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蛛网膜下腔和硬膜外给药后利多卡因的吸收情况。

Absorption of lidocaine following subarachnoid and epidural administration.

作者信息

Giasi R M, D'Agostino E, Covino B G

出版信息

Anesth Analg. 1979 Sep-Oct;58(5):360-3. doi: 10.1213/00000539-197909000-00002.

Abstract

The absorption of lidocaine into the vascular system from the epidural and subarachnoid spaces was determined in 20 patients. Seventy-five milligrams (1.5 ml of a 5% solution) of lidocaine was administered intrathecally to 10 patients for spinal anesthesia and 75 mg (3.75 ml of a 2% solution) was injected epidurally. Venous plasma levels of lidocaine were determined at 2, 5, 10, 15, and 30 minutes after subarachnoid or epidural injection. No significant differences existed between the maximum venous plasma concentrations of lidocaine following epidural injection (0.41 +/- 0.07 microgram/ml) and following subarachnoid injection (0.32 +/- 0.07 microgram/ml). However, the rate of vascular absorption of lidocaine from the subarachnoid space was significantly slower than from the epidural space. By 2, 5, and 10 minutes after injection, venous plasma concentrations of lidocaine were significantly higher following epidural injection than they were after subarachnoid injection. This variation was not attributable to differences in blood pressure folloiwng injection. The differential rate of absorption is probably related to the anatomical arrangement of the venous plexuses in the epidural and subarachnoid spaces.

摘要

在20名患者中测定了利多卡因从硬膜外腔和蛛网膜下腔进入血管系统的吸收情况。10名患者接受鞘内注射75毫克(1.5毫升5%溶液)利多卡因用于脊髓麻醉,另外10名患者接受硬膜外注射75毫克(3.75毫升2%溶液)。在蛛网膜下腔或硬膜外注射后2、5、10、15和30分钟测定静脉血浆中的利多卡因水平。硬膜外注射后利多卡因的最大静脉血浆浓度(0.41±0.07微克/毫升)与蛛网膜下腔注射后(0.32±0.07微克/毫升)之间无显著差异。然而,利多卡因从蛛网膜下腔的血管吸收速率明显慢于从硬膜外腔的吸收速率。注射后2、5和10分钟时,硬膜外注射后静脉血浆中的利多卡因浓度显著高于蛛网膜下腔注射后。这种差异并非归因于注射后血压的差异。吸收速率的差异可能与硬膜外腔和蛛网膜下腔静脉丛的解剖结构有关。

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