Chung J H, deTineo M L, Naclerio R M, Sorrentino J V, Winslow C M, Baroody F M
Otolaryngology-Head and Neck Surgery, Pritzker School of Medicine, University of Chicago, Illinois, USA.
Ann Allergy Asthma Immunol. 1997 Mar;78(3):307-12. doi: 10.1016/S1081-1206(10)63187-0.
Clemastine (1 mg) is currently available over-the-counter for the treatment of allergic rhinitis.
To evaluate the efficacy of half the standard dose of clemastine (0.5 mg) in inhibiting the nasal response to allergen and the cutaneous response to histamine.
Double-blind, placebo-controlled, crossover study of 20 allergic subjects out of season. The subjects received placebo or clemastine administered one, four, and six hours before the challenges. Filter paper discs were used both to challenge the nasal mucosa with diluent and allergen and collect generated secretions. Sneezes, secretion weights, nasal and ocular symptoms, and albumin levels in nasal secretions were monitored for the nasal challenge. Intradermal skin testing was performed with diluent followed by histamine and the wheal and flare reactions were measured.
There was a significant reduction in the number of sneezes after clemastine administered one, four, and six hours prior to challenge compared with placebo (P < .01). Clemastine administered four and six hours before challenge reduced sneezing significantly more than clemastine administered one hour before challenge (P < .05). Antigen-induced increases in secretion weights and symptoms of rhinorrhea were significantly reduced compared with placebo only when clemastine was administered four and six hours prior to challenge (P < .05). Pretreatment with clemastine had no significant inhibitory effects on other nasal symptoms or on albumin levels in nasal secretions, an objective index of increased vascular permeability. Pretreatment with clemastine did not inhibit the histamine-induced wheal skin reaction but showed a tendency, when administered six hours prior to the intradermal challenge, to reduce the flare reaction induced by the lowest dose of histamine (P = .05).
The data show that clemastine, given at half the usual dose four and six hours prior to allergen challenge, provides relief for sneezing and rhinorrhea and suggests that this dose might be useful in the treatment of allergic rhinitis.
氯马斯汀(1毫克)目前可在非处方用于治疗过敏性鼻炎。
评估氯马斯汀标准剂量一半(0.5毫克)抑制鼻腔对过敏原反应及皮肤对组胺反应的疗效。
对20名非季节性过敏受试者进行双盲、安慰剂对照、交叉研究。受试者在激发试验前1、4和6小时接受安慰剂或氯马斯汀。使用滤纸圆盘用稀释剂和过敏原刺激鼻黏膜并收集产生的分泌物。在鼻激发试验中监测喷嚏次数、分泌物重量、鼻和眼部症状以及鼻分泌物中的白蛋白水平。用稀释剂进行皮内皮肤试验,随后用组胺进行试验,并测量风团和红晕反应。
与安慰剂相比,在激发试验前1、4和6小时给予氯马斯汀后,喷嚏次数显著减少(P <.01)。在激发试验前4和6小时给予氯马斯汀比在激发试验前1小时给予氯马斯汀显著更能减少喷嚏次数(P <.05)。仅在激发试验前4和6小时给予氯马斯汀时,与安慰剂相比,抗原诱导的分泌物重量增加和鼻漏症状显著减少(P <.05)。氯马斯汀预处理对其他鼻症状或鼻分泌物中的白蛋白水平(血管通透性增加的客观指标)没有显著抑制作用。氯马斯汀预处理未抑制组胺诱导的风团皮肤反应,但在皮内激发试验前6小时给药时,显示出降低最低剂量组胺诱导的红晕反应的趋势(P =.05)。
数据表明,在过敏原激发试验前4和6小时给予通常剂量一半的氯马斯汀,可缓解喷嚏和鼻漏症状,并表明该剂量可能对治疗过敏性鼻炎有用。