Johns Hopkins Bayview Medical Center, Baltimore, Maryland.
Division of Allergy and Clinical Immunology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Ann Allergy Asthma Immunol. 2014 Jan;112(1):64-70. doi: 10.1016/j.anai.2013.09.028. Epub 2013 Nov 9.
There are limited data regarding alternative treatments for antihistamine refractory chronic idiopathic urticaria (CIU). Patients with recalcitrant skin disease often cannot gain satisfactory symptom control with standard therapies and may require prolonged courses of oral corticosteroids. There is a lack of information describing the degree and duration of sulfasalazine's efficacy, the frequency and nature of adverse reactions, and the appropriate safety monitoring parameters.
To present a case series detailing the efficacy and safety of sulfasalazine therapy in patients with CIU.
A retrospective chart review was conducted of 39 patients with sulfasalazine-treated CIU evaluated at Johns Hopkins Asthma and Allergy Center from October 2007 to March 2012. Eight patients were excluded from the final analysis.
Twenty-six patients (83.9%) showed an improvement in symptoms within the first 3 months, with 51.6% of patients (n = 16) becoming asymptomatic within the first 6 months of starting sulfasalazine. Eleven patients (35.4%) achieved complete relief of symptoms after tapering off sulfasalazine therapy. Five of the 31 patients (16.1%) failed treatment, defined as worsening symptoms and pursuit of an alternative therapy. Six of 31 patients (19.4%) had a modified course of sulfasalazine therapy owing to abnormal hematologic parameters. Serious adverse events leading to drug discontinuation occurred in 6.5% of patients (n = 2) and included a patient with drug-induced leukopenia and one with rhabdomyolysis.
Sulfasalazine is a highly effective treatment for patients with antihistamine resistant CIU. The frequency of adverse events leading to an alteration of sulfasalazine treatment supports the need for close monitoring of these patients.
对于抗组胺药难治性慢性特发性荨麻疹(CIU),替代治疗的相关数据有限。顽固皮肤病患者通常无法通过标准疗法获得满意的症状控制,可能需要长期口服皮质类固醇。目前缺乏描述柳氮磺胺吡啶疗效的程度和持续时间、不良反应的频率和性质以及适当的安全监测参数的信息。
介绍一系列详细描述柳氮磺胺吡啶治疗 CIU 患者的疗效和安全性的病例。
对 2007 年 10 月至 2012 年 3 月在约翰霍普金斯哮喘和过敏中心接受柳氮磺胺吡啶治疗的 39 例 CIU 患者进行回顾性图表分析。最终有 8 例患者被排除在分析之外。
26 例患者(83.9%)在最初 3 个月内症状得到改善,其中 51.6%(n=16)的患者在开始使用柳氮磺胺吡啶的前 6 个月内无症状。11 例患者(35.4%)在逐渐减少柳氮磺胺吡啶治疗后症状完全缓解。5 例患者(16.1%)治疗失败,定义为症状恶化和寻求替代疗法。由于血液学参数异常,31 例患者中有 6 例(19.4%)修改了柳氮磺胺吡啶治疗方案。6.5%(n=2)的患者出现严重不良反应导致停药,包括 1 例药物诱导性白细胞减少和 1 例横纹肌溶解。
柳氮磺胺吡啶是治疗抗组胺药耐药性 CIU 患者的有效药物。导致改变柳氮磺胺吡啶治疗的不良反应的频率支持对这些患者进行密切监测的必要性。