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Conjugated Hyperbilirubinemia in Infants: Is There Still a Role for ERCP
J. Stovicek, S. Hlava, R. Keil, J. Drabek, J. Lochmannova, P. Koptová, M. Wasserbauer, B. Frybova, J. Snajdauf, R. Kotalova, M. Rygl
Jazyk angličtina Země Egypt
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 1987
Directory of Open Access Journals
od 2014
Free Medical Journals
od 2005 do Před 1 rokem
PubMed Central
od 2014
Europe PubMed Central
od 2014
ProQuest Central
od 2013-01-01
Open Access Digital Library
od 1987-01-01
Open Access Digital Library
od 1987-01-01
Open Access Digital Library
od 2014-01-01
Medline Complete (EBSCOhost)
od 2014-01-01
Health & Medicine (ProQuest)
od 2013-01-01
Wiley-Blackwell Open Access Titles
od 1987
ROAD: Directory of Open Access Scholarly Resources
od 2014
PubMed
34258256
DOI
10.1155/2021/9969825
Knihovny.cz E-zdroje
- MeSH
- cholangiopankreatografie endoskopická retrográdní škodlivé účinky MeSH
- choledocholitiáza * diagnostické zobrazování chirurgie MeSH
- cholestáza * etiologie MeSH
- hyperbilirubinemie MeSH
- kojenec MeSH
- lidé MeSH
- pankreatitida * MeSH
- Check Tag
- kojenec MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Over a twenty-year period, we performed 255 ERCP procedures in infants aged up to 1 year. ERCP was indicated in cholestatic infants with suspicion of biliary obstruction. The most common diagnosis was biliary atresia (48%), choledochal cysts (13%), and choledocholithiasis (4%). The procedure complication rate was 13.7%. Hyperamylasemia occurred in 12.9%. More severe complications were rare-0.8% of ERCP procedure. There were no cases of postprocedural pancreatitis or death. Our study has proved that ERCP is a safe and reliable method in this age group. Its high specificity and negative predictive value for extrahepatic biliary atresia can prevent unnecessary surgeries in patients with normal bile ducts or endoscopically treatable pathologies.
Citace poskytuje Crossref.org
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