Hampel Frank, Ratner Paul, Mansfield Lyndon, Meeves Suzanne, Liao Yuning, Georges George
Central Texas Health Research, New Braunfels, Texas 78130, USA.
Ann Allergy Asthma Immunol. 2003 Oct;91(4):354-61. doi: 10.1016/S1081-1206(10)61682-1.
Previous studies have shown that fexofenadine and cetirizine effectively relieve symptoms of seasonal allergic rhinitis (SAR).
To compare the effects of fexofenadine hydrochloride, 180 mg, and cetirizine, 10 mg, on symptoms, drowsiness, and motivation in patients with moderate-to-severe SAR.
In this 2-week multicenter, double-blind, randomized study, 495 subjects with moderate-to-severe SAR received once-daily fexofenadine hydrochloride, 180 mg, or cetirizine, 10 mg, without regard to food intake. Daily 12-hour reflective (AM, PM) and instantaneous (AM) individual symptoms and total symptom score (TSS) were evaluated. Drowsiness and motivation were recorded daily using visual analog scale at 7 AM, 10 AM, and 3 PM.
Between-treatment differences in reduction from baseline in AM instantaneous and 24-hour reflective TSS were -0.18 [95% confidence interval (CI), -0.55 to 0.20) and -0.22 (95% CI, -0.59 to 0.15), respectively. Since CIs for reduction in TSS between treatments fell within a 0.7 margin (defined a priori), treatments were considered statistically equivalent. Patients receiving fexofenadine experienced significantly less overall drowsiness vs baseline than those receiving cetirizine [-2.33 (95% CI, -3.80 to 0.86) vs 0.37 (95% CI, -1.10 to 1.84), P = .0110]. There was a trend toward greater improvements in overall motivation with fexofenadine compared with cetirizine [-2.36 (95% CI, -3.83 to 0.90) vs -0.30 (95% CI, -1.76 to 1.17), P = .0504].
Once-daily fexofenadine hydrochloride, 180 mg, given for 2 weeks caused statistically and clinically equivalent improvement in symptoms and significantly less drowsiness va baseline, compared with cetirizine, 10 mg, in patients with moderate-to-severe SAR.
既往研究表明,非索非那定和西替利嗪可有效缓解季节性变应性鼻炎(SAR)症状。
比较180mg盐酸非索非那定和10mg西替利嗪对中重度SAR患者症状、嗜睡及活力的影响。
在这项为期2周的多中心、双盲、随机研究中,495例中重度SAR患者每日服用一次180mg盐酸非索非那定或10mg西替利嗪,服药时不考虑食物摄入情况。评估每日12小时的回顾性(上午、下午)和即时性(上午)个体症状及总症状评分(TSS)。每天上午7点、10点和下午3点使用视觉模拟量表记录嗜睡和活力情况。
上午即时性TSS和24小时回顾性TSS较基线降低的组间差异分别为-0.18[95%置信区间(CI),-0.55至0.20]和-0.22(95%CI,-0.59至0.15)。由于治疗组间TSS降低的CI落在0.7的范围内(预先定义),因此认为治疗在统计学上等效。与接受西替利嗪的患者相比,接受非索非那定的患者总体嗜睡较基线时显著减轻[-2.33(95%CI,-3.80至0.86)vs0.37(95%CI,-1.10至1.84),P = 0.0110]。与西替利嗪相比,非索非那定在总体活力改善方面有更大改善的趋势[-2.36(95%CI,-3.83至0.90)vs -0.30(95%CI,-1.76至1.17),P = 0.0504]。
对于中重度SAR患者,每日一次服用180mg盐酸非索非那定,持续2周,在症状改善方面与服用10mg西替利嗪在统计学和临床上等效,且较基线时嗜睡显著减轻。