首页> 美国卫生研究院文献>Journal of Allergy >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
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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

机译:一项多中心随机平行分组的试验评估草过敏片对261例草花粉鼻结膜炎患者的依从性耐受性安全性和疗效

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摘要

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.
机译: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。对SLIT的依从性是取得积极临床成果的重要方面。学习目标。要评估是否可以通过提供电子依从性设备(CED)(Memozax;具有可编程的每日声音警报的药片容器)来提高对草过敏免疫治疗片(AIT)的依从性。患者和方法。纳入261例草过敏患者,随机(1:1)使用AED(Grazax)使用CED(A组; n = 122)或不使用CED(B组,n = 139)治疗1年。通过每次访问的片剂计数来测量依从性。结果。 A组的12个月依从性(SD)分别为B组的83%(21)和83%(24)。相较于A组,共有81%的患者报告治疗后症状明显改善。前一年。在研究中没有观察到严重的不良反应。结论。连续12个月给予AIT治疗的依从性总体良好。 CED的使用与更大的合规性无关。 AIT治疗与> 80%具有良好耐受性和安全性的患者的显着临床改善相关。

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