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[氟哌利多、喷他佐辛和氯胺酮全凭静脉麻醉时氯胺酮和喷他佐辛的药代动力学]

[Pharmacokinetics of ketamine and pentazocine during total intravenous anesthesia with droperidol, pentazocine and ketamine].

作者信息

Kudo T, Kudo M, Kimura F, Ishihara H, Matsuki A

机构信息

Department of Anesthesiology, University of Hirosaki School of Medicine.

出版信息

Masui. 1992 Nov;41(11):1772-6.

PMID:1460754
Abstract

Pharmacokinetics was studied in ten surgical patients who underwent various operative procedures of about 4 hours under total intravenous anesthesia with droperidol, pentazocine and ketamine (DPK). Plasma levels of ketamine, its metabolites and pentazocine were determined thirteen times during and after DPK. During anesthesia, ketamine (KO) and norketamine (KMI) levels ranged from 0.7 to 1.0 micrograms.ml-1 and from 0.09 to 0.74 micrograms.ml-1, respectively. A small amount of dehydronorketamine (KM II) was detected only 90 min after the start of DPK anesthesia. Plasma half-lives of ketamine were calculated to be 33 min for distribution phase (alpha phase) and 60 min for elimination phase (beta phase), respectively. Pentazocine levels decreased 300 min after the induction of DPK to 10% of the control level measured 5 min after its injection. Plasma half-lives of pentazocine were 60 min for alpha phase and 140 min for beta phase, respectively. The data obtained in this clinical study show that pharmacokinetics of ketamine during DPK is almost similar to that of DFK.

摘要

对10名接受约4小时各种手术操作的外科患者进行了药代动力学研究,这些患者在氟哌利多、喷他佐辛和氯胺酮(DPK)全静脉麻醉下进行手术。在DPK给药期间及给药后,对氯胺酮、其代谢产物和喷他佐辛的血浆水平进行了13次测定。麻醉期间,氯胺酮(KO)和去甲氯胺酮(KMI)水平分别为0.7至1.0微克/毫升和0.09至0.74微克/毫升。仅在DPK麻醉开始90分钟后检测到少量脱氢去甲氯胺酮(KM II)。氯胺酮的血浆分布半衰期(α相)计算为33分钟,消除半衰期(β相)计算为60分钟。喷他佐辛水平在DPK诱导后300分钟降至注射后5分钟测得的对照水平的10%。喷他佐辛的血浆α相半衰期为60分钟,β相半衰期为140分钟。该临床研究获得的数据表明,DPK期间氯胺酮的药代动力学与DFK的药代动力学几乎相似。

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