Suitestensa RT - Radiotherapy Software rt slide 2 rt slide 3

Suitestensa RT - Radiotherapy Software

SUITESTENSA RT - Radiotherapy Information System and PACS

The point-of-reference RT Information Software and PACS for radiation treatment planning prepared by radiation oncologists, physicists, radiotherapists

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
  • Electronic Patient Record
  • RT Review
  • PACS & Connectivity


SUITESTENSA RT - Radiotherapy Information System and PACS

Plan Treatment, Imaging procedures and follow-ups at a glance

SUITESTENSA RT is a Radiotherapy Information System and PACS integrates data and images from almost all modalities and imaging departments and covers the needs of physicians and radiotherapists during the chemiotherapic and radiation treatment planning. SUITESTENSA RT includes the Electronic Patient Record folder, the Review module for advanced image visualization and reporting, and the PACS system for long-term archive and distribution of diagnostic images related to the oncological patient.

  • Admission and treatment planning, outpatient visits, financial flows and accounting
  • Radiotherapy PACS gathering all related images, and acting as a connector talking with all equipments involved: centering, treatment planning, simulator, etc.

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.


RADIOTHERAPY EPR - Electronic Patient Record

Tailor-made workflow for radiation treatment planning

  • Patient registry and plan treatment, booking and daily observational clinical diary, scheduling, medical notes, planning data and related images storage
  • Chemioterapy Module (treatment programs), Day Hospital, Patient Follow Up management
  • Dedicated Worklists for Simulation Room, Planning Room and Treatment Room
  • Statement of account, final reporting and full administrative tools
  • Import and management of studies, exams, data and measures derived from other diagnostic departments (radiology, laboratory analysis, pathological anatomy, etc.)
  • Powerful search engine, data aggregation and statistical analysis for reporting activities
  • Tele-therapy and Brachytherapy
  • Dose calculations and dose measurements
  • References related RT plan


Simplified Clinical Assessment with specific cards dedicated to the the radiotherapic workflow

The EPR folder of SUITESTENSA RT contains dedicated cards and sections for the management of the radiotherapic workflow:

  • Diagnosis
  • Patient Data
  • First Visit
  • Histology (x-rays, laboratory and surgical procedures, histological and cytological examinations)
  • Staging (anatomical representation of tumor progression stage)
  • Chronology (medical reasons, methods and results of diagnostic procedures executed and of therapeutic protocols applied)
  • Radiotherapy programs (treatments and techniques applied, pathology and priorities of the tumor, CTV-Clinical Target Volume, contrast medium, request for Social and Health Workers, request for urgency or emergency regimen, definition of therapeutic, palliative, symptomatic treatment
  • Chemiotherapy treatment programs

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 RT REVIEW

Image viewing and reporting software specifically dedicated to Radiotherapy

  • Management of all modalities (CT, NMR, CR, DR, RF, US, XA, etc.) with 3D reconstruction, prefetch and comparison from different modalities and/or previous examimations
  • Clip mode visualization for dynamic images, with playback control
  • Integration with Microsoft PowerPoint® for exporting still images and cines
  • Click to show / hide a particular ROI.


RT Image Module

  • Conical Imaging Geometry (Radiographs, Digital Reconstructed Radiographs (DDR), Simulator Images, Portal Images)
  • Pixel spacing on the image plane
  • Exposure Sequence (multiple exposure images, cine images)
  • Information on image generation (gantry angle, field shape)

RT Dose Module

  • Dose distribution and dose volume histograms
  • Grid-based 2D planes
  • Different summation types (plan, fraction, beam, brachy)
  • Isodoses


RT Structure Set Module

  • Regions and Volumes of Interest (ROIs referencing images, ROIs generation algorithm, ROI Observations
  • 3D Objects (e.g. bolus, brachytherapy applicator)
  • Frame of Reference Relationship, Contours, Contour Slab

RT Plan Module

  • Tele-therapy and Brachytherapy
  • Fractionation, Tolerance Tables, Positioning, Plan Relations
  • Reference to Dose Distribution (RT Dose)
  • Control Point Concept (MLC, Dynamic Therapy, IMRT)

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 RT- Radiotherapy Review
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Suietstensa RT - Electronic Patient Record
Suietstensa RT - Electronic Patient Record
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Suitestensa RT - Electronic Patient Record
Suitestensa RT - Electronic Patient Record
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