Institute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Department of Anaesthesiology, University Hospital, LMU Munich, Munich, Germany.
Antimicrob Agents Chemother. 2021 Nov 17;65(12):e0156421. doi: 10.1128/AAC.01564-21. Epub 2021 Sep 27.
Pneumonia is one of the most common infections in intensive care patients, and it is often treated with beta-lactam antibiotics. Even if therapeutic drug monitoring in blood is available, it is unclear whether sufficient concentrations are reached at the target site: the lung. The present study was initiated to fill this knowledge gap. Various compartments from 10 patients' explanted lungs were subjected to laboratory analysis. Meropenem was quantified in serum, bronchoalveolar lavage (BAL) fluid, microdialysate, and homogenized lung tissue with isotope dilution liquid chromatography tandem mass spectrometry (ID-LC-MS/MS). BAL fluid represents diluted epithelial lining fluid (ELF), and microdialysate represents interstitial fluid (IF). Differences between target site and blood concentrations were investigated. The median meropenem concentration in blood, ELF, IF, and tissue were 26.8, 18.0, 12.1, and 9.1 mg/liter, respectively. A total of 37.5% of the target site ELF and IF meropenem concentrations were below the clinical EUCAST breakpoint of 8 mg/liter. The median ELF/serum quotient was 61.8% (interquartile range [IQR], 24.8% to 87.6%), the median IF/serum quotient was 35.4% (IQR, 23.8% to 54.3%), and the median tissue/serum quotient was 34.2% (IQR, 28.3% to 38.2%). We observed a substantial interindividual variability between the blood and the compartments (ELF and IF), whereas the intraindividual variability was relatively low. Target site measurement in different lung compartments was feasible and successfully applied in a clinical setting. A relevant amount of 37.5% of the target site concentrations were below the clinical EUCAST breakpoint, indicating subtherapeutic dosing in high-risk patients receiving perioperative antibiotic prophylaxis in lung transplantation. (This study has been registered at ClinicalTrials.gov under identifier NCT03970265.).
肺炎是重症监护病房患者中最常见的感染之一,常使用β-内酰胺类抗生素进行治疗。即使可以进行血药浓度治疗药物监测,也尚不清楚在目标部位(肺部)是否达到了足够的浓度。本研究旨在填补这一知识空白。对 10 名患者的肺移植标本的不同部位进行了实验室分析。采用同位素稀释液相色谱串联质谱法(ID-LC-MS/MS)对血清、支气管肺泡灌洗液(BAL)、微透析液和匀浆肺组织中的美罗培南进行定量分析。BAL 液代表稀释的上皮衬里液(ELF),微透析液代表间质液(IF)。研究了目标部位与血液浓度之间的差异。血液、ELF、IF 和组织中的美罗培南中位数浓度分别为 26.8、18.0、12.1 和 9.1mg/L。共有 37.5%的目标部位 ELF 和 IF 美罗培南浓度低于临床 EUCAST 8mg/L 的折点。ELF/血清商数中位数为 61.8%(四分位距[IQR],24.8%至 87.6%),IF/血清商数中位数为 35.4%(IQR,23.8%至 54.3%),组织/血清商数中位数为 34.2%(IQR,28.3%至 38.2%)。我们观察到血液与各部位(ELF 和 IF)之间存在很大的个体间变异性,而个体内变异性相对较低。在不同的肺腔室中进行目标部位测量是可行的,并已成功应用于临床环境。有 37.5%的目标部位浓度达到了临床 EUCAST 折点以下,这表明在接受肺移植围手术期抗生素预防的高危患者中,存在治疗剂量不足的情况。(本研究已在 ClinicalTrials.gov 上注册,登记号为 NCT03970265。)