VistA Enterprise Solution
Adverse Reaction Tracking (ART)
The Adverse Reaction Tracking (ART) program provides a standardized and structured system for recording, managing, and validating adverse reaction data. It ensures consistent data entry and allows healthcare providers to document and track adverse drug reactions (ADRs), allergies, and intolerances efficiently.
The module also supports cross-referencing with other clinical systems, ensuring accurate and updated records are available across departments.Additionally, ART facilitates seamless integration with external regulatory bodies, enabling healthcare facilities to report adverse drug reaction data to the Food and Drug Administration (FDA) and other monitoring agencies. This helps in enhancing patient safety, improving pharmacovigilance, and ensuring compliance with medical regulations, making ART an essential component of modern healthcare systems.
VistA Enterprise Solution (Adverse Reaction Tracking )
Features
Patient Allergy Documentation
Records and manages patient allergy and adverse drug reaction data.
VistA Module Integration
Allows other VistA modules to extract and update patient reaction information.
Regulatory Compliance Reporting
Supports VHA Directive 10-92-070 for adverse drug reaction reporting to the FDA.
API for Event Tracking
Includes ART event points in the API to trigger related tasks in other VistA packages.
Advanced Order Processing
Includes quick orders, order sets, and event-delay orders for admissions, discharges.
Progress Note Generation
Creates and displays progress notes for ART events, allowing pre-sign-off edits.
Allergy Inquiry Tracking
Records whether the patient has been asked about allergies and documents their responses.
Patient Chart & ID Band Marking
Tracks when charts and ID bands are marked for specific reactions to ensure patient safety.
Extensive Reporting Capabilities
Provides comprehensive reporting features for analysis and compliance tracking.
