Costing and cost-effectiveness of Cepheid Xpert HIV -1 Qual Assay using whole blood protocol versus PCR by Abbott Systems in Malawi.

Cepheid HIV Malawi TAT Xpert cost

Journal

Journal of global health economics and policy
ISSN: 2806-6073
Titre abrégé: J Glob Health Econ Policy
Pays: Scotland
ID NLM: 9918284149406676

Informations de publication

Date de publication:
2022
Historique:
medline: 1 1 2022
pubmed: 1 1 2022
entrez: 15 9 2023
Statut: ppublish

Résumé

Timely diagnosis of HIV in infants and children is an urgent priority. In Malawi, 40,000 infants annually are HIV exposed. However, gold standard polymerase-chain-reaction (PCR) based testing requires centralised laboratories, causing turn-around times (TAT) of 2 to 3 months and significant loss to follow-up. If feasible and acceptable, minimising diagnostic delays through HIV Point-of-care-testing (POCT) may be cost-effective. We assessed whether POCT Cepheid Xpert HIV-1 Qual assay whole blood (XpertHIV) was more cost-effective than PCR. From July-August 2018, 700 PCR Abbott tests using dried blood spots (DBS) were performed on 680 participants who enrolled on the feasibility, acceptability and performance of the XpertHIV study. Newly identified HIV-positive We conducted a cost-minimisation and cost-effectiveness analysis of XpertHIV against PCR, as the standard of care. A random sample of 200 caregivers from the 680 participants had semi-structured interviews to explore costs from a societal perspective of XpertHIV at Mulanje District Hospital, Malawi. Analysis used TAT as the primary outcome measure. Results were extrapolated from the study period (29 days) to a year (240 working days). Sensitivity analyses characterised individual and joint parameter uncertainty and estimated patient cost per test. During the study period, XpertHIV was cost-minimising at $42.34 per test compared to $66.66 for PCR. Over a year, XpertHIV remained cost-minimising at $16.12 compared to PCR at $27.06. From the patient perspective (travel, food, lost productivity), the cost per test of XpertHIV was $2.45. XpertHIV had a mean TAT of 7.10 hours compared to 153.15 hours for PCR. Extrapolates accounting for equipment costs, lab consumables and losses to follow up estimated annual savings of $2,193,538.88 if XpertHIV is used nationally, as opposed to PCR. This preliminary evidence suggests that adopting POCT XpertHIV will save time, allowing HIV-exposed infants to receive prompt care and may improve outcomes. The Malawi government will pay less due to XpertHIV's cost savings and associated benefits.

Sections du résumé

Background UNASSIGNED
Timely diagnosis of HIV in infants and children is an urgent priority. In Malawi, 40,000 infants annually are HIV exposed. However, gold standard polymerase-chain-reaction (PCR) based testing requires centralised laboratories, causing turn-around times (TAT) of 2 to 3 months and significant loss to follow-up. If feasible and acceptable, minimising diagnostic delays through HIV Point-of-care-testing (POCT) may be cost-effective. We assessed whether POCT Cepheid Xpert HIV-1 Qual assay whole blood (XpertHIV) was more cost-effective than PCR.
Methods UNASSIGNED
From July-August 2018, 700 PCR Abbott tests using dried blood spots (DBS) were performed on 680 participants who enrolled on the feasibility, acceptability and performance of the XpertHIV study. Newly identified HIV-positive We conducted a cost-minimisation and cost-effectiveness analysis of XpertHIV against PCR, as the standard of care. A random sample of 200 caregivers from the 680 participants had semi-structured interviews to explore costs from a societal perspective of XpertHIV at Mulanje District Hospital, Malawi. Analysis used TAT as the primary outcome measure. Results were extrapolated from the study period (29 days) to a year (240 working days). Sensitivity analyses characterised individual and joint parameter uncertainty and estimated patient cost per test.
Results UNASSIGNED
During the study period, XpertHIV was cost-minimising at $42.34 per test compared to $66.66 for PCR. Over a year, XpertHIV remained cost-minimising at $16.12 compared to PCR at $27.06. From the patient perspective (travel, food, lost productivity), the cost per test of XpertHIV was $2.45. XpertHIV had a mean TAT of 7.10 hours compared to 153.15 hours for PCR. Extrapolates accounting for equipment costs, lab consumables and losses to follow up estimated annual savings of $2,193,538.88 if XpertHIV is used nationally, as opposed to PCR.
Conclusions UNASSIGNED
This preliminary evidence suggests that adopting POCT XpertHIV will save time, allowing HIV-exposed infants to receive prompt care and may improve outcomes. The Malawi government will pay less due to XpertHIV's cost savings and associated benefits.

Identifiants

pubmed: 37711180
doi: 10.52872/001c.37787
pmc: PMC10501532
mid: NIHMS1866209
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : FIC NIH HHS
ID : D43 TW010060
Pays : United States
Organisme : Medical Research Council
ID : MR/P020526/1
Pays : United Kingdom

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Auteurs

Maggie Nyirenda-Nyang'wa (M)

University College London, London, UK.
College of Medicine, University of Malawi, Malawi.
Liverpool School of Tropical Medicine, Liverpool, UK.

Gerald Manthalu (G)

Department of Planning and Policy, Ministry of Health, Malawi.

Matthias Arnold (M)

Institute for Applied Health Services Research , Berlin, Germany.
Health Economics Policy Unit (HEPU), College of Medicine, Malawi.

Dominic Nkhoma (D)

Health Economics Policy Unit (HEPU), College of Medicine, Malawi.

Mina C Hosseinipour (MC)

University of North Carolina Project-Malawi, Lilongwe, Malawi.
University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Maganizo Chagomerana (M)

University of North Carolina Project-Malawi, Lilongwe, Malawi.
University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Precious Chibwe (P)

Health Economics Policy Unit (HEPU), College of Medicine, Malawi.

Kevin Mortimer (K)

Liverpool School of Tropical Medicine, Liverpool, UK.

Neil Kennedy (N)

Queen's University Belfast, Belfast, UK.

Derek Fairley (D)

Queen's University Belfast, Belfast, UK.

Victor Mwapasa (V)

College of Medicine, University of Malawi, Malawi.

Chisomo Msefula (C)

College of Medicine, University of Malawi, Malawi.

Henry C Mwandumba (HC)

Liverpool School of Tropical Medicine, Liverpool, UK.
Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.

Jobiba Chinkhumba (J)

College of Medicine, University of Malawi, Malawi.
Malaria Alert Centre, University of Malawi College of Medicine, Blantyre, Malawi.

Nigel Klein (N)

University College London, London, UK.

Dagmar Alber (D)

University College London, London, UK.

Angela Obasi (A)

Liverpool School of Tropical Medicine, Liverpool, UK.
The Royal Liverpool University Hospital NHS Foundation Trust.

Classifications MeSH