Abstract

IntroductionIn developed countries, breastfeeding is not recommended for women living with human immunodeficiency virus (WLWH). However, lactation symptoms can be distressing for women who choose not to breastfeed. There is currently no universal guideline on the most appropriate options for prevention or reduction of lactation symptoms amongst WLWH. This review describes the evidence base for using cabergoline, a dopaminergic agonist, for the post‐partum inhibition of lactation for WLWH.MethodsA scoping review of post‐partum pharmaceutical lactation inhibition specific for WLWH was conducted using searches in PubMed, Medline Ovid, EBM Reviews Ovid, Embase, Web of Science and Scopus until 2019. A narrative review of cabergoline pharmacologic properties, therapeutic efficacy, tolerability data and drug interaction data relevant to lactation inhibition was then conducted.Results and discussionAmong 1366 articles, the scoping review identified 13 relevant publications. Eight guidelines providing guidance regarding lactation inhibition for WLWH and two surveys of medical practice on this topic in UK have been published. Three studies have evaluated the use of pharmaceutical agents in WLWH. Two of these studies evaluated cabergoline and reported it to be an effective method of lactation inhibition in this population. The third study evaluated ethinyl estradiol and bromocriptine use and showed poor efficacy. Cabergoline is a long‐acting dopamine D2 agonist and ergot derivative that inhibits prolactin secretion and suppresses physiologic lactation when given as a single oral dose of 1 mg after delivery. Cabergoline is at least as effective as bromocriptine for lactation inhibition with success rates between 78% and 100%. Transient, mild to moderate adverse events to cabergoline are described in clinical trials. Few drug interactions exist as cabergoline is neither a substrate nor an inducer/inhibitor of hepatic cytochrome P450 isoenzymes. There are no reported clinically significant drug–drug interactions between cabergoline and any antiretroviral medications including protease inhibitors.ConclusionsCabergoline is a safe and effective pharmacologic option for the prevention of physiological lactation and associated physical symptoms in non‐breastfeeding women. Future studies should focus on its safety, efficacy and acceptability among WLWH.

Highlights

  • In developed countries, breastfeeding is not recommended for women living with human immunodeficiency virus (WLWH)

  • In high-income countries, including Canada, the United States (US) and the United Kingdom (UK) where safe alternatives to breast milk are available, exclusive formula feeding is recommended for all infants who are born to women living

  • We have identified eight guidelines or reviews which provide some guidance regarding how to support breastfeeding avoidance in WLWH

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Summary

Introduction

In developed countries, breastfeeding is not recommended for women living with human immunodeficiency virus (WLWH). This review describes the evidence base for using cabergoline, a dopaminergic agonist, for the post-partum inhibition of lactation for WLWH. A narrative review of cabergoline pharmacologic properties, therapeutic efficacy, tolerability data and drug interaction data relevant to lactation inhibition was conducted. Three studies have evaluated the use of pharmaceutical agents in WLWH Two of these studies evaluated cabergoline and reported it to be an effective method of lactation inhibition in this population. Conclusions: Cabergoline is a safe and effective pharmacologic option for the prevention of physiological lactation and associated physical symptoms in non-breastfeeding women. Because maternal cART is likely to reduce only cell-free, and not cell-associated virus, a risk of transmission may still exist [5] and HIV transmission has been reported despite undetectable viral load in maternal plasma and breast milk [6,7]. For women who choose not to breastfeed, the recommendations about lactation inhibition for WLWH are scarce

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