Division of Infectious Diseases, Department of Health Sciences, University of Genova, Genova, Italy.
Division of Infectious Diseases, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
J Antimicrob Chemother. 2024 Apr 2;79(4):835-845. doi: 10.1093/jac/dkae037.
Isavuconazole is first-line treatment of invasive aspergillosis. Therapeutic drug monitoring (TDM) is deemed not necessary, since most patients reached therapeutic levels (>1 mg/L) in large studies. Low levels were reported in some critically ill patients admitted to the ICU. The aim was to compare isavuconazole levels between critically ill and non-critically ill patients.
Retrospective analysis of data from all patients treated with standard-dose isavuconazole between 1 January 2019 and 26 October 2022 was performed. The following data were collected: TDM results from the first 30 days of therapy; ward of admission; demographic and clinical characteristics; continuous renal replacement therapy; extracorporeal membrane oxygenation; and co-administered drugs.
Seventy-two patients (median age 65 years) and 188 TDM measurements (mean number of samples per patient 2.6 ± 1.7) were included; 33 (45.8%) were ICU patients (3 also had haematological disorders); 39 (54.2%) were non-ICU patients, of whom 31 had haematological disorders. In all patients, the mean isavuconazole blood level was 3.33 ± 2.26 mg/L. Significantly lower levels were observed in the ICU versus the non-ICU population: mean 2.02 ± 1.22 versus 4.15 ± 2.31 mg/L (P < 0.001). Significantly higher rates of subtherapeutic levels were observed in ICU patients compared with the non-ICU population: all determinations <2 mg/L in 33.3% versus 7.7%, and all determinations <1 mg/L in 12.1% versus 0%, respectively. Predictors of lower isavuconazole levels were admission to the ICU, BMI > 25 kg/m2, bilirubin > 1.2 mg/dL and the absence of haematological disorder.
ICU patients had significantly lower isavuconazole blood levels compared to non-ICU population. The TDM of isavuconazole for efficacy should be performed in ICU.
伊曲康唑是侵袭性曲霉病的一线治疗药物。由于大多数患者在大型研究中达到了治疗水平(>1mg/L),因此不需要进行治疗药物监测(TDM)。但一些入住 ICU 的危重症患者报告了较低的水平。本研究旨在比较危重症和非危重症患者的伊曲康唑水平。
对 2019 年 1 月 1 日至 2022 年 10 月 26 日期间接受标准剂量伊曲康唑治疗的所有患者的数据进行回顾性分析。收集的资料包括:治疗开始后 30 天内的 TDM 结果、入院科室、人口统计学和临床特征、连续肾脏替代治疗、体外膜氧合和联合使用的药物。
共纳入 72 例患者(中位年龄 65 岁)和 188 次 TDM 测量(每位患者平均样本数 2.6±1.7);33 例(45.8%)为 ICU 患者(其中 3 例还患有血液系统疾病);39 例(54.2%)为非 ICU 患者,其中 31 例患有血液系统疾病。所有患者的伊曲康唑平均血药浓度为 3.33±2.26mg/L。与非 ICU 人群相比,ICU 患者的血药浓度显著较低:平均为 2.02±1.22 与 4.15±2.31mg/L(P<0.001)。与非 ICU 人群相比,ICU 患者的亚治疗水平率显著较高:所有测定值<2mg/L 的比例分别为 33.3%与 7.7%,所有测定值<1mg/L 的比例分别为 12.1%与 0%。伊曲康唑水平较低的预测因素包括入住 ICU、BMI>25kg/m2、胆红素>1.2mg/dL 以及无血液系统疾病。
与非 ICU 人群相比,ICU 患者的伊曲康唑血药水平显著较低。对于 ICU 患者,应进行伊曲康唑的 TDM 以评估疗效。