Results and Complications

Published on 18/03/2015 by admin

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CHAPTER 32 Results and Complications

Reports on the results of reverse shoulder arthroplasty are becoming more common as implantation of this type of shoulder arthroplasty increases. The results vary predominantly by the underlying indication for which the arthroplasty was performed. We have participated in a large European-based study of the reverse prosthesis and continually enroll patients in our own database.1 The results and complications presented in this chapter are drawn from these sources.

RESULTS

The results of reverse shoulder arthroplasty vary mainly with the etiology for which the arthroplasty was performed. The best results are obtained in the treatment of osteoarthritis with a massive rotator cuff tear (rotator cuff tear arthropathy), whereas results are least satisfactory in patients with post-traumatic arthritis. Tables 32-1 and 32-2 detail the results of reverse shoulder arthroplasty for the most common indications for which it is performed. These tables express the results in terms of active mobility; patient satisfaction; the Constant score, a shoulder-specific outcomes device incorporating pain, mobility, activity, and strength; and the age- and gender-adjusted Constant score.2,3

Table 32-1 RESULTS OF REVERSE SHOULDER ARTHROPLASTY ACCORDING TO UNDERLYING ETIOLOGY IN A LARGE EUROPEAN-BASED STUDY

Rights were not granted to include this data in electronic media. Please refer to the printed book.

INTRAOPERATIVE COMPLICATIONS

Intraoperative complications are more common during reverse shoulder arthroplasty than during unconstrained shoulder arthroplasty performed for chronic conditions and may be divided into complications involving the humerus, glenoid, musculotendinous soft tissues (rotator cuff), and neurovascular structures.

Humerus

The most common humeral complication is iatrogenic fracture, which usually results from performing an overly aggressive dislocation maneuver without previous adequate soft tissue release. Many patients undergoing reverse shoulder arthroplasty have moderate to severe osteopenia, thus placing them at increased risk for this complication. Intraoperative tuberosity fractures during glenohumeral dislocation are less common during reverse shoulder arthroplasty than during unconstrained shoulder arthroplasty because of the lack of a rotator cuff attaching to the tuberosities, which could otherwise contribute to fracture during a dislocation maneuver. Fractures involving the humeral diaphysis should be reduced and a long-stem humeral implant placed. Allograft struts and cerclage cables may be added in patients with severe osteopenia (Fig. 32-1).

Intraoperative fractures involving the greater or lesser tuberosities (or both) are usually nondisplaced. Many of these fractures are stable or become stable once the humeral implant is inserted (Fig. 32-2). If a greater tuberosity fracture fragment that has maintained attachment of a substantial portion of the posterior rotator cuff is not satisfactorily stable, suture fixation of the tuberosity is performed and the postoperative rehabilitation adjusted accordingly to allow healing of the tuberosity. A greater tuberosity fracture fragment that is devoid of rotator cuff attachment and is unstable may simply be excised.

Intraoperative lesser tuberosity fractures commonly occur during retraction of the proximal humerus in the course of glenoid preparation and insertion. The thin anterior cortex of the humeral metaphysis, including the lesser tuberosity, may be crushed by the humeral retractor (Fig. 32-3). Creation of this fracture is often necessary to obtain adequate glenoid exposure during insertion of the reverse prosthesis through a deltopectoral approach. This fracture is without clinical consequence and can largely be ignored.

Glenoid

Intraoperative glenoid fractures are more detrimental than humeral injury. Frequently, surgeons who are beginning their experience in reverse shoulder arthroplasty do not have much proficiency in glenoid preparation because they have previously performed hemiarthroplasty for most cases in which shoulder arthroplasty is indicated. Many surgeons initially attempt to ream the glenoid as though it were an acetabulum (i.e., overaggressively), which often leads to obliteration of the glenoid bone, to glenoid fracture, or both. Patients undergoing reverse shoulder arthroplasty are at particular risk for intraoperative glenoid fracture because they tend to have more osteopenia than patients undergoing unconstrained arthroplasty for nonfracture conditions. Fractures may involve only the peripheral glenoid rim or may extend significantly into the central portion of the glenoid. Adequate capsular release helps minimize the risk for glenoid fracture. Additionally, a motorized reamer (not a drill, because the speed and torque are different) should be used for preparation of the glenoid surface. The reamer should be started before the surgeon applies force to engage the reamer onto the glenoid face. This avoids having the reamer “catch” an edge of the glenoid, which may cause a fracture.

Fractures that involve only a small portion of the peripheral rim generally require no treatment, and the glenoid component can be inserted as planned. Glenoid fractures that extend into the central portion of the glenoid should be bone-grafted with the humeral head. The reverse glenoid component can be inserted to help secure the bone graft and internally fix the fracture. If the central post of the reverse component is firmly seated within native glenoid bone, consideration can be given to placing the humeral component in the same surgical setting. If the glenoid component does not seem secure or the central post of the glenoid base plate is not firmly seated in unfractured native glenoid bone, the humeral component should be initially omitted for 6 months to allow the fracture to heal. After 6 months a humeral component can be placed as the second part of a two-stage procedure (Fig. 32-4). Alternatively, if an intraoperative glenoid fracture occurs, the fracture can be bone-grafted and the humeral stem plus a hemiarthroplasty adapter placed (Fig. 32-5). After the fracture has healed and remodeled (around 6 months after the index attempt at reverse shoulder arthroplasty), the second stage of the procedure, consisting of implantation of the glenoid component, may be performed (Fig. 32-6).

Neurovascular Structures

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