Systematic Review of Randomized Controlled Trials Evaluating the Use of Platelet-Rich Plasma for Knee Osteoarthritis: Adherence to Minimum Information for Studies Evaluating Biologics in Orthopaedics

Hirotaka F. Nakagawa, James Kim, Joseph Rinaldi, Judy Rabinowitz, Ken Mautner, Ariana DeMers, Seth Sherman, Joanne Borg-Stein, Walter I. Sussman
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Abstract

Background:The Minimum Information for Studies Evaluating Biologics in Orthopedics (MIBO) guidelines were developed in May 2017 to encourage improved reporting standards, promote increased transparency and reproducibility, and enhance clinical evaluation capabilities. The MIBO guidelines consist of 23 checklist items considered necessary to critically appraise clinical studies evaluating platelet-rich plasma (PRP).Purpose:To assess randomized controlled trials that evaluated PRP for the treatment of knee osteoarthritis in order to systematically review their adherence to the MIBO guidelines.Study Design:Systematic review. Level 1a.Methods:A search was performed following the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. The inclusion criteria were randomized controlled trials reporting on knee osteoarthritis treated with intra-articular PRP. The studies were categorized into pre-, peri-, and post-MIBO groups based on the start date of data collection. The overall MIBO scores, defined as percentage of checklist items out of the 23 checklist items reported in 1 study, individual item scores, defined as percentage of studies reporting the checklist item within a specified group, and overall item score defined as the average of the individual item scores from all the included studies were calculated.Results:The review included 87 studies (7925 patients; 8118 knees). Of these, 51 studies were assigned to the pre-MIBO group, 19 studies to the peri-MIBO group, and 17 studies to the post-MIBO group. The overall MIBO score was 72%. No statistically significant differences in MIBO scores were found among the 3 MIBO groups ( P = .345). The majority of the studies (62 studies; 71%) had MIBO scores <80%. MIBO items with particularly low item scores included reporting of whole-blood characteristics (20%), platelet recovery rate (22%), PRP analysis (30%), and PRP activation (47%). No significant difference among the 3 MIBO groups was found for the item scores except for the reporting of the recipient details ( P = .012).Conclusion:This study highlights the deficiencies in adherence to the MIBO guidelines, particularly in reporting key variables such as whole-blood characteristics, platelet recovery rate, PRP analysis, and PRP activation. These findings suggest that the publication of the MIBO guidelines has not resulted in improved reporting practices in studies investigating intra-articular PRP for the treatment of knee osteoarthritis.
评价富血小板血浆治疗膝骨关节炎的随机对照试验的系统评价:对骨科生物制剂评价研究的最小信息的依从性
背景:《骨科生物制剂研究评估最低信息指南》(MIBO)于2017年5月制定,旨在鼓励改进报告标准,提高透明度和可重复性,增强临床评估能力。MIBO指南包括23个被认为是批判性评估富血小板血浆(PRP)临床研究所必需的检查清单项目。目的:评估评估PRP治疗膝骨关节炎的随机对照试验,以便系统地回顾它们对MIBO指南的遵守情况。研究设计:系统评价。1级。方法:按照PRISMA(系统评价和荟萃分析首选报告项目)指南进行检索。纳入标准是报告关节内PRP治疗膝关节骨性关节炎的随机对照试验。根据数据收集的开始日期,这些研究被分为mibo前、中期和后三组。计算总体MIBO得分(定义为1项研究报告的23个检查表项目中检查表项目的百分比)、单项得分(定义为在指定组中报告检查表项目的研究的百分比)和总体项目得分(定义为所有纳入研究的单项得分的平均值)。结果:纳入87项研究(7925例患者;8118膝盖)。其中51项研究被分配到mibo前组,19项研究被分配到mibo中期组,17项研究被分配到mibo后组。总体MIBO得分为72%。3组间MIBO评分差异无统计学意义(P = .345)。大多数研究(62项研究;71%)的MIBO评分为80%。得分特别低的MIBO项目包括报告全血特征(20%)、血小板回收率(22%)、PRP分析(30%)和PRP激活(47%)。3个MIBO组除报告接受者详细情况外,其他项目得分均无显著差异(P = 0.012)。结论:本研究强调了在遵守MIBO指南方面的不足,特别是在报告全血特征、血小板回收率、PRP分析和PRP激活等关键变量方面。这些发现表明,MIBO指南的发布并没有导致调查关节内PRP治疗膝关节骨关节炎的研究报告实践的改进。
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