Hill Andrew, Clayden Polly, Thorne Claire, Christie Rachel, Zash Rebecca
Department of Translational Medicine, University of Liverpool, UK.
HIV i-Base, London, UK.
J Virus Erad. 2018 Apr 1;4(2):66-71. doi: 10.1016/S2055-6640(20)30247-8.
The integrase strand transfer inhibitor dolutegravir (DTG) is being introduced into low- and middle-income countries (LMICs) as an alternative to first-line treatment with non-nucleoside reverse transcriptase inhibitors. However, DTG is not yet widely recommended for use in pregnant women. The aim of this systematic review was to analyse all available data on birth outcomes and congenital anomalies in the infants of pregnant women treated with DTG.
A PubMed and Embase search was conducted using the terms "dolutegravir" or "DTG" and "pregnancy" or "pregnant" from the earliest available date on the database to 26 July 2017. Any reports involving women who were pregnant, HIV positive and taking DTG were included. The percentage of pregnant women with adverse birth outcomes or congenital anomalies in their infants after taking dolutegravir was compared with five historical control databases.
There were six databases included in the main analysis of birth outcomes and congenital anomalies, with a total of 1200 pregnant women. The percentage of pregnant women taking DTG with adverse birth outcomes and congenital abnormalities was similar to results from historical control studies of HIV-positive women. However, there was significant heterogeneity among the six databases - the percentage of infants with congenital anomalies ranged from 0.0% in Botswana (0/116 infants) to 13.3% in IMPAACT P1026S (2/15 infants).
Up to 15 million people could be on treatment with DTG in LMICs within the next 5 years, of whom a substantial percentage is likely to be women of child-bearing potential. In many countries with large HIV epidemics, unplanned pregnancies are common and access to antenatal clinic facilities may be limited. Continued pharmacovigilance is essential, but it is reassuring that no clear safety signals have been detected, to date, for pregnant women treated with DTG in terms of birth outcomes or congenital anomalies.
整合酶链转移抑制剂多替拉韦(DTG)正被引入低收入和中等收入国家(LMICs),作为非核苷类逆转录酶抑制剂一线治疗的替代方案。然而,DTG尚未被广泛推荐用于孕妇。本系统评价的目的是分析所有关于接受DTG治疗的孕妇所产婴儿的出生结局和先天性异常的可用数据。
在PubMed和Embase数据库中进行检索,检索词为“dolutegravir”或“DTG”以及“pregnancy”或“pregnant”,检索时间从数据库最早可用日期至2017年7月26日。纳入任何涉及怀孕、HIV阳性且服用DTG的女性的报告。将服用多替拉韦后出现不良出生结局或其婴儿出现先天性异常的孕妇百分比与五个历史对照数据库进行比较。
在出生结局和先天性异常的主要分析中纳入了六个数据库,共有1200名孕妇。服用DTG的孕妇出现不良出生结局和先天性异常的百分比与HIV阳性女性的历史对照研究结果相似。然而,六个数据库之间存在显著异质性——先天性异常婴儿的百分比从博茨瓦纳的0.0%(0/116名婴儿)到IMPAACT P1026S研究中的13.3%(2/15名婴儿)不等。
在未来5年内,低收入和中等收入国家多达1500万人可能接受DTG治疗,其中很大一部分可能是具有生育潜力的女性。在许多HIV疫情严重的国家,意外怀孕很常见,且获得产前诊所设施的机会可能有限。持续的药物警戒至关重要,但令人安心的是,迄今为止,就出生结局或先天性异常而言,尚未检测到接受DTG治疗的孕妇有明确的安全信号。