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异丙酚和芬太尼用于主动脉瓣反流患者麻醉诱导的时间较长:一项病例对照前瞻性研究。

Propofol and fentanyl take longer for induction of anesthesia in aortic regurgitation: a case-controlled prospective study.

作者信息

Nath Soumya S, Tripathi Mukesh, Banerjee Sudipto

机构信息

Department of Anesthesiology, Sahara Hospital, Lucknow, India.

Department of Anaesthesiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India.

出版信息

J Cardiothorac Vasc Anesth. 2014 Apr;28(2):290-4. doi: 10.1053/j.jvca.2013.05.038. Epub 2013 Sep 21.

DOI:10.1053/j.jvca.2013.05.038
PMID:24064202
Abstract

OBJECTIVES

This study was conducted to determine if induction time of anesthesia in patients with aortic regurgitation (AR) is different from patients with a normal aortic valve (AV).

DESIGN

A prospective, case-control study.

SETTING

A single institutional study conducted in a tertiary care teaching hospital.

PARTICIPANTS

Twenty-four male patients scheduled for cardiac surgery, group I (n = 12) patients with competent AV and group 2 (n = 12) with severe AR.

INTERVENTIONS

General anesthesia was induced by intravenous infusion of propofol and fentanyl.

MEASUREMENTS AND MAIN RESULTS

Continuous measurements of heart rate, intra-arterial blood pressure, and bispectral index were recorded. Induction doses of propofol and fentanyl were analyzed and compared. There was significant difference between the 2 groups in terms of induction time of anesthesia (mean ± SD 308 ± 68.2 seconds in group 1 v 445 ± 97.9 seconds in group 2). The patients in group 2 (AR) required significantly larger doses of propofol (0.91 ± 0.40 mg/kg) than the patients in group 1 (0.49 ± 0.17 mg/kg). Similarly, fentanyl dose was increased in the group 2 patients (20.8 ± 15.9 µg/kg) compared with the group 1 patients (9.2 ± 2.9 µg/kg).

CONCLUSION

The authors concluded that there was a significant prolongation of the induction time of anesthesia and the need of larger doses of propofol and fentanyl by slow intravenous infusion regimen in patients with AR compared with patients with a competent aortic valve.

摘要

目的

本研究旨在确定主动脉瓣关闭不全(AR)患者的麻醉诱导时间是否与主动脉瓣正常(AV)的患者不同。

设计

一项前瞻性病例对照研究。

地点

在一家三级护理教学医院进行的单机构研究。

参与者

24名计划进行心脏手术的男性患者,第一组(n = 12)为主动脉瓣功能正常的患者,第二组(n = 12)为重度AR患者。

干预措施

通过静脉输注丙泊酚和芬太尼诱导全身麻醉。

测量和主要结果

记录心率、动脉血压和脑电双频指数的连续测量值。分析并比较丙泊酚和芬太尼的诱导剂量。两组在麻醉诱导时间方面存在显著差异(第一组平均±标准差为308±68.2秒,第二组为445±97.9秒)。第二组(AR)患者所需的丙泊酚剂量(0.91±0.40 mg/kg)明显高于第一组患者(0.49±0.17 mg/kg)。同样,与第一组患者(9.2±2.9 µg/kg)相比,第二组患者的芬太尼剂量增加(20.8±15.9 µg/kg)。

结论

作者得出结论,与主动脉瓣功能正常的患者相比,AR患者采用缓慢静脉输注方案时,麻醉诱导时间显著延长,且需要更大剂量的丙泊酚和芬太尼。

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