Heather Melanie R. Ames, Christine Hillestad Hestevik, Patricia Sofia Jacobsen Jardim, Martin Smådal Larsen, Lars Jørun Langøien, Hans Bugge Bergsund, Tiril Cecilie Borge
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引用次数: 0

摘要

使用机器学习功能,如研究设计分类器,自动识别不符合纳入标准的研究,是加快系统审查筛选过程的一种方法。由于定性研究设计分类器尚未开发,因此在筛选过程中,反向使用Cochrane随机对照试验(RCT)分类器是一种可能的方法,可以加快对初级定性研究的识别。本研究的目的是评估Cochrane RCT分类器是否可以用于加速定性证据合成(QES)的研究选择过程。方法我们在首次确定QES的地方进行回顾性评估。然后,我们提取每个QES中纳入的主要定性研究的书目信息,并将参考文献上传到我们的数据管理工具EPPI-Reviewer中。然后,我们对每个QES的每组纳入的研究运行Cochrane RCT分类器。结果共纳入82个QES, 2828个独特的初步研究。56%的初步研究被归类为不太可能是随机对照试验,40%的研究被归类为0-9%可能是随机对照试验。4%被归类为10%或更有可能是随机对照试验。其中,只有1.7%被归类为50%或更有可能成为随机对照试验。结论Cochrane RCT分类器可以作为一种有用的工具来识别具有定性研究设计的初步研究,从而加快QES中的研究选择。然而,作为临床试验的一部分进行的混合方法研究或定性研究可能会被遗漏。需要使用Cochrane RCT分类器对从完整文献检索中检索到的所有参考文献进行进一步评估,以调查节省的时间和资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Can using the Cochrane RCT classifier in EPPI-Reviewer help speed up study selection in qualitative evidence syntheses? A retrospective evaluation

Can using the Cochrane RCT classifier in EPPI-Reviewer help speed up study selection in qualitative evidence syntheses? A retrospective evaluation

Introduction

Using machine learning functions, such as study design classifiers, to automatically identify studies that do not meet the inclusion criteria, is one way to speed up the systematic review screening process. As a qualitative study design classifier is yet to be developed, using the Cochrane randomized controlled trial (RCT) classifier in reverse is one possible way to speed up the identification of primary qualitative studies during screening. The objective of this study was to evaluate whether the Cochrane RCT classifier can be used to speed up the study selection process for qualitative evidence synthesis (QES).

Methods

We performed a retrospective evaluation where we first identified QES. We then extracted the bibliographic information of the included primary qualitative studies in each QES, and uploaded the references into our data management tool, EPPI-Reviewer. We then ran the Cochrane RCT classifier on each group of included studies for each QES.

Results

Eighty-two QES with 2828 unique primary studies were included in the analysis. 56% of the primary studies were classified as unlikely to be an RCT and 40% as being 0–9% likely to be an RCT. 4% were classified as being 10% or more likely to be an RCT. Of these, only 1.7% were classified as being 50% or more likely to be an RCT.

Conclusions

The Cochrane RCT classifier could be a useful tool to identify primary studies with qualitative study designs to speed up study selection in a QES. However, it is possible that mixed methods studies or qualitative studies conducted as part of a clinical trial may be missed. Further evaluations using the Cochrane RCT classifier on all the references retrieved from the complete literature search is needed to investigate time- and resource savings.

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