Efficacy of Preemptive Analgesia on Postoperative Pain Control in Children Who Underwent Full-Mouth Dental Rehabilitation Under General Anesthesia: A Randomized Controlled Clinical Trial.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Sultan Keles, Ozlem Kocaturk, Pinar Demir
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Abstract

Aims: To evaluate the efficacy of intravenous preemptive analgesia on postoperative pain in children undergoing dental rehabilitation under general anesthesia.

Methods: In this prospective randomized clinical trial, 70 children aged 3 to 7 years were scheduled for dental treatment and randomized into two groups: the control group or the preemptive group. Patients received 15 mg/kg of intravenous paracetamol either before the start of treatment (preemptive group, n = 35) or at the end of treatment (control group, n = 35). Postoperative pain scores were recorded at 1, 2, 4, 6, 8, 12, and 24 hours using the Wong-Baker FACES Pain Rating Scale (WBFS). Additionally, the need for rescue analgesic and the total opioid consumption of the patients were recorded during the first 24 hours postoperative.

Results: The pain scores in the preemptive group were significantly lower than those in the control group at the postanesthesia care unit and at 2, 4, and 8 hours postoperative (P < .05). However, there were no statistically significant differences in pain scores between groups at 12 and 24 hours postoperative. Need for rescue analgesics and total intravenous fentanyl consumption were significantly higher in the control group than in the preemptive group (P < .05). The percentage of children who received medication for pain relief at home was higher in the control group than in the preemptive group, but the difference was not statistically significant (P > .05).

Conclusion: Preemptive use of intravenous paracetamol reduces postoperative pain scores and postoperative opioid consumption. However, there is a need to evaluate pain levels in children who receive comprehensive dental treatment under general anesthesia after hospital discharge for effective postoperative pain control.

先发制人镇痛对全麻下全口牙科康复患儿术后疼痛控制的疗效:一项随机对照临床试验。
目的:评价静脉先发制人镇痛对全麻下儿童牙科康复术后疼痛的治疗效果。方法:采用前瞻性随机临床试验,选取70例3 ~ 7岁儿童进行牙科治疗,随机分为对照组和先发制人组。患者在治疗开始前(先发制人组,n = 35)或治疗结束时(对照组,n = 35)接受15 mg/kg静脉注射扑热息痛。术后1、2、4、6、8、12和24小时使用Wong-Baker FACES疼痛评定量表(WBFS)记录疼痛评分。此外,记录患者术后前24小时的救援镇痛药需求和阿片类药物总消耗量。结果:先发制人组在麻醉后护理单元及术后2、4、8 h疼痛评分均显著低于对照组(P < 0.05)。然而,术后12和24小时组间疼痛评分差异无统计学意义。抢救性镇痛药需要量和静脉芬太尼总用量均明显高于抢救性镇痛药组(P < 0.05)。对照组患儿在家接受镇痛药物治疗的比例高于先发制人组,但差异无统计学意义(P > 0.05)。结论:先发制人静脉注射扑热息痛可减少术后疼痛评分和术后阿片类药物的消耗。然而,有必要评估在全麻下接受综合牙科治疗的儿童出院后的疼痛水平,以有效地控制术后疼痛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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