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Maternal and foetal outcomes among 4118 women with HIV infection treated with lopinavir/ritonavir during pregnancy: analysis of population-based surveillance data from the national study of HIV in pregnancy and childhood in the United Kingdom and Ireland
被引:22
|作者:
Tookey, Pat A.
[1
]
Thorne, Claire
[1
]
van Wyk, Jean
[2
]
Norton, Michael
[2
]
机构:
[1] UCL, UCL Inst Child Hlth, 30 Guilford St, London WC1N 1EH, England
[2] AbbVie Inc, 1 North Waukegan Rd, N Chicago, IL 60064 USA
来源:
BMC INFECTIOUS DISEASES
|
2016年
/
16卷
基金:
英国医学研究理事会;
关键词:
Lopinavir/ritonavir;
Pregnancy;
HIV;
Vertical transmission;
Congenital abnormality;
ANTIRETROVIRAL THERAPY;
PRETERM DELIVERY;
TRANSMISSION RATES;
POSITIVE WOMEN;
INCREASED RISK;
MOTHER;
PREVENTION;
BIRTH;
MANAGEMENT;
PROTEASE;
D O I:
10.1186/s12879-016-1400-y
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Background: The National Study of HIV in Pregnancy and Childhood (NSHPC) conducts comprehensive population-based surveillance of pregnancies in women with HIV infection in the United Kingdom/Ireland. Use of antepartum antiretroviral therapy (ART) for prevention of mother-to-child transmission (MTCT) and to treat maternal infection, if required, is standard practise in this population; lopinavir/ritonavir (LPV/r) is commonly used. The study objective was to examine the use of LPV/r among pregnant women with HIV infection to describe maternal and foetal outcomes. Methods: The NSHPC study collected maternal, perinatal and paediatric data through confidential and voluntary obstetric and paediatric reporting schemes. Pregnancies reported to the NSHPC by June 2013, due to deliver 2003-2012 and with LPV/r exposure were included in this analysis, using pregnancy as the unit of observation. Results: Four thousand eight hundred sixty-four LPV/r-exposed pregnancies resulting in 4702 deliveries in 4118 women were identified. Maternal region of birth was primarily sub-Saharan Africa (77 %) or United Kingdom/Ireland (14 %). Median maternal age at conception was 30 years. LPV/r was initiated preconception in 980 (20 %) and postconception in 3884 (80 %) pregnancies; median duration of antepartum LPV/r exposure was 270 and 107 days, respectively. Viral load close to delivery was <50 copies/mL in 73 % and <1000 copies/mL in 94 % of women. 63 % of deliveries were by caesarean section (elective, 62 %; emergency, 38 %). Among singleton live births, 13 % were <37 weeks of gestation (2.5 % <32 weeks) and 15 % had birth weight <2500 g (2.3 % <1500 g). MTCT rates were 1.1 (2003-2007) and 0.5 % (2008-2012). 134 live born children (2.9 %) had >= 1 congenital abnormality. Conclusions: The results of this analysis using real-world data from a large number of pregnant women with HIV infection in the United Kingdom and Ireland who received LPV/r-containing ART regimens demonstrate that these regimens have a good safety profile and are effective for viral suppression during pregnancy, with associated low rates of MTCT.
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