ICAAC: Nevirapine still present in breastmilk two weeks after last dose

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Nevirapine (Viramune) can persist in the breastmilk of HIV-positive women treated with the drug to prevent mother-to-child transmission of HIV for up to 14 days after the last dose of the drug is taken, according to a United States study presented to the 45th Interscience Conference on Antimicrobial Agents and Chemotherapy in Washington DC. The investigators, from Alabama and Los Angeles believe “the persistence of nevirapine in breastmilk may have clinical implications for the development of resistance in women and infants."

Mother-to-child transmission of HIV can occur during pregnancy, labour and via breast-feeding. The non-nucleoside reverse transcriptase analogue (NNRTI) nevirapine has been shown to be highly effective at preventing mother-to-child transmission of HIV when provided to the mother during labour and her infant shortly after. However, the use of nevirapine in this way can lead to the development of resistance to nevirapine and other drugs in the NNRTI class of antiretrovirals. In countries with ready access to anti-HIV therapy, nevirapine monotherapy to prevent vertical transmission of HIV is strongly cautioned against. Nevertheless, its use in resource-limited settings is widespread and recommended.

Nevirapine readily enters breastmilk at high concentrations. Investigators wished to see how long nevirapine persisted in breastmilk after its use was discontinued.

Glossary

concentration (of a drug)

The level of a drug in the blood or other body fluid or tissue.

mother-to-child transmission (MTCT)

Transmission of HIV from a mother to her unborn child in the womb or during birth, or to infants via breast milk. Also known as vertical transmission.

half-life

The amount of time it takes for a concentration in blood to be reduced by 50%. After one half-life, the concentration of a drug in the body amounts to half the starting dose of any drug to be eliminated from the body.

monotherapy

Taking a drug on its own, rather than in combination with other drugs.

nucleoside

A precursor to a building block of DNA or RNA. Nucleosides must be chemically changed into nucleotides before they can be used to make DNA or RNA. 

Samples of breastmilk were collected from the right and left breasts of an HIV-positive woman seven days after she took her last 200mg dose of nevirapine. Additional breastmilk samples were taken from the left breast for a further 15 days.

The investigators then analysed the breastmilk for the presence of nevirapine. They wished to determine the maximum concentration of the drug, the drug’s minimum concentration, the elimination half-life, the area under the curve and clearance of the drug.

Seven days after the last dose of nevirapine, the concentration of the drug was 1.56mg/l in the right breast and 1.49mg/l in the left breast. The last measurable concentration of nevirapine was 14 days after the last dose, and was 0.17mg/l.

The maximum concentrations of the drug were 2.67mg/l for the right breast and 2.78mg/l for the left. The elimination half-life was 40 hours for both the right and left breasts. The area under the curve was 152mgxh/l for the right breast and 153mgxh/l for the left.

Apparent clearance of the drug was similar for both breasts at approximately 2.4 litres per hour.

The extended analysis of the breast milk from the left breast showed that it had an area under the curve of 162mgxh/l. The median estimated area under the curve for both breasts was 57mgxh/l and median 24-hour clearance was 2.1mg/l.

“This is the first evaluation of nevirapine pharmacokinetics in breastmilk to examine the persistence of nevirapine concentrations in both breasts after treatment discontinuation”, note the investigators. They conclude that their findings of persistence of the drug may have clinical implications for both the mother and her infant.

References

Bennetto CJ et al. Persistence of nevirapine concentrations in breast milk. 45th Interscience Conference on Antimicrobial Agents and Chemotherapy, New Orleans, abstract H-1905, 2005.