Liu Yun, Li Binghua, Wu Xiaoran, Xia Bin, Yang Xudong, Cheng Tong
Department of Anesthesiology, National Center for Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory of Digital Stomatology, Peking University School of Stomatology, 22 Zhongguancun South Avenue, Haidian District, Beijing, 100081, China.
Department of Pediatric Dentistry, National Center for Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory of Digital Stomatology, Peking University School of Stomatology, Beijing, 100081, China.
BMC Oral Health. 2025 Jul 2;25(1):1032. doi: 10.1186/s12903-025-06381-9.
To evaluate the safety and efficacy of intranasal dexmedetomidine combined with propofol for pediatric dental sedation, and identify risk factors associated with major adverse events during deep sedation.
From June 2016 to August 2024, children who were unable to cooperate with the short-term oral treatment under non-pharmacological behavior or conscious sedation were selected for inclusion in the study. Intranasal dexmedetomidine 2 µg/kg was administered to facilitate preoperative sedation. Furthermore, a topical anesthetic, lidocaine gel, was applied to the venipuncture site. Once adequate sedation was achieved, venipuncture was performed. If preoperative sedation failed, sevoflurane inhalation was used to facilitate venipuncture. During the oral treatment, continuous target-controlled infusion (TCI) of propofol was administered to maintain a Bispectral index (BIS) of 50-70, ensuring deep sedation.
Major adverse events (hypoxia, tachycardia, and bradycardia).
Less severe events (choking cough, gross body movement, and postoperative agitation) and risk factor exploration (interrelationships between tonsillar hypertrophy, surgery duration, and adverse events).
A total of 513 children (359 boys, 69.98%; 154 girls, 30.02%) were enrolled in the study. Oral treatment was successfully completed in 100% of children. Surgery duration significantly influenced the incidence of major adverse events (p < 0.05), with a receiver operating characteristic (ROC) curve identifying 79 min as the optimal cutoff (AUC = 0.653, 95% CI: 0.573-0.733). Tonsillar hypertrophy was associated with a 4.6-fold increased risk of adverse events (OR = 4.61, 95% CI: 1.2-17.8; P = 0.017), driven by higher rates of hypoxemia (33.3% vs. 3.3%, P < 0.001) and choking cough (9.5% vs. 0%, P < 0.001).
This study establishes intranasal dexmedetomidine premedication followed by target-controlled propofol infusion sedation as a safe, effective alternative to general anesthesia for short-duration pediatric dental procedures (< 2 h).
评估鼻内给予右美托咪定联合丙泊酚用于小儿牙科镇静的安全性和有效性,并确定深度镇静期间与主要不良事件相关的危险因素。
选取2016年6月至2024年8月期间无法在非药物行为或清醒镇静下配合短期口腔治疗的儿童纳入研究。给予鼻内右美托咪定2µg/kg以促进术前镇静。此外,在静脉穿刺部位涂抹局部麻醉药利多卡因凝胶。一旦达到充分镇静,即进行静脉穿刺。如果术前镇静失败,则使用七氟醚吸入以促进静脉穿刺。在口腔治疗期间,持续靶控输注(TCI)丙泊酚以维持脑电双频指数(BIS)在50 - 70,确保深度镇静。
主要不良事件(低氧血症、心动过速和心动过缓)。
较轻微事件(呛咳、全身大动作和术后躁动)以及危险因素探索(扁桃体肥大、手术时间与不良事件之间的相互关系)。
共有513名儿童(359名男孩,69.98%;154名女孩,30.02%)纳入研究。100%的儿童成功完成口腔治疗。手术时间显著影响主要不良事件的发生率(p < 0.05),受试者工作特征(ROC)曲线确定79分钟为最佳截断值(AUC = 0.653,95% CI:0.573 - 0.733)。扁桃体肥大与不良事件风险增加4.6倍相关(OR = 4.61,95% CI:1.2 - 17.8;P = 0.017),原因是低氧血症发生率较高(33.3%对3.3%,P < 0.001)和呛咳发生率较高(9.5%对0%,P < 0.001)。
本研究确立了鼻内给予右美托咪定预处理后靶控输注丙泊酚镇静作为小于2小时的小儿牙科短时间手术全身麻醉的一种安全、有效的替代方法。