Department of Internal Medicine, Dongguk University, Ilsan Hospital, Goyang-si, Gyeonggi-do, Republic of Korea.
Divisions of Pulmonology and Critical Care Medicine, Department of Internal Medicine, Dongguk University, Ilsan Hospital, Goyang-si, Gyeonggi-do, Republic of Korea.
Int J Antimicrob Agents. 2015 Jun;45(6):605-9. doi: 10.1016/j.ijantimicag.2015.01.011. Epub 2015 Feb 25.
Colistimethate sodium (CMS) is increasingly used to treat multidrug-resistant Gram-negative bacilli infections. However, the incidence of CMS-associated nephrotoxicity has not been evaluated in patients with carbapenem-resistant Acinetobacter baumannii (CRAB) pneumonia. This retrospective study included 120 patients with CRAB pneumonia treated with intravenous CMS for ≥72 h. The objective of the study was to determine risk factors for CMS-induced nephrotoxicity and 30-day mortality in patients with CRAB pneumonia. Of the 120 patients with CRAB pneumonia, 61 (51%) developed nephrotoxicity. Multivariate analysis showed that dose per ideal body weight (IBW) [odds ratio (OR)=1.28, 95% confidence interval (CI) 1.01-1.62; P=0.04], Charlson co-morbidity index (OR=1.31, 95% CI 1.06-1.60; P=0.01) and septic shock (OR=3.16, 95% CI 1.32-7.60; P=0.01) were associated with CMS-associated nephrotoxicity. Thirty-day mortality was 33% (39/120). Multivariate analysis showed that higher daily doses of CMS per IBW [hazard ratio (HR)=0.81, 95% CI 0.67-0.98; P=0.03] and longer duration of CMS therapy (HR=0.86, 95% CI 0.79-0.95; P=0.002) were associated with increased survival. Septic shock (HR=3.91, 95% CI 1.95-7.83; P<0.001) and corticosteroid use (HR=3.49, 95% CI 1.67-7.28; P=0.001) were associated with decreased survival in patients with CRAB pneumonia. Higher daily doses of CMS per IBW, Charlson comorbidity index and septic shock were significant risk factors for CMS-associated nephrotoxicity. However, CMS-associated nephrotoxicity does not appear to have an impact on mortality.
黏菌素硫代丁二酸(CMS)越来越多地用于治疗多重耐药革兰氏阴性杆菌感染。然而,在碳青霉烯类耐药鲍曼不动杆菌(CRAB)肺炎患者中,尚未评估 CMS 相关肾毒性的发生率。本回顾性研究纳入了 120 例接受静脉 CMS 治疗≥72 小时的 CRAB 肺炎患者。本研究的目的是确定 CRAB 肺炎患者中 CMS 诱导的肾毒性和 30 天死亡率的危险因素。在 120 例 CRAB 肺炎患者中,61 例(51%)发生肾毒性。多变量分析显示,按理想体重(IBW)计算的剂量[比值比(OR)=1.28,95%置信区间(CI)1.01-1.62;P=0.04]、Charlson 合并症指数(OR=1.31,95%CI 1.06-1.60;P=0.01)和感染性休克(OR=3.16,95%CI 1.32-7.60;P=0.01)与 CMS 相关肾毒性相关。30 天死亡率为 33%(39/120)。多变量分析显示,IBW 更高的 CMS 日剂量[风险比(HR)=0.81,95%CI 0.67-0.98;P=0.03]和更长的 CMS 治疗时间(HR=0.86,95%CI 0.79-0.95;P=0.002)与存活率增加相关。感染性休克(HR=3.91,95%CI 1.95-7.83;P<0.001)和皮质类固醇使用(HR=3.49,95%CI 1.67-7.28;P=0.001)与 CRAB 肺炎患者存活率降低相关。IBW 更高的 CMS 日剂量、Charlson 合并症指数和感染性休克是 CMS 相关肾毒性的显著危险因素。然而,CMS 相关肾毒性似乎不会对死亡率产生影响。