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

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

Affiliations

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

Katja Adamic et al. Wien Klin Wochenschr. 2009.

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.

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References

    1. J Allergy Clin Immunol. 1992 Feb;89(2):529-35 - PubMed
    1. Wien Klin Wochenschr. 1989 Oct 13;101(19):639-52 - PubMed
    1. Ann Allergy Asthma Immunol. 2001 Jul;87(1 Suppl 1):47-55 - PubMed
    1. Ann Allergy Asthma Immunol. 2004 Feb;92(2):225-7 - PubMed
    1. Ann Allergy Asthma Immunol. 2007 Jul;99(1):82-6 - PubMed

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