ECTRIMS eLearning

Workplace difficulties, health-related quality of life and perception of stigma in people with multiple sclerosis with low physical disability
Author(s): ,
J.M. García-Domínguez
Affiliations:
Hospital Universitario Gregorio Marañón, Madrid
,
M.L. Martínez-Ginés
Affiliations:
Hospital Universitario Gregorio Marañón, Madrid
,
N. Canal
Affiliations:
IQVIA, Barcelona
,
N. Medrano
Affiliations:
Medical Department, Roche Farma, Madrid, Spain
J. Maurino
Affiliations:
Medical Department, Roche Farma, Madrid, Spain
ECTRIMS Learn. García-Domínguez J. 10/10/18; 229210; EP1371
José M García-Domínguez
José M García-Domínguez
Contributions
Abstract

Abstract: EP1371

Type: Poster Sessions

Abstract Category: Clinical aspects of MS - MS symptoms

Introduction: In multiple sclerosis (MS), unemployment occurs even at levels of disability, which are not typically associated with overt physical impairment.
Objective: To assess the impact of MS in people with low levels of physical disability.
Methods: A multicenter, non-interventional, cross-sectional study in adult subjects with relapsing-remitting MS (RRMS) or primary progressive MS (PPMS) according to McDonald 2010 criteria was conducted. The 23-item Multiple Sclerosis Work Difficulties Questionnaire (MSWDQ-23), 29-item Multiple Sclerosis Impact Scale (MSIS-29), 8-item Stigma Scale for Chronic Illness (SSCI-8), and Beck Depression Inventory-Fast Screen (BDI-FS) were used to assess working performance, health-related quality of life, perception of stigma and depressive mood, respectively.
Results: A total of 199 subjects were studied (mean age: 43.9 ± 10.5 years, 60.8% female, 86.4% with RRMS). Mean time from diagnosis was 9.6 ± 7.2 years, median EDSS score 2.0 (interquartile range: 1.0-3.5). Employment rate was 47.2% (n=94). Mean physical and psychological MSIS-29 impact sub-scores were 40.38 ± 17.1 and 20.24 ± 7.8, respectively. Forty patients (20.2%) had at least one SSCI-8 item on 4 or 5, suggesting presence of stigma “often” or “always”. Eighty-one patients (40.7%) were depressed, 25 (12.6%) had moderate-to-severe depression. Employed people showed less perception of stigma than unemployed (p=0.001). Patients with higher perception of stigma showed higher physical and psychological impact on health-related quality of life (rho=0.61 and 0.55, respectively; p< 0.001) and more difficulties at work (rho=0.60, p< 0.001). Presence of depressive symptoms was related to working status: pensioner or incapacitated patients had more symptoms of depression (p< 0.001). Moreover, severity of depressive symptoms correlated directly with MSWDQ-23 score, indicating work-related problems influence mood status (rho=0.64, p< 0.001).
Conclusion: Work-related problems, stigma and poor quality of life outcomes are common in people with low physical disability. Using MS-specific patient-reported questionnaires may be a useful complementary strategy to detect early symptoms in clinical practice.
Disclosure: This study was funded by the Medical Department of Roche Farma Spain. N.C is an employee of IQVIA Spain. N.M. and J.M. are employees of Roche Farma Spain. The rest of the authors declared no potential conflict of interest.

Abstract: EP1371

Type: Poster Sessions

Abstract Category: Clinical aspects of MS - MS symptoms

Introduction: In multiple sclerosis (MS), unemployment occurs even at levels of disability, which are not typically associated with overt physical impairment.
Objective: To assess the impact of MS in people with low levels of physical disability.
Methods: A multicenter, non-interventional, cross-sectional study in adult subjects with relapsing-remitting MS (RRMS) or primary progressive MS (PPMS) according to McDonald 2010 criteria was conducted. The 23-item Multiple Sclerosis Work Difficulties Questionnaire (MSWDQ-23), 29-item Multiple Sclerosis Impact Scale (MSIS-29), 8-item Stigma Scale for Chronic Illness (SSCI-8), and Beck Depression Inventory-Fast Screen (BDI-FS) were used to assess working performance, health-related quality of life, perception of stigma and depressive mood, respectively.
Results: A total of 199 subjects were studied (mean age: 43.9 ± 10.5 years, 60.8% female, 86.4% with RRMS). Mean time from diagnosis was 9.6 ± 7.2 years, median EDSS score 2.0 (interquartile range: 1.0-3.5). Employment rate was 47.2% (n=94). Mean physical and psychological MSIS-29 impact sub-scores were 40.38 ± 17.1 and 20.24 ± 7.8, respectively. Forty patients (20.2%) had at least one SSCI-8 item on 4 or 5, suggesting presence of stigma “often” or “always”. Eighty-one patients (40.7%) were depressed, 25 (12.6%) had moderate-to-severe depression. Employed people showed less perception of stigma than unemployed (p=0.001). Patients with higher perception of stigma showed higher physical and psychological impact on health-related quality of life (rho=0.61 and 0.55, respectively; p< 0.001) and more difficulties at work (rho=0.60, p< 0.001). Presence of depressive symptoms was related to working status: pensioner or incapacitated patients had more symptoms of depression (p< 0.001). Moreover, severity of depressive symptoms correlated directly with MSWDQ-23 score, indicating work-related problems influence mood status (rho=0.64, p< 0.001).
Conclusion: Work-related problems, stigma and poor quality of life outcomes are common in people with low physical disability. Using MS-specific patient-reported questionnaires may be a useful complementary strategy to detect early symptoms in clinical practice.
Disclosure: This study was funded by the Medical Department of Roche Farma Spain. N.C is an employee of IQVIA Spain. N.M. and J.M. are employees of Roche Farma Spain. The rest of the authors declared no potential conflict of interest.

By clicking “Accept Terms & all Cookies” or by continuing to browse, you agree to the storing of third-party cookies on your device to enhance your user experience and agree to the user terms and conditions of this learning management system (LMS).

Cookie Settings
Accept Terms & all Cookies