TY - JOUR
T1 - Antiretroviral therapy for prevention of mother-to-child HIV transmission
T2 - Focus on single-dose nevirapine
AU - Giaquinto, Carlo
AU - Rampon, Osvalda
AU - De Rossi, Anita
PY - 2006
Y1 - 2006
N2 - Administration of potent antiretroviral combination therapy in the second and third trimester of pregnancy and during delivery, and for 6 weeks postpartum to the infant, may reduce HIV transmission from the mother to the child to 6 months after delivery or in those who are not severely immunocompromised. Furthermore, studies have shown that adding short-course (up to 7 days) zidovudine or zidovudine/lamivudine prophylaxis after delivery may dramatically reduce the occurrence of nevirapine resistance in both mothers and infants. Until data are available that allow a better understanding of the relevance of antiretroviral drug resistance acquired as a result of mother-to-child HIV transmission prophylaxis, women and children who have previously received single-dose nevirapine as part of a mother-to-child transmission prevention strategy should be considered eligible for NNRTI-based regimens and should not be denied access to antiretroviral therapy.
AB - Administration of potent antiretroviral combination therapy in the second and third trimester of pregnancy and during delivery, and for 6 weeks postpartum to the infant, may reduce HIV transmission from the mother to the child to 6 months after delivery or in those who are not severely immunocompromised. Furthermore, studies have shown that adding short-course (up to 7 days) zidovudine or zidovudine/lamivudine prophylaxis after delivery may dramatically reduce the occurrence of nevirapine resistance in both mothers and infants. Until data are available that allow a better understanding of the relevance of antiretroviral drug resistance acquired as a result of mother-to-child HIV transmission prophylaxis, women and children who have previously received single-dose nevirapine as part of a mother-to-child transmission prevention strategy should be considered eligible for NNRTI-based regimens and should not be denied access to antiretroviral therapy.
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U2 - 10.2165/00044011-200626110-00001
DO - 10.2165/00044011-200626110-00001
M3 - Article
C2 - 17163296
AN - SCOPUS:33750351449
SN - 1173-2563
VL - 26
SP - 611
EP - 627
JO - Clinical Drug Investigation
JF - Clinical Drug Investigation
IS - 11
ER -