Literature DB >> 20357490

Change in referral diagnoses and diagnostic delay in hypogammaglobulinaemic patients during 28 years in a single referral centre.

Jiri Litzman1, Dagmar Stikarovska, Zdenka Pikulova, Tomas Pavlik, Sava Pesak, Vojtech Thon, Pavel Kuklinek, Jindrich Lokaj.   

Abstract

BACKGROUND: The classical clinical manifestation of untreated immunoglobulin deficiency comprises predominantly recurrent and complicated respiratory tract infections. Before the 1980s, little was known about the clinical manifestation of immunodeficiency in the general medical population, and also the availability of serum immunoglobulin laboratory determination was not sufficient, leading to a significant diagnostic delay.
METHODS: We have analysed the diagnostic delay and referral diagnoses in patients in whom any form of primary hypogammaglobulinaemia had been diagnosed at our department, which was established in 1981.
RESULTS: Comparing the diagnostic delay in the 1980s (19 patients, median 5.5 years), the 1990s (37 patients, median 3.5 years) and the years 2001-2008 (33 patients, median 1 year), a significant decrease was observed (p < 0.05, Spearman's correlation coefficient). Also, the median number of pneumonia episodes during the diagnostic delay decreased from 5 in the 1980s, to 1 in the 1990s and to 0 in the period of 2001-2008 (p < 0.05, Spearman's correlation coefficient). While in the 1980s 17 of the 19 patients had pneumonia in their past history, in the period of 2001-2008 only 13 of the 33 patients were concerned.
CONCLUSIONS: Our observation documents improved awareness of immunodeficiencies among physicians. It is supposed that earlier diagnosis will prevent complications, improve the quality of life and even survival of hypogammaglobulinaemic patients. Copyright (c) 2010 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2010        PMID: 20357490     DOI: 10.1159/000301584

Source DB:  PubMed          Journal:  Int Arch Allergy Immunol        ISSN: 1018-2438            Impact factor:   2.749


  4 in total

1.  Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry.

Authors:  Asghar Aghamohammadi; Payam Mohammadinejad; Hassan Abolhassani; Babak Mirminachi; Masoud Movahedi; Mohammad Gharagozlou; Nima Parvaneh; Vaheid Zeiaee; Bahram Mirsaeed-Ghazi; Zahra Chavoushzadeh; Alireza Mahdaviani; Mahboubeh Mansouri; Sedigheh Yousefzadegan; Bahareh Sharifi; Fariborz Zandieh; Ehsan Hedayat; Ali Nadjafi; Roya Sherkat; Behzad Shakerian; Mahnaz Sadeghi-Shabestari; Reza Farid Hosseini; Farahzad Jabbari-Azad; Hamid Ahanchian; Fatemeh Behmanesh; Mohammadreza Zandkarimi; Afshin Shirkani; Taher Cheraghi; Abbas Fayezi; Iraj Mohammadzadeh; Reza Amin; Soheila Aleyasin; Mojgan Moghtaderi; Javad Ghaffari; Saba Arshi; Naser Javahertrash; Mohammad Nabavi; Mohammad Hassan Bemanian; Alireza Shafiei; Najmedin Kalantari; Akefeh Ahmadiafshar; Hossein Ali Khazaei; Lida Atarod; Nima Rezaei
Journal:  J Clin Immunol       Date:  2014-05       Impact factor: 8.317

2.  B-lymphocyte subpopulations in patients with selective IgA deficiency.

Authors:  Jana Nechvatalova; Zdenka Pikulova; Dagmar Stikarovska; Sava Pesak; Marcela Vlkova; Jiri Litzman
Journal:  J Clin Immunol       Date:  2012-02-12       Impact factor: 8.317

3.  Common variable immune deficiency in children--clinical characteristics varies depending on defect in peripheral B cell maturation.

Authors:  Barbara Piątosa; Małgorzata Pac; Katarzyna Siewiera; Barbara Pietrucha; Maja Klaudel-Dreszler; Edyta Heropolitańska-Pliszka; Beata Wolska-Kuśnierz; Hanna Dmeńska; Hanna Gregorek; Irena Sokolnicka; Aneta Rękawek; Katarzyna Tkaczyk; Ewa Bernatowska
Journal:  J Clin Immunol       Date:  2013-02-07       Impact factor: 8.317

4.  Family Physician Perspectives on Primary Immunodeficiency Diseases.

Authors:  Jordan S Orange; Filiz O Seeborg; Marcia Boyle; Christopher Scalchunes; Vivian Hernandez-Trujillo
Journal:  Front Med (Lausanne)       Date:  2016-03-30
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.