Investigation of the Frequency, Causes and Consequences of Cholestasis in Infants Referred to AmirKola Children\'s Hospital During the Years 2012-2022

Background and purpose: Children with cholestasis experience a wide spectrum of disease, ranging from transient liver function abnormalities to life-threatening conditions. These children may require hospitalization or specialized care at various times due to liver enzyme disorders and associated cl...

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Main Authors: Zahra Ghanbari tilami, Sanaz Mehrabani, Mohammadreza Esmaeili Dooki, Maryam Nikpour, Yadollah Zahedpasha, Mousa Ahmadpour, Abbas Hadipour
Format: Article
Language:English
Published: Mazandaran University of Medical Sciences 2024-10-01
Series:Journal of Mazandaran University of Medical Sciences
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Online Access:http://jmums.mazums.ac.ir/article-1-20967-en.pdf
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author Zahra Ghanbari tilami
Sanaz Mehrabani
Mohammadreza Esmaeili Dooki
Maryam Nikpour
Yadollah Zahedpasha
Mousa Ahmadpour
Abbas Hadipour
author_facet Zahra Ghanbari tilami
Sanaz Mehrabani
Mohammadreza Esmaeili Dooki
Maryam Nikpour
Yadollah Zahedpasha
Mousa Ahmadpour
Abbas Hadipour
author_sort Zahra Ghanbari tilami
collection DOAJ
description Background and purpose: Children with cholestasis experience a wide spectrum of disease, ranging from transient liver function abnormalities to life-threatening conditions. These children may require hospitalization or specialized care at various times due to liver enzyme disorders and associated clinical issues. In severe cases, liver damage can lead to acute liver failure, necessitating liver transplantation or resulting in death. Early diagnosis of the etiology of cholestasis can be crucial for improving prognosis. This study aimed to determine the frequency, causes, and outcomes of cholestasis in infants referred to Amir Kola Children's Hospital. Materials and methods: This retrospective descriptive study included all infants with cholestasis admitted to AmirKola Children's Hospital between 2012 and 2022. Inclusion criteria were infants under 2 years of age diagnosed with cholestasis. Infants with incomplete medical records were excluded from the study. Hepatic cholestasis was diagnosed based on the infant's medical history and confirmed by a pediatric gastroenterologist. All infants underwent diagnostic evaluation tests and abdominal ultrasound. Liver biopsy was performed when necessary to assess liver pathology. Short-term outcomes of hepatic cholestasis, including length of hospitalization, frequency of hospitalization, need for special care, liver transplantation, and mortality, were evaluated. Demographic information, along with the causes and outcomes of cholestasis, were reported using measures of central tendency (mean) and dispersion (standard deviation), or as frequencies and percentages. Results: During the study period (2012-2022), 3,650 infants under 2 years of age were admitted to Amir Kola Children's Hospital. The frequency of cholestasis among hospitalized children was 54 (1.47%). The most common symptom of cholestasis was hepatomegaly, observed in 35 (64%) infants. The leading causes of cholestasis included biliary atresia in 21 (38.8%) infants, idiopathic hepatitis in 17 (31.4%) infants, and congenital metabolic disorders in 7 (12.96%) infants. Of the children in the study, 23 (42%) were hospitalized at least once, and 10 (18.5%) were hospitalized twice. Liver biopsy was performed in 32 (60.4%) of the 54 children; 11 had neonatal cholestasis, 7 had normal ultrasound results, and 13 had giant cell hepatitis and neonatal hepatitis (10 with normal ultrasound results), with 2 showing normal pathology reports. Additionally, 20 (37%) of these children died, 24 (44%) recovered, and 9 required liver transplantation. Conclusion: According to the results of this study, more than one-third of children with cholestasis died, with biliary atresia and idiopathic hepatitis identified as the most common causes. Biliary atresia was also the most frequent indication for liver transplantation. These findings highlight the need for timely diagnostic examinations, testing, and specialized evaluations to support early diagnosis and treatment in infancy.
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spelling doaj-art-5b0c5811da4846be8c0adf40067ce9e92024-11-16T05:12:00ZengMazandaran University of Medical SciencesJournal of Mazandaran University of Medical Sciences1735-92601735-92792024-10-01342388185Investigation of the Frequency, Causes and Consequences of Cholestasis in Infants Referred to AmirKola Children\'s Hospital During the Years 2012-2022Zahra Ghanbari tilami0Sanaz Mehrabani1Mohammadreza Esmaeili Dooki2Maryam Nikpour3Yadollah Zahedpasha4Mousa Ahmadpour5Abbas Hadipour6 Medical Student, Student Research Committee, Babol University of Medical Sciences, Babol, Iran Associate Professor, Department of Pediatrics, Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran Professor, Department of Pediatrics, Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran Assistant Professor, Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran Professor, Department of Pediatrics, Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran Professor, Department of Pediatrics, Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran Assistant Professor, Department of Pediatrics, Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran Background and purpose: Children with cholestasis experience a wide spectrum of disease, ranging from transient liver function abnormalities to life-threatening conditions. These children may require hospitalization or specialized care at various times due to liver enzyme disorders and associated clinical issues. In severe cases, liver damage can lead to acute liver failure, necessitating liver transplantation or resulting in death. Early diagnosis of the etiology of cholestasis can be crucial for improving prognosis. This study aimed to determine the frequency, causes, and outcomes of cholestasis in infants referred to Amir Kola Children's Hospital. Materials and methods: This retrospective descriptive study included all infants with cholestasis admitted to AmirKola Children's Hospital between 2012 and 2022. Inclusion criteria were infants under 2 years of age diagnosed with cholestasis. Infants with incomplete medical records were excluded from the study. Hepatic cholestasis was diagnosed based on the infant's medical history and confirmed by a pediatric gastroenterologist. All infants underwent diagnostic evaluation tests and abdominal ultrasound. Liver biopsy was performed when necessary to assess liver pathology. Short-term outcomes of hepatic cholestasis, including length of hospitalization, frequency of hospitalization, need for special care, liver transplantation, and mortality, were evaluated. Demographic information, along with the causes and outcomes of cholestasis, were reported using measures of central tendency (mean) and dispersion (standard deviation), or as frequencies and percentages. Results: During the study period (2012-2022), 3,650 infants under 2 years of age were admitted to Amir Kola Children's Hospital. The frequency of cholestasis among hospitalized children was 54 (1.47%). The most common symptom of cholestasis was hepatomegaly, observed in 35 (64%) infants. The leading causes of cholestasis included biliary atresia in 21 (38.8%) infants, idiopathic hepatitis in 17 (31.4%) infants, and congenital metabolic disorders in 7 (12.96%) infants. Of the children in the study, 23 (42%) were hospitalized at least once, and 10 (18.5%) were hospitalized twice. Liver biopsy was performed in 32 (60.4%) of the 54 children; 11 had neonatal cholestasis, 7 had normal ultrasound results, and 13 had giant cell hepatitis and neonatal hepatitis (10 with normal ultrasound results), with 2 showing normal pathology reports. Additionally, 20 (37%) of these children died, 24 (44%) recovered, and 9 required liver transplantation. Conclusion: According to the results of this study, more than one-third of children with cholestasis died, with biliary atresia and idiopathic hepatitis identified as the most common causes. Biliary atresia was also the most frequent indication for liver transplantation. These findings highlight the need for timely diagnostic examinations, testing, and specialized evaluations to support early diagnosis and treatment in infancy.http://jmums.mazums.ac.ir/article-1-20967-en.pdfcholestasisbilirubininfanthepatitisbiliary atresia
spellingShingle Zahra Ghanbari tilami
Sanaz Mehrabani
Mohammadreza Esmaeili Dooki
Maryam Nikpour
Yadollah Zahedpasha
Mousa Ahmadpour
Abbas Hadipour
Investigation of the Frequency, Causes and Consequences of Cholestasis in Infants Referred to AmirKola Children\'s Hospital During the Years 2012-2022
Journal of Mazandaran University of Medical Sciences
cholestasis
bilirubin
infant
hepatitis
biliary atresia
title Investigation of the Frequency, Causes and Consequences of Cholestasis in Infants Referred to AmirKola Children\'s Hospital During the Years 2012-2022
title_full Investigation of the Frequency, Causes and Consequences of Cholestasis in Infants Referred to AmirKola Children\'s Hospital During the Years 2012-2022
title_fullStr Investigation of the Frequency, Causes and Consequences of Cholestasis in Infants Referred to AmirKola Children\'s Hospital During the Years 2012-2022
title_full_unstemmed Investigation of the Frequency, Causes and Consequences of Cholestasis in Infants Referred to AmirKola Children\'s Hospital During the Years 2012-2022
title_short Investigation of the Frequency, Causes and Consequences of Cholestasis in Infants Referred to AmirKola Children\'s Hospital During the Years 2012-2022
title_sort investigation of the frequency causes and consequences of cholestasis in infants referred to amirkola children s hospital during the years 2012 2022
topic cholestasis
bilirubin
infant
hepatitis
biliary atresia
url http://jmums.mazums.ac.ir/article-1-20967-en.pdf
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