Long-term trajectories of employment status, workhours and disability support pension status, after a first episode of CNS demyelination

Author:

Zarghami Amin1ORCID,van der Mei Ingrid1,Hussain Mohammad Akhtar2,Claflin Suzi B1,Bessing Barnabas1ORCID,Simpson-Yap Steve3ORCID,Ponsonby Anne-Louise4,Lechner-Scott Jeanette5,Broadley Simon6ORCID,Blizzard Leigh1,Taylor Bruce V1,Lucas Robyn,Dear Keith,Dwyer Terry,Kilpatrick Trevor,Williams David,Shaw Cameron,Chapman Caron,Coulthard Alan,Pender Michael P.,Valery Patricia

Affiliation:

1. Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia

2. Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia/Central Coast Public Health Unit, Central Coast Local Health District, New South Wales Health, Gosford, NSW, Australia

3. Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia/Melbourne School of Population and Global Health, The University of Melbourne, Carlton, VIC, Australia

4. The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, Australia/Murdoch Children’s Research Institute, Royal Children’s Hospital, The University of Melbourne, Parkville, VIC, Australia

5. School of Medicine and Public Health, The University of Newcastle, Newcastle, NSW, Australia/Hunter Medical Research Institute, Newcastle, NSW, Australia

6. Menzies Health Institute Queensland, Griffith University, Gold Coast, QLD, Australia

Abstract

Background: People with multiple sclerosis face significant employment-related challenges, with little known of the drivers of these outcomes. Objective: We examined prospective trajectories of employment-related outcomes up to 11 years following a first episode of central nervous system (CNS) demyelination (FCD). Methods: Participants were aged 18–59 years, at FCD, with at least two observations and were employed at study entry or anytime during follow-up ( n = 207). Outcomes were employment status (full-time, part-time and unemployed), average workhours per week and disability support pension (DSP; receiving/not receiving). We used group-based trajectory modelling to identify groups with common trajectories. Factors associated with trajectory membership were explored using log-multinomial regression. Results: Distinct trajectories were identified for employment (4), workhours (4) and DSP (2). Compared with stable full-time, female sex was strongly associated with being in the stable part-time trajectory (risk ratio (RR): 5.35; 95% confidence interval (CI) = 2.56–11.20; p < 0.001). A greater level of disability at 5-year review (RR: 1.35; 95% CI = 1.19–1.53) and having more than two comorbidities at baseline (RR: 2.77; 95% CI = 1.37–5.64) were associated with being in early and late deteriorated employment trajectories, respectively. Compared with the increased part-time trajectory, every additional relapse during the 5 years post-FCD was associated with a 10% increased risk of being in the reduced part-time trajectory (RR = 1.10; 95%CI = 1.00–1.22). For every additional EDSS point at 5-year review, the risk of being in the DSP trajectory increased (RR = 1.21; 95% CI = 1.05–1.41). Conclusion: These trajectories indicate substantial heterogeneity and the complex impact of MS on employment from its earliest timepoints. Understanding these trends could enable better targeting of interventions to facilitate workforce retention, particularly for females, those with a higher number of comorbidities, more frequent relapses and greater rate of disability accrual.

Funder

the National Multiple Sclerosis Society of the United States of America

National Health and Medical Research Council of Australia

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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