Omalizumab in pediatric chronic spontaneous urticaria: A systematic review and meta-analysis of efficacy and safety.

IF 4.5
Omar Alomari, Deniz Ozceker, Muhammed Edib Mokresh, Asli Berivan Topçak, Sinem Nur Ertan, Merve Karaca Şahin, Nilay Çalışkan, Sefika Ilknur Kökcü Karadag, Muhammed Fatih Erbay, Güler Yıldırım, Hamit Bologur, Hilal Güngör, Ozlem Kaplan, Hasan Sarman Tunç, Emek Kocatürk
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Abstract

Chronic spontaneous urticaria significantly impairs quality of life in children, with limited treatment options beyond antihistamines. Omalizumab, an anti-IgE antibody, has shown promise in adults but data on its use in children, especially those under 12, are scarce. This systematic review and meta-analysis aim to evaluate the efficacy and safety of omalizumab in pediatric chronic spontaneous urticaria, providing insights to inform clinical practice and future guidelines. PubMed, Scopus, Embase, Cochrane, and Web of Science databases have been searched for relevant studies. The "R" software has been utilized to analyze the response and relapse rates, changes in urticaria scores, and adverse event rates. Subgroup analyses were also done based on response rate. The assessment of heterogeneity utilized the I2 and chi-squared tests, applying the random effect model. This systematic review included 36 studies met the inclusion criteria. The pooled response rate for omalizumab was 88.0% (95% CI: 80.7%-95.2%; I2 = 61.0%; p = .001), with a complete response rate of 51.0% (95% CI: 32.7%-69.2%; I2 = 90.0%; p < .001). Good or well-controlled response rates were 50.5% (95% CI: 33.9%-67.1%; I2 = 54.2%; p = .068), while poor or partial responses were 20.1% (95% CI: 14.3%-27.3%; I2 = 0.0%; p = .787). Relapse rate were 24.3% (95% CI: 8.1%-40.6%; I2 = 66.6%; p = .006). The Urticaria Activity Score showed a significant mean reduction in symptoms (SMD = -3.08; 95% CI: -5.45 to -0.71; I2 = 89.1%; p < .001). Adverse events occurred in 3.4% of patients, with specific events including urticaria, angioedema, headaches, fatigue, flu-like symptoms, and mild joint pain. In pediatric patients under 12 years, 18 out of 21 achieved complete response, with a median age of 8 years and follow-up durations between 4 and 18 months. Adverse events in this group included serum sickness in one patient. Omalizumab appears to be an effective treatment option for chronic spontaneous urticaria, demonstrating effectiveness in improving symptoms and providing significant relief. The treatment is generally well-tolerated, with adverse events being rare and manageable. Overall, omalizumab contributing to better disease management and quality of life.

Omalizumab治疗儿童慢性自发性荨麻疹:疗效和安全性的系统评价和荟萃分析。
慢性自发性荨麻疹显著损害儿童的生活质量,除抗组胺药外治疗选择有限。Omalizumab是一种抗ige抗体,在成人中显示出希望,但在儿童,特别是12岁以下儿童中的应用数据很少。本系统综述和荟萃分析旨在评估omalizumab治疗儿童慢性自发性荨麻疹的疗效和安全性,为临床实践和未来指南提供见解。检索了PubMed、Scopus、Embase、Cochrane和Web of Science数据库的相关研究。使用“R”软件分析反应和复发率、荨麻疹评分变化和不良事件发生率。根据应答率进行亚组分析。异质性评估采用I2检验和卡方检验,采用随机效应模型。本系统综述纳入了36项符合纳入标准的研究。omalizumab的总有效率为88.0% (95% CI: 80.7%-95.2%;i2 = 61.0%;p = .001),完全缓解率为51.0% (95% CI: 32.7% ~ 69.2%;i2 = 90.0%;p 2 = 54.2%;p = 0.068),不良反应或部分反应占20.1% (95% CI: 14.3%-27.3%;i2 = 0.0%;p = .787)。复发率为24.3% (95% CI: 8.1% ~ 40.6%;i2 = 66.6%;p = .006)。荨麻疹活动评分显示症状显著减轻(SMD = -3.08;95% CI: -5.45 ~ -0.71;i2 = 89.1%;p
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