Department of Otolaryngology-Head and Neck Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Department of Otolaryngology-Head and Neck Surgery, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Clin Otolaryngol. 2022 Jul;47(4):509-515. doi: 10.1111/coa.13933. Epub 2022 Apr 6.
The aim of this study was to assess the effect of topical steroids on acute-onset olfactory dysfunction in patients infected with COVID-19.
Systematic review and meta-analysis of cohort studies.
Patients infected with COVID-19.
PubMed, Embase, the Web of Science, SCOPUS, Cochrane database and Google Scholar were searched for articles up to September 2021. We analysed studies comparing the improvement of olfactory dysfunction between topical steroid treatment and control groups (placebo or no treatment). In addition, we performed a subgroup analysis by study type.
The improvement of olfactory score at 2 (standardised mean difference [SMD] = 0.7272, 95% confidence interval = [0.3851, 1.0692], p < .0001, I = 62.1%) and 4 weeks post-treatment (SMD = 1.0440 [0.6777, 1.4102], p < .0001, I = 61.2%) was statistically greater in the treatment than control group. However, there was no significant difference (odds ratio [OR] = 1.4345 [0.9525, 2.1604], p = .0842, I = 45.4%) in the incidence of fully recovery from anosmia/hyposmia between the treatment and control groups. In subgroup analysis, there were no significant differences in the improvement of olfactory score at 4 weeks post-treatment (OR = 0.6177 [0.1309, 1.1045] vs. 0.1720 [0.8002, 1.5438], p = .0761) or the incidence of full recovery from anosmia/hyposmia (OR = 1.8478 [0.6092, 5.6053] vs. 1.3784 [0.8872, 2.1414], p = .8038) between randomised and non-randomised controlled trials.
Although this meta-analysis found that topical steroids improved the acute-onset olfactory dysfunction caused by COVID-19, there was no difference in the rate of full olfactory recovery between treated and control patients.
本研究旨在评估局部皮质类固醇对 COVID-19 感染患者急性嗅觉功能障碍的影响。
系统评价和队列研究的荟萃分析。
COVID-19 感染患者。
截至 2021 年 9 月,检索 PubMed、Embase、Web of Science、SCOPUS、Cochrane 数据库和 Google Scholar 中的文章。我们分析了比较局部皮质类固醇治疗组与对照组(安慰剂或无治疗)嗅觉功能障碍改善情况的研究。此外,我们还按研究类型进行了亚组分析。
治疗后 2 周(标准化均数差 [SMD] = 0.7272,95%置信区间 [0.3851,1.0692],p <.0001,I ² = 62.1%)和 4 周(SMD = 1.0440 [0.6777,1.4102],p <.0001,I ² = 61.2%)时,治疗组嗅觉评分的改善明显大于对照组。然而,治疗组和对照组完全从嗅觉丧失/嗅觉减退中恢复的发生率(比值比 [OR] = 1.4345 [0.9525,2.1604],p = 0.0842,I ² = 45.4%)无统计学差异。在亚组分析中,治疗后 4 周嗅觉评分的改善(OR = 0.6177 [0.1309,1.1045] 与 0.1720 [0.8002,1.5438],p = 0.0761)或完全从嗅觉丧失/嗅觉减退中恢复的发生率(OR = 1.8478 [0.6092,5.6053] 与 1.3784 [0.8872,2.1414],p = 0.8038)在随机对照试验和非随机对照试验之间均无统计学差异。
尽管这项荟萃分析发现局部皮质类固醇可改善 COVID-19 引起的急性嗅觉功能障碍,但治疗组和对照组患者完全嗅觉恢复的比例无差异。