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Journals / Göztepe Tıp Dergisi / 2008 / Cilt: 23 - Sayı: 3

Hepatobiliary insufficiency-candidate of transplantation newborns and anesthesia (two cases)

Hepatobilier yetmezlikli-transplantasyon adayı neonatal olgular ve anestezi

Verda TOPRAK
Tezcan Gönül KELEŞ
Tülin ÖZTÜRK
Selçuk BULUT
Pages
95–99
Publication Date
2022-10-17
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Early diagnosis and therapy is essential especially for the survival of patients with biliary atresia.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Biliary atresia (BA) is the most common and important neonatal hepatobiliary disorder and is seen in 1 in 8.000 to 1 in 18.000.
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Key Findings & Data:Consequently, 70-80 % of BA patients will eventually require liver transplantation, approximately half in the first 2 y of life.
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Conclusion & Impact:Early diagnosis and therapy is essential especially for the survival of patients with biliary atresia.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Biliary atresia (BA) is the most common and important neonatal hepatobiliary disorder and is seen in 1 in 8.000 to 1 in 18.000. Consequently, 70-80 % of BA patients will eventually require liver transplantation, approximately half in the first 2 y of life. Early diagnosis and therapy is essential especially for the survival of patients with biliary atresia.

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Cite This Article

TOPRAK, V., KELEŞ, T. G., ÖZTÜRK, T., BULUT, S. (2022). Hepatobiliary insufficiency-candidate of transplantation newborns and anesthesia (two cases). Göztepe Tıp Dergisi, Cilt: 23 - Sayı: 3, 95–99. https://ajindex.com/articles/526272

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References (9)

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