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Wiley InterScience | |||||||||
![]() Clinical & Experimental AllergyVolume 34 Issue 4, Pages 650 - 653 Published Online: 1 Mar 2004 © 2010 Blackwell Publishing Ltd The Official Journal of the British Society for Allergy & Clinical Immunology
Abstract | References | Full Text: HTML, PDF (Size: 127K) | Related Articles | Citation Tracking Comparative effects of desloratadine, fexofenadine, and levocetirizine on nasal adenosine monophosphate challenge in patients with perennial allergic rhinitis Copyright © 2004 Blackwell Publishing Ltd KEYWORDS adenosine monophosphate • desloratadine • fexofenadine • H Summary
Background
There are no data directly comparing the relative efficacy of modern H Objective We elected to study the comparative effectiveness of usual clinically recommended doses of desloratadine (DES), fexofenadine (FEX), and levocetirizine (LEV), on nasal adenosine monophosphate (AMP) challenge in patients with perennial allergic rhinitis (PAR). Methods 16 patients with PAR were randomized in double-blind cross-over fashion to receive single doses of DES 5 mg, FEX 180 mg, LEV 5 mg, or placebo (PL), with nasal AMP challenge performed 12 h after dosing. Measurements of peak nasal inspiratory flow (PNIF) were made over 60 min after nasal AMP challenge. Results
Pre-challenge values (mean±SEM) for PNIF (L/min) were not significantly different comparing all groups; DES (129±9), FEX (128±11), LEV (128±13), and PL (128±12). The maximum % PNIF fall from baseline over 60 min after nasal AMP challenge was significantly attenuated (P<0.05) compared to PL (50±4), with DES (32±5), FEX (36±4), and LEV (36±4). The area under the 60-min time–response curve (%.min) was also significantly attenuated (P<0.05) compared to PL (2110±268), with DES (1126±285), FEX (1225±255), and LEV (1261±194). There were no significant differences between the three H Conclusion DES, FEX, and LEV were equally effective in attenuating the response to nasal AMP challenge. However, further long-term studies will be required to study their comparative effects on nasal symptoms, quality of life, as well as on nasal inflammatory cells. Submitted 10 July 2003; revised 20 September 2003; accepted 28 November 2003 |