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      Surgical versus conservative interventions for treating acromioclavicular dislocation of the shoulder in adults

      1 , 2 , 1 , 1 , 1 , 1
      Cochrane Bone, Joint and Muscle Trauma Group
      Cochrane Database of Systematic Reviews
      Wiley

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          Abstract

          Dislocation of the acromioclavicular joint is one of the most common shoulder injuries in a sport‐active population. The question of whether surgery should be used remains controversial. This is an update of a Cochrane Review first published in 2010. To assess the effects (benefits and harms) of surgical versus conservative (non‐surgical) interventions for treating acromioclavicular dislocations in adults. We searched the Cochrane Bone, Joint and Muscle Trauma Group Specialised Register (to June 2019), the Cochrane Central Register of Controlled Trials (CENTRAL) (the Cochrane Library 2019, Issue 6), MEDLINE (1946 to June 2019), Embase (1980 to June 2019), and LILACS (1982 to June 2019), trial registries, and reference lists of articles. There were no restrictions based on language or publication status. We included all randomised and quasi‐randomised trials that compared surgical with conservative treatment of acromioclavicular dislocation in adults. At least two review authors independently performed study screening and selection, 'Risk of bias' assessment, and data extraction. We pooled data where appropriate and used GRADE to assess the quality of evidence for each outcome. We included five randomised trials and one quasi‐randomised trial. The included trials involved 357 mainly young adults, the majority of whom were male, with acute acromioclavicular dislocation. The strength of the findings in all studies was limited due to design features, invariably lack of blinding, that carry a high risk of bias. Fixation of the acromioclavicular joint using hook plates, tunnelled suspension devices, coracoclavicular screws, acromioclavicular pins, or (usually threaded) wires was compared with supporting the arm in a sling or similar device. After surgery, the arm was also supported in a sling or similar device in all trials. Where described in the trials, both groups had exercise‐based rehabilitation. We downgraded the evidence for all outcomes at least two levels, invariably for serious risk of bias and serious imprecision. Low‐quality evidence from two studies showed no evidence of a difference between groups in shoulder function at one year, assessed using the Disability of the Arm, Shoulder, and Hand questionnaire (DASH) (0 (best function) to 100 (worst function)): mean difference (MD) 0.73 points, 95% confidence interval (CI) −2.70 to 4.16; 112 participants. These results were consistent with other measures of function at one‐year or longer follow‐up, including non‐validated outcome scores reported by three studies. There is low‐quality evidence that function at six weeks may be better after conservative treatment, indicating an earlier recovery. Very low‐quality evidence from one trial found no difference between groups in participants reporting pain at one year: risk ratio (RR) 1.32, 95% CI 0.54 to 3.19; 79 participants. There is very low‐quality evidence that surgery may not reduce the risk of treatment failure, usually resulting in non‐routine secondary surgery: 14/168 versus 15/174; RR 0.99, 95% CI 0.51 to 1.94; 342 participants, 6 studies. The main source of treatment failure was complications related to surgical implants in the surgery group and persistent symptoms, mainly discomfort, due to the acromioclavicular dislocation in the conservatively treated group. There is low‐quality evidence from two studies that there may be little or no difference between groups in the return to former activities (sports or work) at one year: 57/67 versus 62/70; RR 0.96, 95% CI 0.85 to 1.10; 137 participants, 2 studies. Low‐quality but consistent evidence from four studies indicated an earlier recovery in conservatively treated participants compared with those treated with surgery. There is low‐quality evidence of no clinically important difference between groups at one year in quality of life scores, measured using the 36‐item or 12‐item Short Form Health Survey (SF‐36 or SF‐12) (0‐to‐100 scale, where 100 is best score), in either the physical component (MD −0.63, 95% CI −2.63 to 1.37; 122 participants, 2 studies) or mental component (MD 0.47 points, 95% CI −1.51 to 2.44; 122 participants). There is very low‐quality and clinically heterogenous evidence of a greater risk of an adverse event after surgery: 45/168 versus 16/174; RR 2.82, 95% CI 1.65 to 4.82; 342 participants, 6 studies; I 2 = 48%. Common adverse outcomes were hardware complications or discomfort (18.5%) and infection (8.7%) in the surgery group and persistent symptoms (7.1%), mainly discomfort, in the conservatively treated group. The majority of surgical complications occurred in older studies testing now‐outdated devices known for their high risk of complications. The very low‐quality evidence from one study (70 participants) means that we are uncertain whether there is a between‐group difference in patient dissatisfaction with cosmetic results. It is notable that the evidence for function, return to former activities, and quality of life came from the two most recently conducted studies, which tested currently used devices and interventions in clearly defined participant populations that represented the commonly perceived population for which there is uncertainty over the use of surgery. There were insufficient data to conduct subgroup analysis relating to type of injury and whether surgery involved ligament reconstruction or not. There is low‐quality evidence that surgical treatment has no additional benefits in terms of function, return to former activities, and quality of life at one year compared with conservative treatment. There is, however, low‐quality evidence that people treated conservatively had improved function at six weeks compared with surgical management. There is very low‐quality evidence of little difference between the two treatments in pain at one year, treatment failure usually resulting in secondary surgery, or patient satisfaction with cosmetic result. Although surgery may result in more people sustaining adverse events, this varied between the trials, being more common in techniques such as K‐wire fixation that are rarely used today. There remains a need to consider the balance of risks between the individual outcomes: for example, surgical adverse events, including wound infection or dehiscence and hardware complication, against risk of adverse events that may be more commonly associated with conservative treatment such as persistent symptoms or discomfort, or both. There is a need for sufficiently powered, good‐quality, well‐reported randomised trials of currently used surgical interventions versus conservative treatment for well‐defined injuries. Surgical versus conservative for treatment for acromioclavicular dislocations of the shoulder in adults This is a summary of research on the effects of surgery compared with non‐surgical (conservative) treatment methods to treat a dislocated acromioclavicular joint. Background The acromioclavicular joint is located at the top of the shoulder. It is the joint between the collarbone and the acromion (a projection from the shoulder blade that is located at the point of the shoulder). Acromioclavicular joint dislocation is one of the most common shoulder injuries treated in a sport‐active population. It is a common shoulder injury in cyclists and contact sports players such as footballers, boxers, and martial arts practitioners. The dislocation typically occurs in young men who fall and suffer a direct impact to the top of the shoulder. Most acromioclavicular dislocations are treated without surgery, especially those with less severe separation between the bones. Non‐surgical or conservative treatment involves immobilisation of the arm. However, the outcome can be less satisfactory when a more serious dislocation occurs. Surgical treatments involve repositioning the joint parts and repairing or reconstructing the ruptured ligaments. Results of the search We searched medical databases up to June 2019 and included six trials involving 357 participants who were mainly young male adults. All studies compared surgical fixation (using either screws, plates, pins, or other devices to stabilise the dislocated joint) with a conservative method (immobilisation with one of three types of slings or a specially designed splint). In all trials the arm was also supported in a sling or similar device after surgery. Where described, both groups had exercise‐based rehabilitation. Key results We found that surgery compared with conservative treatment may not improve shoulder function, return to former activities (sport and work), or quality of life at one year. We found evidence that at six weeks, these outcomes may be better after conservative treatment, indicating an earlier recovery. It is unclear whether there is a difference between surgery and conservative treatment in pain at one year, treatment failure usually resulting in secondary surgery, or patient unhappiness with their shoulder appearance. The review found more complications in the surgery group, which were mainly related to the surgical hardware or infection from the surgery. In contrast, complications in the conservatively treated group were mainly discomfort. The risk of such complications varied amongst the six studies and is likely to depend on the type of surgery used. Surgical complications were more common in the older trials, which used types of surgery rarely used today. Quality of the evidence All six studies had weaknesses that could affect the reliability of their results. We considered the evidence for all outcomes to be either of low or very low quality. Conclusions Low‐quality evidence indicates that surgery may not provide benefits at one year over conservative treatment for acromioclavicular dislocations in adults. Further good‐quality studies may help resolve this uncertainty and change these conclusions.

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          Most cited references57

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          A standardized method for the assessment of shoulder function.

          The American Shoulder and Elbow Surgeons have adopted a standardized form for assessment of the shoulder. The form has a patient self-evaluation section and a physician assessment section. The patient self-evaluation section of the form contains visual analog scales for pain and instability and an activities of daily living questionnaire. The activities of daily living questionnaire is marked on a four-point ordinal scale that can be converted to a cumulative activities of daily living index. The patient can complete the self-evaluation portion of the questionnaire in the absence of a physician. The physician assessment section includes an area to collect demographic information and assesses range of motion, specific physical signs, strength, and stability. A shoulder score can be derived from the visual analogue scale score for pain (50%) and the cumulative activities of daily living score (50%). It is hoped that adoption of this instrument to measure shoulder function will facilitate communication between investigators, stimulate multicenter studies, and encourage validity testing of this and other available instruments to measure shoulder function and outcome. Copyright © 1994 Journal of Shoulder and Elbow Surgery Board of Trustees. Published by Mosby, Inc. All rights reserved.
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            A review of the Constant score: modifications and guidelines for its use.

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              Questionnaire on the perceptions of patients about shoulder surgery.

              We developed a 12-item questionnaire for completion by patients having shoulder operations other than stabilisation. A prospective study of 111 patients was undertaken before operation and at follow-up six months later. Each patient completed the new questionnaire and the SF36 form. Some filled in the Stanford Health Assessment Questionnaire (HAQ). An orthopaedic surgeon assessed the Constant shoulder score. The single score derived from the questionnaire had a high internal consistency. Reproducibility, examined by test-retest reliability, was found to be satisfactory. The validity of the questionnaire was established by obtaining significant correlations in the expected direction with the Constant score and the relevant scales of the SF36 and the HAQ. Sensitivity to change was assessed by analysing the differences between the preoperative scores and those at follow-up. Changes in scores were compared with the patients' responses to postoperative questions about their condition. The standardised effect size for the new questionnaire compared favourably with that for the SF36 and the HAQ. The new questionnaire was the most efficient in distinguishing patients who said that their shoulder was much better from all other patients. The shoulder questionnaire provides a measure of outcome for shoulder operations which is short, practical, reliable, valid and sensitive to clinically important changes.
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                Author and article information

                Journal
                146518
                Cochrane Database of Systematic Reviews
                Wiley
                14651858
                October 11 2019
                Affiliations
                [1 ]Universidade Federal de São Paulo; Department of Orthopaedics and Traumatology; Rua das Rosas, 126 apto 73 São Paulo Sao Paulo Brazil 04038-032
                [2 ]Faculdade Israelita de Ciencias da Saude Albert Einstein and Hospital Israelita Albert Einstein; Orthopaedic Department and School of Medicine; Av. Albert Einstein, 627/701 São Paulo São Paulo Brazil CEP 05651-901
                Article
                10.1002/14651858.CD007429.pub3
                6788812
                31604007
                3ef6c80a-f53c-49f1-8b3a-dd5a103c5707
                © 2019
                History

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