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Journal ArticleDOI

Predictive value of hepatic ultrasound, liver biopsy, and duodenal tube test in the diagnosis of extrahepatic biliary atresia in Serbian infants.

TLDR
A well-coordinated multidisciplinary approach is required in the assessment of suspected cases of biliary atresia, and Histology examination of biopsy specimens plays a pivotal role in the diagnostic evaluation of this disease.
Abstract
Background/aims Extrahepatic biliary atresia (EHBA) is the most important cause of neonatal cholestasis. The validity of different diagnostic methods in the diagnosis of EHBA in developed countries has been presented elsewhere, but data from developing countries with low national incomes are scarce. The aim of this study was to investigate the relative accuracy and roles of abdominal ultrasonography, duodenal tube test (DTT), and liver biopsy in the diagnosis of EHBA in Serbia. Materials and methods The study included 156 infants with cholestasis admitted at the Mother and Child Health Care Institute. Data were collected according to the medical records observation technique. Results Extrahepatic biliary atresia was diagnosed in 72 of 156 infants with cholestasis. The frequency was insignificantly higher in females than in males (1.25:1). Most patients were diagnosed prior to 60 days of life (median 58, range 30-67). In a group of 156 infants with cholestasis, 109 had ultrasound, liver biopsy, duodenal tube test, and intraoperative cholangiography done. Liver biopsy confirmed surgical disease in 71/109 patients and denied it in 38/109 patients (sensitivity- Sn 98%, specificity- Sp 100%, diagnostic efficiency of test- DgEf 99.08%). Duodenal tube test had Sn 97%, Sp 72%, and DgEf 88.99%, and the ultrasound findings showed Sn 78%, Sp 81%, and DgEf 77.92%. Five-year survival rate after Kasai operation was 76%. Conclusion A well-coordinated multidisciplinary approach is required in the assessment of suspected cases of biliary atresia. Histology examination of biopsy specimens is an integral part of the diagnostic algorithm and, therefore, plays a pivotal role in the diagnostic evaluation of this disease.

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Citations
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Journal ArticleDOI

Value of Gamma-Glutamyl Transpeptidase for Diagnosis of Biliary Atresia by Correlation With Age.

TL;DR: Levels of gamma-glutamyl transpeptidase contribute to the diagnosis of BA before 120 days and age must be considered if using GGT levels as a diagnostic test for BA.
Journal ArticleDOI

Early differential diagnosis methods of biliary atresia: a meta-analysis

TL;DR: Combination of multidisciplinary noninvasive diagnosis methods is the first choice for differential diagnosis of BA from other causes of neonatal cholestasis.
Journal ArticleDOI

Development and Validation of Novel Diagnostic Models for Biliary Atresia in a Large Cohort of Chinese Patients

TL;DR: The nomogram has demonstrated better performance for the prediction of BA, holding promise for future clinical application and performance comparison of the three diagnostic models showed that the nomogram displayed better discriminative ability.
Journal ArticleDOI

The value of preoperative liver biopsy in the diagnosis of extrahepatic biliary atresia: A systematic review and meta-analysis☆

TL;DR: Quantitative analysis demonstrated preoperative biopsy to be both highly specific and sensitive in diagnosing EHBA preoperatively, a highly reliable test that offers a means of arriving at an early definitive diagnosis of EH BA.
Journal ArticleDOI

The Role of Endoscopic Retrograde Cholangiopancreatography in the Diagnosis of Biliary Atresia: 14 Years' Experience.

TL;DR: ERCP is safe and accurate in the hands of experts in diagnosing BA if the cause of cholestasis is unclear and the secondary parameters GGT > 250 U/L, bilirubin > 7.3 mg/dL, and the absence of bile traces are risk factors.
References
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Journal ArticleDOI

Impact of Age at Kasai Operation on Its Results in Late Childhood and Adolescence: A Rational Basis for Biliary Atresia Screening

TL;DR: Findings indicate a rational basis for biliary atresia screening to reduce the need for liver transplantations in infancy and childhood and suggest increased age at surgery had a progressive and sustained deleterious effect on the results of the Kasai operation until adolescence.
Book

Liver Disease in Children

TL;DR: Part 1 Pathophysiology of paediatric liver disease: structural and functional development of the liver mechanisms and morphology of cholestasis the cholangiopathies fulminant hepatic failure in children portal hypertension and other conditions and issues in paediatric hepatology.
Journal ArticleDOI

Prognosis of biliary atresia in the era of liver transplantation: French national study from 1986 to 1996

TL;DR: Kasai operation remains the first line treatment of BA, and early performance of Kasai operation and treatment in an experienced center reduces the need for liver transplantation in infancy and childhood and provides children with the best chance of survival.
Journal ArticleDOI

Seamless management of biliary atresia in England and Wales (1999-2002).

TL;DR: The early results suggest that surgical outcome can be improved by centralisation of care to supra-regional centres, and survival is estimated using the Kaplan-Meier method.
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