Comparison of American and European practices in the management of patients with primary immunodeficiencies

Summary Primary immunodeficiency diseases (PIDs) comprise a heterogeneous group of rare disorders. This study was devised in order to compare management of these diseases in the northern hemisphere, given the variability of practice among clinicians in North America. The members of two international...

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Veröffentlicht in:Clinical and experimental immunology 2012-07, Vol.169 (1), p.57-69
Hauptverfasser: Hernandez‐Trujillo, H. S., Chapel, H., Lo Re III, V., Notarangelo, L. D., Gathmann, B., Grimbacher, B., Boyle, J. M., Hernandez‐Trujillo, V. P., Scalchunes, C., Boyle, M. L., Orange, J. S.
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Sprache:eng
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Zusammenfassung:Summary Primary immunodeficiency diseases (PIDs) comprise a heterogeneous group of rare disorders. This study was devised in order to compare management of these diseases in the northern hemisphere, given the variability of practice among clinicians in North America. The members of two international societies for clinical immunologists were asked about their management protocols in relation to their PID practice. An anonymous internet questionnaire, used previously for a survey of the American Academy of Allergy, Asthma and Immunology (AAAAI), was offered to all full members of the European Society for Immunodeficiency (ESID). The replies were analysed in three groups, according to the proportion of PID patients in the practice of each respondent; this resulted in two groups from North America and one from Europe. The 123 responses from ESID members (23·7%) were, in the majority, very similar to those of AAAAI respondents, with > 10% of their practice devoted to primary immunodeficiency. There were major differences between the responses of these two groups and those of the general AAAAI respondents whose clinical practice was composed of
ISSN:0009-9104
1365-2249
DOI:10.1111/j.1365-2249.2012.04588.x