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多替拉韦和依非韦伦方案对有生育潜力的南非 HIV 感染妇女的风险与获益:一项建模研究。

Risks and Benefits of Dolutegravir- and Efavirenz-Based Strategies for South African Women With HIV of Child-Bearing Potential: A Modeling Study.

机构信息

Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts (C.M.D., A.L.C., K.A.F.).

University of Cape Town, Cape Town, South Africa (L.B., L.M., R.W.).

出版信息

Ann Intern Med. 2019 May 7;170(9):614-625. doi: 10.7326/M18-3358. Epub 2019 Apr 2.

Abstract

BACKGROUND

Dolutegravir is superior to efavirenz for HIV antiretroviral therapy (ART) but may be associated with an increased risk for neural tube defects (NTDs) in newborns if used by women at conception.

OBJECTIVE

To project clinical outcomes of ART policies for women of child-bearing potential in South Africa.

DESIGN

Model of 3 strategies: efavirenz for all women of child-bearing potential (EFV), dolutegravir for all women of child-bearing potential (DTG), or World Health Organization (WHO)-recommended efavirenz without contraception or dolutegravir with contraception (WHO approach).

DATA SOURCES

Published data on NTD risks (efavirenz, 0.05%; dolutegravir, 0.67% [Tsepamo study]), 48-week ART efficacy with initiation (efavirenz, 60% to 91%; dolutegravir, 96%), and age-stratified fertility rates (2 to 139 per 1000 women).

TARGET POPULATION

3.1 million South African women with HIV (aged 15 to 49 years) starting or continuing first-line ART, and their children.

TIME HORIZON

5 years.

PERSPECTIVE

Societal.

INTERVENTION

EFV, DTG, and WHO approach.

OUTCOME MEASURES

Deaths among women and children, sexual and pediatric HIV transmissions, and NTDs.

RESULTS OF BASE-CASE ANALYSIS: Compared with EFV, DTG averted 13 700 women's deaths (0.44% decrease) and 57 700 sexual HIV transmissions, but increased total pediatric deaths by 4400 because of more NTDs. The WHO approach offered some benefits compared with EFV, averting 4900 women's deaths and 20 500 sexual transmissions while adding 300 pediatric deaths. Overall, combined deaths among women and children were lowest with DTG (358 000 deaths) compared with the WHO approach (362 800 deaths) or EFV (367 300 deaths).

RESULTS OF SENSITIVITY ANALYSIS

Women's deaths averted with DTG exceeded pediatric deaths added with EFV unless dolutegravir-associated NTD risk was 1.5% or greater.

LIMITATION

Uncertainty in NTD risks and dolutegravir efficacy in resource-limited settings, each examined in sensitivity analyses.

CONCLUSION

Although NTD risks may be higher with dolutegravir than efavirenz, dolutegravir will lead to many fewer deaths among women, as well as fewer overall HIV transmissions. These results argue against a uniform policy of avoiding dolutegravir in women of child-bearing potential.

PRIMARY FUNDING SOURCE

National Institutes of Health, National Institute of Allergy and Infectious Diseases and Eunice Kennedy Shriver National Institute of Child Health and Human Development; Massachusetts General Hospital; and Harvard University Center for AIDS Research.

摘要

背景

与依非韦伦相比,多替拉韦在治疗艾滋病毒方面具有优势(ART),但如果女性在受孕时使用,可能会增加新生儿神经管缺陷(NTD)的风险。

目的

预测南非有生育能力的妇女接受抗逆转录病毒治疗(ART)的临床结果。

设计

三种策略模型:所有有生育能力的妇女使用依非韦伦(EFV)、所有有生育能力的妇女使用多替拉韦(DTG)或世界卫生组织(WHO)推荐的无避孕措施的依非韦伦或有避孕措施的多替拉韦(WHO 方法)。

数据来源

已发表的神经管缺陷风险数据(依非韦伦,0.05%;多替拉韦,0.67%[Tsepamo 研究])、开始或继续一线 ART 时的 48 周 ART 疗效(依非韦伦,60%至 91%;多替拉韦,96%)和年龄分层生育率(每 1000 名妇女中有 2 至 139 名)。

目标人群

310 万感染艾滋病毒的南非妇女(年龄在 15 至 49 岁之间)开始或继续一线 ART 治疗及其子女。

时间范围

5 年。

观点

社会。

干预措施

EFV、DTG 和 WHO 方法。

结果测量

妇女和儿童死亡、性传播和儿科 HIV 传播以及 NTD。

基础分析结果

与 EFV 相比,DTG 避免了 13700 名妇女死亡(减少 0.44%)和 57700 次性传播 HIV,但由于更多的 NTD,儿科总死亡人数增加了 4400 人。与 EFV 相比,WHO 方法提供了一些好处,避免了 4900 名妇女死亡和 20500 次性传播,同时增加了 300 名儿科死亡。总体而言,与 WHO 方法(362800 人死亡)或 EFV(367300 人死亡)相比,DTG 使妇女和儿童的综合死亡人数最低(358000 人死亡)。

敏感性分析结果

除非多替拉韦相关 NTD 风险为 1.5%或更高,否则 DTG 避免的妇女死亡人数超过 EFV 增加的儿科死亡人数。

局限性

在敏感性分析中分别检查了 NTD 风险和多替拉韦在资源有限环境中的疗效的不确定性。

结论

尽管多替拉韦引起的 NTD 风险可能高于依非韦伦,但多替拉韦将导致妇女死亡人数以及总体 HIV 传播人数减少。这些结果反对在有生育能力的妇女中普遍避免使用多替拉韦的政策。

主要资金来源

美国国立卫生研究院、国家过敏和传染病研究所和 Eunice Kennedy Shriver 国立儿童健康与人类发展研究所;马萨诸塞州综合医院;哈佛大学生殖中心艾滋病研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d47/6736740/3a7fb0cc6e8a/nihms-1014331-f0001.jpg

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