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卫生技术评估中纳入的定性证据的范围和质量:对 NICE 和 CADTH 提交材料的审查。

The extent and quality of qualitative evidence included in health technology assessments: a review of submissions to NICE and CADTH.

机构信息

Health Economics and Health Technology Assessment (HEHTA), School of Health and Wellbeing, University of Glasgow, Glasgow, UK.

出版信息

Int J Technol Assess Health Care. 2023 Dec 21;40(1):e6. doi: 10.1017/S0266462323002829.

Abstract

OBJECTIVES

Qualitative methods allow in-depth exploration of patient experiences and can provide context for healthcare decision making. Frameworks for patient-based evidence in health technology assessment (HTA) are expanding; yet, how extensively qualitative methods are currently used is unclear. This review characterized the extent and quality of qualitative data submitted to National Institute for Health and Care Excellence (NICE) and Canadian Agency for Drugs and Technologies in Health (CADTH) for HTA.

METHODS

NICE and CADTH submissions from September 2019 to August 2021 were reviewed. Submission characteristics and features of patient-based evidence included within submissions were extracted. The quality of qualitative reporting was assessed using the CASP checklist.

RESULTS

Patient-based evidence was included in 83/107 NICE and 119/124 CADTH submissions. A small proportion described qualitative data collection (NICE=14; CADTH=24) and analysis (NICE=6; CADTH=9) methods. One-to-one interviews were the most common data collection method, and thematic analysis was exclusively used. Thirty-three percent of NICE submissions scored >7 yes responses on CASP, versus 78 percent of CADTH submissions.

CONCLUSIONS

Although patient-based evidence was common in the submissions reviewed, only 14/107 NICE and 24/124 CADTH submissions involved formal qualitative data collection. Use of formal analysis methods was even rarer and reporting tended to be brief. At present, there is little guidance about qualitative evidence most likely to be informative and therefore to potentially impact decision making. Ensuring, however, that qualitative data are collected and analyzed in a systematic, rigorous way will maximize their usefulness and ensure that patient voices are clearly heard.

摘要

目的

定性方法可以深入探索患者的体验,并为医疗保健决策提供背景。健康技术评估(HTA)中基于患者的证据框架正在扩大;然而,目前定性方法的使用程度尚不清楚。本研究描述了英国国家卫生与保健优化研究所(NICE)和加拿大药物和技术评估机构(CADTH)提交给 NICE 和 CADTH 的 HTA 中定性数据的范围和质量。

方法

审查了 NICE 和 CADTH 从 2019 年 9 月至 2021 年 8 月的提交材料。提取了提交材料的特征以及提交材料中包含的基于患者的证据特征。使用 CASP 清单评估定性报告的质量。

结果

83/107 份 NICE 和 119/124 份 CADTH 提交材料中包含基于患者的证据。只有一小部分描述了定性数据收集(NICE=14;CADTH=24)和分析(NICE=6;CADTH=9)方法。一对一访谈是最常用的数据收集方法,并且专门使用了主题分析。33%的 NICE 提交材料在 CASP 上获得了>7 个“是”的回答,而 78%的 CADTH 提交材料获得了>7 个“是”的回答。

结论

尽管在审查的提交材料中,基于患者的证据很常见,但只有 14/107 份 NICE 和 24/124 份 CADTH 提交材料涉及正式的定性数据收集。更罕见的是使用正式的分析方法,而且报告往往很简短。目前,关于最有可能提供信息并因此可能影响决策的定性证据几乎没有指导。然而,确保以系统和严格的方式收集和分析定性数据将最大限度地提高其有用性,并确保患者的声音得到清晰表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61da/11570126/3247f9cc3c6d/S0266462323002829_fig1.jpg

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