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Multicenter Study
Phase II of the International Study of Asthma and Allergies in Childhood (ISAAC II): rationale and methods.
- S K Weiland, B Björkstén, B Brunekreef, W O C Cookson, E von Mutius, D P Strachan, and International Study of Asthma and Allergies in Childhood Phase II Study Group.
- Dept of Epidemiology, University of Ulm, Helmholzstr. 22, 89081, Ulm, Germany. stephan.weiland@medizin.uni-ulm.de
- Eur. Respir. J. 2004 Sep 1; 24 (3): 406-12.
AbstractInternational comparative studies, investigating whether disease incidence or prevalence rates differ between populations and, if so, which factors explain the observed differences, have made important contributions to the understanding of disease aetiology in many areas. In Phase I of the International Study of Asthma and Allergies in Childhood (ISAAC), the prevalence rates of symptoms of asthma, allergic rhinitis and atopic eczema in 13-14-yr-olds, assessed by standardised questionnaires, were found to differ >20-fold between the 155 study centres around the world. Phase II of ISAAC aims to identify determinants of these differences by studying informative populations. A detailed study protocol was developed for use in community-based random samples of children aged 9-11 yrs. The study modules include standardised questionnaires with detailed questions on the occurrence and severity of symptoms of asthma, allergic rhinitis and atopic eczema, their clinical management, and a broad range of previous and current exposure conditions. In addition, standardised protocols were applied for examination of flexural dermatitis, skin-prick testing, bronchial challenge with hypertonic saline, blood sampling for immunoglobulin E analyses and genotyping, and dust sampling for assessment of indoor exposures to allergens and endotoxin. To date, ISAAC II field work had been completed or started in 30 study centres in 22 countries. The majority of centres are in countries that participated in International Study of Asthma and Allergies in Childhood Phase I and reflect almost the full range of the observed variability in Phase I prevalence rates.
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