Brain Follow-Up - Output Image Review
Having performed the brain follow-up analysis as detailed in the
Introduction, and
Options sections,
you can now review the output image for change.
Several output images are created, with the number depending on the number of time points and
image contrasts analysed. In this simple example, we analysed only two time points and a single
image contrast (proton-density-weighted MR images). The input images are as shown below:
|
|
Baseline |
Two-year follow-up |
These two scans were performed 2 years apart. Although the slices were carefully re-positioned for
the second scan, the patient's head is in a different position.
The Brain Follow-Up tool creates co-registered versions of each of the input images, with names
equal to the input images, but with the prefix 'r'. These co-registered images are shown below:
|
|
Baseline, after co-registration
|
Two-year follow-up, after co-registration
|
At first glance, there appears to be little difference between the images at the two time
points. However, the Brain Follow-Up tool also creates difference images (after correcting any
bias field differences). In this case, we gave the output image base name 'Test', so the
difference between time points 2 and 1 is called 'Test1_2'. This image is shown below for the same
slice:
|
Difference between the 2-year follow-up scan and baseline,
after bias field correction. |
In the difference image, the new periventricular lesion that has formed is readily apparent.
Review of all the image slices would reveal all newly-formed, enlarged, reduced or resolved
lesions. If you use the option
, it is only possible to
distinguish between new and resolved lesions, and between enlarged and reduced lesions by
simultaneously looking at the difference image, together with the two registered time point images.
Review is greatly assisted by loading these three images into
linked, spawned
displays.
Assisted Review
You can get Jim to load these three images (the difference image, together with the two
registered time point images) into three linked display windows by clicking on the
button. This will automatically load the difference image into Jim's main display, and the
registered time point images into two spawned slave displays. The
ROI Toolkits will also be
launched ready for you to make measurements of lesion volume changes on the registered images,
confirming the changes by referring to the difference image.
Note: you can only review the last set of results produced by the Brain Follow-Up tool in
this way, and if you make any changes to the setup between performing the analysis and requesting
the review, then the review may fail to display the correct images.