Department of Pharmacy, Hospital Universitario Central de Asturias, Spain.
Department of Pharmacy, Hospital Universitario San Agustin, Spain.
J Infect Chemother. 2022 Sep;28(9):1249-1254. doi: 10.1016/j.jiac.2022.05.004. Epub 2022 May 14.
Linezolid is an antimicrobial with broad activity against Gram-positive bacteria. Thrombocytopenia is one of its most common side effects often leading to severe complications. The aim of this study is to identify factors related with development of this condition in critically ill patients and to develop and evaluate a predictive machine learning-based model considering easy-to-obtain clinical variables.
Data was obtained from the Medical Information Mart for Intensive Care III. Patients who received linezolid for over three days were considered, excluding those under 18 years and/or lacking laboratory data. Thrombocytopenia was considered as a platelet decrease of at least 50% from baseline.
Three hundred and twenty patients met inclusion criteria of which 63 developed thrombocytopenia and presented significant greater duration of treatment, aspartate-aminotransferase, bilirubin and international normalized ratio; and lower renal clearance and platelet count at baseline. Thrombocytopenia development was associated with a worse outcome (30 days mortality [OR: 2.77; CI95%: 1.87-5.89; P < .001], 60 days mortality [OR: 3.56; CI95%: 2.18-7.26; P < .001]). Thrombocytopenia was also correlated with higher length of hospital stays (35.56 [20.40-52.99] vs 22.69 [10.05-38.61]; P < .001). Median time until this anomaly was of 23 days (CI95%:19.0-NE). Two multivariate models were performed. Accuracy, sensitivity, specificity and AUROC obtained in the best of them were of 0.75, 0.78, 0.62 and 0.80, respectively.
Linezolid associated thrombocytopenia entails greater mortality rates and hospital stays. Although the proposed predictive model has to be subsequently validated in a real clinical setting, its application could identify patients at risk and establish screening and surveillance strategies.
利奈唑胺是一种对革兰氏阳性菌具有广泛活性的抗菌药物。血小板减少症是其最常见的副作用之一,常导致严重并发症。本研究旨在确定与危重症患者发生这种情况相关的因素,并开发和评估一种基于机器学习的预测模型,考虑易于获得的临床变量。
数据来自医疗信息集市 III 重症监护。纳入接受利奈唑胺治疗超过 3 天的患者,排除 18 岁以下和/或缺乏实验室数据的患者。血小板减少症定义为血小板计数比基线至少下降 50%。
320 名患者符合纳入标准,其中 63 名发生血小板减少症,且治疗时间明显延长,天冬氨酸转氨酶、胆红素和国际标准化比值升高,而基线时的肾清除率和血小板计数较低。血小板减少症的发生与不良预后相关(30 天死亡率[OR:2.77;95%CI:1.87-5.89;P<0.001],60 天死亡率[OR:3.56;95%CI:2.18-7.26;P<0.001])。血小板减少症也与更长的住院时间相关(35.56 [20.40-52.99] 与 22.69 [10.05-38.61];P<0.001)。该异常中位时间为 23 天(95%CI:19.0-NE)。进行了两项多变量模型分析。其中最优模型的准确性、敏感度、特异度和 AUC 分别为 0.75、0.78、0.62 和 0.80。
利奈唑胺相关的血小板减少症导致更高的死亡率和住院时间。虽然所提出的预测模型需要在真实临床环境中进一步验证,但它的应用可以识别出有风险的患者,并制定筛查和监测策略。