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تعداد آیتم قابل مشاهده باقیمانده : -11 مورد

Multiple sclerosis disease-modifying therapies and pregnancy washout recommendations

Multiple sclerosis disease-modifying therapies and pregnancy washout recommendations
Disease-modifying therapy Length of disease-modifying therapy washout period per label Length of disease-modifying therapy washout period per pharmacokinetic/
pharmacodynamic placental transfer and potential risks
Characteristics
Self-injectable therapies (platform)
Interferons beta (all brand formulations approved for multiple sclerosis treatments and any generic equivalents) No washout No washout Short half-life, lower efficacy, extensive safety data with no fetotoxicity; may be used up to conception
Glatiramer acetate (brand or any generic formulations) No washout No washout Short half-life, lower efficacy, extensive safety data with no fetotoxicity; may be used up to conception and throughout pregnancy
Oral therapies
Teriflunomide Plasma levels must be <0.02 mg/L, accelerated elimination can be achieved with cholestyramine Accelerated elimination protocol; no washout when used and plasma concentration <0.02 mg/L confirmed Very long half-life, intermediate efficacy, animal evidence of fetotoxicity, not compatible with pregnancy
Sphingosine-1-phosphate (S1P) receptor modulators (fingolimod, ozanimod, ponesimod, siponimod)

2 months for fingolimod

10 days for siponimod

3 months for ozanimod

1 week for ponesimod

2 months for fingolimod High efficacy, long half-life, human evidence of fetotoxicity; rebound multiple sclerosis activity after stopping this disease-modifying therapy
Cladribine 6 months 4 months High efficacy, intermediate half-life, prolonged biologic activity after administration, no human evidence of fetotoxicity
Dimethyl fumarate (brand and generics) No washout No washout Very short half-life, intermediate efficacy, no human evidence of fetotoxicity
Monoclonal antibodies
Alemtuzumab 4 months 4 months Infusion, high efficacy, intermediate half-life but very prolonged biologic activity after administration
B-cell-depleting agents (ocrelizumab, rituximab, and ofatumumab) 6 months 2 months Infusion and self-injectable; high efficacy, intermediate half-life but prolonged biologic activity after administration; emerging safety data with pregnancy exposures reassuring
Natalizumab 3 months No washout Infusion, high efficacy, intermediate half-life; reassuring emerging safety data with pregnancy exposures; rebound multiple sclerosis activity after stopping this disease-modifying therapy
Washout refers to the time period during which the drug has to be stopped before conception attempts can begin.
Adapted with permission from Wolters Kluwer Health, Inc.: Bove RM, Houtchens MK. Pregnancy management in multiple sclerosis and other demyelinating diseases. Continuum (Minneap Minn) 2022; 28(1):12-33. Copyright © 2022 American Academy of Neurology. https://journals.lww.com/continuum/pages/default.aspx.
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