Department of Otorhinolaryngology, University Medical Center Utrecht, Utrecht, The Netherlands.
Otolaryngol Head Neck Surg. 2013 Nov;149(5):668-73. doi: 10.1177/0194599813503791. Epub 2013 Sep 6.
To systematically review the evidence base on the effectiveness of intranasal corticosteroids in adult patients with recurrent acute rhinosinusitis. Data Sources Pubmed, EMBASE, and the Cochrane Library.
A comprehensive search was performed up to March 20, 2013. Two reviewers independently screened publications on title and abstract. Design of selected studies was assessed on directness of evidence and risk of bias. For included studies, risk differences with 95% confidence intervals were extracted or recalculated.
Of 1850 unique records, 3 trials were included. Risk of bias was high and directness of evidence was low for 2 trials, the third trial had low risk of bias with moderate directness of evidence. They found a statistical significant difference for the median number of days to clinical success (defined as patients' report of symptoms to be cured or much improved) favoring intranasal corticosteroids (6 days) over placebo (9 days), while the difference in proportion of patients reporting clinical success after 21 days of treatment was 20% favoring intranasal corticosteroids over placebo.
The evidence for the benefit of intranasal corticosteroids on symptom relief in adult patients with recurrent acute rhinosinusitis is rather limited (ie, 3 trials are available; the best evidence is derived from 1 low risk of bias trial providing moderate directness of evidence that intranasal corticosteroids may speed up relief of symptoms in patients with recurrent acute rhinosinusitis). A large methodologically rigorous randomized trial in antibiotic-naïve patients is needed to provide a more definite recommendation.
系统评价鼻内皮质类固醇治疗成人复发性急性鼻-鼻窦炎的疗效证据。
PubMed、EMBASE 和 Cochrane 图书馆。
全面检索至 2013 年 3 月 20 日。两位评审员独立筛选标题和摘要。对入选研究的设计进行评估,评估指标为证据的直接性和偏倚风险。对纳入研究,提取或重新计算风险差异及其 95%置信区间。
在 1850 条独特记录中,有 3 项试验被纳入。其中 2 项试验的偏倚风险较高,证据的直接性较低,第 3 项试验的偏倚风险较低,证据的直接性为中度。他们发现,在达到临床成功的中位数天数(定义为患者报告症状已治愈或明显改善)方面,鼻内皮质类固醇(6 天)显著优于安慰剂(9 天),而在治疗 21 天后报告临床成功的患者比例方面,鼻内皮质类固醇组(20%)显著优于安慰剂组。
鼻内皮质类固醇治疗成人复发性急性鼻-鼻窦炎症状缓解的证据非常有限(即只有 3 项试验可用;最好的证据来自于 1 项低偏倚风险试验,其提供了中度直接证据,即鼻内皮质类固醇可能加速复发性急性鼻-鼻窦炎患者症状的缓解)。需要一项在未使用抗生素的患者中进行的、方法严谨的大型随机试验,以便提供更明确的推荐。