富血小板血浆治疗膝骨关节炎后的注射方案:系统综述。

IF 2.2 4区 医学 Q1 REHABILITATION PM&R Pub Date : 2024-09-01 Epub Date: 2024-03-25 DOI:10.1002/pmrj.13139
Oscar Paul Levine, Koushik Kondapi, Vehniah Kristin Tjong, Chetan Gohal
{"title":"富血小板血浆治疗膝骨关节炎后的注射方案:系统综述。","authors":"Oscar Paul Levine, Koushik Kondapi, Vehniah Kristin Tjong, Chetan Gohal","doi":"10.1002/pmrj.13139","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Platelet-rich plasma (PRP) use in treating orthopedic conditions has increased, yet evidence of its clinical efficacy is inconsistent and limited by heterogeneity in osteoarthritis (OA) severity, PRP preparations and protocols, and clinical outcome measurement. This review aims to characterize the variations in postinjection protocols in studies assessing the clinical efficacy of PRP for knee OA.</p><p><strong>Literature survey: </strong>A systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. A literature search from database inception to February 2023 of CINAHL, MEDLINE, and EMBASE was conducted.</p><p><strong>Methodology: </strong>Article screening, data extraction, and risk of bias assessments were completed in duplicate by two reviewers. Primary outcomes were presence/absence and timing of the following postinjection protocol components: nonsteroidal anti-inflammatory drug (NSAID) restrictions, non-NSAID analgesic and cryotherapy use, immediate knee flexion/extension, immediate rest, activity restriction, return-to-activity guidelines, and rehabilitation protocols. A descriptive analysis was used to analyze the data. Given study heterogeneity, a meta-analysis was not performed.</p><p><strong>Synthesis: </strong>A total of 187 studies were included for analysis. Half of all studies (51.9%) excluded patients due to preinjection NSAID use, most often within 5 days of blood sampling or injection. Postinjection NSAID restriction was included in 42.8% of studies, ranging from 1 to 1800 days. Few studies (19.4%) that permitted non-NSAID analgesia restricted their use prior to clinical assessments. Postinjection immediate flexion, extension, and immobilization were rarely (8.6%) mentioned. Activity restriction was included in a third of studies (35.3%), with the most frequent length of restriction being 1 day. Postinjection return-to-activity protocols were less common (20.3%), usually with a \"gradual\" and/or \"as tolerated\" recommendation. A minority of studies (16.0%) reported physical therapy protocols and the vast majority (93.3%) were home based.</p><p><strong>Conclusion: </strong>Significant heterogeneity remains in post-PRP injection protocols, with unclear consensus regarding optimal recommendations and limited rationale for the protocols outlined. Further study is necessary to compare protocols directly and to determine which pre- and postinjection recommendations can result in optimal outcomes.</p>","PeriodicalId":20354,"journal":{"name":"PM&R","volume":" ","pages":"1023-1029"},"PeriodicalIF":2.2000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Postinjection protocols following platelet-rich plasma administration for knee osteoarthritis: A systematic review.\",\"authors\":\"Oscar Paul Levine, Koushik Kondapi, Vehniah Kristin Tjong, Chetan Gohal\",\"doi\":\"10.1002/pmrj.13139\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Platelet-rich plasma (PRP) use in treating orthopedic conditions has increased, yet evidence of its clinical efficacy is inconsistent and limited by heterogeneity in osteoarthritis (OA) severity, PRP preparations and protocols, and clinical outcome measurement. This review aims to characterize the variations in postinjection protocols in studies assessing the clinical efficacy of PRP for knee OA.</p><p><strong>Literature survey: </strong>A systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. A literature search from database inception to February 2023 of CINAHL, MEDLINE, and EMBASE was conducted.</p><p><strong>Methodology: </strong>Article screening, data extraction, and risk of bias assessments were completed in duplicate by two reviewers. Primary outcomes were presence/absence and timing of the following postinjection protocol components: nonsteroidal anti-inflammatory drug (NSAID) restrictions, non-NSAID analgesic and cryotherapy use, immediate knee flexion/extension, immediate rest, activity restriction, return-to-activity guidelines, and rehabilitation protocols. A descriptive analysis was used to analyze the data. Given study heterogeneity, a meta-analysis was not performed.</p><p><strong>Synthesis: </strong>A total of 187 studies were included for analysis. Half of all studies (51.9%) excluded patients due to preinjection NSAID use, most often within 5 days of blood sampling or injection. Postinjection NSAID restriction was included in 42.8% of studies, ranging from 1 to 1800 days. Few studies (19.4%) that permitted non-NSAID analgesia restricted their use prior to clinical assessments. Postinjection immediate flexion, extension, and immobilization were rarely (8.6%) mentioned. Activity restriction was included in a third of studies (35.3%), with the most frequent length of restriction being 1 day. Postinjection return-to-activity protocols were less common (20.3%), usually with a \\\"gradual\\\" and/or \\\"as tolerated\\\" recommendation. A minority of studies (16.0%) reported physical therapy protocols and the vast majority (93.3%) were home based.</p><p><strong>Conclusion: </strong>Significant heterogeneity remains in post-PRP injection protocols, with unclear consensus regarding optimal recommendations and limited rationale for the protocols outlined. Further study is necessary to compare protocols directly and to determine which pre- and postinjection recommendations can result in optimal outcomes.</p>\",\"PeriodicalId\":20354,\"journal\":{\"name\":\"PM&R\",\"volume\":\" \",\"pages\":\"1023-1029\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"PM&R\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/pmrj.13139\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/3/25 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"REHABILITATION\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"PM&R","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/pmrj.13139","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/25 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"REHABILITATION","Score":null,"Total":0}
引用次数: 0

摘要

目的:富血小板血浆(PRP)在骨科疾病治疗中的应用日益增多,但其临床疗效的证据并不一致,且受限于骨关节炎(OA)严重程度、PRP制剂和方案以及临床结果测量的异质性。本综述旨在描述在评估 PRP 对膝关节 OA 临床疗效的研究中注射后方案的差异:根据《系统综述和元分析首选报告项目》指南进行了系统综述。文献检索时间从数据库建立之初至 2023 年 2 月,检索范围包括 CINAHL、MEDLINE 和 EMBASE:文章筛选、数据提取和偏倚风险评估由两名审稿人重复完成。主要研究结果为注射后方案中是否包含以下内容以及时间安排:非甾体类抗炎药(NSAID)限制、非NSAID镇痛药和冷冻疗法的使用、立即屈伸膝关节、立即休息、活动限制、恢复活动指南和康复方案。数据分析采用描述性分析方法。鉴于研究的异质性,未进行荟萃分析:共纳入 187 项研究进行分析。半数研究(51.9%)排除了注射前使用非甾体抗炎药的患者,最常见的情况是在抽血或注射后 5 天内使用非甾体抗炎药。42.8%的研究纳入了注射后非甾体抗炎药限制,时间从1天到1800天不等。很少有研究(19.4%)允许在临床评估前限制使用非甾体抗炎镇痛药。很少(8.6%)提到注射后立即屈伸和固定。三分之一的研究(35.3%)提到了活动限制,最常见的限制时间为 1 天。注射后恢复活动的方案较少(20.3%),通常建议 "循序渐进 "和/或 "根据耐受情况"。少数研究(16.0%)报告了物理治疗方案,绝大多数研究(93.3%)以家庭为基础:结论:PRP 注射后的治疗方案仍存在很大的异质性,对最佳建议的共识不明确,概述的治疗方案的合理性有限。有必要开展进一步研究,以直接比较各种方案,并确定哪些注射前和注射后建议可带来最佳疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Postinjection protocols following platelet-rich plasma administration for knee osteoarthritis: A systematic review.

Objective: Platelet-rich plasma (PRP) use in treating orthopedic conditions has increased, yet evidence of its clinical efficacy is inconsistent and limited by heterogeneity in osteoarthritis (OA) severity, PRP preparations and protocols, and clinical outcome measurement. This review aims to characterize the variations in postinjection protocols in studies assessing the clinical efficacy of PRP for knee OA.

Literature survey: A systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. A literature search from database inception to February 2023 of CINAHL, MEDLINE, and EMBASE was conducted.

Methodology: Article screening, data extraction, and risk of bias assessments were completed in duplicate by two reviewers. Primary outcomes were presence/absence and timing of the following postinjection protocol components: nonsteroidal anti-inflammatory drug (NSAID) restrictions, non-NSAID analgesic and cryotherapy use, immediate knee flexion/extension, immediate rest, activity restriction, return-to-activity guidelines, and rehabilitation protocols. A descriptive analysis was used to analyze the data. Given study heterogeneity, a meta-analysis was not performed.

Synthesis: A total of 187 studies were included for analysis. Half of all studies (51.9%) excluded patients due to preinjection NSAID use, most often within 5 days of blood sampling or injection. Postinjection NSAID restriction was included in 42.8% of studies, ranging from 1 to 1800 days. Few studies (19.4%) that permitted non-NSAID analgesia restricted their use prior to clinical assessments. Postinjection immediate flexion, extension, and immobilization were rarely (8.6%) mentioned. Activity restriction was included in a third of studies (35.3%), with the most frequent length of restriction being 1 day. Postinjection return-to-activity protocols were less common (20.3%), usually with a "gradual" and/or "as tolerated" recommendation. A minority of studies (16.0%) reported physical therapy protocols and the vast majority (93.3%) were home based.

Conclusion: Significant heterogeneity remains in post-PRP injection protocols, with unclear consensus regarding optimal recommendations and limited rationale for the protocols outlined. Further study is necessary to compare protocols directly and to determine which pre- and postinjection recommendations can result in optimal outcomes.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
PM&R
PM&R REHABILITATION-SPORT SCIENCES
CiteScore
4.30
自引率
4.80%
发文量
187
审稿时长
4-8 weeks
期刊介绍: Topics covered include acute and chronic musculoskeletal disorders and pain, neurologic conditions involving the central and peripheral nervous systems, rehabilitation of impairments associated with disabilities in adults and children, and neurophysiology and electrodiagnosis. PM&R emphasizes principles of injury, function, and rehabilitation, and is designed to be relevant to practitioners and researchers in a variety of medical and surgical specialties and rehabilitation disciplines including allied health.
期刊最新文献
Percutaneous ultrasound-guided A1 pulley release utilizing a modified 20-gauge spinal needle. Self-perceived preparedness for practice among graduating physical medicine & rehabilitation residents. Knee joint mechanics during gait after anterior cruciate ligament reconstruction using a partial or full thickness quadriceps tendon autograft at 2 years after surgery. Test Smart, Treat Smart-using clinician feedback to adapt a catheter-associated urinary tract infection intervention for spinal cord injury. Racial disparities in prosthesis use, satisfaction, and physical function in upper limb amputation and the impact of veteran status.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1