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制定HIV耐药性流行情况研究报告指南:一项混合方法研究方案

Developing Reporting Guidelines for Studies of HIV Drug Resistance Prevalence: Protocol for a Mixed Methods Study.

作者信息

Garcia Cristian, Rehman Nadia, Lawson Daeria O, Djiadeu Pascal, Mbuagbaw Lawrence

机构信息

Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.

Department of Anesthesia, McMaster University, Hamilton, ON, Canada.

出版信息

JMIR Res Protoc. 2022 May 13;11(5):e35969. doi: 10.2196/35969.

Abstract

BACKGROUND

HIV drug resistance is a global health problem that limits the effectiveness of antiretroviral therapy. Adequate surveillance of HIV drug resistance is challenged by heterogenous and inadequate data reporting, which compromises the accuracy, interpretation, and usability of prevalence estimates. Previous research has found that the quality of reporting in studies of HIV drug resistance prevalence is low, and thus better guidance is needed to ensure complete and uniform reporting.

OBJECTIVE

This paper contributes to the process of developing reporting guidelines for prevalence studies of HIV drug resistance by reporting the methodology used in creating a reporting item checklist and generating key insights on items that are important to report.

METHODS

We will conduct a sequential explanatory mixed methods study among authors and users of studies of HIV drug resistance. The two-phase design will include a cross-sectional electronic survey (quantitative phase) followed by a focus group discussion (qualitative phase). Survey participants will rate the essentiality of various reporting items. This data will be analyzed using content validity ratios to determine the items that will be retained for focus group discussions. Participants in these discussions will revise the items and any additionally suggested items and settle on a complete reporting item checklist. We will also conduct a thematic analysis of the group discussions to identify emergent themes regarding the agreement process.

RESULTS

As of November 2021, data collection for both phases of the study is complete. In July 2021, 51 participants had provided informed consent and completed the electronic survey. In October 2021, focus group discussions were held. Nine participants in total participated in two virtual focus group discussions. As of May 2022, data are being analyzed.

CONCLUSIONS

This study supports the development of a reporting checklist for studies of HIV drug resistance by achieving agreement among experts on what items should be reported in these studies. The results of this work will be refined and elaborated on by a writing committee of HIV drug resistance experts and external reviewers to develop finalized reporting guidelines.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/35969.

摘要

背景

艾滋病毒耐药性是一个全球性的健康问题,它限制了抗逆转录病毒疗法的有效性。艾滋病毒耐药性的充分监测面临着数据报告异质性和不充分的挑战,这损害了流行率估计的准确性、解释性和可用性。先前的研究发现,艾滋病毒耐药性流行率研究中的报告质量较低,因此需要更好的指导以确保完整和统一的报告。

目的

本文通过报告创建报告项目清单所使用的方法,并就重要的报告项目产生关键见解,为制定艾滋病毒耐药性流行率研究的报告指南做出贡献。

方法

我们将在艾滋病毒耐药性研究的作者和使用者中开展一项顺序解释性混合方法研究。两阶段设计将包括一项横断面电子调查(定量阶段),随后进行焦点小组讨论(定性阶段)。调查参与者将对各种报告项目的必要性进行评分。将使用内容效度比分析这些数据,以确定将保留用于焦点小组讨论的项目。这些讨论的参与者将修订这些项目以及任何其他建议的项目,并确定一份完整的报告项目清单。我们还将对小组讨论进行主题分析,以确定有关达成共识过程的新出现主题。

结果

截至2021年11月,该研究两个阶段的数据收集工作均已完成。2021年7月,51名参与者提供了知情同意并完成了电子调查。2021年10月,举行了焦点小组讨论。共有9名参与者参加了两次虚拟焦点小组讨论。截至2022年5月,数据正在分析中。

结论

本研究通过使专家们就这些研究中应报告的项目达成共识,支持制定艾滋病毒耐药性研究的报告清单。艾滋病毒耐药性专家写作委员会和外部评审人员将对这项工作的结果进行完善和阐述,以制定最终的报告指南。

国际注册报告识别号(IRRID):DERR1-10.2196/35969。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abdb/9143765/cae510374ed2/resprot_v11i5e35969_fig1.jpg

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