Endoscopy Center, Peking University People's Hospital, Beijing, People's Republic of China.
Department of Anesthesiology, Peking University People's Hospital, Beijing, People's Republic of China.
Drug Des Devel Ther. 2024 Jul 2;18:2681-2692. doi: 10.2147/DDDT.S454314. eCollection 2024.
Remimazolam is a novel short-acting benzodiazepine used for sedation and general anesthesia. This study aimed to evaluate the efficacy and safety of remimazolam besylate in elderly patients who underwent diagnostic gastrointestinal endoscopy.
A total of 120 patients aged 60-75 years were randomly allocated to one of two groups. Remifentanil 0.3μg/kg was used for analgesia. Patients were administered remimazolam besylate 7 mg (R group) or etomidate 0.1 mg/kg combined with 1% propofol 0.5 mg/kg (EP group) for induction, supplemental repeated doses were given as needed. Some time metrics, vital signs, adverse events were evaluated. Patients' Mini-cog score and recovery questionnaires were compared.
Compared to the EP group, the induction time was slightly longer in the R group (1.50 VS 1.15 minutes) (P<0.05), the time spent in the post-anesthesia care unit (PACU) was shorter (15.17 VS 17.40 minutes) (P<0.05). Compare with EP group, SBP was lower in R group at T15 and T25 time point, but heart rate was higher in T2, T3, T5 (P< 0.05). The Mini-Cog score was higher after the procedure (2.83 VS 2.58) (P<0.05). The incidence of respiratory adverse events was higher in the EP group than R group (18.3% VS 5.0%, P < 0.05). The most common adverse event in R group was hiccups. The sedation satisfaction rate and degree of amnesia were higher in the R group (66.7% VS 11.7%) (P < 0.05), and the effect on patient's life within 24 hours was lower (12.0% VS 30.5%) (P < 0.05).
The safety and efficacy of remimazolam besylate are not inferior to those of etomidate combined with propofol, rendering it a safe option for sedation during gastrointestinal endoscopy in ASA I-II elderly patients, but care should be taken to monitor the occurrence of hiccups.
盐酸瑞马唑仑是一种新型的短效苯二氮䓬类药物,用于镇静和全身麻醉。本研究旨在评估盐酸瑞马唑仑在接受诊断性胃肠内镜检查的老年患者中的疗效和安全性。
120 名 60-75 岁的患者被随机分为两组。瑞芬太尼 0.3μg/kg 用于镇痛。患者给予盐酸瑞马唑仑 7mg(R 组)或依托咪酯 0.1mg/kg 联合 1%丙泊酚 0.5mg/kg(EP 组)诱导,根据需要给予重复补充剂量。评估一些时间指标、生命体征和不良事件。比较患者的 Mini-cog 评分和恢复问卷。
与 EP 组相比,R 组的诱导时间略长(1.50 比 1.15 分钟)(P<0.05),麻醉后监护室(PACU)停留时间更短(15.17 比 17.40 分钟)(P<0.05)。与 EP 组相比,R 组在 T15 和 T25 时间点的 SBP 较低,但 T2、T3、T5 时心率较高(P<0.05)。术后 Mini-cog 评分更高(2.83 比 2.58)(P<0.05)。EP 组的呼吸不良事件发生率高于 R 组(18.3%比 5.0%,P<0.05)。R 组最常见的不良事件是呃逆。R 组的镇静满意度和遗忘程度更高(66.7%比 11.7%)(P<0.05),对患者 24 小时内生活的影响更低(12.0%比 30.5%)(P<0.05)。
盐酸瑞马唑仑的安全性和疗效不劣于依托咪酯联合丙泊酚,对于 ASA I-II 级老年患者胃肠内镜检查时镇静是一种安全的选择,但应注意监测呃逆的发生。