Effect and safety of perioperative ibuprofen administration in pediatric tonsillectomy: A systematic review and meta-analysis

IF 1.8 4区 医学 Q2 OTORHINOLARYNGOLOGY
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引用次数: 0

Abstract

Objectives

This study aimed to evaluate the safety and efficacy of perioperative ibuprofen administration by conducting a meta-analysis of pertinent literature.

Methods

We conducted a comprehensive review of studies sourced from PubMed, SCOPUS, Embase, Web of Science, and Cochrane databases. The studies covered the period from database inception to June 2024. A perioperative ibuprofen administration group was compared to a control group administered either saline, acetaminophen, paracetamol, or opioids. The primary outcome was post-tonsillectomy bleeding that was categorized into overall bleeding and further classified as type 1 (observed at home or evaluated in the emergency department without additional intervention), type 2 (necessitating readmission for observation), and type 3 (requiring a return to the operating room for hemorrhage control). Morbidity incidence rates for postoperative nausea and vomiting were also assessed. The secondary outcomes assessed were postoperative pain management and the frequency of analgesic drug usage. Postoperative pain management was assessed from the incidence of emergency department visits or nurses' calls for pain independent of the presence or absence of dehydration.

Results

Twenty-two studies with 27,149 patients were included and reviewed for this meta-analysis. Post-tonsillectomy bleeding (OR = 0.9954, 95 % CI [0.8800; 1.1260], I2 = 0.0 %) was not significantly higher in the ibuprofen administration group compared to the control group. In subgroup analysis of post-tonsillectomy bleeding severity, ibuprofen caused clinically insignificant type 1 post-tonsillectomy bleeding that did not require intervention (OR = 1.1310 [0.7398; 1.7289]). Clinically significant bleeding requiring hospital admission (type 2) or surgical control (type 3) was not observed. Administration of ibuprofen has demonstrated efficacy in reducing the need for analgesic drugs (OR = 0.4734, 95 % CI [0.2840; 0.7893]; I2 = 19.8 %) and is associated with a significant decrease in the incidence of postoperative nausea and vomiting (OR = 0.4886, 95 % CI [0.3156; 0.7562], I2 = 34.3 %).

Conclusion

This study demonstrated that administration of ibuprofen for pediatric tonsillectomy did not increase the incidence of clinically significant postoperative bleeding. Ibuprofen administration decreased the incidence and severity of postoperative pain, nausea, and vomiting.

小儿扁桃体切除术围手术期布洛芬用药的效果和安全性:系统回顾和荟萃分析。
研究目的本研究旨在通过对相关文献进行荟萃分析,评估围手术期布洛芬用药的安全性和有效性:我们对来自 PubMed、SCOPUS、Embase、Web of Science 和 Cochrane 数据库的研究进行了全面回顾。这些研究的时间跨度从数据库建立之初到 2024 年 6 月。围手术期布洛芬给药组与生理盐水、对乙酰氨基酚、扑热息痛或阿片类药物对照组进行了比较。主要结果是扁桃体切除术后出血,出血分为总体出血和1型(在家观察或在急诊科评估,无需额外干预)、2型(需要再次入院观察)和3型(需要返回手术室控制出血)。此外,还评估了术后恶心和呕吐的发病率。评估的次要结果是术后疼痛管理和镇痛药物的使用频率。术后疼痛管理的评估依据是急诊室就诊率或护士因疼痛呼叫的发生率,与是否存在脱水无关:本次荟萃分析共纳入并审查了 22 项研究,涉及 27,149 名患者。与对照组相比,布洛芬治疗组扁桃体切除术后出血量(OR = 0.9954,95 % CI [0.8800; 1.1260],I2 = 0.0 %)并无明显增加。在扁桃体切除术后出血严重程度的亚组分析中,布洛芬导致的临床不严重的1型扁桃体切除术后出血不需要干预(OR = 1.1310 [0.7398; 1.7289])。未观察到需要入院(2 类)或手术控制(3 类)的临床重大出血。布洛芬可有效减少镇痛药的使用(OR = 0.4734,95 % CI [0.2840;0.7893];I2 = 19.8 %),并显著降低术后恶心和呕吐的发生率(OR = 0.4886,95 % CI [0.3156;0.7562],I2 = 34.3 %):本研究表明,在小儿扁桃体切除术中使用布洛芬不会增加临床意义上的术后出血发生率。布洛芬可降低术后疼痛、恶心和呕吐的发生率和严重程度。
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来源期刊
American Journal of Otolaryngology
American Journal of Otolaryngology 医学-耳鼻喉科学
CiteScore
4.40
自引率
4.00%
发文量
378
审稿时长
41 days
期刊介绍: Be fully informed about developments in otology, neurotology, audiology, rhinology, allergy, laryngology, speech science, bronchoesophagology, facial plastic surgery, and head and neck surgery. Featured sections include original contributions, grand rounds, current reviews, case reports and socioeconomics.
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