一氧化二氮和咪达唑仑用于小儿牙科患者清醒镇静的疗效和安全性的比较评价:一项系统回顾和荟萃分析。

IF 1.2
Manali Khole, Pankaj Chavhan, Arunkumar Sajjanar, Shreya Shah, Prachi Salvi
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引用次数: 0

摘要

儿童对牙科治疗的恐惧会给牙医管理他们的行为带来挑战,这可能会妨碍提供适当的牙科护理。镇静药物的使用可以缓解儿童牙科患者的焦虑和控制行为。一氧化二氮和咪达唑仑是儿童牙科护理行为管理中最常用的两种药物。然而,支持其有效性和安全性的证据尚不清楚。本系统综述和荟萃分析旨在巩固最有力的证据,证明氧化亚氮与咪达唑仑对3至16岁儿童牙科患者有意识镇静的有效性和安全性。按照预定的方案,采用系统的审查方法对电子数据库进行检索。题目和摘要经过筛选,全文由两位作者审阅。纳入的试验比较了氧化亚氮和咪达唑仑作为3至16岁接受牙科治疗的儿童的单一镇静剂。这些试验比较了氧化亚氮与口服、静脉注射、经黏膜或鼻内咪达唑仑。提取有关方法、参与者、干预措施、结局和结果的数据,并对每个试验进行风险偏倚评估。在这七篇文章中,两篇有中等偏倚风险,五篇有高风险。总体结果显示两种干预之间无统计学差异(P = 0.64)。尽管本系统综述和荟萃分析存在局限性,但本研究提供了关于两种镇静剂疗效的重要信息。然而,仍然需要精心设计和充分证明的临床试验。此外,还需要制定关于程序性镇静成功的标准和定义的标准化指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative evaluation of efficacy and safety of nitrous oxide and midazolam for conscious sedation in pediatric dental patients: a systematic review and meta-analysis.

Children's fear of dental treatment can create challenges for dentists in managing their behavior, which may hinder the provision of proper dental care. The use of sedative agents can alleviate anxiety and control behaviors in pediatric dental patients. Nitrous oxide and midazolam are the two most commonly used pharmacological agents for behavioral management in pediatric dental care. However, evidence supporting their efficacy and safety is unclear. This systematic review and meta-analysis aimed to consolidate the most robust evidence on the efficacy and safety of nitrous oxide versus midazolam for conscious sedation in pediatric dental patients aged 3 to 16 years. As per the predefined protocol, a systematic review methodology was employed to search electronic databases. Titles and abstracts were screened, and the full text was reviewed by two authors. The included trials compared nitrous oxide and midazolam as single sedatives in children aged 3 to 16 undergoing dental treatment. These trials compared nitrous oxide with oral, intravenous, transmucosal, or intranasal midazolam. Data on the methods, participants, interventions, outcomes, and results were extracted, and each trial was assessed for risk bias. Of the seven articles, two had a moderate risk of bias and five had a high risk. The overall results showed no statistically significant differences between the two interventions (P = 0.64). Despite the limitations of this systematic review and meta-analysis, the present study provides important information regarding the efficacy of both sedatives. However, well-designed and well-documented clinical trials are still required. In addition, guidelines for the standardization of the criteria and definition of success in procedural sedation need to be developed.

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