TY - JOUR
T1 - Health benefits, costs, and cost-effectiveness of earlier eligibility for adult antiretroviral therapy and expanded treatment coverage: a combined analysis of 12 mathematical models
AU - Eaton, Jeffrey W.
AU - Menzies, Nicolas A.
AU - Stover, John
AU - Cambiano, Valentina
AU - Chindelevitch, Leonid
AU - Cori, Anne
AU - Hontelez, Jan A.C.
AU - Humair, Salal
AU - Kerr, Cliff C.
AU - Klein, Daniel J.
AU - Mishra, Sharmistha
AU - Mitchell, Kate M.
AU - Nichols, Brooke E.
AU - Vickerman, Peter
AU - Bakker, Roel
AU - Bärnighausen, Till
AU - Bershteyn, Anna
AU - Bloom, David E.
AU - Boily, Marie Claude
AU - Chang, Stewart T.
AU - Cohen, Ted
AU - Dodd, Peter J.
AU - Fraser, Christophe
AU - Gopalappa, Chaitra
AU - Lundgren, Jens
AU - Martin, Natasha K.
AU - Mikkelsen, Evelinn
AU - Mountain, Elisa
AU - Pham, Quang D.
AU - Pickles, Michael
AU - Phillips, Andrew
AU - Platt, Lucy
AU - Pretorius, Carel
AU - Prudden, Holly J.
AU - Salomon, Joshua A.
AU - van de Vijver, David A.M.C.
AU - de Vlas, Sake J.
AU - Wagner, Bradley G.
AU - White, Richard G.
AU - Wilson, David P.
AU - Zhang, Lei
AU - Blandford, John
AU - Meyer-Rath, Gesine
AU - Remme, Michelle
AU - Revill, Paul
AU - Sangrujee, Nalinee
AU - Terris-Prestholt, Fern
AU - Doherty, Meg
AU - Shaffer, Nathan
AU - Easterbrook, Philippa J.
AU - Hirnschall, Gottfried
AU - Hallett, Timothy B.
N1 - Funding Information:
The study was funded by the Bill & Melinda Gates Foundation and WHO. We thank Ellen McRobie and Annick Borquez from Imperial College London (London, UK) for coordinating the HIV Modelling Consortium ART Eligibility Guidelines modelling project. We thank Mary Mahy from UNAIDS (Geneva, Switzerland) for providing additional information about UNAIDS' country-level epidemiological estimates. We thank Emmanuela Gakidou and Herbert Duber from the Institute for Health Metrics and Evaluation at the University of Washington (Seattle, WA, USA) for providing information about antiretroviral therapy programmes in South Africa and Zambia. We thank Elliot Raizes from the US Centers for Disease Control and Prevention (CDC, Atlanta, GA, USA) for input on supply-chain management costs for antiretroviral drugs. We thank the Clinton Health Access Initiative (New York, NY, USA) and the Division of Global HIV/AIDS of the CDC for access to unpublished cost estimates. VC and AP acknowledge the University College London Research Computing Services (Legion Cluster; London, UK) and input to the synthesis model from Deborah Ford, Alec Miners, Paul Revill, Fumiyo Nakagawa, and Deenan Pillay. DJK, AB, STC, and BGW thank Bill and Melinda Gates for their active support of this work and their sponsorship through the Global Good Fund. M-CB, SM, EMo, and MP thank all other members of the Strategic Epi-ART in India Modeling team for their contribution to data and model inputs. M-CB, SM, EMo, and MP acknowledge the Canadian Foundation for AIDS (CANFAR, research grant number 023-015) for funding the Belgaum modelling. KMM and HJP acknowledge funding from the Wellcome Trust (086431/Z/08/Z). TC received funding from the US National Institute of General Medical Sciences (U54GM088558; the content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute of General Medical Sciences or the National Institutes of Health). DPW, CCK, QDP, and LZ acknowledge funding from the World Bank, Australian Research Council, University of New South Wales, and AusAID. QDP acknowledges scholarship support from AusAID. RGW acknowledges research funding from the UK Medical Research Council (Methodology Research Fellowship G0802414 and grant MR/J005088/1 ) and the Bill & Melinda Gates Foundation (Consortium to Respond Effectively to the AIDS/TB Epidemic [19790.01] and TB Modelling and Analysis Consortium [ 21675 ]). BEN and DAMCvdV acknowledge research funding from the Aids Fonds (grant 2010-035) in Amsterdam, Netherlands, and the European Union FP7 CHAIN grant (223131). NKM acknowledges funding from a UK National Institute for Health Research postdoctoral fellowship. PV acknowledges funding support from UNAIDS India for modelling work in northeast India. The findings and conclusions in this report are those of the authors and do not necessarily represent the official positions of the CDC or WHO.
PY - 2014/1
Y1 - 2014/1
N2 - Background: New WHO guidelines recommend initiation of antiretroviral therapy for HIV-positive adults with CD4 counts of 500 cells per μL or less, a higher threshold than was previously recommended. Country decision makers have to decide whether to further expand eligibility for antiretroviral therapy accordingly. We aimed to assess the potential health benefits, costs, and cost-effectiveness of various eligibility criteria for adult antiretroviral therapy and expanded treatment coverage. Methods: We used several independent mathematical models in four settings-South Africa (generalised epidemic, moderate antiretroviral therapy coverage), Zambia (generalised epidemic, high antiretroviral therapy coverage), India (concentrated epidemic, moderate antiretroviral therapy coverage), and Vietnam (concentrated epidemic, low antiretroviral therapy coverage)-to assess the potential health benefits, costs, and cost-effectiveness of various eligibility criteria for adult antiretroviral therapy under scenarios of existing and expanded treatment coverage, with results projected over 20 years. Analyses assessed the extension of eligibility to include individuals with CD4 counts of 500 cells per μL or less, or all HIV-positive adults, compared with the previous (2010) recommendation of initiation with CD4 counts of 350 cells per μL or less. We assessed costs from a health-system perspective, and calculated the incremental cost (in US$) per disability-adjusted life-year (DALY) averted to compare competing strategies. Strategies were regarded very cost effective if the cost per DALY averted was less than the country's 2012 per-head gross domestic product (GDP; South Africa: $8040; Zambia: $1425; India: $1489; Vietnam: $1407) and cost effective if the cost per DALY averted was less than three times the per-head GDP. Findings: In South Africa, the cost per DALY averted of extending eligibility for antiretroviral therapy to adult patients with CD4 counts of 500 cells per μL or less ranged from $237 to $1691 per DALY averted compared with 2010 guidelines. In Zambia, expansion of eligibility to adults with a CD4 count threshold of 500 cells per μL ranged from improving health outcomes while reducing costs (ie, dominating the previous guidelines) to $749 per DALY averted. In both countries results were similar for expansion of eligibility to all HIV-positive adults, and when substantially expanded treatment coverage was assumed. Expansion of treatment coverage in the general population was also cost effective. In India, the cost for extending eligibility to all HIV-positive adults ranged from $131 to $241 per DALY averted, and in Vietnam extending eligibility to patients with CD4 counts of 500 cells per μL or less cost $290 per DALY averted. In concentrated epidemics, expanded access for key populations was also cost effective. Interpretation: Our estimates suggest that earlier eligibility for antiretroviral therapy is very cost effective in low-income and middle-income settings, although these estimates should be revisited when more data become available. Scaling up antiretroviral therapy through earlier eligibility and expanded coverage should be considered alongside other high-priority health interventions competing for health budgets. Funding: Bill & Melinda Gates Foundation, WHO.
AB - Background: New WHO guidelines recommend initiation of antiretroviral therapy for HIV-positive adults with CD4 counts of 500 cells per μL or less, a higher threshold than was previously recommended. Country decision makers have to decide whether to further expand eligibility for antiretroviral therapy accordingly. We aimed to assess the potential health benefits, costs, and cost-effectiveness of various eligibility criteria for adult antiretroviral therapy and expanded treatment coverage. Methods: We used several independent mathematical models in four settings-South Africa (generalised epidemic, moderate antiretroviral therapy coverage), Zambia (generalised epidemic, high antiretroviral therapy coverage), India (concentrated epidemic, moderate antiretroviral therapy coverage), and Vietnam (concentrated epidemic, low antiretroviral therapy coverage)-to assess the potential health benefits, costs, and cost-effectiveness of various eligibility criteria for adult antiretroviral therapy under scenarios of existing and expanded treatment coverage, with results projected over 20 years. Analyses assessed the extension of eligibility to include individuals with CD4 counts of 500 cells per μL or less, or all HIV-positive adults, compared with the previous (2010) recommendation of initiation with CD4 counts of 350 cells per μL or less. We assessed costs from a health-system perspective, and calculated the incremental cost (in US$) per disability-adjusted life-year (DALY) averted to compare competing strategies. Strategies were regarded very cost effective if the cost per DALY averted was less than the country's 2012 per-head gross domestic product (GDP; South Africa: $8040; Zambia: $1425; India: $1489; Vietnam: $1407) and cost effective if the cost per DALY averted was less than three times the per-head GDP. Findings: In South Africa, the cost per DALY averted of extending eligibility for antiretroviral therapy to adult patients with CD4 counts of 500 cells per μL or less ranged from $237 to $1691 per DALY averted compared with 2010 guidelines. In Zambia, expansion of eligibility to adults with a CD4 count threshold of 500 cells per μL ranged from improving health outcomes while reducing costs (ie, dominating the previous guidelines) to $749 per DALY averted. In both countries results were similar for expansion of eligibility to all HIV-positive adults, and when substantially expanded treatment coverage was assumed. Expansion of treatment coverage in the general population was also cost effective. In India, the cost for extending eligibility to all HIV-positive adults ranged from $131 to $241 per DALY averted, and in Vietnam extending eligibility to patients with CD4 counts of 500 cells per μL or less cost $290 per DALY averted. In concentrated epidemics, expanded access for key populations was also cost effective. Interpretation: Our estimates suggest that earlier eligibility for antiretroviral therapy is very cost effective in low-income and middle-income settings, although these estimates should be revisited when more data become available. Scaling up antiretroviral therapy through earlier eligibility and expanded coverage should be considered alongside other high-priority health interventions competing for health budgets. Funding: Bill & Melinda Gates Foundation, WHO.
U2 - 10.1016/S2214-109X(13)70172-4
DO - 10.1016/S2214-109X(13)70172-4
M3 - Article
C2 - 25104632
AN - SCOPUS:84890844904
SN - 2214-109X
VL - 2
SP - e23-e34
JO - The Lancet Global Health
JF - The Lancet Global Health
IS - 1
ER -