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

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.

[1]  D. Cella,et al.  Linking outcomes management to quality-of-life measurement. , 1997, Oncology.

[2]  D. Osoba,et al.  Quality of life in oncology practice: prognostic value of EORTC QLQ-C30 scores in patients with advanced malignancy. , 1997, European journal of cancer.

[3]  D. Osoba,et al.  Quality of life scores: An independent prognostic variable in a general population of cancer patients receiving chemotherapy , 2004, Quality of Life Research.

[4]  Bryan R Luce,et al.  Rethinking Randomized Clinical Trials for Comparative Effectiveness Research: The Need for Transformational Change , 2009, Annals of Internal Medicine.

[5]  Amy P Abernethy,et al.  Management of gastrointestinal symptoms in advanced cancer patients: the rapid learning cancer clinic model , 2010, Current opinion in supportive and palliative care.

[6]  Nancy A Dreyer,et al.  Why observational studies should be among the tools used in comparative effectiveness research. , 2010, Health affairs.

[7]  Asif Ahmad,et al.  Electronic Patient-Reported Data Capture as a Foundation of Rapid Learning Cancer Care , 2010, Medical care.

[8]  A. Abernethy,et al.  Correlates of quality of life‐related outcomes in breast cancer patients participating in the Pathfinders pilot study , 2011, Psycho-oncology.

[9]  R. Deyo,et al.  A primary care-based interdisciplinary team approach to the treatment of chronic pain utilizing a pragmatic clinical trials framework , 2012, Translational behavioral medicine.

[10]  S. Silow-Carroll,et al.  Using electronic health records to improve quality and efficiency: the experiences of leading hospitals. , 2012, Issue brief.

[11]  Dean F Sittig,et al.  A Survey of Informatics Platforms That Enable Distributed Comparative Effectiveness Research Using Multi-institutional Heterogenous Clinical Data , 2012, Medical care.

[12]  A. Abernethy,et al.  Importance of health information technology, electronic health records, and continuously aggregating data to comparative effectiveness research and learning health care. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[13]  Jennifer G. Robinson,et al.  Electronic health records based phenotyping in next-generation clinical trials: a perspective from the NIH Health Care Systems Collaboratory. , 2013, Journal of the American Medical Informatics Association : JAMIA.

[14]  Next-Generation Registries: Fusion of Data for Care, and Research , 2013, AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science.

[15]  B. Coller,et al.  Assessing participant-centered outcomes to improve clinical research. , 2013, The New England journal of medicine.

[16]  E. Basch Toward patient-centered drug development in oncology. , 2013, The New England journal of medicine.

[17]  Incorporating the patient's voice in the continuum of care. , 2013, Journal of the National Comprehensive Cancer Network : JNCCN.

[18]  Robert Hauser,et al.  CancerLinQ and the future of cancer care. , 2013, American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting.

[19]  A. Abernethy,et al.  Real-world outcomes in metastatic renal cell carcinoma: insights from a Joint Community-Academic Registry. , 2014, Journal of oncology practice.

[20]  Suzanne E. Maddux,et al.  Patient-reported outcome performance measures in oncology. , 2014, Journal of oncology practice.