Department of Paediatrics, The Chinese University of Hong Kong, Shatin, Hong Kong & Department of Paediatrics and adolescent Medicine, the Hong Kong Children's Hospital, Shatin, Hong Kong.
Centre for Learning Enhancement and Research, The Chinese University of Hong Kong, Shatin, Hong Kong.
Expert Opin Pharmacother. 2021 Mar;22(4):497-509. doi: 10.1080/14656566.2020.1829593. Epub 2021 Feb 22.
Chronic spontaneous urticaria (CSU) refers to urticaria (wheals) or angioedema, which occur for a period of six weeks or longer without an apparent cause. The condition may impair the patient's quality of life.
Treatment for CSU is mainly symptomatic. Both AAAAI/ACAAI practice parameters and EAACI/GA2LEN/EDF/WAO guidelines suggest CSU management in a stepwise manner. First-line therapy is with second-generation H-antihistamines. Treatment should be stepped up along the algorithm if symptoms are not adequately controlled. Increasing the dosage of second-generation H-antihistamines, with the addition of first-generation H-antihistamines, H antagonist, omalizumab, ciclosporin A, or short-term corticosteroid may be necessary. New medications are being developed to treat refractory CSU. They include spleen tyrosine kinase inhibitor, Bruton tyrosine kinase inhibitor, prostaglandin D receptor inhibitor, H-antihistamine, and other agents. The authors discuss these treatments and provide expert perspectives on the management of CSU.
Second-generation H-antihistamines remain the first-line therapeutic options for the management of CSU. For patients not responding to higher-dose H-antihistamines, international guidelines recommend the addition of omalizumab. Efficacy and safety data for newer agents are still pending. Large-scale, well-designed, randomized, double-blind, placebo-controlled trials will further provide evidence on the safety profile and efficacy of these agents in patients with CSU.
慢性自发性荨麻疹(CSU)是指荨麻疹(风团)或血管性水肿,持续六周或更长时间而无明显原因。这种情况可能会降低患者的生活质量。
CSU 的治疗主要是对症治疗。美国过敏、哮喘和免疫学学会/美国过敏、哮喘和免疫学学院实践参数以及欧洲过敏与临床免疫学会/全球过敏与哮喘欧洲网络/欧洲变态反应与临床免疫学会/世界变态反应组织指南均建议采用逐步治疗方法管理 CSU。一线治疗是第二代 H1 抗组胺药。如果症状不能得到充分控制,应根据算法逐步升级治疗。增加第二代 H1 抗组胺药的剂量,同时加用第一代 H1 抗组胺药、H 受体拮抗剂、奥马珠单抗、环孢素 A 或短期皮质类固醇可能是必要的。正在开发新的药物来治疗难治性 CSU。它们包括脾酪氨酸激酶抑制剂、布鲁顿酪氨酸激酶抑制剂、前列腺素 D 受体抑制剂、H1 抗组胺药和其他药物。作者讨论了这些治疗方法,并就 CSU 的管理提供了专家意见。
第二代 H1 抗组胺药仍然是 CSU 管理的一线治疗选择。对于对高剂量 H1 抗组胺药无反应的患者,国际指南建议加用奥马珠单抗。新型药物的疗效和安全性数据仍在等待中。大规模、精心设计、随机、双盲、安慰剂对照试验将进一步提供这些药物在 CSU 患者中的安全性和疗效的证据。