Sarala Nicholas
Médecins Sans Frontières
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Featured researches published by Sarala Nicholas.
Emerging Infectious Diseases | 2013
Andrea Minetti; Matthew Kagoli; Agnes Katsulukuta; Helena Huerga; Amber Featherstone; Hazel Chiotcha; Delphine Noel; Cameron Bopp; Laurent Sury; Renzo Fricke; Marta Iscla; Northan Hurtado; Tanya Ducomble; Sarala Nicholas; Storn Kabuluzi; Rebecca F. Grais; Francisco J. Luquero
Supplementary immunization activities are crucial to reduce the number of susceptible children.
Journal of the International AIDS Society | 2011
Laurence Ahoua; Chantal Umutoni; Helena Huerga; Andrea Minetti; Elisabeth Szumilin; Suna Balkan; David Olson; Sarala Nicholas; Mar Pujades-Rodriguez
BackgroundAmong people living with HIV/AIDS, nutritional support is increasingly recognized as a critical part of the essential package of care, especially for patients in sub-Saharan Africa. The objectives of the study were to evaluate the outcomes of HIV-positive malnourished adults treated with ready-to-use therapeutic food and to identify factors associated with nutrition programme failure.MethodsWe present results from a retrospective cohort analysis of patients aged 15 years or older with a body mass index of less than 17 kg/m2 enrolled in three HIV/AIDS care programmes in Africa between March 2006 and August 2008. Factors associated with nutrition programme failure (patients discharged uncured after six or more months of nutritional care, defaulting from nutritional care, remaining in nutritional care for six or more months, or dead) were investigated using multiple logistic regression.ResultsOverall, 1340 of 8685 (15.4%) HIV-positive adults were enrolled in the nutrition programme. At admission, median body mass index was 15.8 kg/m2 (IQR 14.9-16.4) and 12% received combination antiretroviral therapy (ART). After a median of four months of follow up (IQR 2.2-6.1), 524 of 1106 (47.4%) patients were considered cured. An overall total of 531 of 1106 (48.0%) patients failed nutrition therapy, 132 (11.9%) of whom died and 250 (22.6%) defaulted from care. Men (OR = 1.5, 95% CI 1.2-2.0), patients with severe malnutrition at nutrition programme enrolment (OR = 2.2, 95% CI 1.7-2.8), and those never started on ART (OR = 4.5, 95% CI 2.7-7.7 for those eligible; OR = 1.6, 95% CI 1.0-2.5 for those ineligible for ART at enrolment) were at increased risk of nutrition programme failure. Diagnosed tuberculosis at nutrition programme admission or during follow up, and presence of diarrhoeal disease or extensive candidiasis at admission, were unrelated to nutrition programme failure.ConclusionsConcomitant administration of ART and ready-to-use therapeutic food increases the chances of nutritional recovery in these high-risk patients. While adequate nutrition is necessary to treat malnourished HIV patients, development of improved strategies for the management of severely malnourished patients with HIV/AIDS are urgently needed.
Journal of Acquired Immune Deficiency Syndromes | 2011
Sarala Nicholas; K Sabapathy; Cecilia Ferreyra; F Varaine; Mar Pujades-Rodriguez
Setting:Eight HIV programs in sub-Saharan Africa. Objective:To describe the incidence of pulmonary and extrapulmonary tuberculosis before and after the start of combined antiretroviral therapy (ART) and investigate associated risk factors. Design:Multicohort study. Adults enrolled between January 2006 and September 2008. Results:A total of 30,134 patients contributed 25,916 person-years of follow-up. The incidence of tuberculosis was 10.5 per 100 person-years during the pre-ART and 5.4 during the ART period. For all types of tuberculosis, incidence was similar in the pre-ART period and initial 3 months of ART but declined over time receiving ART (from 13 per 100 person-years in the first 3 months to 1.5 per 100 person-years after 12 months of therapy). Throughout follow-up, rates of pulmonary tuberculosis remained 2-fold to 3-fold higher than extrapulmonary tuberculosis rates. Smear-negative pulmonary tuberculosis was higher than smear-positive incidence and varied greatly across sites during the pre-ART period. Incidence was lower in rural sites, women, patients without prior history of tuberculosis, body mass index ≥18.5 kg/m2, and ≥200 nadir CD4 cells per microliter. Recurrence rate was 1.7 per 100 person-years (95% confidence interval: 1.0 to 2.8). Conclusions:Our findings show the high burden that tuberculosis represents for HIV programs and highlight the importance of earlier ART start and the need to implement intensified tuberculosis finding, isoniazide prophylaxis, and infection control.
AIDS | 2012
David Maman; Mar Pujades-Rodriguez; Sarala Nicholas; Megan McGuire; Elisabeth Szumilin; René Ecochard; Jean-François Etard
Objective:We investigated the association between immune response and mortality in four HIV African programs supported by Médecins Sans Frontières. Design:Multicentric retrospective cohort study. Methods:All antiretroviral therapy (ART) naive adults (>15 years) who initiated therapy between March 2001 and November 2010 and receiving therapy for 9 months or more were included. We described the evolution of mortality over time. Mixed Poisson models were used to assess the effect of updated CD4 cell counts and other potential risk factors on mortality. Findings:A total of 24 037 patients, of which 68% were women, contributed 69 516.2 person-years of follow-up. At ART initiation, 5718 patients (23.7%) were classified as WHO clinical stage 4, 1587 (6.6%) had a BMI below 16 kg/m2 and 2568 (10.7%) had CD4 cell count below 50 cells/&mgr;l. A total of 568 (2.4%) deaths were recorded during the study period. In the CD4 response categories 500 cells/&mgr;l or more, 350–499, 200–349, 50–199 cells/&mgr;l and less than 50 cells/&mgr;l, unadjusted mortality rates were 0.36; 0.58; 0.88; 1.91 and 7.43 per 100 person-years, respectively. In multivariate analysis, higher mortality was observed in patients with CD4 response levels 350–499 cells/&mgr;l [adjusted hazard ratio (aHR) 1.70, 95% confidence interval (CI) 1.26–2.30] and for those between 200–349 (aHR 2.56; 95% CI 1.93–3.38), compared to those with 500 cells/&mgr;l or more. Interpretation:The observed higher survival of patients with a CD4 response to ART higher than 500 cells/&mgr;l supports the need of further research to evaluate the individual benefit of initiating ART at higher CD4 levels in sub-Saharan Africa.
International Journal of Social Psychiatry | 2011
Renato Souza; Klaudia Porten; Sarala Nicholas; Rebecca F. Grais
Background: There is little evidence to describe the feasibility and outcomes of services for the care of street children and youth in low-income countries. Aims: To describe the outcomes of a multidisciplinary case management approach delivered in a drop-in centre for street children and youth. Methods: A longitudinal study of street children and youth followed in an urban drop-in centre. Four hundred (400) street children and youth received a multidisciplinary case management therapeutic package based on the community reinforcement approach. The main outcomes were changes in psychological distress, substance abuse and social situation scores. Results: The median follow-up time for the cohort was 18 months. There were reductions in the levels of psychological distress (p = 0.0001) and substance abuse (p ≤ 0.0001) in the cohort as well as an improvement in the social situation of street children and youth (p = 0.0001). There was a main effect of gender (p < 0.001) and a significant interaction of gender over time (p < 0.001) on improvements in levels of psychological distress. Survival analysis showed that the probability of remaining on substances at 12 months was 0.76 (95% CI: 0.69–0.81) and 0.51 (95% CI: 0.42–0.59) at 24 months. At 12 months, fewer female patients remained using substances compared to male (p < 0.01). Conclusion: To be most effective, programmes and strategies for children and youth in street situations in developing countries should target both their health and social needs.
PLOS Neglected Tropical Diseases | 2015
Anne Laure Page; Iza Ciglenecki; Ernest Robert Jasmin; Laurence Desvignes; Francesco Grandesso; Jonathan Polonsky; Sarala Nicholas; Kathryn Alberti; Klaudia Porten; Francisco J. Luquero
Background In 2010 and 2011, Haiti was heavily affected by a large cholera outbreak that spread throughout the country. Although national health structure-based cholera surveillance was rapidly initiated, a substantial number of community cases might have been missed, particularly in remote areas. We conducted a community-based survey in a large rural, mountainous area across four districts of the Nord department including areas with good versus poor accessibility by road, and rapid versus delayed response to the outbreak to document the true cholera burden and assess geographic distribution and risk factors for cholera mortality. Methodology/Principal Findings A two-stage, household-based cluster survey was conducted in 138 clusters of 23 households in four districts of the Nord Department from April 22nd to May 13th 2011. A total of 3,187 households and 16,900 individuals were included in the survey, of whom 2,034 (12.0%) reported at least one episode of watery diarrhea since the beginning of the outbreak. The two more remote districts, Borgne and Pilate were most affected with attack rates up to 16.2%, and case fatality rates up to 15.2% as compared to the two more accessible districts. Care seeking was also less frequent in the more remote areas with as low as 61.6% of reported patients seeking care. Living in remote areas was found as a risk factor for mortality together with older age, greater severity of illness and not seeking care. Conclusions/Significance These results highlight important geographical disparities and demonstrate that the epidemic caused the highest burden both in terms of cases and deaths in the most remote areas, where up to 5% of the population may have died during the first months of the epidemic. Adapted strategies are needed to rapidly provide treatment as well as prevention measures in remote communities.
Tropical Medicine & International Health | 2012
Heidi Spillane; Sarala Nicholas; Zhirong Tang; Elisabeth Szumilin; Suna Balkan; Mar Pujades-Rodriguez
Objectives To identify factors influencing mortality in an HIV programme providing care to large numbers of injecting drug users (IDUs) and patients co‐infected with hepatitis C (HCV).
PLOS Neglected Tropical Diseases | 2015
Lise Grout; Isabel Martinez-Pino; Iza Ciglenecki; Sakoba Keita; Alpha Amadou Diallo; Balla Traore; Daloka Delamou; Oumar Toure; Sarala Nicholas; Barbara Rusch; Nelly Staderini; Micaela Serafini; Rebecca F. Grais; Francisco J. Luquero
Introduction Since 2010, WHO has recommended oral cholera vaccines as an additional strategy for cholera control. During a cholera episode, pregnant women are at high risk of complications, and the risk of fetal death has been reported to be 2–36%. Due to a lack of safety data, pregnant women have been excluded from most cholera vaccination campaigns. In 2012, reactive campaigns using the bivalent killed whole-cell oral cholera vaccine (BivWC), included all people living in the targeted areas aged ≥1 year regardless of pregnancy status, were implemented in Guinea. We aimed to determine whether there was a difference in pregnancy outcomes between vaccinated and non-vaccinated pregnant women. Methods and Findings From 11 November to 4 December 2013, we conducted a retrospective cohort study in Boffa prefecture among women who were pregnant in 2012 during or after the vaccination campaign. The primary outcome was pregnancy loss, as reported by the mother, and fetal malformations, after clinical examination. Primary exposure was the intake of the BivWC vaccine (Shanchol) during pregnancy, as determined by a vaccination card or oral history. We compared the risk of pregnancy loss between vaccinated and non-vaccinated women through binomial regression analysis. A total of 2,494 pregnancies were included in the analysis. The crude incidence of pregnancy loss was 3.7% (95%CI 2.7–4.8) for fetuses exposed to BivWC vaccine and 2.6% (0.7–4.5) for non-exposed fetuses. The incidence of malformation was 0.6% (0.1–1.0) and 1.2% (0.0–2.5) in BivWC-exposed and non-exposed fetuses, respectively. In both crude and adjusted analyses, fetal exposure to BivWC was not significantly associated with pregnancy loss (adjusted risk ratio (aRR = 1.09 [95%CI: 0.5–2.25], p = 0.818) or malformations (aRR = 0.50 [95%CI: 0.13–1.91], p = 0.314). Conclusions In this large retrospective cohort study, we found no association between fetal exposure to BivWC and risk of pregnancy loss or malformation. Despite the weaknesses of a retrospective design, we can conclude that if a risk exists, it is very low. Additional prospective studies are warranted to add to the evidence base on OCV use during pregnancy. Pregnant women are particularly vulnerable during cholera episodes and should be included in vaccination campaigns when the risk of cholera is high, such as during outbreaks.
American Journal of Tropical Medicine and Hygiene | 2016
Paul Loubet; Romain Palich; Richard Kojan; Olivier Peyrouset; Christine Danel; Sarala Nicholas; Mamoudou Conde; Klaudia Porten; Augustin Augier; Yazdan Yazdanpanah
BMC Research Notes | 2014
Silvia Mancini; Matthew E. Coldiron; Sarala Nicholas; Augusto E. Llosa; Isabelle Mouniaman-Nara; Joseph Ngala; Rebecca F. Grais; Klaudia Porten