Highlights
- •Multiple sclerosis (MS) patients completed a vocational survey every three months.
- •Stably employed patients, those who lost work and healthy controls are compared.
- •Before job loss, group differences were noted in clinical and workplace variables.
- •MS patients who lost work were more likely to report negative work events.
- •Evaluation of negative work events can be used in timely vocational intervention.
Abstract
Purpose
Determine if a recently validated online survey of negative work events can predict
future job loss among multiple sclerosis (MS) patients.
Method
Evaluated were 284 employed individuals (63 healthy controls, 221 MS patients), every
three months, using an online vocational monitoring tool. Job loss rates in MS patients
were compared with the healthy controls. Survey responses from MS patients suffering
job loss (n = 23) were then compared to those maintaining employment. Analyses focused on the frequency
of negative work events.
Results
While 23 (10%) of MS patients lost their job after baseline, there was no job loss
among the healthy controls. Compared to stably employed patients, those suffering
job loss had been diagnosed with MS later in life, were more likely to report a progressive
disease course, and had greater physical disability as measured by the Patient Derived
Disease Steps (PDDS). Declining patients were also more likely to report negative
work events within three months of job loss (e.g., verbal criticism for errors or
removal of responsibilities). Stepwise logistic regression predicting MS job loss
retained the PDDS, age at diagnosis, years working for employer and reporting a negative
work event.
Conclusions
The results show that physical disability and patient reported risk factors for job
loss can be monitored using an online survey tool. The tool can trigger clinical assessments
to help prevent unemployment and assist patients in procuring disability benefits.
Keywords
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Article info
Publication history
Published online: July 23, 2015
Accepted:
July 21,
2015
Received in revised form:
July 11,
2015
Received:
May 22,
2015
Identification
Copyright
© 2015 Elsevier B.V. Published by Elsevier Inc. All rights reserved.