Shoulder and Elbow Arthroplasty


Reconstructive Procedures of the Shoulder

Prosthetic replacement of the glenohumeral joint has become accepted as a successful treatment for a variety of degenerative, traumatic, and posttraumatic conditions around the shoulder. Multiple studies with long-term follow-up have demonstrated improvements in pain and function with excellent longevity. As experience with primary arthroplasty has accumulated, improved techniques for revision surgery have evolved as well. In the past 2 decades, the emergence of the reverse total shoulder arthroplasty has added another option for the treatment of patients with advanced glenohumeral conditions associated with end-stage rotator cuff dysfunction and/or glenoid deformity. This chapter discusses the indications, surgical technique, outcomes, and complications of shoulder arthroplasty.

History

The earliest known report of shoulder arthroplasty dates back to 1893, when a French surgeon, Péan, substituted a platinum and rubber implant for a glenohumeral joint destroyed by tuberculosis. In the early 1950s, Neer introduced a humeral head prosthesis that he planned to use for complex shoulder fractures. In 1951, he reported his initial results of replacement of the humeral head with an unconstrained cobalt-chromium alloy (Vitallium) prosthesis. In 1974, the Neer II humeral prosthesis, which was modified to articulate with a glenoid component, was introduced. In the early 1990s, Paul Grammont introduced an improved design of a semiconstrained shoulder replacement using a metal sphere implanted into the glenoid and a polyethylene liner and stem into the humerus: the reverse total shoulder arthroplasty. Although implant design factors continue to evolve, the primary features of this prosthesis are retained in current iterations of reverse arthroplasty.

Glenoid components for anatomic total shoulder arthroplasty were initially designed for cementless fixation using screws and porous coating on metal backing with a polyethylene shell. But long-term studies have shown an unacceptably high complication rate, and as such these implants have been largely abandoned. Subsequently, more emphasis was placed on restoring normal kinematics with anatomic location and orientation of the glenoid joint surface, advanced soft-tissue balancing techniques, and physiologic stabilization of the joint. Most current glenoid implants are polyethylene and use cement for fixation with either a pegged or keeled configuration on the backside of the component. Use of anchor-pegged devices to improve glenoid fixation and encourage bony ingrowth also has become a popular implant design.

Anatomy and Biomechanics

The anatomy of the shoulder joint permits more mobility than any other joint in the body. Although it often is described as a ball-and-socket joint, the large humeral head articulates against and not within the small glenoid cavity. The glenohumeral joint depends on the static and dynamic stabilizers for movement and stability, especially the rotator cuff, which not only stabilizes the glenohumeral joint while allowing greater freedom of motion but also fixes the fulcrum of the upper extremity against which the deltoid can contract and elevate the humerus. The rotator cuff must act simultaneously and synergistically, however, with the deltoid muscle for normal function.

Restoration of glenohumeral anatomy is essential for a good functional outcome in shoulder replacement. Anatomic studies have defined the humeral geometry further and suggested applications to shoulder arthroplasty prosthesis design and surgical techniques ( Fig. 12.1 and Table 12.1 ). The articular surface of the humeral head is essentially spherical, with an arc of approximately 160 degrees covered by articular cartilage. The radius of curvature is approximately 25 mm and is slightly larger in men than in women. The glenoid articular surface radius of curvature is 2 to 3 mm larger than that of the humeral head. The average neck-shaft angle is 45 degrees (±5 degrees), with a range of 30 to 50 degrees. Murthi et al. found that arthritic shoulders have a flatter neck-shaft angle close to 50 degrees. CT studies found that the normal position of the glenoid surface in relation to the axis of the scapular body ranged from 2 degrees of anteversion to 7 degrees of retroversion.

FIGURE 12.1, Family tree of shoulder arthroplasty prostheses.

TABLE 12.1
Anatomic Characteristics of the Shoulder Important for Prosthesis Design
Glenoid diameter
Superior anteroposterior 18-30 mm
Inferior anteroposterior 21-35 mm
Superoinferior (height) 30-48 mm
Inclination
Glenoid Average 4.2 degrees (−7 to 20 degrees)
Humeral head 30-55 degrees
VERSION
Glenoid 1.5 degrees retroversion (10.5-9.5 degrees anteversion)
Humeral head 0-55 degrees retroversion (dependent on measurement method; highly variable among individuals)
Surface area
Glenoid 4-6 mm
Humeral head 11-19 mm
Cartilage Thickness
Glenoid 2.16 mm
Humeral head 1.44 mm
Radius of Curvature
Glenoid 22-28 mm
Humeral head 23-28 mm (smaller in women than men)
Humeral Offset
Medial (coronal) 4-14 mm
Posterior (transverse) −2 to 10 mm
Head-shaft angle 30-55 degrees

The superior margin of the humeral head articular surface normally is superior to the top of the greater tuberosity by 8 to 10 mm ( Fig. 12.2 ). Restoring the center of rotation for the humeral head in relation to the axis of the humeral diaphysis may play a role in prolonging glenoid fixation and decreasing polyethylene wear. The distance from the lateral base of the coracoid process to the lateral margin of the greater tuberosity is called the lateral humeral offset. Maintaining this distance is important because a significant decrease reduces the lever arms for the deltoid and supraspinatus muscles, which weakens abduction and impairs function. A significant increase causes excessive tension on the soft tissues (“overstuffing” of the joint), which results in loss of motion and also likely accelerates polyethylene wear. A biomechanical cadaver study determined that humeral articular malposition of more than 4 mm led to increased subacromial contact and that offset of 8 mm in any direction significantly decreased passive range of motion. The authors suggested that anatomic reconstruction of the humeral head/humeral shaft offset should be within 4 mm of normal to minimize subacromial contact and maximize glenohumeral motion.

FIGURE 12.2, Normal glenohumeral relationships. Humeral offset is depicted by distance F to H, thickness of humeral head from B to C, and center of humeral head at C. Note superior position of humeral head proximal to greater tuberosity (D to E).

Based on the clinical success of the Neer II implant, numerous modular designs were developed to improve implant fixation and durability. Detailed studies of shoulder anatomy found not only that normal shoulder anatomy aligned differently than the commonly used prostheses, but also that normal anatomy varied greatly among individuals. Modularity allows a better fit for individual patients because various stem and head sizes can be “mixed and matched” to an individual’s anatomy. Biomechanical studies also showed that shoulder biomechanics are adversely affected by the use of a prosthetic head that is too thick, too thin, or shifted too far from its original position along the plane of the anatomic humeral neck. Other characteristics of shoulder anatomy that are important in prosthesis design are retroversion, head-shaft angle, offset, radius of curvature, and humeral head height. Proximal humeral retroversion is highly variable, ranging from 0 to 55 degrees, depending on the method used for measurement. The proximal and the distal axes used to define retroversion have various definitions. For the proximal reference axis, the plane of the articular surface, a line connecting the center of rotation and the central point of the articular surface, and a line from the greater tuberosity to the central point of the articular surface have been used. For the distal reference axis, the trochlear axis, a line between epicondyles, and the forearm itself have been used. The inclination of the proximal humeral articular surface relative to the humeral shaft is the neck-shaft angle; it ranges from 30 to 55 degrees, depending on the method of measurement. The humeral offset defines the position of the proximal humeral articular surface relative to the humeral shaft; it is measured as the distance from the center of rotation of the proximal humeral articular surface to the central axis of the humeral canal. The medial offset (coronal plane) ranges from 4 to 14 mm, and the anteroposterior offset (transverse plane) ranges from −2 to 10 mm. Reported values for the radius of curvature of the proximal humeral articular surface range from 20 to 30 mm; smaller radii typically are reported in women, and some authors have reported that the radius of curvature is larger in the coronal plane than in the sagittal plane.

Prosthesis Design

Most current systems are modular with varying humeral head diameters and neck lengths to allow more accurate coverage of the cut surface of the humeral neck and improve the ability to establish correct position of the joint line and rotator cuff tension. Some designs allow independent sizing of head thickness and head diameter to make soft-tissue balancing easier. Most stems are made of cobalt-chrome or titanium alloy and have proximal porous ingrowth coating to allow insertion without cement.

In an effort to match the proximal humeral anatomy as closely as possible, several implant systems offer concentric and offset humeral heads. In an anatomic dissection study, Boileau and Walch found that the center of the humeral head was 2.6 mm posterior and 6.9 mm medial to the center of the humeral shaft, and Robertson et al., using CT, noted similar measurements of 2.2 and 7.4 mm.

Anatomic positioning of the humeral head prosthesis is best done with an eccentric locking position of the Morse taper, which allows adjustments to the variable medial offset and any posterior offset. Curiously, postoperative kinematics after total shoulder arthroplasty do not mimic those of the native shoulder. Massimini et al. found that the posterosuperior quadrant of the glenoid is the primary contact location and that the replaced shoulder is not subject to traditional kinematic conceptions. Nevertheless, positioning the head too far superiorly puts additional tension on the overlying supraspinatus tendon and can cause impingement between the head and the acromion. Positioning the head too far inferiorly may cause abutment of the greater tuberosity on the acromion or internal impingement on the rim of the glenoid. Positioning the head too far anteriorly or posteriorly can result in abutment of the uncovered humeral neck on the corresponding glenoid rim and excessive tension on the overlying subscapularis or posterior rotator cuff tendons. Most current systems offer humeral heads that are offset by 3 or 4 mm; some allow several discrete positions, and some allow free rotation around the taper.

Most stems can be inserted with a press-fit or cemented technique. In a cadaver study, micromotion was found to be significantly less with proximal cement than with press-fit; no difference was found between proximal cementation and full cementation, and full cementation did not increase rotational stability over proximal cementation. One study found a very low rate of radiolucencies around proximal porous-coated stems and no clinical signs of loosening. Clinically significant loosening of the humeral component in the absence of infection is uncommon regardless of fixation methods. Due to improved design concepts and ingrowth technology, the use of shorter stems and stemless implants to preserve proximal humeral bone also has become more popular.

Cemented all-polyethylene components remain the gold standard for glenoid component fixation, but designs remain in evolution. Both inlay and onlay glenoid components are available, and many systems now employ bone ingrowth technology to reduce reliance on the bone-cement-implant interface. Regardless of these design features, most components now have an increased radius of curvature (i.e., nonconforming glenoid components ) compared with the humeral head (2 to 6 mm larger) to allow translation during movement and to decrease edge loading. Several studies have shown that translation accompanies glenohumeral rotation after total shoulder arthroplasty. Such translation in a perfectly congruent or conforming joint may have a potential for localized wear and loosening (rocking-horse effect); however, increased loosening and polyethylene wear have not been reported to occur when the radii of curvature of the glenoid component and the humeral head are matched within 2 mm. In a multicenter study of 319 total shoulder arthroplasties using the same type of prosthesis, Walch et al. noted fewer radiolucencies with mismatches between the glenoid and humeral head diameters of more than 5.5 mm (6 to 10 mm). Current opinion seems to suggest that a nonconforming glenoid with a radius curvature of 2 to 4 mm larger than the humeral head allows normal translation during rotation without rim loading or risk of loosening ( Fig. 12.3 ).

FIGURE 12.3, A, When radii of curvature of glenoid component and humeral head conform, translation results in glenoid component rim loading. B, Slight increase in diameter of curvature of glenoid component over that of humeral head allows some translation before rim loading occurs.

A larger glenoid component results in an increased risk for volumetric polyethylene wear similar to what is seen in hip and knee arthroplasty, but this risk has not been substantiated clinically. However, larger components have been linked with improved stability. In a biomechanical study, Tammachote et al. demonstrated improved stability with increasing sizes of glenoid components. Specifically, transverse plane stability improved 17% between the small and medium components and then improved 10% between the medium and large components.

All-polyethylene glenoid components generally are cemented into place. A biomechanical study found that cemented all-polyethylene designs had an overall stress pattern closer to that of an intact glenoid than did uncemented metal-backed components. In a report of 408 shoulder arthroplasties using a standard glenoid component and followed for more than 2 years, Neer reported that only three (0.07%) required reoperation because of glenoid loosening. More recently, Hopkins et al. found that bone quality was important in achieving solid glenoid component fixation. They also stressed the importance of proper implant positioning.

Polyethylene glenoid components generally have a central keel or multiple peripheral pegs for fixation into the glenoid vault. The preponderance of biomechanical evidence suggests an advantage to pegged designs, however. Lacroix et al., using a three-dimensional model and finite element analysis, found that bone stresses were not much affected by prosthesis design except at the tip of the central peg or keel. They did conclude, however, that pegged prostheses were better for normal bone. As understanding of glenoid deformities has improved, augmented glenoid components also have been developed to accommodate commonly seen glenoid wear patterns. Although long-term studies are not yet available, short-term outcomes have been promising.

The biomechanics of reverse total shoulder arthroplasty revolve around recruitment of the deltoid to restore active motion in a rotator cuff-deficient shoulder. All reverse arthroplasty designs medialize the center of rotation to some degree and generally lengthen the deltoid to increase its lever arm to power forward elevation. The original Grammont style reverse total shoulder arthroplasty design medialized the center of rotation at the glenoid face and used a valgus neck-shaft angle of 155 degrees in the humeral component to provide straight line vertical pull of the deltoid. Although this implant improved loosening rates over prior designs and was reliable for the restoration of forward elevation, the return of external rotation was less reliable, and concerns developed over impingement between the polyethylene humeral bearing surface and glenoid neck with resultant scapular notching. Therefore, implant designers turned toward developing “lateralized” (i.e., less-medialized) components in which the center of glenohumeral rotation is placed lateral to the glenoid face. This can be done through the glenosphere or with bone graft (so-called medial humerus-lateral glenoid constructs) or the humeral bearing surface (lateral humerus-medial glenoid constructs). Because most current systems employ modular design concepts that often allow conversion between anatomic total shoulder arthroplasty and reverse total shoulder arthroplasty, constructs that employ a lateral humerus and lateral glenoid design are available, but uncommonly used. Nevertheless, these convertible systems offer an advantage in the revision setting because they often allow preservation of the humeral stem without the need for removal.

The biomechanical data on lateralization in reverse total shoulder arthroplasty suggest an improvement in remaining rotator cuff torque, which may be helpful for restoration of internal and external rotation. In addition, a systematic review concluded that lateralized constructs reduce scapular notching rates as well as improve external rotation. In general, larger glenospheres are thought to improve range of motion and decrease scapular notching as well. Additional investigation has focused on the position of the humeral component in reverse total shoulder arthroplasty. Placing the humeral stem in neutral version demonstrated the least amount of intraarticular and extraarticular impingement, but stems placed in 40 degrees of retroversion allowed the greatest range of motion in a simulator study. To balance these two priorities, most authorities recommend placing the humeral stem in 20 to 30 degrees of retroversion for reverse total shoulder arthroplasty.

Clinical Presentation and Radiographic Evaluation

The clinical appearance of advanced glenohumeral degeneration was initially described by Neer. Patients typically present with global pain about the shoulder with difficulty performing overhead activities and, often, activities of daily living. On physical examination, diminished active and passive range of motion may be observed, and patients may have previously been diagnosed with adhesive capsulitis. In patients with intact rotator cuff tendons, strength is often preserved but may be diminished secondary to pain. Palpable crepitus often can be elicited with passive internal and external rotation of the glenohumeral joint and/or with strength testing. The acromioclavicular joint and biceps tendon should be carefully evaluated because symptomatic acromioclavicular degeneration and/or biceps tendinitis may also be present.

Standard radiographs include anteroposterior views with a 40-degree posterior oblique view in neutral position and internal and external rotation and an axillary lateral view. Radiographs of the opposite, uninvolved shoulder and humerus are helpful in unusual situations, such as when a custom implant is indicated for large humeral or glenoid deficiencies.

The radiographic appearance varies with the patient’s pathologic process. Those with osteoarthritis reliably demonstrate subchondral sclerosis and a large osteophyte on the inferior aspect of the humeral head ( Fig. 12.4 ). This so-called “goat’s beard” is pathognomonic of advanced glenohumeral degeneration. These osteophytes can enlarge the humeral head to twice its normal size, resulting in capsular distention ( Fig. 12.5 ). Joint space narrowing, which is so reliably seen in hip and knee osteoarthritis, is not commonly seen in the shoulder until very late in the disease process owing to the non-weight-bearing position of the shoulder under standard radiography. Axillary lateral radiographs typically demonstrate posterior subluxation of the humeral head on the glenoid, and a wear pattern in the posterior glenoid may be present ( Fig. 12.6 ). Patients with capsulorrhaphy arthropathy have a similar radiographic appearance except that loose bodies and osteophytes tend to be more common and numerous ( Fig. 12.7 ) than in standard osteoarthritis.

FIGURE 12.4, Subchondral sclerosis and large osteophyte on inferior aspect of humeral head.

FIGURE 12.5, “Goat’s beard” is pathognomonic of advanced glenohumeral degeneration.

FIGURE 12.6, Axillary radiograph (A) and CT scan (B) showing severe degenerative arthritis.

FIGURE 12.7, Radiograph showing capsulorrhaphy arthropathy; note numerous loose bodies and osteophytes.

Malunions of proximal humeral fractures can make shoulder arthroplasty more difficult. A varus malunion between the head and shaft can complicate positioning of components, but osteotomy usually is unnecessary as newer short-stem and stemless designs allow accommodation of these deformities. Patients with inflammatory arthritis often do not have an inferior osteophyte on radiographs and, instead, demonstrate a more symmetrical pattern of joint space narrowing with periarticular osteopenia. The wear pattern is more commonly central in the glenoid, and posterior subluxation of the humeral head is less common. Cystic change is also common. Rotator cuff tears are more common in patients with rheumatoid arthritis than in patients with osteoarthritis: full-thickness rotator cuff tears have been identified in 25% to 50% of patients undergoing shoulder arthroplasty. Most of these tears are in the superior rotator cuff.

MRI can be a useful preoperative planning tool in this population. In patients with strength deficits that could be caused by either arthritic pain or a torn rotator cuff, MRI can help determine the status of the tendons. Whereas rotator cuff tendinopathy is common in this setting, full-thickness tears are uncommon and are seen in only about 10% of patients. MRI also typically demonstrates advanced cartilage degeneration and may show numerous other findings, including thinning of the subscapularis and degenerative changes in the biceps tendon. Increased capsular volume posteriorly and capsular contraction anteriorly are usual changes as well. Finally, in patients with precollapse osteonecrosis, MRI is useful for visualizing the area of dead bone and is often the best tool to make the diagnosis ( Fig. 12.8 ).

FIGURE 12.8, Magnetic resonance image showing precollapse osteonecrosis.

CT is also a valuable asset in the evaluation and preoperative planning for patients with advanced glenohumeral degeneration. The scans give an excellent picture of the patient’s glenoid bone stock and the pattern of glenoid wear, which is essential for determining if standard glenoid components can be used or if a bone graft will be needed. Loose bodies may be seen in the axillary or subscapularis recess or attached to the synovium. In the case of malunions or nonunions, three-dimensional reconstruction helps to precisely show the bony deformities and defects before surgery. CT arthrography often is useful to evaluate both the bony architecture of the shoulder and the rotator cuff in patients with contraindications to MRI.

Preoperative Planning

Once the patient is determined to have advanced glenohumeral degeneration and has consented to a shoulder arthroplasty, preoperative planning includes careful evaluation of the radiographs and the CT scans, if obtained. As noted earlier, CT gives a clear view of the glenoid bone stock and wear pattern. Viewing these changes preoperatively allows the surgeon to prepare for the possibility that glenoid bone grafting, augmented components, or glenoid recontouring procedures may be necessary to correct the deformity. The role of preoperative planning based on three-dimensional CT scans to optimize implant position, size, and range of motion is an evolving area of investigation. Most reports have concluded that preoperative planning software using CT scans results in more accurate glenoid component placement with either conventional or patient-specific implants. In particular, shoulders with significant posterior glenoid erosion tend to benefit from implant reaming and targeting systems.

In patients who have had previous shoulder surgery, infection can be evaluated by laboratory tests including erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and complete blood cell count. Aspiration and culture of glenohumeral joint fluid, holding the culture for at least 14 days to isolate Cutibacterium acnes ( formerly Propionibacterium acnes) , is essential if infection is suspected. Electromyography and nerve conduction studies should be obtained preoperatively in patients with suspected deficits. Finally, preoperative medical clearance often is warranted in this typically elderly population.

Hemiarthroplasty

Indications

The predominant indication for shoulder hemiarthroplasty is end-stage joint degeneration in a patient with a contraindication to glenoid resurfacing. The preponderance of evidence indicates that total shoulder arthroplasty is superior to hemiarthroplasty regarding pain, function, activity level, long-term survival, and revision rate and, therefore, the glenoid should be resurfaced if at all possible in patients with bipolar arthritis. However, young laborers, patients with glenoid bone stock insufficiency, patients with high activity levels, and those with preserved glenoid cartilage may benefit from hemiarthroplasty. Also, rotator cuff tears remain a contraindication to prosthetic glenoid resurfacing. Although excellent pain relief and moderate improvements in function and motion have been reported after total shoulder arthroplasty in patients with irreparable rotator cuff tears, some long-term follow-up studies noted an association between glenoid component loosening and irreparable rotator cuff tears. Eccentric loading of the glenoid caused by superior migration of the humeral component has been cited as a cause of glenoid loosening (the “rocking-horse effect”).

Historically, hemiarthroplasty was recommended for patients in whom a massive, long-standing tear of the rotator cuff caused progressive degenerative changes of the glenohumeral joint (cuff tear arthropathy). However, reverse total shoulder arthroplasty has emerged as a more reliable option to reestablish shoulder level function in these patients.

Matsen et al. listed five situations in which hemiarthroplasty should be considered: (1) the humeral joint surface is rough, but the cartilaginous surface of the glenoid is intact, and there is sufficient glenoid arc to stabilize the humeral head; (2) there is insufficient bone to support a glenoid component; (3) there is fixed upward displacement of the humeral head relative to the glenoid (as in cuff tear arthropathy or severe rheumatoid arthritis); (4) there is a history of remote joint infection; and (5) heavy demands would be placed on the joint (anticipated heavy loading from occupation, sport, or lower extremity paresis).

Contraindications to hemiarthroplasty are recent sepsis, a neuropathic joint, a paralytic disorder of the joint, deficiencies in shoulder cuff and deltoid muscle function, and lack of patient cooperation. Remote infection may not be an absolute contraindication, but the operation should be undertaken only after thorough workup to document sterilization of the glenohumeral joint and careful consideration by the surgeon and the patient of all the potential hazards involved.

Surgical Technique

The goal of hemiarthroplasty is restoration of the humeral articular surface to its normal location and configuration. Because the glenoid is not replaced, the size, radius, and orientation of the prosthetic joint surface must duplicate that of the original biologic humeral head. Radiographs of the contralateral shoulder can provide information about a patient’s normal humeral head anatomy. Care should be taken to avoid a “big head” humeral prosthesis that can “overstuff” the joint ( Fig. 12.9 ).

FIGURE 12.9, Use of humeral head component that is too large results in overstuffing of joint, which can limit range of motion and lead to rotator cuff failure.

Hemiarthroplasty

Technique 12.1

  • Place the patient in the beach chair position to allow positioning of the patient at the top and edge of the table ( Fig. 12.10A ). Pad all bony prominences. The medial border of the scapula should be free and off the table, allowing full adduction to gain access to the intramedullary canal.

    FIGURE 12.10, Hemiarthroplasty technique (see text). A, Beach-chair position with arm extended off table. B, Incision. C, Axillary nerve is identified. D, Darrach retractor is used to lift head of humerus out of glenoid fossa. SEE TECHNIQUE 12.1.

  • Secure the patient’s head to the headrest, holding the head in a position that avoids hyperextension or tilting of the neck, which can cause compression of the cervical roots.

  • Prepare the arm and drape it widely. We recommend using occlusive dressings to cover the entire surgical field.

  • Make an incision anteriorly, approximately one third to halfway between the coracoid and the lateral aspect of the acromion ( Fig. 12.10B ). Carry dissection down to the deltoid and raise medial and lateral flaps to mobilize the deltoid.

  • Open the deltopectoral interval and allow the cephalic vein to fall medially.

  • Perform subdeltoid, subcoracoid, and subacromial releases to release the proximal humerus. In the subcoracoid space, locate the axillary nerve by passing the volar surface of the index finger down along the anterior surface of the subscapularis muscle ( Fig. 12.10C ). If scarring and adhesions make identification of the nerve difficult, pass an elevator along the anterior surface of the subscapular muscle to create an interval between the muscle and the nerve. Great care must be taken in this step to avoid plunging into the brachial plexus. After the axillary nerve is identified, carefully retract and hold it out of the way, especially during the crucial steps of releasing the anteroinferior capsule.

  • We prefer to perform a biceps tenodesis before incising the subscapularis. A figure-of-eight stitch is placed between the biceps and pectoralis major tendons. The biceps is then divided, and the proximal portion is later resected before making the humeral head osteotomy.

  • Incise the subscapularis 1 cm medial to the lesser tuberosity. Place two retention sutures in the subscapularis to be used as traction sutures when freeing the rest of the tendon from the underlying capsule and scar tissue. Some authors prefer either a lesser tuberosity osteotomy or a release of the subscapularis directly off of bone. If external rotation is markedly limited, the subscapularis also can be reattached to the proximal humerus more medially to allow increased external rotation. Alternatively, the tendon can be lengthened with a coronal Z-plasty technique.

  • Incise the rotator interval, directing the cut medially toward the glenoid. Typically, a large amount of synovial fluid escapes as the joint is entered.

  • Release the anteroinferior capsule from the humerus and externally rotate the arm to bring the inferior aspect of the shoulder capsule into view. Take care to stay directly on bone so as not to injure the axillary nerve during the capsular release. The importance of the inferior capsule release cannot be overstated and must be thoroughly carried out to at least the 7 o’clock position to dislocate the humeral head and gain access to the glenoid.

  • Once the capsule is adequately released, place a large Darrach retractor in the joint and gently externally rotate, adduct, and extend the arm to deliver the humeral head up and out of the glenoid fossa ( Fig. 12.10D ). If the humeral head cannot be delivered in this fashion, the inferior capsule must be released further.

  • Prepare the humeral canal, using the humeral axis to reference the osteotomy. Initially, open the canal with a high-speed burr at the base of the rotator cuff footprint and ream it to a size where appropriate fit is felt. Do not use motorized equipment for reaming, and be careful not to overream the canal, which could create a stress riser or cause a fracture.

  • We prefer to use a cutting guide that employs extramedullary referencing, using the axis of the forearm as the reference point, with the cutting guide pinned into position at 30 degrees of retroversion. Other surgeons may prefer a free-hand, anatomic neck-cutting technique. Regardless of the cutting technique, care must be taken to avoid violating the rotator cuff.

  • Complete the osteotomy with an oscillating saw. If any inferior humeral head osteophyte remains, remove it with a rongeur.

  • After the head cut, broach the humeral canal to the same size as the reamed canal. It is imperative to confirm proper position of the broaches in 30 degrees of retroversion during this step to prevent component malposition.

  • Inspect the glenoid to confirm there is enough glenoid cartilage to provide an adequate bearing surface for the metal humeral head. After this inspection, check the humeral trial stem to ensure it is seated securely within the humeral canal. If so, tap the component stem into position, taking care to keep the stem in 30 degrees of retroversion.

  • If cementing is deemed necessary because of a previous surgical procedure, fracture, osteoporosis, rheumatoid arthritis, or degenerative cysts, place a cement restrictor or a cortical bone plug from the resected humeral head 2 cm inferior to the tip of the prosthesis.

  • Place a trial humeral head and reduce the glenohumeral joint using internal rotation and gentle traction. With the arm in neutral rotation, check the height of the humeral head to confirm anatomic reconstruction. As a rule of thumb, the most superior aspect of the humeral head should be 1 cm superior to the greater tuberosity.

  • Also check the version to confirm that the humeral head rests directly across from the glenoid. With a thumb on the lesser tuberosity, push the humeral head posteriorly and then release it: 50% posterior excursion with immediate “bounce back” of the humeral head is optimal. Evaluate forward elevation and internal rotation.

  • Once the checks have been performed, thoroughly clean the Morse taper, impact the humeral head into position, and reduce the joint for the final time.

  • Perform a tight closure of the rotator interval and the subscapularis with heavy nonabsorbable suture. Both transosseous and tendon-to-tendon repair techniques are reasonable. If the tendon was divided or lengthened, repair and secure it with heavy nonabsorbable sutures to allow immediate passive movement beginning the day after surgery. If a lesser tuberosity osteotomy is preferred, robust fixation of the bone back to the humeral shaft is critical. Place a drain in the deltopectoral interval and close it with No. 0 sutures. Close the skin in standard fashion and place the arm in a soft sterile dressing and a sling while the patient is still upright and before being aroused from anesthesia.

Postoperative Care

Patients are instructed in a gentle home exercise program with passive forward elevation to 90 degrees and passive external rotation to neutral. Patients typically are discharged from the hospital on the morning after surgery and are encouraged to use a pillow behind the elbow while recumbent in the sling to support the extremity. Full-time sling immobilization continues for 6 weeks, followed by 6 weeks of sling use only in unprotected environments. Therapy progresses to full passive range of motion by 6 to 12 weeks and to isometric strengthening at 10 weeks.

Outcomes

Hemiarthroplasty has been reported to initially relieve pain in 75% to 95% of patients with glenohumeral arthritis and severe rotator cuff deficiency, with more modest improvements in range of motion and strength. However, long-term results have been compromised by persistent pain from glenoid arthrosis, anterosuperior instability, and progressive bone loss.

The best results of shoulder hemiarthroplasty are in patients with osteonecrosis, in whom hemiarthroplasty has been reported to provide consistently good pain relief in 90%, with an almost normal preoperative range of motion ( Table 12.2 ). Results are not quite as good in patients with rheumatoid arthritis, osteoarthritis, glenoid dysplasia, or posttraumatic glenohumeral arthrosis but are satisfactory in most patients, although range of motion is decreased. In particular, one long-term report found that only 25% of patients were satisfied with stemmed hemiarthroplasty for shoulder osteoarthritis at an average of 17 years follow-up.

TABLE 12.2
Reported Results of Shoulder Hemiarthroplasty for Rotator Cuff Tear Arthropathy
  • Modified from Sanchez-Sotelo J: Shoulder arthroplasty for cuff-tear arthropathy. In Morrey BF, editor: Joint replacement arthroplasty , ed 3, Philadelphia, 2003, Churchill Livingstone. NR , Not reported.

  • Copyright of Mayo Foundation.

Study No Mean Age (Range) Mean Follow-Up, Years (Range) No Pain or Mild Postoperative Pain Active Elevation Preoperative/Postoperative Mean, Degrees (Range) Successful Results Comments
Arntz et al. (1993) 18 71 (54-84) 2 (2-10) 11 (61%) 66 (44-90)/112 (70-160) NR Two reoperations for symptomatic glenoid erosion, one for symptomatic instability, one for postoperative traumatic fracture of the acromion
Williams and Rockwood (1996) 21 72 (59-80) 4 (2-7) 18 (86%) 70 (0-155)/120 (15-160) 18 (86%) No instability or reoperation reported
Field et al. (1997) 16 74 (62-83) 3 (2-5) 13 (81%) 60 (40-80)/100 (80-130) 10 (62%) One intraoperative humeral shaft fracture; 4 patients with instability, 2 of whom required reoperation for subscapularis advancement (1) and resection arthroplasty (1)
Zuckerman et al. (2000) 15 73 (65-81) 2 (1-5) 7 (47%) 69 (20-140)/86 (45-140) NR Eleven of 15 patients satisfied with operation; 1 had anterior instability
Sanchez-Sotelo: Mayo Clinic series (2003) 33 69 (50-87) 5 (2-11) 24 (73%) 72 (30-150)/91 (40-165) 22 (67%) One intraoperative humeral shaft fracture; 7 patients with anterosuperior instability
Goldberg et al. (2008) 34 72 (48-90) 4 (2-12) 26 (76%) 78 (20-165)/111 (40-180) 26 (76%) One patient required reoperation for osteophyte removal; no problems related to implant failure, loosening, infection, or fracture

Modified Hemiarthroplasty: Interposition Arthroplasty and Glenoidplasty (Ream and Run)

As it has become clear that glenoid arthritis continues to be a long-term concern for patients undergoing isolated shoulder hemiarthroplasty, some authors have explored various types of glenoid resurfacing procedures, particularly for younger, higher-demand patients. These interposition techniques aim to allow the metal humeral head to articulate with a cushioning surface rather than with the native glenoid in an effort to minimize arthritic progression and subsequent pain. Although most interposition procedures have demonstrated early success, intermediate-term outcome studies have been disappointing.

Fascial interposition hemiarthroplasty (biologic resurfacing) has been recommended for use in young, active patients with osteoarthritis. The glenoid is resurfaced using the anterior capsule sewn over the glenoid face, a free fascia lata graft, or commercially available patch devices. Good long-term outcomes have been reported with this biologic glenoid resurfacing technique. Other studies, however, have noted a high number of failures and poor outcomes using Achilles tendon allograft as a resurfacing material with hemiarthroplasty.

Lateral meniscal allografts also have been used as an interposition material. In this procedure, the anterior and posterior horns of the allograft are sewn to each other to form a circular surface for articulation with the humeral head. The allograft is laid onto the glenoid and secured, typically with suture anchors. Despite initially positive results, intermediate-term outcomes have been inferior to standard hemiarthroplasty.

A third technique that has been advanced involves concentric reaming of the glenoid combined with shoulder hemiarthroplasty, the “ream and run” procedure. Intermediate-term outcomes have demonstrated range-of-motion and Simple Shoulder Test scores to be significantly improved after this procedure, with a revision rate of 16%. However, it should be noted that strict patient selection criteria should be used and that an intensive and extended rehabilitation program is associated with this procedure.

Resurfacing Hemiarthroplasty

In an attempt to preserve proximal humeral bone stock, shoulder resurfacing procedures have been developed. Resurfacing implants do not use a stem for intramedullary fixation but instead form a cap over the humeral articular surface and are typically stabilized with a smaller post in the metaphysis. This implant design has been reported to more closely replicate humeral head geometry and reduce eccentric glenoid loading compared with stemmed hemiarthroplasty ( Fig. 12.11 ). Outcomes of humeral resurfacing have generally been successful, with patient satisfaction rates as high as 93% and overall results similar to that of stemmed prostheses. Several series have reported similar success in specific patient cohorts with rheumatoid arthritis, osteoarthritis, and cuff tear arthropathy; however, the reported revision rate of humeral head resurfacing is higher than that of stemmed hemiarthroplasty.

FIGURE 12.11, Stemmed shoulder hemiarthroplasty.

Total Shoulder Arthroplasty

Total shoulder arthroplasty is a well-established procedure with an excellent long-term track record of pain relief and functional improvements. Long-term results have been reported that are equivalent to those after replacement of the knee and hip. In a meta-analysis of series that included 646 shoulder arthroplasties done for osteoarthritis, Wilde found that 89% had complete or nearly complete relief of pain; 91% of patients with rheumatoid arthritis reported satisfactory relief.

Indications

The primary indication for total shoulder arthroplasty is end-stage glenohumeral joint degeneration with an intact rotator cuff. This encompasses a number of conditions, including osteoarthritis, rheumatoid arthritis, osteonecrosis, posttraumatic arthritis, and capsulorrhaphy arthropathy. Contraindications to shoulder arthroplasty include active or recent infection and irreparable rotator cuff tears. Paralysis with complete loss of function of the deltoid is also a contraindication. Debilitating medical status and uncorrectable glenohumeral instability are additional contraindications to shoulder arthroplasty.

Other patient-specific factors should be considered before total shoulder arthroplasty: morbidly obese patients are known to have a higher rate of medical complications and to incur higher costs; diabetes is reported to correlate with a higher rate of perioperative medical complications; and hepatitis C also has been established as an independent factor correlating with increased complications, including infection and need for revision. Therefore, although perioperative mortality is only approximately 1%, careful medical optimization and patient selection are recommended before shoulder arthroplasty.

Surgical Technique

Total Shoulder Arthroplasty

Technique 12.2

  • Approach the glenohumeral joint as described in Technique 12.1. Once the trial broach is tapped into position, remove the retractors from about the humerus. Of note, stemless humeral components for total shoulder arthroplasty have been investigated and approved by the United States Food and Drug Administration (FDA).

  • Expose the glenoid by placing a retractor on the posterior aspect of the glenoid to sublux the humerus posteriorly.

  • Debride the glenoid vault of all remaining labral tissue and articular cartilage.

  • Release the anterior capsule and place a flat Darrach retractor on the anterior glenoid neck to aid exposure.

  • The glenoid is not adequately exposed until the anterior, posterior, superior, and inferior aspects of the glenoid can be seen. Once this is accomplished, inspect the glenoid for wear and bone defects. Typically, there is posterior erosion of the glenoid, and the anterior rim of the glenoid needs to be lowered to reestablish correct version ( Fig. 12.12 ). This can be done by eccentric reaming. Alternatively, glenoid bone grafting or augmented glenoid components can elevate the posterior glenoid to re-establish version. A preoperative CT scan with or without planning software can aid in understanding glenoid orientation and morphology.

    FIGURE 12.12, Problem of and solution for uneven wear and erosion of glenoid. A, Area of wear. B, If glenoid component is inserted without correction of slope, anchoring device passes out of medullary canal; tilt and loss of height also make implant unstable. C and D, Severe erosion is corrected by bone grafting. Piece of humeral head is secured to scapula with 4-mm AO navicular screw. Lesser erosion can be offset by building up low side with acrylic cement or lowering high side. Building up with cement is not recommended because of feared cement loosening. Lowering high side often requires shortening holding device of glenoid component and creates laxity between components, which can make implant temporarily unstable and requires special postoperative care. Alternatively, an augmented glenoid component can be used to correct glenoid version. SEE TECHNIQUE 12.2.

  • Once the glenoid vault is debrided, make a centering hole, typically with a guide. It often is helpful to confirm adequate depth and position of the starting hole with a small curet. After the starting hole is made, proceed with glenoid reaming until the sclerotic bone of the arthritic glenoid is removed and the subchondral plate is seen. With the common posterior wear pattern of osteoarthritis, reaming typically is done in an eccentric fashion so that the anterior lip of the glenoid is planed down. If posterior rim wear is significant and the anterior rim has not been lowered, the component sits excessively retroverted, and anterior glenoid neck perforation is likely. Take care also not to ream too aggressively medially and thereby compromise the glenoid bone stock, as this may result in component subsidence.

  • When reaming is complete, prepare the glenoid for the implant. Systems vary in their instrumentation but involve precise placement of the anchoring pegs or keel. To provide secure fixation and reduce the risk of loosening, the glenoid trial must sit securely against the subchondral bone of the glenoid without any rocking after the glenoid is prepared. Cement cannot be used to adjust for poor seating of the glenoid component.

  • Prepare the glenoid vault for cementing with pulsed lavage to remove debris and blood. Thoroughly dry the peg holes or keel before cementation.

  • Tuberculin syringes are helpful to pressurize the cement. Pack cement into the syringe and then inject it into the peg holes or into the keel.

  • Next, insert the glenoid component and maintain thumb pressure until the cement has hardened. Most shoulder systems also come with an instrument to hold the glenoid component in place while the cement hardens. This method allows excellent pressurization and interdigitation of the cement into the cancellous bone of the glenoid vault, and postoperative radiolucent lines seen with other cementing techniques are minimized. Some systems use a polyethylene or metal ingrowth post to provide a press-fit of the glenoid component, which provides immediate stability so that the component does not rely solely on digital pressure while the cement is curing ( Fig. 12.13 ). Although totally uncemented, metal-backed glenoid components exist, they are associated with higher revision and failure rates.

    FIGURE 12.13, A, Degenerative joint disease of left shoulder. B, Anatomic total shoulder arthroplasty with a stemless humeral component and ingrowth glenoid implant. SEE TECHNIQUE 12.2.

  • After the cement has hardened, check the broach to ensure that it is still secure within the humeral canal. If so, insert the humeral prosthesis as described in Technique 12.1. Head height, range of motion, and soft-tissue balancing are critical to providing an optimal outcome. With posterior pressure on the lesser tuberosity, the ideal cuff tension allows the humeral head to translate approximately 50% of the glenoid component width and then recenter it when pressure is removed. If the humeral head dislocates posteriorly with this maneuver, it must be corrected with a larger and/or thicker head. Most current systems use modular heads with a variety of diameters and thicknesses to accomplish this goal.

  • Once the appropriate head is selected, dry the Morse taper and tap the head into position. Reduce the glenohumeral joint and close the wound as described in Technique 12.1.

Postoperative Care

Postoperative care and rehabilitation are essentially the same as after shoulder hemiarthroplasty (see Technique 12.1) and are governed by protection of the subscapularis repair.

See also .

Outcomes

The preponderance of evidence in randomized and nonrandomized studies suggests that, although hemiarthroplasty can provide pain relief and increased range of motion in patients with osteoarthritis and a concentric glenoid, total shoulder arthroplasty generally provides superior results in terms of patient satisfaction, function, and strength, especially at longer-term follow-up. A Cochrane Database systemic review of seven studies found that total shoulder arthroplasty is associated with better shoulder function than hemiarthroplasty but does not provide any other significant clinical benefits. Mather et al. found that in elderly patients (≥64 years) with osteoarthritis, total shoulder arthroplasty with a cemented glenoid component was more cost effective than hemiarthroplasty in improving quality of life. In addition, an economic decision model concluded that total shoulder arthroplasty was a more cost-effective intervention compared to hemiarthroplasty in young patients with shoulder arthritis.

Results after total shoulder arthroplasty have been predictable in producing pain relief and functional improvements for patients with a variety of degenerative glenohumeral conditions, with good results reported in 65% to 95% of patients. Loosening of the glenoid component, however, has been reported in almost half of shoulders at more than 10-year follow-up and is often associated with pain. The best functional results are obtained in patients with osteoarthritis because the rotator cuff usually is intact and of good quality and the bone stock is typically adequate. In patients with rheumatoid arthritis, the quality of the rotator cuff directly influences the functional result.

The durability of total shoulder replacement is similar to that of hip and knee replacements. Results at long-term follow-up in several series have reported 85% component retention at 20 years of follow-up and revision rates for all causes averaging less than 10%. Loosening of the glenoid component has been reported in almost half of shoulders at more than 10-year follow-up and often is associated with pain; however, glenoid component loosening has averaged 4.3% over multiple studies.

Osteoarthritis

Most total shoulder arthroplasties are done in patients with osteoarthritis or rheumatoid arthritis. Few (<10%) patients with osteoarthritis have complete rotator cuff tears, but contracture of the subscapularis tendon is common. A large multicenter study reported significant improvements in Constant scores and range of motion at 10-year follow-up. Glenoid component survivorship with revision as the end point was 94.5%. In patients older than 80 years, total shoulder arthroplasty remains a reliable option, with 80% attaining an excellent or satisfactory result at an average of 5.5 years, even though there is an increased risk for perioperative medical complications. In patients younger than 50 years, one report with a 20-year minimum follow-up found over 75% component retention, but clinical outcomes tended to decline, ultimately with a large number of unsatisfactory results. This and other similar studies, including a systematic review, suggest caution in performing total shoulder arthroplasty in younger patients.

Inflammatory Arthritis

Total shoulder replacement also is effective in patients with inflammatory arthritis, resulting in significant improvements in pain, range of motion, function, and quality of life. The frequency of perioperative complications in patients with rheumatoid arthritis is similar to that in patients who have total shoulder arthroplasty for other indications; in fact, patients with rheumatoid arthritis have been reported to have shorter average hospital stays and a higher likelihood of routine discharge. Satisfactory pain relief also was reported in 11 shoulders severely affected by juvenile rheumatoid arthritis, although improvements in range of motion were minor.

If shoulder and ipsilateral elbow replacements are necessary, the most painful joint should be replaced first. Function may not be significantly improved in patients with severe rheumatoid arthritis until the second joint is replaced. If the shoulder is operated on first, and if a cemented prosthesis is chosen, a cement restrictor or canal plug must be used to prevent cement from entering the distal medullary canal. A stress riser can occur in the humeral diaphysis between the tips of the two humeral components. If shoulder arthroplasty is done first, a short-stem prosthesis should be used; if a long-stem component is in place at either joint, the cement column for the second arthroplasty should extend to and include the cement column of the first arthroplasty. If shorter components are used, a long length (∼360 mm) of unfilled humerus should be left between the cement columns.

Posttraumatic Arthritis and Posttraumatic Sequelae

Shoulder arthroplasty for arthritis secondary to chronic displaced fractures and fracture-dislocations of the glenohumeral joint is particularly difficult because of contractures and scarring of the soft tissues, malunion or nonunion of the tuberosities, and possible nerve injuries. Axillary nerve injuries can significantly impair motion and strength due to loss of deltoid function.

Anatomic shoulder arthroplasty also has been described for proximal humeral malunions. In a mixed cohort of hemiarthroplasty and total shoulder arthroplasty, an average forward elevation of 109 degrees and improvements in pain were reported. However, postoperative instability because of rotator cuff dysfunction or capsular injury was a common complication.

Osteonecrosis

The most common causes of osteonecrosis of the humeral head are heavy corticosteroid use, sickle cell disease, and alcoholism; less common causes include dysbarism, Gaucher disease, and systemic lupus erythematosus. Idiopathic osteonecrosis also is fairly common. Cruess classified osteonecrosis of the humeral head into five stages of increasing severity ( Fig. 12.14 ). Symptomatic progression of the osteonecrosis is almost certain in those with stage IV or stage V. Both total shoulder arthroplasty and hemiarthroplasty have been successful in obtaining subjective improvement in most patients with humeral head osteonecrosis.

FIGURE 12.14, Stages of osteonecrosis of humeral head. Stage I changes are invisible on plain radiographs, and they are not discernible on gross examination. Stage II is marked by sclerotic changes and evidence of bone remodeling, but shape and sphericity of humeral head are maintained. Stage III is differentiated from stage II by presence of subchondral bone collapse or fracture, resulting in loss of humeral head sphericity. In stage IV, humeral head has area of collapsed articular surface; fragment may become displaced intraarticularly. In stage V, there are osteoarthritic changes in the glenoid fossa.

Most patients with osteonecrosis are relatively young, with good bone quality, and secure press-fit fixation of the humeral component can be obtained. The need for a glenoid component (see section on hemiarthroplasty) is based on the condition of the glenoid fossa, the amount of deformity present, and the degree of articular cartilage loss. In many patients with intact glenoid cartilage, humeral head replacement alone is satisfactory, whereas most patients with stage V disease require a glenoid component because of extensive articular cartilage loss.

Capsulorrhaphy Arthropathy and Arthropathy of Recurrent Instability

Advanced glenohumeral arthritis can be a late sequela of anterior instability surgery. It is more common after nonanatomic repairs and in younger patients than typical glenohumeral arthritis and is characterized by severe internal rotation contracture and a severely osteophytic arthritis. Excessive soft-tissue tension on the side of the dislocation may produce a fixed subluxation of the humeral head in the posterior direction, requiring release of the iatrogenic soft-tissue contracture to restore joint balance and mobility. Subscapularis lengthening, anterior capsular release, or posterior capsular plication may be required to correct soft-tissue contractures. Although total shoulder arthroplasty can improve function in patients with glenohumeral degeneration associated with shoulder instability or instability surgery, a complication rate of 40% has been reported, particularly subscapularis insufficiency, with 20% of patients requiring additional surgery. Comparative studies have demonstrated equivalent functional outcomes but lower complication rates when reverse total shoulder arthroplasty is employed for this disorder.

Reverse Total Shoulder Arthroplasty

In 1983, Neer, Craig, and Fukuda described “cuff-tear arthropathy” as a distinct form of osteoarthritis associated with a massive chronic tear of the rotator cuff. Clinically, rotator cuff arthropathy is characterized by pain, poor active motion, near-normal passive motion, crepitus, weakness, and occasionally significant fluid buildup under the deltoid. Radiographic changes include elevation of the humeral head, formation of an acromiohumeral pseudoarticulation, and loss of joint space at the glenohumeral joint. The radiographic pattern of degenerative changes can vary, and not all patients with rotator cuff arthropathy have pain or limited motion.

The glenohumeral instability resulting from this condition is manifested as proximal migration of the humerus relative to the glenoid, resulting in erosion of the superior glenoid and the caudal surface of the acromion. Rotator cuff tears have been implicated in early glenoid component loosening in total shoulder replacements, and irreparable tears are a contraindication to traditional glenoid resurfacing. Until the introduction of reverse total shoulder arthroplasty, patients with cuff tear arthropathy were generally treated with hemiarthroplasty, which was a durable, if imperfect, solution that provided adequate pain relief but did not restore forward elevation.

Indications

The primary indication for reverse total shoulder arthroplasty is a nonfunctional rotator cuff. This encompasses a number of disease processes, including cuff tear arthropathy, pseudoparalysis caused by massive rotator cuff tear without arthritis, multiple failed rotator cuff repairs with poor function and anterosuperior instability, three- and four-part proximal humeral fractures in the elderly, proximal humeral nonunions, greater tuberosity malunions, and failed shoulder arthroplasty with rotator cuff insufficiency. Reverse total shoulder arthroplasty is most appropriate for patients with an intact deltoid, adequate bone stock to support the glenoid component, no evidence of infection, no severe neurologic deficiency (Parkinson disease, Charcot joints, syringomyelia), and no excessive demands on the shoulder joint ( Box 12.1 ).

BOX 12.1
Indications for Reverse Total Shoulder Arthroplasty
From Sanchez-Sotelo J: Reverse total shoulder arthroplasty. In Morrey BF, ed: Joint replacement arthroplasty: basic science, elbow and shoulder , Philadelphia, 2011, Wolters Kluwer, p 277.

  • Cuff-tear arthropathy

  • Massive rotator cuff tear with pseudoparalysis

  • Severe inflammatory arthritis with a massive cuff tear

  • Failed shoulder arthroplasty

    • Absence of tuberosities (failed hemiarthroplasty for fracture/nonunion)

    • Absence of cuff (failed hemiarthroplasty for cuff-tear arthropathy)

    • Instability

  • Proximal humeral fracture

  • Proximal humeral nonunion

  • Reimplantation for deep periprosthetic infection

  • Reconstruction after tumor removal

Contraindications generally include loss or inactivity of the deltoid and excessive glenoid bone loss that would not allow secure implantation of the glenoid component. Some authors have suggested that the procedure is unsuitable for patients younger than 70 years old; however, current opinion has moved more toward accepting use of the reverse prosthesis in younger patients for some end-stage disorders. Surgeon inexperience also is a relative contraindication to reverse total shoulder arthroplasty. One study demonstrated a volume-value relationship in which costs and hospital length of stay were minimized in specialized, high-volume shoulder arthroplasty centers.

Surgical Technique

Biomechanically, the reverse prosthesis works by reestablishing a fulcrum around which the deltoid muscle can power shoulder motion. With standard prostheses, absence of the rotator cuff allows the humeral head to subluxate superiorly during deltoid muscle contraction. The reverse prosthesis corrects this by moving the center of rotation of the shoulder medially and distally and reestablishing a semiconstrained fulcrum around that fixed point ( Fig. 12.15 ).

FIGURE 12.15, A, In a shoulder with no rotator cuff tendons there are few restraints to anterosuperior subluxation of the humeral head when patient attempts to raise the arm. Pull of the deltoid muscle worsens this by pulling superiorly and medially (arrow). B, With reverse arthroplasty, deltoid muscle lever arm is restored, providing a fulcrum around which the deltoid can pull to restore forward elevation (arrow).

Because the reverse prosthesis places high shear stresses across the glenoid, several investigators have sought to define the factors most important in maximizing glenoid fixation. Parsons et al. stressed that proper orientation of the baseplate and placement of the screws in optimal position were important for fixation. Others have found that the inferior screw faces the highest shear stress and is key to prevent loosening, whereas others have recommended screw placement in areas with the highest quality bone: the coracoid base, the scapular spine, or the inferior pillar. A device with a lateralized center of rotation was shown to obtain adequate fixation despite a 69% greater moment at the baseplate-glenoid interface.

Glenoid wear is common in rotator cuff-deficient conditions. Frankle et al. (2009) studied 216 glenoids with plain radiographs and CT scans before operative intervention and found that 37.5% of the glenoids had abnormal morphology. They classified the wear patterns as posterior (17.6%), superior (9.3%), global (6.5%), and anterior (4.2%). These wear patterns were found to affect surgical technique, often requiring placement of the center screw along an alternate center line along the scapular spine. In a later follow-up study of 143 of these patients, all 56 shoulders with abnormal glenoids had center screw placement along the alternative center line, and 22 had bone grafting procedures; larger glenospheres also were used more often than in shoulders with normal glenoids. Outcomes were not significantly different between the two groups. Augmented glenoid components and bone grafting procedures also are available to treat glenoid deficiency.

Reverse Total Shoulder Arthroplasty

Technique 12.3

  • Approach the proximal humerus and prepare it for stem implantation as described in Technique 12.1. Some authors recommend a superior approach, but we prefer the deltopectoral approach because of its versatility and easily extensive nature. However, there are some important differences in humeral preparation from a total shoulder arthroplasty or hemiarthroplasty. First, because of the common superior subluxation deformity of rotator cuff-deficient shoulders, a larger humeral head cut is often required. Second, some authors advocate placing the stem in less retroversion (∼20 degrees) to prevent impingement and maximize rotation; however, we believe that stem placement in 30 degrees of retroversion is not only acceptable but also preferable to prevent the more common instability in adduction and extension seen with the reverse prosthesis. Although stems were initially cemented in reverse total shoulder arthroplasty, the use of uncemented and shorter stems has been reported with clinical success. Once the glenoid vault is adequately debrided and all four borders are visible, identify the centering point. Move the starting point inferiorly 1 to 2 mm to allow inferior placement of the baseplate to prevent scapular notching. Most authors recommend placing the baseplate with the inferior aspect flush with the inferior surface of the bony glenoid.

  • Place a guide pin through this centering hole using a guide. Take care to place the guide pin in 10 to 15 degrees of inferior tilt, again to prevent scapular notching.

  • Ream the glenoid until the “smiley face” is achieved, with bleeding cancellous bone inferiorly and hard sclerotic bone superiorly ( Fig. 12.16 ). This confirms adequate inferior tilt of the baseplate.

    FIGURE 12.16, Some authorities prefer reaming the glenoid to create an “inferior smile,” with bleeding cancellous bone at the bottom of glenoid to provide inferior tilt of baseplate. SEE TECHNIQUE 12.3.

  • Impact the baseplate and secure it with screws. The peripheral screws are ideally placed in the “pillars” of densest cortical bone—the coracoid base, inferior pillar, and scapular spine. We have found screw placement to be inconsistent in the scapular spine; however, fixed-angle locking screws can be reliably positioned in the coracoid base and inferior pillar by internally rotating a circular baseplate approximately 10 degrees.

  • Dry the Morse taper and impact the glenosphere into position.

  • Place the humeral stem as described in Technique 12.1, using trial components to test for stability and motion. Reduction and dislocation of the glenohumeral joint typically are more difficult than with standard shoulder arthroplasty. Reduction involves a combination of longitudinal traction and forward elevation on the arm. The deltoid tension should be slightly greater than before joint relocation, but take care not to overlengthen the deltoid, which can result in dehiscence and/or acromial fracture. There can be 2 to 3 mm of gapping in the glenohumeral articulation once the joint is reduced without loss of stability.

  • To dislocate the glenohumeral joint, place the dislocation instrument between the bearing surface and glenosphere to disrupt the articulation. Then pull the humerus anteriorly (shoulder extension) to deliver the bearing surface.

  • Once the proper bearing surface is chosen, dry the Morse taper and impact it into position. Reduce the glenohumeral joint for a final time. Close the wound as described in Technique 12.1. The importance of subscapularis repair after reverse total shoulder arthroplasty remains controversial. One study found no correlation between subscapularis integrity and outcome. Another large study found that outcomes were not inferior when the subscapularis was left free compared to when it was repaired. However, closure of the subscapularis has been found to correlate with improved stability in traditional Grammont style prostheses but is likely less important for lateralized designs.See also .

Postoperative Care

Postoperative care is as described for Technique 12.1.

Outcomes

In the past decade, multiple authors have reported the outcomes of reverse total shoulder arthroplasty done for a number of indications. In general, outcomes vary by etiology, with posttraumatic conditions and revision procedures having worse outcomes and a higher complication rate. Fatty infiltration or absence of the teres minor has also been shown to compromise outcomes. Overall, good and excellent results have been reported in 67% to 82% of patients, with significant increases in functional scores and average forward elevation between 100 and 138 degrees. Longer-term survivorship studies are emerging with implant survival rates of over 90% at 10 years and 87% at 15 years of follow-up. Survivorship for glenoid loosening has been reported at 84% over the same period. Although the acceptable postoperative activity level that the reverse prosthesis can tolerate is unknown, a high percentage of patients nevertheless report medium- and high-demand use of the operative limb after surgery.

Cuff Tear Arthropathy

Several large studies have reported good results for reverse total shoulder arthroplasty done for rotator cuff arthropathy. In a multicenter study of 80 shoulders observed for an average of 44 months, 96% of patients reported no or minimal pain, and there was an increase in active forward elevation from 73 to 138 degrees. Forty-nine patients (64%) had medial component encroachment and scapular notching, however, without evidence of loosening. Another study reported that 78% of 45 patients were satisfied with their results at midterm follow-up (average 40 months); 67% had no or slight pain. Results were significantly better in patients who had primary arthroplasty for cuff tear arthropathy than in patients who had revision of a failed standard arthroplasty. Frankle et al. (2006) reported their results with reverse total shoulder arthroplasty at an average 33-month follow-up of 60 patients who had severe rotator cuff deficiency. Significant improvements were found in pain and function scores; 41 (68%) of the 60 patients rated their outcomes as excellent or good, 16 (27%) were satisfied, and three (5%) were dissatisfied. Seven patients required revision surgery to another reverse total shoulder arthroplasty (five patients) or hemiarthroplasty (two patients). Finally, comparative studies have found reverse total shoulder arthroplasty to be superior to hemiarthroplasty for the treatment of cuff tear arthropathy.

Rotator Cuff Dysfunction Without Arthritis

More recently, indications have been expanded from cuff tear arthropathy to include other conditions of rotator cuff insufficiency. Mulieri et al. reported 90% implant survivorship at a little over 4 years after surgery of 72 shoulders with rotator cuff dysfunction without glenohumeral arthritis; 20% of patients had a complication. Ek et al. and Ernstbrunner et al. have reported similar series of younger patient cohorts with clinical improvements that were maintained up to 10 years after surgery; however, the complication rate remains high as in the series reported by Mulieri et al.

Proximal Humeral Fractures

Several authors have reported the use of reverse total shoulder arthroplasty to treat proximal humeral fractures in the elderly. Results have been satisfactory, with average forward elevation of approximately 100 degrees but a high rate of scapular notching. A growing body of evidence supports the use of reverse total shoulder arthroplasty over hemiarthroplasty in the treatment of comminuted proximal humeral fractures in elderly patients; two meta-analyses have found reverse total shoulder arthroplasty to be superior to hemiarthroplasty for proximal humeral fractures in this population. One survey study demonstrated a consensus that reverse total shoulder arthroplasty is the preferred surgical treatment for four-part fractures in the older population. Other studies have compared the results of reverse total shoulder arthroplasty with nonoperative treatment for comminuted proximal humeral fractures in the elderly and reported mixed results with no clear advantage to reverse total shoulder arthroplasty. However, in one study functional outcomes were reported to be slightly better with reverse total shoulder arthroplasty.

Rheumatoid Arthritis with Rotator Cuff Tear

Two studies have reported the use of reverse total shoulder arthroplasty in patients with rheumatoid arthritis. At an average follow-up of 2 years, John et al. reported improvements in all outcomes scores in 17 patients. Scapular notching occurred in roughly one fourth of patients, but there were no radiologic signs of loosening. Holcomb et al. also reported significant improvements in all outcomes measurements in 21 shoulders observed for an average of 3 years. The complication rate was 14%, and 18 patients rated their results as either good or excellent. Young et al. found similar clinical results but noted a high rate of intraoperative and postoperative fractures in this population.

Salvage Procedures

In general, the outcomes of reverse total shoulder arthroplasty for revision of failed shoulder arthroplasty have been less satisfactory than those for primary reverse total shoulder arthroplasty for other conditions. Cuff et al. reported the outcomes of reverse total shoulder arthroplasty in the treatment of 22 shoulders that had either one- or two-staged irrigation, debridement, and conversion to reverse total shoulder arthroplasty. There were no recurrent infections and motion was significantly improved; however, the average forward elevation was only 80 degrees. Boileau et al. reported that, although results were not as good as for primary reverse total shoulder arthroplasty, 93% of 40 patients were satisfied with their results. Average forward elevation was 123 degrees at final follow-up, and the complication rate was 12%. The authors stressed that reverse total shoulder arthroplasty in patients with more than 90 degrees of forward elevation before surgery risks loss of motion in this plane and decreased patient satisfaction.

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