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肠内乙酰半胱氨酸在重症监护病房的药代动力学特征和生物利用度。

The Pharmacokinetic Profile and Bioavailability of Enteral N-Acetylcysteine in Intensive Care Unit.

机构信息

Institute of Pharmacy, University of Tartu, Nooruse 1, 50411 Tartu, Estonia.

Pharmacy Department, Tartu University Hospital, L. Puusepa 8, 50406 Tartu, Estonia.

出版信息

Medicina (Kaunas). 2021 Nov 8;57(11):1218. doi: 10.3390/medicina57111218.

Abstract

: N-acetylcysteine (NAC) is a mucolytic agent used to prevent ventilator-associated pneumonia in intensive care units. This study aimed to evaluate the oral bioavailability of NAC in critically ill patients with pneumonia, isolated acute brain injury and abdominal sepsis. : This quantitative and descriptive study compared NAC's pharmacokinetics after intravenous and enteral administration. 600 mg of NAC was administered in both ways, and the blood levels for NAC were measured. : 18 patients with pneumonia, 19 patients with brain injury and 17 patients with abdominal sepsis were included in the population pharmacokinetic modelling. A three-compartmental model without lag-time provided the best fit to the data. Oral bioavailability was estimated as 11.6% (95% confidence interval 6.3-16.9%), similar to bioavailability in healthy volunteers and patients with chronic pulmonary diseases. : The bioavailability of enteral NAC of ICU patients with different diseases is similar to the published data on healthy volunteers.

摘要

N-乙酰半胱氨酸(NAC)是一种黏液溶解剂,用于预防重症监护病房中的呼吸机相关性肺炎。本研究旨在评估肺炎、孤立性急性脑损伤和腹部脓毒症的重症患者中 NAC 的口服生物利用度。

这是一项定量和描述性研究,比较了静脉内和肠内给予 NAC 后的药代动力学。两种途径均给予 600mg 的 NAC,并测量 NAC 的血药浓度。

将 18 例肺炎、19 例脑损伤和 17 例腹部脓毒症患者纳入群体药代动力学建模。无滞后时间的三房室模型为数据提供了最佳拟合。口服生物利用度估计为 11.6%(95%置信区间 6.3-16.9%),与健康志愿者和慢性肺部疾病患者中的生物利用度相似。

不同疾病的 ICU 患者肠内给予 NAC 的生物利用度与健康志愿者的已发表数据相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b727/8620940/e6e2bc929773/medicina-57-01218-g001.jpg

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