Patient Experience – Using Tiny Data to Make a BIG Difference!
Patient Experience Questions One of the earliest benefits of patient-reported outcome data collection is achieved through...
PRO Terms Glossary
A Reliable and Valid Glossary – PRO Testing, Measurement, and Stats Terms You Need to Know
Challenges Facing Joint Replacement Registries
What are the challenges facing Joint Replacement Registries? With the number of total joint replacement (TJRs) performed and...
California Joint Replacement Registry (CJRR)
There are several aspects of the CJRR that make it unique. In addition to clinical information, CJRR collects information directly from patients about how they are functioning both before and after surgery by using validated patient-reported outcome tools. It was one of the first Level III orthopedic data registries in the nation.
Patient-Reported Outcome Data For Private Practices
Private practices love the CODE PRO Platform because it allows you the ability to quickly build a high-quality private data registry. Patient-reported outcome data differentiates your practice by shifting the focus from the pure cost-reduction model implemented by your competitors, to a complete value-based model.
Patient-Reported Outcome Data Collection for Hospitals
Hospitals love the CODE PRO Platform because it allows the ability to quickly build a high-quality private data registry. Patient-reported outcome data differentiates your hospital by shifting the focus from the pure cost-reduction model implemented by your competitors, to a complete value-based model.
American Joint Replacement Registry (AJRR)
American Joint Replacement Registry (AJRR) is a not-for-profit organization, created in partnership with the American Academy of Orthopedic Surgeons (AAOS) in 2009 to create a national center for primary and revision hip and knee replacement data collection.
N²QOD – National Neurosurgery Quality Outcomes Database
Tracking outcomes is a top priority for spine surgeons. The neurosurgical community has continued to push for the collection of outcomes through a national data registry formerly known as the National Neurosurgery Quality and Outcomes Database (N²QOD). It’s now referred to as the Quality Outcomes Database (QOD).
MARCQI – Michigan Arthroplasty Registry Collaborative Quality Initiative
MARCQI is a Blue Cross Blue Shield of Michigan (BCBSM) and Blue Care Network supported group that began in 2012. Dedicated to improving the quality of care for patients undergoing hip and knee replacement surgery in Michigan, MARCQI has built a statewide hip and knee replacement data registry for hospitals and ambulatory surgery centers.
Optimize Bundled Payment Programs with Outcomes
Comprehensive Care for Joint Replacement (CJR) Beginning in 2016, the Centers for Medicare and Medicaid Services have mandated...
Feasibility Study of Collecting Orthopedic Patient-Reported Outcome Data in Clinic
Patient-Reported Outcomes Collection Feasibility Study We are pleased to see the release of the study validating the feasibility...
Why Surgeons Need to Track Total Joint Complications
Why is tracking complications so important? Millions of total joint replacement surgeries are performed each year in the US....