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Risk factors for mortality of children with zoonotic visceral leishmaniasis in Central Tunisia
BACKGROUND: Zoonotic visceral leishmaniasis (ZVL) caused by Leishmania infantum is endemic with an epidemiological profile of a paediatric disease in Tunisia. In the context of a high fatality rate, identifying risk factors for in-hospital mortality in children treated for ZVL is of major epidemiolo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5747430/ https://www.ncbi.nlm.nih.gov/pubmed/29287082 http://dx.doi.org/10.1371/journal.pone.0189725 |
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author | Ben Helel, Khaled Ben Rejeb, Mohamed Habboul, Zakia Khattat, Nizar Mejaouel, Houssain Said-Latiri, Houyem Kaabi, Belhassen Zhioua, Elyes |
author_facet | Ben Helel, Khaled Ben Rejeb, Mohamed Habboul, Zakia Khattat, Nizar Mejaouel, Houssain Said-Latiri, Houyem Kaabi, Belhassen Zhioua, Elyes |
author_sort | Ben Helel, Khaled |
collection | PubMed |
description | BACKGROUND: Zoonotic visceral leishmaniasis (ZVL) caused by Leishmania infantum is endemic with an epidemiological profile of a paediatric disease in Tunisia. In the context of a high fatality rate, identifying risk factors for in-hospital mortality in children treated for ZVL is of major epidemiological importance. DESIGN: A retrospective (case-control) study included 230 immuno-competent children diagnosed and confirmed with primary ZVL in the paediatric department of the University Hospital of Kairouan between 2004 and 2014. Forty-seven per cent (47%) were children under 18 months of age, and with a male ⁄ female ratio of 1.01:1. RESULTS: The overall case-fatality was 6% (n = 14). The risk factors for in-hospital death identified by a multivariate analysis were: bleeding at admission (OR = 25.5, 95% CI: 2.26–287.4; p = 0.009), white cell count less than 4000/mm3 (OR = 5.66, 95% CI: 1.16–27.6; p = 0.032), cytolysis (OR = 28.13, 95% CI: 4.55–173.6; p < 0.001), and delay between onset of symptoms and admission ≥ 15 days (OR = 11, 95% CI: 1.68–72; p = 0.012). CONCLUSION: The results strongly suggest that paediatric patients admitted 15 days after onset of symptoms, with bleeding, white cell counts below 4,000/mm(3), and cytolysis at admission should be considered severe cases and subsequently, they are at high risk of mortality. A better understanding of factors associated with death of children from ZVL may contribute to decrease mortality. |
format | Online Article Text |
id | pubmed-5747430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-57474302018-01-26 Risk factors for mortality of children with zoonotic visceral leishmaniasis in Central Tunisia Ben Helel, Khaled Ben Rejeb, Mohamed Habboul, Zakia Khattat, Nizar Mejaouel, Houssain Said-Latiri, Houyem Kaabi, Belhassen Zhioua, Elyes PLoS One Research Article BACKGROUND: Zoonotic visceral leishmaniasis (ZVL) caused by Leishmania infantum is endemic with an epidemiological profile of a paediatric disease in Tunisia. In the context of a high fatality rate, identifying risk factors for in-hospital mortality in children treated for ZVL is of major epidemiological importance. DESIGN: A retrospective (case-control) study included 230 immuno-competent children diagnosed and confirmed with primary ZVL in the paediatric department of the University Hospital of Kairouan between 2004 and 2014. Forty-seven per cent (47%) were children under 18 months of age, and with a male ⁄ female ratio of 1.01:1. RESULTS: The overall case-fatality was 6% (n = 14). The risk factors for in-hospital death identified by a multivariate analysis were: bleeding at admission (OR = 25.5, 95% CI: 2.26–287.4; p = 0.009), white cell count less than 4000/mm3 (OR = 5.66, 95% CI: 1.16–27.6; p = 0.032), cytolysis (OR = 28.13, 95% CI: 4.55–173.6; p < 0.001), and delay between onset of symptoms and admission ≥ 15 days (OR = 11, 95% CI: 1.68–72; p = 0.012). CONCLUSION: The results strongly suggest that paediatric patients admitted 15 days after onset of symptoms, with bleeding, white cell counts below 4,000/mm(3), and cytolysis at admission should be considered severe cases and subsequently, they are at high risk of mortality. A better understanding of factors associated with death of children from ZVL may contribute to decrease mortality. Public Library of Science 2017-12-29 /pmc/articles/PMC5747430/ /pubmed/29287082 http://dx.doi.org/10.1371/journal.pone.0189725 Text en © 2017 Ben Helel et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Ben Helel, Khaled Ben Rejeb, Mohamed Habboul, Zakia Khattat, Nizar Mejaouel, Houssain Said-Latiri, Houyem Kaabi, Belhassen Zhioua, Elyes Risk factors for mortality of children with zoonotic visceral leishmaniasis in Central Tunisia |
title | Risk factors for mortality of children with zoonotic visceral leishmaniasis in Central Tunisia |
title_full | Risk factors for mortality of children with zoonotic visceral leishmaniasis in Central Tunisia |
title_fullStr | Risk factors for mortality of children with zoonotic visceral leishmaniasis in Central Tunisia |
title_full_unstemmed | Risk factors for mortality of children with zoonotic visceral leishmaniasis in Central Tunisia |
title_short | Risk factors for mortality of children with zoonotic visceral leishmaniasis in Central Tunisia |
title_sort | risk factors for mortality of children with zoonotic visceral leishmaniasis in central tunisia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5747430/ https://www.ncbi.nlm.nih.gov/pubmed/29287082 http://dx.doi.org/10.1371/journal.pone.0189725 |
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