Literature DB >> 26360615

Burden of illness in multiple sclerosis (DEFENSE) study: the costs and quality-of-life of Finnish patients with multiple sclerosis.

Juhani Ruutiainen1, Anna-Mari Viita2, Jarmo Hahl3, Jesse Sundell4, Helena Nissinen2.   

Abstract

OBJECTIVE: Although multiple sclerosis (MS) is one of the most common causes of non-traumatic disability among young adults, no published data on its economic and health-related quality-of-life (HRQoL) burden is available from Finland. The DEFENSE study aimed to estimate the costs and HRQoL of patients with MS (PwMS) in Finland and explore how these variables are influenced by disease severity and relapses.
METHODS: Overall, 553 PwMS registered with the Finnish Neuro Society, a national patient association in Finland, completed a self-administered questionnaire capturing information on demographics, disease characteristics and severity (Expanded Disease Severity Scale [EDSS]), relapses, resource consumption and HRQoL.
RESULTS: The PwMS had a mean EDSS score of 4.0. Overall, 44.1% had relapsing-remitting form of the disease (RRMS). The mean age was 53.8 years and 55.7% had retired prematurely due to MS. Disease-modifying therapies (DMTs) were used by 42.7% of the study population, and 21.5% across all disease types and severities had experienced relapses during the previous year. The mean total annual cost of MS was €46,994, which increased with advancing disease from €10,835 (EDSS score = 0) to €109,901 (EDSS score = 8-9). The mean utility was 0.644. HRQoL decreased with increasing disease severity. Relapses imposed an additional utility decrement among the PwMS with RRMS and EDSS ≤5 and had a trend-like effect on total costs. LIMITATIONS: The cross-sectional setting did not allow assessment of the significance of relapses in early MS or the use of DMTs on the prognosis of the disease.
CONCLUSION: The study confirms previous findings from other countries regarding a significant disease burden associated with MS and provides, for the first time, published numerical estimates from Finland. Treatments that slow disease progression and help PwMS retain employment for a longer duration have the highest potential to reduce the disease burden associated with MS.

Entities:  

Keywords:  Burden of illness; Costs; Finland; MS; Multiple sclerosis; Quality of life; Utilities

Mesh:

Year:  2015        PMID: 26360615     DOI: 10.3111/13696998.2015.1086362

Source DB:  PubMed          Journal:  J Med Econ        ISSN: 1369-6998            Impact factor:   2.448


  10 in total

1.  Costs of illness of multiple sclerosis in Sweden: a population-based register study of people of working age.

Authors:  Hanna Gyllensten; Michael Wiberg; Kristina Alexanderson; Anders Norlund; Emilie Friberg; Jan Hillert; Olivia Ernstsson; Petter Tinghög
Journal:  Eur J Health Econ       Date:  2017-05-09

2.  Costs and quality of life by disability among people with multiple sclerosis: a register-based study in Sweden.

Authors:  Hanna Gyllensten; Andrius Kavaliunas; Kristina Alexanderson; Jan Hillert; Petter Tinghög; Emilie Friberg
Journal:  Mult Scler J Exp Transl Clin       Date:  2018-07-09

3.  Costs of illness progression for different multiple sclerosis phenotypes: a population-based study in Sweden.

Authors:  Hanna Gyllensten; Andrius Kavaliunas; Chantelle Murley; Kristina Alexanderson; Jan Hillert; Petter Tinghög; Emilie Friberg
Journal:  Mult Scler J Exp Transl Clin       Date:  2019-06-28

4.  Cost Effectiveness of Cladribine Tablets for the Treatment of Relapsing-Remitting Multiple Sclerosis in The Netherlands.

Authors:  Renée Else Michels; Maria de Fransesco; Koshu Mahajan; Gerald J D Hengstman; Krijn M H Schiffers; Sangeeta Budhia; Gerard Harty; Marieke Krol
Journal:  Appl Health Econ Health Policy       Date:  2019-12       Impact factor: 2.561

5.  The socioeconomic impact of multiple sclerosis in France: Results from the PETALS study.

Authors:  A Bouleau; C Dulong; C A Schwerer; R Delgrange; K Bouaou; T Brochu; S Zinai; K Švecová; M J Sá; A Petropoulos; S Aly; P Labauge
Journal:  Mult Scler J Exp Transl Clin       Date:  2022-04-21

6.  Treatment Status and Healthcare Cost Trends for Patients with Multiple Sclerosis in Japan: A Claims Database Analysis.

Authors:  Izumi Kawachi; Hiromichi Otaka; Kosuke Iwasaki; Tomomi Takeshima; Kengo Ueda
Journal:  Neurol Ther       Date:  2022-06-17

7.  Preliminary testing of a patient decision aid for patients with relapsing-remitting multiple sclerosis.

Authors:  Nick Bansback; Judy A Chiu; Rebecca Metcalfe; Emmanuelle Lapointe; Alice Schabas; Marilyn Lenzen; Anthony Traboulsee; Larry D Lynd; Robert Carruthers
Journal:  Mult Scler J Exp Transl Clin       Date:  2021-07-15

8.  Validity and reliability of the Finnish version of the Multiple Sclerosis Impact Scale-29.

Authors:  Eija Rosti-Otajärvi; Päivi Hämäläinen; Anna Wiksten; Tanja Hakkarainen; Juhani Ruutiainen
Journal:  Brain Behav       Date:  2017-05-17       Impact factor: 2.708

9.  Validity and reliability of the Fatigue Severity Scale in Finnish multiple sclerosis patients.

Authors:  Eija Rosti-Otajärvi; Päivi Hämäläinen; Anna Wiksten; Tanja Hakkarainen; Juhani Ruutiainen
Journal:  Brain Behav       Date:  2017-06-09       Impact factor: 2.708

10.  A Principal Component Analysis Approach to Estimate the Disability Status for Patients with Multiple Sclerosis Using Japanese Claims Data.

Authors:  Izumi Kawachi; Hiromichi Otaka; Kosuke Iwasaki; Tomomi Takeshima; Kengo Ueda
Journal:  Neurol Ther       Date:  2022-01-22
  10 in total

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