TOOL AND METHOD FOR IMPLANTING FUSION DEVICE INTO SACROILIAC JOINT
20240315708 ยท 2024-09-26
Inventors
Cpc classification
A61B17/17
HUMAN NECESSITIES
A61B17/1739
HUMAN NECESSITIES
A61F2/4603
HUMAN NECESSITIES
A61B17/8894
HUMAN NECESSITIES
International classification
A61B17/17
HUMAN NECESSITIES
A61B17/88
HUMAN NECESSITIES
Abstract
Tools for positioning an implant into the sacroiliac joint. A directional cannula includes a main body having a bore that receives the implant. A cut-out, allowing access to the joint, is formed in a leading end of the main body. A pair of parallel prongs extend from the leading end of the main body in transversely spaced apart relation to one another. A drill guide has a main body of rectangular transverse cross-section and a cylindrical head formed integrally with the main body. A transverse width-reducing step is formed in the main body near its distal end. First and second bores are formed in the cylindrical head and in the main body. Both bores are eccentric relative to the drill guide longitudinal axis of symmetry. The drill guide is rotated 180? after first and second drilling operations, prior to third and fourth drilling operations.
Claims
1.-5. (canceled)
6. A method of positioning an implant into a sacroiliac joint, comprising the steps of: providing said cannula with a cylindrical main body having a longitudinally-extending central bore formed therein, said central bore having a transverse profile that matches a transverse profile of said implant; providing said cannula with a cut-out formed in its leading end; providing a drill bit having a positive stop and inserting said drill bit into the cannula and drilling said drill bit in the sacral and ilium until said drill bit reaches said positive stop; withdrawing said drill bit from said cannula; inserting said implant into said central bore; tamping said implant until said implant reaches said positive stop so that said implant is positioned inside the cavity drilled into the sacrum and ilium by said drilling; and withdrawing said cannula.
7. A method of positioning an implant into a sacroiliac joint, comprising the steps of: inserting a first guide wire into said sacroiliac joint; positioning a joint locator over said first guide wire in ensleeving relation to said first guide wire; positioning a directional cannula over said joint locator in ensleeving relation to said joint locator; providing said directional cannula with a cylindrical main body having a longitudinally-extending central bore formed therein, said central bore having a transverse profile that matches a transverse profile of said implant; forming a cut-out in a leading end of said directional cannula; forming a pair of parallel, transversely spaced apart prongs that extend from said leading end of said directional cannula; inserting said prongs into the sacroiliac joint; retracting said joint locator and said first guide wire from said lumen of said directional cannula, leaving said directional cannula with said prongs disposed in the sacroiliac joint; providing a drill guide having an elongate main body of rectangular cross-section and having a pair of parallel, longitudinally extending bores formed in said main body in eccentric relation to a longitudinal axis of symmetry of said drill guide; providing a drill guide head that is enlarged relative to said main body; forming a step in said main body that reduces the transverse extent of said main body near a leading end thereof, said step exposing a drill bit-accommodating semi-circular groove in each side of the leading end of said drill guide, said leading end being the part of said main body that extends distal of said step; inserting said drill guide into the central bore of said directional cannula to verify placement of said directional cannula into said sacroiliac joint, said central bore of said directional cannula having a profile that enables it to slidingly receive said drill guide in the center of the larger implant-receiving central bore; providing a drill bit having a positive stop and inserting said drill bit into a first bore of said eccentric bores and advancing said drill bit towards the ilium until it abuts the ilium; drilling a first cavity in said ilium until said drill bit reaches said positive stop; withdrawing said drill bit from said first bore and inserting said inserting drill bit into said second bore and drilling a second cavity in the ilium until said drill bit reaches said positive stop; retracting said drill guide from said central bore of said directional cannula; rotating said drill guide one hundred eighty degrees (180?) about its longitudinal axis of symmetry; inserting said drill bit a second time into said first bore of said eccentric bores and advancing said drill bit towards the sacrum until it abuts the sacrum; drilling a first cavity in said sacrum until said drill bit reaches said positive stop; withdrawing said drill bit from said first bore and inserting said drill bit into said second bore a second time and drilling a second cavity in the sacrum until said drill bit reaches said positive stop; said first and second ilium cavities merging with said first and second sacrum cavities to form a single cavity adapted to receive said fusion implant therein; withdrawing said drill guide from said central bore of said directional cannula; inserting said implant into said central bore; tamping said implant until said implant reaches said positive stop so that said implant is positioned inside the cavity drilled into the sacrum and ilium by said first, second, third and fourth drillings; and withdrawing said directional cannula.
8. (canceled)
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0019] For a fuller understanding of the nature and objects of the invention, reference should be made to the following detailed disclosure, taken in connection with the accompanying drawings, in which:
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DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
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[0058] The novel method steps include the steps of taking anterior, posterior, and lateral X-ray views of the sacroiliac (SI) area to identify the anatomy that is causing pain in a patient.
[0059] An entry point is established to gain access to the SI joint with an oblique (approximately thirty five degree (35?) angle) and a Ferguson angle measurement of curvature which is approximately ten to fifteen degrees (10-15?).
[0060] As depicted in
[0061] As depicted in
[0062] A third guide wire 20, as depicted in
[0063] Three incision points are then marked on the skin, as depicted in
[0064] Center incision point 24 is midway between the points where the second and third lines 18 and 22 cross first line 12 and is spaced in the medial direction about three to five millimeters (3-5 mm) from first line 12.
[0065] Superior incision point 26 is spaced in the medial direction about three to five millimeters (3-5 mm) from the intersection of first line 12 and second line 14.
[0066] Inferior incision point 28 is spaced in the medial direction about three to five millimeters (3-5 mm) from the intersection of first line 12 and third line 22.
[0067] As depicted in
[0068] Joint locator 50, depicted in
[0069] Directional cannula 52, depicted in
[0070] Directional cannula 52 has a cylindrical main body 52a having longitudinally-extending central bore 52b formed therein. Central bore 52b has a transverse profile that matches the transverse profile of a fusion implant. A leading end of central bore 52b is exposed to view by cut-out or notch 52c. Two prongs 52d and 52e extend from said leading end in transversely spaced, parallel relation to one another. Prongs 52d and 52e enter the sacroiliac joint when directional cannula 52 is in use. Barb 52f is formed in the leading end of main body 52a as depicted in
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[0072] Joint locator 50 and guide wire 30 are then retracted, leaving directional cannula 52 in position. When so positioned, prongs 52d, 52e are disposed in sacroiliac joint 10. Barb 52f engages the sacrum to hold directional cannula 52 in position as aforesaid.
[0073] Drill guide 54, depicted in
[0074] Drill guide 54 is inserted into the central bore or lumen of directional cannula 52 towards the sacrum to verify placement of directional cannula 52 into the SI joint. The lumen of directional cannula 52 has a profile that enables it to slidingly receive drill guide 54 in the center of the larger implant-receiving lumen.
[0075] Drill bit 56, depicted in
[0076] The distance from the proximal end of head 54c of drill guide 54 to the lower side of positive stop 56a is then measured. Directional cannula 52 is properly seated in the SI joint if the measured distance is between twenty-five to thirty millimeters (25-30 mm). The proper seating can also be confirmed with a lateral X-ray view that shows the leading end of directional cannula 52 disposed flush with the sacrum.
[0077] Drill bit 56 is then inserted into eccentric drill guide bore 54a and a first cavity is created in the ilium by a first drilling, until positive stop 56a abuts the proximal end of directional cannula 52. Drill bit 56 is then withdrawn from bore 54a, placed into bore 54b, and a second cavity is formed in the ilium by a second drilling. The second drilling continues until drill bit 56 reaches positive stop 56a.
[0078] Drill guide 54 is then retracted from directional cannula 52 and rotated one hundred eighty degrees (180?). Drill bit 56 is then inserted into eccentric drill guide bore 54a and a first cavity is created in the sacrum by a third drilling that continues until drill bit 56 reaches positive stop 56a. Drill bit 56 is then withdrawn from bore 54a, placed into bore 54b, and a second cavity is formed in the sacrum by a fourth drilling. The fourth drilling continues until drill bit 56 reaches positive stop 56a. Drill bit 56 is then removed.
[0079] Due to the eccentricity of the bores and the rotation of the drill guide, all four cavities merge into a single cavity that accommodates the fusion implant.
[0080] When the drilling is completed, drill guide 54 is retracted from directional cannula 52 and fusion implant 58, depicted in
[0081] Fusion implant 58 may take many forms and may be as simple as a dowel having a circular cross-section, i.e., the oval shape of main body 58a, upper and lower fins 58b, 58c, and the swept back leading edge 58d of said fins are not critical parts of the fusion implant.
[0082] Implant tamp 60, depicted in
[0083] As perhaps best understood in connection with
[0084] A guide wire is then inserted through superior incision point 26 at a superior/interior angle about forty-five degrees (45?) towards superior. The medial/lateral angle is the same as the oblique angle on the C-arm, which is approximately thirty-five degrees (35?).
[0085] The guide wire is then guided into the SI joint. A second incision is made when the guide wire is properly positioned. The steps that follow the first incision are then repeated, i.e., joint locator 50 is inserted over the guide wire, directional cannula 52 is paced over the joint locator, and so on.
[0086] The procedure is concluded by inserting a guide wire through inferior incision point 28 at a superior/interior angle about forty-five degrees (45?) towards inferior. The medial/lateral angle is the same as the oblique angle on the C-arm, which is approximately thirty-five degrees (35?).
[0087] The guide wire is then guided into the SI joint. A third incision is made when the guide wire is properly positioned. The steps that follow the first and second incisions are then repeated, i.e., joint locator 50 is inserted over the guide wire, directional cannula 52 is paced over the joint locator, and so on.
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[0089] It will thus be seen that the objects set forth above, and those made apparent from the foregoing disclosure, are efficiently attained and since certain changes may be made in the above construction without departing from the scope of the invention, it is intended that all matters contained in the foregoing disclosure or shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.
[0090] It is also to be understood that the following claims are intended to cover all of the generic and specific features of the invention herein described, and all statements of the scope of the invention that, as a matter of language, might be said to fall therebetween.