Suitestensa MG - Mammography Software MG slide 2 mg slide 3

Suitestensa MG - Mammography Software

SUITESTENSA MG - Mammography Information System and PACS

The Mammography Information Software and PACS for Mammographic Screening programs and complete digital mammography workflow.

Technology and features are system/configuration dependent. Specifications subject to change without notice. Information might refer to products or modalities not yet approved in all countries.
  • Overview
  • MG Screening
  • MG Review
  • PACS & Connectivity


SUITESTENSA MG - Mammography Information System and PACS

Breast Cancer Screening Programs in integrated HIS, RIS PACS environment

  • Double-blind reading protocols, review process with automatic arbitration and reassignment of the study
  • External ergonomic Mammo Keypad, to visualize exams in a click
  • Structured reporting performed directly on the images, with PDF report and CD patient printing
  • Computer Aided Detection (CAD), to automatically highlight spots of calcifications within dense breast tissue
  • Advanced visualization tools and image processing, with differences’ contrast-enhancement filterings


Specific Integration Standards and PACS Features for SUITESTENSA MG solution

  • Compliance to DICOM IHE interoperability/integration protocols with different modalities (CR, DR, MG, US, MR, XA, Multislice CT, Elastosonography, Tomosynthesis), and Regional Screening Programs in HIS, RIS PACS environments
  • BI-RADS codes
  • Multi-user multi-department, multi-modality, multi-vendor integrated management

Technology and features are system/configuration dependent. Specifications subject to change without notice. For further details, please contact your EBIT sales representative.

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.

Technology and features are system/configuration dependent. Specifications subject to change without notice. Information might refer to products or modalities not yet approved in all countries. For further details, please contact your EBIT sales representative.

SUITESTENSA MG - Screening

 

All medical history data in a unified working environment fully configurable and customizable.

 

  • Patients registry, administrative hospital acceptance and full administrative tools
  • Structured representation of medical data (previous examinations and interventions, signs and symptoms, observations and measurements) and insertion of alarms (heredity, surgical operations, delays in reporting examinations with positive result, diverging readings)
  • Fully customizable reports layouts and digital signature
  • Follow-up module, with automatic generation of recalling lists and forwarding module to modalities
  • Traceability of tests and data executed by technologist
  • Powerful search engine, data aggregation and statistical analysis for reporting activities

Technology and features are system/configuration dependent. Specifications subject to change without notice. For further details, please contact your EBIT sales representative.

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.

Technology and features are system/configuration dependent. Specifications subject to change without notice. Information might refer to products or modalities not yet approved in all countries. For further details, please contact your EBIT sales representative.


SUITESTENSA MG REVIEW

Structured Reporting directly on the images and in Double-Blind

Together with all the functionalities of SUITESTENSA Review, SUITESTENSA MG Review features advanced tools for the management and post-processing of mammographic data and images, with particular attention to an ergonomic, functional and automated comparison with images of previous studies.

  • PDF Structured Report (printable on CD/DVD) containing text, images, measurements, postprocessing and filterings, digital signature and time stamp
  • External ergonomic Mammo Keypad, to visualize exams in a click
  • Customizable double-blind reporting according to the rule: "multiple accesses / unique examination"


  • Automatic request for reviewing of conflicting readings (Third Reading/Arbitration)
  • Reassignment of a temporary/pending reading to another operator/reader, and final validation management
  • Evidence digital mark-up and insertion of annotations directly on the diagnostic images displayed (thanks to DICOM
  • Structured Reports in HTML format)
  • Real time loading/unloading worklists, divided into reading status /modality/operator and real time state-of-completion of the readings
  • Automatic comparative examination of the current and previous study with dedicated Current/Prior workspace, even belonging to different series and different patients
  • Powerful search engine, Statistics tools and data export to JPEG, TIFF , BMP , XML, CSV, etc.

 

A dedicated Mammo Workspace

 

  • MG Navigator tool, to sequentially displaying the different sections in which the image is automatically divided
  • Ergonomic workspace selection for RMLO-LMO/RCC-LCC
  • Simultaneous scrolling and symmetrical panning for images that belong to the same series and which have the same type of acquisition but are of opposite laterality
  • Related lines of reference between the two laterality
  • Alarm warning of any hidden image related to images displayed
  • Vertical alignment and auto-zoom to the chest wall, True Size mode (monitor size equal to body size)
  • Magnification, rotation, mirroring, inversion (chest wall justification, symmetrical lens, reverse, etc.), contrast-enhancement filtering

  • Overlays, remarks texts, signs and measurement of regions of interest, even for statistical purposes (calibration, angle, distance, density, ROI, area, etc.)
  • Automatic removal of bone tissue and patient table
  • IHE Mammo Profile: Patient Orientation, Image Laterality, View Code Sequence, View Modifier Code Sequence
  • Computer Aided Detection (CAD), to automatically highlight spots of calcifications within dense breast tissue
  • "Marker CAD" parallel reading protocol, with contextual, selective and informative dedicated menu
  • Mammography CAD results (SR visualization and management of CAD findings, ON/OFF display of the findings)

Technology and features are system/configuration dependent. Specifications subject to change without notice. For further details, please contact your EBIT sales representative.

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.

Technology and features are system/configuration dependent. Specifications subject to change without notice.
For further details, please contact your EBIT sales representative.

SUITESTENSA PACS: Workflow, Processing, Integration, Scalability beyond all limits

SUITESTENSA PACS is the enterprise-wide server system for radiology and cardiology diagnostic image acquisition, archiving, distribution and management over local or remote networks of multi-departmental and multi-site healthcare departments. Based on the latest web technologies, SUITESTENSA PACS integrates with HIS-Hospital Information Systems and all imaging modalities thanks to DICOM 3.0, HL7 and FDA-XML standard communication protocols, supporting systems’ interoperability and avoiding data duplication.

  • A vendor-neutral approach: modality-and-film independent
  • Powerful SEARCH ENGINE, data extraction tools and filters for multi-parametric queries
  • Customizable Case Report Forms (CRFs) for supporting clinical trials: cases can be indexed, anonymized and exported into logical archives
  • Remote and web system administration tools: parameters and configuration settings; monitoring; adding / removing / editing DICOM nodes and links; view statistics

SUITESTENSA Quality Control: Integration Goes Extreme

SUITESTENSA Quality Control Server is the exclusive software that streamlines the integration among PACS, HIS, RIS or CVIS, and it is natively integrated into all SUITESTENSA Products Family. QCS establishes configurable, firm and strong rules for true systems integration, while managing and monitoring systems interaction:

  • Automatic association of HIS services with PACS exams
  • Management of human errors and out-of-the-systems workflows (manual association and editing)

SUITESTENSA PACS DPA: The effectiveness of digital preservation and archiving

SUITESTENSA PACS DPA is the software dedicated to electronic storage, on removable media or hard disk, of images and reports, as specified by national and international laws.

  • Digital preservation of images and reports, digital signature (Italian CNIPA 11/2004, UNI 11386: 2010)
  • European directives on privacy and secure archiving policies
  • Archiving and indexing backup

SUITESTENSA WEB PACS: See all your DICOM images via the Internet or Intranet

  • For complex multi-departments needs with more than 150.000 services (imaging)/per year
  • Running on “standard” PC
  • tele-cardiology/radiology and tele-consultation functions; Specialists and General Practitioners distribution
  • Streaming "progressive" decoding engine: as soon as the web pacs has downloaded enough of the DICOM file, the diagnostic image is progressively decoded, displayed, and manipulated, so it is not necessary to wait for the entire file to be downloaded
  • Window/Level, zoom, rotation, flip, coloring, enhancement filters; distances, angles, density, graphical tools for annotations
  • Cine-sequences of multi-frame playback
  • Hanging Protocols
  • Reference lines (or Scout Lines) and 3D localizer cursor for MRI and CT scans
  • Compatibility with the main web browsers: Internet Explorer 7 or later, Google Chrome, Mozilla Firefox 3 or later, Safari

Suitestensa Mobile: The Newest Frontiers of Mobile PACS Connection Anytime, Anywhere

  • Works on modern web browsers, IOS & Android mobile devices, Laptop and desktop computers
  • Supported Operating Systems: Windows, Mac OS
  • Unparalleled security: no downloads mean no risk of data loss (it works with existing image and reporting archives)
  • Collaborations for teaching and teleconsultancy
  • Query and retrieve of images (DICOM standard)
  • Possibility to manage simultaneously the same image from different access points
  • Predefined workspaces and display of annotations, measurements and other data as previously assigned to the image modality
  • Interactive 2D, 3D & MIP/MPR diagnostic (slab variation up to 50 mm), 3D Volume Rendering
  • Scouts and positional references
  • Digital slow motion (XA , US/Echo)
  • Analysis and measurements tools: dynamic control of contrast and brightness (W/L), distance, angle, density, magnifying glass (for IOS), zoom, pan

Radiotherapy PACS

Dedicated visualitazion protocols specific for SUITESTENSA RT Radiotherapy

  • Prefetch and comparison from different modalities and/or previous examimations
  • Central Repository for all DICOM treatment data
  • Full integration of cone-beam CTs and other simulators, portal images, treatment planning systems (TPS and LINAC )

Compliance with all DICOM RT-related objects:

  • RT Structure Set (VOIs, Contours, Dose Reference Point)
  • RT Plan (Treatment Plans, Fractionation, Patient setup)
  • RT Image (Simulator, DRR, Portale Image)
  • RT Dose (Dose Points, Isodoses, DVH)
  • RT Treatment Records: (Beams, Brachy, Summary)

Mammographic PACS

Specific Integration Standards and PACS Features for SUITESTENSA MG solution

  • Compliance to DICOM IHE interoperability/integration with different modalities (CR, DR, MG, US, MR, XA, Multislice CT, Elastosonography, Tomosynthesis), and Regional Screening Programs in HIS, RIS PACS environments
  • BI-RADS codes for integration with Regional Screening Programs in Hospital Information Systems, RIS and PACS environments
  • Multi-user multi-department, multi-modality, multi-vendor integrated management

Connectivity - DICOM Conformance Statements and IHE Integration Statements

In a fast-changing world where the value of information is increased by the possibility of sharing it, the highest level of clinical data management has to be offered to meet today’s medical needs.
The worldwide medical imaging community has entered a new era of communication opportunities. These developments enable imaging professionals to reach diagnoses more effectively and efficiently, which in turn can raise the level of overall healthcare provided. From the very beginning of IT diffusion in the medical environment, Esaote has been recognized as a world leader in IT Solutions providing a solid contribution to the revolution that is bringing the medical world to an unexpected level of efficiency.
Information technology in Esaote has developed innovative systems for the management of diagnostic images, whose goal is connectivity of all diagnostic modalities, medical devices and imaging workstations, where data and digital images flow in a fully standard, filmless environment.
Complete and integrated management of US (images and clips) and ECG traces, possibility of archiving data on media (with indexing support and external jukebox compatibility), exporting multimedia files, in standard Windows® and DICOM format (available on network folder and CD), automatically forwarding to external PACS are just a few opportunities Esaote can offer.
Our product portfolio consists today in a wide range of DICOM and HL7 compliant solutions for effective management of medical images in paper and film-less hospital, all conforming with IHE interoperability project. 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. All products are in full compliance with DICOM standards and are supplied, on request, with the corresponding DICOM Conformance Statement. All products are in full compliance with one or more of the IHE integration profiles and are supplied, on request, with the corresponding IHE Integration Statement.

 

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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.

Technology and features are system/configuration dependent. Specifications subject to change without notice.
For further details, please contact your EBIT sales representative.

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Suitestensa MG Mammography Information System and PACS
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Suitestensa MG Mammography Information System and PACS
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Suitestensa MG Mammography Information System and PACS
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Suitestensa MG Mammography Information System and PACS
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Suitestensa MG Mammography Information System and PACS
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