151. Pediatric living donor liver transplantation for biliary atresia with hepatopulmonary syndrome: the gift of a second wind
- Author
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Masanobu Hyodo, Yasunaru Sakuma, Shuji Hishikawa, Koichi Mizuta, Taizen Urahashi, T. Fujiwara, Hideo Kawarasaki, Taiichi Wakiya, Yukihiro Sanada, Minoru Umehara, and Yoshikazu Yasuda
- Subjects
Adult ,Male ,Parents ,medicine.medical_specialty ,Tissue and Organ Procurement ,Adolescent ,medicine.medical_treatment ,Liver transplantation ,Gastroenterology ,Liver disease ,Biliary Atresia ,Biliary atresia ,Internal medicine ,Pediatric surgery ,Living Donors ,medicine ,Humans ,Child ,Hepatopulmonary syndrome ,Retrospective Studies ,integumentary system ,business.industry ,Retrospective cohort study ,General Medicine ,medicine.disease ,eye diseases ,Liver Transplantation ,Transplantation ,Child, Preschool ,Pediatrics, Perinatology and Child Health ,Female ,Surgery ,Complication ,business ,Follow-Up Studies ,Hepatopulmonary Syndrome - Abstract
Hepatopulmonary syndrome (HPS) is a progressive, deteriorating complication of end-stage liver disease (ESLD) that occurs in 13-47% of liver transplant candidates. Although LT is the only therapeutic option for HPS, it has a high morbidity and mortality, especially in patients with severe hypoxemia before transplantation, but the course of HPS after living donor liver transplantation (LDLT), especially for biliary atresia (BA) patients is not well established.The present study evaluated 122 patients who received an LDLT for BA and of these, 3 patients had HPS at the time of LDLT in a single-center series.Two patients of the HPS patients them had biliary and/or vascular complications, but they recovered uneventfully with interventional treatment. None of the patients required supplemental oxygen and had no residual cardiopulmonary abnormalities at a follow-up of more than 24 months.Although a series of three patients is too small for definitive conclusion and further investigations must be conducted, pediatric LDLT can be a favorable therapeutic option for HPS.
- Published
- 2011
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