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新西兰与药物相关的肝脏反应:21年经验

Drug associated hepatic reactions in New Zealand: 21 years experience.

作者信息

Pillans P I

机构信息

Centre for Adverse Reactions Monitoring, National Toxicology Group, University of Otago Medical School, Dunedin.

出版信息

N Z Med J. 1996 Aug 23;109(1028):315-9.

PMID:8816722
Abstract

AIMS

To review spontaneous reports of drug-associated adverse hepatic reactions.

METHODS

Reports of drug-associated adverse hepatic reactions received by the New Zealand Centre for Adverse Reactions Monitoring over the 21 year period January 1974 to December 1994 were reviewed. Subdivision into three 7 year periods was undertaken to compare patterns.

RESULTS

Of a total of 22,455 adverse medicine reaction (AMR) reports there were 943 reports of liver injury (4.2%). Two hundred and five drugs were associated with hepatic reactions. The top 20 drugs accounted for 57% of all liver reactions. Fifty-seven percent were reported in females. Hepatotoxicity was most commonly reported among patients 50-80 years old. Liver reactions were associated with a 3.3% mortality, but were responsible for 7.4% of all fatal occurrences. There was a steady increase in the number of reports over the 21 years. Although the largest number of reports of liver injury were received between 1988 and 1994, mortality was lowest during this period. There were substantial differences in the medicines associated with hepatic reactions during each of the three periods, although erythromycin was the commonest cause throughout. Erythromycin was associated with two deaths. Halothane and perhexilene were the most frequent cause of death and were two of the most important causes of liver injury during the first and second periods. Diclofenac, Augmentin and flucloxacillin were important causes of hepatotoxicity during period 3 but were not associated with a fatal outcome.

CONCLUSION

Hepatic reactions accounted for 4.2% of all adverse medicine reactions and 7.4% of all fatal occurrences. The top 20 drugs were responsible for 57% of all liver reactions. Despite a steady increase in the number of reports during the 21 years, mortality was lowest during the last 7 years. Differences in the medicines causing liver injury during the three periods influenced the number of fatalities. Erythromycin was the most commonly reported cause of hepatic reactions but was usually associated with a favourable outcome. There were no reported deaths with diclofenac, Augmentin or flucloxacillin.

摘要

目的

回顾药物相关不良肝反应的自发报告。

方法

对新西兰不良反应监测中心在1974年1月至1994年12月这21年期间收到的药物相关不良肝反应报告进行回顾。将其细分为三个7年时间段以比较模式。

结果

在总共22455份药物不良反应(AMR)报告中,有943份肝损伤报告(4.2%)。205种药物与肝反应有关。排名前20的药物占所有肝反应的57%。57%的报告发生在女性中。肝毒性最常报告于50至80岁的患者中。肝反应与3.3%的死亡率相关,但占所有致命事件的7.4%。在这21年中报告数量稳步增加。尽管1988年至1994年期间收到的肝损伤报告数量最多,但该期间死亡率最低。在三个时间段中,与肝反应相关的药物存在很大差异,尽管红霉素在整个期间都是最常见的原因。红霉素与两例死亡相关。氟烷和哌克昔林是最常见的死亡原因,并且是第一和第二个时间段中肝损伤的两个最重要原因。双氯芬酸、阿莫西林克拉维酸钾和氟氯西林是第三个时间段中肝毒性的重要原因,但未与致命结果相关。

结论

肝反应占所有药物不良反应的4.2%,占所有致命事件的7.4%。排名前20的药物占所有肝反应的57%。尽管在这21年中报告数量稳步增加,但最后7年死亡率最低。三个时间段中导致肝损伤的药物差异影响了死亡人数。红霉素是最常报告的肝反应原因,但通常与良好结局相关。双氯芬酸、阿莫西林克拉维酸钾或氟氯西林未报告有死亡病例。

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