thedrill guide sleeve2 can be removed and thesuture22 fed directly into thesecond tunnel portion13. Thesuture22 or wire may be fed into thesecond tunnel portion13 by any appropriate suture inserter known in the art, including a needle, an alligator clamp, a wire loop, or other known means. Thesuture22 is inserted a distance such that thesuture22 interacts with theguide component10 such that thesuture22 can be seized by theguide component10. In a preferred embodiment, thesuture22 interacts with thetarget ring17 on theinterior end16 of theguide component10, namely is inserted through thetarget ring17, and is seized when a suture clamping component, such assuture seizing pestle18, in effect clamps thesuture22 against thetarget ring17, as disclosed below in conjunction withFIG. 15.Trigger mechanism21 or scissor handles40 move thesuture seizing pestle18 into the fixedtarget ring17, or alternatively, move thetarget ring17 toward the fixedsuture seizing pestle18. Thesuture22 seized by theguide component10 is pulled through and out of the angled osteal tunnel4 when theguide component10 is removed from thesecond tunnel portion13 while thetrigger mechanism21 or the scissor handles40 are engaged or squeezed. Such aguide component10 therefore allows for the intraosseous retrieval of sutures. This is, thesuture22 is within thebone5, in the angledosteal tunnel12,13, and theguide component10 allows for the retrieving of thesuture22 from within thebone5 without having to look within thebone5.
• In one illustrative embodiment, the suture seizing mechanism of theguide component10 is a grip andtrigger mechanism21, wherein the trigger is movable relative to the grip and the trigger is operatively connected to the suture seizing component, such assuture seizing pestle18, whereby moving the trigger relative to the grip causes the movement of the suture seizing component. In another illustrative embodiment, the suture seizing mechanism is a hinged scissors handle40 mechanism wherein one scissor handle is movable relative to another scissor handle and one scissor handle is operatively connected to the suture seizing component, such assuture seizing pestle18, whereby moving the scissor handles relative to each other grip causes the movement of the suture seizing component.
• Referring now toFIG. 5, theguide component10 is left in place in thefirst tunnel portion12 and asuture22 is inserted into the length of thesecond tunnel portion13, in a manner and/or using a device as already disclosed, so as to reach the guide component10 (seeFIG. 4). Once inserted into and through thesecond tunnel portion13, thesuture22 passes into thetarget ring17, which has been left in place in thefirst tunnel portion12. Once thefirst tunnel portion12 is drilled and theguide component10 is inserted, thetarget ring17 is aligned with the direction of thedrill guide sleeve2 such that both a drill bit3 and asuture22 fed into thesecond tunnel portion13 through thedrill guide sleeve2 will communicate with and be inserted into thetarget ring17 when inserted to the proper depth.
• Referring now toFIG. 6, once thesuture22 is inserted to a proper depth so as to enter into thetarget ring17, thesuture22 is seized and firmly held by the interaction of thetarget ring17 and thesuture seizing pestle18 when thegrip20 andtrigger mechanism21 are engaged by squeezing them together, or alternatively, when the scissor handles40 are engaged. It should be understood that other preferred embodiments of the suture seizing mechanism may employ other means known in the art to move thesuture seizing pestle18 within thetarget ring17 to grasp asuture22 including electronically-operated mechanisms. With thegrip20 andtrigger mechanism21 in the engaged or squeezed position, thesuture22 is pulled through and out of thefirst tunnel portion12 where it can be tied or otherwise secured within the osteal tunnel4 or outside of thebone5. For example, one end of thesuture22 can be attached to the ligament or muscle in known manners, and another end of thesuture22 can be attached to thebone5 in known manners. Alternatively, the attachment methods and means of the present invention, as disclosed in conjunction withFIGS. 10-14 and19, are preferred.
• FIGS. 7,8, and9 show illustrative alternatives of the method for drilling or punching osteal tunnels4, including drilling multiple osteal tunnels4 connected by one intersecting osteal tunnel4 and drilling multiple angled osteal tunnels4 emanating from one entrance point at the surface of thebone5. The present invention allows the user to more easily drill multiple osteal tunnels4 and multiple intersectingosteal tunnels12,13 so as to provide a better anchor for ligaments, tendons and muscle.
• Referring now toFIG. 7, an alternate method for drilling angled osteal tunnels4 of the present invention is shown. A firstsecond tunnel portion25 and a secondsecond tunnel portion26 can be drilled in a linear configuration. The multiplesecond tunnel portions25,26 intersect and connect with a singlefirst tunnel portion12. For example, a singlefirst tunnel portion12 can be drilled or punched free-hand as disclosed previously at a desiredfirst surface12aof the bone. After thefirst tunnel portion12 is drilled, theguide component10 is inserted into thefirst tunnel portion12 a certain first distance. Thedrill guide sleeve2 then is moved to a desired location at a firstsecond surface25 of thebone5 and is adjusted on the rack7 at the desired firstsecond surface25aof thebone5 to allow for a drilling location, angle and distance desired for a firstsecond tunnel portion25. This firstsecond tunnel portion25 then is drilled using thedrill guide sleeve2,guide component10, and rack7 configuration as disclosed previously so as to intersect and connect with thefirst tunnel portion12 at a first intersecting point4a. Theguide component10 then can be moved axially within thefirst tunnel portion12 a certain second distance, different than the first distance. Thedrill guide sleeve2 then is moved to a second first surface26aof thebone5 and is adjusted on the rack7 to allow for a drilling location, angle and distance desired for a secondsecond tunnel portion26. This secondsecond tunnel portion26 then is drilled using thedrill guide sleeve2,guide component10, and rack7 configuration in the same manner as the firstsecond tunnel portion25 so as to intersect and connect with thefirst tunnel portion12 at a second intersecting point4b. Theguide component10 and thedrill guide sleeve2 then can be moved to drill third and additional second tunnel portions (not shown), all of which can intersect with thefirst tunnel portion12 at other intersecting points.Sutures22 can be inserted into each of thesecond tunnel portions13,25,26, etc., seized one at a time by the suture seizing mechanism, and pulled through thefirst tunnel portion12, to be secured using the methods and devices disclosed herein. The second tunnel portions can be parallel to each other, as shown inFIG. 7, in parallel planes to each other, or at angles to each other, as desired or required by the circumstances.
• Referring now toFIG. 8, another alternate method for drilling angled osteal tunnels4 of the present invention is shown. A firstsecond tunnel portion25, a secondsecond tunnel portion26, and a thirdsecond tunnel portion27 can be drilled in a fan-shaped configuration, or any geometric configuration relative to thefirst tunnel portion12. This method includes drilling a number ofsecond tunnel portions25,26,27, and more if desired, for intersecting with a smaller number offirst tunnel portions12 such that at least onefirst tunnel portion12 intersects and connects with at least twosecond tunnel portions25,26, for example. This alternative is similar to the alternative disclosed above, but at least threesecond tunnel portions25,26,27 are drilled, with at least two of the second tunnel portions,25,26, for example, intersecting and connecting with one of thefirst tunnel portions12. Athird tunnel portion28 also can be drilled to intersect with one of the second tunnel portions. Various configurations of intersecting first, second, and third tunnel portions are envisioned to enhance the anchoring of the tendons, ligaments or muscles. One limitation to the number of tunnels drilled is, of course, the size and thickness of thebone5 and the available area with which to work, and the ability to pass sutures through the connecting tunnel portions.
• As shown inFIG. 8,third tunnel portion28 intersects with thirdsecond tunnel portion27 but not with thefirst tunnel portion12. As described above, thefirst tunnel portion12 is drilled free-hand. Theguide component10 is inserted into thefirst tunnel portion12 and thedrill guide sleeve2 is positioned to create thirdsecond tunnel portion27. Then, theguide component10 is inserted into thirdsecond tunnel portion27 and thedrill guide sleeve2 is positioned to createthird tunnel portion28 which does not intersectfirst tunnel portion12.Sutures22 then can be pulled through the various tunnel portions as described above.
• Referring now toFIG. 9, in still another illustrative alternate method for drilling angled osteal tunnels4, multiple first tunnel portions,30,31,32, are drilled free-hand. Theguide component10 is inserted into firstfirst tunnel portion30, and thedrill guide sleeve2 is positioned above anentrance point33 to create a firstsecond portion30a. Theguide component10 is next inserted into secondfirst tunnel portion31, and thedrill guide sleeve2 is again positioned aboveentrance point33 to create second second tunnel portion31a. Similarly, theguide component10 is inserted into thirdfirst tunnel portion32, and thedrill guide sleeve2 is positioned aboveentrance point33 so that thirdsecond tunnel portion32acan be drilled. Thus, all of thesecond tunnel portions30a,31a,32aexit thebone5 at thesame location33. This configuration also can be done in reverse, with each of the first tunnel portions having the same entrance point. In this example, first tunnel portions would be shown byreference numerals30a,30b,30c, and second tunnel portions would be shown byreference numerals30,31,32. Usingentrance point33, firstfirst tunnel portion30a, second first tunnel portion30b, and third first tunnel portion30cwould all be drilled free-hand fromentrance point33.Guide component10 is inserted into firstfirst tunnel portion30a, and thedrill guide sleeve2 is positioned proximal tobone5 so as to be able to drill firstsecond tunnel portion30.Guide component10 then is inserted into second first tunnel portion30b, and thedrill guide sleeve2 is positioned proximal tobone5 so as to be able to drill secondsecond tunnel portion31.Guide component10 then is inserted into third first tunnel portion30c, and thedrill guide sleeve2 is positioned proximal tobone5 so as to be able to drill thirdsecond tunnel portion32.Sutures22 then can be pulled through the various tunnel portions as described above.
• In each of the preferred and alternate methods disclosed herein, sutures22 can be tied together to the ends ofother sutures22 extending out of other osteal tunnels4, or anchored together withsutures22 extending out of other osteal tunnels4 using the novel anchor29 (seeFIGS. 10-14) and anchoring method of the present invention. A suture can also by tied off in a “mattress” tying method, by looping a suture around a torn ligament or tendon in a mattress suture pattern, and then pulling the suture, and with it, the tendon, into the tunnel.
• Referring now toFIGS. 10-14, the present invention also includes ananchor29 and method for anchoring sutures. In theanchor29 and anchoring method, ananchor29 is depressed or deformed about asuture22 needing to be anchored proximal to abone5 to prevent thesuture22 from being pulled back through thebone5. Thisanchor29 eliminates the need for the introduction of an invasive anchoring device into thebone5 itself, such as a staple, or the elaborate tying of the ends of thesutures22 in knots or to other anchoring devices lodged within or outside of thebone5.
• Referring now toFIG. 10, at least onesuture22 or a wire extending through an angled osteal tunnel4 can be secured using ananchor29, thus avoiding the use of knots or a staple into thebone5. Anillustrative anchor29 is an oval device through which at least onesuture22 can extend. As shown inFIG. 11,multiple sutures22 can be threaded through oneanchor29. As shown inFIG. 12, after at least onesuture22 is threaded through theanchor29, theanchor29 is then compressed or deformed to anchor29 the at least onesuture22, thus preventing the at least onesuture22 from being pulled back through the osteal tunnel4. In the multi-tunnel embodiments, as depicted inFIGS. 7,8, and9, themultiple sutures22 all can be passed through asingle anchor29. As shown inFIG. 13, aftermultiple sutures22 are pulled through an angled osteal tunnel4, the ends of thesutures22 are drawn through theanchor29. As shown inFIG. 14, when theanchor29 is depressed or deformed aboutsutures22, thesutures22 are prevented from being pulled back into the osteal tunnels4.
• Anchor29 preferably is manufactured out of a deformable or malleable metal or material, which, after being deformed, resists both further deformation and returning to the original shape. Representative shapes of theanchor29 include a round or oval ring. Other preferred shapes include a U-shape or other open-ended or self-threading shape. Any other shape known in the art suitable for accommodating asuture22 within is acceptable. Theanchor29 also can have a curved shape that mimics or is similar to the curve of the surface of abone5, such that if theanchor29 is pulled back against thebone5 by thesutures22, theanchor29 can lie relatively flush against the surface of thebone5. Theanchor29 can be deformed using pliers, forceps, tweezers, or other means for applying pressure from opposing sides. Theanchor29 is deformed until it tightly grips thesuture22.
• In another exemplary alternate embodiment of the suture anchoring method of the present invention, asuture22 is threaded through ananchor29, and then a tendon, ligament or muscle is also threaded through ananchor29. Theanchor29 is then depressed or deformed about thesuture22 and tendon, ligament or muscle. Thesuture22 may be threaded through an osteal tunnel4, and the other end of thesuture22 can be anchored on the outside of thebone5 with anotheranchor29. Also, ananchor29 can be used to join together to the ends ofother sutures22 to increase their length by threading one end through theanchor29 and then threading the end of anothersuture22 into theanchor29 and deforming or depressing theanchor29 to secure the ends of thesutures22.
• FIG. 15A illustrates a cross-sectional side view of anillustrative guide component10 showing an illustrative suture seizing mechanism. The scissor handles40 are positioned on theexterior end19 and operate asuture seizing pestle18 within theguide component10, preferably within a hollow cylinder or another form suitably-shaped for insertion into anosteal tunnel11. As also shown inFIG. 15B, thesuture seizing pestle18 is within the cylinder when the scissor handles40 are not squeezed or engaged such that it does not block the opening of thetarget ring17. As also shown inFIG. 15C, when engaged, the scissor handles40 move thesuture seizing pestle18 toward theawl tip16aof the cylinder and through the opening of thetarget ring17, which securely presses thesuture seizing pestle18 against the tip of the cylinder or the edge of thetarget ring17 on theinterior end16, thus trapping thesuture22. As a result, the end of asuture22 fed into anosteal tunnel11 is directed into thetarget ring17, and can be gripped by thesuture seizing pestle18 when thesuture22 is pinched between thesuture seizing pestle18 and the wall, ring, or tip of theinterior end16 when the scissor handles40 are engaged. This allows thesuture22 to be easily pulled through an angledosteal tunnel11. It should be understood to those skilled in the art that the scissor handles40 orgrip20 andtrigger mechanism21 used to engage thesuture seizing pestle18 in thetarget ring17 are only examples of embodiments of the present invention, and that any suitable means for engaging thesuture seizing pestle18 can be used.
• Thetarget ring17 is on theinterior end16 of theguide component10 and, in one embodiment of thesurgical tool8 of the present invention, is a circular or oval hole in cylindrical guide component10 (FIGS. 2A and 4). The circular or oval void defined by thetarget ring17 is suitable for accommodating a typical drill bit3 so that the drill bit3 is directed into the void so that the drill bit3 does not drill into or damage the body of theguide component10.
• In an alternate embodiment of the present invention, thesuture seizing pestle18 is stationary and fixed to theguide component10, and thetarget ring17 is engaged by squeezing or compressing thegrip20 andtrigger mechanism21 or scissor handles40 to draw thetarget ring17 toward the fixedsuture seizing pestle18 so as to pin thesuture22 against the inner surface of thetarget ring17, thus seizing thesuture22. Similarly, as theguide component10 is removed from thefirst tunnel portion12, thesuture22 is pulled through the angledosteal tunnel11.
• FIG. 16 illustrates an alternate embodiment of the invention shown inFIG. 2A having amovable guide component10 and a straight rod41 and plunger42 suture seizing mechanism. Theguide component10 is slidably or removably mounted to the rack7, which may be arcuate in shape, and is capable of being securely positioned about the rack7 toward either end. Theguide component10 can be fixed into a desired position by engagingclamp23 with tighteningscrew24. In this embodiment,drill guide sleeve2 remains fixed to an end of the rack7. In this alternate embodiment, thegrip20 andtrigger mechanism21 is replaced with a straight rod41 and plunger42. The straight rod41 functions as asuture seizing pestle18 and has one end attached to the plunger42, and the other end is a free end. The straight rod41 is slidably received within a cylinder43 and moves out through the cylinder43 as the plunger42 is pulled outward, and moves into the cylinder43 as the plunger42 is depressed. Asuture22 is seized within thetarget ring17 by squeezing thesuture22 between thetarget ring17 and the free end of the straight rod41 as the plunger42 is depressed.
• FIG. 17 illustrates an alternate embodiment of the invention shown inFIG. 2A having a movabledrill guide sleeve2 and amovable guide component10. Theguide component10 and thedrill guide sleeve2 are each slidably or removably mounted to the rack7, which may be arcuate in shape, and are capable of being securely positioned about the rack7 in a desired position. Theguide component10 and thedrill guide sleeve2 can be fixed in a position on the rack7 by engagingclamp23 with tighteningscrew24.
• FIGS. 18A and 18B are close-up views of theclamp23 and tighteningscrew24 in accordance with the present invention. Theclamp23 is attached to an adjustable portion of the surgical drill guide1. The adjustable portion preferably is theexterior end19 of theguide component10, but alternatively may be thedrill guide sleeve2. Rack7 is slidably disposed withinclamp23 such thatclamp23 andguide component10 can be positioned about rack7. Tighteningscrew24 moves clamp23 toward rack7 as it is turned one way, fixingclamp23 andguide component10 to the rack7. When turned in an opposite direction, the tighteningscrew24 moves theclamp23 away from the rack7, making theclamp23 loose and adjustable.
• Referring now toFIG. 19, an alternate method for tying and anchoring aligament44 with asuture22 between osteal tunnels4 is shown. Using this method,first tunnel portion12 andsecond tunnel portion13 are drilled or punched in the manners described above. Asuture22 or wire is drawn through the osteal tunnels4, with one free end of thesuture22 extending from thefirst tunnel portion12, and one free end of thesuture22 extending from thesecond tunnel portion13. The free end ofsuture22 extending from the second tunnel portion is wrapped around ligament44 (or tendon or muscle) andbone5, such thatligament44 is sandwiched betweensuture22 andbone5 between the entrance points of thefirst tunnel portion12 and thesecond tunnel portion13 on the surface of thebone5. The free end of thesuture22 extending from thesecond tunnel portion13 is then tied or anchored using thenovel anchor29 of the present invention to the free end of thesuture22 extending from thefirst tunnel portion12. Alternatively, the free end of thesuture22 extending from thefirst tunnel portion12 can be drawn over theligament44, and the suture can be secured at any point between the entrance points of thefirst tunnel portion12 andsecond tunnel portion13.
• Other methods of fixating thesutures22 also are contemplated for use with the present invention. For example, one can tie sutures exiting from different tunnels to each other. One can use an interference type of device, such as a plug, placed in the exiting tunnel so as to frictionally engage the suture against the tunnel wall. One can tie the sutures form the exiting tunnel over a button having a larger diameter than the tunnel. Various other known methods for tying sutures also can be utilized.
• Referring now toFIG. 20, asuture feeding sleeve70 as a part of the present invention is shown. Suture feedingsleeve70 is a generallytubular structure72 having ahollow interior82, anouter diameter74 smaller thantunnel portions12,13 in general, and smaller thansecond tunnel portion13 in particular, and aninner diameter76 large enough to accommodate a variety ofsutures22. Further, theouter diameter74 also preferably is larger than the diameter of the opening oftarget ring17 to prevent thesuture feeding sleeve70 from entering thetarget ring17 when in use, as disclosed in more detail below. Suture feedingsleeve70 can have a roundedinsertion edge78 for ease of insertion intotunnel portion12,13, and a flangedouter edge80 for ease of gripping and removing.
• Referring now toFIG. 21, in one illustrative embodiment,suture feeding sleeve70 is inserted into eithersecond tunnel portion13 orfirst tunnel portion12 whileguide component10 remains in eitherfirst tunnel portion12 orsecond tunnel portion13, respectively. As theouter diameter74 of suture feeding sleeve is larger than the diameter of the opening oftarget ring17,suture feeding sleeve70 will contactguide component10, but will not entertarget ring17.Suture22 then can be fed down through thehollow interior82 ofsuture feeding sleeve70 and into thetarget ring17 wheresuture22 can be seized, as disclosed above. In another illustrative embodiment,suture22 can be fed down through thehollow interior82 ofsuture feeding sleeve70 prior to the insertion of thesuture feeding sleeve70 into thetunnel portion12,13. In this embodiment,suture22 can be fed through thehollow interior82 so as to extend out of the insertion edge78 a certain desired distance, the distance being chosen to allow just enough of thesuture22 to extend out of thehollow interior82 so that just enough ofsuture22 can extend intotarget ring17 and be seized, without having to estimate the amount ofsuture22 to be fed intohollow interior82. Suture feedingsleeve70 can be appropriately calibrated for such distances.
• Thus, in use, the present devices and methods allow for tunnels providing robust bony bridges even with minimal distance between the surface points of entry and exit on the bone. The osteal tunnels can be created through limited exposure of the muscle, tendons, and bone (i.e., limited exposure of the subdermal structures), and the technique may be performed arthroscopically. For example, arthroscopic surgery of the shoulder to repair a torn rotator cuff involves fixation of the torn tendon to bone. Straight tunnels are precluded because the closer the point of entry and exit, the more shallow the tunnel and the weaker the bony bridge. The present invention addresses this issue.
• Further, the present devices and methods allow for the blind intraosseous preparation of osteal tunnels and retrieval of sutures, without the need for direct visualization of the tunnels or the sutures. The ability to prepare osteal tunnels and retrieve sutures from within the tunnels without direct visualization can help simplify this type of surgery and reduce surgical errors.
• It is to be understood that the present invention is by no means limited to the particular constructions and method steps herein disclosed or shown in the drawings, but also comprises any modifications or equivalents within the scope of the claims known in the art. It will be appreciated by those skilled in the art that the devices and methods herein disclosed will find utility with respect to multiple bones, joints, and the like.

Claims (37)

1. A surgical drill guide device for drilling an angled osteal tunnel comprising:

a) an support rack having a first end and a second end;

b) a drill guide sleeve having a passage for receiving a drill therethrough, the drill guide sleeve being adjustably securable and positionable on the rack between the first end and the second end of the rack; and

c) a guide component secured on the first end of said rack, the guide component having a suture seizing mechanism for seizing a suture.

2. The surgical drill guide device as claimed inclaim 1, wherein the suture seizing mechanism comprises a suture seizing pestle and a target ring having an opening.

3. The surgical drill guide device as claimed inclaim 1, wherein the guide component comprises an interior end to be inserted into the osteal tunnel and an exterior end attached to the rack.

4. The surgical drill guide device as claimed inclaim 1, further comprising an activating mechanism on the exterior end of the guide component for engaging the suture seizing mechanism.

5. The surgical drill guide device as claimed inclaim 1, further comprising a clamp and tightening screw whereby the positioning of the drill guide sleeve is adjustable about the length of the rack.

6. The surgical drill guide device as claimed inclaim 3, wherein the suture seizing mechanism is located on the interior end.

7. The surgical drill guide device as claimed inclaim 3, wherein the drill guide sleeve comprises a generally cylindrical structure through which a drill can be inserted and guided to drill into the bone.

8. The surgical drill guide device as claimed inclaim 7, wherein the drill guide sleeve and the guide component cooperate with each other to allow the drilling of the second tunnel portion and to guide the drill bit so that the second tunnel portion intersects at an angle with the first tunnel portion within the bone.

9. The surgical drill guide device as claimed inclaim 8, wherein:

the guide component and the drill guide sleeve are selectively positionable relative to each other on the rack between the first end and the second end of the rack such that when the interior end of the guide component is located intraosteal within a first tunnel portion drilled into the bone, the drill guide sleeve directs the drill towards the target ring,

whereby a second tunnel portion drilled into the bone intersects at an angle to the first tunnel portion.

10. The surgical device as claimed inclaim 9, wherein the angle is greater than 0° and less than 180°.

11. The surgical device as claimed inclaim 9, wherein the angle is between approximately 10° and approximately 170°.

12. The surgical device as claimed inclaim 9, wherein the angle is between approximately 45° and approximately 135°.

13. The surgical device as claimed inclaim 9, wherein the interior end of the guide component comprises an awl tip and the exterior end of the guide component comprises a tamping plate for forming the tunnel portions.

14. The surgical drill guide device as claimed inclaim 8, wherein the suture seizing pestle is moved toward the target ring when the activating mechanism is activated, wherein the movement of the suture seizing pestle closes the opening of the target ring and securely presses against the tip of the interior end of the guide component or the edge of the target ring, whereby a suture is pinched and secured between the suture seizing pestle and the tip of the interior end of the guide component or the edge of the target ring.

15. The surgical drill guide device as claimed inclaim 2, further comprising a suture feeding sleeve having a generally tubular structure having a hollow interior, an outer diameter smaller than the osteal tunnel, and an inner diameter large enough to accommodate the sutures.

16. The surgical drill guide device as claimed inclaim 15, wherein the outer diameter of the suture feeding sleeve is larger than the opening of the target ring.

17. A surgical drill guide device for drilling an angled osteal tunnel comprising:

a) an arcuate support rack having a first end and a second end;

b) a drill guide sleeve having a passage for receiving a drill therethrough; and

c) a guide component having an interior end and an exterior end, wherein the interior end is for inserting into an osteal tunnel and comprises a target ring and a suture seizing mechanism, and wherein the exterior end comprises an activating mechanism for activating the suture seizing mechanism,

wherein the guide component and the drill guide sleeve are selectively positionable relative to each other on the rack between the first end and the second end of the rack such that when the interior end of the guide component is located within a first tunnel portion drilled into the bone, the drill guide sleeve directs the drill towards the target ring,

whereby a second tunnel portion drilled into the bone intersects at an angle to the first tunnel portion.

18. The surgical drill guide device as claimed inclaim 17, wherein the guide component is a hollow cylinder.

19. The surgical drill guide device as claimed inclaim 17, wherein the activating mechanism can be squeezed to force the suture seizing pestle axially in the cylinder and into the target ring so as to pin a suture against an inner surface of the target ring, thus seizing the suture.

20. The surgical drill guide device as claimed inclaim 17, further comprising a rack rigidly attached to the guide component, the rack having a radius of curvature, and a drill guide sleeve attached to the rack, wherein the drill guide sleeve is attached such that is can be selectively positioned along the rack.

21. The surgical drill guide device as claimed inclaim 18, wherein the suture seizing mechanism comprises a suture seizing pestle located within the cylinder, and wherein the target ring and suture seizing pestle are structured to accommodate a drill bit and to receive a suture.

22. The surgical drill guide device as claimed inclaim 20, further comprising a clamp and tightening screw whereby the positioning of the drill guide sleeve is adjustable about the length of the rack.

23. The surgical drill guide device as claimed inclaim 21, wherein said suture seizing pestle is moved toward the target ring when the activating mechanism is activated, wherein the movement of the suture seizing pestle closes the opening of the target ring and securely presses against the tip of the interior end of the guide component or the edge of the target ring, whereby a suture is pinched and secured between the suture seizing pestle and the tip of the interior end of the guide component or the edge of the target ring.

24. The surgical device as claimed inclaim 20, wherein the angle is greater than 0° and less than 180°.

25. The surgical device as claimed inclaim 20, wherein the angle is between approximately 10° and approximately 170°.

26. The surgical device as claimed inclaim 20, wherein the angle is between approximately 45° and approximately 135°.

27. The surgical drill guide device as claimed inclaim 17, further comprising a suture feeding sleeve having a generally tubular structure having a hollow interior, an outer diameter smaller than the osteal tunnel, and an inner diameter large enough to accommodate the sutures.

28. The surgical drill guide device as claimed inclaim 27, wherein the outer diameter of the suture feeding sleeve is larger than an opening of the target ring.

29. A surgical drill guide device for drilling osteal tunnels for the repair of tom tendons and ligaments comprising:

a) a rack having a first and second end;

b) a drill guide sleeve adjustably secured on the rack, wherein the drill guide sleeve can be positioned between the first end and the second end of the rack;

c) a guide component secured on the first end of the rack;

d) a suture seizing mechanism attached to the guide component, wherein the suture seizing mechanism comprises a cooperating target ring and suture seizing mechanism, and wherein the target ring has an opening complimentary to a suture inserted therein; and

e) an actuating mechanism for causing the engagement of the suture seizing mechanism and the target ring, wherein the suture seizing mechanism is engaged when the actuating mechanism is activated.

30. The surgical drill guide device as claimed inclaim 29, wherein the guide component is a cylinder.

31. The surgical drill guide device as claimed inclaim 30, further comprising a clamp and tightening screw whereby the positioning of the drill guide sleeve is adjustable about the length of the rack.

32. The surgical drill guide device as claimed inclaim 31, wherein the suture seizing mechanism comprises a suture seizing pestle that is movable toward the target ring when the activating mechanism is activated, wherein the movement of the suture seizing pestle closes the opening of the target ring and securely presses against the tip of the interior end of the guide component or the edge of the target ring, whereby a suture is pinched and secured between the suture seizing pestle and the tip of the interior end of the guide component or the edge of the target ring.

33. The surgical device as claimed inclaim 32, wherein the angle is greater than 0° and less than 180°.

34. The surgical device as claimed inclaim 32, wherein the angle is between approximately 10° and approximately 170°.

35. The surgical device as claimed inclaim 32, wherein the angle is between approximately 45° and approximately 135°.

36. The surgical drill guide device as claimed inclaim 29, further comprising a suture feeding sleeve having a generally tubular structure having a hollow interior, an outer diameter smaller than the osteal tunnel, and an inner diameter large enough to accommodate the sutures.

37. The surgical drill guide device as claimed inclaim 36, wherein the outer diameter of the suture feeding sleeve is larger than the opening of the target ring.

Images