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RESEARCH ARTICLE

HIV in pregnant women and prevention of perinatal transmission

Michelle Giles
+ Author Affiliations
- Author Affiliations

Department of Infectious Diseases
Monash University and The Alfred Hospital
Level 2, Burnet Institute
85 Commercial Road
Prahran, Vic. 3004, Australia
Fax: +61 3 9076 2431
Email: m.giles@alfred.org.au

Microbiology Australia 36(4) 182-184 https://doi.org/10.1071/MA15064
Published: 19 October 2015

Women with HIV who have access to treatment can expect to have a normal life expectancy. With effective antiretroviral therapy, an undetectable viral load, and avoidance of breastfeeding, the rate of perinatal transmission is extremely low (<1%). A Caesarean section is no longer routinely recommended nor is intrapartum zidovudine. Women living with HIV should be supported in their decision regarding parenthood given their excellent prognosis, low risk of perinatal transmission and reproductive rights. If interventions to reduce perinatal HIV transmission during pregnancy and post-partum are embraced, women can expect to have an uninfected infant.


This article provides a succinct review of women, HIV and pregnancy and is focused on the resource rich setting. Differences exist in management and access to interventions in the resource-poor setting but this will not be discussed in this manuscript.

Women with HIV who have access to lifelong combination antiretroviral therapy can expect to have a normal life expectancy. This combined with extremely low rates of perinatal transmission has resulted in many women now contemplating plans for parenthood. In addition, the risk of HIV transmission to their partner through the process of conception can be significantly reduced by use of antiretroviral therapy (by the HIV infected woman) or by pre exposure prophylaxis (by the uninfected male partner) if they choose to conceive via condomless sex. Alternatively self-insemination can be utilised for conception if the HIV infected partner is the woman, posing no risk of HIV transmission to the uninfected partner, or assisted reproduction may be utilised if there are fertility issues. Once pregnant, the risk of perinatal transmission can be reduced to <1% if the woman takes combination antiretroviral therapy during the pregnancy and the neonate has four weeks of antiretroviral monotherapy, combined with avoidance of breastfeeding. A Caesarean section is no longer routinely recommended nor is intrapartum intravenous zidovudine.


Conception

The prognosis of adults living with HIV has continued to improve in the past two decades with the use of combination antiretroviral therapy. Mathematical modelling now suggests that for an adult newly diagnosed with HIV in a resource rich setting, with access to lifelong medication, life expectancy approaches that of HIV uninfected adults1. This combined with the extremely low rates of perinatal transmission reported2 many women living with HIV are contemplating their options for parenthood. One important step in this decision-making is the optimal and safest method of conception. Options for conception need to take into account the HIV status of the partner and fertility issues. Women who are infected with HIV have the option of condomless sex with their partner, self-insemination or assisted reproduction depending on availability and any existing fertility issues. The most important intervention to reduce transmission of HIV to the uninfected partner is treatment with antiretroviral therapy, either as treatment for prevention to the HIV infected partner3 or as pre exposure prophylaxis (PrEP) in the HIV-uninfected partner4,5. Data regarding the use of PrEP for conception are limited to observational studies6.


Management during pregnancy

The most important intervention to reduce perinatal HIV transmission is antiretroviral therapy for the mother7. It has been well established that combination therapy (rather than monotherapy) is the most effective method for reducing maternal viral load, the most important predictor of perinatal transmission8. Recent data suggest that the earlier treatment is started, the lower the transmission rate2 and if women enter pregnancy already on antiretrovirals then these should be continued2. Although safety data are still lacking on some of the newer antiretrovirals, the antiretroviral pregnancy registry provides reassuring data excluding teratogenicity for the majority of prescribed first line antiretrovirals9. Historically, elective Caesarean section was recommended as an intervention to reduce perinatal transmission, although the data to support this were primarily before the advent of combination therapy with more recent analyses suggesting the risk of perinatal HIV transmission is comparable in women with an undetectable viral load10,11. Today, vaginal birth is the recommended mode of delivery in women with an undetectable viral load (defined as either <50 copies/mL in guidelines from the United Kingdom to <1000 copies/mL in guidelines from the United States)12,13 unless there is an obstetric indication for a Caesarean section. Similarly, intrapartum zidovudine was previously prescribed routinely but is now reserved for women with a viral load at the time of delivery of >1000 copies/mL12,13. In addition to antiretrovirals for the mother, it is recommended that exposed neonates receive four weeks of monotherapy to further reduce the risk of HIV transmission.


Breastfeeding

When considering breastfeeding, the individual setting needs to be taken into account as guidelines regarding breastfeeding differ significantly between resource rich and resource poor settings. HIV has been found in breast milk and the only way to guarantee that HIV will not be transmitted after birth is for complete avoidance of breastfeeding. However when this is not possible or safe, recent studies have confirmed that with the use of antiretroviral therapy to either the mother or the infant for the duration of breastfeeding, rates of transmission can be reduced1416. This has re-ignited debate regarding the support of women especially in resource rich settings who desire to breast feed despite the availability of safe, affordable, culturally appropriate alternatives. In this setting, although the recommendation remains avoidance of breastfeeding, it is becomingly increasingly recognised that if a well informed woman elects to breastfeed, knowing the potential risk associated with this, that she should be supported in this decision making process to maximize the likelihood of adherence to antiretroviral therapy rather than it be seen as a child protection issue17.


Management of the neonate

It is essential that infants born to HIV infected mothers are appropriately followed up and tested after birth. The options for testing include a p24 antigen, HIV RNA, and/or an HIV proviral DNA. The choice of test depends on local availability. For diagnosis of HIV in the neonate, all these tests are suitable and appropriate. The most important issue is that the infant has follow up testing, rather than which test is available, given the equivalent performance of these tests in experienced hands. The recommended timing of testing also varies depending on the individual setting but commonly accepted protocols for follow up testing includes testing in the first week of life, at six weeks, and then three months provided no ongoing exposure via breastfeeding occurs.


Conclusion

Women living with HIV should be supported in their decision regarding parenthood given their excellent prognosis, low risk of perinatal transmission and reproductive rights. Importantly however, these women need to be well informed regarding the interventions available to reduce risk of HIV transmission to their partners (if they are HIV negative) and to their infant. If these are embraced women can have normal vaginal births and expect to have an uninfected infant.



References

[1]  Samji, H. et al. (2013) Closing the gap: increases in life expectancy among treated HIV-positive individuals in the United States and Canada. PLoS One 8, e81355.
Closing the gap: increases in life expectancy among treated HIV-positive individuals in the United States and Canada.Crossref | GoogleScholarGoogle Scholar | 24367482PubMed |

[2]  Mandelbrot, L. et al. (2015) No perinatal transmission of HIV-1 from women with effective antiretroviral therapy starting before conception. Clin. Infect. Dis. , civ578.
No perinatal transmission of HIV-1 from women with effective antiretroviral therapy starting before conception.Crossref | GoogleScholarGoogle Scholar | 26197844PubMed |

[3]  Cohen, M.S. et al. (2011) Prevention of HIV-1 infection with early antiretroviral therapy. N. Engl. J. Med. 365, 493–505.
Prevention of HIV-1 infection with early antiretroviral therapy.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhtVars7jF&md5=6140aaa04d514bf049cf3a65e46d8270CAS | 21767103PubMed |

[4]  Baeten, J.M. et al. (2012) Antiretroviral prophylaxis for HIV-1 prevention among heterosexual men and women. N. Engl. J. Med. 367, 399–410.
Antiretroviral prophylaxis for HIV-1 prevention among heterosexual men and women.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhtlSltrbK&md5=1b1ba52eeedbfc675f8e62e0bee64e36CAS | 22784037PubMed |

[5]  Thigpen, M.C. et al. (2012) Antiretroviral preexposure prophylaxis for heterosexual HIV transmission in Botswana N. Engl. J. Med. 367, 423–434.
Antiretroviral preexposure prophylaxis for heterosexual HIV transmission in BotswanaCrossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhtlSltrbE&md5=63b29a69462ae3d70df595d4c378d6beCAS | 22784038PubMed |

[6]  Vernazza, P.L. et al. (2011) Pre-exposure prophylaxis and timed intercourse for HIV-serodiscordant couples willing to conceive a child AIDS 25, 2005–2008.
Pre-exposure prophylaxis and timed intercourse for HIV-serodiscordant couples willing to conceive a childCrossref | GoogleScholarGoogle Scholar | 21716070PubMed |

[7]  Siegfried, N. et al. (2011) Antiretrovirals for reducing the risk of mother-to-child transmission of HIV infection. Cochrane Database Syst. Rev. , CD003510.
Antiretrovirals for reducing the risk of mother-to-child transmission of HIV infection.Crossref | GoogleScholarGoogle Scholar | 21735394PubMed |

[8]  Cooper, E.R. et al. (2002) Combination antiretroviral strategies for the treatment of pregnant HIV-1-infected women and prevention of perinatal HIV-1 transmission. J. Acquir. Immune Defic. Syndr. 29, 484–494.
Combination antiretroviral strategies for the treatment of pregnant HIV-1-infected women and prevention of perinatal HIV-1 transmission.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XjvFSrt7s%3D&md5=0d3c6227e49cc9b93333e5608b986df7CAS | 11981365PubMed |

[9]  Antiretroviral Pregnancy Registry Steering Committee (2015) Antiretroviral Pregnancy Registry International Interim Report for 1 January 1989 through 31 January 2015. Willington, NC: Registry Coordinating Centre. www.APRegistry.com

[10]  Briand, N. et al. (2013) Cesarean section for HIV-infected women in the combination antiretroviral therapies era, 2000–2010. Am. J. Obstet. Gynecol. 209, 335.e1–335.e12.
Cesarean section for HIV-infected women in the combination antiretroviral therapies era, 2000–2010.Crossref | GoogleScholarGoogle Scholar |

[11]  Read, J.S. and Newell, M.K. (2005) Efficacy and safety of cesarean delivery for prevention of mother-to-child transmission of HIV-1 Cochrane Database Syst. Rev. , CD005479.
| 1:STN:280:DC%2BD28%2FhtFaktg%3D%3D&md5=1748ab55369125f72d33a41a409d974eCAS | 16235405PubMed |

[12]  British HIV Association (2014) British HIV Association guidelines for the management of HIV infection in pregnant women 2012 (2014 interim review). HIV Med. 15, 1–77.
| 25604045PubMed |

[13]  Panel on Treatment of HIV-Infected Pregnant Women and Prevention of Perinatal Transmission (2015) Recommendations for use of antiretroviral drugs in pregnant HIV-1-infected women for maternal health and interventions to reduce perinatal HIV transmission in the United States. http://aidsinfo.nih.gov/contentfiles/lvguidelines/PerinatalGL.pdf

[14]  White, A.B. et al. (2014) Antiretroviral interventions for preventing breast milk transmission of HIV. Cochrane Database Syst. Rev. , CD011323.
Antiretroviral interventions for preventing breast milk transmission of HIV.Crossref | GoogleScholarGoogle Scholar | 25280769PubMed |

[15]  Jamieson, D.J. et al. (2012) Maternal and infant antiretroviral regimens to prevent postnatal HIV-1 transmission: 48-week follow-up of the BAN randomised controlled trial. Lancet 379, 2449–2458.
Maternal and infant antiretroviral regimens to prevent postnatal HIV-1 transmission: 48-week follow-up of the BAN randomised controlled trial.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xmt1Gkurw%3D&md5=846ca8400482a71799c24182274d33daCAS | 22541418PubMed |

[16]  The Kesho Bora Study Group de Vincenzi, I. (2011) Triple antiretroviral compared with zidovudine and single-dose nevirapine prophylaxis during pregnancy and breastfeeding for prevention of mother-to-child transmission of HIV-1 (Kesho Bora study): a randomised controlled trial. Lancet Infect. Dis. 11, 171–180.
Triple antiretroviral compared with zidovudine and single-dose nevirapine prophylaxis during pregnancy and breastfeeding for prevention of mother-to-child transmission of HIV-1 (Kesho Bora study): a randomised controlled trial.Crossref | GoogleScholarGoogle Scholar | 21237718PubMed |

[17]  British HIV Association (BHIVA) and Children’s HIV Association (CHIVA) (2010) Position Statement on Infant Feeding in the UK. November.


Biography

Dr Giles is an Associate Professor in the Department of Obstetrics and Gynaecology and Department of Infectious Diseases at Monash University. She completed her PhD on the topic of ‘HIV, Women and Reproduction in Australia’ and works clinically as an infectious diseases specialist with an interest in infections in pregnancy. She is Director of the Infections in Pregnancy service and Deputy Director of HIV services at Monash Health.