'If I am on ART, my new-born baby should be put on treatment immediately': Exploring the acceptability, and appropriateness of Cepheid Xpert HIV-1 Qual assay for early infant diagnosis of HIV in Malawi.


Journal

PLOS global public health
ISSN: 2767-3375
Titre abrégé: PLOS Glob Public Health
Pays: United States
ID NLM: 9918283779606676

Informations de publication

Date de publication:
2023
Historique:
received: 31 05 2022
accepted: 13 01 2023
entrez: 24 3 2023
pubmed: 25 3 2023
medline: 25 3 2023
Statut: epublish

Résumé

Early infant diagnosis of HIV (EID-HIV) is key to reducing paediatric HIV mortality. Traditional approaches for diagnosing HIV in exposed infants are usually unable to optimally contribute to EID. Point-of-care testing such as Cepheid Xpert HIV-1 Qual assay-1 (XPertHIV) are available and could improve EID-HIV in resource constrained and high HIV burden contexts. We investigated the acceptability and perceived appropriateness of XpertHIV for EID-HIV in Mulanje Hospital, Malawi. Qualitative cross-sectional study using semi-structured interviews (SSI) among caregivers and health care workers at Mulanje District Hospital. The qualitative study was nested within a larger diagnostic study that evaluated the performance of XpertHIV using whole-blood-sample in a resource limited and high burden setting. A total of 65 SSIs were conducted among caregivers (n = 60) and health care providers (n = 5). Data were coded using deductive and inductive approaches while thematic approach was used to analyse data. Point-of-care XPertHIV was perceived to be acceptable among caregivers and health care providers. Caregivers' motivations for accepting XPertHIV HIV-testing for their infants included perceived risk of HIV emanating from child's exposure and validation of caregiver's own HIV sero-status. Although concerns about pain of testing and blood sample volumes taken from an infant remained amplified, overall, both caregivers and health care providers felt XpertHIV was appropriate because of its quick result turn-around-time which decreased anxiety and stress, the prospect of early treatment initiation and reduction in hospital visits and related costs. Implementation of XpertHIV has a great potential to improve EID-HIV in Malawi because of its quick turn-around-time and associated benefits including overcoming access-related barriers. Scaled implementation of this diagnostic technology require a robust community engagement strategy for managing caregivers and community myths and misconceptions towards the amount of blood sample collected from infants.

Identifiants

pubmed: 36962982
doi: 10.1371/journal.pgph.0001135
pii: PGPH-D-22-00882
pmc: PMC10021387
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e0001135

Informations de copyright

Copyright: © 2023 Nyirenda-Nyang'wa et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Maggie Nyirenda-Nyang'wa (M)

Department of Infection, Immunity, Inflammation, Institute of Child Health, University College London, London, United Kingdom.
Department of Paediatrics, Kamuzu University of Health Sciences, Blantyre, Malawi.
Department of International Public Health, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.

Moses Kelly Kumwenda (MK)

Gender in Health Associate Group and Maternal and Fetal Health, Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
Department of Pathology, Helse Nord TB Initiative, Kamuzu University of Health Sciences, Blantyre, Malawi.

Shona Horter (S)

Department of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Mina C Hosseinipour (MC)

University of North Carolina Project-Malawi, Lilongwe, Malawi.
Department of Medicine, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, United States of America.

Maganizo Chagomerana (M)

University of North Carolina Project-Malawi, Lilongwe, Malawi.
Department of Medicine, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, United States of America.

Neil Kennedy (N)

Centre for Medical Education, Queen's University Belfast, Belfast, United Kingdom.

Derek Fairley (D)

Department of microbiology, Belfast Health & Social Care Trust, Belfast, United Kingdom.
Wellcome Wolfson institute, Queen's University Belfast, Belfast, United Kingdom.

Kevin Mortimer (K)

Department of International Public Health, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Respiratory Medicine, Aintree University Hospital, Liverpool University Hospitals NHS Foundation, Liverpool, United Kingdom.
Department of Medicine, University of Cambridge, Cambridge, United Kingdom.

Victor Mwapasa (V)

Department of Community and Environmental Health, Kamuzu University of Health Sciences, Blantyre, Malawi.

Chisomo Msefula (C)

Department of Pathology, Kamuzu University of Health Sciences, Blantyre, Malawi.

Nigel Klein (N)

Department of Infection, Immunity, Inflammation, Institute of Child Health, University College London, London, United Kingdom.

Dagmar Alber (D)

Department of Infection, Immunity, Inflammation, Institute of Child Health, University College London, London, United Kingdom.

Angela Obasi (A)

Department of International Public Health, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
AXESS Sexual Health, Liverpool University Hospitals NHS Foundation Trust, Liverpool, United Kingdom.

Classifications MeSH