Factors associated with health care utilization in pediatric multiple sclerosis

2020 ◽  
Vol 38 ◽  
pp. 101511
Author(s):  
Ruth Ann Marrie ◽  
Julia O'Mahony ◽  
Colleen Maxwell ◽  
Vicki Ling ◽  
Christine Till ◽  
...  
PLoS ONE ◽  
2019 ◽  
Vol 14 (6) ◽  
pp. e0218215 ◽  
Author(s):  
Ruth Ann Marrie ◽  
Julia O’Mahony ◽  
Colleen J. Maxwell ◽  
Vicki Ling ◽  
E. Ann Yeh ◽  
...  

2020 ◽  
pp. 135245852096388
Author(s):  
Ruth Ann Marrie ◽  
Randy Walld ◽  
James M Bolton ◽  
Jitender Sareen ◽  
Scott B Patten ◽  
...  

Background: Little is known about the effects of changes in the presence or absence of psychiatric disorders on health care utilization in multiple sclerosis (MS). Objective: To evaluate the association between “active” mood and anxiety disorders (MAD) and health care utilization in MS. Methods: Using administrative data from Manitoba, Canada, we identified 4748 persons with MS and 24,154 persons without MS matched on sex, birth year, and region. Using multivariable general linear models, we evaluated the within-person and between-person effects of any “active” MAD on annual physician visits, hospital days, and number of drug classes dispensed in the following year. Results: Annually, the MS cohort had an additional two physician visits, two drug classes, and nearly two more hospital days versus the matched cohort. Individuals with any MAD had more physician visits, had hospital days, and used more drug classes than individuals without a MAD. Within individuals, having an “active” MAD was associated with more utilization for all outcomes than not having an “active” MAD, but the magnitude of this effect was much smaller for visits and drugs than the between-person effect. Conclusion: Within individuals with MS, changes in MAD activity are associated with changes in health services use.


Author(s):  
Sheri L. Pohar ◽  
C. Allyson Jones ◽  
Sharon Warren ◽  
Karen V.L. Turpin ◽  
Kenneth Warren

Background:Persons with multiple sclerosis (MS) represent a small segment of the population, but given the progression of the disease, they experience substantial physical, psychosocial and economic burdens.Objective:The primary aim was to compare demographic characteristics, health status, health behaviours, health care resource utilization and access to health care of the community dwelling populations with and without MS.Methods:Cross-sectional survey using data from the Canadian Community Health Survey (CCHS 1.1). Adjusted analyses were performed to assess differences between persons with MS and the general population, after controlling for age and sex. Normalized sampling weights and bootstrap variance estimates were used.Results:Respondents with MS were 7.6 times (95% CI: 5.4, 10.7) more likely to have health-related quality of life scores that reflected severe impairment than respondents without MS. Respondents with MS were 12.2 times (95% CI: 8.6, 17.2) to rate their health as ‘poor’ or ‘fair’ than the general population. Urinary incontinence and chronic fatigue syndrome were 18.7 times (95% CI: 12.5, 28.2) and 21.9 times (95% CI: 11.9, 40.3), more likely to be reported by respondents with MS than those without. Differences between the two populations also existed in terms of health care resource utilization and access and health behaviours.Conclusion:Large discrepancies in health status and health care utilization existed between persons with MS who reside in the community and the general population according to all indicators used. Health care needs of persons with MS were also not met.


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