Measurement Best Practices
Measurement tells the story of your palliative care service: what it does, whom it serves, and its impact on outcomes important to patients, families, leaders, decision makers, funders/payers, and other stakeholders.
This toolkit provides guidance on measurement so that your program can:
- Demonstrate value to stakeholders
- Align your services with national palliative care quality standards
- Manage your program operations
- Perform continuous quality improvement
What’s in the Toolkit
How and What to Measure
Recommendations for program measures that are feasible to collect and that produce data that the program can use to achieve its goals.
Recommendations for measures and approaches to evaluating palliative care services that enable growth and improvement.
PCQC is a membership organization that operates a national unified palliative care registry, which captures both program and patient-level data. Membership allows palliative care teams to track their performance over time, benchmark against their peers, and participate in quality improvement offerings.
This Virtual Office Hour explores best practices in evaluating your program and engaging stakeholders.
Synthesize data to manage the program efficiently, perform continuous quality improvement, and demonstrate value to stakeholders.
Tools to make the case for palliative care resources and financial partnerships, including the palliative care evidence base and downloadable tools for presenting the case.
Webinar presentation on how to leverage measurement for quality improvement and to demonstrate value.
Diane E. Meier, MD, FACP, FAAHPM
Founder, Director Emerita and Strategic Medical Advisor, Center to Advance Palliative Care
Maggie Rogers, MPH
Director, Research and Analytics
J. Brian Cassel, PhD
Palliative Care Research Director; Associate Professor, VCU School of Medicine
Faculty, Palliative C…
Brynn Bowman, MPA
Chief Executive Officer, Center to Advance Palliative Care
Allison Silvers, MBA
Chief Health Care Transformation Officer