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Mortality in esophageal atresia: Assessment of probable risk factors (10 years’ experience)

BACKGROUND: Esophageal atresia (EA) is a common congenital anomaly. In this study, we evaluated the mortality and its risk factors in patients born with esophageal atresia. METHODS AND MATERIALS: A database of 206 consecutive patients treated for EA was developed in ST-Zahra hospital of Isfahan betw...

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Autores principales: Davari, Heidar A., Hosseinpour, Mehrdad, Nasiri, Gilda M., Kiani, Gelare
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634291/
https://www.ncbi.nlm.nih.gov/pubmed/23626630
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author Davari, Heidar A.
Hosseinpour, Mehrdad
Nasiri, Gilda M.
Kiani, Gelare
author_facet Davari, Heidar A.
Hosseinpour, Mehrdad
Nasiri, Gilda M.
Kiani, Gelare
author_sort Davari, Heidar A.
collection PubMed
description BACKGROUND: Esophageal atresia (EA) is a common congenital anomaly. In this study, we evaluated the mortality and its risk factors in patients born with esophageal atresia. METHODS AND MATERIALS: A database of 206 consecutive patients treated for EA was developed in ST-Zahra hospital of Isfahan between 1994 and 2004. RESULTS: In this study, 206 patients were evaluated. The most common type of EA was type C (86.4%). Mortality rate was 56%; it was more common in patients with congenital malformation, in late operation and in low birth weight and premature babies. Sepsis was the most common cause of death. CONCLUSIONS: For improvement of EA survival, we should improve operation techniques, supportive care, and ICU management. It is also important to operate these patients as soon as possible.
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spelling pubmed-36342912013-04-26 Mortality in esophageal atresia: Assessment of probable risk factors (10 years’ experience) Davari, Heidar A. Hosseinpour, Mehrdad Nasiri, Gilda M. Kiani, Gelare J Res Med Sci Original Article BACKGROUND: Esophageal atresia (EA) is a common congenital anomaly. In this study, we evaluated the mortality and its risk factors in patients born with esophageal atresia. METHODS AND MATERIALS: A database of 206 consecutive patients treated for EA was developed in ST-Zahra hospital of Isfahan between 1994 and 2004. RESULTS: In this study, 206 patients were evaluated. The most common type of EA was type C (86.4%). Mortality rate was 56%; it was more common in patients with congenital malformation, in late operation and in low birth weight and premature babies. Sepsis was the most common cause of death. CONCLUSIONS: For improvement of EA survival, we should improve operation techniques, supportive care, and ICU management. It is also important to operate these patients as soon as possible. Medknow Publications & Media Pvt Ltd 2012-06 /pmc/articles/PMC3634291/ /pubmed/23626630 Text en Copyright: © Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Davari, Heidar A.
Hosseinpour, Mehrdad
Nasiri, Gilda M.
Kiani, Gelare
Mortality in esophageal atresia: Assessment of probable risk factors (10 years’ experience)
title Mortality in esophageal atresia: Assessment of probable risk factors (10 years’ experience)
title_full Mortality in esophageal atresia: Assessment of probable risk factors (10 years’ experience)
title_fullStr Mortality in esophageal atresia: Assessment of probable risk factors (10 years’ experience)
title_full_unstemmed Mortality in esophageal atresia: Assessment of probable risk factors (10 years’ experience)
title_short Mortality in esophageal atresia: Assessment of probable risk factors (10 years’ experience)
title_sort mortality in esophageal atresia: assessment of probable risk factors (10 years’ experience)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634291/
https://www.ncbi.nlm.nih.gov/pubmed/23626630
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