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[前列腺素E1或阿方那特诱导低血压期间硬膜外给予布比卡因的药代动力学]

[Pharmacokinetics of epidurally administered bupivacaine during prostaglandin E1- or trimetaphan-induced hypotension].

作者信息

Takasaki M, Sakimura S, Takeshita M, Hamakawa T

机构信息

Department of Anesthesiology, Miyazaki Medical College.

出版信息

Masui. 1992 May;41(5):779-84.

PMID:1608154
Abstract

The effects of prostaglandin E1 (PGE1) and trimetaphan (TMP) on the plasma concentrations and derived pharmacokinetic parameters of bupivacaine were studied in 14 women after its epidural administration. Patients, whose ages ranging from 35 to 60 years for mastectomy, received 50 mg of bupivacaine without epinephrine injected into the cervical epidural space during PGE1- or TMP-induced hypotension (80-90 mmHg of the systolic arterial pressure) under general anesthesia with nitrous oxide, oxygen and isoflurane 0.3-0.5%. No significant differences in pharmacokinetic parameters for the absorption and distribution of bupivacaine were found between the two groups. However, the mean elimination half-life of bupivacaine was significantly longer in patients with TMP [5.0 +/- 1.7 (SD) hr] compared with those with PGE1 (3.1 +/- 1.4 hr). The total clearance of bupivacaine was greater in patients with PGE1 (345 +/- 150 ml.min-1) compared with those with TMP (248 +/- 66 ml.min-1). The results of this pharmacokinetic study indicate that the plasma bupivacaine concentration decreases more rapidly during PGE1-induced hypotension than during TMP-induced hypotension.

摘要

在14名女性患者硬膜外给予布比卡因后,研究了前列腺素E1(PGE1)和咪噻芬(TMP)对其血浆浓度及相关药代动力学参数的影响。年龄在35至60岁之间行乳房切除术的患者,在氧化亚氮、氧气和0.3 - 0.5%异氟烷全麻下,于PGE1或TMP诱导的低血压(收缩压80 - 90 mmHg)期间,将50 mg不含肾上腺素的布比卡因注入颈段硬膜外间隙。两组间布比卡因吸收和分布的药代动力学参数无显著差异。然而,与PGE1组患者(3.1±1.4小时)相比,TMP组患者布比卡因的平均消除半衰期显著延长[5.0±1.7(标准差)小时]。与TMP组患者(248±66 ml·min⁻¹)相比,PGE1组患者布比卡因的总清除率更高(345±150 ml·min⁻¹)。这项药代动力学研究结果表明,PGE1诱导低血压期间血浆布比卡因浓度下降速度比TMP诱导低血压期间更快。

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