Copyright © 2007 by The Journal of Bone and Joint Surgery, Inc.

Commentary & Perspective

Commentary & Perspective on
"Arthroscopic Repair of Traumatic Combined Rotator Cuff Tears Involving the Subscapularis Tendon"
by Junji Ide, MD, et al.

Commentary & Perspective by
Joseph P. Iannotti MD, PhD*,
Cleveland Clinic and Lerner College of Medicine of Case Western Reserve University, Cleveland, Ohio

Posted November 2007

The paper by Ide et al. describes the clinical and anatomic outcome after arthroscopic repair of anterosuperior rotator cuff tears in a prospective clinical series of patients. The arthroscopic procedure was performed by a single surgeon who used a standard surgical procedure and postoperative protocol. Twenty patients had a minimum of two years of follow-up with magnetic resonance imaging. All patients had a full-thickness tear of a portion of the superior two-thirds of the subscapularis tendon. Thirteen patients had a supraspinatus tear in addition to the subscapularis tear (a total of two tendon tears), and seven patients had a supraspinatus tear and an infraspinatus tear in addition to the subscapularis tear (a total of three tendon tears). All tears were repairable and were associated with a traumatic event, thereby defining a time that the tear occurred. In all instances, the tear was repaired within six months of the injury, with an average time until repair of 2.7 months. Patients with stage-3 or 4 atrophy of the muscle were excluded from this study. These anatomic and patient parameters are ideal criteria for repair of large and massive tears of the rotator cuff involving the subscapularis tendon. The arthroscopic surgical techniques were performed by an experienced surgeon. Postoperatively, the arm was supported in a sling with an abduction pillow, and only passive or active-assisted range-of-motion exercises were permitted for six weeks after surgery. Despite these favorable conditions, one third of the tears failed to heal.

This study, like others, correlates healing of the repaired rotator cuff tendons to better clinical outcome1-4, size of the tear2,5, the degree of muscle atrophy1,6,7, tendon retraction1, and age of the patients8,9. The study was comprised of a well-defined group of patients who underwent a uniformly applied surgical technique and postoperative rehabilitation protocol in which clinical as well as anatomic parameters were defined at follow-up. This paper establishes a standard by which other series can be compared.

Approximately one-third of the tears had a persistent full-thickness defect, noted on magnetic resonance imaging, at the time of follow-up. The anatomical and clinical results reported in this paper are equal to the best results reported in the literature for patients with two or three tendon tears1,10. Tendon failure after repair relates to many biomechanical factors, such as the initial strength of the repair, the tension on the repair, and the quality of the tendon and bone. None of the repairs in this series demonstrated failure of the anchors from bone. This suggests that the structural defects were related to failure at the tendon-suture interface. In this series, larger tears with more severe retraction of the tendon resulted in the largest number of failures, suggesting that the tension of the repair is a major factor associated with failure of the tendon to remain attached to bone. Early failure of the repair will not allow for sufficient time to achieve an increase in mechanical strength of the repair by the deposition of new tissue. An opportunity to achieve better results may exist through the use of improved methods of fixation of the repair by augmentation of the tendon with a graft material11, better methods to protect the repair against high tensile loads after surgery, or growth factors to accelerate the rate or quality of the healing process12. All of these methods to enhance the mechanical and biologic potential of these tendons to heal after surgical repair are active areas of research in preclinical and clinical trials11,12.

In summary, this paper provides excellent clinical information because it is a well-documented, well-defined clinical case series. It thereby provides sufficient clinical data, as a historical control, for developing the study design criteria of a clinical trial to evaluate the efficacy of any new method of cuff repair when using this surgical technique for this type of tear.

*The author did not receive any outside funding or grants in support of his research for or preparation of this work. Neither he nor a member of his immediate family received payments or other benefits or a commitment or agreement to provide such benefits from a commercial entity. No commercial entity paid or directed, or agreed to pay or direct, any benefits to any research fund, foundation, division, center, clinical practice, or other charitable or nonprofit organization with which the author, or a member of his immediate family, is affiliated or associated.

References

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