Learn More About the Palliative Care Quality Collaborative

The Palliative Care Quality Collaborative (PCQC) is a 501(c)3 organization, lead by a board of directors, that will house a new national palliative care data registry system, which will capture both program and patient-level quality data.

With support from the Gordon and Betty Moore Foundation and the Cambia Health Foundation, the National Palliative Care Registry, the Palliative Care Quality Network (PCQN), and the Global Palliative Care Quality Alliance (GPCQA) will combine into one unified national registry system under the PCQC. This opportunity incorporates the best practices of each system, improves comparison reports, aligns with national standards, informs research and quality improvement, and explores EHR integration. The goal is to have the new system operational during the summer of 2020.

Current PCQN, GPCQA, and National Palliative Care Registry™ members can anticipate similar functionality and quality of services as the current registry systems. The PCQC will:

  • work to minimize any interruptions in your service during the transition,
  • have a pricing structure that offers both free program-level services (similar to the current offerings in the National Palliative Care Registry™) and paid patient-level services (similar to the current offerings in GPCQA and PCQN) to meet the needs of the field
  • incorporate your feedback to provide a strong registry
  • maintain some continuity to the current registry systems’ data elements while identifying best practices for each data element.

PCQC was created through a partnership between the American Academy of Hospice and Palliative Medicine (AAHPM), the Center to Advance Palliative Care (CAPC), the National Palliative Care Research Center (NPCRC), the Palliative Care Quality Network (PCQN), the Global Palliative Care Quality Alliance (GPCQA), and Four Seasons.

Download this PCQC powerpoint to learn more or visit our FAQ page.

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