下肢受损儿童的患者和代理报告结果的质量:采用基于共识的健康测量工具选择标准方法进行系统性审查

T. Saris, J. R. Kalle, I. Sierevelt, Denise Eygendaal, C. V. van Bergen
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引用次数: 0

摘要

患者报告的结果测量已成为对患者进行临床评估的关键。在年轻人群中适当选择测量工具对于提供以患者为中心的循证医疗服务至关重要。本系统性综述采用基于共识的健康测量工具选择标准方法,对针对下肢受损的儿科骨科患者的患者报告结果测量方法进行了严格的评估。我们对电子数据库进行了系统性检索,以确定对评估下肢受损儿童的患者报告结果测量方法的开发和/或验证进行报告的原始研究。数据提取、质量评估和偏倚风险评估均按照《基于共识的健康测量工具选择标准》指南和《系统综述和元分析首选报告项目》声明进行。共筛选出 6919 篇文章。共纳入 33 项研究,报告了 13 种不同的患者报告结果测量方法和 20 种翻译方法的测量特性。四项研究报告了内容效度和患者报告结果测量指标的开发。关于结构效度、内容效度或患者报告结果测量指标开发的研究,其方法学质量大多被评为 "可疑 "或 "很好"。有关测量特性的证据质量差异明显,大多数研究需要提高方法学质量,以证明其结果的合理性。本综述广泛概述了针对小儿骨科下肢损伤患者的所有可用患者报告结果测量方法。我们谨慎地建议使用四种患者报告结果测量方法。然而,有关内容有效性和患者报告结果测量方法开发的研究很少,这就突出了未来研究工作的一个领域,以提高我们对目前可用的患者报告结果测量方法的认识。诊断级别 1
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quality of patient- and proxy-reported outcomes for children with impairment of the lower extremity: A systematic review using the COnsensus-based Standards for selection of health Measurement INstruments methodology
Patient-reported outcome measures have become crucial in the clinical evaluation of patients. Appropriate selection, in a young population, of the instrument is vital to providing evidence-based patient-centered healthcare. This systematic review applies the COnsensus-based Standards for selection of health Measurement INstruments methodology to provide a critically appraised overview of patient-reported outcome measures targeted at pediatric orthopedic patients with lower limb impairment. A systematic search of electronic databases was performed to identify original studies reporting the development and/or validation of patient-reported outcome measures evaluating children with impairment of the lower extremity. Data extraction, quality assessment, and risk of bias evaluation were performed following the COnsensus-based Standards for selection of health Measurement INstruments guidelines and Preferred Reporting Items for Systematic reviews and Meta-Analyses statement. A total of 6919 articles were screened. Thirty-three studies were included, reporting evidence on the measurement properties of 13 different patient-reported outcome measures and 20 translations. Four studies reported on content validity and patient-reported outcome measure development. The methodological quality of studies on structural validity, content validity, or patient-reported outcome measure development was mostly rated as “doubtful” or “very good.” The quality of evidence on measurement properties varied noticeably, with most studies needing to perform improve their methodological quality to justify their results. This review provides an extensive overview of all available patient-reported outcome measures for patients with lower extremity impairment within pediatric orthopedics. We cautiously advise the use of four patient-reported outcome measures. However, the scarce availability of research on content validity and patient-reported outcome measure development highlights an area for future research endeavors to improve our knowledge on the currently available patient-reported outcome measures. Diagnostic level 1
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