Department of Internal Medicine, Division of Allergy and Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390-8859, USA.
Am J Clin Dermatol. 2011 Dec 1;12(6):361-76. doi: 10.2165/11591130-000000000-00000.
The effects of urticaria are predominantly mediated by histamine release; therefore, H1-antihistamines are the mainstay of treatment. Second-generation H1-antihistamines, compared with their first-generation counterparts, have demonstrated improved peripheral H1-receptor selectivity and decreased lipophilicity (which minimizes CNS adverse effects), and antiallergic properties in addition to being histamine inverse agonists. Evidence of clinical efficacy and tolerability of second-generation H1-antihistamines available in the US for the treatment of chronic urticaria (CU) was analyzed using the GRADE system to develop the strength of recommendations for particular therapies. The evidence for the safety and efficacy of the majority of second-generation H1-antihistamines available in the US is of high quality and leads to a strong recommendation for their use in CU. There is a limited amount of data of variable quality comparing the efficacy between various second-generation H1-antihistamines in CU leading to weak recommendations for using cetirizine over fexofenadine and levocetirizine over desloratadine. Limited data of variable quality exist for the efficacy of higher doses of second-generation H1-antihistamines in CU patients not responsive to standard doses. These limited data lead to a strong recommendation that higher than recommended doses of fexofenadine do not offer greater efficacy in control of CU and a weak recommendation that higher doses of levocetirizine and desloratadine are more effective in CU unresponsive to standard doses. More studies of higher quality are required to make any firm recommendations regarding second-generation H1-antihistamines in the treatment of physical urticarias. All second-generation H1-antihistamines appear to be very well tolerated in CU patients, with rare reports of adverse effects. Due to the relatively large gaps in the quantity and quality of evidence, particularly for choice of H1-antihistamines, use of higher doses, and use in physical urticarias, greater emphasis in management decisions should be based on the risk/benefit ratio and the patient's personal values and preferences (including cost) in clinical decision making.
荨麻疹的主要影响因素是组胺释放;因此,H1 抗组胺药是治疗的主要方法。与第一代 H1 抗组胺药相比,第二代 H1 抗组胺药具有改善的外周 H1 受体选择性和降低的亲脂性(最大限度地减少中枢神经系统不良反应),以及除了作为组胺反向激动剂之外的抗过敏特性。使用 GRADE 系统分析了美国可用于治疗慢性荨麻疹 (CU) 的第二代 H1 抗组胺药的临床疗效和耐受性证据,以制定特定治疗方法的建议强度。美国大多数第二代 H1 抗组胺药的安全性和有效性证据质量较高,强烈推荐将其用于 CU。比较各种第二代 H1 抗组胺药在 CU 中的疗效的大量数据质量参差不齐,导致仅对西替利嗪优于非索非那定,左西替利嗪优于地氯雷他定的弱推荐。在对标准剂量无反应的 CU 患者中,更高剂量的第二代 H1 抗组胺药的疗效数据有限,且质量参差不齐。这些有限的数据强烈推荐,高于推荐剂量的非索非那定在控制 CU 方面没有更大的疗效,而弱推荐是更高剂量的左西替利嗪和地氯雷他定在治疗对标准剂量无反应的 CU 方面更有效。需要进行更多高质量的研究,以便就第二代 H1 抗组胺药治疗物理性荨麻疹提出任何确切建议。所有第二代 H1 抗组胺药在 CU 患者中似乎都非常耐受,不良反应罕见。由于证据的数量和质量存在较大差距,特别是在 H1 抗组胺药的选择、高剂量使用和物理性荨麻疹的使用方面,在管理决策中应更加强调基于风险/效益比以及患者的个人价值观和偏好(包括成本)。