School of Health Preservation and Rehabilitation, Chengdu University of Traditional Chinese Medicine, Chengdu, 610000, Sichuan, China.
Acupuncture and Tuina School, Chengdu University of Traditional Chinese Medicine, No. 37 Shierqiao Road, Jinniu District, Chengdu, 610075, Sichuan, China.
BMC Pharmacol Toxicol. 2023 Apr 6;24(1):23. doi: 10.1186/s40360-023-00665-y.
Standard doses of second-generation H-antihistamines (sgAHs) as first-line treatment are not always effective in treating chronic spontaneous urticaria (CSU), and hence an increase in the dose of sgAHs is recommended. However, literature evaluating the efficacy and safety of this treatment remains inconclusive, highlighting the need for a systematic review and meta-analysis. The aim of this systematic review and meta-analysis was to evaluate the efficacy and safety of high-dose sgAHs compared with standard-dose sgAHs in treating CSU.
A systematic literature search of double-blind, randomized controlled trials (RCT) utilizing multiple doses of sgAHs was performed by searching the electronic databases Medline, Embase, PsycInfo, Cochrane databases, and Web of Science. Bibliographies were also manually searched. The Cochrane Risk of Bias Tool for assessing risk of bias was used to assess the quality of randomized controlled trials (RCTs). Two reviewers screened studies, extracted data, and evaluated the risk of bias independently. The response rate, the number of adverse events, somnolence, and withdrawal due to adverse events were extracted from each article. The data were combined and analyzed to quantify the safety and efficacy of the treatment. RevMan (V5.3) software was used for data synthesis.
A total of 13 studies were identified, seven of which met the eligibility criteria for the meta-analysis. Our pooled meta-analyses showed that high-dose sgAHs was associated with a significantly higher response rate than standard-dose (RR 1.13, 95% CI 1.02 to 1.26; P = 0.02). Conversely, high doses of sgAHs were associated with significantly higher somnolence rates than standard dose (RD 0.05, 95% CI 0.01 to 0.09; P = 0.02). There was no significant difference in adverse events or withdrawal due to adverse events between standard- and high-dose treatments.
Our analyses showed that a high dose of sgAHs (up to two times the standard dose) might be more effective than a standard dose in CSU treatment. High-dose and standard-dose sgAHs showed similar adverse events, except for somnolence, where incidence was found to be dose-dependent in some studies. However, given the limited number of studies, our meta-analysis results should be interpreted with caution.
标准剂量的第二代 H1 抗组胺药(sgAHs)作为一线治疗药物,在治疗慢性自发性荨麻疹(CSU)时并不总是有效,因此建议增加 sgAHs 的剂量。然而,评估这种治疗方法的疗效和安全性的文献仍然没有定论,这突出表明需要进行系统评价和荟萃分析。本系统评价和荟萃分析的目的是评估高剂量 sgAHs 与标准剂量 sgAHs 治疗 CSU 的疗效和安全性。
通过检索 Medline、Embase、PsycInfo、Cochrane 数据库和 Web of Science 等电子数据库,对使用多种 sgAHs 剂量的双盲随机对照试验(RCT)进行了系统文献检索。还手动搜索了参考文献。使用 Cochrane 偏倚风险工具评估随机对照试验(RCTs)的偏倚风险。两位评审员独立筛选研究、提取数据并评估偏倚风险。从每篇文章中提取应答率、不良反应的数量、嗜睡和因不良反应而退出的数量。合并数据并进行分析以量化治疗的安全性和疗效。RevMan(V5.3)软件用于数据综合。
共确定了 13 项研究,其中 7 项符合荟萃分析的纳入标准。我们的汇总荟萃分析显示,高剂量 sgAHs 与标准剂量相比,应答率显著更高(RR 1.13,95%CI 1.02 至 1.26;P=0.02)。相反,高剂量 sgAHs 与标准剂量相比,嗜睡发生率显著更高(RD 0.05,95%CI 0.01 至 0.09;P=0.02)。标准剂量和高剂量治疗之间的不良反应或因不良反应而退出没有显著差异。
我们的分析表明,高剂量 sgAHs(高达标准剂量的两倍)可能比 CSU 治疗中的标准剂量更有效。高剂量和标准剂量的 sgAHs 表现出相似的不良反应,但嗜睡除外,一些研究发现嗜睡发生率与剂量有关。然而,由于研究数量有限,我们的荟萃分析结果应谨慎解释。