The Secrets to Making Data Your Friend: How AAPM&R Registry Participants are Using Their Data to Improve Care for Stroke and Low Back Pain Patients (2023)-Session Presentation

Video Transcription

Video Summary

The transcript is a summary of a presentation about the AAPMNR Registry, which is a database that collects data on patients with stroke and low back pain in order to improve patient care. The registry collects both clinical data from electronic health records and patient-reported data. The presentation includes an overview of the registry, as well as information on the challenges in clinical practice, the goals and benefits of the registry, and some examples of data collected. The speakers discuss the demographics of the patients included in the registry and present scorecards showing the progress of patients over time. They also talk about the challenges of collecting patient-reported outcomes and the need for better integration with electronic health records. The speakers highlight the importance of physician and patient engagement, as well as the need for training and support to ensure successful implementation of the registry. They also discuss the future plans for the registry, including the development of new modules and the expansion of the data collection to include other conditions and patient populations. Overall, the presentation emphasizes the value of the registry in improving patient care and driving quality and research efforts in physiatry.

Keywords

AAPMNR Registry

database

patient care

clinical data

electronic health records

patient-reported data

challenges in clinical practice

goals and benefits

demographics of patients

progress of patients