确定雷马唑仑抑制成人上消化道内窥镜插入应答的90%有效剂量:一项采用偏置硬币上下序贯方法的双盲研究

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Journal of Clinical Pharmacy and Therapeutics Pub Date : 2023-09-19 DOI:10.1155/2023/9391407
Pengfei Yin, Xian Zhao, Chaoliang Zhang, Yi Shi, Weiwei Sheng, Binwei Hu, Hui Li, Mi Wang, Xianhui Kang
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The first patient was given a dose of 0.3 mg/kg of remimazolam and was next randomized according to a biased coin design (BCD) method, and each patient received a dose of remimazolam depending on the response of the previous patient. A positive reaction was defined as no choking cough, nausea and vomiting, and/or motor response during placement of the upper GI endoscope into pharyngeal cavity or within 3 minutes after placement; otherwise, it was a negative reaction. If positive, randomize the next patient’s dose of remimazolam to be unchanged or decrease by 0.05 mg/kg. If negative, increase the next patient’s dose of remimazolam by 0.05 mg/kg. According to the study protocol, at least 45 patients with positive reactions were needed to suspend the trial while monitoring anesthesia-related adverse events. Results. The ED90 of remimazolam for upper gastrointestinal endoscopy insertion was 0.556 mg/kg (95% CI: 0.399–0.578). 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引用次数: 0

摘要

背景。雷马唑仑是一种具有临床优势的苯二氮卓类镇静剂,用于胃肠道内窥镜检查麻醉。然而,准确的临床剂量仍有待研究。本研究旨在探讨雷马唑仑在90%有效剂量(ED90)下对上消化道内镜插入反应的抑制作用,并评价其在上消化道内镜诊治中的有效性和安全性。方法。本研究共纳入54例在程序性镇静下接受上消化道内镜检查的成年患者,并采用静脉注射雷马唑仑麻醉。第一名患者给予0.3 mg/kg剂量的雷马唑仑,然后根据有偏硬币设计(BCD)方法随机分组,根据前一名患者的反应,每位患者接受一次剂量的雷马唑仑。阳性反应定义为上消化道内窥镜置入咽腔时或置入后3分钟内无呛咳、恶心、呕吐和/或运动反应;否则,这就是一个负面反应。如果阳性,随机分配下一个患者的雷马唑仑剂量不变或减少0.05 mg/kg。如果阴性,下一个病人的雷马唑仑剂量增加0.05 mg/kg。根据研究方案,至少有45例阳性反应患者需要暂停试验,同时监测麻醉相关不良事件。结果。雷马唑仑用于上消化道内镜插入的ED90为0.556 mg/kg (95% CI: 0.399 ~ 0.578)。镇静期间,所有患者血液循环稳定,无严重不良事件发生。患者满意度为4.89±0.69分,麻醉医师满意度为4.57±0.96分,内镜医师满意度为4.67±0.87分(满分5分,最低1分)。结论。使用雷马唑仑进行上消化道内窥镜检查是安全有效的,ED90剂量为0.556 mg/kg的单次静脉注射可抑制该手术的反应。
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Determining the 90% Effective Dose of Remimazolam Inhibiting Responses to Upper Gastrointestinal Endoscopy Insertion in Adults: A Double-Blind Study Utilizing a Biased Coin Up-and-Down Sequential Method
Background. Remimazolam, a benzodiazepine sedative with clinical advantages, is used for anesthesia during GI endoscopy. However, the accurate clinical dosage remains understudied. This study aims to investigate the 90% effective dose (ED90) of remimazolam in inhibiting responses to upper GI endoscopy insertion and evaluate its efficacy and safety for upper GI endoscopic diagnosis and treatment. Methods. A total of 54 adult patients undergoing upper GI endoscopy under procedural sedation were included, and they were anesthetized with an intravenous bolus of remimazolam. The first patient was given a dose of 0.3 mg/kg of remimazolam and was next randomized according to a biased coin design (BCD) method, and each patient received a dose of remimazolam depending on the response of the previous patient. A positive reaction was defined as no choking cough, nausea and vomiting, and/or motor response during placement of the upper GI endoscope into pharyngeal cavity or within 3 minutes after placement; otherwise, it was a negative reaction. If positive, randomize the next patient’s dose of remimazolam to be unchanged or decrease by 0.05 mg/kg. If negative, increase the next patient’s dose of remimazolam by 0.05 mg/kg. According to the study protocol, at least 45 patients with positive reactions were needed to suspend the trial while monitoring anesthesia-related adverse events. Results. The ED90 of remimazolam for upper gastrointestinal endoscopy insertion was 0.556 mg/kg (95% CI: 0.399–0.578). All patients maintained stable circulation and no serious adverse events were observed during sedation. Patient satisfaction was 4.89 ± 0.69 points, anesthesiologist satisfaction was 4.57 ± 0.96 points, and endoscopist satisfaction was 4.67 ± 0.87 points (full score 5 points, minimum 1 point). Conclusion. The use of remimazolam for upper gastrointestinal endoscopy was safe and effective, with a single intravenous bolus at an ED90 dose of 0.556 mg/kg inhibiting responses to the procedure.
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
226
审稿时长
6 months
期刊介绍: The Journal of Clinical Pharmacy and Therapeutics provides a forum for clinicians, pharmacists and pharmacologists to explore and report on issues of common interest. Reports and commentaries on current issues in medical and pharmaceutical practice are encouraged. Papers on evidence-based clinical practice and multidisciplinary collaborative work are particularly welcome. Regular sections in the journal include: editorials, commentaries, reviews (including systematic overviews and meta-analyses), original research and reports, and book reviews. Its scope embraces all aspects of clinical drug development and therapeutics, including: Rational therapeutics Evidence-based practice Safety, cost-effectiveness and clinical efficacy of drugs Drug interactions Clinical impact of drug formulations Pharmacogenetics Personalised, stratified and translational medicine Clinical pharmacokinetics.
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