Identification of an effective and safe bolus dose and lockout time for patient-controlled sedation (PCS) using dexmedetomidine in dental treatments: a randomized clinical trial.

Seung-Hyun Rhee, Young-Seok Kweon, Dong-Ok Won, Seong-Whan Lee, Kwang-Suk Seo
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Abstract

Background: This study investigated a safe and effective bolus dose and lockout time for patient-controlled sedation (PCS) with dexmedetomidine for dental treatments. The depth of sedation, vital signs, and patient satisfaction were investigated to demonstrate safety.

Methods: Thirty patients requiring dental scaling were enrolled and randomly divided into three groups based on bolus doses and lockout times: group 1 (low dose group, bolus dose 0.05 µg/kg, 1-minute lockout time), group 2 (middle dose group, 0.1 µg/kg, 1-minute), and group 3 (high dose group, 0.2 µg/kg, 3-minute) (n = 10 each). ECG, pulse, oxygen saturation, blood pressure, end-tidal CO2, respiratory rate, and bispectral index scores (BIS) were measured and recorded. The study was conducted in two stages: the first involved sedation without dental treatment and the second included sedation with dental scaling. Patients were instructed to press the drug demand button every 10 s, and the process of falling asleep and waking up was repeated 1-5 times. In the second stage, during dental scaling, patients were instructed to press the drug demand button. Loss of responsiveness (LOR) was defined as failure to respond to auditory stimuli six times, determining sleep onset. Patient and dentist satisfaction were assessed before and after experimentation.

Results: Thirty patients (22 males) participated in the study. Scaling was performed in 29 patients after excluding one who experienced dizziness during the first stage. The average number of drug administrations until first LOR was significantly lower in group 3 (2.8 times) than groups 1 and 2 (8.0 and 6.5 times, respectively). The time taken to reach the LOR showed no difference between groups. During the second stage, the average time required to reach the LOR during scaling was 583.4 seconds. The effect site concentrations (Ce) was significantly lower in group 1 than groups 2 and 3. In the participant survey on PCS, 8/10 in group 3 reported partial memory loss, whereas 17/20 in groups 1 and 2 recalled the procedure fully or partially.

Conclusion: PCS with dexmedetomidine can provide a rapid onset of sedation, safe vital sign management, and minimal side effects, thus facilitating smooth dental sedation.

确定牙科治疗中使用右美托咪定进行患者控制镇静(PCS)的有效安全注射剂量和锁定时间:随机临床试验。
背景:本研究调查了牙科治疗中使用右美托咪定进行患者控制镇静(PCS)的安全有效的栓剂剂量和锁定时间。研究还调查了镇静深度、生命体征和患者满意度,以证明其安全性:招募了 30 名需要洗牙的患者,并根据栓剂剂量和锁定时间随机分为三组:第一组(低剂量组,栓剂剂量 0.05 µg/kg,锁定时间 1 分钟)、第二组(中等剂量组,0.1 µg/kg,1 分钟)和第三组(高剂量组,0.2 µg/kg,3 分钟)(每组 10 人)。测量并记录心电图、脉搏、血氧饱和度、血压、潮气末二氧化碳、呼吸频率和双谱指数(BIS)。研究分两个阶段进行:第一阶段是在不进行牙科治疗的情况下使用镇静剂,第二阶段是在洗牙的情况下使用镇静剂。患者被要求每隔 10 秒按一次药物需求按钮,入睡和醒来的过程重复 1-5 次。在第二阶段,患者在洗牙时被要求按下药物需求按钮。失去反应能力(LOR)的定义是对听觉刺激六次都没有反应,从而确定睡眠开始。实验前后对患者和牙医的满意度进行了评估:30 名患者(22 名男性)参加了研究。在排除了一名在第一阶段出现头晕的患者后,对 29 名患者进行了洗牙。第 3 组(2.8 次)到第一次 LOR 的平均用药次数明显低于第 1 组和第 2 组(分别为 8.0 次和 6.5 次)。各组达到 LOR 所需的时间没有差异。在第二阶段,缩放过程中到达 LOR 所需的平均时间为 583.4 秒。效果点浓度(Ce)在第 1 组明显低于第 2 组和第 3 组。在关于 PCS 的受试者调查中,第 3 组的 8/10 名受试者表示部分记忆丧失,而第 1 组和第 2 组的 17/20 名受试者则能完全或部分回忆起手术过程:结论:使用右美托咪定的 PCS 可以提供快速起效的镇静、安全的生命体征管理和最小的副作用,从而促进牙科镇静的顺利进行。
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