Table 3.
Incidence of cross sensitivity to NSAIDs among patients with aspirin induced asthma
Trial | Study design | Age (years) | Study population | Authors' definition of positive response | Maximum challenge dose (mg) | Subjects tested | Positive outcome | Incidence (%) | Sensitivity previously proved by challenge |
---|---|---|---|---|---|---|---|---|---|
Ibuprofen: | |||||||||
Chafee and Settipane 197428 | Double blind, placebo controlled | 16-60 | Allergy and clinical immunology department | Reduction in peak expiratory flow > 15% (positive reactions ranged from 19-68%) | 300 | 18 | 18 | 100 | Yes |
Szczeklik et al 19771 | Double blind, placebo controlled | 16-68 | Allergy and clinical immunology department | Reduction in peak expiratory flow 16-25% and clinical symptoms of bronchial obstruction or reduction in in peak expiratory flow > 25% with no symptoms | 400 | 31 | 30 | 97 | Yes |
Total (95% CI)* | — | Not available | — | — | Not available | — | — | 98 (90 to 100)† | — |
Naproxen: | |||||||||
Szczeklik et al 10771 | Double blind, placebo controlled | 16-68 | Allergy and clinical immunology department | Reduction in peak expiratory flow 16-25% and clinical symptoms of bronchial obstruction or reduction in peak expiratory flow > 25% with no symptoms | 100 | 11 | 11 | 100 | Yes |
Falliers 197329 | Double blind, placebo controlled | Mean 39 | Allergy and clinical immunology department | Reduction in peak expiratory flow > 20% up to four hours after dose | 80 | 11 | 11 | 100 | Yes |
Total (95% CI)* | — | — | — | — | Not available | — | — | 100 (83 to 100)† | — |
Diclofenac: | |||||||||
Szczeklik et al 19771 | Double blind, placebo controlled | 16-68 | Allergy and clinical immunology department | Reduction in peak expiratory flow 16-25% and clinical symptoms of bronchial obstruction or reduction in peak expiratory flow > 25% with no symptoms | 40 | 14 | 12 | 86 | Yes |
Falliers 197329 | Double blind, placebo controlled | Mean 39 | Allergy and clinical immunology department | Reduction in peak expiratory flow > 20% up to four hours after dose | 25 | 11 | 11 | 100 | Yes |
Total (95% CI)* | — | Not available | — | — | Not available | — | — | 93 (76 to 100)† | — |
Calculated from pooling incidence rate in individual studies.
Upper bound truncated at 100.