膝关节骨性关节炎的注射后治疗方案:随机对照试验的系统回顾

Anna L. Park , Zachary P. Bailowitz , Peter M. DeJong , Zainab Shirazi , Nicholas Tsitsilianos , Kristian J. von Rickenbach , Christine E. Townsend , Drew A. Lansdown , Alfred C. Gellhorn , Anthony Luke
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引用次数: 0

摘要

背景:目前对于使用富血小板血浆(PRP)治疗膝关节骨性关节炎(OA)尚无明确的注射后推荐。本文系统地回顾了PRP治疗膝关节OA的随机对照试验的注射后方案,特别关注非甾体抗炎药(NSAIDs)的限制、活动限制和康复方案。数据来源我们在PubMed和Embase数据库中检索了截止到2024年2月的术语“膝关节骨关节炎”、“PRP”、“富血小板血浆”或“自体”,得到了1156篇独特的文章。纳入研究资格标准、受试者和干预措施,纳入10名以上受试者使用PRP治疗膝关节OA的随机对照试验。71项研究符合纳入标准。研究评价和综合方法提取和总结非甾体抗炎药限制、活动限制和康复方案的数据。使用Cochrane risk of bias 2工具评估偏倚风险。结果54.9%的文献提供了注射后限制使用非甾体抗炎药的信息,最常见的限制时间超过4周。33.8%的人提供了有关负重限制的信息。两项研究报告了详细的康复方案。局限性:PRP注射治疗膝关节OA的随机对照试验在注射后方案的报告中存在显著的可变性和缺陷。关键发现的结论和意义注射后方案中报告的缺失和潜在的异质性限制了比较研究结果的能力。系统评审注册号crd42024509022
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Postinjection protocols following platelet rich plasma injection for knee osteoarthritis: a systematic review of randomized controlled trials

Background

There are currently no established postinjection recommendations for the use of platelet-rich plasma (PRP) as a treatment for knee osteoarthritis (OA).

Objectives

This paper systematically reviews postinjection protocols for randomized controlled trials of PRP for knee OA, with a particular focus on nonsteroidal anti-inflammatory drugs (NSAIDs) restrictions, activity limitations, and rehabilitation protocols.

Data sources

We searched the PubMed and Embase databases through February 2024 for the terms “knee osteoarthritis,” and “PRP,” “platelet rich plasma,” or “autologous,” resulting in 1156 unique articles.

Study eligibility criteria, participants, and interventions

Studies were included if they were randomized controlled trials with more than 10 participants using PRP for knee OA. Seventy-one studies met the inclusion criteria.

Study appraisal and synthesis methods

Data on NSAID restrictions, activity limitations, and rehabilitation protocols were extracted and summarized. The risk of bias was assessed using the Cochrane Risk of Bias 2 tool.

Results

Exactly 54.9% of the reviewed articles provided information about postinjection NSAID restriction, with the most common time frame being longer than 4 weeks. Exactly 33.8% provided information about weight-bearing restrictions. Two studies reported detailed rehabilitation protocols.

Limitations

Randomized controlled trials for PRP injections for knee OA have significant variability and deficits in the reporting of postinjection protocols.

Conclusions and implications of key findings

Lack of reporting and potential heterogeneity in postinjection protocols limits the ability to compare results between studies.

Systematic review registraiton number

CRD42024509022
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