HIV viral load non-suppression and associated factors among pregnant and postpartum women in rural northeastern South Africa: a cross-sectional survey.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
10 03 2022
Historique:
entrez: 11 3 2022
pubmed: 12 3 2022
medline: 28 4 2022
Statut: epublish

Résumé

We aimed to measure the prevalence of maternal HIV viral load (VL) non-suppression and assess associated factors, to evaluate progress towards United Nations-AIDS (UNAIDS) targets. Cross-sectional study. The eight largest community health centres of Ehlanzeni, a rural district in northeast South Africa. Pregnant women living with HIV (WLHIV) in their third trimester and postpartum WLHIV and their biological infants, recruited equally across all stages of the first 24 months post partum, were included. A sample of 612 mothers participated from a target of 1000. The primary outcome was maternal VL (mVL) non-suppression (defined here as mVL >1000 copies/mL). We collected information on antiretroviral use, healthcare visits and sociodemographics through interviews and measured plasma mVL. Descriptive statistics, χ All mothers (median age: 30 years) were on antiretroviral therapy (ART) and 24.9% were on ART ≤12 months. The prevalence of mVL non-suppression was 14.7% (95% CI: 11.3% to 19.0%), while 13.8% had low-level viraemia (50-1000 copies/mL). Most (68.9%) women had initiated breast feeding and 37.6% were currently breast feeding their infants. Being younger than 25 years (adjusted odds ratio (AOR): 2.6 (95% CI: 1.1 to 6.4)), on first-line ART (AOR: 2.3 (95% CI: 1.1 to 4.6)) and married/cohabiting (AOR: 1.9 (95% CI: 1.0 to 3.7)) were significantly associated with increased odds of mVL non-suppression. The prevalence of mVL ≤1000 copies/mL of 85.3% among pregnant and postpartum WLHIV and attending public healthcare centres in this rural district is below the 2020 90-90-90 and 2030 95-95-95 UNAIDS targets. Given that low-level viraemia may also increase the risk of vertical HIV transmission, we recommend strengthened implementation of the new guidelines which include better ART options, improved ART regimen switching and mVL monitoring schedules, and intensified psychosocial support for younger women, while exploring district-level complementary interventions, to sustain VLs below 50 copies/mL among all women.

Identifiants

pubmed: 35273061
pii: bmjopen-2021-058347
doi: 10.1136/bmjopen-2021-058347
pmc: PMC8915310
doi:

Substances chimiques

Anti-HIV Agents 0
Anti-Retroviral Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e058347

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 108065/Z/15/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 222075/Z/20/Z
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Nobubelo Kwanele Ngandu (NK)

HIV Prevention Research Unit, South African Medical Research Council, Cape Town, South Africa nobubelo.ngandu@mrc.ac.za.

Carl J Lombard (CJ)

Division of Epidemiology and Biostatistics, University of Stellenbosch, Cape Town, South Africa.
Biostatistics Unit, South African Medical Research Council, Cape Town, South Africa.

Thandiwe Elsie Mbira (TE)

HIV Prevention Research Unit, South African Medical Research Council, Cape Town, South Africa.

Adrian Puren (A)

Centre for HIV and STI, National Institute for Communicable Diseases, Johannesburg, South Africa.

Catriona Waitt (C)

Faculty of Health and Life Sciences, Department of Pharmacology, University of Liverpool, Liverpool, UK.
Infectious Diseases Institute, Makerere University College of Health Sciences, Kampala, Uganda.

Andrew J Prendergast (AJ)

Blizard Institute, Queen Mary University of London, London, UK.
Zvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe.

Thorkild Tylleskär (T)

Centre for International Health, Universitetet i Bergen, Bergen, Norway.

Philippe Van de Perre (P)

Pathogenesis and Control of Chronic and Emerging Infections, University of Montpellier INSERM, Montpellier, France.
CHU, Montpellier, Montpellier, France.
Etablissement Français du Sang, Antilles University, Paris, France.

Ameena Ebrahim Goga (AE)

HIV Prevention Research Unit, South African Medical Research Council, Cape Town, South Africa.

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