Safety of high-dose daptomycin in obese patients: a multicentric retrospective study.

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES
Vasco Dias Meireles, Clémentine Airaud, Elouan Demay, Charles Cazanave, Fabien Xuereb, Pauline Lazaro, Astrid Bacle, Marin Lahouati
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引用次数: 0

Abstract

Purpose: Obese patients treated with daptomycin at 4 mg/kg have a 30% increased drug exposure, potentially raising the risk of adverse events (AEs) like rhabdomyolysis. Given limited data on the safety of higher doses (10 mg/kg) in this population, this study aimed to assess the safety of high-dose daptomycin in obese patients and to identify potential AEs risk factors.

Methods: This multicenter, retrospective observational study was conducted from June 2021 to May 2022 using medical records. Patients with a BMI > 30 kg/m2 were classified as obese. AEs assessed included: CK elevation (> 5x upper limit of normal), severe elevation (> 10x upper limit), eosinophilic pneumonia, and elevated liver enzymes. Both univariate and multivariate analyses were conducted.

Results: A total of 1 303 patients were included: 970 non-obese and 333 Ob patients. These patients received an average daptomycin dose of 9.9 mg/kg based on actual body weight for an average treatment duration of 8.27 days. One-third of the patients had CK monitoring. AEs rates were 3.5% for the n-Ob group vs. 8.7% in the Ob group (p < 0.01). Ob patients had significantly higher CK levels (n-Ob, 9.5%; Ob, 20.3%; p = 0.001), and severe elevation (n-Ob, 5.2%; Ob, 10.9%; p = 0.03). Factors increasing AE risk included obesity, concomitant prescriptions of drugs with risk of rhabdomyolysis, eGFR 30-60 mL/min, and daptomycin duration (OR = 2.42; 4.34; 2.03 and 1.05, respectively, p < 0.001). On the opposite, consultation with an infectious disease specialist reduced risk (OR = 0.52, p = 0.024).

Conclusion: This study highlights that obese patient has a significantly increased risk of AEs with high dose of daptomycin compared to non-obese patients. Adjusted body weight dosing may be considered to reduce AEs risk.

大剂量达托霉素在肥胖患者中的安全性:一项多中心回顾性研究。
目的:肥胖患者接受4 mg/kg剂量的达托霉素治疗时,药物暴露量增加了30%,可能会增加横纹肌溶解等不良事件(AEs)的风险。鉴于有关肥胖患者使用大剂量(10 mg/kg)达托霉素安全性的数据有限,本研究旨在评估肥胖患者使用大剂量达托霉素的安全性,并确定潜在的不良反应风险因素:这项多中心回顾性观察研究是在 2021 年 6 月至 2022 年 5 月期间利用医疗记录进行的。体重指数大于 30 kg/m2 的患者被归类为肥胖。评估的不良反应包括肌酸激酶升高(大于正常值上限的 5 倍)、严重升高(大于上限的 10 倍)、嗜酸性粒细胞肺炎和肝酶升高。研究人员进行了单变量和多变量分析:共纳入 1 303 名患者:结果:共纳入 1 303 名患者:970 名非肥胖患者和 333 名肥胖患者。根据实际体重,这些患者接受的达托霉素平均剂量为 9.9 毫克/千克,平均疗程为 8.27 天。三分之一的患者接受了 CK 监测。N-Ob组的AEs发生率为3.5%,而Ob组为8.7%(P 结论:N-Ob组的AEs发生率为3.5%,而Ob组为8.7%:本研究强调,与非肥胖患者相比,肥胖患者在使用大剂量达托霉素时发生 AEs 的风险明显增加。可考虑调整体重剂量以降低AEs风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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