Literature DB >> 31732910

Quality of life in primary care patients with moderate medically unexplained physical symptoms.

P E van Westrienen1,2,3, M F Pisters4,5,6, S A J Toonders4,5,6, M Gerrits7, N J de Wit7, C Veenhof5,6,8.   

Abstract

PURPOSE: Medically Unexplained Physical Symptoms (MUPS) have a large impact on patient's quality of life. Most studies have been limited to chronic MUPS and thus, little is known about moderate MUPS. Improved knowledge concerning determinants influencing quality of life in moderate MUPS patients can be helpful in managing MUPS. This study is aimed at describing the common characteristics seen in moderate MUPS patients and compare them with characteristics seen in chronic MUPS patients and general population. We also identified determinants of the physical and mental components of quality of life in moderate MUPS patients.
METHODS: In a cross-sectional study, moderate MUPS patients (n = 160) were compared with chronic MUPS patients (n = 162) and general population (n = 1742) based on demographic characteristics and patient's quality of life. Multivariable linear regression analyses were performed to identify determinants associated with a patient's quality of life, assessed with the RAND-36.
RESULTS: Moderate MUPS patients experienced a better quality of life than chronic MUPS patients, but a worse quality of life as compared to the general population. Determinants associated with the physical and mental components of quality of life explain 49.1% and 62.9% of the variance, respectively.
CONCLUSION: Quality of life of patients with MUPS varies with MUPS disease stage. Based on their quality of life scores, moderate MUPS patients would be adequately distinguished from chronic MUPS patients. Half of the variance in the physical component and almost two thirds of the mental component would be explained by a number of MUPS-related symptoms and perceptions.

Entities:  

Keywords:  Medically Unexplained Physical Symptoms; Primary care; Quality of life; SF-36

Mesh:

Year:  2019        PMID: 31732910     DOI: 10.1007/s11136-019-02358-8

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  49 in total

1.  Association of different levels of depressive symptoms with symptomatology, overall disease severity, and quality of life in women with fibromyalgia.

Authors:  Alberto Soriano-Maldonado; Kirstine Amris; Francisco B Ortega; Víctor Segura-Jiménez; Fernando Estévez-López; Inmaculada C Álvarez-Gallardo; Virginia A Aparicio; Manuel Delgado-Fernández; Marius Henriksen; Jonatan R Ruiz
Journal:  Qual Life Res       Date:  2015-06-14       Impact factor: 4.147

2.  Somatization increases medical utilization and costs independent of psychiatric and medical comorbidity.

Authors:  Arthur J Barsky; E John Orav; David W Bates
Journal:  Arch Gen Psychiatry       Date:  2005-08

3.  The association of socioeconomic status and symptom severity in persons with fibromyalgia.

Authors:  Mary-Ann Fitzcharles; Emmanouil Rampakakis; Peter A Ste-Marie; John S Sampalis; Yoram Shir
Journal:  J Rheumatol       Date:  2014-06-15       Impact factor: 4.666

4.  Outcome in general medical patients presenting with common symptoms: a prospective study with a 2-week and a 3-month follow-up.

Authors:  K Kroenke; J L Jackson
Journal:  Fam Pract       Date:  1998-10       Impact factor: 2.267

5.  Do patients with unexplained physical symptoms pressurise general practitioners for somatic treatment? A qualitative study.

Authors:  Adele Ring; Christopher Dowrick; Gerry Humphris; Peter Salmon
Journal:  BMJ       Date:  2004-03-31

Review 6.  Exercise for treating fibromyalgia syndrome.

Authors:  A J Busch; K A R Barber; T J Overend; P M J Peloso; C L Schachter
Journal:  Cochrane Database Syst Rev       Date:  2007-10-17

7.  Illness perceptions in patients with fibromyalgia and their relationship to quality of life and catastrophizing.

Authors:  C Paul van Wilgen; Miriam W van Ittersum; Ad A Kaptein; Marten van Wijhe
Journal:  Arthritis Rheum       Date:  2008-11

Review 8.  The health status burden of people with fibromyalgia: a review of studies that assessed health status with the SF-36 or the SF-12.

Authors:  D L Hoffman; E M Dukes
Journal:  Int J Clin Pract       Date:  2007-11-24       Impact factor: 2.503

9.  Determinants of quality of life in patients with fibromyalgia: A structural equation modeling approach.

Authors:  Jeong-Won Lee; Kyung-Eun Lee; Dong-Jin Park; Seong-Ho Kim; Seong-Su Nah; Ji Hyun Lee; Seong-Kyu Kim; Yeon-Ah Lee; Seung-Jae Hong; Hyun-Sook Kim; Hye-Soon Lee; Hyoun Ah Kim; Chung-Il Joung; Sang-Hyon Kim; Shin-Seok Lee
Journal:  PLoS One       Date:  2017-02-03       Impact factor: 3.240

10.  Patients with persistent medically unexplained symptoms in general practice: characteristics and quality of care.

Authors:  Anja J E Dirkzwager; Peter F M Verhaak
Journal:  BMC Fam Pract       Date:  2007-05-31       Impact factor: 2.497

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