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孕早期硫喷妥钠需求量降低。

Decreased thiopental requirements in early pregnancy.

作者信息

Gin T, Mainland P, Chan M T, Short T G

机构信息

Department of Anaesthesia and Intensive Care, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong.

出版信息

Anesthesiology. 1997 Jan;86(1):73-8. doi: 10.1097/00000542-199701000-00011.

Abstract

BACKGROUND

Anesthetic requirements for inhalational agents are decreased during pregnancy, but there are no data regarding requirements for intravenous agents. The quantal dose-response curves for thiopental were calculated for 70 nonpregnant women having gynecologic surgery and for 70 pregnant women of 7-13 weeks' gestation having elective abortions.

METHODS

Groups of 10 patients were given 2, 2.4, 2.8, 3.3, 3.8, 4.5, or 5.3 mg/kg thiopental as a bolus dose during a period of 10 s. Two minutes later, patients were asked to open their eyes as a test for hypnosis. Patients who did not open their eyes were given a 10-s, 50-Hz, 80-mA transcutaneous tetanic electrical stimulus to the ulnar nerve as a test for anesthesia. Purposeful movement indicated that there was no anesthesia. Log dose-response curves for hypnosis and anesthesia were calculated after logit transformation.

RESULTS

In the nonpregnant women, the median effective doses (ED50s) (95% confidence interval) for hypnosis and anesthesia were 3.1 (2.8-3.4) mg/kg and 4.9 (4.5-5.4) mg/kg, whereas in the pregnant women the corresponding ED50s were 2.6 (2.3-2.8) mg/kg and 4 (3.7-4.4) mg/kg. In the non-pregnant women, the ED95s (95% CI) for hypnosis and anesthesia were 4.4 (3.9-5.4) mg/kg and 6.4 (5.7-7.9) mg/kg, whereas in the pregnant women the corresponding ED95s were 3.7 (3.3-4.5) mg/kg and 5.2 (4.7-6.3) mg/kg. The pregnant to nonpregnant relative median potency (95% CI) ratio for hypnosis was 0.83 (0.67-0.96) and for anesthesia it was 0.82 (0.62-0.94).

CONCLUSIONS

The dose of thiopental for hypnosis was 17% less and that for anesthesia was 18% less in pregnant women of 7-13 weeks' gestation compared with that in nonpregnant women.

摘要

背景

孕期吸入性麻醉药的需求降低,但关于静脉麻醉药需求的数据尚无报道。计算了70例接受妇科手术的非孕妇女以及70例妊娠7至13周行选择性流产的孕妇硫喷妥钠的质反应剂量-反应曲线。

方法

每组10例患者在10秒内静脉推注2、2.4、2.8、3.3、3.8、4.5或5.3mg/kg硫喷妥钠。两分钟后,要求患者睁眼以测试催眠效果。未睁眼的患者给予50Hz、80mA的经皮强直电刺激尺神经10秒以测试麻醉效果。有目的的运动表明无麻醉作用。经对数转换后计算催眠和麻醉的对数剂量-反应曲线。

结果

非孕妇女催眠和麻醉的半数有效剂量(ED50s)(95%置信区间)分别为3.1(2.8 - 3.4)mg/kg和4.9(4.5 - 5.4)mg/kg,而孕妇相应的ED50s分别为2.6(2.3 - 2.8)mg/kg和4(3.7 - 4.4)mg/kg。非孕妇女催眠和麻醉的95%有效剂量(ED95s)(95%CI)分别为4.4(3.9 - 5.4)mg/kg和6.4(5.7 - 7.9)mg/kg,而孕妇相应的ED95s分别为3.7(3.3 - 4.5)mg/kg和5.2(4.7 - 6.3)mg/kg。孕妇与非孕妇女催眠的相对半数效价(95%CI)比为0.83(0.67 - 0.96),麻醉的相对半数效价比为0.82(0.62 - 0.94)。

结论

与非孕妇女相比,妊娠7至13周的孕妇硫喷妥钠的催眠剂量降低17%,麻醉剂量降低18%。

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