Literature DB >> 11567202

[Diagnostic management of patients with rare genetic diseases: example of five pathologies].

V Godet1, I Hirtzlin, N Costet.   

Abstract

BACKGROUND: Orphan diseases are serious and unknown chronic diseases, for which a rapid diagnosis may provide a better access to healthcare. The aim of this study was to describe the procedures of diagnosis for patients with such ailments.
METHODS: Self-administered questionnaires describing patient's behavior, medical examinations until the final diagnosis, as well as received medical care and financial support, were directly sent to the patients through patient associations and special examinations dedicated to rare diseases.
RESULTS: 532 patients were included, suffering from 5 different diseases. Although the average delay between the appearance of symptoms and diagnosis is 2 years and 8 months, this hides great disparities (from 0 to 40 years) and half of the patients were diagnosed within 4 months. The study shows that the diagnosis management is influenced by the illness and its symptoms as well as by the characteristics of the first medical examination.
CONCLUSIONS: The diagnosis management of patients with rare diseases is strongly determined by personnel initiatives or exceptional opportunities, rather than by a real organisational strategy of the healthcare system.

Entities:  

Mesh:

Year:  2001        PMID: 11567202

Source DB:  PubMed          Journal:  Rev Epidemiol Sante Publique        ISSN: 0398-7620            Impact factor:   1.019


  1 in total

1.  What, if anything, is specific about having a rare disorder? Patients' judgements on being ill and being rare.

Authors:  Caroline Huyard
Journal:  Health Expect       Date:  2009-10-14       Impact factor: 3.377

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.