Abnormal Elevation of Serum ALT Level Induced by Multiple Administrations of Unfractionated Heparin in Healthy Japanese Volunteers
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概要
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Objective: Although often described abroad, heparin-induced hepatotoxicity is seldom recognized in clinical practice in Japan. We evaluated the safety of multiple doses of unfractionated heparin using healthy Japanese volunteers, with the primary focus on serum transaminase levels.<BR>Methods: Eight healthy males, aged between 20 and 24 years, participated in the study. Six of the 8 volunteers received subcutaneous administration of 5000 IU unfractionated calcium heparin (UFH) for 9 days. The remaining two volunteers received subcutaneous saline injections in place of UFH. A follow-up survey was conducted for 7 days following the final administration. Laboratory measurements, including the levels of hepatic enzymes, were taken during the administration of UFH.<BR>Results: Administration of UFH to five of the six volunteers had to be stopped within the first week. Administration in one subject was discontinued on day 3 due to prolonged activated partial thromboplastin time ; the other four were due to an abnormal elevation of ALT above the level considered to be safe. This abnormal elevation continued for 2 days, despite cessation of administration. The levels then gradually decreased, and within 6 weeks returned to pre-administration levels.<BR>Conclusion: An abnormal elevation of transaminase levels following repeated injections of UFH was observed in Japanese as is reported in Caucasians. As we have shown, it is highly probable that this abnormal elevation of transaminase levels, during repeated administration of UFH, could be observed in the clinical setting in Japan. Monitoring of serum transaminase levels at periodic intervals should thus be encouraged during multiple injections of UFH even though clinically relevant symptoms may not be noticed.
- 一般社団法人 日本臨床薬理学会の論文
- 2004-03-31
著者
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Maruyama Toru
Institute Of Health Science Kyushu University
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OKADA Mitsuko
医療法人相生会臨床薬理センター
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NAKANO Shigeyuki
大分医科大学臨床薬理学
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Nakano Shigeyuki
Department Of Clinical Pharmacology And Therapeutics Oita Medical University
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Hayashi Masamiti
Department Of Cardiology Tokyo Women's Medical University
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Urae Akinori
Kyushu Pharmacology Research Clinic
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Hashiguchi Masayuki
Department Of Medication Use Analysis And Clinical Research Meiji Pharmaceutical University
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Tanaka Takanori
Clinical Pharmacology Center Osaki Clinic
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HASHIGUCHI Masayuki
Division for Evaluation and Analysis of Drug Information, Faculty of Pharmacy, Keio University
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TANAKA Takanori
Medical Co. LTA Clinical Pharmacology Center
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IRIE Shin
Medical Co. LTA Clinical Pharmacology Center
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Hashiguchi Masayuki
Division For Evaluation And Analysis Of Drug Information Faculty Of Pharmacy Keio University
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URAE Akinori
Clinical Pharmacology Center, LTA Medical Corporation
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OKADA Mitsuko
Clinical Pharmacology Center, LTA Medical Corporation
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INADA Kenichi
Clinical Pharmacology Center, LTA Medical Corporation
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KOTAKE Midori
Clinical Pharmacology Center, LTA Medical Corporation
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IRIE Shin
Clinical Pharmacology Center, LTA Medical Corporation
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Kotake Midori
Clinical Pharmacology Center Lta Medical Corporation
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Inada Kenichi
Clinical Pharmacology Center Lta Medical Corporation
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Okada Mitsuko
Clinical Pharmacology Center Lta Medical Corporation
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