Literature DB >> 16457060

[Clinical and psychosocial characteristics of subjects with fibromyalgia. Impact of the diagnosis on patients' activities].

Maria del Carmen Ubago Linares1, Isabel Ruiz Pérez, Maria José Bermejo Pérez, Antonio Olry de Labry Lima, Juncal Plazaola Castaño.   

Abstract

BACKGROUND: Little is known today about the characteristics of individuals diagnosed with fibromyalgia, their degree of disability and the health system response system response to this condition. The objectives of this work include: to establish the sociodemographic, clinical and psychosocial profile of male and female patients with fibromyalgia. To describe the response they receive from the health service, and to study the repercussions of this syndrome on the daily activities of subjects who suffer it, including its effects on their work environment.
METHODS: Descriptive cross-sectional study. The information was received from telephone interviews of individuals diagnosed with fibromyalgia in the Hospital Universitario Virgen de las Nieves in Granada during 2003.
RESULTS: 92.1% of those interviewed were women. Fibromyalgia caused work absenteeism in 31.4% of cases; and 64% regarded their health as poor or very poor. Fibromyalgia was associated with other diseases in 52.3% of cases. The family doctor is the specialist consulted before diagnosis in 92.1% of cases. A total of 50.5% had a history of psychiatric disorders, these were still present at the time of interview in 36.4%. Around 71% of the sample received family support, and 70.1% of cases considered the disease to seriously affect their environment.
CONCLUSIONS: Fibromyalgia was mainly diagnosed in women. Subjects with this syndrome have a poor perception of their own health and work situation, and it negatively affects their family environment.

Entities:  

Mesh:

Year:  2005        PMID: 16457060     DOI: 10.1590/s1135-57272005000600008

Source DB:  PubMed          Journal:  Rev Esp Salud Publica        ISSN: 1135-5727


  5 in total

1.  [Fibromyalgia: no psychosomatic dialogue, no doctor-psychiatrist dialogue].

Authors:  José Miguel Ribé Buitrón
Journal:  Aten Primaria       Date:  2010-06-08       Impact factor: 1.137

2.  Analysis of the impact of fibromyalgia on quality of life: associated factors.

Authors:  Ma Del Carmen Ubago Linares; Isabel Ruiz-Pérez; Ma José Bermejo Pérez; Antonio Olry de Labry-Lima; Elisa Hernández-Torres; Juncal Plazaola-Castaño
Journal:  Clin Rheumatol       Date:  2007-10-02       Impact factor: 2.980

3.  Work, family and social environment in patients with Fibromyalgia in Spain: an epidemiological study: EPIFFAC study.

Authors:  Antonio Collado; Emili Gomez; Rosa Coscolla; Ruth Sunyol; Emília Solé; Javier Rivera; Emília Altarriba; Jordi Carbonell; Xavier Castells
Journal:  BMC Health Serv Res       Date:  2014-11-11       Impact factor: 2.655

Review 4.  A review of chronic pain impact on patients, their social environment and the health care system.

Authors:  María Dueñas; Begoña Ojeda; Alejandro Salazar; Juan Antonio Mico; Inmaculada Failde
Journal:  J Pain Res       Date:  2016-06-28       Impact factor: 3.133

5.  [Application of an uncertainty model for fibromyalgia].

Authors:  Ángeles Triviño Martínez; M Carmen Solano Ruiz; José Siles González
Journal:  Aten Primaria       Date:  2015-08-12       Impact factor: 1.137

  5 in total

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