艾司洛尔用于控制硫喷妥酮和琥珀胆碱后气管插管期间心率和血压升高。

P L Liu, S Gatt, L D Gugino, S R Mallampati, B G Covino
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引用次数: 87

摘要

艾司洛尔是一种超短效心脏选择性β -肾上腺素能阻滞剂,在一项双盲前瞻性研究中,研究了其在硫贲妥和琥珀酰胆碱治疗后控制气管插管相关血流动力学反应的能力。30例ASA身体状态为I的患者接受12分钟的艾司洛尔输注(500微克X kg-1 X min-1持续4分钟,然后300微克X kg-1 X min-1持续8分钟)或生理盐水。药物/安慰剂输注开始5分钟后,用4 mg X kg-1硫喷妥诱导麻醉,随后用琥珀酰胆碱气管插管。在诱导之前,艾司洛尔显著降低心率(HR)(9.3% +/- 1.8%)和心率压产物(RPP)(13.1% +/- 1.8%)、收缩压(SAP)(4.3% +/- 1.5%)和平均动脉压(MAP)(1.7% +/- 2.0%)。与服用安慰剂的患者相比,服用艾司洛尔的患者插管后HR、SAP和RPP的增加大约减少了50%。当最大艾司洛尔插管后反应与最大安慰剂反应比较时,HR (p < 0.0001)和RPP (p < 0.0005)有极显著差异,SAP (p < 0.05)有显著差异。在本研究中使用的剂量输注艾司洛尔显著减弱,但没有完全消除对插管的心血管反应。
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Esmolol for control of increases in heart rate and blood pressure during tracheal intubation after thiopentone and succinylcholine.

Esmolol, an ultra-short-acting cardioselective beta-adrenergic blocker, was investigated in a double-blind prospective protocol for its ability to control haemodynamic responses associated with tracheal intubation after thiopentone and succinylcholine. Thirty ASA physical status I patients received a 12-minute infusion of esmolol (500 micrograms X kg-1 X min-1 for four minutes, then 300 micrograms X kg-1 X min-1 for 8 minutes) or saline. Five minutes after the start of the drug/placebo infusion, anaesthesia was induced with 4 mg X kg-1 thiopentone followed by succinylcholine for tracheal intubation. Prior to induction esmolol produced significant decreases in heart rate (HR) (9.3 +/- 1.8 per cent) and rate-pressure product (RPP) (13.1 +/- 1.8 per cent), systolic blood pressure (SAP) (4.3 +/- 1.5 per cent) and mean arterial blood pressure (MAP) (1.7 +/- 2.0 per cent). Increases in HR, SAP and RPP after intubation were approximately 50 per cent less in patients given esmolol compared to patients given placebo. There were highly significant differences in HR (p less than 0.0001), and RPP (p less than 0.0005) and significant differences in SAP (p less than 0.05) when the maximal esmolol post-intubation response was compared to the maximal placebo response. Infusion of esmolol in the dose utilized in this study significantly attenuated but did not completely eliminate cardiovascular responses to intubation.

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