逃离过敏性鼻炎的陷阱。

Q2 Medicine
Clinical and Molecular Allergy Pub Date : 2015-08-04 eCollection Date: 2015-01-01 DOI:10.1186/s12948-015-0023-y
Oliviero Rossi, Ilaria Massaro, Marco Caminati, Cristina Quecchia, Filippo Fassio, Enrico Heffler, Giorgio Walter Canonica
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引用次数: 8

摘要

鼻炎通常是过敏的第一症状,但经常被忽视,并归类为讨厌的条件。具有讽刺意味的是,由于它对工作和日常生活的影响,它在世界范围内造成了最大的社会经济负担。然而,患者似乎不愿寻求专业建议,只有在症状变得“无法忍受”时才去看医生,而且通常是在他们的常规治疗无效时。显然,是时候开发新的更有效的过敏性鼻炎治疗方法了。MP29-02 (Dymista®;Meda, Solna, Sweden)是治疗中度至重度季节性和常年性变应性鼻炎的一类新药物,如果单用鼻内抗组胺药或鼻内皮质类固醇治疗不充分。MP29-02是由盐酸氮唑elastine (AZE)和丙酸氟替卡松(FP)组成的新制剂。它不仅受益于两种活性剂的掺入,而且受益于一种新的配方;其黏度低,液滴尺寸小,体积大(137 μl),喷雾角度宽,对鼻黏膜的覆盖和滞留效果最佳,有助于提高临床疗效。在临床试验中,接受MP29-02治疗的患者的症状缓解是接受FP和AZE治疗的患者的两倍,而后者的症状缓解又明显大于安慰剂患者。事实上,MP29-02相对于FP的优势与FP相对于安慰剂的优势大致相同。MP29-02的优势在鼻塞为主的患者中尤为明显,MP29-02的鼻塞缓解效果是FP的3倍(p = 0.0018), AZE的5倍(p = 0.0001)。此外,接受MP29-02治疗的患者比单独接受FP或AZE治疗的患者更快达到每项反应,在现实生活中,2名患者中有1名在仅3天后就报告了疾病控制良好的感觉。在常年性变应性鼻炎和非变应性鼻炎患者中,MP29-02较FP的长期优势也很明显,从治疗第一天起就有统计学意义,治疗差异维持了整整一年。综上所述,这些数据表明MP29-02可能会改善许多患者的生活,使他们最终摆脱过敏性鼻炎的陷阱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Escaping the trap of allergic rhinitis.

Escaping the trap of allergic rhinitis.

Escaping the trap of allergic rhinitis.

Escaping the trap of allergic rhinitis.

Rhinitis is often the first symptom of allergy but is frequently ignored and classified as a nuisance condition. Ironically it has the greatest socioeconomic burden worldwide caused by its impact on work and on daily life. However, patients appear reticent to seek professional advice, visiting their doctor only when symptoms become 'intolerable' and often when their usual therapy proves ineffective. Clearly, it's time for new and more effective allergic rhinitis treatments. MP29-02 (Dymista®; Meda, Solna, Sweden) is a new class of medication for moderate to severe seasonal and perennial allergic rhinitis if monotherapy with either intranasal antihistamine or intranasal corticosteroids is not considered sufficient. MP29-02 is a novel formulation of azelastine hydrochloride (AZE) and fluticasone propionate (FP). It benefits not only from the incorporation of two active agents, but also from a novel formulation; its lower viscosity, smaller droplet size, larger volume (137 μl) and wider spray angle ensure optimal coverage of, and retention on the nasal mucosa and contribute to its clinical efficacy. In clinical trials, patients treated with MP29-02 experienced twice the symptom relief as those treated with FP and AZE, who in turn exhibited significantly greater symptom relief than placebo-patients. Indeed, the advantage of MP29-02 over FP was approximately the same as that shown for FP over placebo. The advantage of MP29-02 was particularly evident in those patients for whom nasal congestion is predominant, with MP29-02 providing three times the nasal congestion relief of FP (p = 0.0018) and five times the relief of AZE (p = 0.0001). Moreover, patients treated with MP29-02 achieved each and every response up to a week faster than those treated with FP or AZE alone and in real life 1 in 2 patients reported the perception of well-controlled disease after only 3 days. MP29-02's superiority over FP was also apparent long-term in patients with perennial allergic rhinitis or non-allergic rhinitis, with statistical significance noted from the first day of treatment, with treatment difference maintained for a full year. Taken together, these data suggest that MP29-02 may improve the lives of many of our patients, enabling them to finally escape the allergic rhinitis trap.

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来源期刊
Clinical and Molecular Allergy
Clinical and Molecular Allergy Medicine-Immunology and Allergy
CiteScore
8.20
自引率
0.00%
发文量
11
审稿时长
13 weeks
期刊介绍: Clinical and Molecular Allergy is an open access, peer-reviewed, online journal that publishes research on human allergic and immunodeficient disease (immune deficiency not related to HIV infection/AIDS). The scope of the journal encompasses all aspects of the clinical, genetic, molecular and inflammatory aspects of allergic-respiratory (Type 1 hypersensitivity) and non-AIDS immunodeficiency disorders. However, studies of allergic/hypersensitive aspects of HIV infection/AIDS or drug desensitization protocols in AIDS are acceptable. At the basic science level, this includes original work and reviews on the genetic and molecular mechanisms underlying the inflammatory response.
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