小儿扁桃体切除术和腺扁桃体切除术疼痛治疗随机临床试验的范围界定综述。

Q2 Medicine
World Journal of OtorhinolaryngologyHead and Neck Surgery Pub Date : 2022-04-18 eCollection Date: 2023-03-01 DOI:10.1002/wjo2.54
Michael C Shih, Barry D Long, Phayvanh P Pecha, David R White, Yi-Chun C Liu, Emily Brennan, Mariam I Nguyen, Clarice S Clemmens
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引用次数: 0

摘要

目的:研究小儿扁桃体切除术和腺扁桃体切除术药物止痛的随机临床试验的数量、主题和报告趋势,并确定需要进一步研究的领域:研究小儿扁桃体切除术和腺扁桃体切除术药物止痛的随机临床试验文献的数量、主题和报告趋势,并确定需要进一步研究的领域:数据来源:PubMed(美国国家医学图书馆和美国国立卫生研究院)、Scopus(Elsevier)、CINAHL(EBSCO)和 Cochrane Library(Wiley):对四个数据库进行了系统检索。方法:对四个数据库进行了系统检索,只纳入了研究小儿扁桃体切除术或腺样体切除术中药物干预对疼痛改善作用的随机对照试验或对比试验。收集的数据包括人口统计学、疼痛相关结果、镇静评分、恶心/呕吐、术后出血、比较药物的类型、给药方式、给药时间以及研究药物的特性:结果:共纳入 189 项研究进行分析。大多数研究采用了经过验证的疼痛量表,其中大多数研究采用了视觉辅助量表(49.21%)。较少的研究对术后 24 小时后的疼痛进行了检查(24.87%),很少有研究采用了有效的镇静量表(12.17%)。研究对药物治疗的几个不同方面进行了比较,包括不同的药物、给药时间、给药方式和剂量。只有 23 项(12.17%)研究对术后用药进行了检查,只有 29 项(15.34%)研究对口服药物进行了检查。对乙酰氨基酚只有四项自我比较:我们的研究首次对疼痛和小儿扁桃体切除术进行了范围界定。考虑到药物的安全性,文献中没有足够的数据来确定哪种治疗方案能更好地控制小儿扁桃体切除术的疼痛。即使是对乙酰氨基酚和布洛芬等常见药物也需要进一步研究,以优化扁桃体切除术后疼痛的治疗。研究设计和比较的异质性削弱了潜在的系统综述和荟萃分析的结论。未来的研究方向包括更多独特比较的非劣效性研究和更多检查术后口服药物的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A scoping review of randomized clinical trials for pain management in pediatric tonsillectomy and adenotonsillectomy.

A scoping review of randomized clinical trials for pain management in pediatric tonsillectomy and adenotonsillectomy.

A scoping review of randomized clinical trials for pain management in pediatric tonsillectomy and adenotonsillectomy.

A scoping review of randomized clinical trials for pain management in pediatric tonsillectomy and adenotonsillectomy.

Objectives: To examine the volume, topics, and reporting trends in the published literature of randomized clinical trials for pharmacologic pain management of pediatric tonsillectomy and adenotonsillectomy and to identify areas requiring further research.

Data sources: PubMed (National Library of Medicine and National Institutes of Health), Scopus (Elsevier), CINAHL (EBSCO), and Cochrane Library (Wiley).

Methods: A systematic search of four databases was conducted. Only randomized controlled or comparison trials examining pain improvement with a pharmacologic intervention in pediatric tonsillectomy or adenotonsillectomy were included. Data collected included demographics, pain-related outcomes, sedation scores, nausea/vomiting, postoperative bleeding, types of drug comparisons, modes of administration, timing of administration, and identities of the investigated drugs.

Results: One hundred and eighty-nine studies were included for analysis. Most studies included validated pain scales, with the majority using visual-assisted scales (49.21%). Fewer studies examined pain beyond 24 h postoperation (24.87%), and few studies included a validated sedation scale (12.17%). Studies have compared several different dimensions of pharmacologic treatment, including different drugs, timing of administration, modes of administration, and dosages. Only 23 (12.17%) studies examined medications administered postoperatively, and only 29 (15.34%) studies examined oral medications. Acetaminophen only had four self-comparisons.

Conclusion: Our work provides the first scoping review of pain and pediatric tonsillectomy. With drug safety profiles considered, the literature does not have enough data to determine which treatment regimen provides superior pain control in pediatric tonsillectomy. Even common drugs like acetaminophen and ibuprofen require further research for optimizing the treatment of posttonsillectomy pain. The heterogeneity in study design and comparisons weakens the conclusions of potential systematic reviews and meta-analyses. Future directions include more noninferiority studies of unique comparisons and more studies examining oral medications given postoperatively.

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