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The Catalonia MS Registry is a population-based surveillance tool to determine disease incidence, geographical distribution, time trends and survival studies.  It is continously updated and in provides useful data that contributes to decision-making in health policy and resource allocation. 

The Registry started in January 2009 after completing a three month pilot phase. It is a multicentric initiative based on the collaboration of several hospitals specialized in the management of MS and representative of different regions throughout Catalonia. New MS cases are notified on-line using an specific software with secure access. The diagnosis validity is  high due to the  systems automatic diagnostic criteria application.  Information completeness is assured by the periodical evaluation by the staff of the registry and feedback to collaborating centers. The Registry ensures fulfilment of actual requirements in patients data confidentiality. 

 

Highlights

By january 2012, The MS Registry of Catalonia includes over 600 patients.

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An European Registry of MS (EUReMS) is starting. The European Multiple Sclerosis Platform (EMSP) is coordinating the project EUReMS, carried out by a multidisciplinary team and funded from the European Commission. The CEM-Cat has been selected by the European Multiple Sclerosis Platform as one of the centers participating in the project. Learn more.

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