Literature DB >> 22076953

The association of illness perceptions with physical and mental health in systemic sclerosis patients: an exploratory study.

Seher Arat1, Patrick Verschueren, Ellen De Langhe, Vanessa Smith, Marie Vanthuyne, Luwis Diya, Koen Van den Heede, Daniel Blockmans, Filip De Keyser, Frédéric A Houssiau, René Westhovens.   

Abstract

OBJECTIVE: The aim of the present study was to evaluate the association between illness perceptions and the ability to cope with physical and mental health problems in a large cohort of systemic sclerosis (SSc) patients.
METHODS: This was a cross-sectional study in 217 systemic sclerosis patients from the Belgian Systemic Sclerosis Cohort. Illness perception and coping were measured by the Revised Illness Perception Questionnaire and a coping questionnaire--the Coping Orientation of Problem Experience inventory (COPE). Physical and mental health-related quality of life was measured by the 36-item short-form health survey (SF-36), as were disease activity and several severity parameters. The relationship between illness perceptions and the ability to cope with physical/mental health problems was examined using multiple linear regression analysis.
RESULTS: According to LeRoy's classification, 49 patients had limited SSc (lSSc), 129 had limited cutaneous SSc (lcSSc) and 39 had diffuse cutaneous SSc (dcSSc). Median disease duration was five years and the modified Rodnan skin score was 4. Good physical health was significantly associated with the lcSSc subtype and low disease activity (p < 0.01 and p < 0.05, respectively). The perception of 'serious consequences' and strong 'illness identity' correlated with poor physical health (p < 0.001). Good mental health was associated with low illness identity scores and low 'emotional response' scores (p < 0.001). Coping variables were less significantly correlated with physical and mental health compared with the illness perception items.
CONCLUSION: Illness representations contribute more than classical disease characteristics to physical and mental health.
Copyright © 2011 John Wiley & Sons, Ltd.

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Mesh:

Year:  2011        PMID: 22076953     DOI: 10.1002/msc.223

Source DB:  PubMed          Journal:  Musculoskeletal Care        ISSN: 1478-2189


  10 in total

1.  Associations between illness duration and health-related quality of life in specified mental and physical chronic health conditions: results from a population-based survey.

Authors:  Lucy Busija; Jeretine Tan; Kerrie M Sanders
Journal:  Qual Life Res       Date:  2017-05-12       Impact factor: 4.147

2.  Quality of life in SSc-ILD patients: Understanding the impact of the ILD and the needs of the SSc-ILD patients and their need for caregivers in France.

Authors:  Yannick Allanore; Joel Constans; Dominique Godard; Gerard de Pouvourville; Stephane Bouee; Viviane Jeanbat; Clement Teissier; Katell Le Lay; Julien Chollet; Eric Hachulla
Journal:  J Scleroderma Relat Disord       Date:  2021-06-21

3.  Health-related quality of life in patients with systemic sclerosis: evolution over time and main determinants.

Authors:  Nina M van Leeuwen; Jacopo Ciaffi; Sophie I E Liem; Tom W J Huizinga; Jeska K de Vries-Bouwstra
Journal:  Rheumatology (Oxford)       Date:  2021-08-02       Impact factor: 7.580

4.  Psychiatric symptoms and quality of life in systemic sclerosis.

Authors:  G Mura; Krishna M Bhat; A Pisano; G Licci; Mg Carta
Journal:  Clin Pract Epidemiol Ment Health       Date:  2012-04-20

5.  Illness representations of systemic lupus erythematosus and systemic sclerosis: a comparison of patients, their rheumatologists and their general practitioners.

Authors:  Seher Arat; Jan L Lenaerts; Ellen De Langhe; Patrick Verschueren; Philip Moons; Joris Vandenberghe; Veerle Taelman; Rene Westhovens
Journal:  Lupus Sci Med       Date:  2017-11-14

6.  Patients' views and needs about systemic sclerosis and its management: a qualitative interview study.

Authors:  Luc Mouthon; Sophie Alami; Anne-Sophie Boisard; Benjamin Chaigne; Eric Hachulla; Serge Poiraudeau
Journal:  BMC Musculoskelet Disord       Date:  2017-05-30       Impact factor: 2.362

7.  Illness perceptions, risk perceptions and worries in patients with early systemic sclerosis: A focus group study.

Authors:  Nina M van Leeuwen; Maaike Boonstra; Tom W J Huizinga; Ad A Kaptein; Jeska K de Vries-Bouwstra
Journal:  Musculoskeletal Care       Date:  2020-01-26

8.  Prospective associations between illness perceptions and health outcomes in patients with systemic sclerosis and systemic lupus erythematosus: a cross-lagged analysis.

Authors:  Seher Arat; Jessica Rassart; Philip Moons; Koen Luyckx; Joris Vandenberghe; René Westhovens
Journal:  Rheumatol Adv Pract       Date:  2018-03-06

9.  Quality of life as measured by the short-form 36 (SF-36) questionnaire in patients with early systemic sclerosis and undifferentiated connective tissue disease.

Authors:  Michele Iudici; Giovanna Cuomo; Serena Vettori; Manuela Avellino; Gabriele Valentini
Journal:  Health Qual Life Outcomes       Date:  2013-02-25       Impact factor: 3.186

10.  Development and preliminary evaluation of the validity and reliability of a revised illness perception questionnaire for healthcare professionals.

Authors:  Seher Arat; Anke Van den Zegel; Maity Van Rillaer; Philip Moons; Joris Vandenberghe; Ellen De Langhe; René Westhovens
Journal:  BMC Nurs       Date:  2016-06-01
  10 in total

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