Clinica Pediatrica, Azienda Ospedaliero-Universitaria, Department of Medicine and Surgery, University of Parma, Via Gramsci 14, 43126 Parma, Italy.
Medicina (Kaunas). 2024 Apr 25;60(5):704. doi: 10.3390/medicina60050704.
The guidelines for chronic urticaria in children contain recommendations that are often based on adult studies. The diagnostic pathway has not been standardized and the effectiveness of anti-H1, omalizumab, montelukast, and systemic glucocorticoids is rarely reported in the pediatric population. There is a wide variation in the rate of remission of chronic urticaria between studies. The aim of this study is to enhance our understanding of pediatric chronic urticaria. This study enrolled 37 children with chronic urticaria aged from 0 to 18 years. Demographic parameters, medical history, clinical features, laboratory data and treatment information were collected. Children were treated with the recommended dosage of second-generation H1-antihistamines, which was increased by up to twofold. Omalizumab was added for refractory anti-H1 patients. A three-day course with systemic glucocorticoids was administered for severe exacerbations. Montelukast was administered to some children. : Wheals without angioedema were common. Chronic urticaria was spontaneous in 32 children (86.48%), inducible in 2 (5.41%), induced by a parasite in 1 and vasculitic in 2. Treatment of the potential causes of chronic urticaria was of no benefit, except for eradication of Dientamoeba fragilis. Chronic urticaria was resolved within three years in 45.9% of cases. Allergic diseases were present in nine children (24.32%) and autoimmune diseases were present in three (8.11%). All children were treated with anti-H1 at the licensed dose or at a higher dose. A partial or complete response to anti-H1 was observed in 29 (78.38%) patients. Montelukast showed no benefit. All children treated with omalizumab responded. Systemic glucocorticoids were successfully used to treat exacerbations. Our findings indicate that laboratory tests should not be routinely performed in children with chronic urticaria without clinical suspicion. However, comorbidities such as thyroid autoimmune disease and coeliac disease are suggested to be monitored over the chronic urticaria course. These clinical conditions could be diagnosed from the diagnostic framework of chronic urticaria. Increasing the dosage of anti-H1 and omalizumab was effective in children resistant to standard treatment but we still need further studies to generate a standard patient-centered treatment.
儿童慢性荨麻疹指南包含了许多基于成人研究的建议。其诊断途径尚未标准化,儿童人群中抗组胺 H1 药物、奥马珠单抗、孟鲁司特和全身糖皮质激素的疗效也鲜有报道。不同研究中慢性荨麻疹的缓解率差异很大。本研究旨在提高我们对儿科慢性荨麻疹的认识。本研究纳入了 37 名 0 至 18 岁的慢性荨麻疹患儿。收集了人口统计学参数、病史、临床特征、实验室数据和治疗信息。患儿接受了推荐剂量的第二代 H1 抗组胺药治疗,最大剂量可增加至两倍。对抗 H1 治疗无效的患儿加用奥马珠单抗。严重发作时给予 3 天疗程的全身糖皮质激素。部分患儿给予孟鲁司特。无血管性水肿的风团很常见。32 例(86.48%)患儿慢性荨麻疹为自发性,2 例(5.41%)为诱导性,1 例由寄生虫引起,2 例为血管炎。除了根除脆弱双核阿米巴外,治疗慢性荨麻疹的潜在病因没有获益。3 年内痊愈的患儿占 45.9%。9 例患儿(24.32%)存在过敏性疾病,3 例患儿(8.11%)存在自身免疫性疾病。所有患儿均按许可剂量或更高剂量接受 H1 抗组胺治疗。29 例(78.38%)患儿有部分或完全反应。孟鲁司特无效。所有接受奥马珠单抗治疗的患儿均有反应。全身糖皮质激素成功用于治疗发作。我们的研究结果表明,对于无临床怀疑的慢性荨麻疹患儿,实验室检查不应常规进行。然而,建议在慢性荨麻疹病程中监测甲状腺自身免疫性疾病和乳糜泻等合并症。这些临床情况可以从慢性荨麻疹的诊断框架中诊断出来。增加 H1 抗组胺药和奥马珠单抗的剂量对标准治疗抵抗的患儿有效,但我们仍需要进一步的研究来制定以患者为中心的标准治疗方案。