Department of Pharmacy, First People's Hospital of Linping District, Hangzhou, China.
Department of Pharmacy, Yuecheng District People's Hospital of Shaoxing, Shaoxing, China.
BMC Pharmacol Toxicol. 2024 Jul 10;25(1):39. doi: 10.1186/s40360-024-00760-8.
Statins are widely used in cardiovascular disease (CVD) as a common lipid-lowering drug, while quinolones are widely used for the treatment of infectious diseases. It is common to see CVD in combination with infectious diseases, therefore it is often the case that statins and quinolones are used in combination. Data suggest combinations of statin and quinolone may be associated with potentially life-threatening myopathy, rhabdomyolysis and acute hepatitis. This systematic review aims to characterize data regarding patients affected by the statin-quinolone interaction.
The purpose of this systematic review was to collect and evaluate the evidence surrounding statin-quinolone drug interactions and to discuss related risk mitigation strategies. The following databases were searched: PubMed (Medline), Embase, Scopus, and Cochrane Library. The systematic electronic literature search was conducted with the following search terms. In this study, three types of search terms were used: statins-related terms, quinolones-related terms, and drug interactions-related terms.
There were 16 case reports that met the criteria for qualitative analysis. Patients were involved in the following adverse reactions: rhabdomyolysis (n = 12), acute hepatitis (n = 1), muscle weakness (n = 1), hip tendinopathy (n = 1), or myopathy (n = 1). In the included literature, patients vary in the dose and type of statins they take, including simvastatin (n = 10) at a dose range of 20-80 mg/d and atorvastatin (n = 4) at a dose of 80 mg/d. There were 2 patients with unspecified statin doses, separately using simvastatin and atorvastatin. The quinolones in combination were ciprofloxacin (n = 9) at a dose range of 800-1500 mg/d, levofloxacin (n = 6) at a dose range of 250-1000 mg/d, and norfloxacin (n = 1) in an unspecified dose range. 81% of the case patients were over 60 years of age, and about 1/3 had kidney-related diseases such as diabetic nephropathy, post-transplantation, and severe glomerulonephritis. Nearly two-third of the patients were on concomitant cytochrome P450 3A4 (CYP3A4) inhibitors, P-glycoprotein (P-gp) inhibitors, or organic anion transporting polypeptide 1B1 (OATP1B1) inhibitors.
Patients treated with statin-quinolone combination should be monitored more closely for changes in aspartate aminotransferase or creatine kinase (CK) levels, and muscle symptoms, especially in patients with ciprofloxacin or levofloxacin, with simvastatin and high-dose atorvastatin, over 60 years of age, with kidney-related diseases, and on concomitant CYP3A4 inhibitors.
他汀类药物作为一种常见的降脂药物,广泛用于心血管疾病(CVD);而喹诺酮类药物则广泛用于治疗传染病。CVD 常合并传染病,因此他汀类药物和喹诺酮类药物常联合使用。有数据表明,他汀类药物和喹诺酮类药物联合使用可能与潜在威胁生命的肌病、横纹肌溶解和急性肝炎有关。本系统评价旨在描述他汀类药物-喹诺酮类药物相互作用患者的数据。
本系统评价的目的是收集和评估他汀类药物-喹诺酮类药物药物相互作用的证据,并讨论相关的风险缓解策略。检索了以下数据库:PubMed(Medline)、Embase、Scopus 和 Cochrane 图书馆。系统地进行了电子文献检索,使用了以下搜索词。在这项研究中,使用了三种类型的搜索词:他汀类药物相关术语、喹诺酮类药物相关术语和药物相互作用相关术语。
有 16 份病例报告符合定性分析的标准。患者涉及以下不良反应:横纹肌溶解(n=12)、急性肝炎(n=1)、肌肉无力(n=1)、髋关节腱病(n=1)或肌病(n=1)。在纳入的文献中,患者服用的他汀类药物剂量和类型各不相同,包括辛伐他汀(n=10)剂量范围为 20-80mg/d 和阿托伐他汀(n=4)剂量为 80mg/d。有 2 名患者未说明他汀类药物的剂量,分别使用辛伐他汀和阿托伐他汀。联合使用的喹诺酮类药物有环丙沙星(n=9)剂量范围为 800-1500mg/d、左氧氟沙星(n=6)剂量范围为 250-1000mg/d 和诺氟沙星(n=1)剂量范围不明确。81%的病例患者年龄在 60 岁以上,约 1/3 患有与肾脏相关的疾病,如糖尿病肾病、移植后和严重肾小球肾炎。近三分之二的患者同时服用细胞色素 P450 3A4(CYP3A4)抑制剂、P-糖蛋白(P-gp)抑制剂或有机阴离子转运蛋白 1B1(OATP1B1)抑制剂。
接受他汀类药物-喹诺酮类药物联合治疗的患者应更密切监测天冬氨酸氨基转移酶或肌酸激酶(CK)水平的变化,以及肌肉症状,特别是在使用环丙沙星或左氧氟沙星、高剂量辛伐他汀和阿托伐他汀、年龄在 60 岁以上、与肾脏相关的疾病以及同时服用 CYP3A4 抑制剂的患者中。