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Aktualnosci Neurologiczne ; 21(3):131-136, 2021.
Article in Polish | Web of Science | ID: covidwho-1771883

ABSTRACT

Multiple sclerosis patients are by definition more susceptible to infections, which dependents on the use of disease-modifying treatments. Depending on the mechanism of action, individual disease-modifying treatments carry different risks. As a result, patients require an individualised approach to initiating and continuing new treatments. This problem became very important during the COVID-19 pandemic. In the case of drugs with different mechanisms of action on the immune system, the impact of therapy on susceptibility to SARS-CoV-2 infections and the course of COVID-19 should be considered. Based on the risk/benefit analysis for the patient, individual therapies have been assigned recommendations: 1) low-risk therapies (glatiramer acetate, interferons, dimethyl fumarate, teriflunomide) - discontinuation of therapy and delay of treatment initiation is not recommended;2) moderate-risk therapies (fingolimod, natalizumab, ocrelizumab, cladribine) - require caution, individual risk/benefit assessment, risk analysis of multiple sclerosis symptom exacerbation after drug discontinuation;3) high-risk therapies (alemtuzumab, mitoxantrone, haematopoietic stem cells transplantation) - treatment initiation is not recommended, administration of subsequent doses requires extreme caution. The article reviews the recommendations and publications from the last 2 years, taking into account the changing views on the treatment of multiple sclerosis in the time of COVID-19 pandemic.

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