Limited Evidence to Support the Use of Intra-Articular Injection of Hyaluronic Acid for the Management of Hallux Rigidus: A Systematic Review.

Foot & Ankle Orthopaedics Pub Date : 2024-07-29 eCollection Date: 2024-07-01 DOI:10.1177/24730114241265109
James J Butler, Hayden Hartman, Amanda Mener, Nathaniel P Mercer, Grace W Randall, Stephen Petropoulos, Andrew J Rosenbaum, John G Kennedy
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引用次数: 0

Abstract

Background: The purpose of this systematic review was to evaluate outcomes following intra-articular injection of hyaluronic acid (HA) for the treatment of hallux rigidus.

Methods: During April 2024, a systematic review of the MEDLINE, EMBASE, and Cochrane Library databases was performed based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Data collected and analyzed were number of patients, patient age, follow-up, subjective clinical outcomes, complications, and failures.

Results: Five studies were included. In total, 218 patients (218 feet) underwent intra-articular injection of HA at a weighted mean follow-up time of 4.4 ± 1.4 months (range, 3-6). There was an improvement in postinjection visual analog scale (VAS) pain at rest scores, VAS pain during activity scores, American Orthopaedic Foot & Ankle Society (AOFAS) scores, and Foot Health Status Questionnaire (FHSQ) scores. In total, 21 complications (10.0%) were observed, the most common of which was transient postinjection pain in 20 patients (9.6%). There were 7 patients (3.2%) who underwent secondary procedures (3.2%). One randomized control trial (RCT) demonstrated no difference in outcomes between an intra-articular injection of HA compared to an intra-articular injection of saline. One RCT demonstrated superior FHSQ scores following between an intra-articular injection of HA compared to an intra-articular injection of triamcinolone acetonide.

Conclusion: This systematic review suggests that intra-articular injection of HA for the treatment of hallux rigidus may lead to improved clinical outcomes with a low complication rate at short-term follow-up. However, the low level and quality of evidence underscores the need for further high-quality studies to be conducted to identify the precise role of HA in the treatment of hallux rigidus.

支持关节腔内注射透明质酸治疗拇指外翻的证据有限:系统回顾
背景:本系统性综述旨在评估关节内注射透明质酸(HA)治疗硬下疳的疗效:本系统综述旨在评估关节内注射透明质酸(HA)治疗硬下疳的疗效:方法:2024 年 4 月,根据《系统综述和元分析首选报告项目》(Preferred Reporting Items for Systematic Reviews and Meta-Analyses,PRISMA)指南,对 MEDLINE、EMBASE 和 Cochrane Library 数据库进行了系统综述。收集和分析的数据包括患者人数、患者年龄、随访情况、主观临床结果、并发症和失败:结果:共纳入五项研究。共有218名患者(218只脚)接受了HA关节内注射,加权平均随访时间为4.4±1.4个月(3-6个月)。注射后静息时疼痛视觉模拟量表(VAS)评分、活动时疼痛视觉模拟量表(VAS)评分、美国骨科足踝协会(AOFAS)评分和足部健康状况问卷(FHSQ)评分均有改善。共观察到 21 例并发症(10.0%),其中最常见的是 20 例患者(9.6%)注射后出现短暂疼痛。有 7 名患者(3.2%)接受了二次手术(3.2%)。一项随机对照试验(RCT)显示,关节内注射 HA 与关节内注射生理盐水的结果没有差异。一项随机对照试验显示,与关节内注射曲安奈德相比,关节内注射HA后的FHSQ评分更高:本系统性综述表明,关节内注射HA治疗僵直性拇指外翻可改善临床疗效,且短期随访的并发症发生率较低。然而,由于证据的水平和质量较低,因此需要进一步开展高质量的研究,以确定 HA 在治疗僵直性拇指外翻中的确切作用。
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
Foot & Ankle Orthopaedics
Foot & Ankle Orthopaedics Medicine-Orthopedics and Sports Medicine
CiteScore
1.20
自引率
0.00%
发文量
1152
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