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不同方案减少正颌术后疼痛的效果:系统评价和荟萃分析。

Effectiveness of different protocols to reduce postoperative pain following orthognathic surgery: A systematic review and meta-analysis.

机构信息

Department of Oral and Maxillofacial Surgery, King Abdulaziz Medical City, National Guard, 14611 Riyadh, Saudi Arabia.

Department of Oral and Maxillofacial Surgery, King Abdulaziz Medical City, National Guard, 14611 Riyadh, Saudi Arabia.

出版信息

Br J Oral Maxillofac Surg. 2022 Sep;60(7):e1-e10. doi: 10.1016/j.bjoms.2022.03.013. Epub 2022 Apr 23.

Abstract

Pain management in orthognathic surgery is essential to enhance recovery, reduce hospital stay, and improve the whole experience of the patient. The aim of this systematic review was to evaluate current evidence on pain management in orthognathic surgery. A systematic review of the literature was performed following PRISMA guidelines, and PubMed, EMBASE, and the Cochrane Controlled Trials Registry were searched to retrieve randomised clinical trials (RCTs) published until July 2020. RCTs that compared different pre-emptive analgesia and low-level laser therapy (LLLT) with placebo after orthognathic surgery were included. Outcome variables were pain scores and duration of surgery. The quality of evidence was rated according to Cochrane's tool for assessing risk of bias. Standardised mean difference (SMD) or mean difference (MD) was used to analyse continuous data. There was significant pain reduction within the first 48 hours after pre-emptive analgesia (very low quality evidence, SMD: -1.329; confidence interval (CI): -2.030 to -0.628; p = 0.001) and LLLT (very low quality evidence, SMD: -0.690; CI: -1.172 to -0.207; p = 0.005) versus placebo. Evidence to support pre-emptive analgesia or LLLT effectively reducing pain scores within the first postoperative 48 hours after orthognathic surgery when compared with placebo, was of low quality.

摘要

正颌外科中的疼痛管理对于促进康复、缩短住院时间和改善患者整体体验至关重要。本系统评价的目的是评估正颌外科中疼痛管理的现有证据。按照 PRISMA 指南进行系统文献检索,并检索 PubMed、EMBASE 和 Cochrane 对照试验登记处,以获取截至 2020 年 7 月发表的随机临床试验 (RCT)。纳入了比较不同预防性镇痛和低水平激光治疗 (LLLT) 与正颌手术后安慰剂的 RCT。结局变量为疼痛评分和手术持续时间。根据 Cochrane 评估偏倚风险工具对证据质量进行评级。采用标准化均数差 (SMD) 或均数差 (MD) 分析连续数据。预防性镇痛 (极低质量证据,SMD:-1.329;置信区间 [CI]:-2.030 至 -0.628;p = 0.001) 和 LLLT (极低质量证据,SMD:-0.690;CI:-1.172 至 -0.207;p = 0.005) 后 48 小时内疼痛明显减轻。与安慰剂相比,预防性镇痛或 LLLT 有效降低正颌手术后 48 小时内疼痛评分的证据质量为低质量。

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