| Literature DB >> 15502939 |
Koh-ichi Sugimoto1, Masami Ohmori, Akio Fujimura, Koh-ichi Sakamoto, Shuji Hishikawa, Koichi Mizuta, Yoshiaki Kita, Takeji Uno, Hideo Kawarasaki.
Abstract
Reductions in hepatic oxygen supply may reduce the oxidative metabolism of drugs, including tacrolimus. We encountered a patient (2.3-year-old girl) with hypoxemia [arterial oxygen tension (PaO2) 40.9 mmHg in room air] due to hepatopulmonary syndrome who had undergone living related liver transplantation. After transplantation, tacrolimus was initially administered by continuous intravenous infusion, and her PaO2 was maintained at more than 50 mmHg [72.8+/-10.4 (SD) mmHg] by oxygen supplementation. Apparent clearance of tacrolimus (calculated as: the infusion rate of tacrolimus/blood concentration) in the patient (0.075 l/h per kg) was comparable to those of non-hypoxemic control pediatric cases (0.092+/-0.014 l/h per kg, n=7, mean age 2.2 years, PaO2 149.2+/-41.5 mmHg), except for the acute decline in the early period after transplantation. These findings suggest that the reduction in tacrolimus clearance is negligible when arterial oxygen tension is maintained at more than 50 mmHg, even in patients with hypoxemia.Entities:
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Year: 2004 PMID: 15502939 DOI: 10.1007/s00147-004-0761-0
Source DB: PubMed Journal: Transpl Int ISSN: 0934-0874 Impact factor: 3.782