Mother-To-Child Transmission of HIV in Adolescents and Young Women: Findings From a National Prospective Cohort Survey, Zimbabwe, 2013-2014.


Journal

The Journal of adolescent health : official publication of the Society for Adolescent Medicine
ISSN: 1879-1972
Titre abrégé: J Adolesc Health
Pays: United States
ID NLM: 9102136

Informations de publication

Date de publication:
04 2020
Historique:
received: 13 05 2019
revised: 21 09 2019
accepted: 18 10 2019
pubmed: 23 1 2020
medline: 22 6 2021
entrez: 23 1 2020
Statut: ppublish

Résumé

We assessed 18-month cumulative mother-to-child HIV transmission (MTCT) risk and risk factors for no antiretroviral medication use during pregnancy among adolescent, young women, and adult mothers in Zimbabwe. We analyzed data from a prospective survey of 1,171 mother-infant pairs with HIV-exposed infants aged 4-12 weeks who were recruited from 151 immunization clinics from February to August 2013. HIV-exposed infants were followed until diagnosed with HIV, death, or age 18 months. Findings were weighted and adjusted for complex survey design and nonresponse. The 18-month cumulative MTCT risk was highest among adolescent aged ≤19 years (12%) followed by young women aged 20-24 years (7.5%) and adult women aged ≥25 years (6.9%). Across these groups, more than 94% had ≥1 antenatal care visit by 21 weeks of gestation, more than 95% had ≥1 HIV test, and more than 98% knew their HIV status. Of known HIV-positive mothers, maternal antiretroviral medication coverage during pregnancy was 76.8% (95% confidence interval: 65.1-85.5), 83.8% (78.6-87.9), and 87.8% (84.6-90.4) among adolescent, young women, and adult mothers, respectively. Among HIV-positive mothers diagnosed prenatally, the adjusted odds ratio of no ARV use during pregnancy was increased among those who had no antenatal care attendance (adjusted odds ratio: 7.7 [3.7-16.0]), no HIV testing (7.3 [2.3-23.5]), no prepartum CD4 count testing (2.1 [1.3-3.4]), and maternal HIV identification during pregnancy (2.9 [1.8-4.8]). Age was not a risk factor. With similar coverage of prevention of MTCT services, the 18-month cumulative MTCT risk was higher among adolescents and young women, compared with adults. Additional research should examine the causes to develop targeted interventions.

Identifiants

pubmed: 31964611
pii: S1054-139X(19)30874-2
doi: 10.1016/j.jadohealth.2019.10.023
pmc: PMC8740363
mid: NIHMS1681349
pii:
doi:

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

455-463

Subventions

Organisme : CGH CDC HHS
ID : U2G GH000315
Pays : United States
Organisme : PEPFAR
Pays : United States

Informations de copyright

Published by Elsevier Inc.

Références

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Auteurs

Amanda B Burrage (AB)

Division of Global HIV and TB, U.S. Centers for Disease Control and Prevention, Center for Global Health, Atlanta, Georgia.

Angela Mushavi (A)

AIDS and TB Department, Ministry of Health and Child Care of Zimbabwe, Harare, Zimbabwe.

Ray W Shiraishi (RW)

Division of Global HIV and TB, U.S. Centers for Disease Control and Prevention, Center for Global Health, Atlanta, Georgia.

Beth Tippett Barr (BT)

Division of Global HIV/AIDS, U.S. Centers for Disease Control and Prevention, Center for Global Health, Harare, Zimbabwe.

Geral Shambira (G)

Department of Community Health, University of Zimbabwe, Harare, Zimbabwe.

Justice Nyakura (J)

Department of Community Health, University of Zimbabwe, Harare, Zimbabwe.

Shirish Balachandra (S)

Division of Global HIV/AIDS, U.S. Centers for Disease Control and Prevention, Center for Global Health, Harare, Zimbabwe.

Peter H Kilmarx (PH)

Division of Global HIV and TB, U.S. Centers for Disease Control and Prevention, Center for Global Health, Atlanta, Georgia; Division of Global HIV/AIDS, U.S. Centers for Disease Control and Prevention, Center for Global Health, Harare, Zimbabwe.

Thu-Ha Dinh (TH)

Division of Global HIV and TB, U.S. Centers for Disease Control and Prevention, Center for Global Health, Atlanta, Georgia. Electronic address: dvt1@cdc.gov.

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