Patient-Centered Outcomes

Patient-Centered Outcomes

Co-chairs:

Patient-centered outcomes (PCOs) comprise measurable health outcomes that are important, impactful, and/or meaningful to patients. PCOs include data collected directly from patients – patient reported outcomes (PROs) – and data collected through other sources, such as electronic health records (EHRs), registries, and claims data. Capturing PCOs well in embedded pragmatic clinical trials raises challenges that go beyond measure selection, including integrating data collection with EHRs, building partnerships with health systems, and developing analytic methods to derive and validate PCOs from existing data. The Core works across all of these areas.

PCOs are comprised of variables collected directly from patients and variables collected through other sources

This figure shows a list of Patient Reported Outcomes. They are Health-related quality of life, symptoms, function, satisfaction with care or symptoms, adherence to prescribed medications or other therapy, and preceived value of treatment.PRO data are defined by the FDA as “any report of the status of a patient’s health condition that comes directly from the patient, without interpretation of the patient’s response by a clinician or anyone else.” These data are increasingly used to inform and guide patient-centered care, clinical decision-making, and health policy decisions and are an important component of many of the Collaboratory’s NIH Collaboratory Trials.

Areas of Focus

The Patient-Centered Outcomes Core works closely with the Collaboratory to create guidelines and define best practices with respect to

  • Selecting, compiling, and curating the most appropriate PCO measures, including PRO measures and outcomes derived from other data sources.

  • Stimulating the development of new instruments when new solutions are needed.

  • Creating efficient, high-quality data collection and integration systems compatible with EHRs and registries, and building partnerships with health systems to support this integration.

  • Developing and applying analytic methods for deriving PCOs from existing data (eg, EHRs, registries, claims) and assessing their validity.
  • Conducting statistical analyses of PCO endpoints.

Interview

During the NIH Pragmatic Trials Collaboratory 2024 Steering Committee meeting, Drs. Emily O'Brien and Christy Zigler discussed challenges and lessons learned in collecting patient-centered outcome data in pragmatic clinical trials.

As part of this work, the Core conducts interviews with clinicians and other investigators using PROs, including NIH Collaboratory Trial principle investigators, to determine how PROs are currently used in the field, brainstorm solutions to challenges, and monitor progress with PRO implementation and data collection.

The Core has written a PCOs Living Textbook chapter, a white paper Strategies for Overcoming Barriers to Patient-Reported Outcomes Measures, and a chapter on including PROs in registries as a part of the AHRQ handbook on registries. It also helped lead the development of an Effectiveness Guidance Document (EGD) for incorporating PROs into comparative effectiveness research in adult oncology and held a workshop to help clinicians implement the NIH Patient Reported Outcomes Measurement Information System (PROMIS).

News and Interviews


View More

Products and Publications

View More

Presentations

View More

Back to top