Linked Patient-Reported Outcomes Data From Patients With Multiple Sclerosis Recruited on an Open Internet Platform to Health Care Claims Databases Identifies a Representative Population for Real-Life Data Analysis in Multiple Sclerosis.
Valery RissonBhaskar GhodgeIan C BonzaniJonathan R KornJennie MedinTanmay SaraykarSouvik SenguptaDeepanshu SainiMelvin Skip OlsonPublished in: Journal of medical Internet research (2016)
Linking patient-reported outcomes data, from a Web-based survey of US patients with MS recruited on open Internet platforms, to health care utilization information from claims databases may enable rapid generation of a large population of representative patients with MS suitable for outcomes analysis.