Author
Listed:
- Andrew Phillips
(University College London)
- Amir Shroufi
(Southern Africa Medical Unit (SAMU), Medecins sans Frontieres (MSF) SA)
- Lara Vojnov
(Clinton Health Access Initiative)
- Jennifer Cohn
(Médecins Sans Frontières, Access Campaign)
- Teri Roberts
(Médecins Sans Frontières, Access Campaign)
- Tom Ellman
(Southern Africa Medical Unit (SAMU), Medecins sans Frontieres (MSF) SA)
- Kimberly Bonner
(Médecins Sans Frontières)
- Christine Rousseau
(Bill and Melinda Gates Foundation)
- Geoff Garnett
(Bill and Melinda Gates Foundation)
- Valentina Cambiano
(University College London)
- Fumiyo Nakagawa
(University College London)
- Deborah Ford
(MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology)
- Loveleen Bansi-Matharu
(University College London)
- Alec Miners
(Health Services Research & Policy, London School of Hygiene and Tropical Medicine)
- Jens D. Lundgren
(CHIP, Rigshospitalet, University of Copenhagen)
- Jeffrey W. Eaton
(Imperial College London)
- Rosalind Parkes-Ratanshi
(Infectious Diseases Institute (IDI), College of Health Sciences, Makerere University)
- Zachary Katz
(Clinton Health Access Initiative)
- David Maman
(Southern Africa Medical Unit (SAMU), Medecins sans Frontieres (MSF) SA)
- Nathan Ford
(HIV/AIDS and Global Hepatitis Programme, World Health Organization)
- Marco Vitoria
(HIV/AIDS and Global Hepatitis Programme, World Health Organization)
- Meg Doherty
(HIV/AIDS and Global Hepatitis Programme, World Health Organization)
- David Dowdy
(Johns Hopkins Bloomberg School of Public Health)
- Brooke Nichols
(Erasmus Medical Center)
- Maurine Murtagh
(International Diagnostics Centre, London School of Hygiene & Tropical, Medicine)
- Meghan Wareham
(Clinton Health Access Initiative)
- Kara M. Palamountain
(Kellogg School of Management, Northwestern University)
- Christine Chakanyuka Musanhu
(WHO Country Office)
- Wendy Stevens
(University of the Witwatersrand)
- David Katzenstein
(Division of Infectious Disease
Stanford University Medical Center)
- Andrea Ciaranello
(Massachusetts General Hospital Division of Infectious Diseases)
- Ruanne Barnabas
(Medicine, Global Health and Epidemiology, University of Washington (UW))
- R. Scott Braithwaite
(New York University School of Medicine)
- Eran Bendavid
(Division of General Medical Disciplines, Department of Medicine Stanford University)
- Kusum J. Nathoo
(University of Zimbabwe, College of Health Sciences)
- David van de Vijver
(Erasmus Medical Center)
- David P. Wilson
(University of New South Wales
UNSW Campus)
- Charles Holmes
(Centre for Infectious Disease Research in Zambia)
- Anna Bershteyn
(Institute for Disease Modeling)
- Simon Walker
(Centre for Health Economics, University of York)
- Elliot Raizes
(Care and Treatment Branch Center for Global Health, CDC)
- Ilesh Jani
(Instituto Nacional de Saúde (INS), Ministry of Health)
- Lisa J. Nelson
(The Office of the US Global AIDS Coordinator and Health Diplomacy (S/GAC))
- Rosanna Peeling
(London School of Hygiene and Tropical Medicine)
- Fern Terris-Prestholt
(London School of Hygiene and Tropical Medicine)
- Joseph Murungu
(Ministry of Health and Child Care)
- Tsitsi Mutasa-Apollo
(Ministry of Health and Child Care)
- Timothy B. Hallett
(Imperial College London)
- Paul Revill
(Centre for Health Economics, University of York)
Abstract
There are inefficiencies in current approaches to monitoring patients on antiretroviral therapy in sub-Saharan Africa. Patients typically attend clinics every 1 to 3 months for clinical assessment. The clinic costs are comparable with the costs of the drugs themselves and CD4 counts are measured every 6 months, but patients are rarely switched to second-line therapies. To ensure sustainability of treatment programmes, a transition to more cost-effective delivery of antiretroviral therapy is needed. In contrast to the CD4 count, measurement of the level of HIV RNA in plasma (the viral load) provides a direct measure of the current treatment effect. Viral-load-informed differentiated care is a means of tailoring care so that those with suppressed viral load visit the clinic less frequently and attention is focussed on those with unsuppressed viral load to promote adherence and timely switching to a second-line regimen. The most feasible approach to measuring viral load in many countries is to collect dried blood spot samples for testing in regional laboratories; however, there have been concerns over the sensitivity and specificity of this approach to define treatment failure and the delay in returning results to the clinic. We use modelling to synthesize evidence and evaluate the cost-effectiveness of viral-load-informed differentiated care, accounting for limitations of dried blood sample testing. We find that viral-load-informed differentiated care using dried blood sample testing is cost-effective and is a recommended strategy for patient monitoring, although further empirical evidence as the approach is rolled out would be of value. We also explore the potential benefits of point-of-care viral load tests that may become available in the future. This article has not been written or reviewed by Nature editors. Nature accepts no responsibility for the accuracy of the information provided.
Suggested Citation
Andrew Phillips & Amir Shroufi & Lara Vojnov & Jennifer Cohn & Teri Roberts & Tom Ellman & Kimberly Bonner & Christine Rousseau & Geoff Garnett & Valentina Cambiano & Fumiyo Nakagawa & Deborah Ford & , 2015.
"Sustainable HIV treatment in Africa through viral-load-informed differentiated care,"
Nature, Nature, vol. 528(7580), pages 68-76, December.
Handle:
RePEc:nat:nature:v:528:y:2015:i:7580:d:10.1038_nature16046
DOI: 10.1038/nature16046
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