Department of Nephrology, Beaumont Hospital, Dublin, Ireland.
Am J Kidney Dis. 2010 Nov;56(5):e11-5. doi: 10.1053/j.ajkd.2010.07.011.
Rhabdomyolysis is a known complication of statin therapy and may be triggered by a pharmacokinetic interaction between a statin and a second medication. Fatal statin-induced rhabdomyolysis has an incidence of 0.15 deaths/million prescriptions. We describe 4 cases of severe rhabdomyolysis with the common feature of atorvastatin use and coadministration of fusidic acid. All cases involved long-term therapy with atorvastatin; fusidic acid was introduced for treatment of osteomyelitis or septic arthritis. Three cases occurred in the setting of diabetes mellitus, with 2 in patients with end-stage renal disease, suggesting increased susceptibility to atorvastatin-fusidic acid-induced rhabdomyolysis in these patient populations. Of the 4 patients in this series, 3 died. Fusidic acid is a unique bacteriostatic antimicrobial agent with principal antistaphylococcal activity. There have been isolated reports of rhabdomyolysis attributed to the interaction of statins and fusidic acid, the cause of which is unclear. Fusidic acid does not inhibit the cytochrome P450 3A4 isoenzyme responsible for atorvastatin metabolism; increased atorvastatin levels due to inhibition of the glucuronidation pathway may be responsible. Considering the low frequency of fusidic acid use, the appearance of 4 such cases within a short time and in a small population suggests the probability that development of this potentially fatal complication may be relatively high.
横纹肌溶解症是他汀类药物治疗的已知并发症,可能是由他汀类药物与第二种药物之间的药代动力学相互作用引发的。致命性他汀类药物引起的横纹肌溶解症的发病率为每百万处方 0.15 例死亡。我们描述了 4 例具有阿托伐他汀使用和伴随应用夫西地酸的共同特征的严重横纹肌溶解症病例。所有病例均涉及阿托伐他汀的长期治疗;夫西地酸用于治疗骨髓炎或脓毒性关节炎。3 例发生在糖尿病患者中,其中 2 例发生在终末期肾病患者中,这表明这些患者群体对阿托伐他汀-夫西地酸引起的横纹肌溶解症的敏感性增加。在本系列的 4 例患者中,有 3 例死亡。夫西地酸是一种具有独特抑菌作用的抗菌药物,主要具有抗葡萄球菌活性。有孤立的报道称,横纹肌溶解症归因于他汀类药物和夫西地酸的相互作用,但原因尚不清楚。夫西地酸不抑制负责阿托伐他汀代谢的细胞色素 P450 3A4 同工酶;由于抑制葡萄糖醛酸化途径,可能导致阿托伐他汀水平升高。考虑到夫西地酸的使用频率较低,在短时间内和小范围内出现 4 例这样的病例表明,这种潜在致命并发症的发展可能性相对较高。