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Institution

International Centre for Diarrhoeal Disease Research, Bangladesh

FacilityDhaka, Bangladesh
About: International Centre for Diarrhoeal Disease Research, Bangladesh is a facility organization based out in Dhaka, Bangladesh. It is known for research contribution in the topics: Population & Vibrio cholerae. The organization has 3103 authors who have published 5238 publications receiving 226880 citations. The organization is also known as: SEATO Cholera Research Laboratory & Bangladesh International Centre for Diarrhoeal Disease Research.


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Journal ArticleDOI
Elisabeth Njamkepo1, Nizar Fawal1, Alicia Tran-Dien1, Jane Hawkey2, Nancy Strockbine3, Claire Jenkins4, Kaisar A. Talukder5, Raymond Bercion1, Konstantin V. Kuleshov, Renáta Kolínská, Julie E. Russell4, Lidia Kaftyreva1, Marie Accou-Demartin1, Andreas Karas6, Olivier Vandenberg7, Alison E. Mather8, Alison E. Mather9, Carl J. Mason, Andrew J. Page9, Thandavarayan Ramamurthy, Chantal Bizet1, Andrzej Gamian, Isabelle Carle1, Amy Gassama Sow1, Christiane Bouchier1, Astrid Louise Wester10, Monique Lejay-Collin1, Marie-Christine Fonkoua, Simon Le Hello1, Martin J. Blaser11, Cecilia Jernberg12, Corinne Ruckly1, Audrey Mérens, Anne-Laure Page, Martin Aslett9, Peter Roggentin, Angelika Fruth13, Erick Denamur14, Malabi M. Venkatesan15, Herve Bercovier16, Ladaporn Bodhidatta, Chien-Shun Chiou3, Dominique Clermont1, Bianca Colonna17, S. A. Egorova1, Gururaja P. Pazhani, Analia V. Ezernitchi18, Ghislaine Guigon1, Simon R. Harris9, Hidemasa Izumiya19, Agnieszka Korzeniowska-Kowal, Anna Lutyńska, Malika Gouali1, Francine Grimont1, Céline Langendorf, Monika Marejková, Lorea A. M. Peterson20, Guillermo I. Perez-Perez11, Antoinette Ngandjio, Alexander Podkolzin, Erika Souche1, M. A. Makarova1, German A. Shipulin, Changyun Ye21, Helena Žemličková22, Mária Herpay, Patrick A. D. Grimont1, Julian Parkhill9, Philippe J. Sansonetti1, Kathryn E. Holt2, Sylvain Brisse23, Sylvain Brisse1, Nicholas R. Thomson9, Nicholas R. Thomson24, François-Xavier Weill9, François-Xavier Weill1 
TL;DR: It is shown that Shigella dysenteriae type 1 has existed since at least the eighteenth century and that it swept the globe at the end of the nineteenth century, diversifying into distinct lineages associated with the First World War, Second World War and various conflicts or natural disasters across Africa, Asia and Central America.
Abstract: Together with plague, smallpox and typhus, epidemics of dysentery have been a major scourge of human populations for centuries(1). A previous genomic study concluded that Shigella dysenteriae type 1 (Sd1), the epidemic dysentery bacillus, emerged and spread worldwide after the First World War, with no clear pattern of transmission(2). This is not consistent with the massive cyclic dysentery epidemics reported in Europe during the eighteenth and nineteenth centuries(1,3,4) and the first isolation of Sd1 in Japan in 1897(5). Here, we report a whole-genome analysis of 331 Sd1 isolates from around the world, collected between 1915 and 2011, providing us with unprecedented insight into the historical spread of this pathogen. We show here that Sd1 has existed since at least the eighteenth century and that it swept the globe at the end of the nineteenth century, diversifying into distinct lineages associated with the First World War, Second World War and various conflicts or natural disasters across Africa, Asia and Central America. We also provide a unique historical perspective on the evolution of antibiotic resistance over a 100-year period, beginning decades before the antibiotic era, and identify a prevalent multiple antibiotic-resistant lineage in South Asia that was transmitted in several waves to Africa, where it caused severe outbreaks of disease.

67 citations

Journal ArticleDOI
TL;DR: During the period under study, perinatal mortality declined regularly and significantly over time in an area covered by an intensive Family Planning and Health Services programme, but not in the adjacent control area, raising the issue of the impact of such a programme upon perinnatal mortality.
Abstract: In 1986 as part of the ongoing Demographic Surveillance System of the International Centre for Diarrhoeal Disease Research Bangladesh health workers regularly visited households in Matlab district to record vital events and other demographic data. They recorded 497 fetal deaths and early neonatal deaths. Low birth weight contributed to 25% of fetal deaths followed by prolonged labor (19%) maternal medical problems (13%) malpresentation at term (12%) and twins (2%). The cause of fetal death for 28% could not be determined. Similarly low birth weight causes 63% of very early neonatal deaths followed by prolonged labor (31%) and 37% and 15% respectively in 4-7 day old neonates. The 2nd leading cause of death for 4-7 day old neonates was neonatal tetanus (25%w0. Males were more likely to die from tetanus than females (relative risk=4.3; p=.015). The women at lowest risk included those 20-24 years old who were pregnant for the 2nd-3rd time those 25-29 years old who were pregnant for the 4th-5th time and those 30-34-years old who were pregnant for the 6th-7th time. Even though the perinatal mortality rates in the study and comparison areas in Matlab did not significantly differ (74 and 75 total births/1000) the rate fell significantly from 82 (1979) to 65 (1986) in the area where maternal and child health and family planning services (MCH-FP) existed (p<.001). Further the rate declined significantly more in the 2nd half of the study period (1983-1986) than in the 1st half (1979-1982) in the MCH-FP area (p<.002). Moreover the difference between the 2 areas was only significant in the 2nd half (p<.04). Perinatal mortality was highest from August to December. The researchers credit the tetanus toxoid as having more of an impact on reducing the perinatal mortality in the study area than family planning interventions.

67 citations

Journal ArticleDOI
16 Sep 2014-PLOS ONE
TL;DR: Post-discharge mortality was common in Bangladeshi children following inpatient care for severe malnutrition and pneumonia, and the underlying contributing factors require a better understanding to inform the potential of interventions that could improve survival.
Abstract: Background: Post-discharge mortality among children with severe illness in resource-limited settings is under-recognized and there are limited data. We evaluated post-discharge mortality in a recently reported cohort of children with severe malnutrition and pneumonia, and identified characteristics associated with an increased risk of death.Methods: Young children (< 5 years of age) with severe malnutrition (WHO criteria) and radiographic pneumonia on admission to Dhaka Hospital of icddr, b over a 15-month period were managed according to standard protocols. Those discharged were followed-up and survival status at 12 weeks post-discharge was determined. Verbal autopsy was requested from families of those that died.Results: Of 405 children hospitalized with severe malnutrition and pneumonia, 369 (median age, 10 months) were discharged alive with a follow-up plan. Of these, 32 (8.7%) died in the community within 3 months of discharge: median 22 (IQR 9-35) days from discharge to death. Most deaths were reportedly associated with acute onset of new respiratory or gastrointestinal symptoms. Those that died following discharge were significantly younger (median 6 [IQR 3,12] months) and more severely malnourished, on admission and on discharge, than those that survived. Bivariate analysis found that severe wasting on admission (OR 3.64, 95% CI 1.66-7.97) and age,12 months (OR 2.54, 95% CI 1.1-8.8) were significantly associated with post-discharge death. Of those that died in the community, none had attended a scheduled follow-up and care-seeking from a traditional healer was more common (p, 0.001) compared to those who survived.Conclusion and Significance: Post-discharge mortality was common in Bangladeshi children following inpatient care for severe malnutrition and pneumonia. The underlying contributing factors require a better understanding to inform the potential of interventions that could improve survival.

67 citations

Journal ArticleDOI
TL;DR: The antidiarrheal effects of green banana and pectin are mediated by improvement of small intestinal permeability in addition to their known colonotrophic effects.
Abstract: To evaluate the effects of green banana and pectin (nondigestible, dietary sources of colonic short-chain fatty acids [SCFA]) on intestinal permeability, 57 boys (5–12 months) with persistent diarrhea (≥14 days) were given a week's treatment with a rice-based diet containing either cooked green banana (n=19), pectin (n=17), or rice diet alone (n=21). Intestinal permeability was assessed before and after treatment by giving a lactulose–mannitol (LM) drink and measuring urinary recovery after 5 hr. Treatment with banana significantly (P<0.05) reduced lactulose recovery, increased mannitol recovery, and decreased the LM ratio, indicating improvement of permeability. Pectin produced similar results. Permeability changes were associated with a 50% reduction in stool weights which correlated strongly (green banana, r2 = 0.84, pectin, r2 = 0.86) with the LM ratio. Green banana-derived and SCFA-mediated stimulation of colonic as well as small bowel absorption is responsible for their antidiarrheal effects. The antidiarrheal effects of green banana and pectin are mediated by improvement of small intestinal permeability in addition to their known colonotrophic effects.

67 citations

Journal ArticleDOI
TL;DR: The high attack rate suggesting that the infection was new to this area, and the increased risk among adult women suggests that risk of transmission may have been higher around households, suggests that this outbreak was due to Chikungunya.
Abstract: Background The first identified Chikungunya outbreak occurred in Bangladesh in 2008. In late October 2011, a local health official from Dohar Sub-district, Dhaka District, reported an outbreak of undiagnosed fever and joint pain. We investigated the outbreak to confirm the etiology, describe the clinical presentation, and identify associated vectors.

67 citations


Authors

Showing all 3121 results

NameH-indexPapersCitations
Stanley Falkow13434962461
Myron M. Levine12378960865
Roger I. Glass11647449151
Robert F. Breiman10547343927
Harry B. Greenberg10043334941
Barbara J. Stoll10039042107
Andrew M. Prentice9955046628
Robert H. Gilman9690343750
Robert E. Black9220156887
Johan Ärnlöv9138690490
Juan Jesus Carrero8952266970
John D. Clemens8950628981
William A. Petri8550726906
Toshifumi Hibi8280828674
David A. Sack8043723320
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20235
202234
2021494
2020414
2019391
2018334