Implantable tendon protection systems and related kits and methods
An implantable tendon protection system includes a body adapted to be implanted within a bursa overlying a tendon of a patient to protect the tendon. The body may be fixed to the tendon with adhesive, sutures, staples, and/or anchors. A surgical kit is provided with such a tendon protection system and an insertion cannula. Methods of protecting a tendon of a patient are also disclosed.
1. A method of implanting an implant in a shoulder region of a patient comprising:
inserting a distal end of an implant delivery device into a shoulder region of the patient proximate a supraspinatus muscle, the implant delivery device comprising:
a sheath defining a lumen; and
an implant disposed within the lumen of the sheath;
transitioning the implant from an undeployed state within the sheath to a deployed state outside of the sheath;
positioning the implant over a partial thickness tear of a supraspinatus tendon of the patient;
attaching the implant to the supraspinatus tendon of the patient while the implant is positioned over the partial thickness tear of the supraspinatus tendon of the patient.
2. The method of claim 1 , further comprising inserting the distal end of the implant delivery device into a subacromial bursa of the patient.
3. The method of claim 1 , further comprising attaching the implant to the supraspinatus tendon using staples.
4. The method of claim 1 , further comprising attaching the implant to the supraspinatus tendon using an adhesive.
5. The method of claim 4 , wherein the implant comprises a least one channel and a plurality apertures, and the method further comprising:
injecting the adhesive into the at least one channel.
6. The method of claim 5 , wherein the adhesive elutes through the plurality of apertures after being injected into the at least one channel.
7. The method of claim 1 , further comprising attaching the implant to the supraspinatus tendon such that at least a portion of the implant overlays the supraspinatus tendon and at least a portion of the implant overlays a humerus bone.
8. The method of claim 1 , wherein the implant comprises a bioabsorbable material.
9. The method of claim 1 , further comprising retracting the sheath to transition the implant from the undeployed state to the deployed state.
10. The method of claim 1 , wherein the implant comprises:
a first layer having a sliding surface; and
a second layer opposite the first layer and configured to engage the supraspinatus tendon, the second layer comprising a biocompatible material and a plurality of pores for encouraging tissue growth.
11. A method of attaching an implant to a supraspinatus tendon of a patient comprising:
inserting a sheet-like implant into a subacromial bursa of the patient;
positioning the implant so that at least a portion of the implant covers a partial thickness tear of the supraspinatus tendon; and
securing the implant to the supraspinatus tendon while at least a portion of the implant is covering the partial thickness tear of the supraspinatus tendon.
12. The method of claim 11 , further comprising positioning the implant so that at least a portion of the implant covers a humerus bone.
13. The method of claim 11 , further comprising:
inserting the implant into the subacromial bursa in a folded configuration; and
unfolding the implant while in the subacromial bursa.
14. The method of claim 13 , wherein the implant is inserted into the subacromial bursa within a sheath of a delivery device.
15. The method of claim 11 , wherein the implant comprises at least one channel in fluid communication with a plurality of apertures on a tendon-engaging surface of the implant.
16. The method of claim 11 , wherein securing the implant to the supraspinatus tendon comprises inserting one or more staples through the implant and into the supraspinatus tendon.
17. A method of treating a rotator cuff of a shoulder of a patient comprising:
inserting a distal end of an implant delivery device into a subacromial bursa within the shoulder of the patient, the implant delivery device comprising:
a sheath; and
an implant disposed within the sheath in a folded configuration;
advancing the implant beyond the distal end of the implant delivery device into the subacromial bursa;
transitioning the implant from the folded configuration to an unfolded configuration within the subacromial bursa;
positioning the implant so that at least a portion of the implant covers a partial thickness tear of a supraspinatus tendon of the patient; and
attaching the implant to the supraspinatus tendon while at least a portion of the implant is covering the partial thickness tear of the supraspinatus tendon of the patient.
18. The method of claim 17 , where the implant is attached to the supraspinatus tendon by inserting one or more staples through the implant and into the supraspinatus tendon.
19. The method of claim 17 , further comprising positioning the implant so that at least a portion of the implant covers a humerus bone of the patient.
20. The method of claim 17 , where in the unfolded configuration the implant assumes a concave shape.