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在 vvECMO 治疗期间接受高剂量利奈唑胺治疗的 COVID-19 相关 ARDS 患者的血小板减少症风险:一项观察性研究。

Thrombocytopenia risks in ARDS COVID-19 patients treated with high-dose linezolid during vvECMO therapy: an observational study.

机构信息

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.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2024 Oct;397(10):7747-7756. doi: 10.1007/s00210-024-03136-1. Epub 2024 May 7.

DOI:10.1007/s00210-024-03136-1
PMID:38713258
Abstract

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.

摘要

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。

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本文引用的文献

1
What's new in therapeutic drug monitoring of antimicrobials?抗菌药物治疗药物监测有哪些新进展?
Intensive Care Med. 2023 Jul;49(7):857-859. doi: 10.1007/s00134-023-07060-5. Epub 2023 May 3.
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Treatment and outcome of gram-positive bacteremia in patients receiving extracorporeal membrane oxygenation.体外膜肺氧合患者革兰阳性菌血症的治疗和转归。
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Hematological toxicities associated with linezolid therapy in adults: key findings and clinical considerations.
成人利奈唑胺治疗相关的血液学毒性:主要发现及临床考量
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Extracorporeal membrane oxygenation for COVID-19-related acute respiratory distress syndrome: a narrative review.用于治疗新型冠状病毒肺炎相关急性呼吸窘迫综合征的体外膜肺氧合:一篇叙述性综述
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Individualised dosing of antibiotics in ICU patients: timing, target and model selection matter.重症监护病房患者抗生素的个体化给药:时机、目标和模型选择很重要。
Intensive Care Med. 2023 Apr;49(4):475-476. doi: 10.1007/s00134-023-06990-4. Epub 2023 Jan 31.
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Expert consensus statement on therapeutic drug monitoring and individualization of linezolid.专家共识声明:利奈唑胺的治疗药物监测与个体化用药
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7
Global Challenges to Public Health Care Systems during the COVID-19 Pandemic: A Review of Pandemic Measures and Problems.新冠疫情期间全球公共卫生保健系统面临的挑战:疫情应对措施与问题综述
J Pers Med. 2022 Aug 7;12(8):1295. doi: 10.3390/jpm12081295.
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Sepsis and Thrombocytopenia: A Nowadays Problem.脓毒症与血小板减少症:当今的一个问题。
Cureus. 2022 May 27;14(5):e25421. doi: 10.7759/cureus.25421. eCollection 2022 May.
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Antibiotics and ECMO in the Adult Population-Persistent Challenges and Practical Guides.成人人群中的抗生素与体外膜肺氧合——持续挑战与实用指南
Antibiotics (Basel). 2022 Mar 4;11(3):338. doi: 10.3390/antibiotics11030338.
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Evidence-Based Mechanical Ventilatory Strategies in ARDS.急性呼吸窘迫综合征基于证据的机械通气策略
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