Jeffrey W. Eaton
Imperial College London
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Featured researches published by Jeffrey W. Eaton.
The Lancet | 2013
Laura Robertson; Phyllis Mushati; Jeffrey W. Eaton; Lovemore Dumba; Gideon Mavise; Jeremiah C. Makoni; Christina Schumacher; Tom Crea; Roeland Monasch; Lorraine Sherr; Geoffrey P. Garnett; Constance Nyamukapa; Simon Gregson
Summary Background Cash-transfer programmes can improve the wellbeing of vulnerable children, but few studies have rigorously assessed their effectiveness in sub-Saharan Africa. We investigated the effects of unconditional cash transfers (UCTs) and conditional cash transfers (CCTs) on birth registration, vaccination uptake, and school attendance in children in Zimbabwe. Methods We did a matched, cluster-randomised controlled trial in ten sites in Manicaland, Zimbabwe. We divided each study site into three clusters. After a baseline survey between July, and September, 2009, clusters in each site were randomly assigned to UCT, CCT, or control, by drawing of lots from a hat. Eligible households contained children younger than 18 years and satisfied at least one other criteria: head of household was younger than 18 years; household cared for at least one orphan younger than 18 years, a disabled person, or an individual who was chronically ill; or household was in poorest wealth quintile. Between January, 2010, and January, 2011, households in UCT clusters collected payments every 2 months. Households in CCT clusters could receive the same amount but were monitored for compliance with several conditions related to child wellbeing. Eligible households in all clusters, including control clusters, had access to parenting skills classes and received maize seed and fertiliser in December, 2009, and August, 2010. Households and individuals delivering the intervention were not masked, but data analysts were. The primary endpoints were proportion of children younger than 5 years with a birth certificate, proportion younger than 5 years with up-to-date vaccinations, and proportion aged 6–12 years attending school at least 80% of the time. This trial is registered with ClinicalTrials.gov, number NCT00966849. Findings 1199 eligible households were allocated to the control group, 1525 to the UCT group, and 1319 to the CCT group. Compared with control clusters, the proportion of children aged 0–4 years with birth certificates had increased by 1·5% (95% CI −7·1 to 10·1) in the UCT group and by 16·4% (7·8–25·0) in the CCT group by the end of the intervention period. The proportions of children aged 0–4 years with complete vaccination records was 3·1% (−3·8 to 9·9) greater in the UCT group and 1·8% (−5·0 to 8·7) greater in the CCT group than in the control group. The proportions of children aged 6–12 years who attended school at least 80% of the time was 7·2% (0·8–13·7) higher in the UCT group and 7·6% (1·2–14·1) in the CCT group than in the control group. Interpretation Our results support strategies to integrate cash transfers into social welfare programming in sub-Saharan Africa, but further evidence is needed for the comparative effectiveness of UCT and CCT programmes in this region. Funding Wellcome Trust, the World Bank through the Partnership for Child Development, and the Programme of Support for the Zimbabwe National Action Plan for Orphans and Vulnerable Children.
The Lancet Global Health | 2014
Jeffrey W. Eaton; Nicolas A. Menzies; John Stover; Valentina Cambiano; Leonid Chindelevitch; Anne Cori; Jan A.C. Hontelez; Salal Humair; Cliff C. Kerr; Daniel J. Klein; Sharmistha Mishra; Kate M. Mitchell; Brooke E. Nichols; Peter Vickerman; Roel Bakker; Till Bärnighausen; Anna Bershteyn; David E. Bloom; Marie-Claude Boily; Stewart T. Chang; Ted Cohen; Peter J. Dodd; Christophe Fraser; Chaitra Gopalappa; Jens D. Lundgren; Natasha K. Martin; Evelinn Mikkelsen; Elisa Mountain; Quang D. Pham; Michael Pickles
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
Aids and Behavior | 2011
Jeffrey W. Eaton; Timothy B. Hallett; Geoffrey P. Garnett
) 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 countrys 2012 per-head gross domestic product (GDP; South Africa:
AIDS | 2009
Georges Reniers; Jeffrey W. Eaton
8040; Zambia:
PLOS ONE | 2014
Anne Cori; Helen Ayles; Nulda Beyers; Ab Schaap; Sian Floyd; Kalpana Sabapathy; Jeffrey W. Eaton; Katharina Hauck; Peter C. Smith; Sam Griffith; Ayana T. Moore; Deborah Donnell; Sten H. Vermund; Sarah Fidler; Richard Hayes; Christophe Fraser
1425; India:
Nature | 2015
Andrew N. Phillips; Amir Shroufi; Lara Vojnov; Jennifer Cohn; Teri Roberts; Tom Ellman; Kimberly Bonner; Christine Rousseau; Geoff P. Garnett; Valentina Cambiano; Fumiyo Nakagawa; Deborah Ford; Loveleen Bansi-Matharu; Alec Miners; Jens D. Lundgren; Jeffrey W. Eaton; Rosalind Parkes-Ratanshi; Zachary Katz; David Maman; Nathan Ford; Marco Vitoria; Meg Doherty; David Dowdy; Brooke E. Nichols; Maurine Murtagh; Meghan Wareham; Kara M. Palamountain; Christine Chakanyuka Musanhu; Wendy Stevens; David Katzenstein
1489; Vietnam:
PLOS Medicine | 2012
Marie-Claude Boily; Benoı̂t Mâsse; Ramzi Alsallaq; Nancy S. Padian; Jeffrey W. Eaton; Juan F. Vesga; Timothy B. Hallett
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
Journal of Acquired Immune Deficiency Syndromes | 2013
Timothy B. Hallett; Jeffrey W. Eaton
237 to
PLOS Medicine | 2012
Wim Delva; Jeffrey W. Eaton; Fei Meng; Christophe Fraser; Richard G. White; Peter Vickerman; Marie-Claude Boily; Timothy B. Hallett
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
AIDS | 2013
David A. M. C. van de Vijver; Brooke E. Nichols; Ume L. Abbas; Charles A. Boucher; Valentina Cambiano; Jeffrey W. Eaton; Robert Glaubius; Katrina A. Lythgoe; John W. Mellors; Andrew N. Phillips; Kim C. E. Sigaloff; Timothy B. Hallett
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