Literature DB >> 25006149

Assessing the value of patient-generated data to comparative effectiveness research.

Lynn Howie1, Bradford Hirsch2, Tracie Locklear3, Amy P Abernethy4.   

Abstract

The goal of comparative effectiveness research is to assess medical therapies and allow patients, health care providers, payers, and policy makers to make evidence-based decisions about the most appropriate therapies in routine clinical practice. To conduct this type of research and to inform health care delivery, data about the impact of interventions on patient outcomes are needed. Methods of generating evidence for comparative effectiveness research provide opportunities to engage patients and understand their experiences with illness and its treatment. In this article we assess the need for, uses of, and strengths and weaknesses of patient-generated data. We also review in brief federal and medical society efforts to create new streams of patient-generated data for clinical and research use. We observe that the key to high-quality patient-generated data is to have immediate and actionable data so that patients experience the importance of the data for their own care as well as research purposes. We conclude that leveraging the emerging wealth of "big data" being generated by patient-facing technologies such as systems to collect patient-reported outcomes data and patient-worn sensors is critical to developing the evidence base that informs decisions made by patients, providers, and policy makers in pursuit of high-value medical care. Project HOPE—The People-to-People Health Foundation, Inc.

Entities:  

Keywords:  Evidence-Based Medicine; Information Technology; Medical technology; Organization and Delivery of Care; Quality Of Care

Mesh:

Year:  2014        PMID: 25006149     DOI: 10.1377/hlthaff.2014.0225

Source DB:  PubMed          Journal:  Health Aff (Millwood)        ISSN: 0278-2715            Impact factor:   6.301


  23 in total

1.  Current use of routinely collected health data to complement randomized controlled trials: a meta-epidemiological survey.

Authors:  Lars G Hemkens; Despina G Contopoulos-Ioannidis; John P A Ioannidis
Journal:  CMAJ Open       Date:  2016-04-06

2.  Adapting the stage-based model of personal informatics for low-resource communities in the context of type 2 diabetes.

Authors:  Meghan Reading Turchioe; Marissa Burgermaster; Elliot G Mitchell; Pooja M Desai; Lena Mamykina
Journal:  J Biomed Inform       Date:  2020-09-20       Impact factor: 6.317

3.  Mobile apps for real-world evidence in health care.

Authors:  Madison Milne-Ives; Michelle Helena van Velthoven; Edward Meinert
Journal:  J Am Med Inform Assoc       Date:  2020-06-01       Impact factor: 4.497

Review 4.  What is the future of patient-reported outcomes in sickle-cell disease?

Authors:  Sharon A Singh; Nitya Bakshi; Prashant Mahajan; Claudia R Morris
Journal:  Expert Rev Hematol       Date:  2020-10-15       Impact factor: 2.929

5.  A Systematic Review of Patient-Facing Visualizations of Personal Health Data.

Authors:  Meghan Reading Turchioe; Annie Myers; Samuel Isaac; Dawon Baik; Lisa V Grossman; Jessica S Ancker; Ruth Masterson Creber
Journal:  Appl Clin Inform       Date:  2019-10-09       Impact factor: 2.342

Review 6.  Patient-reported outcomes in cancer care - hearing the patient voice at greater volume.

Authors:  Thomas W LeBlanc; Amy P Abernethy
Journal:  Nat Rev Clin Oncol       Date:  2017-10-04       Impact factor: 66.675

Review 7.  Quality of Life Outcomes for Bladder Cancer Patients Undergoing Bladder Preservation with Radiotherapy.

Authors:  Michael A Feuerstein; Anuj Goenka
Journal:  Curr Urol Rep       Date:  2015-11       Impact factor: 3.092

8.  Factors Influencing Sustained Engagement with ECG Self-Monitoring: Perspectives from Patients and Health Care Providers.

Authors:  Meghan Reading; Dawon Baik; Melissa Beauchemin; Kathleen T Hickey; Jacqueline A Merrill
Journal:  Appl Clin Inform       Date:  2018-10-10       Impact factor: 2.342

Review 9.  Applying a community-based participatory research framework to patient and family engagement in the development of patient-centered outcomes research and practice.

Authors:  Simona C Kwon; Shiv Darius Tandon; Nadia Islam; Lindsey Riley; Chau Trinh-Shevrin
Journal:  Transl Behav Med       Date:  2018-09-08       Impact factor: 3.046

10.  Patient-Centered Outcomes Measurement: Does It Require Information From Patients?

Authors:  Leif I Solberg; Stephen E Asche; John Butler; David Carrell; Christine K Norton; Jeffrey G Jarvik; Rebecca Smith-Bindman; Juliana O Tillema; Robin R Whitebird; Ann M Werner; Jeanette Y Ziegenfuss
Journal:  J Patient Cent Res Rev       Date:  2017-11-06
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