Siddappa Prajwal, Kamath Shaila Surendra
Department of Anaesthesiology, Kasturba Medical College, Mangalore, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Ann Afr Med. 2025 Apr 1;24(2):474-480. doi: 10.4103/aam.aam_106_24. Epub 2024 Dec 17.
Dexmedetomidine has been administered as an intravenous infusion for maintenance dose following a loading dose, however, there is no study conducted so far that has compared the effectiveness of dexmedetomidine administered as bolus intravenously. The study aimed to compare the hemodynamic stability between intravenous infusion and intravenous bolus injection dexmedetomidine.
A comparative observational study was conducted among 60 participants aged 20-60 years with American Society of Anesthesiologists physical status I/II, scheduled to undergo elective ear, nose, and throat surgeries. Participants were divided into Group A (received a loading dose of 0.5 µg/kg followed by 0.3 µg/kg/h intravenous infusion of dexmedetomidine) and Group B (an intravenous bolus of dexmedetomidine 0.5 µg/kg) 15 min before the induction of anesthesia. Hemodynamic variables, anesthetic requirement, blood loss, volume of intravenous fluid, recovery time, pain scores, rescue analgesia required, and any adverse events were recorded.
Heart rate, blood pressure (BP), and mean arterial pressure were found to be significantly higher among participants receiving dexmedetomidine in the bolus group ( P = 0.001). Diastolic BP was higher 90 min after intubation. Mean propofol administered, total blood loss, and total intravenous fluid volume were significantly higher in the bolus group ( P = 0.001). Pain scores were higher in the bolus group after 2 h and infusion group after 12 h. Participants in the infusion group took more time to recover from anesthesia.
Almost all outcome variables were significantly higher among the bolus group. The recovery time was nonetheless reduced. There were no adverse events reported in both groups.
右美托咪定在给予负荷剂量后一直以静脉输注的方式给予维持剂量,然而,迄今为止尚未有研究比较静脉推注右美托咪定的有效性。本研究旨在比较静脉输注和静脉推注右美托咪定之间的血流动力学稳定性。
对60名年龄在20 - 60岁、美国麻醉医师协会身体状况分级为I/II级、计划接受择期耳鼻喉手术的参与者进行了一项比较观察性研究。参与者被分为A组(接受0.5μg/kg的负荷剂量,随后以0.3μg/kg/h的速度静脉输注右美托咪定)和B组(在麻醉诱导前15分钟静脉推注0.5μg/kg右美托咪定)。记录血流动力学变量、麻醉需求、失血量、静脉输液量、恢复时间、疼痛评分、所需的补救性镇痛以及任何不良事件。
在推注组接受右美托咪定的参与者中,心率、血压(BP)和平均动脉压显著更高(P = 0.001)。插管后90分钟舒张压更高。推注组给予的丙泊酚平均剂量、总失血量和总静脉输液量显著更高(P = 0.001)。推注组在2小时后疼痛评分更高,输注组在12小时后疼痛评分更高。输注组的参与者从麻醉中恢复所需的时间更长。
推注组几乎所有的结局变量都显著更高。然而,恢复时间缩短了。两组均未报告不良事件。