Sophie Dunmall, Lucylynn Lizarondo, Romy Menghao Jia, Eng Hooi Ooi
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引用次数: 0
摘要
目的:本综述旨在评估选择性COX-2抑制剂在扁桃体切除术患者中的安全性。扁桃体切除术后的恢复是痛苦的,需要强有力的多模式镇痛来管理;然而,非甾体类抗炎药(NSAIDs)存在出血风险。选择性COX-2抑制剂理论上是安全的,因为COX-1抗血小板作用很小;然而,尽管有多项已发表的实验研究,但它们作为扁桃体切除术患者药物亚类的安全性尚未得到很好的证实。纳入标准:本综述将考虑评估接受扁桃体切除术或腺扁桃体切除术的任何年龄患者,使用非甾体抗炎药治疗COX-2比COX-1更具选择性的研究。主要的相关结果是扁桃体切除术后出血的发生率。方法:本综述将遵循JBI方法对有效性进行系统评价。搜索策略将包括检索CINAHL、Cochrane图书馆、Embase、MEDLINE、SciELO和Web of Science。研究将由2名独立审稿人根据纳入标准进行评估。任何日期、语言或方法学质量的研究都可以纳入数据提取。将使用JBI标准的批判性评价方法。效应量将以优势比表示,亚组分析将用于识别和管理研究设计和患者队列的差异。将采用GRADE方法对证据的确定性进行分级。评审注册:PROSPERO: CRD42024577071。
Safety of selective COX-2 inhibitors in tonsillectomy patients: a systematic review protocol.
Objective: This review aims to assess the safety of selective COX-2 inhibitors in tonsillectomy patients.
Introduction: Recovery after tonsillectomy is painful and requires robust multimodal analgesia to manage; however, there is a concern for bleeding risk with non-steroidal anti-inflammatory drugs (NSAIDs). Selective COX-2 inhibitors are theoretically safe due to minimal COX-1 anti-platelet effect; however, their safety as a subclass of medication in tonsillectomy patients has not been well established despite multiple published experimental studies.
Inclusion criteria: The review will consider studies that assess patients of any age undergoing tonsillectomy or adenotonsillectomy, treated with an NSAID that is more selective for COX-2 than COX-1. The primary relevant outcome is the incidence of post-tonsillectomy bleeding.
Methods: The review will follow the JBI methodology for systematic reviews of effectiveness. The search strategy will include searches of CINAHL, the Cochrane Library, Embase, MEDLINE, SciELO, and Web of Science. Studies will be assessed by 2 independent reviewers against inclusion criteria. Studies of any date, language, or methodological quality may be included for data extraction. The standard JBI methodology for critical appraisal will be used. Effect sizes will be expressed as odds ratios, and sub-group analyses will be used to identify and manage differences in study design and patient cohorts. The GRADE approach for grading certainty of evidence will be followed.