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Arthroscopic acromioplasty may not be efficacious for shoulder impingement syndrome
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SHOULDER & ELBOW

Which patients do not recover from shoulder impingement syndrome, either with operative treatment or with nonoperative treatment?
Verified
This report has been verified by one or more authors of the original publication.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2016;4(6):45 Acta Orthop. 2015 Dec;86(6):641-6

140 patients with shoulder impingement syndrome were randomized to either a supervised exercise program alone or to arthroscopic acromioplasty followed with a similar exercise program. The purpose of this subgroup analysis study was to determine which patients (from either the arthroscopic acromioplasty and exercise therapy group, or the group treated solely with exercise therapy) are effectively treated for shoulder impingement syndrome when followed up at 2 and 5 years. Findings showed similar results between the patients who underwent operative treatment and the group that underwent conservative treatment. Furthermore, arthroscopic acromioplasty did not appear to improve results in patients who were originally allocated to exercise therapy alone and were unsatisfied with outcome following conservative management.


出版資金提供の詳細 +
資金提供:
Non-Industry funded
スポンサー:
Professor of medicine Y. T. Konttinen from Helsinki University Central Hospital
コンフリクト:
None disclosed

バイアスのリスク

4/10

報告基準

16/20

脆弱性指数

N/A

Was the allocation sequence adequately generated?

Was allocation adequately concealed?

Blinding Treatment Providers: Was knowledge of the allocated interventions adequately prevented?

Blinding Outcome Assessors: Was knowledge of the allocated interventions adequately prevented?

Blinding Patients: Was knowledge of the allocated interventions adequately prevented?

Was loss to follow-up (missing outcome data) infrequent?

Are reports of the study free of suggestion of selective outcome reporting?

Were outcomes objective, patient-important and assessed in a manner to limit bias (ie. duplicate assessors, Independent assessors)?

Was the sample size sufficiently large to assure a balance of prognosis and sufficiently large number of outcome events?

Was investigator expertise/experience with both treatment and control techniques likely the same (ie.were criteria for surgeon participation/expertise provided)?

はい = 1

不確実=0.5

無関係 = 0

いいえ = 0

報告基準評価では、著者が出版物内で試験の方法論的特徴や試験特性を報告する際の透明性を評価します。評価は以下の5つのカテゴリーに分類されます。

3/4

Randomization

1/4

Outcome Measurements

4/4

Inclusion / Exclusion

4/4

Therapy Description

4/4

Statistics

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

Fragility Indexは、重要な所見の解釈を助けるツールで、結果の強さの尺度を提供します。Fragility Indexは、その所見が有意でなくなるために、二項対立の結果に追加する必要がある連続した事象の数を表します。数値が小さいほど弱い所見を表し、数値が大きいほど強い所見を表します。

なぜ今この研究が必要なのですか?

Shoulder impingement syndrome is a common source of shoulder pain and functional deficit. Both operative and non-operative methods have been used to treat shoulder impingement syndrome. Despite previous literature suggesting that arthroscopic acromioplasty may not offer any significant advantages over exercise therapy, the use of arthroscopic acromioplasty in the treatment of shoulder impingement has been increasing over the past years. . This subgroup analysis was conducted to identify the individuals within the sample population that would benefit from operative treatment.

主な研究課題は何ですか?

What differences, if any, exist between subgroups of patients treated with acromioplasty and exercise therapy versus exercise therapy alone in the management of shoulder impingement syndrome, as assessed over a 5-year follow-up period?

研究の特徴 +
人口:
140 patients (18-60 years of age) with shoulder impingement syndrome. To be eligible for inclusion, patients must have symptoms that were unresponsive to previous nonoperative treatments, as well as a lack of previous shoulder surgery. (n=140; Mean age: 47 years; 52M/88F)
介入:
Combined group: patients in this group underwent combined treatment of arthroscopic acromioplasty followed by a structured exercise program. An arthroscopic decompression was initially performed for these patients. All patients were under regional anesthesia, and the operation was performed using a burr drill. (n=70; Mean age: 46.4 [Range: 23.3 to 60]; 41F/29M; 57 completed follow-up)
比較:
Exercise therapy group: patients randomized to this group only took part in the supervised exercise program. (n=70; Mean age: 47.8 [Range: 26.8 to 59.2]; 47F/23M; 52 completed follow-up)
アウトカム:
The primary outcome of this study was self-reported pain measured by a visual analogue scale (VAS). The number of pain-free patients was also determined by the criteria of having a VAS score of 3 or less from a scale of 0 to 10. Secondary outcomes consisted of disability measurements, working ability, VAS pain at night, shoulder disability questionnaire (SDQ) score and a number of reported days with pain before follow-up.
方法:
RCT; single-center
時間:
Follow up was conducted at 2 and 5 years after randomization.

重要な知見は?

  • Both the operative and non-operative groups reported significant improvements compared to baseline for self-reported pain, disability, working ability, pain at night, SDQ score and reported days with pain. Outcomes were similar between the groups.
  • Patients who were dissatisfied in the non-operative group and later received operative treatment reported worse values compared to patients in the other groups.
  • Overall in the entire cohort, 86 patients were pain-free and 48 patients reported pain (>3 on a visual analog scale) at 2-year follow-up. At 5 years, 82 patients were pain-free and 27 patients reported pain.
  • A number of factors were identified as having a statistically significant impact on pain. At 2-year follow-up factors included: living alone (Odds ratio 3.29 [95%CI 1.39-7.78]), lack of professional education (OR 3.67 [95%CI 1.20-11.2]), moderate load lifted per day (20-100kg) (OR 4.36 [95%CI 1.38-13.8]), and sick leave prior to randomization exceeding 2 weeks (OR 2.52 [95%CI 1.10-10.22]). At 5-year follow-up factors included: living alone (OR 2.77 [95%CI 1.02-7.55]), moderate-heavy load lifted per day (100-500kg) (OR 4.35 [95%CI 1.13-18.1]), and sick leave prior to randomized exceeding 2 weeks (OR 3.83 [95%CI 1.35-10.9]).
  • Overall satisfaction at work demonstrated a statistically significant effect on pain at 2-year follow-up (p=0.01), and requirement/challenges at work demonstrated a statistically significant effect on pain at 5 years (p=0.01).
最も覚えておくべきことは?

In the treatment of shoulder impingement syndrome, similar results for self-reported pain, disability, working ability, pain at night, SDQ score, and reported days with pain were demonstrated between arthroscopic acromioplasty with exercise therapy compared to exercise therapy alone. Patients initially in the exercise therapy group that later wanted arthroscopic acromioplasty did not show postoperative improvement.

それが私の患者ケアにどのように影響するか?

Based on the results of this analysis, arthroscopic acromioplasty may not offer any significant difference in clinical outcome when compared to supervised exercise therapy, or in cases of pursued surgery following supervised exercise therapy. The authors also reported that there does not appear to be a specific subgroup of patients to guide the decision between supervised exercise therapy and arthroscopic acromioplasty. Future research should consider possible patient subgroups as enrollment criteria in order to prospectively analyze outcomes between supervised exercise therapy and arthroscopic acromioplasty with a more narrow focus, as opposed to a secondary analysis with low sample sizes for multiple variables.

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引用方法 ACE Report

OrthoEvidence. Arthroscopic acromioplasty may not be efficacious for shoulder impingement syndrome. OE Journal. 2016;4(6):45. Available from: https://myorthoevidence.com/AceReport/Show/

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