specific to the EPDI v3.0 dataset upgrade, as well as a review of inclusion criteria. The EP Device Implant Registry v3.0 offers the ability to capture new devices and placement locations, and track procedure participation of fellows in training. The streamlined data collection uses procedure-specific pathways, robust parent-child data element relationships, dynamic lists, and incorporates the set-to-know functionality to reduce the data collection effort while continuing to offer data-driven knowledge and insight. The EP Device Implant Registry establishes a national standard for understanding patient characteristics, treatments, outcomes, device safety, and the overall quality of care for internal cardiac defibrillators, permanent pacemakers, and cutting-edge devices of left and ventricular endocardial and cardiac contractility modulation procedures, while also delivering benchmarking data. Participating facilities can submit data for either permanent pacemaker procedures, or submit data for ICD procedures, or submit data for both permanent pacemakers and ICD procedures. The registry plays an important role in providing data-driven knowledge and insight for optimizing patient care. The EP Device Implant Registry v3.0 offers three procedure submission options. Each one captures all patients undergoing the relevant procedure or procedures. Facilities are encouraged to submit all procedures so they can receive the most data and feedback about the patient care and outcomes at their facility. The procedure population selected informs reporting of executive summary measures and metrics on the facility dashboard, and impacts the ability of a facility to engage with public reporting. Once a facility chooses to submit either internal defibrillator procedures, or permanent pacemaker procedures, or both ICD and permanent pacemaker procedures, the facility must designate the category of patient types in the site profile. The procedure population selected will be reflected with each submission to the Data Quality Report, or DQR. A facility may change their procedure population at any time. The procedure submission option selected is effective immediately, and is applied to all future data submissions and resubmissions. The EP Device Implant Registry is streamlined to provide concise data abstraction. This is achieved by incorporating procedure pathways, robust parent-child data elements, incorporating more dynamic lists, and incorporating the set-to- know functionality. Each patient record abstracted in the registry will indicate the procedures performed in Sequence 15826, EP Device Implant Pathway. The selection will identify the device pathway and determine which data elements are available for coding, thus streamlining the data collection process and reducing abstraction effort. Set-to-know is a feature that allows users to set sequence numbers 14264, 14268, and 9002 to know while still coding yes for the patient's historical or current intra- or post-procedure event data. This structure ensures comprehensive tracking of patient information while reducing data abstraction effort. This functionality is available for the History Risk Factor section for both conditional history and procedural history, and for the intra- and post-procedure events, potentially saving 56 total clicks. Dynamic lists, which are not shown here, can be modified as needed to ensure selections are up-to-date and comprehensive for a specific data element. Thank you for taking the time to view this presentation.

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EP Device Implant Registry

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patient care