A healthcare organization interested in comparing its cardiac care outcomes with other organizations should consider participating in a registry. A registry collects and stores data on specific patient populations, treatments, and outcomes from multiple organizations, allowingparticipants to benchmark their performance against others. This comparison can help identify areas for improvement and validate the quality of care provided.

Network (B): A network might facilitatecollaboration or sharing best practices but does not provide the detailed comparative data that a registry offers.

Research (C): Participating in research could help generate new knowledge, but it is not specifically designed for benchmarking outcomes.

Certification (D): Certification ensures that an organization meets specific standards but does not provide comparative outcome data.

References

NAHQ Body of Knowledge: Data Analytics and Benchmarking in Quality Improvement

NAHQ CPHQ Exam Preparation Materials: Using Registries for Outcome Comparisons