Medical Intensive Care Unit, University Clinical Centre of the Republic of Srpska, Dvanaest Beba Bb, 78000, Banja Luka, The Republic of Srpska, Bosnia and Herzegovina.
Faculty of Medicine, University of Banja Luka, Save Mrkalja 14, 78000, Banja Luka, Bosnia and Herzegovina.
Naunyn Schmiedebergs Arch Pharmacol. 2024 Oct;397(10):7747-7756. doi: 10.1007/s00210-024-03136-1. Epub 2024 May 7.
Patients treated with ECMO are at great risk of nosocomial infections, and around 10% of isolates are gram-positive pathogens. Linezolid (LZD) is effective in the treatment of these infections but appropriate dosing is challenging. The aim was to evaluate the occurrence of thrombocytopenia during ECMO when treated with LZD. An LZD trough concentration of 8 mg/L was set as the cutoff value for thrombocytopenia occurrence among critically ill patients who received parenteral LZD therapy at a dose of 600 mg every 8 h during ECMO. Eleven patients were included in this prospective observational study. Median LZD trough concentrations were 7.85 (interquartile range (IQR), 1.95-11) mg/L. Thrombocytopenia was found in 81.8% of patients. Based on the median LZD trough concentrations cutoff value, patients were divided into two groups, 1.95 (IQR, 0.91-3.6) and 10.3 (IQR, 9.7-11.7) mg/L, respectively. Median platelet values differed significantly between groups on admission, ECMO day 0, ECMO day 1, and LZD sampling day [194 and 152.5, (p < 0.05)], [113 and 214, (p < 0.05)], [76 and 147.5, (p < 0.01)], and [26 and 96.5, (p < 0.01)], respectively. Duration of LZD therapy was similar between the groups. Significant platelet reduction was observed in both groups, emphasizing the need for closer monitoring to prevent LZD-associated thrombocytopenia.
接受 ECMO 治疗的患者存在严重的医院感染风险,约 10%的分离株为革兰阳性病原体。利奈唑胺(LZD)在治疗这些感染方面有效,但合适的剂量颇具挑战性。本研究旨在评估 ECMO 治疗期间使用 LZD 时血小板减少症的发生情况。将 LZD 谷浓度 8mg/L 设定为接受静脉注射 LZD 治疗的危重症患者发生血小板减少症的截断值,剂量为每 8 小时 600mg。11 例患者纳入本前瞻性观察研究。LZD 谷浓度中位数为 7.85(四分位距(IQR),1.95-11)mg/L。81.8%的患者发生血小板减少症。根据 LZD 谷浓度截断值,患者分为两组,分别为 1.95(IQR,0.91-3.6)和 10.3(IQR,9.7-11.7)mg/L。入院时、ECMO 第 0 天、ECMO 第 1 天和 LZD 采样日两组间血小板值中位数差异有统计学意义[194 和 152.5,(p<0.05)]、[113 和 214,(p<0.05)]、[76 和 147.5,(p<0.01)]和[26 和 96.5,(p<0.01)]。两组 LZD 治疗持续时间相似。两组均观察到显著的血小板减少,强调需要更密切的监测以预防 LZD 相关的血小板减少症。