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两例患者在联合使用大环内酯类抗生素后出现辛伐他汀相关性横纹肌溶解症。

Simvastatin-associated rhabdomyolysis after coadministration of macrolide antibiotics in two patients.

作者信息

Molden Espen, Andersson Kirsti Svendsen

机构信息

Department of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway.

出版信息

Pharmacotherapy. 2007 Apr;27(4):603-7. doi: 10.1592/phco.27.4.603.

Abstract

Two men, aged 83 and 78 years, who received stable therapy with simvastatin 80 mg/day were hospitalized 1-2 weeks after completion of short-term treatment with erythromycin and clarithromycin, respectively. Both patients were admitted with myalgia, muscle weakness, functional disability (inability to raise arms and legs), and serum creatine kinase levels more than 60 times the upper limit of normal (ULN). Substantial elevations in aspartate aminotransferase (> 30 times the ULN) and alanine aminotransferase (> 7 times the ULN) levels were also observed. Rhabdomyolysis was diagnosed in both patients. Both recovered, but the combined events resulted in almost 40 days of hospitalization, the cost of which is considerable. According to the Naranjo adverse drug reaction probability scale, the likelihood that the rhabdomyolysis was secondary to a simvastatin-macrolide interaction was probable. Four cases of rhabdomyolysis after therapy with combined simvastatin and clarithromycin have been reported previously, but this is apparently the first report of rhabdomyolysis after coadministration of erythromycin. The interacting mechanism likely was inhibited cytochrome P450 (CYP) 3A4 metabolism and possibly P-glycoprotein transport of simvastatin as well. Previous reports of simvastatin-clarithromycin-related events involved additional drugs that inhibited CYP3A4 and P-glycoprotein. However, this was not the situation with our two patients. To prevent future events, it is crucial that clinicians recognize the interaction risk associated with concurrent use of simvastatin and clarithromycin or erythromycin. The risk could be managed by temporary interruption of simvastatin treatment or administration of a noninteracting antimicrobial agent.

摘要

两名分别为83岁和78岁的男性,正在接受每天80毫克辛伐他汀的稳定治疗,在分别完成短期红霉素和克拉霉素治疗后的1至2周内住院。两名患者均因肌痛、肌肉无力、功能障碍(无法抬起手臂和腿部)入院,血清肌酸激酶水平超过正常上限(ULN)的60倍以上。还观察到天冬氨酸转氨酶(> ULN的30倍)和丙氨酸转氨酶(> ULN的7倍)水平大幅升高。两名患者均被诊断为横纹肌溶解症。两人均康复,但这些综合事件导致住院近40天,费用相当可观。根据Naranjo药物不良反应概率量表,横纹肌溶解症继发于辛伐他汀-大环内酯类药物相互作用的可能性很大。此前曾有4例联合使用辛伐他汀和克拉霉素治疗后发生横纹肌溶解症的报告,但这显然是首次报告红霉素合用后发生横纹肌溶解症。相互作用机制可能是抑制细胞色素P450(CYP)3A4代谢,也可能是抑制辛伐他汀的P-糖蛋白转运。此前关于辛伐他汀-克拉霉素相关事件的报告涉及其他抑制CYP3A4和P-糖蛋白的药物。然而,我们的两名患者并非这种情况。为防止未来发生此类事件,临床医生必须认识到同时使用辛伐他汀和克拉霉素或红霉素相关的相互作用风险。可以通过暂时中断辛伐他汀治疗或使用无相互作用的抗菌药物来管理这种风险。

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