| Literature DB >> 26262118 |
Anthony Solomonides1, Satyender Goel2, Denise Hynes3, Jonathan C Silverstein1, Bala Hota4, William Trick5, Francisco Angulo5, Ron Price6, Eugene Sadhu3, Susan Zelisko6, James Fischer3, Brian Furner7, Andrew Hamilton8, Jasmin Phua9, Wendy Brown10, Samuel F Hohmann11, David Meltzer12, Elizabeth Tarlov3, Frances M Weaver6, Helen Zhang5, Thomas Concannon13, Abel Kho2.
Abstract
CAPriCORN, the Chicago Area Patient Centered Outcomes Research Network, is one of the eleven PCORI-funded Clinical Data Research Networks. A collaboration of six academic medical centers, a Chicago public hospital, two VA hospitals and a network of federally qualified health centers, CAPriCORN addresses the needs of a diverse community and overlapping populations. To capture complete medical records without compromising patient privacy and confidentiality, the network created policies and mechanisms for patient consultation, central IRB approval, de-identification, de-duplication, and integration of patient data by study cohort, randomization and sampling, re-identification for consent by providers and patients, and communication with patients to elicit patient-reported outcomes through validated instruments. The paper describes these policies and mechanisms and discusses two case studies to prove the feasibility and effectiveness of the network.Entities:
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Year: 2015 PMID: 26262118
Source DB: PubMed Journal: Stud Health Technol Inform ISSN: 0926-9630