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临床艾滋病毒护理中的患者报告结局:丹麦单中心多阶段混合方法研究方案。

Patient-reported outcomes in clinical HIV care: protocol for a single-centre, multistage, mixed-methods study in Denmark.

机构信息

Department of Infectious Diseases, Hvidovre Hospital, Copenhagen University Hospital, Hvidovre, Denmark

Department of Infectious Diseases, Hvidovre Hospital, Copenhagen University Hospital, Hvidovre, Denmark.

出版信息

BMJ Open. 2023 Sep 13;13(9):e077303. doi: 10.1136/bmjopen-2023-077303.

Abstract

INTRODUCTION

People with HIV-1 (PWH) have worse health-related quality of life (HRQoL) compared with the general population. Using patient-reported outcomes (PROs) may help reorient the focus of HIV care towards improving HRQoL. This study aims to develop, implement and evaluate the use of PROs in HIV care.

METHODS AND ANALYSIS

This is a Danish single-centre, multistage mixed-methods study consisting of four substudies (studies I-IV). Study I is a qualitative focus group interview study aiming to identify relevant PRO domains, and barriers and benefits to PRO use. Participants are 5-10 PWH and 5-10 HIV healthcare providers (HCPs). Data are thematically analysed. Results will guide the design of a PRO measure (PROM). Study II is a quantitative study aiming to assess PWH's willingness and ability to engage with PRO. All PWH are consecutively invited to complete the PROMs before their next consultations. Demographic data are collected at enrolment. Differences between PWH who do/do not complete the PROMs are assessed. Study III is a quantitative before-and-after study aiming to assess the impact of PRO use on HCP awareness. Participants are all who complete the PROMs in Study II. In contrast to study II, HCPs are notified of the PROM results. The number of problems documented by the HCP in patients' medical records during studies II and III are compared using χ tests. Multiple regression models are used to identify factors associated with HCP awareness. Study IV is a qualitative study aiming to explore PWH and HCP experiences of using PROs. Participants are 15-20 PWH and 10-15 HCP. Data are collected from participant observation of PRO consultations and individual interviews. Data are analysed thematically.

ETHICS AND DISSEMINATION

This study is approved by the Danish Data Protection Agency. Participants will provide written consent prior to participation. Results will be published in peer-reviewed journals.

摘要

简介

与一般人群相比,HIV-1(HIV)感染者的健康相关生活质量(HRQoL)更差。使用患者报告的结局(PROs)可能有助于将 HIV 护理的重点重新调整为改善 HRQoL。本研究旨在开发、实施和评估 PRO 在 HIV 护理中的应用。

方法和分析

这是一项丹麦单中心、多阶段混合方法研究,包括四项子研究(研究 I-IV)。研究 I 是一项定性焦点小组访谈研究,旨在确定相关的 PRO 领域,以及 PRO 使用的障碍和益处。参与者是 5-10 名 HIV 感染者和 5-10 名 HIV 医护人员(HCPs)。数据进行主题分析。结果将指导 PRO 测量工具(PROM)的设计。研究 II 是一项定量研究,旨在评估 HIV 感染者参与 PRO 的意愿和能力。所有 HIV 感染者在下一次就诊前都会被邀请连续填写 PROM。在登记时收集人口统计学数据。评估完成和未完成 PROM 的 HIV 感染者之间的差异。研究 III 是一项前后对照研究,旨在评估 PRO 使用对 HCP 意识的影响。参与者是在研究 II 中完成 PROM 的所有人。与研究 II 不同的是,HCPs 会被告知 PROM 的结果。使用 χ 检验比较研究 II 和 III 期间 HCP 在患者病历中记录的问题数量。使用多元回归模型确定与 HCP 意识相关的因素。研究 IV 是一项定性研究,旨在探讨 HIV 感染者和 HCP 使用 PRO 的经验。参与者是 15-20 名 HIV 感染者和 10-15 名 HCP。数据通过对 PRO 咨询的参与式观察和个人访谈收集。数据进行主题分析。

伦理和传播

本研究已获得丹麦数据保护局的批准。参与者将在参与前提供书面同意。研究结果将发表在同行评议的期刊上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d699/10503392/42abc573f66d/bmjopen-2023-077303f01.jpg

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