Cardiac Device Surveillance
As more patients receive pacemakers, implantable cardioverter defibrillators (ICDs), and cardiac resynchronization therapy systems, Cardiac Device Surveillance has become a cornerstone of long-term cardiovascular care. This session focuses on how structured in-clinic and remote follow-up can detect lead malfunctions, battery depletion, programming issues, arrhythmias, and early signs of infection before they result in clinical deterioration. Participants will explore how device data—ranging from stored electrograms and arrhythmia counters to thoracic impedance and activity logs—can be used to optimize therapy and guide timely interventions. The session is designed for cardiologists, electrophysiologists, device nurses, and technologists who manage growing device populations across diverse practice settings.
Clinicians around the world increasingly search for a cardiology conference as remote monitoring platforms, connectivity standards, and alert workflows rapidly evolve. This session reviews best practices for enrolling patients in remote monitoring, configuring alerts to minimize noise while capturing critical events, and integrating reports into electronic health records. Attendees will learn how proactive surveillance can shorten time to clinical decision-making in response to arrhythmias, lead alerts, or device parameter changes. Real case examples will illustrate how early detection of lead fracture, inappropriate shocks, rising thresholds, or fluid overload trends can prevent hospitalizations and improve quality of life.
A major emphasis is on developing robust CIED follow-up programs (cardiac implantable electronic device follow-up) that combine technology with clear processes and roles. Participants will examine workflow models for device clinics, including triage of incoming alerts, division of responsibilities between clinicians and device specialists, and documentation standards that support billing, compliance, and quality reporting. The session also explores patient-facing aspects such as education on transmitter use, expectations around contact and follow-up, and strategies for engaging patients who have limited digital literacy or connectivity.
Future developments, including fully cloud-based ecosystems, AI-assisted alert prioritization, and integration with broader remote cardiac monitoring, will also be discussed. By the end, attendees will have a practical roadmap for designing or refining device surveillance services that are efficient, scalable, and patient-centered, ensuring the full benefits of device therapy are realized over the long term.
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Submit Your Abstract Here →Key Priorities in Cardiac Device Surveillance
Routine Follow-Up and Remote Monitoring
- Establishing scheduled in-clinic visits complemented by continuous remote data review.
- Ensuring all eligible patients are enrolled, connected, and consistently transmitting device information.
Alert Management and Triage
- Configuring alerts to highlight clinically relevant events while limiting low-value notifications.
- Developing clear triage rules so that urgent issues are escalated quickly to the right clinician.
Performance and Longevity Assessment
- Tracking battery status, lead integrity, and pacing or shock statistics over time.
- Recognizing subtle parameter changes that signal impending device or lead malfunction.
Data Integration and Documentation
- Incorporating device reports into electronic health records with standardized summaries.
- Documenting clinical decisions linked to device findings for legal, regulatory, and billing needs.
Clinical and Operational Benefits
Earlier Detection of Device Problems
Proactive surveillance identifies malfunctions and infections before they become emergencies.
Reduced Hospitalizations and ER Visits
Prompt outpatient responses to arrhythmias and fluid trends avert decompensations.
Improved Patient Confidence and Engagement
Patients feel supported knowing their device is being monitored between visits.
More Efficient Use of Clinic Time
Structured workflows and remote monitoring free in-person visits for complex issues.
Better Quality Metrics and Accreditation Readiness
Reliable follow-up data support performance reporting and adherence to guidelines.
Stronger Collaboration Across the Care Team
Device specialists, nurses, and physicians work from a shared information platform.
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