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This chapter discusses the indications and techniques for arthrodesis of the shoulder and elbow joints as well as the most common tendon transfers performed around the shoulder. Because of the limited function and morbidity after shoulder and elbow arthrodesis, as well as the development of more reliable alternatives, the indications for arthrodesis are becoming increasingly rare. Unlike arthrodesis, tendon transfers around the shoulder continue to be viable alternatives in young, high-demand patients with irreparable rotator cuff tears for which arthroplasty may not be an option.
Historically, shoulder arthrodesis was a relatively common procedure. Indications in the past were mainly upper extremity paralysis caused by poliomyelitis or arthropathy caused by tuberculosis. Because of the success of the procedure, the list of indications grew over the next several decades. The earliest techniques did not use internal or external fixation devices. A purely extraarticular technique of shoulder arthrodesis was recommended for tuberculous infection to prevent systemic dissemination from the infected joint. With the advent of antitubercular drugs, however, this technique became unnecessary. Later procedures placed various types of bone grafts into the beds of the decorticated glenohumeral or acromiohumeral joints, or both. These procedures all required prolonged spica casting.
External fixation has been used to apply compression across the fusion site, with the external fixator removed at 6 weeks and a spica cast worn for 3 months. Although fusion rates with external fixation alone are generally poor, it is still useful in carefully selected patients, especially if infection is present or trauma has occurred with significant soft-tissue injury.
With the advancement of internal fixation techniques, shoulder arthrodesis has continued to evolve because external support alone is unable to provide adequate compression and stabilization of the contact surfaces to promote fusion. Also, if rigid internal fixation is obtained, the use of prolonged immobilization is avoided, allowing early functional use. Various techniques of internal fixation have been described, including isolated screw fixation, external fixation combined with screws, as well as single and double plating ( Fig. 13.1 ). A biomechanical study of fixation techniques used for shoulder arthrodesis found that double plating using 4.5-mm dynamic compression plates had the highest bending strength and torsional stiffness, followed by (in order of decreasing strength) single plating, external fixation combined with screws, external fixation alone, and screws alone. Conversely, a cadaver study comparing various six-screw configurations with a reconstruction plate found that certain screw configurations were as mechanically stable as a 16-hole reconstruction plate, with no significant difference in construct strength between the two groups. The use of a pelvic reconstruction plate instead of a dynamic compression plate has the advantages of greater intraoperative contouring and less implant prominence and is a more common technique performed today. This also allows excellent intraarticular (glenohumeral) and extraarticular (acromiohumeral) stabilization. Advantages of screw-only fixation over plate fixation include less soft-tissue dissection, a lower infection rate, a decreased rate of postoperative humeral fractures, and less frequent need to remove painful implants. Disadvantages of screw fixation are a higher nonunion rate and a greater need for postoperative immobilization.
Recently, all-arthroscopic and arthroscopically assisted techniques for shoulder arthrodesis have been described. These techniques are minimally invasive, decreasing the morbidity associated with large dissection and with fusion rates, outcomes, and complications that are comparable to traditional open procedures.
The goal of shoulder arthrodesis is to give the humerus stability in a functional position that allows optimal use of the distal upper extremity. The indications for shoulder arthrodesis have declined over time given the success with shoulder arthroplasty to treat a wide variety of end-stage shoulder conditions as well as the near eradication of poliomyelitis and tuberculosis, and improved techniques to treat shoulder fractures and instability. However, shoulder arthrodesis remains a successful treatment option for certain conditions including paralytic conditions, combined insufficiency of the rotator cuff and deltoid, recalcitrant instability, and chronic infections. Given the advancements in shoulder arthroplasty, other less common indications include failed shoulder arthroplasty, arthritic conditions in young, active patients unsuitable for arthroplasty, and neoplastic lesions. Current indications are listed in Box 13.1 .
One of the most common indications, currently, for shoulder arthrodesis is paralytic disorders of the upper extremity, including obstetrical brachial plexus injuries and traumatic brachial plexus injuries. When nerve repair, nerve grafting, and tendon transfers have failed or are contraindicated, shoulder arthrodesis may be indicated. Obstetrical brachial plexus injuries can be treated with arthrodesis near skeletal maturity when growth arrest and position changes are less of a concern. Some authors recommend combining shoulder arthrodesis with transhumeral amputation and prosthetic fitting in patients with complete brachial plexus palsy. Although a minimum age of 10 to 12 years has been suggested, in a review of shoulder arthrodesis in 102 patients, significant growth arrest occurred in only one child. Early arthrodesis has been advocated for children older than 6 years of age who have an irreversible flail shoulder with adequate scapulothoracic muscles, intact elbow flexors, and a functional hand with skin sensation. Finally, shoulder arthrodesis can be used in adult patients with flail limbs caused by persistent traumatic brachial plexus injuries. Wong et al. reported glenohumeral arthrodesis using a reconstruction plate in 6 patients, all of whom achieved fusion, with 5 reporting satisfactory pain relief. Ruhmann et al. reported 77 patients with persistent brachial plexus palsies treated with either trapezius transfer or shoulder arthrodesis. In the 14 patients who had arthrodesis, average abduction improved from 9.6 to 59.3 degrees and average forward elevation improved from 11.4 to 50.7 degrees postoperatively. Complications that necessitated multiple revisions and ultimately led to a poor outcome occurred in 1 patient.
In patients with combined deltoid and rotator cuff paralysis or insufficiency, arthrodesis is indicated over arthroplasty. With deltoid deficiency, the muscle power required to achieve adequate function after arthroplasty is lacking and complication rates are high. In patients with chronic infections, arthroplasty is contraindicated, and arthrodesis with limited internal fixation, with or without external fixation, often is the preferred salvage option. In these patients, though, it is important to adequately debride the shoulder of any infected tissue or bony sequestra in an attempt to minimize the infectious load and increase the chance of successful union. Patients with persistent shoulder instability after multiple failed procedures generally have deficiency of all capsulolabral structures with or without deltoid deficiency. These patients generally have inferior subluxation of the humeral head leading to painful instability, and arthrodesis in these patients gives a stable shoulder with low levels of pain.
Shoulder arthrodesis may be indicated after malignant tumor resection when soft tissues do not allow endoprosthetic reconstruction. Bone graft is required, and Bilgin et al. described the use of a vascularized free fibular autograft to augment bony healing in this situation. Massive bone loss also may be encountered in arthrodesis following failed shoulder arthroplasty when revision is impossible. Scalise and Iannotti described the use of different bone graft techniques to achieve shoulder arthrodesis. Additional procedures frequently are required to obtain union, and caution should be used in these complex patients. Others have reported acceptable outcomes with resection arthroplasty, which may be preferable to arthrodesis because of the technical difficulties associated with that procedure. In general, a physical laborer who is not required to routinely perform overhead lifting is the ideal candidate for shoulder arthrodesis.
Success after shoulder arthrodesis requires a functional scapulothoracic articulation. Given this, functional scapular stabilizers, including the trapezius, serratus anterior, and levator scapulae, are paramount, and paralysis of this musculature is a contraindication to shoulder arthrodesis. In particular, the trapezius and levator scapulae are responsible for shoulder abduction and the serratus anterior is responsible for forward elevation after shoulder arthrodesis. Other contraindications include ipsilateral elbow arthrodesis or contralateral shoulder arthrodesis, which produce significant functional deficits with activities of daily living, and Charcot arthropathy, which has an unacceptable nonunion rate.
The proper position of the arm at the time of arthrodesis ( Fig. 13.2 ) remains controversial ( Table 13.1 ). Currently, most authors prefer 10 to 20 degrees of abduction, 10 to 20 degrees of flexion, and 35 to 45 degrees of internal rotation. This position allows the patient to reach the mouth, waist, back pocket, and contralateral shoulder, facilitating activities of daily living. The position of rotation is the most crucial factor in obtaining optimal function. One study found that more than 15 degrees of flexion and rotation of either less than 40 degrees or more than 60 degrees constituted a malposition that required operative treatment. Another study suggested that abduction of approximately 35 degrees and forward elevation of 30 degrees provided optimal functional results, but that internal rotation of more than 45 degrees should be avoided to prevent problems with hand-to-face activities.
AOA committee (1942) | 50 degrees abduction 15-25 degrees flexion 25 degrees internal rotation |
Rowe (1974) | 20-25 degrees abduction and flexion ∼40 degrees internal rotation |
Cofield and Briggs (1979) | 45 degrees abduction 25 degrees flexion 21 degrees internal rotation |
Hawkins and Neer (1987) | 25-40 degrees abduction 20-30 degrees flexion 25-30 degrees internal rotation |
Richards et al. (1988) | ∼30 degrees abduction, forward flexion, internal rotation |
Jónsson et al. (1989) | 20-30 degrees abduction, forward flexion, internal rotation |
Groh et al. (1997) | 10-15 degrees abduction 10-15 degrees flexion 45 degrees internal rotation |
Matsen et al. (2004) | ∼15 degrees abduction, forward flexion 40 degrees internal rotation |
Clare et al. (2001) | 10-15 degrees abduction 10-15 degrees flexion 45 degrees internal rotation |
Nagy et al. (2004) | 15-30 degrees of flexion 35-45 degrees of abduction 30-40 degrees internal rotation |
Safran and Iannotti (2006) | 20 degrees flexion 20 degrees abduction 40 degrees internal rotation |
Scalise and Iannotti (2009) | 10-20 degrees abduction 10-20 degrees flexion 35-45 degrees internal rotation |
Abduction can be determined at the time of surgery by clinically measuring the angle formed by the body and the humerus. Alternatively, this angle can be determined by obtaining an anteroposterior radiographic view using the spine rather than the border of the scapula as a landmark. Flexion is determined by observing the angle that the humerus forms with the horizontal plane in a supine patient. After the positions of abduction and flexion have been determined, the elbow is flexed to 90 degrees. The hand is positioned over the ipsilateral area of the chest between the sternum and axilla so that further flexion of the elbow allows the top of the thumb to touch the chin ( Fig. 13.3 ).
Fusion of the glenohumeral joint, as well as between the humeral head and undersurface of the acromion, should be attempted, and numerous techniques have been described. Stable internal fixation can reduce the need for bone grafting, external fixation, or prolonged immobilization. Postoperative use of a premade custom orthosis to hold the position of the arm until fusion has been achieved is generally well tolerated by most patients and can be used for any of these techniques.
Shoulder arthrodesis without implants is primarily of historical interest. The techniques of Watson-Jones, Putti, Steindler, Brett, and Gill are not included in this edition because they are rarely indicated. For details of these techniques, the reader may refer to earlier editions of this textbook or the original articles.
Charnley originally described a procedure to accomplish shoulder arthrodesis by applying external compression. External fixation, preferably with screw supplementation, should be considered when an arthrodesis is indicated in a patient with significant soft-tissue loss or deficiency. This technique is also useful in patients with recalcitrant infections.
(CHARNLEY AND HOUSTON)
Preoperatively, fit a prefabricated shoulder orthosis to the patient in the intended position of fusion. Adjustments can be made in the operating room while the patient is still under anesthesia. Alternatively, before the operation, apply the trunk portion of a shoulder spica cast with the patient awake, allow it to harden, and then bivalve it and save it for use later.
Position the patient in a semireclining or beach-chair posture and make a “saber cut” incision centered over the lateral border of the acromion.
Using electrocautery, take down the anterior and lateral deltoid muscle and then tag and retract this muscle.
Excise the soft tissue from the subacromial space. Denude the upper half of the glenoid fossa of articular cartilage and the undersurface of the acromion to bleeding bone. Remove the articular cartilage from the humeral head and reduce the joint.
With an osteotome or oscillating saw, resect the greater tuberosity and humeral head bone to allow articulation superiorly against the undersurface of the acromion and the superior part of the glenoid fossa. Use the resected bone as graft material around the fusion. Insert a 4-mm pin from the posterior superior aspect of the acromion into the scapular neck deep to the glenoid fossa ( Fig. 13.4 ). Another pin can be placed in the base of the coracoid process. Alternatively, 3 pins can be placed into the scapular spine.
Insert a second set of 2 or 3 similar pins into the surgical neck of the humerus posterolaterally perpendicular to the shaft of the humerus.
Additionally, 6.5-mm cannulated screws can be placed intraarticularly and extraarticularly to augment compression and fixation.
Construct an external frame of adjustable pin clamps and bars and connect it to the pins for application of compression with the arm in the desired position for arthrodesis.
Reattach the deltoid to the acromion and close the wound in layers over a drain.
Apply the external shoulder orthosis or previously made shoulder spica cast with the patient still under anesthesia, incorporating the external fixator.
The pins and external fixator are removed after 6 to 8 weeks. Immobilization is continued until the arthrodesis is solid.
The AO group described a double plating technique for rigid stabilization in glenohumeral arthrodesis. This is particularly useful in humeral head resection in which a second plate significantly aids stability. The disadvantage of this technique is the possible need for a second procedure to remove symptomatic implants after the arthrodesis is solid.
(AO GROUP)
Place the patient in the lateral decubitus position.
Make an incision along the spine of the scapula, over the acromion, and along the proximal third of the humerus. Expose the scapular spine, glenoid fossa, and proximal third of the humerus.
Denude the glenoid fossa and humeral head of all cartilage.
Decorticate the undersurface of the acromion and the lateral portion of the humerus for contact with the acromion.
An osteotomy of the acromion may be necessary to increase surface contact between the plate and bones.
Position the humeral head in the desired position in the glenoid fossa.
Use a malleable template to determine the contour for a standard broad AO plate and contour the plate with bending press and irons. The plate is to lie along the scapular spine, over the acromion, and against the proximal third of the humerus ( Fig. 13.5 ).
Fasten the plate initially with a long cortical screw inserted vertically into the scapular neck. Insert the remaining proximal screws into the scapula using standard AO technique.
Displace the humerus superiorly and medially to lie against the acromion and glenoid fossa in the desired position for arthrodesis.
Fix the plate distally with two screws that pass through it and the humeral head and into the glenoid fossa and scapular neck. Insert at least two more screws to fix the plate to the humerus. If the plate does not achieve complete stability at the arthrodesis site, apply a second plate posteriorly from the scapular spine to the humerus (see Fig. 13.5 ).
Apply bone grafts as desired. Close the wound in layers over drains.
A Velpeau dressing is applied. The sutures are removed at 2 weeks if nonabsorbable. Active rehabilitation of the elbow, wrist, and hand is begun within the first few days after surgery, but care should be taken not to place stress on the fusion site.
To overcome the technical difficulties of contouring the AO plate and the occasional problems caused by prominent screws, Richards et al. used a malleable pelvic reconstruction plate, obtaining successful fusion in 11 patients without the need for plate removal. Chun and Byein also reported success with this technique in eight patients followed for approximately 4 years. This is our preferred method to achieve shoulder fusion.
(MODIFICATION OF RICHARDS ET AL.)
Place the patient in a modified beach-chair position with the head of the bed approximately at 45 degrees and drape the arm free. Ensure the entire ipsilateral scapula is exposed.
Make an incision extending from the spine of the scapula to the midpoint on the lateral aspect of the acromion and distally on the lateral aspect of the humeral shaft.
Split the deltoid muscle and extend dissection distally to ensure adequate exposure for the entire length of the intended plate.
Resect the rotator cuff. Decorticate the glenoid fossa, the undersurface of the acromion, and the head of the humerus. While the humeral head is dislocated, glenoid reamers can aid in decorticating the glenoid.
Support the shoulder in 30 degrees of flexion, 30 degrees of abduction, and 30 degrees of internal rotation, and measure abduction from the side of the body. Bring the head of the humerus proximally to appose the decorticated undersurface of the acromion. Abducting and flexing the humerus 30 degrees apposes the head of the humerus to the undersurface of the acromion and the glenoid fossa. Make sure adequate bony contact between all intended fusion sites is obtained.
Maintain the position by supporting the arm with folded sterile sheets and have an assistant maintain this position while the plate is contoured. Alternatively, the use of an arm positioner can aid in this process.
Use hand-held bending irons to contour a 4.5-mm reconstruction plate along the spine of the scapula, over the acromion, and down onto the shaft of the humerus. This generally requires a 12- to 16-hole plate. Bend the plate gently 60 degrees over the acromion and twist it 20 to 25 degrees just distal to the bend to appose the shaft of the humerus ( Fig. 13.6 ).
Two independent partially threaded 6.5-mm cancellous screws with washers can be placed through the lateral aspect of the humeral head and into the glenoid vault to achieve compression of the glenohumeral joint. This aids in provisional fixation while positioning the plate.
Place the plate onto the scapular spine and onto the lateral aspect of the humerus. Place 4.5-mm cortical or locking screws through the plate and into the scapular spine as well as the humerus. Direct a cortical screw from the spine of the scapula into the base of the coracoid process. Place a 6.5-mm cancellous screw across the acromiohumeral site of fusion and an additional screw across the glenohumeral joint.
Do not osteotomize the acromion because it is used to augment the fixation of the scapula to the humerus.
Pack the residual space with corticocancellous bone chips to augment fusion.
Close the wound in layers over a drain.
The operative extremity is placed into a “gunslinger” orthosis in the intended fusion position for 6 weeks, with elbow, wrist, and hand range of motion exercises only. If there are no signs of implant loosening, the arm is transitioned to a simple sling. Strenuous activity is delayed for at least 16 weeks after surgery.
Although not a common indication for shoulder arthrodesis, the combination of a failed shoulder arthroplasty with rotator cuff and deltoid dysfunction has few other reconstructive options. Because of proximal humeral bone loss, soft-tissue deficiencies, and multiple previous operations, shoulder arthrodesis in this situation is associated with high rates of nonunion and revision surgery, but it does represent a salvage option for selected patients for whom other reconstruction options are unlikely to be of benefit.
(SCALISE AND IANNOTTI)
Before surgery, determine whether a bone graft will be needed and, if so, what type of bone graft will be most appropriate. Large segmental defects may require a vascularized autogenous fibular graft. If the volume of bone graft needed cannot be obtained from the patient, allografts such as a femoral head should be available.
Place the patient in a modified beach-chair position that allows the involved extremity to be fully adducted and extended and provides full access to the posterior aspect of the shoulder.
After induction of general anesthesia and administration of an interscalene block, make an incision over the spine of the scapula and curve it anteriorly toward the midportion of the acromion lateral to the acromioclavicular joint and then distally to the level of the deltoid tuberosity, incorporating deltopectoral incisions from previous surgeries if present ( Fig. 13.7A ).
Develop the deltopectoral interval and identify the atrophic or detached deltoid. Resect this sclerotic tissue from the distal end of the clavicle and the anterolateral aspect of the acromion.
Retract the detached deltoid tissue distally to expose the entire proximal end of the humerus.
Typically, much of the rotator cuff envelope is deficient. Release any remaining inferior portion of the subscapularis from its humeral insertion.
Place a large Darrach retractor in the glenohumeral joint and a bent Hohmann retractor in the subacromial space behind the humeral head. Dislocate the proximal end of the humerus anterosuperiorly with adduction, extension, and external rotation, and remove the prosthetic components. If the humeral bone is thin and osteopenic, take care to avoid fracture.
If implant removal is difficult, use an oscillating saw to create a unicortical longitudinal osteotomy. Place a broad osteotome in this gap to gently expand the diameter of the diaphysis to loosen osseous on-growth or disrupt the bone-cement interface.
For removal of the glenoid implant, circumferentially excise the scar and devitalized tissue surrounding the glenoid, as well as any within the glenoid vault.
With the entire glenoid rim and vault exposed, use a high-speed burr to plane the undersurface of the acromion flat to determine the best placement of the bone graft to maximize osseous contact.
With the proximal end of the humerus apposed to the glenoid and the underside of the acromion, place two 3-mm Steinmann pins to provide temporary fixation while the optimal position of the fusion is determined. Place one pin laterally from the humerus into the glenoid and one superiorly through the acromion into the humerus ( Fig. 13.7B ).
Remove and replace the Steinmann pins as needed while the position of the humerus is adjusted to obtain optimal fusion position.
When the appropriate position is determined, use an oscillating saw to cut the medial portion of the proximal end of the humerus parallel to the glenoid face to maximize osseous contact. If necessary, temporarily remove the Steinmann pin during this step. Save the resected bone for graft material.
Replace the Steinmann pins with 6.5-mm partially threaded screws, compressing the humerus to the glenoid first, followed by screw fixation of the humerus to the acromion.
Contour a 4.5-mm pelvic reconstruction plate to the spine of the scapula, the lateral surface of the acromion, and the lateral aspect of the proximal end of the humerus. The plate should extend far enough proximally to allow placement of at least three bicortical screws in the scapula. Distally, the plate should have at least three bicortical screws in the humeral shaft.
Compression of the humerus to the glenoid results in relative medialization of the humeral shaft. Shape the femoral head allograft to fit the gap between the undersurface of the plate and the lateral cortex of the proximal end of the humerus. Stabilize the graft with interfragmentary compression screws.
Secure the neutralization plate to the spine of the scapula and to the humerus with screws, transfixing the graft, humerus, and glenoid ( Fig. 13.7C ).
If a vascularized fibular autograft is to be used to span a large humeral defect, harvest a length of fibula that is 6 cm longer than the defect.
Strip the fibular graft of its soft tissue so that it can be inserted in the canal of the remaining part of the humerus. Provisionally fix the graft with one or two interfragmentary 4.5-mm lag screws.
To maximize contact with the glenoid, use a high-speed burr to create a slot on the face of the glenoid to allow the fibula to be recessed at the proper orientation to provide the appropriate humeral position.
Place the bulk allograft and secure it laterally to the fibular graft with interfragmentary screws.
Contour a large-fragment reconstruction plate and secure it to the surface of the scapula, acromion, fibular graft, and distal humerus ( Fig. 13.7D ).
For a vascularized graft, revascularization of the fibula is done by the microvascular team once the graft is stabilized, using end-to-side anastomosis of the peroneal artery and either an end-to-side or end-to-end venous anastomosis.
Use either an autologous iliac crest bone marrow aspirate mixed with an allograft matrix or a traditional iliac crest cancellous autograft to pack around both the proximal and distal osteosynthesis sites.
Repair any remaining deltoid to the acromion through bone tunnels to maximize soft-tissue coverage.
Place a drain in the deep space, close the soft tissue in layers, and apply a hinged shoulder immobilizer that maintains the position of the arthrodesis. As an alternative, a shoulder spica cast can be used.
The shoulder is immobilized for 12 to 16 weeks or until union is verified radiographically. Range of motion of the hand, wrist, and elbow is allowed immediately. Scapulothoracic range-of-motion exercises, with progression to strengthening of the scapular stabilizers, are begun after union has been obtained, typically by 8 to 12 weeks. If union is not established by 12 weeks, bone grafting of the fusion site should be considered to prevent failure of the implants.
Lenoir et al. described arthroscopic shoulder arthrodesis with external fixation in eight patients; glenohumeral fusion was achieved in all eight at a mean of 3 months. Two 6.5-mm cannulated screws are placed for intraarticular compression. If bone quality is poor, a third 6.5-mm cannulated screw can be placed from the acromion to the humeral head under imaging. The only two complications, a superficial wound infection and migration of an acromiohumeral screw, did not compromise the final outcome.
(LENOIR)
Place the patient in the beach-chair position. Obtain fluoroscopic anteroposterior and Bernageau profile views of the glenoid before the start of surgery.
Place three pins of the external fixator percutaneously in the scapular spine and three pins in the humeral shaft ( Fig. 13.8 ).
Establish standard anterior and posterior arthroscopic portals, and remove the glenohumeral ligament and labral complex with radiofrequency ablation. Remove the glenoid and humeral head cartilage and subchondral bone with a 5-mm arthroscopic bur.
Place the arm in 30 degrees of forward flexion, 30 degrees of abduction, and 30 degrees of internal rotation and assemble the external fixator. Check the position by placing the patient’s hand at the forehead and ipsilateral buttock.
Debride the rotator cuff by enlarging the percutaneous screw incisions. The humeral head can be moved up to directly contact the acromion or alternatively bone graft can be used in the subacromial space.
Place 2 parallel guidewires percutaneously through the humeral head into the glenoid under fluoroscopic imaging. Place 26.5-mm cannulated screws for intraarticular compression. If bone quality is poor, a third 6.5-mm cannulated screw can be placed from the acromion to the humeral head under imaging.
The shoulder is immobilized with an abduction pillow for 4 weeks. After immobilization, active-assisted exercises are performed to mobilize the scapulothoracic joint. The external fixator is removed 2 months postoperatively.
Complications associated with shoulder arthrodesis are listed in Box 13.2 . Immediate postoperative complications are uncommon and mainly involve wound problems, such as infection, skin breakdown, and wound hematoma. The surgeon must also be mindful of pressure sores if a spica cast is used. Loss of elbow motion has been reported but is usually temporary as long as the elbow is not immobilized for more than 2 weeks.
Infection
Wound hematoma
Skin slough
Pressure sores under spica cast
Pseudarthrosis/nonunion
Painful hardware
Malposition
Ipsilateral humeral fracture
Traction neuritis
Periscapular muscle strain
Acromioclavicular arthritis
Epiphyseal problems/growth arrest
Later postoperative complications are more prevalent. Malunion has been reported in up to a third of patients with shoulder arthrodesis. Malposition can lead to a traction neuritis or periscapular muscle strain, especially when the arm is positioned in too much abduction. A recent study reported an overall complication rate of 28%. Specifically, pseudarthrosis was more common when screw fixation was used, whereas infection, periprosthetic fracture, and symptomatic implants were more common when plates were used.
Nonunion rates in most modern series are less than 10%. Union is generally achieved with autologous bone grafting. Secondary degenerative arthritis of the acromioclavicular joint is common. If any signs of acromioclavicular arthritis are present preoperatively, a concurrent distal clavicle excision should be performed.
Ipsilateral humeral fractures after shoulder fusion have been reported in 25% of patients in some series. Most authors recommend nonoperative treatment with a shoulder spica or orthosis in these patients.
There has been a paucity of literature detailing the long-term outcomes of shoulder arthrodesis. Dimmen and Madsen reported 18 patients who had shoulder fusion using plate fixation. All obtained full or partial arthrodesis, and at an average 8-year follow-up the mean Oxford shoulder score was 32 and the mean American Shoulder and Elbow Surgeons (ASES) score was 59. Complications were uncommon: one patient required reoperation because of severe pain and one for a postoperative humeral shaft fracture; one patient had complex regional pain syndrome. In 21 patients who had shoulder arthrodesis as a primary or secondary procedure after tumor resection, Fuchs et al. found no local recurrences and no metastatic disease at an average 11-year follow-up. The average Toronto Extremity Salvage Score was 81% and the average Musculoskeletal Tumor Society score was 23. However, 43% of patients developed a complication that required additional surgical intervention. Another study by Miller et al. (2011) reported the outcomes of shoulder arthrodesis in 11 children (13 procedures) with flail shoulders caused by polio. At an average follow-up of 41 months, all patients were satisfied and pain free with improved shoulder function. Six patients underwent implant removal, and two shoulders required humeral osteotomy for malrotation. In a larger series of 54 patients undergoing shoulder arthrodesis for brachial plexus palsy, Atlan et al. reported an ultimate fusion rate of 94% and average active abduction of 59 degrees at an average follow-up of approximately 3 years. Arthrodesis rates were improved with the use of a subacromial bone graft.
Although total elbow arthroplasty has become an accepted treatment for a variety of degenerative and traumatic elbow conditions, concerns regarding its durability in young and/or high-demand patients make elbow arthrodesis an acceptable alternative in this population. Although partially mitigated by the ability of adjacent joints to compensate for lack of elbow motion, significant functional disability, particularly with self-care and activities of daily living, is common. As a result, total elbow arthroplasty, fascial arthroplasty, or even resection arthroplasty in the presence of functional musculature often provides better function of the upper extremity than does elbow arthrodesis.
Indications for elbow arthrodesis are listed in Box 13.3 . In general, elbow arthrodesis is reserved for patients with painful arthritis who are not candidates for total elbow arthroplasty, especially individuals who place high demands on the upper extremities, such as manual laborers. Elbow fusion also is indicated for persistent infection, including tuberculosis, which historically was the main indication for this procedure. More recently, elbow arthrodesis has also become recognized as the optimal treatment for massive upper extremity trauma seen on the battlefield. Typically, a combined internal and external fixation technique is recommended because of the extensive soft-tissue injury that is usually associated with such injuries.
Infection
Failed total joint arthroplasty
Posttraumatic arthritis
Arthritic diseases unsuitable for arthroplasty
Severely comminuted intraarticular fractures
For unilateral arthrodesis of the elbow, a position of 90 to 100 degrees of flexion is desirable to provide the most powerful grip strength. There is no ideal fusion position for all patients; the optimal position depends on whether occupational activity or self-care is the primary goal, as well as on the mobility of the contralateral arm. Simulation of arthrodesis by use of preoperative splints or casts set at varying degrees of flexion has been recommended.
Bilateral elbow arthrodesis rarely is indicated because of resultant functional limitations. If indicated, one elbow should be placed in 110 to 120 degrees of flexion to permit the patient to reach the mouth, and the other should be placed in 45 to 65 degrees to aid in personal hygiene. These positions can be varied to meet the requirements of the patient’s occupation.
Arthrodesis of the elbow joint is difficult because of the unique bony anatomy of the elbow and the long lever arm of the upper extremity distal to the elbow. For successful elbow arthrodesis, adequate bone stock must be present, although resection of the radial head may be necessary to preserve pronation and supination, and internal or external fixation with bone grafting is typically required.
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