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埃索美拉唑在危重症患者中的药代动力学

Pharmacokinetics of Esomeprazole in Critically Ill Patients.

作者信息

Xu Yanyan, Tian Xin, Wang Wei, Tian Weiqiang, Zhang Tao, Sun Jian, Zhou Qingyun, Shao Chuxiao

机构信息

Department of Pharmacy, Lishui Municipal Central Hospital, Lishui, China.

Department of Intensive Care Medicine, Lishui Municipal Central Hospital, Lishui, China.

出版信息

Front Med (Lausanne). 2022 Feb 7;8:621406. doi: 10.3389/fmed.2021.621406. eCollection 2021.

Abstract

BACKGROUND

Esomeprazole, a potent proton pump inhibitor (PPI), is widely used for the prevention of stress ulcers in intensive care unit (ICU) patients.

OBJECTIVE

This study investigates the pharmacokinetics (PK) of esomeprazole in critically ill patients.

METHODS

The study included eligible adult ICU patients who received endotracheal intubation assisted mechanical ventilation for more than 48 h and had at least an extra risk factor for stress ulcers. All enrolled patients received once-daily intravenous (IV) esomeprazole 40 mg. After the first dose of esomeprazole was administrated, serial blood samples were collected at 3, 5, 15, 30 min and 1, 2, 4, 6, 8, and 10 h. The total sample concentrations of esomeprazole were measured by UPLC-MS/MS. Esomeprazole PK parameters were analyzed using noncompartmental analysis.

RESULTS

A total of 30 patients were evaluable. Mean age and body mass index (BMI) were 61.97 years and 23.14. PK sampling on the first dose resulted in the following median (IQR) parameters: AUC 8.06 (6.65-9.47) mg·h/L; MRT 4.70 (3.89-5.51) h; t 3.29 (2.7-3.87) h; V 24.89 (22.09-27.69) L; CL 6.13 (5.01-7.26) L/h; and C 2.56 (2.30-2.82) mg/L.

CONCLUSIONS

According to the label of esomeprazole, our study showed different esomeprazole PK parameters in ICU patients compared with healthy volunteers. Esomeprazole has unique pharmacokinetic parameters in critically ill patients.

摘要

背景

埃索美拉唑是一种强效质子泵抑制剂(PPI),广泛用于预防重症监护病房(ICU)患者的应激性溃疡。

目的

本研究调查埃索美拉唑在危重症患者中的药代动力学(PK)。

方法

该研究纳入了符合条件的成年ICU患者,这些患者接受气管插管辅助机械通气超过48小时,且至少有一个应激性溃疡的额外危险因素。所有入选患者每天接受一次静脉注射(IV)埃索美拉唑40mg。在首次给予埃索美拉唑后,于3、5、15、30分钟以及1、2、4、6、8和10小时采集系列血样。采用超高效液相色谱-串联质谱法(UPLC-MS/MS)测定埃索美拉唑的总样本浓度。使用非房室分析方法分析埃索美拉唑的PK参数。

结果

共有30例患者可进行评估。平均年龄和体重指数(BMI)分别为61.97岁和23.14。首次给药后的PK采样得出以下中位数(IQR)参数:AUC 8.06(6.65 - 9.47)mg·h/L;MRT 4.70(3.89 - 5.51)小时;t 3.29(2.7 - 3.87)小时;V 24.89(22.09 - 27.69)L;CL 6.13(5.01 - 7.26)L/小时;以及C 2.56(2.30 - 2.82)mg/L。

结论

根据埃索美拉唑的标签说明,我们的研究显示ICU患者与健康志愿者相比,埃索美拉唑的PK参数有所不同。埃索美拉唑在危重症患者中具有独特的药代动力学参数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b640/8858832/ad811ff9aa66/fmed-08-621406-g0001.jpg

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