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首页> 外文期刊>Otolaryngology--head and neck surgery: official journal of American Academy of Otolaryngology-Head and Neck Surgery >Long-term efficacy of specific immunotherapy on house dust mite-induced allergic rhinitis in China.
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Long-term efficacy of specific immunotherapy on house dust mite-induced allergic rhinitis in China.

机译:特异性免疫疗法对中国尘螨诱发的过敏性鼻炎的长期疗效。

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摘要

Although the effect of specific immunotherapy (SIT) on allergic rhinitis (AR) has been well documented in developed countries, its long-term efficacy in patients in developing countries (such as China) is poorly understood. This study investigated the long-term therapeutic and preventive effects of SIT on house dust mite (HDM)-induced AR in patients from China.Historical cohort study.University hospital.One hundred forty-six AR patients with/without asthma allergic to HDM were investigated for 5 years after initiation of a 3-year course of subcutaneous SIT (SIT group, n = 106) or no SIT (control group, n = 40). The clinical responses of all patients were evaluated at baseline, the stop point of SIT (third year), and 2 years after SIT termination (fifth year), by clinical index including symptom and rescue medication scores (SMS), visual analog scale (VAS), total immunoglobulin E (tIgE), and specific IgE (sIgE). Asthma was assessed by clinical evaluation.The decrease of SMS and VAS from baseline was significantly improved in the SIT group compared with controls at both the third and fifth year. For patients without asthma at baseline, the odds ratio for no asthma was 3.57 (95% confidence interval, 1.05-12.91; P < .05) in favor of SIT. The serum sIgE/tIgE ratio was significantly increased after SIT treatment in the SIT group, but it was not related to SIT efficacy.SIT has a long-term effect of improving clinical symptoms and reducing the risk of development of asthma in Chinese AR patients.
机译:尽管在发达国家已充分证明了特异性免疫疗法(SIT)对变应性鼻炎(AR)的作用,但对于发展中国家(例如中国)患者的长期疗效尚不甚了解。本研究调查了SIT对中国房尘螨(HDM)诱发的AR的长期治疗和预防作用。历史队列研究。大学医院.146例对HDM过敏的哮喘患者(无哮喘)在开始3年皮下SIT治疗(SIT组,n = 106)或不进行SIT(对照组,n = 40)后进行了5年的研究。通过包括症状和急救药物评分(SMS),视觉模拟量表(VAS)在内的临床指标,在基线,SIT停止点(第三年)和SIT终止后两年(第五年)评估所有患者的临床反应。 ),总免疫球蛋白E(tIgE)和特异性IgE(sIgE)。通过临床评估评估哮喘.SIT组与对照组相比,在第三和第五年,SMS和VAS从基线的下降均明显改善。对于基线时无哮喘的患者,无哮喘的优势比为3.57(95%置信区间为1.05-12.91; P <.05),有利于SIT。在SIT组中,SIT治疗后血清sIgE / tIgE比值显着增加,但与SIT疗效无关.SIT对改善中国AR患者的临床症状和减少哮喘风险具有长期影响。

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