Suppr超能文献

脊柱融合手术中 FDA 调查器械豁免试验的脆弱指数和反向脆弱指数:一项系统评价。

The fragility index and reverse fragility index of FDA investigational device exemption trials in spinal fusion surgery: a systematic review.

机构信息

Tufts University School of Medicine, 145 Harrison Ave, Boston, MA, 02111, USA.

Department of Orthopedic Surgery, Tufts Medical Center, Tufts University School of Medicine, 800 Washington St, Tufts MC Box #306, Boston, MA, 02111, USA.

出版信息

Eur Spine J. 2024 Jul;33(7):2594-2603. doi: 10.1007/s00586-024-08317-3. Epub 2024 May 27.

Abstract

PURPOSE

FDA investigational device exemption (IDE) studies are considered a gold standard of assessing safety and efficacy of novel devices through RCTs. The fragility index (FI) has emerged as a means to assess robustness of statistically significant study results and inversely, the reverse fragility index (RFI) for non-significant differences. Previous authors have defined results as fragile if loss to follow up is greater than the FI or RFI. The aim of this study was to assess the FI, RFI, and robustness of data supplied by IDE studies in spinal surgery.

METHODS

This was a systematic review of the literature. Inclusion criteria included randomized controlled trials with dichotomous outcome measures conducted under IDE guidelines between 2000 and 2023. FI and RFI were calculated through successively changing events to non-events until the outcome changed to non-significance or significance, respectively. The fragility quotient (FQ) and reverse fragility quotient (RFQ) were calculated by dividing the FI and RFI, respectively, by the sample size.

RESULTS

Thirty-two studies met inclusion criteria with a total of 40 unique outcome measures; 240 outcomes were analyzed. Twenty-six studies reported 96 statistically significant results. The median FI was 6 (IQR: 3-9.25), and patients lost to follow up was greater than the FI in 99.0% (95/96) of results. The average FQ was 0.027. Thirty studies reported 144 statistically insignificant results and a median RFI of 6 (IQR: 4-8). The average RFQ extrapolated was 0.021, and loss to follow up was greater than the RFI in 98.6% (142/144) of results.

CONCLUSIONS

IDE studies in spine surgery are surprisingly fragile given their reputations, large sample sizes, and intent to establish safety in investigational devices. This study found a median FI and RFI of 6. The number of patients lost to follow-up was greater than FIand RFI in 98.8% (237/240) of reported outcomes. FQ and RFQ tell us that changes of two to three patients per hundred can flip the significance of reported outcomes. This is an important reminder of the limitations of RCTs. Analysis of fragility in future studies may help clarify the strength of the relationship between reported data and their conclusions.

摘要

目的

FDA 研究性设备豁免 (IDE) 研究被认为是通过 RCT 评估新型设备安全性和有效性的金标准。脆弱指数 (FI) 已成为评估统计学显著研究结果稳健性的一种手段,相反,反向脆弱指数 (RFI) 则用于评估非显著差异。之前的作者将失访率大于 FI 或 RFI 的结果定义为脆弱。本研究旨在评估脊柱外科 IDE 研究提供的数据的 FI、RFI 和稳健性。

方法

这是一项文献系统评价。纳入标准包括 2000 年至 2023 年间根据 IDE 指南进行的、具有二分类结局测量的随机对照试验。通过连续将事件更改为非事件,直到结局变为非显著或显著,分别计算 FI 和 RFI。脆弱性商数 (FQ) 和反向脆弱性商数 (RFQ) 分别通过将 FI 和 RFI 除以样本量计算得出。

结果

32 项研究符合纳入标准,共有 40 个独特的结局指标;分析了 240 个结局。26 项研究报告了 96 个统计学显著的结果。FI 的中位数为 6(IQR:3-9.25),99.0%(96/96)的结果中失访率大于 FI。平均 FQ 为 0.027。30 项研究报告了 144 个统计学上不显著的结果,RFI 的中位数为 6(IQR:4-8)。平均 RFQ 推断为 0.021,98.6%(144/144)的结果中失访率大于 RFI。

结论

鉴于其声誉、大样本量和旨在确定研究设备安全性的意图,脊柱外科 IDE 研究令人惊讶地脆弱。本研究发现 FI 和 RFI 的中位数分别为 6。在报告的结局中,失访率大于 FI 和 RFI 的比例为 98.8%(237/240)。FQ 和 RFQ 告诉我们,每 100 名患者中增加 2 到 3 名患者就可以改变报告结果的显著性。这提醒我们 RCT 存在局限性。未来研究中对脆弱性的分析可能有助于阐明报告数据与其结论之间的关系强度。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验