Provision of HIV viral load testing services in Zimbabwe: Secondary data analyses using data from health facilities using the electronic Patient Monitoring System.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 11 01 2020
accepted: 02 12 2020
entrez: 22 1 2021
pubmed: 23 1 2021
medline: 16 6 2021
Statut: epublish

Résumé

Routine viral load (VL) testing among persons living with Human Immunodeficiency Virus (PLHIV) enables earlier detection of sub-optimal antiretroviral therapy (ART) adherence and for appropriate management of treatment failure. Since adoption of this policy by Zimbabwe in 2016, the extent of implementation is unclear. Therefore we set out to determine among PLHIV ever enrolled on ART from 2004-2017 and in ART care for ≥12 months at health facilities providing ART in Zimbabwe: numbers (proportions) with VL testing uptake, VL suppression and subsequently switched to 2nd-line ART following confirmed virologic failure. We used retrospective data from the electronic Patient Monitoring System (ePMS) in which PLHIV on ART are registered at 525 public and 4 private health facilities. Among the 392,832 PLHIV in ART care for ≥12 months, 99,721 (25.4%) had an initial VL test done and results available of whom 81,932 (82%) were virally suppressed. Among those with a VL>1000 copies/mL; 6,689 (37.2%) had a follow-up VL test and 4,086 (61%) had unsuppressed VLs of whom only 1,749 (42.8%) were switched to 2nd-line ART. Lower age particularly adolescents (10-19 years) were more likely (ARR 1.34; 95%CI: 1.25-1.44) to have virologic failure. The study findings provide insights to implementation gaps including limitations in VL testing; low identification of high- risk PLHIV in care and lack of prompt utilization of test results. The use of electronic patient-level data has demonstrated its usefulness in assessing the performance of the national VL testing program. By end of 2017 implementation of VL testing was sub-optimal, and virological failure was relatively common, particularly among adolescents. Of concern is evidence of failure to act on VL test results that were received. A quality improvement initiative has been planned in response to these findings and its effect on patient management will be monitored.

Identifiants

pubmed: 33481931
doi: 10.1371/journal.pone.0245720
pii: PONE-D-20-00956
pmc: PMC7822242
doi:

Substances chimiques

Anti-Retroviral Agents 0

Types de publication

Clinical Trial Journal Article Multicenter Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0245720

Subventions

Organisme : FIC NIH HHS
ID : D43 TW009539
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Tsitsi Apollo (T)

Department of HIV and TB, Ministry of Health and Child Care, Harare, Zimbabwe.
Department of Medicine, University of Zimbabwe College of Health Sciences, Harare, Zimbabwe.

Kudakwashe C Takarinda (KC)

Department of HIV and TB, Ministry of Health and Child Care, Harare, Zimbabwe.
Centre for Operations Research, International Union Against TB and Lung Disease, Paris, France.

Andrew Phillips (A)

Institute for Global Health, UCL, London, United Kingdom.

Chiratidzo Ndhlovu (C)

Department of Medicine, University of Zimbabwe College of Health Sciences, Harare, Zimbabwe.

Frances M Cowan (FM)

Centre for Sexual Health and HIV/AIDS Research (CeSHHAR), Harare, Zimbabwe.
Liverpool School of Tropical Medicine, Liverpool, United Kingdom.

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