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Rarely, arthrodesis is done to stabilize the glenohumeral joint after many failed attempts at shoulder reconstruction.. Arthrodesis for failed prosthetic arthroplasty or tumor resection

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Shoulder arthrodesis is an end-stage salvage option for the failing, painful joint that cannot undergo or has failed reconstruction It is indicated for irreversible and nonreconstructible massive rotator cuff tears and deltoid muscle denervation as well as for detachment

of the deltoid from its origin Rarely, arthrodesis is done to stabilize the glenohumeral joint after many failed attempts at shoulder reconstruction Arthrodesis for failed prosthetic arthroplasty or tumor resection presents additional challenges because of the associated bone loss on the humeral and/or glenoid side of the joint Primary arthrodesis requires rigid internal plate fixation and both an extra- and an intra-articular site of fusion Depending on bone volume and quality needed, the patient may require bracing for 8 to 10 weeks, autogenous or allograft bone grafting, or a vascularized fibular bone graft to reconstruct the bone deficiency, along with prolonged spica cast immobilization The optimal

position for arthrodesis is 20° of forward flexion, 20° of abduction, and 40° of internal rotation, with modifications based on patient

body size or other patient-specific factors Bone fusion is attained

in nearly all patients, with marked pain reduction and improved function Postoperatively, the patient should be able to lift the arm

to near shoulder height and to reach the top of the head, the mouth, the ipsilateral back pocket, and the groin Complications include nonunion, malposition, pain associated with prominent hardware, and periarticular fractures

The development of prosthetic shoulder arthroplasty has nearly eliminated the need for arthrodesis in primary arthritic joints Arthrodesis has become an end-stage salvage pro-cedure for shoulder pain, weakness, and instability not suitable for soft-tissue or prosthetic reconstruction.1

The principal indications include conditions that result in severe and irreparable deltoid and rotator cuff deficiency, caused by irreversible pa-ralysis of these muscles with preser-vation of the scapular muscles In such refractory cases, arthrodesis may offer significant pain reduction

and some functional use of the upper extremity in what would otherwise

be an unsolvable situation

Indications

Currently, shoulder arthrodesis is in-dicated for brachial plexus injury, failed prosthetic arthroplasty, recon-struction after tumor resection, chronic infection, and refractory in-stability and pseudoparalysis of the shoulder secondary to combined ro-tator cuff and deltoid muscle dys-function

Motor vehicle accidents account

Ori Safran, MD

Joseph P Iannotti, MD, PhD

Dr Safran is Senior Orthopaedic

Surgeon, Department of Orthopaedic

Surgery, Hadassah-Hebrew University

Medical School, Jerusalem, Israel Dr.

Iannotti is Professor and Chairman,

Department of Orthopaedic Surgery,

The Cleveland Clinic Foundation,

Cleveland Clinic Lerner School of

Medicine of Case Western Reserve

University, Cleveland, OH.

None of the following authors or the

departments with which they are

affiliated has received anything of value

from or owns stock in a commercial

company or institution related directly or

indirectly to the subject of this article:

Dr Safran and Dr Iannotti.

Reprint requests: Dr Iannotti, The

Cleveland Clinic Foundation, 9500

Euclid Avenue, Cleveland, OH 44195.

J Am Acad Orthop Surg

2006;14:145-153

Copyright 2006 by the American

Academy of Orthopaedic Surgeons.

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for most traumatic brachial plexus

injuries These devastating injuries

affect young patients in almost 90%

of cases.2When spontaneous

recov-ery of the deltoid and rotator cuff

muscles does not occur, procedures

such as neurolysis, nerve grafting,

and muscle transfer are warranted in

an effort to reestablish shoulder

function Shoulder arthrodesis may

be considered in the presence of

se-verely restricted shoulder passive

range of motion, significant bone

loss, or failed prior reconstructive

measures.3 Because the trapezius

and levator scapulae muscles are

al-most always intact after traumatic

brachial plexus injury, active arm

abduction can occur through the

scapulothoracic articulation When

the serratus anterior is preserved,

forward elevation of the arm

through scapular rotation is also

pos-sible.4

Severe humeral and glenoid bone

loss, poor deltoid and rotator cuff

function, and refractory instability

(after multiple surgical procedures)

may render functional improvement

or pain relief via revision

arthroplas-ty impossible in patients with failed

shoulder arthroplasty When

arthro-desis is considered for these patients,

special techniques are needed to

compensate for the significant

gle-noid and humeral bone loss

Limb-sparing resection for

malig-nant and locally destructive tumors

of the proximal humerus may result

in significant tissue deficiency The

choice between prosthetic

recon-struction and glenohumeral

arthrode-sis is made based on the quality of the

soft tissue and bone after completion

of the curative resection Frequently,

tissue loss is severe, and arthrodesis

is the only valid option for regaining

shoulder stability.5,6To achieve fusion

in these patients, vascularized

au-tograft or bulk allograft must be used

to compensate for bone deficiency

Patients with the combination of

infection and a painful, damaged

joint present a difficult challenge

Prosthetic reconstruction is

con-traindicated when the septic process

is not eradicated Surgical débride-ment and glenohumeral fusion may yield a painless stable joint in many patients.7

Most unstable shoulder pathology

is managed through one or a combi-nation of the following procedures:

soft-tissue balancing, muscle trans-fer, and bone block With persistent refractory instability after multiple failed stabilization procedures, pa-tients may be left with a painful, dysfunctional shoulder devoid of competent soft-tissue or bony straints Fusion is one option for re-gaining stability and some degree of function in these patients.8

Arthropathy resulting from rota-tor cuff tear alone has not been con-sidered an indication for shoulder fu-sion Currently, patients with a rotator cuff tear may be treated suc-cessfully with shoulder hemiarthro-plasty or reverse total shoulder ar-throplasty with acceptable results

However, in the presence of irrepara-ble rotator cuff tear coinciding with irreparable deficiency of the deltoid muscle or dysfunction, some au-thors recommend fusion.9,10Fusion

is especially advocated in younger patients with demands for substan-tial strength at low angles of shoul-der flexion

Glenohumeral arthrodesis is gen-erally contraindicated in patients who lack functional scapulothoracic motion, which may be caused by pa-ralysis of the trapezius, levator scap-ulae, and serratus anterior muscles

Fusion is a less favorable option in patients at high risk of pseudarthro-sis, such as those with Charcot arthropathy.10-12 Patients with ad-vanced bilateral shoulder disease should not undergo bilateral arthro-desis because positioning cannot be achieved to allow the normal perfor-mance of activities of daily living (ADLs) Finally, elderly patients or those with progressive neurologic disease generally do not achieve sat-isfactory results with shoulder ar-throdesis

Surgical Considerations

A variety of periarticular fusion techniques, fixation methods, and immobilization strategies have been advocated for shoulder arthrodesis

Shoulder Position

The ideal position for shoulder ar-throdesis remains a matter of debate Most surgeons agree that the proper position of shoulder arthrodesis should enable the patient to reach the face for washing, the midline for dressing and hygiene, and the back pocket (Figure 1) It is important to minimize scapular winging in the resting position in order to minimize fatigue and periscapular muscle pain.10

The exact position of fusion re-mains elusive It is difficult to objec-tively and accurately measure the different angles, and the ideal posi-tion depends on patient body size One of the first guidelines was made

in 1942 by a committee of the Amer-ican Orthopaedic Association,13

which recommended 50° of abduc-tion, 15° to 25° of flexion, and 25° of internal rotation This recommenda-tion was later disputed by Rowe,14

who found that the degree of abduc-tion suggested by the committee caused periscapular muscle pain be-cause of excessive loads and winging

of the scapula in the resting position

He explained that excessive abduc-tion shifted the extremity away from the fulcrum of the shoulder, thus weakening its lifting and functional strength Rowe suggested 20° to 25°

of abduction (just enough to clear the axilla), 30° of forward flexion, and 45° to 50° of internal rotation to get to the midline of the body Elbow flexion, in his opinion, would allow the patient to reach the head and face.14,15

In contrast, in their review of 71 shoulder fusions, Cofield and Briggs16

found that the amount of abduction and flexion did not correlate with ei-ther periscapular pain or patient sat-isfaction and ADL function They did

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find a correlation between the

amount of internal rotation and

var-ious ADLs Later studies supported

Rowe’s findings, although they

fa-vored less internal rotation.12,17,18

Groh et al19advocated a lesser degree

of abduction and forward flexion of

10° to 15°, compensated with 45° of

internal rotation, enabling the

pa-tient to reach the mouth, belt buckle,

and contralateral shoulder and axilla

Fusion of the shoulder joint in 20°

of abduction, 20° of forward flexion,

and 40° of internal rotation in most

mesomorphic patients usually

al-lows acceptable position In obese

patients, significantly greater

abduc-tion is both required and

well-toler-ated; the body habitus will not allow

<20° of abduction In all patients, at

the conclusion of the procedure the

surgeon should be able to bring the

hand to the forehead with a

combi-nation of shoulder elevation and

el-bow flexion In addition, the

pa-tient’s arm should be able to rest at

the side without excessive scapular

winging

Extra-articular Versus Intra-articular Fusion

Shoulder arthrodesis may be ac-complished by fusing the glenohu-meral joint, the acromiohuglenohu-meral in-terface, or both Extra-articular fusion involves fusion between the proximal humerus and the undersur-face of the acromion, scapula, and clavicle without entering the gleno-humeral joint Extra-articular fusion alone was one of the first methods of shoulder arthrodesis The technique involved decorticating the upper part of the proximal humerus, the undersurface of the acromion, the lateral portion of the spine of the scapula, and the distal clavicle This procedure was initially advocated for treating tuberculosis patients with glenohumeral joint destruction dur-ing the era in which anti-tuberculosis antibiotics were not available.20 Extra-articular fusions are rarely done as isolated proce-dures today

Intra-articular fusion involves preserving the rotator cuff tendons

without attempting to fuse the hu-merus to the acromion Limited in-ternal fixation is used to preserve most of the bone architecture and soft tissues Some surgeons recom-mend intra-articular fusion for younger patients with glenohumeral joint destruction and intact rotator cuff tendons, with the expectation of possible future revision into shoul-der arthroplasty.21In 1992, Morgan and Casscells22 reported on an arthroscopically assisted intra-articular glenohumeral arthrodesis

in a 39-year-old woman with refrac-tory multidirectional shoulder insta-bility, intractable pain, and deltoid paralysis After aggressive arthro-scopic débridement and decortica-tion of the glenohumeral joint, two cannulated compression screws were inserted across the glenohu-meral joint, followed by an acromio-humeral screw for extra-articular stabilization The patient was placed

in a foam abduction pillow for 4 weeks Radiographs at 10 weeks confirmed solid glenohumeral bony

Figure 1

The arthrodesis position should enable the patient to reach the face and hair for washing and combing (A), the midline for dressing (B), and the back pocket (C).

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union The patient was pain-free and

able to perform ADLs with the fused

shoulder

Currently, combined extra- and

intra-articular fusion techniques are

most commonly used.4,10,12,16-18,23

Decorticating the humeral head,

gle-noid, and acromion maximizes the

surface area for bone contact,

there-by increasing the probability of

achieving solid fusion

Fixation Methods

Arthrodesis fixation methods

have undergone marked evolution

Historically, postoperative spica

casting for 3 to 4 months was the

only so-called fixation used, and loss

of position was common In 1964,

Charnley and Houston24introduced

external bone compression for

achieving solid fusion of the

shoul-der Later, Beltran et al25introduced

glenohumeral compression screws,

which reduced the length of

postop-erative immobilization to 4 weeks

Subsequently, compression screws

became the accepted standard,12,15,16

but most patients still required

rela-tively prolonged periods of

postoper-ative spica cast immobilization In

the past two decades, the additional

stability provided by the

combina-tion of compression screws and

plates has minimized the need for

strict postoperative immobilization

without a concurrent increase in

nonunion rates; this has become the

accepted standard for glenohumeral

arthrodesis.4,7,8,10,18,23

Richards et al4used a single

con-toured 4.5-mm dynamic

compres-sion plate (DCP) placed over the

spine of the scapula, the acromion,

and the lateral portion of the

humer-al shaft for shoulder arthrodesis in

14 patients Postoperatively, patients

were placed in a spica cast for an

av-erage of 8 weeks All patients

achieved solid fusion; the two who

had only acromiohumeral fusion

re-mained stable and asymptomatic

Five years later, Richards et al23

re-ported their use of a single 4.5-mm

pelvic reconstruction plate on 11

pa-tients with brachial plexus palsy who underwent shoulder arthrode-sis; they were immobilized postoper-atively in a spica cast for 6 weeks

All achieved union by 5 months

The authors concluded that the more malleable reconstruction plate provided sufficient stability, a high union rate, and minimal skin prob-lems

Stark et al18used a long DCP in 15 patients undergoing arthrodesis, with no postoperative immobiliza-tion aside from an abducimmobiliza-tion pillow

Fusion was achieved in 14 of 15 pa-tients, and extremity position was lost in only one patient, in whom fixation was inadequate Four pa-tients had local skin irritation and pain, with two ultimately requiring removal of the screws but not the plate Clare et al10recommended the routine use of a 4.5-mm reconstruc-tion plate but favored the 4.5-mm DCP plate for patients weighing more than 100 kg Use of the ex-tremity was allowed as soon as tol-erated Routine use of compression screws traversing the plate and crossing the glenohumeral joint were used by all authors

External fixators also have been used in shoulder arthrodesis Charn-ley and Houston24used an external fixator, achieving union in 18 of 19 patients, most with tuberculous joint destruction Postoperatively, spica casts were used for additional stability in all patients Johnson et

al26 and, later, Kocialkowski and Wallace,27reported using a combina-tion of compression glenohumeral screws and an external fixator

Johnson et al26 used a Hoffman ex-ternal fixator and compression screws in four patients without addi-tional immobilization, and all fused

The fixator was removed 7 to 14 weeks after surgery; the authors re-ported only one pin tract infection (which responded to antibiotics and local wound care) and one fracture after frame removal Nagano et al28

reported on 11 patients who under-went shoulder arthrodesis for

brachi-al plexus injury using an externbrachi-al fixator and temporary internal fixa-tion All patients had solid fusion within 3 months, and the external fixator was removed 3 months after surgery No complications were re-ported

Technique

Preoperative planning is crucial for successful arthrodesis Often, shoulder arthrodesis is performed af-ter several failed previous surgical attempts or in conjunction with a radical bone and soft-tissue resec-tion Extensive bone loss may exist because of injury, infection, osteoly-sis after shoulder arthroplasty, or tu-mor resection Consideration should

be given to careful assessment of re-maining bone stock and soft-tissue deficiencies Small cancellous bone deficiencies may be managed with local or iliac cancellous bone graft More substantial deficits may re-quire a structural graft, such as a tri-cortical iliac graft, structural al-lograft, or vascularized fibular graft The patient is anesthetized using

a combination of a scalene block and general anesthesia, followed by su-pine beach chair positioning An in-cision is made over the spine of the scapula, curving it anteriorly over the midacromion toward the antero-lateral corner of the acromion, then continuing over the lateral aspect of the arm toward the deltoid tuberos-ity The deltopectoral interval is identified and developed The

anteri-or and middle panteri-ortions of the deltoid are detached from the lateral third of the clavicle, anterior acromion, and lateral acromion The deltoid is then retracted laterally and distally, hinged on its neurovascular pedicle The subscapularis tendon is sharply dissected from the lesser tuberosity, and the supraspinatus tendon is ex-cised from its musculotendinous junction to the greater tuberosity The glenoid is prepared by remov-ing its articular cartilage and cuttremov-ing its bony surface flat and parallel with its original plane The humeral

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head is placed in contact with the

prepared glenoid fossa, and the arm

is placed in the preferred position

and temporarily held in place by two

Steinmann pins Proper positioning

is examined by taking the arm

through a range of scapulothoracic

motion, verifying a functional range

With the arm in the correct position,

an oscillating saw is used to cut the

medial portion of the humeral head

The undersurface of the acromion is

cut to a flat decorticated surface, and

the superior portion of the humeral

head is cut parallel with it (Figure 2,

A and B)

A 4.5-mm pelvic reconstruction

plate is contoured to accommodate

the spine of the scapula, the lateral

surface of the acromion, and the

lat-eral portion of the proximal

humer-us Under fluoroscopic guidance,

two partially threaded cancellous

screws are placed through the

hu-meral head into the glenoid surface

and neck; at least one is placed

through the plate One or two

simi-lar screws are inserted through the

acromion into the humeral head,

with at least one through the plate

An additional screw is placed

through the plate and spine of the

scapula into the base of the glenoid

neck The remaining screws are

placed through the plate into the

spine of the scapula and proximal

humerus using a standard AO

tech-nique (Figure 2, C and D) The fusion

site is packed with local morcellized

bone using pieces of bone removed

during humeral and acromial

prepa-ration The subscapularis is then

re-paired to the lesser tuberosity The

deltoid is reattached to the clavicle

and to the anterior and lateral

por-tions of the acromion through bone

holes, as well as to the trapezius

fas-cia

In the presence of severe bone

stock deficiency (eg, after failed

ar-throplasty), augmentation of the

bone stock is needed In these cases,

bone contact may be improved by

using the tuberosities as a local

vas-cularized bone graft; they are fixed to

the fusion region between the gle-noid and neck Further stability may

be achieved by adding a structural graft of tricortical iliac bone or al-lograft between the lateral humeral shaft and the decorticated undersur-face of the acromion A pelvic recon-struction plate is used to fix the al-lograft in place (Figure 3)

When >6 cm of the proximal hu-meral shaft is missing, vascularized fibular grafts are used to replace the absent segment, along with addi-tional iliac bone graft or allograft For optimal docking, the fibular graft should be 4 to 5 cm longer than the humeral length needed The distal 3

cm of the fibular graft is stripped of its soft tissue and is either placed in

the humeral medullary canal or at-tached to the humeral outer cortex and fixed with cortical screws The proximal part of the fibular graft is keyed into a trough burred within the glenoid fossa The construct is stabilized with a 4.5-cm pelvic recon-struction plate Partially threaded cancellous screws are placed through the fibula into the glenoid (Figures 4 and 5) After stable fixation is achieved, the fibular graft is revascu-larized Thereafter, augmentation is done with autologous graft or frac-tionated bone marrow aspirate mixed with demineralized cortical fibers and cancellous chips The material is used to fill the space between the proximal fibula, the glenoid, and the

Figure 2

Stages of bone preparation and fixation A, The medial aspect of the humeral head

is cut parallel with the glenoid surface The glenohumeral pins are removed before

completing the cut B, The undersurface of the acromion and superior surface of the humeral head are cut in parallel C, A 4.5-mm pelvic reconstruction plate is used

to firmly stabilize the arthrodesis Partially threaded screws are used to compress

the humerus to the glenoid and acromion D, Anteroposterior radiograph taken a

few weeks after arthrodesis (Panels A, B, and C copyright Cleveland Clinic Foundation, 2003.)

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undersurface of the acromion.

After surgery, the shoulder is

im-mobilized using a Southern

Califor-nia Orthopaedic Institute (SCOI)

brace (DonJoy, Vista, CA), abduction

pillow, or spica cast The extent of

immobilization depends on the

qual-ity and quantqual-ity of bone as well as

the stability of the fixation In a

pri-mary fusion with good bone stock

and stable fixation, the SCOI brace

or abduction pillow is used for 8 to

10 weeks In complex cases with

poor bone quality, poor fixation, or

structural grafting, the patient is

im-mobilized in a spica cast for 3 to 4

months or until there is

radiograph-ic evidence of fusion When it is dif-ficult to determine bony fusion on radiographs, computed tomography scan reconstructions may be neces-sary Scapular exercises for range of motion and strength are started after radiographic signs of fusion are found

Functional Results

The objective of shoulder arthrode-sis is a painless, functional

extremi-ty sufficient for most ADLs Studies indicate that most patients report

marked pain relief after surgery, al-though few are completely pain-free Hawkins and Neer12 reported that only 4 of their 16 patients were pain-free, whereas 9 needed analgesics on

a daily basis for moderate or severe pain Cofield and Briggs16 reported better pain control in their series Of the 65 patients, 25 (38%),were pain free, 24 (36%) had mild pain, 15 (23%) had moderate pain, and only 2 (3%) had severe pain Of the 17 pa-tients with moderate or severe pain,

10 (59%) had pain located to the sur-gical area, 5 (29%) had pain in the periscapular region, and 2 (12%) had diffuse pain Extremity function was limited by pain in most of the pa-tients with moderate or severe pain Rouholamin et al29described ex-cellent pain relief in 10 of 15 pa-tients with brachial plexus injury

Figure 3

A 65-year-old man presented with failed humeral arthroplasty of the right shoulder,

an irreparable rotator cuff tear, and impaired deltoid muscle function

A,Preoperative anteroposterior radiograph demonstrating noticeable prosthetic

loosening B, Postoperative anteroposterior radiograph after application of a pelvic

reconstruction plate C and D, Functional range of motion was achieved.

Figure 4

Arthrodesis with large proximal humeral bone deficiency The fibular graft is 4

to 5 cm longer than the humeral length needed, for optimal docking The proximal part of the fibular graft is keyed into a burred trough in the glenoid The trough is fashioned to optimize bone contact and allow sufficient abduction (Copyright Cleveland Clinic Foundation, 2003.)

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who underwent shoulder fusion.

Three patients reported aching with

prolonged use of the arm; the pain

was relieved with rest Two patients

with preoperatively diagnosed

neu-rogenic pain continued to have pain

Excellent pain relief also was

report-ed by Rybka et al30in their series of

41 patients with rheumatoid

arthri-tis Only four patients reported

tran-sitory pain, which was thought to be

caused by increased strain on the

periscapular muscles In a recent

study, Wick et al7reported marked

pain reduction after arthrodesis in 15

patients with septic arthritis

Four-teen of the 15 patients had active

in-fection (positive cultures) at the time

of arthrodesis Ninety percent of

pa-tients reported marked pain

reduc-tion; however, no patient was

pain-free

Functional outcome after

shoul-der arthrodesis has lagged behind

pain improvement Of the 17

pa-tients in the Hawkins and Neer

study,125 functioned reasonably well

at head level (eg, hair combing, face

washing), while 4 others had great

difficulty Fourteen patients could

use their hands satisfactorily at

waist level, but only 3 could reach

the hand behind the back for

hy-giene Overall, 7 of the 17 patients

were dissatisfied because of

func-tional disability Wick et al7 found

that patients were unable to reach

behind the back, and most of them

had difficulty with ADLs around the

face In contrast, Cofield and

Briggs16reported that, of the 65

pa-tients available for follow-up, 70%

could lift moderate weights, dress

themselves, tend to personal

hy-giene, and eat using the extremity

with the fused shoulder Although

only 21% could use their arm for

light work at shoulder level, 82%

found their arthrodesis to be

func-tionally beneficial

Richards and colleagues4,23 and

Rouholamin et al29 reported

func-tional results similar to those of

Cofield and Briggs.16All of their

pa-tients (except those with distal

ex-tremity paralysis or amputees) could easily reach the mouth Although none of Richards’ patients could per-form overhead work, all were satis-fied with their functional improve-ment Hawkins and Neer12reported that no patient was able to work overhead or with the arms abducted (eg, hammering, painting, climbing a ladder) Four of 17 patients could not return to jobs requiring manual la-bor Five of the 17 patients returned

to manual labor, but not at their

pre-injury level It is worth noting that Hawkins and Neer12 as well as Cofield and Briggs16found extreme internal rotation to be detrimental for shoulder function

Complications

Among the complications of shoul-der arthrodesis are nonunion, mal-positioning of the fused shoulder, perifusion fractures, infection, con-tinued pain, and soft-tissue irritation

Figure 5

A 21-year-old man presented several years after resection of the right proximal humerus for osteogenic sarcoma The proximal humerus was reconstructed with

segmental allograft and a custom-made total shoulder prosthesis A, Preoperative

anteroposterior radiograph demonstrating dislocation of the shoulder arthroplasty

as well as a recent periprosthetic fracture, necessitating shoulder arthrodesis

B,Postoperative radiograph demonstrating a long vascularized fibular graft compensating for a deficient humerus and arthrodesis of the acromion, glenoid,

and fibula C and D, Functional range of motion was achieved after fusion.

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caused by prominent fixation

devic-es The frequency of these

complica-tions is related to the quality and

quantity of bone available for fusion

as well as to the condition of the

soft-tissue envelope

Nonunion

In most series, the rate of

20%.4,7,8,12,16,23,30The relatively small

number of patients in most studies,

along with the complexity of the

ini-tial diagnosis, makes it difficult to

compare results between studies

With modern fixation methods,

however, the nonunion rate is

clos-er to 10%, with the exception of

fu-sion after septic arthritis, which

re-mains at 20%.7

Most reported nonunions were

symptomatic, painful, and required

further treatment Revision surgery

with secondary bone grafting and/or

refixation achieved union in most

patients Only a small percentage of

patients demonstrated partial fusion

of either the glenohumeral or the

acromiohumeral articulation In

nearly all cases, the fusion mass was

stable, the shoulder was functional,

and no further treatment was

neces-sary

Malposition of the Fused

Shoulder

It is difficult to define

malposi-tion because no consensus exists as

to optimal position However,

sever-al guidelines may assist in making

this assessment Painful winging of

the scapula with the arm in the

rest-ing position is a functional

defini-tion of malposidefini-tion associated with

excessive abduction or flexion of the

fusion In addition, in the absence of

other causes, inability to reach the

face or anterior midline is most

like-ly the result of rotational

malposi-tion of the arthrodesis Surgical

cor-rection should be sought when the

malposition causes scapular pain or

leads to dysfunction in ADLs A

closing wedge corrective osteotomy

distal to the fusion mass combined

with plate fixation and grafting is recommended for managing a signif-icant and symptomatic malposi-tioned fusion.10Groh et al19reported that osteotomy markedly improved pain and function in all nine patients who underwent corrective

osteoto-my for malpositioned shoulder fu-sion

Periarthrodesis Fractures

Elimination of motion at the gle-nohumeral joint combined with lo-cal osteopenia increases the proba-bility that relatively minor trauma will cause fracture around the ar-throdesis Typically, fracture occurs distal to the fusion mass either at the point at which the plate fixation ends or at the entry point of the most distal compression screws

Cofield and Briggs16 reported on eight postoperative humeral frac-tures in their series of 71 patients, with most occurring in paralytic pa-tients All fractures healed with ex-ternal immobilization In their se-ries of 41 patients, Rybka et al30

reported only one late postoperative humeral neck fracture, which oc-curred after a fall 1.5 years after sur-gery No fractures were reported by Richards and colleagues4,23 or by Stark et al.18Nondisplaced humeral fractures are managed with immobi-lization; displaced or unstable frac-tures require internal fixation for solid union to occur.17

Prominence of Fixation Device

The superficial location of inter-nal fixation devices, particularly compression screws and plates, may cause local skin problems and skin penetration Typically, this occurs over the spine of the scapula and acromion because of a poor soft-tissue envelope secondary to muscle atrophy and multiple surgeries In many cases, partial or complete re-moval of the fixation device after consolidation of the fusion mass is necessary to solve the problem

Cofield and Briggs16 reported late

screw removal in 17 of 71 shoulder operations (compression screws were used) Higher rates of soft-tissue prominence have been reported when DCP plates were used Rich-ards et al4had to remove eight DCP plates from their 14 patients (57%) Stark et al18reported four symptom-atic plate removals in 15 patients In the later study by Richards et al,23

lower rates of metal-related symp-toms were reported when recon-struction plates were used However,

in a series using only reconstruction plates for fixation, local discomfort

or prominence necessitated hard-ware removal in five of eight pa-tients.8

Summary

Shoulder arthrodesis is an end-stage salvage procedure for managing pain and loss of function when other joint-sparing reconstructive options have been exhausted It is an alterna-tive to resection arthroplasty in the patient who desires the ability to lift

to chest or shoulder level A solid fu-sion achieves good pain relief and ac-ceptable ADL function in most pa-tients Return to work is less consistently achieved, however Both the surgeon and the patient should be aware of the limitations of shoulder arthrodesis and set realistic goals With proper indications and surgical techniques, solid shoulder fusion and a satisfactory result are achieved in the vast majority of

cas-es, with improvement in pain and functional outcome

References

Evidence-based Medicine: Evidence-based reports consist of level III (case-contracted studies) or level IV (case series) only

Citation numbers printed in bold

type indicate references published

within the past 5 years

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