The trial version allows you to test all features of VueBox ® Research beside the export and saving of results. Additionally, only a set of perfusion parameters is available and this version expires 30 days after activation.

• New licences are active for 2 years from the date of delivery. 
  If you wish a specific date of delivery, please include it in your quote request; otherwise, the software will be delivered after the order has been processed.
• Renewal licences are active for 1 year from the previous date of expiration.
   

Please note that an IRB-approved or IRB-exempt research must be in place throughout the period of use of VueBox Research.

VueBox Research ® can be run on Mac OS providing that a virtual machine application with Windows OS is installed (e.g. VMWare, Parallels, etc.).

Each license can be used to activate VueBox® Research on 2 different computers in the same institution. 

Yes. 
First, deactivate the licence from the current computer by starting VueBox ® Research > Help > About > Deactivate License. 
Then, activate VueBox ® Research on the new computer using the same Serial Key. 
 

In order to improve visualization of the useful information contained in the echo signal, ultrasound system manufacturers enhance the lower amplitude echo signals.
As a result, the video signal (i.e., the pixel values) is no more directly proportional to the local concentration of the contrast agent in the corresponding pixel locations, thus no quantification can be performed on the raw date.
To recover data linearization, specific calibration data must be acquired for the specific ultrasound system and acquisition settings.

You can find more information on linearization here: Linearization

Advanced System Recognition (ASR)-compatible ultrasound scanners are systems where the calibration data are directly embedded by the manufacturers in the DICOM files.

With ASR-compatible systems, manual selection of a calibration file is not required, as the parameters are automatically loaded by VueBox® Research. 
 

Yes. If your system is not ASR-compatible, quantification with VueBox® Research may still possible by importing a specific calibration file in the software.

Please ensure that your acquisition system and settings are supported before requesting your copy of VueBox ® Research. 
You can find an updated list of supported not-ASR systems here: Supported Ultrasound Systems.

VueBox® Research can be made compatible with virtually any ultrasound system providing that a calibration file is available.

If an ultrasound system or a specific setting does not appear in the list, contact the Bracco customer support at vuebox-research@bracco.com.

VueBox® Research converts video data (pixel intensity in grey levels) into echo-power data (arbitrary units or [a.u.]), a quantity directly proportional to the instantaneous concentration of contrast agent at each location in the field of view.

This conversion process, called linearization, takes into account color or greyscale rendering, the dynamic range of log-compression used during the clip acquisition and compensates for contrast gain, as long as pixel intensity is not truncated or saturated.

However, echo-power values, either expressed in [a.u.] or in [dB], are absolute values and are tricky to compare as such with data acquired on different systems (and different manufacturers) or from different subjects as

(1) the video data compression laws differ from one manufacturer to another. Thus, the comparison of absolute echo-power values, obtained after the decompression of video data using a dedicated calibration setting, is not recommended. Indeed, such values could differ by a factor, which changes according to the system, probe, dynamic range, and colormap used,

(2) and more importantly, the comparison of absolute echo-power values suffers from differences in morphology between subjects (e.g. acoustic windows, input functions), which currently, cannot be compensated for.

Therefore, we strongly recommend, whenever possible, to use relative measurements, by selecting a reference ROI (such as an artery, or healthy surrounding tissue), see Instructions for use for more information. This way, the results obtained become independent of the system used as well as the subject's morphology.

When a reference ROI is selected (checkbox next to ROI names in parameters table), values of amplitude parameters are displayed in [a.u.], [%] and [dB]. In this case, the [dB] column contains values that are relative to this reference and computed as follows:

value_dB = 10 * log10 ( value_au / value_ref_au)

When no reference ROI is selected, values of amplitude parameters are displayed in [a.u.] and [dB]. And in this case, the [dB] are relative to the value 1:

value_dB = 10 * log10 ( value_au / 1)

Thus, without reference ROI, the values expressed in [dB] are likely to vary between patients and US systems, just like [a.u.] ones.

VueBox^® Research features an automatic contrast arrival detection to help determine the best time origin. However, it is important to note that

• the time origin detected is a suggestion only and should be reviewed by the user before pressing the OK button.
• the time origin will affect mainly 1 perfusion parameter, i.e. the time-related parameter named TTP (Time To Peak), which expresses the time in seconds from the time origin to the peak of the fitted curve.

The time-related parameter named TTP (Time To Peak) expresses the time in seconds from the time origin to the peak of the fitted curve, while RT (Rise Time) expresses the time from TI (the instant at which the maximum slope tangent intersects the x-axis) to the peak of the fitted curve, and is thus independent of the time origin. More information can be found in the user manual (Perfusion models).