Adamic Katja, Zidarn Mihaela, Bajrovic Nissera, Erzen Renato, Kopac Peter, Music Ema
University Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.
Wien Klin Wochenschr. 2009;121(9-10):357-60. doi: 10.1007/s00508-009-1172-0.
Although immunotherapy is effective in allergic rhinitis, conjunctivitis, asthma and stinging insect hypersensitivity, it carries a risk of anaphylactic reactions.
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.
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.
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.
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。
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。
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。
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。