Primary Immunodeficiency Diseases in Aguascalientes, Mexico: Results from an Educational Program.
J Clin Immunol
; 36(3): 173-8, 2016 Apr.
Article
em En
| MEDLINE
| ID: mdl-26898367
ABSTRACT
PURPOSE:
Primary immunodeficiencies (PIDs) are a heterogeneous group of disorders characterized mainly by recurrent infections. Late diagnosis remains as one of the main issues to solve. We aimed to increase PID diagnosis in Aguascalientes, a 1.3 million inhabitants state in the center of Mexico, and to describe the clinical features of such patients.METHODS:
We developed an educational program for health personnel and general public; patients with possible PID were referred to a State University clinical center from December 2011 to December 2012. The patients were evaluated at the clinic and their definitive diagnosis pursued through laboratory, molecular and genetic assays. We describe the findings of those patients and analyze the impact of the program in terms of number of referrals.RESULTS:
After 41 talks and 12 media appearances 151 patients were referred for evaluation. Fifteen (9.9%) were diagnosed with PID five (33%) had antibody deficiencies, seven (47%) Well-defined syndromes, two (13%) Severe combined Immunodeficiency (SCID) and one case (7%) of an innate immune deficiency. All of the 15 PID patients had been referred by physicians, as opposed to the public. We estimated a "number needed to teach" of 75 physicians to get one PID patient referral.CONCLUSION:
Educational programs are a fundamental part of the global efforts to increase PID diagnosis and care. To be successful, such programs should include public relations, reach for first-contact physicians, and aim to develop an efficient referral network with molecular diagnostic capability. Enhancing medical knowledge on PID is a successful strategy to improve early diagnosis and treatment.Palavras-chave
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Base de dados:
MEDLINE
Assunto principal:
Sistema de Registros
/
Conhecimentos, Atitudes e Prática em Saúde
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Síndromes de Imunodeficiência
Idioma:
En
Ano de publicação:
2016
Tipo de documento:
Article