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The hemodynamic effect of an intravenous antispasmodic on propofol requirements during colonoscopy: A randomized clinical trial

机译:静脉内解痉药对结肠镜检查期间异丙酚需求的血流动力学影响:一项随机临床试验

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Purpose: Hemodynamic status during induction of anesthesia may modify the amount of propofol needed to induce loss of consciousness (LOC). This study was aimed to evaluate the effect of antispasmodic-induced tachycardia on the concentration of propofol at the effect-site for inducing LOC when deep sedation was executed for colonoscopy. Methods: One hundred and sixteen adult patients were randomly assigned to receive either 20 mg of the antispasmodic Buscopan intravenously (Buscopan group; n = 58) or normal saline (control group; n = 58) for colonoscopy. After administration of Buscopan, the antispasmodic or normal saline, propofol was given by means of target-controlled infusion to induce LOC. We recorded patient characteristics, hemodynamic profiles, effect-site propofol concentration upon LOC, total propofol dosage for colonoscopy, and colonoscopy outcomes. Results: There were no significant differences in the characteristics between the two groups. Although the patients receiving Buscopan had a higher heart rate than those of the control group (101 +/- 15 beats/minute vs. 77 +/- 13 beats/minute; p < 0.001), we found no significant difference between two groups in the effect-site propofol concentration for inducing LOC (3.9 +/- 0.6 @mg/mL vs. 3.8 +/- 0.6 @mg/mL; p = 0.261) nor total propofol dosage required for colonoscopy (3.2 +/- 1.4 mg/kg vs. 3.1 +/- 1.1 mg/kg; p = 0.698). Both groups had comparable colonoscopy outcomes, including percentage of patients completing the procedure and total procedure time. Conclusion: The hemodynamic responses to intravenous Buscopan neither affected the effect-site propofol concentration needed to induce LOC, nor the total propofol dosage required for colonoscopy in this study. There is no need to modify the dosage of propofol in patients subject to Buscopan premedication in colonoscopy.
机译:目的:麻醉诱导期间的血流动力学状态可能会改变诱导意识丧失(LOC)所需的异丙酚量。本研究旨在评估深层镇静用于结肠镜检查时,解痉诱导的心动过速对诱导LOC的丙泊酚浓度的影响。方法:116名成年患者被随机分配接受20 mg的抗痉挛性Buscopan静脉内(Buscopan组; n = 58)或生理盐水(对照组; n = 58)进行结肠镜检查。在给予解痉剂或生理盐水Buscopan后,通过靶标控制输注丙泊酚以诱导LOC。我们记录了患者的特征,血流动力学特征,LOC上的影响部位丙泊酚浓度,用于结肠镜检查的丙泊酚总剂量以及结肠镜检查的结果。结果:两组之间的特征无显着差异。尽管接受Buscopan的患者的心率高于对照组(101 +/- 15次/分钟vs. 77 +/- 13次/分钟; p <0.001),但我们发现两组之间在心律上无显着差异诱导LOC的作用部位丙泊酚浓度(3.9 +/- 0.6 @ mg / mL与3.8 +/- 0.6 @ mg / mL; p = 0.261)或结肠镜检查所需的总丙泊酚剂量(3.2 +/- 1.4 mg / mL)千克vs.3.1 +/- 1.1毫克/千克; p = 0.698)。两组的结肠镜检查结果相当,包括完成手术的患者百分比和总手术时间。结论:本研究对静脉内Buscopan的血液动力学反应既不影响诱导LOC所需的作用部位丙泊酚浓度,也不影响结肠镜检查所需的总丙泊酚剂量。在结肠镜检查中接受Buscopan药物治疗的患者无需更改丙泊酚的剂量。

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