The Effects of Long-Term Treatment by Immunotherapy and Fluticazone on Broncial Hyperreactivity

Author:

Ilonidis G.1,Anogianakis G.2,Trakatelli Chr.3,Anogeianaki A.2,Giavazis J.1,Trakatellis M.4,Michalis I.1

Affiliation:

1. Fourth Department of Medicine, Pneumology - Allergology Laboratory, Faculty of Medicine, Aristotle University of Thessaloniki, Hippokratio Hospital, Greece

2. Laboratory of Experimental Physiology, Faculty of Medicine, Aristotle University of Thessaloniki, Greece

3. Department of Internal Medicine, Georgios Gennimatas Hospital, Thessaloniki, Greece

4. Department of Biochemistry, Faculty of Medicine, Aristotle University of Thessaloniki, Greece

Abstract

Thirty subjects (20 female and 10 male), all allergic to the mites D. Pteronyssinus and D. Farinae, participated in the present study which covered a period of four years. The subjects were randomly divided in two groups. Group I included 10 female and 5 male subjects, with an average age of 25.8 (+/− 3.5) years who received immunotherapy only. Group II had an average age of 31.5 (+/− 4) years and they received immunotherapy along with fluticazone propionate (1000mcg/day). The protocol for immunotherapy was the same for both groups. The basis FEV1 was determined for each subject of both Groups I and II and afterwards they were subjected to provocation tests of nebulized methacholine solution administered in consecutively larger concentrations until a drop in FEV1 >20 % (PC20), was observed. Three years later, when their therapy was completed, all subjects were subjected to the same provocation test and a significant reduction in bronchial hyperactivity was documented for both groups. In particular, for Group I, the percentage of change in FEV1 values was 27.25 +/- 5.23 % and PC20 5.11 +/− 2.64 mg/ml before immunotherapy, while after immunotherapy the same indicators were 22.22 +/- 7.08 % (P<0.05) and 6.85 +/− 4.03 mg/ml, (P<0.05) respectively. For Group II, the percentage of change in FEV1 values was 26.28 +/− 2.5 % and PC20 5.42 +/− 2.5 mg/ml before immunotherapy, while after immunotherapy the same indicators were 12.27 +/- 2.49 % (P<0.01)and 11.64 +/− 5.14 mg/ml, P<0.01 respectively. It is concluded that although significant reduction in hyperreactivity can be achieved through immunotherapy, the combination of immunotherapy with daily fluticazone propionate administration shows the most promising results.

Publisher

SAGE Publications

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