Factors associated with delay to medical recognition in two Canadian multiple sclerosis cohorts
- PMID: 20202651
- DOI: 10.1016/j.jns.2010.02.007
Factors associated with delay to medical recognition in two Canadian multiple sclerosis cohorts
Abstract
Long referral and diagnostic delays can impact both the opportunity for early therapeutic intervention and estimates of MS incidence and prevalence. We investigated factors associated with diagnostic or referral delays within two geographically distinct MS Canadian cohorts and the association between referral delay and disability at first clinic visit. Adult-onset MS patients were selected from the population-based British Columbian MS (BCMS) (n=5705) and the clinic-based Hôpital Notre-Dame, Quebec (CHUM) (n=1489) databases. Referral delay (BCMS) and diagnostic delay (CHUM) were examined by sex, onset age, disease course (primary progressive (PPMS) vs. relapsing at onset), onset symptoms (BCMS only) and year of first clinic visit/diagnosis. Cohorts were analyzed separately by stratified analyses and multivariable linear modeling. The relationship between referral delay and initial disability was examined by multiple ordinal regression in the BCMS cohort. Younger at onset patients or those with PPMS exhibited significantly longer delays (p<0.001). Delays decreased over the 20+ year period, but reductions varied by clinical course, onset age and sex. Long referral delays were associated with greater disability at first clinic visit (p<0.001). If early intervention at mild disability levels is warranted in MS, then the extended delays to medical recognition for young adult-onset and PPMS patients must be addressed.
Copyright 2010 Elsevier B.V. All rights reserved.
Similar articles
-
Is late-onset multiple sclerosis associated with a worse outcome?Neurology. 2006 Sep 26;67(6):954-9. doi: 10.1212/01.wnl.0000237475.01655.9d. Neurology. 2006. PMID: 17000960
-
The natural history of primary progressive multiple sclerosis.Neurology. 2009 Dec 8;73(23):1996-2002. doi: 10.1212/WNL.0b013e3181c5b47f. Neurology. 2009. PMID: 19996074
-
Changes in the ascertainment of multiple sclerosis.Neurology. 2005 Oct 11;65(7):1066-70. doi: 10.1212/01.wnl.0000178891.20579.64. Neurology. 2005. PMID: 16217060
-
[Primary progressive forms of multiple sclerosis: application of the new diagnostic criteria in French].Rev Neurol (Paris). 2002 Mar;158(3):341-5. Rev Neurol (Paris). 2002. PMID: 11976594 French.
-
The clinical course of multiple sclerosis.Handb Clin Neurol. 2014;122:343-69. doi: 10.1016/B978-0-444-52001-2.00014-5. Handb Clin Neurol. 2014. PMID: 24507525 Review.
Cited by
-
The Prevalence of Bipolar Disorders and Association With Quality of Life in a Cohort of Patients With Multiple Sclerosis.J Neuropsychiatry Clin Neurosci. 2017 Winter;29(1):45-51. doi: 10.1176/appi.neuropsych.15120403. Epub 2016 Aug 19. J Neuropsychiatry Clin Neurosci. 2017. PMID: 27539374 Free PMC article.
-
Multiple sclerosis diagnostic delay and its associated factors in Upper Egyptian patients.Sci Rep. 2023 Feb 8;13(1):2249. doi: 10.1038/s41598-023-28864-x. Sci Rep. 2023. PMID: 36754987 Free PMC article.
-
The Multiple Sclerosis Prodrome: Evidence to Action.Front Neurol. 2022 Jan 31;12:761408. doi: 10.3389/fneur.2021.761408. eCollection 2021. Front Neurol. 2022. PMID: 35173664 Free PMC article.
-
Genetic susceptibility for autoimmune diseases and white blood cell count.Sci Rep. 2023 Apr 11;13(1):5852. doi: 10.1038/s41598-023-32799-8. Sci Rep. 2023. PMID: 37041293 Free PMC article.
-
Functional neurological disorder and multiple sclerosis: a systematic review of misdiagnosis and clinical overlap.J Neurol. 2022 Feb;269(2):654-663. doi: 10.1007/s00415-021-10436-6. Epub 2021 Feb 21. J Neurol. 2022. PMID: 33611631 Free PMC article.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical