Intranasal Fentanyl Combined with Oral Midazolam for Pediatric Dental Sedation: A Controlled Randomized Blinded Crossover Clinical Trial.

IF 1.5 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Pediatric dentistry Pub Date : 2022-07-15
Roaa I Alhaidari, Maha AlSarheed, Saad A Sheta, Mohammed Aldhubaiban
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Abstract

Purpose: The purpose of this study was to compare the effectiveness of intranasal fentanyl combined with oral midazolam to oral midazolam alone in pediatric dental patients. Methods: Thirty-two uncooperative healthy children aged three to six years old, who met the inclusion criteria, were randomly assigned to receive oral midazolam (0.7 mg/kg) with either intranasal fentanyl (one μg/kg) or intranasal placebo (saline). A controlled, randomized, double-blinded, crossover clinical trial design was followed so that each child received both regimens. Data collected included the onset of sedation, working time, sedation and behavior assessment, and occurrence of side effects. Results: The onset of sedation time was not statistically different between the two groups (P=0.62), while the median working time of the midazolam/fentanyl sedation was sig- nificantly longer than the midazolam sedation (P<0.001). Sedation scores were significantly better with the midazolam/fentanyl sedation regimen at separation from parents (P=0.032), local anesthesia administration (P=0.018), rubber dam application (P=0.035), after five minutes of dental treatment (P=0.035), after 10 minutes (P=0.039), after 15 minutes (P=0.012), and after 20 minutes (P=0.038). Behavior scores were significantly better with the midazolam/fentanyl sedation only at local anesthesia administration (P=0.021), rubber dam placement (P=0.004), and after five minutes of dental treatment (P=0.049). Minor side effects occurred in 12.5 percent of sedation procedures and were not significantly associated with either of the two groups (P=0.70). Conclusion: The combination of oral midazolam with intranasal fentanyl sedation, when compared to oral midazolamas a single agent, significantly improved sedation and behavior during local anesthesia and operative dentistry for healthy three- to six-year-old children in addition to prolonged sedation working time.

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芬太尼鼻内联合口服咪达唑仑用于小儿牙科镇静:一项对照随机盲法交叉临床试验。
目的:本研究的目的是比较芬太尼鼻内联合口服咪达唑仑与单独口服咪达唑仑对小儿牙科患者的疗效。方法:32例符合纳入标准的3 ~ 6岁不合作健康儿童,随机分为口服咪达唑仑(0.7 mg/kg)和鼻内芬太尼(1 μg/kg)或鼻内安慰剂(生理盐水)两组。遵循对照、随机、双盲、交叉临床试验设计,以便每个孩子都接受两种方案。收集的数据包括镇静的开始时间,工作时间,镇静和行为评估,以及副作用的发生。结果:两组患者的镇静起效时间差异无统计学意义(P=0.62),而咪达唑仑/芬太尼镇静的中位工作时间明显长于咪达唑仑镇静(P)。与单剂口服咪达唑仑相比,口服咪达唑仑联合鼻内芬太尼镇静可显著改善3 - 6岁健康儿童在局麻和牙科手术期间的镇静和行为,并延长镇静工作时间。
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来源期刊
Pediatric dentistry
Pediatric dentistry DENTISTRY, ORAL SURGERY & MEDICINEPEDIATRI-PEDIATRICS
CiteScore
1.20
自引率
6.20%
发文量
74
审稿时长
>12 weeks
期刊介绍: Pediatric Dentistry is the official publication of the American Academy of Pediatric Dentistry, the American Board of Pediatric Dentistry and the College of Diplomates of the American Board of Pediatric Dentistry. It is published bi-monthly and is internationally recognized as the leading journal in the area of pediatric dentistry. The journal promotes the practice, education and research specifically related to the specialty of pediatric dentistry. This peer-reviewed journal features scientific articles, case reports and abstracts of current pediatric dental research.
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