Rational approach to aspirin dosing during oral challenges and desensitization of patients with aspirin-exacerbated respiratory disease

Background Aspirin desensitization improves clinical outcomes in most patients with aspirin-exacerbated respiratory disease. Most protocols for desensitization are time-consuming. Objective Our objective was to use historical information about the course of aspirin desensitization to enhance the eff...

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Bibliographic Details
Published inJournal of allergy and clinical immunology Vol. 123; no. 2; pp. 406 - 410
Main Authors Hope, Andrew P., MD, Woessner, Katharine A., MD, Simon, Ronald A., MD, Stevenson, Donald D., MD
Format Journal Article
LanguageEnglish
Published New York, NY Mosby, Inc 01.02.2009
Elsevier
Elsevier Limited
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Summary:Background Aspirin desensitization improves clinical outcomes in most patients with aspirin-exacerbated respiratory disease. Most protocols for desensitization are time-consuming. Objective Our objective was to use historical information about the course of aspirin desensitization to enhance the efficiency of the desensitization protocol. Methods Four hundred twenty subjects with suspected aspirin-exacerbated respiratory disease underwent oral aspirin challenges. Their clinical characteristics were analyzed in relation to features of reactions during aspirin challenges. Results Large (FEV1 decrease >30%) and moderate (FEV1 decrease 21% to 30%) bronchial reactions occurred in 9% and 20% of subjects, respectively. Multivariate analysis identified risk factors associated with these larger reactions, including lack of leukotriene modifier use, baseline FEV1 of less than 80% of predicted value, and previous asthma-related emergency department visits. Seventy-five percent of patients reacted to a provoking dose of either 45 or 60 mg. Only 3% of initial reactions occurred after 150- or 325-mg provoking doses, and none occurred after the 650-mg dose. Conclusions Most bronchial and naso-ocular reactions during oral aspirin challenges occurred within a narrow dosing range (45-100 mg). Only 1 of 26 patients without risk factors had a moderate reaction.
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ISSN:0091-6749
1097-6825
DOI:10.1016/j.jaci.2008.09.048