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David Brandling-Bennett

Bio: David Brandling-Bennett is an academic researcher from Pan American Health Organization. The author has contributed to research in topics: Chagas disease & Measles. The author has an hindex of 3, co-authored 6 publications receiving 749 citations.

Papers
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01 Jan 2015
TL;DR: The Global Technical Strategy for Malaria 2016-2030 emphasizes the need for universal coverage of core malaria interventions for all populations at risk and highlights the importance of using high-quality surveillance data for decision-making.
Abstract: The Global Technical Strategy for Malaria 2016–2030 was adopted by the World Health Assembly in May 2015. It provides a comprehensive framework to guide countries in their efforts to accelerate progress towards malaria elimination. The strategy sets the target of reducing global malaria incidence and mortality rates by at least 90% by 2030. It emphasizes the need for universal coverage of core malaria interventions for all populations at risk and highlights the importance of using high-quality surveillance data for decision-making. It also identifies areas where innovative solutions will be essential for attaining the goals, and summarizes the estimated global costs of implementation. The WHO strategy was developed in close alignment with the Roll Back Malaria Partnership's Action and Investment to defeat Malaria 2016-2030 – for a malaria-free world to ensure shared goals and complementarity.

580 citations

Journal ArticleDOI
17 Jan 1996-JAMA
TL;DR: The strategy currently used to control measles in most countries has been to immunize each successive birth cohort through the routine health services delivery system, while measles vaccine coverage has increased markedly, significant measles outbreaks have continued to recur.
Abstract: The strategy currently used to control measles in most countries has been to immunize each successive birth cohort through the routine health services delivery system. While measles vaccine coverage has increased markedly, significant measles outbreaks have continued to recur. During the past 5 years, experience in the Americas suggests that measles transmission has been interrupted in a number of countries (Cuba, Chile, and countries in the English-speaking Caribbean and successfully controlled in all remaining countries. Since 1991 these countries have implemented one-time "catch-up" vaccination campaigns (conducted during a short period, usually 1 week to 1 month, and targeting all children 9 months through 14 years of age, regardless of previous vaccination status or measles disease history). These campaigns have been followed by improvements in routine vaccination services and in surveillance systems, so that the progress of the measles elimination efforts can be sustained and monitored. Follow-up mass vaccination campaigns for children younger than 5 years are planned to take place every 3 to 5 years. ( JAMA . 1996;275:224-229)

250 citations

Journal ArticleDOI
01 May 1996-JAMA
TL;DR: It is agreed that an epidemiologically based mathematical model could provide valuable guidance in determining the appropriate interval for follow-up campaigns and that the longer the intervals between such campaigns, the more economical and feasible such a strategy would be.
Abstract: In Reply. —We thank Mr Gay and Dr Nokes for their comments concerning our article. In their letter, they question the use of the Pan American Health Organization's operational criterion of the accumulation of 1 birth cohort of susceptible preschool-aged children for determining the proper interval between follow-up campaigns. We agree with Gay and Nokes that an epidemiologically based mathematical model could provide valuable guidance in determining the appropriate interval for follow-up campaigns and that the longer the intervals between such campaigns, the more economical and feasible such a strategy would be. As noted, however, a more conservative strategy is currently recommended that for most countries will call for a "followup" campaign every 4 to 5 years. The present strategy was adopted for 2 principal reasons. Most important is the fact that, until now, measles transmission has never been interrupted over any large contiguous area for more than a matter

27 citations

Journal ArticleDOI

2 citations


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Journal ArticleDOI
08 Oct 2015-Nature
TL;DR: It is found that Plasmodium falciparum infection prevalence in endemic Africa halved and the incidence of clinical disease fell by 40% between 2000 and 2015, and interventions have averted 663 (542–753 credible interval) million clinical cases since 2000.
Abstract: Since the year 2000, a concerted campaign against malaria has led to unprecedented levels of intervention coverage across sub-Saharan Africa. Understanding the effect of this control effort is vital to inform future control planning. However, the effect of malaria interventions across the varied epidemiological settings of Africa remains poorly understood owing to the absence of reliable surveillance data and the simplistic approaches underlying current disease estimates. Here we link a large database of malaria field surveys with detailed reconstructions of changing intervention coverage to directly evaluate trends from 2000 to 2015, and quantify the attributable effect of malaria disease control efforts. We found that Plasmodium falciparum infection prevalence in endemic Africa halved and the incidence of clinical disease fell by 40% between 2000 and 2015. We estimate that interventions have averted 663 (542-753 credible interval) million clinical cases since 2000. Insecticide-treated nets, the most widespread intervention, were by far the largest contributor (68% of cases averted). Although still below target levels, current malaria interventions have substantially reduced malaria disease incidence across the continent. Increasing access to these interventions, and maintaining their effectiveness in the face of insecticide and drug resistance, should form a cornerstone of post-2015 control strategies.

2,135 citations

Book ChapterDOI
01 Jan 2008
TL;DR: This article is reproduced from the previous edition, volume 3, pp. 59–71, of Elsevier Inc.
Abstract: Reliable, comparable information about the main causes of disease and injury in populations, and how these are changing, is a critical input for debates about priorities in the health sector. Traditional sources of information about the descriptive epidemiology of diseases, injuries, and risk factors are generally incomplete, fragmented, and of uncertain reliability and comparability. The Global Burden of Disease (GBD) Study has provided a conceptual and methodological framework to quantify and compare the health of populations using a summary measure of both mortality and disability, the disability-adjusted life year (DALY). This article describes key features of the Global Burden of Disease analytic approach, the evolution of the GBD starting from the first study for the year 1990, and summarizes the methodological improvements incorporated into GBD revisions carried out by the World Health Organization. It also reviews controversies and criticisms, and examines priorities and issues for future GBD updates.

1,011 citations

Journal ArticleDOI
TL;DR: This report reviews the developmental arc of theoretical epidemiology with emphasis on vaccination, as it led from classical models assuming homogeneously mixing populations and ignoring human behavior, to recent models that account for behavioral feedback and/or population spatial/social structure.

789 citations

Journal ArticleDOI
TL;DR: In a systematic review and meta-analysis, Amitabh Suthar and colleagues describe the evidence base for different HIV testing and counseling services provided outside of health facilities.
Abstract: Background: Effective national and global HIV responses require a significant expansion of HIV testing and counselling (HTC) to expand access to prevention and care. Facility-based HTC, while essential, is unlikely to meet national and global targets on its own. This article systematically reviews the evidence for community-based HTC. first-time testers (RR 1.23, 95% CI 1.06-1.42), and the proportion of participants with CD4 counts above 350 cells/ml (RR 1.42, 95% CI 1.16-1.74), and obtained a lower positivity rate (RR 0.59, 95% CI 0.37-0.96), relative to facility-based approaches. 80% (95% CI 75%-85%) of 5,832 community-based HTC participants obtained a CD4 measurement following HIV diagnosis, and 73% (95% CI 61%-85%) of 527 community-based HTC participants initiated antiretroviral therapy following a CD4 measurement indicating eligibility. The data on linking participants without HIV to prevention services were limited. In low- and middle-income countries, the cost per person tested ranged from US$2-US$126. At the population level, community- based HTC increased HTC coverage (RR 7.07, 95% CI 3.52-14.22) and reduced HIV incidence (RR 0.86, 95% CI 0.73-1.02), although the incidence reduction lacked statistical significance. No studies reported any harm arising as a result of having been tested. Conclusions: Community-based HTC achieved high rates of HTC uptake, reached people with high CD4 counts, and linked people to care. It also obtained a lower HIV positivity rate relative to facility-based approaches. Further research is needed to further improve acceptability of community-based HTC for key populations. HIV programmes should offer community- based HTC linked to prevention and care, in addition to facility-based HTC, to support increased access to HIV prevention, care, and treatment. Review Registration: International Prospective Register of Systematic Reviews CRD42012002554 Please see later in the article for the Editors' Summary.

346 citations