Optimizing outcomes in multiple sclerosis: consensus guidelines for the diagnosis and treatment of multiple sclerosis in Latin America
- PMID: 22164189
- PMCID: PMC3229255
- DOI: 10.1177/1756285611423560
Optimizing outcomes in multiple sclerosis: consensus guidelines for the diagnosis and treatment of multiple sclerosis in Latin America
Abstract
Objective: The prevalence of multiple sclerosis (MS) in Latin America varies across different studies but an intermediate risk and increased frequency of the disease have been reported in recent years. The circumstances of Latin American countries are different from those of Europe and North America, both in terms of differential diagnoses and disease management.
Methods: An online survey on MS was sent to 855 neurologists in nine Latin American countries. A panel of nine experts in MS analyzed the results.
Results: Diagnostic and therapeutic recommendations were outlined with special emphasis on the specific needs and circumstances of Latin America. The experts proposed guidelines for MS diagnosis, treatment, and follow up, highlighting the importance of considering endemic infectious diseases in the differential diagnoses of MS, the identification of patients at high risk of developing MS in order to maximize therapeutic opportunities, early treatment initiation, and cost-effective control of treatment efficacy, as well as global assessment of disability.
Conclusions: The experts recommended that healthcare systems allocate a longer consultation time for patients with MS, which must be conducted by neurologists trained in the management of the disease. All drugs currently approved must be available in all Latin American countries and must be covered by healthcare plans. The expert panel supported the creation of a permanent forum to discuss future clinical and therapeutic recommendations that may be useful in Latin American countries.
Keywords: glatiramer acetate; immunomodulators; interferon-beta; mitoxantrone; multiple sclerosis; natalizumab.
Conflict of interest statement
Dr Carrá is on the Advisory Board of Teva, Teva-Tuteur Argentina, and Biogen-Idec Argentina. Dr Correale is a board member of Merck-Serono Argentina, Biogen-Idec LATAM, and Merck-Serono LATAM. He has received reimbursement for developing educational presentations for Merck-Serono Argentina, Merck-Serono LATAM, Biogen-Idec Argentina, and Teva-Tuteur Argentina as well as professional travel/accommodation stipends. Dr Gabbai received honoraria for participating in meetings sponsored by Bayer Schering, Biogen-Idec, Merck Serono, Novartis, and Teva. Dr Duriez has received fees for conferences from Stendhal and TEVA, as well as fees for projects of investigation for Bayer Schering and Merck Serono. Dr Macías-Islas received fees for being on the Advisory Board for Teva Neurosciences Mexico, Merck Serono, and Bayer Schering. Dr Vizcarra-Escobar has received compensation as a member of the Advisory Board for Stendhal, fees from Abbot and Pfizer for his participation at research projects, and fees from Pfizer and MEDCO for teaching conferences.
Dr García-Bonitto, Dr Vergara-Edwards and Dr Bolaña have nothing to disclose.
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