Davies B H, Mullins J
Asthma and Allergy Unit, Sully Hospital, Penarth, South Glamorgan, UK.
Allergy. 1993 Oct;48(7):519-24. doi: 10.1111/j.1398-9995.1993.tb01108.x.
The efficacy, tolerability, and adverse-effect profile of the recently developed, topical antihistamine levocabastine were compared with those of sodium cromoglycate in a 4-week double-blind, placebo-controlled trial in 95 patients with seasonal allergic conjunctivitis. At the end of the trial, global therapeutic efficacy was considered to be excellent or good in 87% of levocabastine-treated patients, as compared with 68% of sodium cromoglycate-treated patients (P = 0.006) and 63% of those who received placebo (P = 0.05). After 4 weeks of treatment, levocabastine patients had experienced significantly greater relief from their most severe ocular symptom than patients in the sodium cromoglycate group (P < 0.05). Furthermore, 37% of levocabastine-treated patients were virtually symptom-free for at least 75% of the treatment period, as compared with only 6% of patients in the sodium cromoglycate group (P < 0.01) and 4% of those who received placebo (P < 0.01). Moreover, this trend was maintained on days when the pollen count was high, when the corresponding figures were 33%, 6% (P = 0.02), and 4% (P = 0.02), respectively. Levocabastine was well tolerated. Indeed, the incidence of adverse reactions was no greater in the levocabastine group than in the placebo group. Topical levocabastine is an effective and well-tolerated drug for the prophylaxis and treatment of seasonal allergic conjunctivitis.
在一项针对95例季节性变应性结膜炎患者的为期4周的双盲、安慰剂对照试验中,将新研发的局部用抗组胺药左卡巴斯汀的疗效、耐受性和不良反应情况与色甘酸钠进行了比较。试验结束时,87%接受左卡巴斯汀治疗的患者总体治疗效果被认为极佳或良好,相比之下,接受色甘酸钠治疗的患者为68%(P = 0.006),接受安慰剂治疗的患者为63%(P = 0.05)。治疗4周后,左卡巴斯汀组患者最严重眼部症状的缓解程度显著大于色甘酸钠组患者(P < 0.05)。此外,37%接受左卡巴斯汀治疗的患者在至少75%的治疗期间几乎无症状,相比之下,色甘酸钠组患者仅为6%(P < 0.01),接受安慰剂治疗的患者为4%(P < 0.01)。而且,在花粉计数高的日子里这一趋势依然存在,相应的数字分别为33%、6%(P = 0.02)和4%(P = 0.