首页> 外文期刊>American journal of therapeutics >A Phase IIIb, randomized, double-blind, placebo-controlled, multicenter study evaluating the safety and efficacy of dexmedetomidine for sedation during awake fiberoptic intubation.
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A Phase IIIb, randomized, double-blind, placebo-controlled, multicenter study evaluating the safety and efficacy of dexmedetomidine for sedation during awake fiberoptic intubation.

机译:一项IIIb期,随机,双盲,安慰剂对照的多中心研究,评估了右美托咪定在清醒光纤插管期间镇静的安全性和有效性。

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摘要

GABA-mediated sedatives have respiratory depressant properties that may be detrimental in patients with difficult airways. In this randomized, double-blind, multicenter, Phase IIIb Food and Drug Administration study, safety and efficacy of dexmedetomidine compared with placebo were evaluated as the primary sedative for awake fiberoptic intubation (AFOI). Patients were randomized to receive dexmedetomidine or saline. Patients were sedated with dexmedetomidine or rescue midazolam to achieve targeted sedation (Ramsay Sedation Scale >/= 2) before topicalization and throughout AFOI. Primary efficacy endpoint was percentage of patients requiring rescue midazolam; secondary efficacy endpoints were total dose of rescue midazolam, percentage requiring additional rescue nonmidazolam medications, anesthesiologist's assessment of ease of subject care, and patient recall and satisfaction 24 hours postoperatively. Less rescue midazolam was required to maintain Ramsay Sedation Scale >/=2 (47.3% vs. 86.0%, P < 0.001), and supplemental midazolam dose was lower (1.07 +/- 1.5 mg vs. 2.85 +/- 3.0 mg, P < 0.001) with dexmedetomidine compared with placebo. More Mallampati Class IV patients treated with dexmedetomidine were successfully intubated without midazolam than with placebo (66.7% vs. 8.3%, P = 0.009). Dexmedetomidine decreased blood pressure and heart rate compared with placebo patients sedated with midazolam. Patients and anesthesiologists showed favorable satisfaction responses in both groups. Adverse events and patient recall were similar in both groups. Dexmedetomidine is effective as the primary sedative in patients undergoing AFOI. Some patients may require small supplemental doses of midazolam, in addition to dexmedetomidine, to achieve sufficient sedation for AFOI. Dexmedetomidine provides another AFOI option for sedation of patients with difficult airways.
机译:GABA介导的镇静剂具有呼吸抑制特性,可能对呼吸困难的患者有害。在这项随机,双盲,多中心,IIIb期食品和药物管理局研究中,右美托咪定与安慰剂相比的安全性和有效性被评估为清醒光纤插管(AFOI)的主要镇静剂。患者被随机分配接受右美托咪定或生理盐水。在局部麻醉之前和整个AFOI期间,患者使用右美托咪定或抢救的咪达唑仑镇定以达到靶向镇静作用(Ramsay镇静等级> / = 2)。主要疗效终点是需要急救的咪达唑仑患者的百分比;次要疗效终点为抢救性咪达唑仑的总剂量,需要额外抢救性非咪达唑仑药物的百分比,麻醉学家对受试者易于护理的评估以及术后24小时的患者召回率和满意度。维持Ramram镇静等级> / = 2所需的抢救咪达唑仑较少(47.3%vs. 86.0%,P <0.001),补充咪达唑仑的剂量较低(1.07 +/- 1.5 mg vs. 2.85 +/- 3.0 mg,P与安慰剂相比,右美托咪定的<0.001)。与未使用安慰剂的患者相比,使用右美托咪定治疗的Mallampati IV类患者成功进行了插管术,未使用咪达唑仑的比例更高(66.7%比8.3%,P = 0.009)。与使用咪达唑仑镇静的安慰剂患者相比,右美托咪定降低了血压和心率。两组患者和麻醉医生的满意度均令人满意。两组的不良事件和患者回忆均相似。右美托咪定在接受AFOI的患者中作为主要的镇静剂有效。除右美托咪定外,某些患者可能还需要补充小剂量的咪达唑仑,以达到对AFOI足够的镇静作用。右美托咪定为患有困难气道的患者镇静提供了另一种AFOI选项。

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