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J Am Acad Orthop Surg, Vol 14, No 3, March 2006, 145-153.
© 2006 the American Academy of Orthopaedic Surgeons

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Arthrodesis of the Shoulder

Ori Safran, MD and Joseph P. Iannotti, MD, PhD

Dr. Safran is Senior Orthopaedic Surgeon, Department of Orthopaedic Surgery, Hadassah-Hebrew University Medical School, Jerusalem, Israel. Dr. Iannotti is Professor and Chairman, Department of Orthopaedic Surgery, The Cleveland Clinic Foundation, Cleveland Clinic Lerner School of Medicine of Case Western Reserve University, Cleveland, OH.

None of the following authors or the departments with which they are affiliated has received anything of value from or owns stock in a commercial company or institution related directly or indirectly to the subject of this article: Dr. Safran and Dr. Iannotti.

Reprint requests: Dr. Iannotti, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195.

Shoulder arthrodesis is an end-stage salvage option for the failing, painful joint that cannot undergo or has failed reconstruction. It is indicated for irreversible and nonreconstructible massive rotator cuff tears and deltoid muscle denervation as well as for detachment of the deltoid from its origin. Rarely, arthrodesis is done to stabilize the glenohumeral joint after many failed attempts at shoulder reconstruction. Arthrodesis for failed prosthetic arthroplasty or tumor resection presents additional challenges because of the associated bone loss on the humeral and/or glenoid side of the joint. Primary arthrodesis requires rigid internal plate fixation and both an extra- and an intra-articular site of fusion. Depending on bone volume and quality needed, the patient may require bracing for 8 to 10 weeks, autogenous or allograft bone grafting, or a vascularized fibular bone graft to reconstruct the bone deficiency, along with prolonged spica cast immobilization. The optimal position for arthrodesis is 20° of forward flexion, 20° of abduction, and 40° of internal rotation, with modifications based on patient body size or other patient-specific factors. Bone fusion is attained in nearly all patients, with marked pain reduction and improved function. Postoperatively, the patient should be able to lift the arm to near shoulder height and to reach the top of the head, the mouth, the ipsilateral back pocket, and the groin. Complications include nonunion, malposition, pain associated with prominent hardware, and periarticular fractures.







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Copyright © 2006 by the American Academy of Orthopaedic Surgeons.