MyMS: An Interface for Patient-Reported Outcomes for Finnish Individuals With Multiple Sclerosis
The patient interface of the Finnish MS Register consists of data from 17 of 21 counties with well-being services. The interface is used by 10% of Finnish individuals with MS. The addition of the PREDSS, EQ-5D, FSMC, and MSNQ to the interface has increased health care professional and patient interest in the use of PROMs. We suggest that PROs should be integrated into electronic health records to improve shared decision-making and diminish documentation burden.
Authors
- Hanna Kuusisto (ORCID: https://orcid.org/0000-0002-3697-4961)
- Merja Soilu‐Hänninen (ORCID: https://orcid.org/0000-0001-6930-0229)
- Juhani Ruutiainen
- Päivi Hämäläinen (ORCID: https://orcid.org/0000-0001-7968-2179)
- Matias Viitala (ORCID: https://orcid.org/0000-0003-2854-2410)
Institutions
- University of Turku (FI)
- University of Eastern Finland (FI)
- Turku University Hospital (FI)
- Finnish Youth Research Society (FI)
- Tampere University Hospital (FI)
- Tampere University (FI)
Publication Details
- Journal
- International Journal of MS Care
- Published
- 2024-10-07
- DOI
- https://doi.org/10.7224/1537-2073.2023-082
- Citations
- 9
- Primary Topic
- Multiple Sclerosis Research Studies
- Type
- article
- Field-Weighted Citation Impact
- 3.82