Examines the feasibility of establishing national outcomes databases to help patients and providers make more informed treatment decisions.
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Cheryl Damberg (Ph.D., Rand Graduate School of Policy Studies) is a Health Policy Fellow. Research interests include employmentbased health insurance, health care reform, quality of care, health promotion/disease prevention. Matthias Schonlau (Ph.D. Statistics, University of Waterloo, Ontario) is an associate statistician at Rand. Elizabeth A. McGlynn (Ph.D., Public Policy, Rand Graduate School) is Director of the Rand Center for Research on Quality in Health Care.
This report examines issues surrounding the establishment of a national patient outcomes database that would be used by patients and providers to make more informed treatment decisions. It focuses on prostate cancer and surgery for osteoarthritis.
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