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Dive into the research topics where Claire M. Wagner is active.

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Featured researches published by Claire M. Wagner.


BMJ | 2013

Reduced premature mortality in Rwanda: lessons from success.

Paul Farmer; Cameron T Nutt; Claire M. Wagner; Claude Sekabaraga; Tej Nuthulaganti; Jonathan Weigel; Didi Bertrand Farmer; Antoinette Habinshuti; Soline Dusabeyesu Mugeni; Jean-Claude Karasi; Peter Drobac

Rwanda’s approach to delivering healthcare in a setting of post-conflict poverty offers lessons for other poor countries, say Paul Farmer and colleagues


The New England Journal of Medicine | 2013

The Human Resources for Health Program in Rwanda — A New Partnership

Agnes Binagwaho; Patrick Kyamanywa; Paul Farmer; Tej Nuthulaganti; Benoite Umubyeyi; Soline Dusabeyesu Mugeni; Anita Asiimwe; Uzziel Ndagijimana; Helen Lamphere McPherson; Jean de Dieu Ngirabega; Anne Sliney; Agnes Uwayezu; Vincent Rusanganwa; Claire M. Wagner; Cameron T Nutt; Mark Eldon-Edington; Corrado Cancedda; Ira C. Magaziner; Eric Goosby

The authors discuss the Human Resources for Health Program, which is working to improve the quality and quantity of health professionals in Rwanda by means of sustained collaborations with U.S. schools of medicine, nursing, dentistry, and public health.


The Lancet | 2014

Rwanda 20 years on: investing in life

Agnes Binagwaho; Paul Farmer; Sabin Nsanzimana; Corine Karema; Michel Gasana; Jean de Dieu Ngirabega; Fidele Ngabo; Claire M. Wagner; Cameron T Nutt; Thierry Nyatanyi; Maurice Gatera; Yvonne Kayiteshonga; Cathy Mugeni; Placidie Mugwaneza; Joseph Shema; Parfait Uwaliraye; Erick Gaju; Marie Aimee Muhimpundu; Theophile Dushime; Florent Senyana; Jean Baptiste Mazarati; Celsa Muzayire Gaju; Lisine Tuyisenge; Vincent Mutabazi; Patrick Kyamanywa; Vincent Rusanganwa; Jean Pierre Nyemazi; Agathe Umutoni; Ida Kankindi; Christian R Ntizimira

Two decades ago, the genocide against the Tutsis in Rwanda led to the deaths of 1 million people, and the displacement of millions more. Injury and trauma were followed by the effects of a devastated health system and economy. In the years that followed, a new course set by a new government set into motion equity-oriented national policies focusing on social cohesion and people-centred development. Premature mortality rates have fallen precipitously in recent years, and life expectancy has doubled since the mid-1990s. Here we reflect on the lessons learned in rebuilding Rwandas health sector during the past two decades, as the country now prepares itself to take on new challenges in health-care delivery.


Global health, science and practice | 2014

Nationwide implementation of integrated community case management of childhood illness in Rwanda

Catherine Mugeni; Adam C. Levine; Richard B. Mark Munyaneza; Epiphanie Mulindahabi; Hannah Cockrell; Justin Glavis-Bloom; Cameron T Nutt; Claire M. Wagner; Erick Gaju; Alphonse Rukundo; Jean Pierre Habimana; Corine Karema; Fidele Ngabo; Agnes Binagwaho

Between 2008 and 2011, Rwanda introduced iCCM of childhood illness nationwide. One year after iCCM rollout, community-based treatment for diarrhea and pneumonia had increased significantly, and under-5 mortality and overall health facility use had declined significantly. Between 2008 and 2011, Rwanda introduced iCCM of childhood illness nationwide. One year after iCCM rollout, community-based treatment for diarrhea and pneumonia had increased significantly, and under-5 mortality and overall health facility use had declined significantly. ABSTRACT Background: Between 2008 and 2011, Rwanda introduced integrated community case management (iCCM) of childhood illness nationwide. Community health workers in each of Rwandas nearly 15,000 villages were trained in iCCM and equipped for empirical diagnosis and treatment of pneumonia, diarrhea, and malaria; for malnutrition surveillance; and for comprehensive reporting and referral services. Methods: We used data from the Rwanda health management information system (HMIS) to calculate monthly all-cause under-5 mortality rates, health facility use rates, and community-based treatment rates for childhood illness in each district. We then compared a 3-month baseline period prior to iCCM implementation with a seasonally matched comparison period 1 year after iCCM implementation. Finally, we compared the actual changes in all-cause child mortality and health facility use over this time period with the changes that would have been expected based on baseline trends in Rwanda. Results: The number of children receiving community-based treatment for diarrhea and pneumonia increased significantly in the 1-year period after iCCM implementation, from 0.83 cases/1,000 child-months to 3.80 cases/1,000 child-months (P = .01) and 0.25 cases/1,000 child-months to 5.28 cases/1,000 child-months (P<.001), respectively. On average, total under-5 mortality rates declined significantly by 38% (P<.001), and health facility use declined significantly by 15% (P = .006). These decreases were significantly greater than would have been expected based on baseline trends. Conclusions: This is the first study to demonstrate decreases in both child mortality and health facility use after implementing iCCM of childhood illness at a national level. While our study design does not allow for direct attribution of these changes to implementation of iCCM, these results are in line with those of prior studies conducted at the sub-national level in other low-income countries.


Nature Reviews Cancer | 2014

Bringing cancer care to the poor: experiences from Rwanda.

Lawrence N. Shulman; Tharcisse Mpunga; Neo Tapela; Claire M. Wagner; Temidayo Fadelu; Agnes Binagwaho

The knowledge and tools to cure many cancer patients exist in developed countries but are unavailable to many who live in the developing world, resulting in unnecessary loss of life. Bringing cancer care to the poor, particularly to low-income countries, is a great challenge, but it is one that we believe can be met through partnerships, careful planning and a set of guiding principles. Alongside vaccinations, screening and other cancer-prevention efforts, treatment must be a central component of any cancer programme from the start. It is also critical that these programmes include implementation research to determine programmatic efficacy, where gaps in care still exist and where improvements can be made. This article discusses these issues using the example of Rwandas expanding national cancer programme.


Academic Medicine | 2014

Enhancing formal educational and in-service training programs in rural Rwanda: a partnership among the public sector, a nongovernmental organization, and academia.

Corrado Cancedda; Paul Farmer; Patrick Kyamanywa; Robert Riviello; Joseph Rhatigan; Claire M. Wagner; Fidele Ngabo; Manzi Anatole; Peter Drobac; Tharcisse Mpunga; Cameron T Nutt; Jean Baptiste Kakoma; Joia S. Mukherjee; Chadi Cortas; Jeanine Condo; Fabien Ntaganda; Gene Bukhman; Agnes Binagwaho

Global disparities in the distribution, specialization, diversity, and competency of the health workforce are striking. Countries with fewer health professionals have poorer health outcomes compared with countries that have more. Despite major gains in health indicators, Rwanda still suffers from a severe shortage of health professionals. This article describes a partnership launched in 2005 by Rwanda’s Ministry of Health with the U.S. nongovernmental organization Partners In Health and with Harvard Medical School and Brigham and Women’s Hospital. The partnership has expanded to include the Faculty of Medicine and the School of Public Health at the National University of Rwanda and other Harvard-affiliated academic medical centers. The partnership prioritizes local ownership and—with the ultimate goals of strengthening health service delivery and achieving health equity for poor and underserved populations—it has helped establish new or strengthen existing formal educational programs (conferring advanced degrees) and in-service training programs (fostering continuing professional development) targeting the local health workforce. Harvard Medical School and Brigham and Women’s Hospital have also benefited from the partnership, expanding the opportunities for training and research in global health available to their faculty and trainees. The partnership has enabled Rwandan health professionals at partnership-supported district hospitals to acquire new competencies and deliver better health services to rural and underserved populations by leveraging resources, expertise, and growing interest in global health within the participating U.S. academic institutions. Best practices implemented during the partnership’s first nine years can inform similar formal educational and in-service training programs in other low-income countries.


Globalization and Health | 2013

Shared learning in an interconnected world: innovations to advance global health equity

Agnes Binagwaho; Cameron T Nutt; Vincent Mutabazi; Corine Karema; Sabin Nsanzimana; Michel Gasana; Peter Drobac; Michael W. Rich; Parfait Uwaliraye; Jean Pierre Nyemazi; Michael R. Murphy; Claire M. Wagner; Andrew Makaka; Hinda Ruton; Gita N. Mody; Danielle R. Zurovcik; Jonathan A. Niconchuk; Cathy Mugeni; Fidele Ngabo; Jean de Dieu Ngirabega; Anita Asiimwe; Paul Farmer

The notion of “reverse innovation”--that some insights from low-income countries might offer transferable lessons for wealthier contexts--is increasingly common in the global health and business strategy literature. Yet the perspectives of researchers and policymakers in settings where these innovations are developed have been largely absent from the discussion to date. In this Commentary, we present examples of programmatic, technological, and research-based innovations from Rwanda, and offer reflections on how the global health community might leverage innovative partnerships for shared learning and improved health outcomes in all countries.


Journal of the International AIDS Society | 2012

HIV-free survival among nine- to 24-month-old children born to HIV-positive mothers in the Rwandan national PMTCT programme: a community-based household survey

Hinda Ruton; Placidie Mugwaneza; Nadine Shema; Alexandre Lyambabaje; Jean Bizimana; Landry Tsague; Elevanie Nyankesha; Claire M. Wagner; Vincent Mutabazi; Jean Pierre Nyemazi; Sabin Nsanzimana; Corine Karema; Agnes Binagwaho

BackgroundOperational effectiveness of large-scale national programmes for the prevention of mother to child transmission (PMTCT) of HIV in sub-Saharan Africa remains limited. We report on HIV-free survival among nine- to 24-month-old children born to HIV-positive mothers in the national PMTCT programme in Rwanda.MethodsWe conducted a national representative household survey between February and May 2009. Participants were mothers who had attended antenatal care at least once during their most recent pregnancy, and whose children were aged nine to 24 months. A two-stage stratified (geographic location of PMTCT site, maternal HIV status during pregnancy) cluster sampling was used to select mother-infant pairs to be interviewed during household visits. Alive children born from HIV-positive mothers (HIV-exposed children) were tested for HIV according to routine HIV testing protocol. We calculated HIV-free survival at nine to 24 months. We subsequently determined factors associated with mother to child transmission of HIV, child death and HIV-free survival using logistic regression.ResultsOut of 1448 HIV-exposed children surveyed, 44 (3.0%) were reported dead by nine months of age. Of the 1340 children alive, 53 (4.0%) tested HIV positive. HIV-free survival was estimated at 91.9% (95% confidence interval: 90.4-93.3%) at nine to 24 months. Adjusting for maternal, child and health system factors, being a member of an association of people living with HIV (adjusted odds ratio: 0.7, 95% CI: 0.1-0.995) improved by 30% HIV-free survival among children, whereas the maternal use of a highly active antiretroviral therapy (HAART) regimen for PMTCT (aOR: 0.6, 95% CI: 0.3-1.07) had a borderline effect.ConclusionsHIV-free survival among HIV-exposed children aged nine to 24 months is estimated at 91.9% in Rwanda. The national PMTCT programme could achieve greater impact on child survival by ensuring access to HAART for all HIV-positive pregnant women in need, improving the quality of the programme in rural areas, and strengthening linkages with community-based support systems, including associations of people living with HIV.


Journal of Clinical Oncology | 2016

Proposing Essential Medicines to Treat Cancer: Methodologies, Processes, and Outcomes

Lawrence N. Shulman; Claire M. Wagner; Ronald Barr; Gilberto Lopes; Giuseppe Longo; Jane Robertson; Gilles Forte; Julie Torode; Nicola Magrini

PURPOSE A great proportion of the worlds cancer burden resides in low- and middle-income countries where cancer care infrastructure is often weak or absent. Although treatment of cancer is multidisciplinary, involving surgery, radiation, systemic therapies, pathology, radiology, and other specialties, selection of medicines that have impact and are affordable has been particularly challenging in resource-constrained settings. In 2014, at the invitation of the WHO, the Union for International Cancer Control convened experts to develop an approach to propose essential cancer medicines to be included in the WHO Model Essential Medicines Lists (EML) for Adults and for Children, as well as a resulting new list of cancer medicines. METHODS Experts identified 29 cancer types with potential for maximal treatment impact, on the basis of incidence and benefit of systemic therapies. More than 90 oncology experts from all continents drafted and reviewed disease-based documents outlining epidemiology, diagnostic needs, treatment options, and benefits and toxicities. RESULTS Briefing documents were created for each disease, along with associated standard treatment regimens, resulting in a list of 52 cancer medicines. A comprehensive application was submitted as a revision to the existing cancer medicines on the WHO Model Lists. In May 2015, the WHO announced the addition of 16 medicines to the Adult EML and nine medicines to the Childrens EML. CONCLUSION The list of medications proposed, and the ability to link each recommended medicine to specific diseases, should allow public officials to apply resources most effectively in developing and supporting nascent or growing cancer treatment programs.


PLOS ONE | 2013

Prevention of Mother-To-Child Transmission of HIV: Cost-Effectiveness of Antiretroviral Regimens and Feeding Options in Rwanda

Agnes Binagwaho; Elisabetta Pegurri; Peter Drobac; Placidie Mugwaneza; Sara Stulac; Claire M. Wagner; Corine Karema; Landry Tsague

Background Rwandas National PMTCT program aims to achieve elimination of new HIV infections in children by 2015. In November 2010, Rwanda adopted the WHO 2010 ARV guidelines for PMTCT recommending Option B (HAART) for all HIV-positive pregnant women extended throughout breastfeeding and discontinued (short course-HAART) only for those not eligible for life treatment. The current study aims to assess the cost-effectiveness of this policy choice. Methods Based on a cohort of HIV-infected pregnant women in Rwanda, we modelled the cost-effectiveness of six regimens: dual ARV prophylaxis with either 12 months breastfeeding or replacement feeding; short course HAART (Sc-HAART) prophylaxis with either 6 months breastfeeding, 12 months breastfeeding, or 18 months breastfeeding; and Sc-HAART prophylaxis with replacement feeding. Direct costs were modelled based on all inputs in each scenario and related unit costs. Effectiveness was evaluated by measuring HIV-free survival at 18 months. Savings correspond to the lifetime costs of HIV treatment and care avoided as a result of all vertical HIV infections averted. Results All PMTCT scenarios considered are cost saving compared to “no intervention.” Sc-HAART with 12 months breastfeeding or 6 months breastfeeding dominate all other scenarios. Sc-HAART with 12 months breastfeeding allows for more children to be alive and HIV-uninfected by 18 months than Sc-HAART with 6 months breastfeeding for an incremental cost per child alive and uninfected of 11,882 USD. This conclusion is sensitive to changes in the relative risk of mortality by 18 months for exposed HIV-uninfected children on replacement feeding from birth and those who were breastfed for only 6 months compared to those breastfeeding for 12 months or more. Conclusion Our findings support the earlier decision by Rwanda to adopt WHO Option B and could inform alternatives for breastfeeding duration. Local contexts and existing care delivery models should be part of national policy decisions.

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Sabin Nsanzimana

Swiss Tropical and Public Health Institute

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Fidele Ngabo

Université libre de Bruxelles

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