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The management of HIV infection during pregnancy is complex, and the scenario box on this page illustrates the complexities involved. In 2005, UNAIDS (the Joint United Nations Programme on HIV/AIDS) estimated that 38.6 million people had HIV, of whom 17.3 million were women (with most being in their reproductive years). At least 3.28 million pregnant women infected with HIV are estimated to give birth each year, with more than 75% of these in sub-Saharan Africa; this is where most of the annual 700000 new infections of HIV in children occur.
A 27 year old woman is referred to the antenatal clinic at 16 weeks of pregnancy. This is her second pregnancy—her first child, delivered by caesarean section, is now 8 years old. The mother was diagnosed with HIV four years ago when she developed herpes zoster. She has been taking zidovudine, lamivudine, and nevirapine for four weeks through an antiretroviral treatment access programme. At the time of starting treatment, her CD4 count was 124×106 cells/l, her viral load 50000 copies/ml, and her haemoglobin 104 g/l. She had received a negative screening result for tuberculosis and was receiving daily co-trimoxazole prophylaxis for preventing opportunistic infections. At the 16 week visit she was found to have a haemoglobin concentration of 87 g/l. She is from an African community and has not disclosed her HIV status to her family; she is concerned about the possible stigma associated with not breast feeding her infant.
Perinatal transmission of HIV can occur in utero, during labour and delivery, or postnatally through breastfeeding.1w1 Most transmission occurs during the intrapartum period.1 Transmission will vary from less than 2% in the developed world (with its access to antiretroviral therapy, caesarean section, and formula milk) to more than 30% in the developing world (where access to therapy is limited and breastfeeding is prolonged). w2 Observational studies have shown that the risk of perinatal transmission is affected by maternal stage of disease; duration of rupture of membranes; increased genital secretion of HIV associated with sexually transmitted infections such as herpes simplex virus; and other factors such as prematurity. Large randomised controlled studies have shown that mother to child transmission can be reduced by the use of antiretroviral therapy, elective caesarean section, and exclusive formula feeding.2
Pregnancy does not adversely affect HIV progression or survival.3w3-w7 Dual infection with HIV and malaria has been associated with increased risk of maternal, perinatal, and early infant death.w8 Improved access to care, treatment, and nutritional support in resource limited settings may help to reduce poor pregnancy outcomes. The decline in the CD4 cell count during pregnancy normally resolves in the postpartum period and is attributed to haemodilution.4 5w9-w11 Although HIV RNA levels seem to remain stable during pregnancy, some studies have shown an increase in viral load in the postpartum period.w11
In developed countries, with easy access to specialist care, HIV infection is a rare cause of maternal mortality. In contrast, HIV infection has become an important contributing cause of maternal mortality in Africa.6w12 In areas of high HIV prevalence, the infection has become a leading cause of maternal mortality. Several reports from southern African countries have shown this trend, including maternal mortality rates that are fivefold higher in HIV infected women than in uninfected women.6w12 In South Africa's confidential inquiry into maternal deaths for 2002-46 HIV/AIDS was reported to be the leading cause of death, responsible for 20.1% of all deaths, higher than any direct obstetric cause. This figure may underestimate the problem as HIV status was only known for about half of the maternal deaths.
Observational studies have shown that HIV infection is associated with varying rates of adverse pregnancy outcomes, such as increased spontaneous abortion, stillbirth, perinatal and infant mortality, intrauterine growth retardation, low birth weight, and chorioamnionitis.w13-w16 HIV infection may also reduce fertility, irrespective of stage of infection.w17 In Uganda HIV infected women have lower pregnancy rates and more pregnancy losses than uninfected women.w17 Some studies have found larger intervals between pregnancies and an association between high viral loads and difficulty in conceiving.w18
Antenatal care provides an opportunity to counsel pregnant women about HIV risk and offer HIV testing. The management of a pregnant woman with HIV infection will depend on the resources available and the individual needs of the woman; a multidisciplinary team of clinicians, psychologists, and social workers will optimise care. In women who know their HIV status, prepregnancy counselling may optimise medical care and minimise adverse outcomes.
In many resource poor areas, tuberculosis is a common opportunistic infection in pregnant women with HIV, so it should be excluded in these settings or in women who have recently arrived in a developed country from a developing one. Laboratory investigations, in addition to routine tests in pregnancy, should include liver function tests, complete blood count (including platelet count and lymphocyte subsets), plasma HIV RNA viral load, and screening for sexually transmitted infections. Where hepatitis screening is not one of the routine investigations, then hepatitis B testing should be offered to women from areas with a high prevalence of HIV infection, and hepatitis C screening should be considered if intravenous drug use is common.
Antiretroviral therapy can be used in pregnancy (according to a country's guidelines) when indicated as an ongoing treatment for maternal health; when not needed for this indication, it can be provided for preventing mother to child transmission. If antiretrovirals are indicated for maternal health, the choice of regimen should ensure that maternal side effects and risks to the infants are minimised. Dosage modification is not required for nucleoside reverse transcriptase inhibitors and nevirapine. Efavirenz should be avoided during early pregnancy because of teratogenic neural tube defects seen in both primates and humans.7 The combination of didanosine and stavudine should be avoided in pregnancy because of lactic acidosis. Nevirapine should be avoided in women with CD4 counts >250×106 cells/l.8 When antiretroviral therapy is used for preventing mother to child transmission, regimens range from the use of triple antiretroviral therapy to zidovudine started antenatally, with or without peripartum nevirapine (box 1). Post-exposure prophylaxis should be started at birth (box 2).
The British HIV Association recommends an elective caesarean section for women receiving zidovudine alone; those receiving combination therapy with detectable viraemia; and those with HIV and hepatitis C coinfection.9 Observational data have shown that caesarean section may be associated with a slightly higher risk of postoperative complications in women with HIV than in uninfected women and that frequent complications such as postpartum fever, endometritis, wound infection, and pneumonia occur significantly more often in infected women.w19-w21
Although the use of elective caesarean section has been a major factor in reducing the rates of mother to child transmission in well resourced settings, it may not be a feasible option in many less resourced areas of high HIV prevalence. In these areas, some cases might merit a lowered threshold for caesarean section; such cases would include any pregnancies where labour is expected to be prolonged or where other obstetric complications may be associated with increased transmission risk (such as abruptio placentae and preterm rupture of membranes). Depending on the available facilities, this may also apply to women who had had previous caesarean sections or breech presentations.
When caesarean section is not performed, care in labour should focus on minimising the risk of mother to child transmission. This risk is increased with increased duration of rupture of membranes. As artificial rupture of membranes has little obstetric benefit in normal labour, it should not be done routinely in women who are known to be HIV positive or in areas of high HIV prevalence. In the case of premature rupture of membranes, with or without labour, the risk of HIV transmission must be balanced against the risk of premature delivery.
Invasive fetal monitoring techniques such as penetrating or spiral scalp electrodes and fetal scalp blood sampling may create a portal of entry for the virus and ought to be avoided. Episiotomy may increase the exposure of the infant to HIV during delivery and increase the risk of transmission. Routine episiotomy is not recommended, and it should be reserved for those cases with a clear obstetric indication. Assisted delivery by forceps or vacuum extraction carries a theoretical possibility of increasing the risk of transmission through damage to the baby's skin. Little information exists on the contribution of obstetric procedures to the risk of transmission in the presence of antiretroviral therapy.
In most HIV positive women the postnatal course will be uncomplicated and no special medical care will be needed. Postpartum complications encountered more often in HIV positive women include puerperal sepsis, infected episiotomies, massive condylomata acuminata, urinary tract infections, pneumonia, fever, tuberculosis, and unusual infections.
Breast feeding is an important route of transmission. In the United Kingdom, where safe infant feeding alternatives are available, HIV infected women are advised to refrain from breast feeding. In resource poor settings where breast feeding is essential for infant survival, exclusive breast feeding for four to six months may be justified.
In non-breastfed infants, HIV infection can be diagnosed definitively at age 6-12 weeks using DNA polymerase chain reaction. In some settings, such testing is done at birth to exclude in utero transmission of HIV-1, and this test is repeated at age 6 weeks and 12 weeks to exclude transmission that may have occurred in the intrapartum and postpartum period. If the mother is breast feeding her infant, HIV testing can start one month after weaning, with a second test eight weeks later.10
Preventing HIV infection in children has become possible in the past decade. Interventions exist for minimising mother to child transmission of HIV, both in the developed and the developing world. If these are widely implemented in the next decade, they will result in a substantial decline in the number of children acquiring this devastating disease from their mothers.mothers.
This is one of a series of occasional articles about how to manage a pre-existing medical condition during pregnancy. If you would like to suggest a topic for this series please email Kirsten Patrick (firstname.lastname@example.org)
Contributors: GE Gray was responsible for the conception, development, and overall writing of the article; she is also the guarantor. JAMcI provided the case report, gave obstetrical input, and helped to edit the manuscript.
Competing interests: None declared.
Provenance and peer review: Commissioned; externally peer reviewed.