A multicenter, randomized, parallel-group trial assessing compliance, tolerability, safety, and efficacy to treatment with grass allergy tablets in 261 patients with grass pollen rhinoconjunctivitis.

Journal of allergy Pub Date : 2012-01-01 Epub Date: 2011-11-09 DOI:10.1155/2012/673502
Roberta Alesina, Massimo Milani, Silvia Pecora
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引用次数: 10

Abstract

Background. Allergen-specific sublingual immunotherapy (SLIT) is considered a causal treatment of respiratory allergies. Compliance to the SLIT is an important aspect for a positive clinical outcome. Study Aim. To evaluate if compliance with grass Allergy Immunotherapy Tablet (AIT) can be increased by providing an electronic compliance device (CED) (Memozax; a tablet-container with a programmable daily acoustic alarm). Patients and Methods. 261 patients with grass allergy were enrolled and randomized (1 : 1) to 1-year treatment with AIT (Grazax) using a CED (group A; n = 122) or without (Group B, n = 139). Compliance was measured through tablet count at each visit. Results. The 12-month compliance, mean (SD), in group A was 83% (21) and 83% (24) in group B. A total of 81% of patients reported a significant clinical improvement of symptoms after treatment in comparison with the previous year. No severe adverse reactions were observed in the study. Conclusion. Compliance to the treatment with AIT administered for 12 consecutive months is in general good. The use of CED is not associated with a greater compliance. AIT treatment was associated with a significant clinical improvement in >80% of patients with a good tolerability and safety profile.

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一项多中心、随机、平行组试验评估261例草花粉鼻结膜炎患者草过敏片治疗的依从性、耐受性、安全性和有效性。
背景。过敏原特异性舌下免疫疗法(SLIT)被认为是呼吸道过敏的因果治疗。遵守SLIT是积极临床结果的一个重要方面。研究的目标。为了评估是否可以通过提供电子依从性装置(CED)来增加对草过敏免疫治疗片(AIT)的依从性。一种带有可编程每日声音警报的平板容器)。患者和方法:261例草过敏患者被纳入研究,随机(1:1)接受为期1年的AIT (Grazax)治疗,并使用CED (a组;n = 122)或无(B组,n = 139)。依从性通过每次就诊时的片剂数量来衡量。结果。A组12个月的平均(SD)依从性为83%(21例),b组为83%(24例)。与前一年相比,共有81%的患者报告治疗后症状有显着的临床改善。本研究未见严重不良反应。结论。连续12个月接受AIT治疗的依从性一般良好。使用CED并不意味着更强的遵从性。AIT治疗与>80%具有良好耐受性和安全性的患者的显著临床改善相关。
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