首页> 外文期刊>Annals of allergy, asthma, and immunology >Efficacy of diphenhydramine vs desloratadine and placebo in patients with moderate-to-severe seasonal allergic rhinitis.
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Efficacy of diphenhydramine vs desloratadine and placebo in patients with moderate-to-severe seasonal allergic rhinitis.

机译:苯海拉明与去氯雷他定和安慰剂在中度至重度季节性变应性鼻炎患者中的疗效。

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BACKGROUND: Previous studies have shown that diphenhydramine and desloratadine effectively relieve symptoms of seasonal allergic rhinitis (SAR). OBJECTIVE: To compare the relative efficacy of 50 mg of diphenhydramine hydrochloride, 5 mg of desloratadine, and placebo in relieving symptoms in patients with moderate-to-severe SAR. METHODS: In this 1-week, multicenter, parallel-group, randomized, double-blind, double-dummy, placebo-controlled study, 610 patients with moderate-to-severe SAR received 50 mg of diphenhydramine hydrochloride 3 times daily, 5 mg of desloratadine once daily, or placebo. Daily 24-hour reflective total nasal symptom scores (TNSSs) (primary end point), total symptom scores, and individual symptom scores were evaluated. A global evaluation of response to treatment was conducted at 2 posttreatment visits. RESULTS: The mean reduction from baseline in 24-hour reflective TNSSs relative to the placebo response was 77.6% for the diphenhydramine group (P < .001) and 21.0% for the desloratadine group (P = .12). A TNSS between-treatment difference of -1.81 (46.7%; P < .001) was observed when comparing diphenhydramine with desloratadine. A similar between-treatment difference was observed for the 24-hour reflective total symptom score comparing diphenhydramine to desloratadine (-3.35; 45.5%; P < .001). Diphenhydramine provided clinically and statistically significant reductions vs placebo and desloratadine in all individual symptoms, including nasal congestion. Desloratadine had a tendency toward improvement compared with placebo for most individual symptom scores. However, a statistically significant result was reached only for sneezing (-0.27; 33.9%; P = .04). CONCLUSIONS: Diphenhydramine, 50 mg, given for 1 week provided statistically significant and clinically superior improvements in symptoms compared with 5 mg of desloratadine in patients with moderate-to-severe SAR. Somnolence occurred more frequently with diphenhydramine (22.1%) compared with desloratadine (4.5%) and placebo (3.4%).
机译:背景:以前的研究表明苯海拉明和去氯雷他定可以有效缓解季节性变应性鼻炎(SAR)的症状。目的:比较50 mg盐酸苯海拉明,5 mg去氯雷他定和安慰剂缓解中重度SAR患者症状的相对疗效。方法:在这项为期1周的多中心,平行组,随机,双盲,双虚拟,安慰剂对照研究中,610例中度至重度SAR患者每天接受50 mg盐酸苯海拉明3次,每次5 mg每天一次使用地洛雷他定或安慰剂。每天评估24小时反射性总鼻症状评分(TNSSs)(主要终点),总症状评分和个别症状评分。在两次治疗后就诊时对治疗反应进行了总体评估。结果:相对于安慰剂反应,苯海拉明组的24小时反射性TNSS相对于基线的平均减少量为77.6%(P <.001),而去氯雷他定组的平均减少量为21.0%(P = .12)。当比较苯海拉明和去氯雷他定时,TNSS治疗间差异为-1.81(46.7%; P <.001)。比较苯海拉明与去氯雷他定,24小时反射总症状评分观察到相似的治疗间差异(-3.35; 45.5%; P <.001)。与安慰剂和地氯雷他定相比,苯海拉明在所有个体症状(包括鼻充血)方面均在临床和统计学上均显着降低。与安慰剂相比,地氯雷他定在大多数个体症状评分中都有改善的趋势。但是,仅在打喷嚏时才达到统计学上的显着结果(-0.27; 33.9%; P = .04)。结论:中度至重度SAR患者给予50 mg苯海拉明1周,与5 mg去氯雷他定相比,在统计学上具有统计学上的显着改善,并且在临床上有较好的改善。与去氯雷他定(4.5%)和安慰剂(3.4%)相比,苯海拉明(22.1%)的嗜睡发生率更高。

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