Department of Pharmacy, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Division of Infectious Diseases, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
J Clin Pharm Ther. 2021 Apr;46(2):363-368. doi: 10.1111/jcpt.13289. Epub 2020 Oct 5.
Daptomycin is associated with a number of adverse effects including eosinophilic pneumonia, hypersensitivity reaction, myopathy, rhabdomyolysis, headache and transaminitis. The adverse effects of high-dose daptomycin have not been fully evaluated in patients with end-stage renal disease (ESRD).
To determine the incidence and characteristics of significant adverse effects in patients receiving high-dose daptomycin with severe renal dysfunction.
A single-centre, retrospective study was conducted to assess safety outcomes of high-dose daptomycin in patients with an estimated creatinine clearance less than 30 mL/min. Adult patients aged 18 to 89 years admitted between 1 July 2015 and 1 July 2019 were eligible for inclusion. Patients must have received definitive daptomycin therapy with doses greater than or equal to 7.5 mg/kg based on actual body weight. The primary outcome was overall incidence of creatine phosphokinase (CK) elevation, myopathy and rhabdomyolysis.
A total of 74 patients who received daptomycin therapy were screened with 50 included in the study. The population was well distributed in terms of gender (48% male, n = 24) with a median age of 61 (IQR, 48-67) years. The primary indication for daptomycin use was Gram-positive bacteremia. The median daptomycin dose was 750 (IQR, 600-875) mg, or 8.46 (IQR, 7.92-9.96) mg/kg based on actual body weight, with a median patient weight of 81 (IQR, 65-113) kg. The median duration of therapy was 27 (IQR, 14-42) days. One patient experienced significant CK elevation while on daptomycin therapy with rhabdomyolysis; however, daptomycin was continued as there was an alternative explanation for an elevated CK. One patient experienced daptomycin discontinuation due to CK elevation without meeting the definition for significant CK elevation.
In a cohort of patients with severe renal dysfunction treated with daptomycin 7.5 mg/kg or greater, significant CK elevation on daptomycin therapy was infrequently observed. Future research should confirm these findings, with special consideration for higher mg/kg dosages and/or obese populations.
达托霉素与多种不良反应相关,包括嗜酸性肺炎、过敏反应、肌病、横纹肌溶解、头痛和转氨基酶升高。在终末期肾病(ESRD)患者中,尚未充分评估高剂量达托霉素的不良反应。
确定严重肾功能障碍患者接受高剂量达托霉素治疗时,发生显著不良反应的发生率和特征。
对 2015 年 7 月 1 日至 2019 年 7 月 1 日期间,在单中心进行的回顾性研究,评估估计肌酐清除率<30 ml/min 的患者接受高剂量达托霉素治疗的安全性结局。纳入年龄 18-89 岁的成年患者。患者必须接受基于实际体重,剂量大于或等于 7.5mg/kg 的达托霉素治疗。主要结局是肌酸磷酸激酶(CK)升高、肌病和横纹肌溶解的总发生率。
对 74 例接受达托霉素治疗的患者进行了筛查,其中 50 例纳入研究。患者性别分布均衡(48%为男性,n=24),中位年龄为 61(IQR,48-67)岁。达托霉素使用的主要适应证为革兰阳性菌血症。达托霉素的中位剂量为 750(IQR,600-875)mg,或基于实际体重的 8.46(IQR,7.92-9.96)mg/kg,中位患者体重为 81(IQR,65-113)kg。中位治疗持续时间为 27(IQR,14-42)天。1 例患者在达托霉素治疗期间出现显著 CK 升高伴横纹肌溶解,但因 CK 升高有其他解释而继续使用达托霉素。1 例患者因 CK 升高而停用达托霉素,但不符合显著 CK 升高的定义。
在严重肾功能障碍接受达托霉素 7.5mg/kg 或以上剂量治疗的患者队列中,达托霉素治疗期间 CK 显著升高的情况很少见。未来的研究应证实这些发现,特别要考虑更高的 mg/kg 剂量和/或肥胖人群。