Health benefits, costs, and cost-effectiveness of earlier eligibility for adult antiretroviral therapy and expanded treatment coverage: a combined analysis of 12 mathematical models

被引:162
作者
Eaton, Jeffrey W. [2 ]
Menzies, Nicolas A. [3 ]
Stover, John [6 ]
Cambiano, Valentina [7 ]
Chindelevitch, Leonid [4 ]
Cori, Anne [1 ]
Hontelez, Jan A. C. [8 ,10 ,11 ]
Humair, Salal [4 ]
Kerr, Cliff C. [12 ]
Klein, Daniel J. [13 ]
Mishra, Sharmistha [2 ,14 ]
Mitchell, Kate M. [15 ]
Nichols, Brooke E. [9 ]
Vickerman, Peter [15 ]
Bakker, Roel [8 ]
Baernighausen, Till [4 ,10 ]
Bershteyn, Anna [13 ]
Bloom, David E. [4 ]
Boily, Marie-Claude [2 ]
Chang, Stewart T. [13 ]
Cohen, Ted [5 ,17 ]
Dodd, Peter J. [16 ]
Fraser, Christophe [1 ]
Gopalappa, Chaitra [6 ]
Lundgren, Jens [18 ,19 ]
Martin, Natasha K. [15 ,20 ]
Mikkelsen, Evelinn [11 ]
Mountain, Elisa [2 ]
Pham, Quang D. [12 ]
Pickles, Michael [2 ]
Phillips, Andrew [7 ]
Platt, Lucy [15 ]
Pretorius, Carel [6 ]
Prudden, Holly J. [15 ]
Salomon, Joshua A. [3 ,4 ]
van de Vijver, David A. M. C. [9 ]
de Vlas, Sake J. [8 ]
Wagner, Bradley G. [13 ]
White, Richard G. [16 ]
Wilson, David P. [12 ]
Zhang, Lei [12 ]
Blandford, John [21 ]
Meyer-Rath, Gesine [22 ,23 ]
Remme, Michelle [15 ]
Revill, Paul [24 ]
Sangrujee, Nalinee [21 ]
Terris-Prestholt, Fern [15 ]
Doherty, Meg [25 ]
Shaffer, Nathan [25 ]
Easterbrook, Philippa J. [25 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, MRC Ctr Outbreak Anal & Modelling, London W2 1PG, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Infect Dis Epidemiol, London W2 1PG, England
[3] Harvard Univ, Sch Publ Hlth, Ctr Hlth Decis Sci, Boston, MA 02115 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Global Hlth & Populat, Boston, MA 02115 USA
[5] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[6] Futures Inst, Glastonbury, CT USA
[7] UCL, Res Dept Infect & Populat Hlth, London, England
[8] Univ Med Ctr Rotterdam, Erasmus MC, Dept Publ Hlth, Rotterdam, Netherlands
[9] Univ Med Ctr Rotterdam, Erasmus MC, Dept Virol, Rotterdam, Netherlands
[10] Univ KwaZulu Natal, Africa Ctr Hlth & Populat Studies, Mtubatuba, South Africa
[11] Radboud Univ Nijmegen, Med Ctr, Dept Primary & Community Care, Nijmegen Int Ctr Hlth Syst Anal & Educ NICHE, NL-6525 ED Nijmegen, Netherlands
[12] Univ New S Wales, Kirby Inst, Sydney, NSW, Australia
[13] Inst Dis Modelling, Intellectual Ventures Lab, Bellevue, WA USA
[14] Univ Toronto, St Michaels Hosp, Div Infect Dis, Toronto, ON, Canada
[15] London Sch Hyg & Trop Med, Social & Math Epidemiol Grp, London WC1, England
[16] London Sch Hyg & Trop Med, Dept Infect Dis Epidemiol, London WC1, England
[17] Brigham & Womens Hosp, Div Global Hlth Equ, Boston, MA 02115 USA
[18] Copenhagen Univ Hosp, Rigshosp, Ctr Viral Dis, Dept Infect Dis, Copenhagen, Denmark
[19] Univ Copenhagen, Fac Hlth Sci, Copenhagen, Denmark
[20] Univ Bristol, Sch Social & Community Med, Bristol, Avon, England
[21] US Ctr Dis Control & Prevent, Div Global HIV AIDS, Atlanta, GA USA
[22] Boston Univ, Ctr Global Hlth & Dev, Boston, MA 02215 USA
[23] Univ Witwatersrand, Dept Med, Hlth Econ & Epidemiol Res Off, Fac Hlth Sci, ZA-2001 Johannesburg, South Africa
[24] Univ York, Ctr Hlth Econ, York YO10 5DD, N Yorkshire, England
[25] WHO, Dept HIV AIDS, CH-1211 Geneva, Switzerland
基金
英国惠康基金; 英国医学研究理事会; 比尔及梅琳达.盖茨基金会; 澳大利亚研究理事会;
关键词
HIV-PREVENTION PROGRAM; IMPACT; INFECTION; RISK; SEX; ART; PREVALENCE; BEHAVIOR; OUTCOMES; AFRICA;
D O I
10.1016/S2214-109X(13)70172-4
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background New WHO guidelines recommend initiation of antiretroviral therapy for HIV-positive adults with CD4 counts of 500 cells per mu L 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 mu L or less, or all HIV-positive adults, compared with the previous (2010) recommendation of initiation with CD4 counts of 350 cells per mu L 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 mu L 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 mu L 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 mu L 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.
引用
收藏
页码:E23 / E34
页数:12
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