U.S. claims data suggest a high rate of relapse after delivery and low use of MS therapies in the years before and after pregnancy.
To examine use of disease-modifying drugs for multiple sclerosis (MS) before, during, and after pregnancy, researchers used the 2006 to 2015 IQVIA Real World Data Adjudicated Claims–US database, which is designed to be representative of U.S. commercially insured individuals younger than 65. Inclusion criteria were women with an MS diagnosis code and a pregnancy-related code.
Of 205,466 women with MS, a pregnancy diagnosis claim was entered for 10,630, of whom 2158 had a live birth with 1 year of continuous insurance eligibility prepregnancy and 1 year postpregnancy. Compared with the prepregnancy period, odds of relapse declined to 0.62 during pregnancy, increased to 1.71 in the puerperium (delivery through 6 weeks), and ended higher in the …
Reviewing Author
DisclosuresConsultant/Advisory BoardAlexion Pharmaceuticals; Amgen; Astoria; Biogen; Bristol Myers Squibb; Celltrion; Genentech; Hoffmann-La Roche; Genzyme; EMD Serono; Immpact-Bio; Immunic Therapeutics; Kyverna; Lundbeck; Novartis; Sandoz; TG Therapeutics
Grant/Research SupportNational Institutes of Health; National Multiple Sclerosis Society; U.S. Department of Defense
Leadership Positions in Professional SocietiesConsortium of Multiple Sclerosis Centers (Treasurer)
DisclosuresConsultant/Advisory BoardAlexion Pharmaceuticals; Amgen; Astoria; Biogen; Bristol Myers Squibb; Celltrion; Genentech; Hoffmann-La Roche; Genzyme; EMD Serono; Immpact-Bio; Immunic Therapeutics; Kyverna; Lundbeck; Novartis; Sandoz; TG Therapeutics
Grant/Research SupportNational Institutes of Health; National Multiple Sclerosis Society; U.S. Department of Defense
Leadership Positions in Professional SocietiesConsortium of Multiple Sclerosis Centers (Treasurer)