Objective: To assess survival and all-cause mortality among MS patients in a large US database and a MS patient registry compared to a non-MS population. Background Although MS is a generally well-characterized condition, survival and cause of mortality data within US populations is limited. Design/Methods: 28,845 MS and 86,129 non-MS patients were selected from a large US claims database affiliated with i3. Inclusion in the MS cohort required ≥2 ICD-9-340 codes ≥30 days apart, or a combination of 1 ICD-9-340 and ≥1 disease modifying treatment (DMT) code, all with ≥3 consecutive months of database reporting. Inclusion in the non-MS cohort required absence of ICD-9-340 and DMT codes throughout the database reporting. Non-MS patients were matched based on age at index year (year subjects first identified as having MS), sex, and residence region at index year. From NARCOMS (a US volunteer-based MS registry), 34,777 MS participants were selected. Patients9 vital status was achieved by matching their information to the National Death Index (NDI) and the Social Security Administration Death Master File. Analyses focused on overall mortality rates and survival patterns since birth within and among populations. Results: In the i3-affiliated database, a K-M survival analysis showed that participants with MS had a significant survival disadvantage compared to non-MS controls (p Conclusions: Patients with MS have a significant survival disadvantage compared to non-MS populations and have mortality rates 2- to 3-fold higher than those without MS. Supported by: Bayer HealthCare Pharmaceuticals, Inc. Disclosure: Ms. Reshef has received personal compensation for activities with Bayer HealthCare Pharmaceuticals as an employee. Dr. Cutter has received personal compensation for activities with Sanofi-Aventis Pharmaceuticals, Inc., Cleveland Clinic, Daiichi Pharmaceutical Corporation, GlaxoSmithKline, Inc., Genmab Biopharmaceuticals, Eli Lilly & Company, Medivation, Modigenetech, Ono Pharmaceutical, PTC Therapeutics, Teva Neuroscience, Vivus, University of Pennsylvania, NHLBI, NINDS, NMSS, Alexion, Bayhill Therapeutics, Bayer Pharmaceuticals Corporation, Celgene, Novartis, Consortium of MS Centers, Genzyme Corporation, Klein-Buendel Incorporated, Nuron Biotech, Peptimmune, Somnus Pharmaceuticals, Sandoz, University of Texas Southwestern and Visioneering Technologies, Inc. Dr. Cutter has received compensation for serving on the board of Pythagoras, INC. Dr. Cutter has received research support from various pharmaceutical corporations. Dr. Golub has received personal compensation for activities with Bayer Pharmaceuticals Corporation. Dr. Brueckner has received personal compensation for activities with Bayer HealthCare Pharmaceuticals as an employee. Dr. Knappertz has received personal compensation for activities with Bayer Pharmaceuticals Corporation as an employee.
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