Gupta Keshav Kumar, Balai Edward, Tang Ho Tsun, Ahmed Abiya Amna, Doshi Jayesh R
University Hospitals Birmingham NHS Foundation Trust, Heartlands Hospital, Bordesley Green East, Birmingham B9 5SS, United Kingdom.
University Hospitals Coventry and Warwickshire, Clifford Bridge Road, Coventry CV2 2DX, United Kingdom.
Otol Neurotol. 2023 Apr 1;44(4):310-316. doi: 10.1097/MAO.0000000000003823. Epub 2023 Jan 28.
Bell's palsy is typically treated with oral corticosteroids (40-60 mg daily). Concomitant antivirals are currently not recommended. The objective of this systematic review and meta-analysis was to examine the effect of high-dose versus standard-dose corticosteroids, without antivirals, in the management of Bell's palsy.
Embase, MEDLINE, PubMed, CINAHL, Cochrane Library.
A systematic review and meta-analysis was performed according to PRISMA guidelines. Studies comparing high-dose (≥80 mg) or standard-dose (40-60 mg) corticosteroid therapy for Bell's palsy were included. Exclusion criteria were coexisting antiviral treatment, nonoral drug delivery, and facial palsy due to other causes. Risk of bias was assessed using ROBINS-I. A weighted estimate of treatment effects across trials as odds ratios (OR) using a Mantel-Haenzel random-effects model was calculated.
Three articles were included in the analysis, representing 485 patients. There was a significant decrease in nonrecovery with high-dose, compared with standard-dose, corticosteroids at 6 months follow-up (OR = 0.17, 95% confidence interval = 0.05-0.56, p = 0.004). Overall adverse events were 5.8% (n = 28), all reported in one study in the high-dose group (transient elevated liver enzymes and fecal occult blood).
Our analysis shows a favorable effect of high-dose corticosteroid in the treatment of Bell's palsy. It is the first to evaluate this effect without the use of antivirals in keeping with current treatment recommendations. As all included studies had a serious risk of bias, future research should focus on larger trials with more robust methodology. This will allow for more up-to-date and large-scale analyses where more valid conclusions can be drawn that may potentially influence treatment protocols.
贝尔面瘫通常采用口服皮质类固醇(每日40 - 60毫克)进行治疗。目前不推荐同时使用抗病毒药物。本系统评价和荟萃分析的目的是研究在不使用抗病毒药物的情况下,高剂量与标准剂量皮质类固醇治疗贝尔面瘫的效果。
Embase、MEDLINE、PubMed、CINAHL、Cochrane图书馆。
根据PRISMA指南进行系统评价和荟萃分析。纳入比较高剂量(≥80毫克)或标准剂量(40 - 60毫克)皮质类固醇治疗贝尔面瘫的研究。排除标准为同时存在抗病毒治疗、非口服给药以及由其他原因引起的面瘫。使用ROBINS - I评估偏倚风险。采用Mantel - Haenzel随机效应模型计算各试验治疗效果的加权估计值,以比值比(OR)表示。
分析纳入了3篇文章,共485例患者。在6个月随访时,与标准剂量皮质类固醇相比,高剂量皮质类固醇治疗后未恢复的情况显著减少(OR = 0.17,95%置信区间 = 0.05 - 0.56,p = 0.004)。总体不良事件发生率为5.8%(n = 28),均在高剂量组的一项研究中报告(短暂性肝酶升高和粪便潜血)。
我们的分析表明高剂量皮质类固醇治疗贝尔面瘫有良好效果。这是首次按照当前治疗建议在不使用抗病毒药物的情况下评估这种效果。由于所有纳入研究都存在严重的偏倚风险,未来研究应侧重于方法更可靠的大型试验。这将有助于进行更及时、大规模的分析,从而得出更有效的结论,可能会影响治疗方案。