Building Data Capacity
for Patient-Centered
Outcomes Research
INTERIM REPORT 2-
Data Standards, Methods, and Policy
Committee on Building Data Capacity for
Patient-Centered Outcomes Research:
An Agenda for 2021 to 2030
Committee on National Statistics
Division of Behavioral and Social Sciences and Education
Board on Health Care Services
Health and Medicine Division
Computer Science and Telecommunications Board
Division on Engineering and Physical Sciences
A Consensus Study Report of
THE NATIONAL ACADEMIES PRESS
Washington, DC
www.nap.edu
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This activity was supported by a contract between the National Academy of Sciences and the U.S. Department of Health and Human Services (award #HHSP233201400020B/75P00120F37102). Any opinions, findings, conclusions, or recommendations expressed in this publication do not necessarily reflect the views of any organization or agency that provided support for the project.
International Standard Book Number-13: 978-0-309-27262-9
International Standard Book Number-10: 0-309-27262-9
Digital Object Identifier: https://doi.org/10.17226/26298
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Suggested citation: National Academies of Sciences, Engineering, and Medicine. (2022). Building Data Capacity for Patient-Centered Outcomes Research: Interim Report 2—Data Standards, Methods, and Policy. Washington, DC: The National Academies Press. https://doi.org/10.17226/26298.
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COMMITTEE ON BUILDING DATA CAPACITY FOR PATIENT-CENTERED OUTCOMES RESEARCH: AN AGENDA FOR 2021 TO 2030
GEORGE ISHAM (Chair), HealthPartners Institute
JOHN F.P. BRIDGES, The Ohio State University
JULIE BYNUM, University of Michigan
ANGELA DOBES, IBD Plexus, Crohn’s & Colitis Foundation
DEBORAH ESTRIN, Cornell Tech
OLUWADAMILOLA FAYANJU, University of Pennsylvania
CONSTANTINE GATSONIS, Brown University
ROBERT GOERGE, Chapin Hall, University of Chicago
GEORGE HRIPCSAK, Columbia University
LISA IEZZONI, Massachusetts General Hospital
S. CLAIBORNE JOHNSTON, The University of Texas at Austin
MIGUEL MARINO, Oregon Health & Science University
ELIZABETH McGLYNN, Kaiser Permanente
DAVID MELTZER, University of Chicago
PAUL TANG, Stanford University and Palo Alto Medical Foundation
KRISZTINA MARTON, Study Director
CRYSTAL BELL, Associate Program Officer
RUTH COOPER, Associate Program Officer
MARY GHITELMAN, Senior Program Assistant
BRIAN HARRIS-KOJETIN, Director, Committee on National Statistics
SHARYL NASS, Director, Board on Health Care Services
JON EISENBERG, Director, Computer Science and Telecommunications Board
SAUL RIVAS, National Academy of Medicine Fellow, University of Texas Rio Grande Valley
COMMITTEE ON NATIONAL STATISTICS
ROBERT M. GROVES (Chair), Georgetown University
ANNE C. CASE, Princeton University
MICK P. COUPER, University of Michigan
JANET M. CURRIE, Princeton University
DIANA FARRELL, JPMorgan Chase Institute
ROBERT GOERGE, Chapin Hall at the University of Chicago
ERICA L. GROSHEN, Cornell University
HILARY HOYNES, University of California, Berkeley
DANIEL KIFER, The Pennsylvania State University
SHARON LOHR, Arizona State University, emerita
JEROME P. REITER, Duke University
JUDITH A. SELTZER, University of California, Los Angeles
C. MATTHEW SNIPP, Stanford University
ELIZABETH A. STUART, Johns Hopkins University
JEANETTE WING, Columbia University
BRIAN A. HARRIS-KOJETIN, Director
CONSTANCE F. CITRO, Senior Scholar
BOARD ON HEALTH CARE SERVICES
DAVID BLUMENTHAL (Chair), The Commonwealth Fund
ANDREW BINDMAN, Kaiser Foundation Health Plan, Inc.
NIRANJAN BOSE, Gates Ventures
MELINDA J. BEEUWKES BUNTIN, Vanderbilt University School of Medicine
NEIL S. CALMAN, The Institute for Family Health
PAUL CHUNG, Kaiser Permanente School of Medicine
PATRICIA M. DAVIDSON, Johns Hopkins University School of Nursing
MARTHA DAVIGLUS, University of Illinois at Chicago
JENNIFER E. DeVOE, Oregon Health & Science University
R. ADAMS DUDLEY, University of Minnesota
RICHARD G. FRANK, Harvard Medical School
TERRY FULMER, John A. Hartford Foundation
CINDY GILLESPIE, Arkansas Department of Human Services
ELMER HUERTA, The George Washington University Cancer Center
SHARON INOUYE, Harvard Medical School
JOHN LUMPKIN, BlueCross BlueShield of North Carolina Foundation
FAITH MITCHELL, The Urban Institute
DAVID B. PRYOR, Ascension Health
TRISH RILEY, National Academy for State Health Policy
WILLIAM SAGE, The University of Texas at Austin
HARDEEP SINGH, Baylor College of Medicine
SHARYL NASS, Director
COMPUTER SCIENCE AND TELECOMMUNICATIONS BOARD
LAURA HAAS (Chair), University of Massachusetts Amherst
DAVID CULLER, University of California, Berkeley
ERIC HORVITZ, Microsoft Corporation
CHARLES ISBELL, Georgia Institute of Technology
BETH MYNATT, Georgia Institute of Technology
CRAIG PARTRIDGE, Colorado State University
DANIELA RUS, Massachusetts Institute of Technology
FRED B. SCHNEIDER, Cornell University
MARGO SELTZER, The University of British Columbia
NAMBIRAJAN SESHADRI, University of California, San Diego
MOSHE VARDI, Rice University
JON EISENBERG, Senior Board Director
Acknowledgments
This Consensus Study Report was reviewed in draft form by individuals chosen for their diverse perspectives and technical expertise. The purpose of this independent review is to provide candid and critical comments that will assist the National Academies of Sciences, Engineering, and Medicine in making each published report as sound as possible and to ensure that it meets the institutional standards for quality, objectivity, evidence, and responsiveness to the study charge. The review comments and draft manuscript remain confidential to protect the integrity of the deliberative process.
We thank the following individuals for their review of this report: Rebecca A. Hubbard, Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania; Sue Jinks-Robertson, Department of Molecular Genetics and Microbiology, Duke University; Harold Lehman, Division of General Internal Medicine, Department of Medicine, Johns Hopkins University School of Medicine; Vincent X. Liu, Division of Research, Kaiser Permanente; Keith Marsolo, Population Health Sciences, Duke University School of Medicine; Emily O’Brien, Department of Population Health Sciences, Duke Clinical Research Institute, Duke University School of Medicine; and Jerome Reiter, Department of Statistical Science, Duke University.
Although the reviewers listed above provided many constructive comments and suggestions, they were not asked to endorse the conclusions of this report, nor did they see the final draft before its release. The review of this report was overseen by Andrew B. Bindman, Chief Medical Officer, Kaiser Foundation Health Plan and Hospitals, and Alicia L. Carriquiry, Department of Statistics, Iowa State University. They were responsible for
making certain that an independent examination of this report was carried out in accordance with the standards of the National Academies and that all review comments were carefully considered. Responsibility for the final content rests entirely with the authoring committee and the National Academies.
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Boxes and Figures
BOXES
1-2 Building Blocks of the Patient-Centered Outcomes Research Data Infrastructure
1-3 Statement of Task for the Overall Study
2-1 A Perspective on Data Required for Patient-Centered Outcomes Research and Standards to Consider
FIGURES
1-1 Patient-Centered Outcomes Research Trust Fund: Three streams of work and funding
1-2 ASPE’s strategic framework for the patient-centered outcomes research data infrastructure
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