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毒液和吸入性变应原皮下免疫疗法的局部和全身副作用。

The local and systemic side-effects of venom and inhaled-allergen subcutaneous immunotherapy.

作者信息

Adamic Katja, Zidarn Mihaela, Bajrovic Nissera, Erzen Renato, Kopac Peter, Music Ema

机构信息

University Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.

出版信息

Wien Klin Wochenschr. 2009;121(9-10):357-60. doi: 10.1007/s00508-009-1172-0.

Abstract

BACKGROUND

Although immunotherapy is effective in allergic rhinitis, conjunctivitis, asthma and stinging insect hypersensitivity, it carries a risk of anaphylactic reactions.

METHODS

In a 4-year retrospective survey, we investigated 1257 adult patients who had received venom or inhaled-allergen subcutaneous immunotherapy. The dose-increase phase was performed as the 2-day rush protocol for venom immunotherapy and the 6-week protocol for inhaled-allergen immunotherapy.

RESULTS

A total of 904 patients received venom immunotherapy and 353 patients inhaled-allergen immunotherapy. The prevalence of systemic reactions was 13.6%. The frequency of systemic reactions was higher during the maintenance phase than in the dose-increase phase (9.6% vs. 5.9%) and was highest in both phases of treatment with honeybee venom (P < 0.001). The majority of systemic reactions were mild. Five (0.4%) patients had reaction with a fall of blood pressure and were treated with adrenaline. There was no fatal outcome. The systemic side-effects during the dose-increase phase of venom immunotherapy occurred at a median dose of 46 microg (range 2-100 microg). Large local reactions occurred in 13.9% of patients without any significant difference between the allergens.

CONCLUSIONS

We have shown that systemic reactions are not rare even during maintenance phase in patients with a well tolerated dose-increase phase of treatment. The most prominent risk factor for systemic reactions was immunotherapy with honeybee extract.

摘要

背景

尽管免疫疗法在过敏性鼻炎、结膜炎、哮喘和蜂蜇过敏反应中有效,但它存在过敏反应的风险。

方法

在一项为期4年的回顾性调查中,我们调查了1257例接受毒液或吸入性变应原皮下免疫疗法的成年患者。剂量增加阶段采用毒液免疫疗法的2天快速方案和吸入性变应原免疫疗法的6周方案。

结果

共有904例患者接受毒液免疫疗法,353例患者接受吸入性变应原免疫疗法。全身反应的发生率为13.6%。维持阶段全身反应的频率高于剂量增加阶段(9.6%对5.9%),且在蜂毒治疗的两个阶段中均最高(P<0.001)。大多数全身反应为轻度。5例(0.4%)患者出现血压下降反应并接受肾上腺素治疗。无死亡病例。毒液免疫疗法剂量增加阶段的全身副作用发生时的中位剂量为46微克(范围2-100微克)。13.9%的患者出现严重局部反应,不同变应原之间无显著差异。

结论

我们已经表明,即使在治疗剂量增加阶段耐受性良好的患者的维持阶段,全身反应也并不罕见。全身反应最突出的危险因素是蜜蜂提取物免疫疗法。

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