Literature DB >> 9223881

[Living related liver transplantation for patients with ornithine transcarbamylase deficiency].

M Tazuke1, M Murakawa, S Nakao, K Mukaida, H Toda, K Mori.   

Abstract

Ornithine transcarbamylase deficiency (OTCD) is an inborn error of urea synthesis inherited as an X-linked trait, a clinical manifestation of which is a repeated episodes of hyperammonemic coma. Recently, liver transplantations have been performed in these patients in the USA and Europe. We experienced the anesthetic managements of liver transplantations in two OTCD patients, who had been suffering from several episodes of hyperammonemic decompensation despite a restricted protein diet with administration of sodium benzoate. Anesthesia was induced and maintained with a combination of fentanyl and midazolam in both cases. Their postoperative courses were good without any neurological damages, though one patient had hyperammonemic attack during the operation.

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Year:  1997        PMID: 9223881

Source DB:  PubMed          Journal:  Masui        ISSN: 0021-4892


  2 in total

1.  [Patients with ornithine transcarbamylase deficiency. Anaesthesiological and intensive care management].

Authors:  J Schmidt; M Schroth; A Irouschek; T Birkholz; M Kurzai; S Kröber; M Meisner; S Albrecht
Journal:  Anaesthesist       Date:  2005-12       Impact factor: 1.041

2.  Anesthesia management in living-donor liver transplantation in a patient with carbamoyl phosphate synthetase deficiency: a case report.

Authors:  Hiroki Matsushita; Tetsushiro Fujiyoshi; Koichiro Yoshimaru; Toshiharu Matsuura; Yuichi Mushimoto; Yuji Karashima; Ken Yamaura
Journal:  JA Clin Rep       Date:  2022-09-07
  2 in total

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