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Primary Immunodeficiency Diseases at Reference and High-Specialty Hospitals in the State of Guanajuato, Mexico

Background. In general, primary immunodeficiency diseases (PIDs) are underdiagnosed in most countries. The objective of this study was to describe the frequency and clinical spectrum of PID in the most important tertiary hospitals in our region. Methods. An observational, cross-sectional, with retro...

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Autores principales: Guaní-Guerra, Eduardo, García-Ramírez, Ulises Noel, Jiménez-Romero, Ana Isabel, Velázquez-Ávalos, José Manuel, Gallardo-Martínez, Gabriela, Mendoza-Espinoza, Francisco-Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3773974/
https://www.ncbi.nlm.nih.gov/pubmed/24073395
http://dx.doi.org/10.1155/2013/187254
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author Guaní-Guerra, Eduardo
García-Ramírez, Ulises Noel
Jiménez-Romero, Ana Isabel
Velázquez-Ávalos, José Manuel
Gallardo-Martínez, Gabriela
Mendoza-Espinoza, Francisco-Javier
author_facet Guaní-Guerra, Eduardo
García-Ramírez, Ulises Noel
Jiménez-Romero, Ana Isabel
Velázquez-Ávalos, José Manuel
Gallardo-Martínez, Gabriela
Mendoza-Espinoza, Francisco-Javier
author_sort Guaní-Guerra, Eduardo
collection PubMed
description Background. In general, primary immunodeficiency diseases (PIDs) are underdiagnosed in most countries. The objective of this study was to describe the frequency and clinical spectrum of PID in the most important tertiary hospitals in our region. Methods. An observational, cross-sectional, with retrospective chart, review study was conducted. A total of 26 patients were included and grouped according to the updated classification of PIDs. Results. PIDs spectra were as follows: predominantly antibody deficiency diseases were the most common category (65.38%), followed by other well-defined immunodeficiency syndromes (11.55%), congenital defects of phagocyte number and/or function (7.69%), complement deficiencies (3.85%), combined T- and B-cell immunodeficiencies (3.85%), and defects in innate immunity (3.85%). The mean time elapsed from the onset of symptoms to the reference and diagnosis by a tertiary hospital was of 4.65 ± 6.95 years. Conclusions. Predominant antibody deficiency disease was the most common group of PIDs, agreeing with international reports. Awareness of underdiagnosis by physicians is crucial for a prompt diagnosis and treatment, which in turn should improve the quality of life among patients with PIDs.
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spelling pubmed-37739742013-09-26 Primary Immunodeficiency Diseases at Reference and High-Specialty Hospitals in the State of Guanajuato, Mexico Guaní-Guerra, Eduardo García-Ramírez, Ulises Noel Jiménez-Romero, Ana Isabel Velázquez-Ávalos, José Manuel Gallardo-Martínez, Gabriela Mendoza-Espinoza, Francisco-Javier Biomed Res Int Clinical Study Background. In general, primary immunodeficiency diseases (PIDs) are underdiagnosed in most countries. The objective of this study was to describe the frequency and clinical spectrum of PID in the most important tertiary hospitals in our region. Methods. An observational, cross-sectional, with retrospective chart, review study was conducted. A total of 26 patients were included and grouped according to the updated classification of PIDs. Results. PIDs spectra were as follows: predominantly antibody deficiency diseases were the most common category (65.38%), followed by other well-defined immunodeficiency syndromes (11.55%), congenital defects of phagocyte number and/or function (7.69%), complement deficiencies (3.85%), combined T- and B-cell immunodeficiencies (3.85%), and defects in innate immunity (3.85%). The mean time elapsed from the onset of symptoms to the reference and diagnosis by a tertiary hospital was of 4.65 ± 6.95 years. Conclusions. Predominant antibody deficiency disease was the most common group of PIDs, agreeing with international reports. Awareness of underdiagnosis by physicians is crucial for a prompt diagnosis and treatment, which in turn should improve the quality of life among patients with PIDs. Hindawi Publishing Corporation 2013 2013-09-01 /pmc/articles/PMC3773974/ /pubmed/24073395 http://dx.doi.org/10.1155/2013/187254 Text en Copyright © 2013 Eduardo Guaní-Guerra et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Guaní-Guerra, Eduardo
García-Ramírez, Ulises Noel
Jiménez-Romero, Ana Isabel
Velázquez-Ávalos, José Manuel
Gallardo-Martínez, Gabriela
Mendoza-Espinoza, Francisco-Javier
Primary Immunodeficiency Diseases at Reference and High-Specialty Hospitals in the State of Guanajuato, Mexico
title Primary Immunodeficiency Diseases at Reference and High-Specialty Hospitals in the State of Guanajuato, Mexico
title_full Primary Immunodeficiency Diseases at Reference and High-Specialty Hospitals in the State of Guanajuato, Mexico
title_fullStr Primary Immunodeficiency Diseases at Reference and High-Specialty Hospitals in the State of Guanajuato, Mexico
title_full_unstemmed Primary Immunodeficiency Diseases at Reference and High-Specialty Hospitals in the State of Guanajuato, Mexico
title_short Primary Immunodeficiency Diseases at Reference and High-Specialty Hospitals in the State of Guanajuato, Mexico
title_sort primary immunodeficiency diseases at reference and high-specialty hospitals in the state of guanajuato, mexico
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3773974/
https://www.ncbi.nlm.nih.gov/pubmed/24073395
http://dx.doi.org/10.1155/2013/187254
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