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莫桑比克使用多替拉韦为基础的抗逆转录病毒方案的队列患者主动安全性监测方案。

Protocol for active safety monitoring of a cohort of patients using a dolutegravir-based antiretroviral regimen in Mozambique.

机构信息

Pharmacovigilance Unit, National Directorate of Pharmacy, Maputo, Mozambique.

National HIV/AIDS Division, MISAU, Maputo, Mozambique.

出版信息

BMJ Open. 2021 Sep 7;11(9):e050671. doi: 10.1136/bmjopen-2021-050671.

Abstract

INTRODUCTION

Dolutegravir-based antiretroviral therapy (ART) is increasingly being used as the preferred first-line regimen for the treatment of HIV in low-income and middle-income countries. The National Program for the Control of STI/HIV/AIDS in Mozambique has planned a phased introduction of the tenofovir/lamivudine/dolutegravir (TLD) regimen. In 2019, concerns about a potential safety signal identified with dolutegravir identified in the results of the Tsepamo study, conducted in Botswana, led the National Directorate of Pharmacy and the National Program for the Control of STI/HIV/AIDS to establish an active pharmacovigilance surveillance system among newly placed patients on a TLD regimen. This activity aims to establish an active pharmacovigilance system to monitor adverse events in patients on a TLD regimen to support the effectiveness of Mozambique's public health programmes in improving the process of care and treatment outcomes for people with HIV/AIDS.

METHODS AND ANALYSIS

This is a prospective, non-interventional, descriptive cohort study to monitor HIV patients managed with TLD at 10 sentinel health centres in Mozambique. The cohort consists of HIV-infected patients commencing treatment with TLD, either as treatment naïve patients or switched from other ART regimens. Patients have monthly routine follow-up visits for the first 3 months after starting HIV treatment with TLD, and subsequently every 3 months for a total period of 1 year. Patients are monitored to identify possible adverse events during the follow-up period. The intended size of the cohort is 3000 patients.

ETHICS AND DISSEMINATION

Ethical approval was obtained from the National Commission on Bioethics in Health in Mozambique. Written informed consent is obtained from each participant who agrees to participate to have their information collected, analysed and stored. Findings will be reported to the Ministry of Health and participating health centres to inform policy and practice as well as disseminated by peer-review publications.

摘要

引言

在低收入和中等收入国家,基于多替拉韦的抗逆转录病毒疗法(ART)正日益被用作治疗 HIV 的首选一线方案。莫桑比克性传播感染/艾滋病控制国家规划已计划分阶段引入替诺福韦/拉米夫定/多替拉韦(TLD)方案。2019 年,在博茨瓦纳开展的 Tsepamo 研究结果中发现多替拉韦存在潜在安全性信号,这引起了国家药剂管理局和性传播感染/艾滋病控制国家规划的关注,促使他们在开始使用 TLD 方案的新患者中建立了一个主动药物警戒监测系统。该活动旨在建立一个主动药物警戒系统,以监测 TLD 方案患者的不良事件,从而支持莫桑比克公共卫生计划改善艾滋病毒/艾滋病患者的护理和治疗结果的有效性。

方法和分析

这是一项在莫桑比克 10 个哨点卫生中心开展的、监测使用 TLD 方案治疗的 HIV 患者的前瞻性、非干预性、描述性队列研究。该队列包括开始接受 TLD 治疗的 HIV 感染患者,包括初治患者和从其他 ART 方案转换而来的患者。患者在开始 TLD 治疗后的前 3 个月每月进行常规随访,此后每 3 个月随访一次,总随访期为 1 年。在随访期间监测患者以识别可能发生的不良事件。该队列的预期规模为 3000 名患者。

伦理和传播

该研究已获得莫桑比克国家卫生生物伦理委员会的伦理批准。每位同意参与并同意收集、分析和存储其信息的参与者都将获得书面知情同意。研究结果将报告给卫生部和参与的卫生中心,以便为政策和实践提供信息,并通过同行评审出版物进行传播。

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