Standard compared with fracture-specific components in reverse shoulder arthroplasty for proximal humerus fractures : a meta-analysis of clinical outcomes.

IF 4.6 1区 医学 Q1 ORTHOPEDICS
Adinun Apivatgaroon, Tanawan Kongmalai, Pinkawas Kongmalai
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引用次数: 0

Abstract

Aims: Reverse total shoulder arthroplasty (RSA) is a well-established treatment for proximal humerus fractures in elderly patients. However, the clinical advantages of standard humeral components compared to fracture-specific components remain unclear. This meta-analysis compares the clinical outcomes and complication rates of standard compared with fracture-specific components in RSA.

Methods: A systematic review and meta-analysis were conducted according to the PRISMA guidelines. PubMed, Scopus, and Cochrane Library databases were searched from inception to 12 August 2024. Comparative studies reporting clinical outcomes between standard components and fracture-specific components in RSA for proximal humerus fractures were included. Data on functional scores, range of motion, tuberosity healing, and complications were extracted. Meta-analyses were performed using fixed or random-effects models based on heterogeneity, and risk of bias was assessed using the Newcastle-Ottawa Scale (NOS) and the Cochrane Risk of Bias Tool (RoB2). Weighted mean difference (WMD) was used as the effect size estimator for continuous outcomes, and risk ratio (RR) for dichotomous outcomes. Sensitivity analysis was performed to assess the robustness of the findings.

Results: Six studies involving 436 patients (142 with standard components and 294 with fracture-specific components) were included. The pooled analysis found no significant differences between the two component types in functional outcomes (visual analogue scale (VAS): WMD 0.22; American Shoulder and Elbow Surgeons (ASES): WMD -7.43; Constant score: WMD -3.08) or postoperative range of motion (abduction: WMD 1.08°; internal rotation: WMD 0.35°; external rotation: WMD -2.76°; forward flexion: WMD -4.27°). Complication rates, including tuberosity failure (RR 1.34), scapular notching (RR 1.09), and component loosening (RR 1.64), were also comparable.

Conclusion: This meta-analysis demonstrates no significant differences in clinical outcomes or complication rates between standard components and fracture-specific components in RSA, suggesting comparable performance in the treatment of proximal humerus fractures. While the findings offer potentially useful insights, they should be interpreted in the context of the limited number of included studies and possible risk of bias.

肱骨近端骨折逆行肩关节置换术与骨折特异性部件的标准比较:临床结果的荟萃分析。
目的:反向全肩关节置换术(RSA)是一种成熟的治疗老年患者肱骨近端骨折的方法。然而,标准肱骨假体与骨折特异性假体相比的临床优势尚不清楚。本荟萃分析比较了RSA中标准和骨折特异性组件的临床结果和并发症发生率。方法:根据PRISMA指南进行系统评价和荟萃分析。检索了PubMed、Scopus和Cochrane图书馆数据库,检索时间从创建到2024年8月12日。比较研究报告了肱骨近端骨折RSA中标准假体和骨折特异性假体的临床结果。提取功能评分、活动范围、结节愈合和并发症的数据。采用基于异质性的固定效应或随机效应模型进行meta分析,并使用纽卡斯尔-渥太华量表(NOS)和Cochrane偏倚风险工具(RoB2)评估偏倚风险。采用加权平均差(WMD)作为连续结局的效应量估计,采用风险比(RR)作为二分类结局的效应量估计。进行敏感性分析以评估研究结果的稳健性。结果:纳入6项研究,涉及436例患者(142例使用标准组件,294例使用骨折特异性组件)。合并分析发现两种成分类型在功能结局方面无显著差异(视觉模拟评分(VAS): WMD 0.22;美国肩肘部外科医生(ASES): WMD -7.43;恒定评分:WMD -3.08)或术后活动范围(外展:WMD 1.08°;内旋:WMD 0.35°;外旋:WMD -2.76°;前屈:WMD -4.27°)。并发症发生率,包括结节失败(RR 1.34),肩胛骨缺口(RR 1.09)和部件松动(RR 1.64),也具有可比性。结论:该荟萃分析显示,RSA标准假体与骨折特异性假体在临床结果或并发症发生率方面无显著差异,提示其治疗肱骨近端骨折的效果相当。虽然这些发现提供了潜在的有用见解,但它们应该在有限的纳入研究数量和可能的偏倚风险的背景下进行解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bone & Joint Journal
Bone & Joint Journal ORTHOPEDICS-SURGERY
CiteScore
9.40
自引率
10.90%
发文量
318
期刊介绍: We welcome original articles from any part of the world. The papers are assessed by members of the Editorial Board and our international panel of expert reviewers, then either accepted for publication or rejected by the Editor. We receive over 2000 submissions each year and accept about 250 for publication, many after revisions recommended by the reviewers, editors or statistical advisers. A decision usually takes between six and eight weeks. Each paper is assessed by two reviewers with a special interest in the subject covered by the paper, and also by members of the editorial team. Controversial papers will be discussed at a full meeting of the Editorial Board. Publication is between four and six months after acceptance.
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