Clinical evaluation of subcutaneous immunotherapy with a polymerized molecular allergoid of Alt a 1 in patients with allergic rhinoconjunctivitis and/or allergic asthma caused by the mould Alternaria alternata.

IF 2.6 Q2 ALLERGY
Á Ferrer Torres
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引用次数: 2

Abstract

Summary: This is a retrospective analysis of the clinical evolution of 14 patients diagnosed with allergic rhinoconjunctivitis (AR) and/or allergic asthma (AA) caused by Alternaria alternata, who were attended by the allergology service of Vega Baja Hospital of Orihuela (Alicante, Spain). The purpose was to assess the clinical impact and safety of 1-year of subcutaneous immunotherapy with a polymerized molecular allergoid of Alt a 1. Impact of the treatment on allergic diseases (mean number AR/AA episodes and ARIA/GINA classifications), changes in symptoms and prescribed medication, change in the global subjective clinical status of patients and satisfaction with the treatment were also evaluated. Adverse reactions were also recorded and analyzed. After 1-year of treatment, fewer AR and AA episodes (p less than 0.05) and improvements in ARIA/GINA classifications were observed. Significant improvements of symptoms (p less than 0.05) and a resulting general reduction of the medication prescribed was also detected. Improvements in the global subjective clinical status and good satisfaction rates were observed. Only 1 patient presented a local and not clinically relevant adverse reaction. The treatment showed promising effects with a significant improvement in the clinical status of all patients with a good safety profile.

Altera 1聚合分子变应原皮下免疫治疗由Alternaria alternata霉菌引起的过敏性鼻结膜炎和/或过敏性哮喘患者的临床评价。
摘要:这是对14名被诊断为由Alternaria alternata引起的过敏性鼻结膜炎(AR)和/或过敏性哮喘(AA)的患者的临床演变的回顾性分析,这些患者由奥里胡埃拉Vega Baja医院(西班牙阿利坎特)的变态反应科服务就诊。目的是评估用聚合分子变应原Alt a 1进行1年皮下免疫治疗的临床影响和安全性。还评估了治疗对过敏性疾病的影响(平均AR/AA发作次数和ARIA/GINA分类)、症状和处方药的变化、患者整体主观临床状态的变化以及对治疗的满意度。还记录和分析了不良反应。治疗1年后,观察到AR和AA发作次数减少(p<0.05),ARIA/GINA分级有所改善。症状也有显著改善(p小于0.05),处方药也普遍减少。观察到整体主观临床状况的改善和良好的满意度。只有1名患者出现局部且与临床无关的不良反应。The治疗显示出良好的疗效,所有患者的临床状况都有显著改善,安全性良好。
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CiteScore
4.00
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102
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