SUITESTENSA CVIS PACS Software from Esaote

The New Cardiology Comprehensive Approach

SUITESTENSA is the CVIS PACS imaging & information management software platform developed by EBIT, the Esaote’s Company dedicated to healthcare IT diagnostic processes.

By encompassing all cardiology specialties into one single platform, SUITESTENSA allows for achieving a better workflow from patient admission to exam execution, reporting, administration and distribution.

SUITESTENSA cardiology folder contains all exams performed in the cardiology department: cath-lab, echo, ECG, EP, and can be connected to other diagnostic examinations to get the entire clinical history of a patient simply as just one click.

• Tight integration with HISs (ADT, EPR, Lab, Repositories, etc.)
• Emergency management
• Possibility of integration with central hospital warehouse and real-time stock and inventory Lab management (immediate cost per procedure, order filler and order management)
• Multi-parametric data extraction, analysis and statistics
• Customizable Case Report Forms (CRFs) for clinical trials: cases can be indexed, anonymized and exported into logical archives
• 2D, 3D & 4D advanced clinical packages for image processing and reconstruction

Compliant with the Most Relevant Regulations, Directives & Standards

• Data security, data integrity and disaster recovery
• Full traceability of involved personnel and implanted devices per procedure
• Compliance with datasets rules of national and international reference associations: ESC, ASE, ANMCO, GISE, SIEC, AIAC
• Compliant with cath-lab quality standards validation (Italian initiative GISENetwork: Outcome Survey of Coronary Angioplasty)
• Compliant with SIEC & ASE recommendations for standardized adult trans-thoracic report
• Possibility of mapping data into other national registries

Structured Report

Shape The Future Of Cardiology Reporting: SUITESTENSA has innovated the way Cardiologists produce and distribute reports.

Certifications

SUITESTENSA RIS CVIS PACS, manufactured by Esaote, complies with the Medical Device Directive (MDD) 93\42\EEC as amended by the 2007/47/EC.

In accordance with this directive, SUITESTENSA RIS CVIS PACS is classified as Class IIa devices.

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