Impact of breastfeeding, maternal antiretroviral treatment and health service factors on 18-month vertical transmission of HIV and HIV-free survival: results from a nationally representative HIV-exposed infant cohort, South Africa.


Journal

Journal of epidemiology and community health
ISSN: 1470-2738
Titre abrégé: J Epidemiol Community Health
Pays: England
ID NLM: 7909766

Informations de publication

Date de publication:
12 2020
Historique:
received: 21 12 2019
revised: 02 05 2020
accepted: 07 07 2020
pubmed: 28 9 2020
medline: 3 9 2021
entrez: 27 9 2020
Statut: ppublish

Résumé

We analysed the impact of breastfeeding, antiretroviral drugs and health service factors on cumulative (6 weeks to 18 months) vertical transmission of HIV (MTCT) and 'MTCT-or-death', in South Africa, and compared estimates with global impact criteria to validate MTCT elimination: (1) <5% final MTCT and (2) case rate ≤50 (new paediatric HIV infections/100 000 live births). 9120 infants aged 6 weeks were enrolled in a nationally representative survey. Of 2811 HIV-exposed uninfected infants (HEU), 2644 enrolled into follow-up (at 3, 6, 9, 12, 15 and 18 months). Using Kaplan-Meier analysis and weighted survey domain-based Cox proportional hazards models, we estimated cumulative risk of MTCT and 'MTCT or death' and risk factors for time-to-event outcomes, adjusting for study design and loss-to-follow-up. Cumulative (final) MTCT was 4.3% (95% CI 3.7% to 5.0%); case rate was 1290. Postnatal MTCT (>6 weeks to 18 months) was 1.7% (95% CI 1.2% to 2.4%). Cumulative 'MTCT-or-death' was 6.3% (95% CI 5.5% to 7.3%); 81% and 62% of cumulative MTCT and 'MTCT-or-death', respectively, occurred by 6 months. Postnatal MTCT increased with unknown maternal CD4-cell-count (adjusted HR (aHR 2.66 (1.5-5.6)), undocumented maternal HIV status (aHR 2.21 (1.0-4.7)) and exclusive (aHR 2.3 (1.0-5.2)) or mixed (aHR 3.7 (1.2-11.4)) breastfeeding. Cumulative 'MTCT-or death' increased in households with 'no refrigerator' (aHR 1.7 (1.1-2.9)) and decreased if infants used nevirapine at 6 weeks (aHR 0.4 (0.2-0.9)). While the <5% final MTCT target was met, the case rate was 25-times above target. Systems are needed in the first 6 months post-delivery to optimise HEU health and fast-track ART initiation in newly diagnosed mothers.

Sections du résumé

BACKGROUND
We analysed the impact of breastfeeding, antiretroviral drugs and health service factors on cumulative (6 weeks to 18 months) vertical transmission of HIV (MTCT) and 'MTCT-or-death', in South Africa, and compared estimates with global impact criteria to validate MTCT elimination: (1) <5% final MTCT and (2) case rate ≤50 (new paediatric HIV infections/100 000 live births).
METHODS
9120 infants aged 6 weeks were enrolled in a nationally representative survey. Of 2811 HIV-exposed uninfected infants (HEU), 2644 enrolled into follow-up (at 3, 6, 9, 12, 15 and 18 months). Using Kaplan-Meier analysis and weighted survey domain-based Cox proportional hazards models, we estimated cumulative risk of MTCT and 'MTCT or death' and risk factors for time-to-event outcomes, adjusting for study design and loss-to-follow-up.
RESULTS
Cumulative (final) MTCT was 4.3% (95% CI 3.7% to 5.0%); case rate was 1290. Postnatal MTCT (>6 weeks to 18 months) was 1.7% (95% CI 1.2% to 2.4%). Cumulative 'MTCT-or-death' was 6.3% (95% CI 5.5% to 7.3%); 81% and 62% of cumulative MTCT and 'MTCT-or-death', respectively, occurred by 6 months. Postnatal MTCT increased with unknown maternal CD4-cell-count (adjusted HR (aHR 2.66 (1.5-5.6)), undocumented maternal HIV status (aHR 2.21 (1.0-4.7)) and exclusive (aHR 2.3 (1.0-5.2)) or mixed (aHR 3.7 (1.2-11.4)) breastfeeding. Cumulative 'MTCT-or death' increased in households with 'no refrigerator' (aHR 1.7 (1.1-2.9)) and decreased if infants used nevirapine at 6 weeks (aHR 0.4 (0.2-0.9)).
CONCLUSIONS
While the <5% final MTCT target was met, the case rate was 25-times above target. Systems are needed in the first 6 months post-delivery to optimise HEU health and fast-track ART initiation in newly diagnosed mothers.

Identifiants

pubmed: 32980812
pii: jech-2019-213453
doi: 10.1136/jech-2019-213453
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1069-1077

Subventions

Organisme : NCHHSTP CDC HHS
ID : U2G PS001137
Pays : United States
Organisme : PEPFAR
Pays : United States
Organisme : CGH CDC HHS
ID : U2G GH001150
Pays : United States

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Ameena Ebrahim Goga (AE)

Health Systems Research Unit, South African Medical Research Council, Tygerberg, South Africa Ameena.Goga@mrc.ac.za.
HIV Prevention Research Unit, South African Medical Research Council, Tygerberg, South Africa.
Department of Paediatrics and Child Health, University of Pretoria, Pretoria, South Africa.

Carl Lombard (C)

Biostatistics Research Unit, South African Medical Research Council, Tygerberg, South Africa.
Division of Epidemiology and Biostatistics, University of Stellenbosch Faculty of Science, Tygerberg, South Africa.

Debra Jackson (D)

University of the Western Cape, Bellville, South Africa.
UNICEF, New York, USA.

Vundli Ramokolo (V)

Health Systems Research Unit, South African Medical Research Council, Tygerberg, South Africa.

Nobubelo Kwanele Ngandu (NK)

Health Systems Research Unit, South African Medical Research Council, Tygerberg, South Africa.

Gayle Sherman (G)

Centre for HIV and STI, National Institute for Communicable Diseases, Johannesburg, South Africa.
Department of Paediatrics and Child Health, University of the Witwatersrand Faculty of Health Sciences, Johannesburg, South Africa.

Adrian Puren (A)

Centre for HIV and STI, National Institute for Communicable Diseases, Johannesburg, South Africa.
Division of Virology and Communicable Diseases, University of the Witwatersrand, Johannesburg-Braamfontein, South Africa.

Witness Chirinda (W)

Medical Research Council of South Africa, Tygerberg, South Africa.

Sanjana Bhardwaj (S)

UNICEF, Abuja, Nigeria.

Nobuntu Makhari (N)

Health Systems Research Unit, South African Medical Research Council, Tygerberg, South Africa.

Trisha Ramraj (T)

Health Systems Research Unit, South African Medical Research Council, Tygerberg, South Africa.

Vuyolwethu Magasana (V)

Health Systems Research Unit, South African Medical Research Council, Tygerberg, South Africa.

Yagespari Singh (Y)

Health Systems Research Unit, South African Medical Research Council, Tygerberg, South Africa.

Yogan Pillay (Y)

National Department of Health, Pretoria, South Africa.

Thu-Ha Dinh (TH)

Center for Global Health, CDC, Atlanta, Georgia, USA.

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