eFilmLite UserGuide
eFilmLite UserGuide
V 4.2
USER’S GUIDE
Merge Healthcare
900 Walnut Ridge Drive,
Hartland, WI 53029
USA
© Copyright 2018 Merge Healthcare Incorporated, an IBM Company.
The content of this document is confidential information of Merge Healthcare Incorporated and its use and
disclosure is subject to the terms of the agreement pursuant to which you obtained the software that
accompanies the documentation.
Merge Healthcare® is a registered trademark of Merge Healthcare Inc.
The Merge Healthcare logo is a trademark of Merge Healthcare Inc.
All other names are trademarks or registered trademarks of their respective companies.
This product is a "Commercial Item" offered with "Restricted Rights." The Government's rights to use,
modify, reproduce, release, perform, display or disclose this documentation are subject to the restrictions
set forth in Federal Acquisition Regulation ("FAR") 12.211 and 12.212 for civilian agencies and in DFARS
227.7202-3 for military agencies. Contractor is Merge Healthcare.
eFilm Lite is a software application that is used for viewing medical images.
eFilm Lite receives digital images and data from various sources (including but not limited to CT, MR, US,
RF units, computed and direct radiographic devices, secondary capture devices, scanners, imaging
gateways or imaging sources).
eFilm Lite can be used to communicate, process and display medical images.
Users have access to various image processing and measurement tools to assist them in viewing images.
In addition, users can overlay templates on medical images to aid in preoperative planning.
eFilm Lite can be integrated with an institution’s existing HIS or RIS for a fully integrated electronic patient
record.
Typical users of eFilm Lite are trained medical professionals, including but not limited to radiologists,
technologists and clinicians.
CAUTION: U.S. Federal law restricts this device to sale by or on the order of a
physician.
NOTE: The eFilm software complies with the MDD Council Directive 93/42/EEC of 14
June 1993.
Viewing Studies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Arranging Study Series in Panes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Viewing Study Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Setting the Encryption Password . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Adjusting the Screen Layout . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Selecting Images and Series . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Selecting Images. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Selecting Series . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Closing Studies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
• understand the layout of the eFilm Lite workspace (see “eFilm Lite Window” on
page 10);
• customize the eFilm Lite toolbar and access the Mini bar (see “Using the Toolbar” on
page 11); and
• understand the functions of the tools in the eFilm Lite toolbar (see “Using Tools” on
page 13).
Precautions
Due to limitations in data acquisition, eFilm cannot guarantee that the measurements are
accurate for Digital Radiography (DX), Computed Radiography (CR), Intra-oral Radiography
(IO) and Mammography (MG) images.
WARNING: eFilm cannot guarantee that the calibration data received from the
modality is accurate. We cannot guarantee that manual calibration
performed by users were done accurately.
NOTE: There is an inherent magnification effect and distortion when taking x-ray images.
NOTE: The application displays a warning that the measurement is approximate when
measuring on any projectional images.
System Requirements
This section describes the hardware and software required to run eFilm Lite.
Required Hardware
eFilm Lite must run on a computer that meets the following hardware requirements at a
minimum:
• 2GB RAM
When choosing computer hardware, users should note that the most substantial performance
gains result when RAM is increased. In order to prevent poor performance of the software,
Merge Healthcare recommends that eFilm Lite be run on more powerful systems than that
listed above.
NOTE: The eFilm application is tested with the English language version of the operating
systems noted above.
A video display adapter with at least 128 MB of video RAM that fully supports DirectX 9 or
later.
Refer to the product help files and the Merge Healthcare Web site at www.merge.com for the
most up-to-date system requirements.
NOTE: eFilm Lite should launch automatically when you insert a CD with DICOMDIR
images burned on it. If it does not launch, navigate to your CDROM directory and
double-click eFilmLt.exe.
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This window can contain more than one image at a time, each in a separate pane arranged in
a grid. The menu bar appears at the top of the window, and the status bar will appear at the
bottom (if enabled). By default, the tool bar appears at the top of the window directly beneath
the menu bar, but you can move it by following the procedure outlined in “Customizing the
Toolbar” on page 11.
To view the description of a tool, hold the cursor over its icon. Full descriptions of the tools can
be found in “Using Tools” on page 13.
• access the Mini Bar (see “Accessing the Mini Bar” on page 12)
11
NOTE: All tools are also found in the Tools menu; however, not all tools listed in this
menu are available on the toolbar.
Option Description
Standard Displays all of the toolbar icons relevant to the modality of the
study displayed in the eFilm Lite window.
Small, Medium, Large Adjusts the size of the buttons in the toolbar.
Status Bar Shows or hides the status bar at the bottom of the window.
By default, the Mini Bar includes the following six tools: Stack, Pan, Zoom, Window/Level,
Measurement Tool - Line and Reset Image Settings. This tool set is predefined; tools cannot
be added to the Mini Bar, but if you remove a tool from the toolbar, it will also not appear in the
Minibar (i.e., a tool will only appear on the Minibar if it is part of the eFilm toolbar). If the toolbar
is customized not to display any of the tools in this set, then those tools will not be displayed in
the Mini Bar. All of the tools on the Mini Bar can be assigned to either the left or right mouse
button except the Reset Image Settings tool.
Hold the right-mouse button and then click the left-mouse button. The Mini Bar pops up in the
area of the window where you clicked both mouse buttons.
12
Using Tools
eFilm Lite includes a large selection of tools to help you navigate and manipulate study
images. In this section, you will learn about the tools located on the toolbar. The tools are
grouped as follows:
• Common – apply to all modality types, including window/level settings, layout settings,
and other image viewing tools (see “Common Tools” on page 14)
• Multiplanar – work with MultiPlanar Reformatting (MPR) images (see “Multiplanar Tools”
on page 16)
• Image Manipulation – rotate, flip, and invert images, and related functions (see “Image
Manipulation Tools” on page 16)
• Volume – view and manipulate images in three dimensions (see “Volume Tools” on
page 17)
Main Tools
13
Common Tools
14
Next/Previous Tools
Measurement Tools
15
Multiplanar Tools
Show All Reference Lines Shows the location of all the images with
reference lines.
Show First and Last Shows the location of the first and last images.
Reference Lines
Show Current Reference Shows the location of the currently active image.
Line
Auto Series Synchronizes images that are related to each
Synchronization other spatially and scanned during the same
exam. For example, it will not synchronize images
from the same patient from different studies.
Flip Horizontal Flips the selected image from left to right about the
vertical axis.
Flip Vertical Flips the selected image from top to bottom about
the horizontal axis.
Rotate Left 90 Degrees Rotates the selected image 90 degrees counter
clockwise.
Rotate Right 90 Degrees Rotates the selected image 90 degrees clockwise.
16
Volume Tools
17
NOTE: When you have changed your preferences, you must re-select the study in eFilm
Lite for the changes to take effect to the image you are currently viewing.
NOTE: Your changes are saved when you exit, and your new preferences are the default
the next time that you use eFilm Lite.
• Change the default display settings for each modality (see “Customizing Modality
Settings” on page 18).
• Change your monitor setup (see “Customizing System Preferences” on page 22).
• Specify where and how to display image markers on images (see “Using Image
Markers” on page 23).
• Specify settings for images displayed as volumes (see “Customizing Volume Settings”
on page 25).
• The default layout for a modality (see “Changing Modality Layouts” on page 19).
• Advanced image display settings for a modality (see “Customizing Advanced User
Settings for a Modality” on page 20).
18
NOTE: This feature is useful for CR skeletal surveys where eFilm Lite loads the images in
survey mode. You can then follow the procedure outlined in “Exploding Series”
on page 58 to move between individual images and the survey mode.
2. Click the Modality Settings tab, and then click the Layout tab.
NOTE: If you want eFilm Lite to automatically create as many viewports that are
necessary to display all the series in an exam, select the AutoFormat check
boxes.
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2. Click the Modality Settings tab, and then click the Advanced tab.
4. Adjust the settings as required by selecting the options provided in the Advanced User
Settings pane. The defaults for each modality are Bilinear Interpolation and Simple
Window & Level algorithm.
20
• Mode:
• Select Bilinear Interpolation for a good compromise between speed and quality.
• Split multi-phase – Select whether eFilm Lite displays the original series after
splitting it into individual phases.
• Allow window leveling of individual images – Select if you want to be able to alter
the window/level settings independently for each image for this modality. Clear the
check box to have window/level settings apply to the entire series.
• Simple – Select to have the window and level values set to a mid-point between
the minimum and maximum values in the image.
• Histogram Analysis – Select to have the window and level values automatically
adjust based on image characteristics. This feature only works if the scanner
sending the image does not define the window and level settings.
• Hide stacking scrollbar – Select to hide the scrollbar for multi-image series (see
“Stacking Images” on page 40). This is recommended for modalities such as CR,
DX, and MG.
• Select the Preserve Presentation Intent in Viewports check box if you want to
preserve the presentation intent of the following image manipulation tools.
NOTE: The “Preserve Presentation Intent in Viewports” option is only for use with
Hanging Protocols.
21
• In Hardcopy, suppress the scale marker – Select this option to prevent the scale
marker from appearing on images you print.
NOTE: eFIlm now displays the standardized uptake values (SUV) for positron emission
tomography images when pixel value measurements are taken using the pixel
value tools. Four methods of SUV calculation are supported. You may manually
enter the information needed for these calculations.
22
3. To configure your monitor setup, select either the Single or Dual radio button, whichever
reflects the setup of your monitors.
WARNING: eFilm is not approved for FFDM diagnostic review. All digital
mammography images are for reference only.
23
NOTE: Digital mammography scanners attach image markers to their studies so that
breast images can be properly identified. The default setting for this tab is set to
display image markers. If you do not want image markers, then clear the Show
marker on Mammogram (MG) images check box.
1. Select either the By pixel offsets or By percentage offsets radio button, which position
the image marker either by pixels or by percentage respectively.
2. Move the position of the image marker by inserting values in the Horizontally and
Vertically fields. The preview screen refreshes according to your selection.
3. Select the corner from which the image marker is oriented by selecting the corresponding
corner. The preview screen refreshes according to your selection.
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• If you want to remove the border, clear the Show border around marker check box.
• If you want to keep the border, but change its size, select the Show border around
marker check box, and clear the Allow marker to calculate dimensions
automatically check box. The Width and Height fields are activated, so that you can
specify custom border dimensions.
NOTE: You can change the upper information font, select the Upper information option,
and select a font from the drop-down list. To change the lower information font,
repeat this step with the Lower information option.
2. To change the font size, clear the Use default size check box and select the appropriate
font size from the Size drop-down list.
25
1. Change the Angle value to increase or decrease the strength of the stereo effect.
NOTE: Increasing the angle increases the shift between the red and blue images.
2. Change the Z Offset value to make the stereo volume appear to float in front of or behind
the display surface. The default value places the stereo volume at the center of the
screen’s surface.
NOTE: To return the stereo settings to their default values, click Restore Defaults.
26
1. Select the Hide bounding box when not cropping. check box to hide the wire frame
surrounding the volume when it is not in crop mode.
2. Select the Suppress creation of oblique MPR view to keep eFilm Lite from generating
this view when Auto-Generate MPR is selected.
3. Change the Slice Separation for MPR Series (mm) value to adjust the slice spacing
used to create your MPR views.
4. Change the Initial location of range limit settings to adjust the default MPR range limits.
27
• Use the eFilm Lite viewer (see “Using the eFilm Lite Viewer” on page 28).
• Select individual or multiple images and series (see “Selecting Images and Series” on
page 35).
2. The pane lists the studies that are stored in DICOMDIR format on your CD.
Click a header to sort the list according to that heading. For example, click Name to sort the
list alphabetically, or click Patient ID to sort the list numerically.
NOTE: Clicking the header field again sorts the list in the reverse order.
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Click and hold the header you want to move, and drag-and-drop it to a new location.
Viewing Studies
Studies can be viewed using the procedures for the four exam tabs outlined in previous
sections. This section provide a general reiteration of those procedures. In addition to learning
how to view a study, this section describes how to:
• Arrange study series in the main window (see “Arranging Study Series in Panes” on
page 31).
• View information for a study (see “Viewing Study Information” on page 32).
• Set an encryption password (see “Setting the Encryption Password” on page 33).
• Change the layout of the screen (see “Adjusting the Screen Layout” on page 33).
29
To view a study
Select a study from the list and double-click it to view it automatically, or select a study from
the list and click View. The study opens in the main window, and the toolbar is activated.
NOTE: Images appear side-by-side in a grid (default setting = 1x2), like the films mounted
beside each other on a light box. This grid configuration can be adjusted by
following the procedure outlined in “Adjusting the Screen Layout” on page 33.
30
1. Right-click the pane where you wish to place the series. A menu appears, identifying the
series that is currently occupying the pane.
NOTE: When you load a study the right-click menu is first populated with a list of related
studies. The studies themselves are then loaded, starting with the most recent
studies and working backward to the oldest studies.
NOTE: The menu displays all the studies belonging to a patient, provided they are
available as local or Image Channel exams that correspond with the Patient ID.
3. If the series is currently displayed and you want to move it to another pane, hold Shift,
select the series you wish to move, and drag-and-drop it in a different pane.
31
NOTE: If confidential patient data is encrypted, you can decrypt it by entering the
encryption password (see “Setting the Encryption Password” on page 33).
NOTE: If the patient’s History field has more than 64 characters, only the first 52
characters appear, and <TRUNCATED> appears at the end of the line to indicate
that the field has been truncated for display.
32
1. Select Utility > Set Password. The Encryption Password dialog box opens.
3. Click OK to set the encryption password, or click Cancel to exit without setting it.
1. Choose one of the following options to access the Screen Layout dialog box:
33
• Click .
The Series layout determines the format of the panes in the window. Each pane can
contain one series. The Image layout determines the format of the images within the
active series.
2. Select a layout for the series/image, or define the values for rows and columns, and click
Apply.
NOTE: Different series may have different image formats. For example, a CT exam with
two series (one scout, one axial) may be displayed using a 1x2 series layout.
Furthermore, the images in the scout series may be displayed in a 1x1 format,
and the axials in a 2x2 format.
34
• A single image, multiple images, and all images in a series (see “Selecting Images” on
page 35).
• A single series, multiple series, and all series in a study (see “Selecting Series” on
page 36).
Selecting Images
These procedures enable you to select a single image, multiple images, or all images in a
series.
2. Select the selection box in the lower right corner of the image. The selection box fills in
orange to indicate that it is selected.
Selection
Box
1. View the first image that you want to select in any pane.
2. Select the selection box in the lower right corner of the image. The selection box fills in
orange to indicate that it is selected.
35
NOTE: Selected images remain selected as you scroll through the series. You can select
every other image in the series by clicking Select Every 2nd Image In Series on
the Edit menu.
1. Click a series in any pane in the window. The border around the selected series turns
green.
• Click .
Selecting Series
These procedures enable you to select a single series, multiple series, or all series in a study.
Click a series in any pane in the window. The border around the selected series turns green.
Hold Ctrl and click a number of series in any pane in the window. The borders around all of the
selected series turn green.
• Click .
• Press Ctrl + A.
36
NOTE: This tool only selects all currently displayed series. To select all series in a study,
adjust the screen layout to display the whole study (that is, all series) in the
window.
Closing Studies
After you are finished viewing a study, you can close the study without exiting eFilm Lite.
To close a study
• Click .
37
• Navigate through images in a series (see “Moving Through Images” on page 38).
• Navigate through series in a study (see “Moving Through Series” on page 42).
• Next/Previous Image: Enables you to move through the images of a series one at a time
(see “Using the Toolbar to Move Through Images” on page 39).
• Scrollbar: Enables you to either move through images one at a time or easily scroll
though the images of a series (see “Using the Scrollbar to Move Through Images” on
page 39).
• Stacking: Enables you to quickly and easily move through the images of a series (see
“Stacking Images” on page 40).
• Cine: Dynamically displays the stacked images for a video display viewing (see “Using
the Cine Tool” on page 41).
38
4. Specify the image order number and click Goto to display the required image.
Click the Up or Down arrow to move to the next or previous image in the series.
39
Click and hold the Up or Down scrollbar arrow to scroll forward or backward through the stack,
or click and drag the scrollbar bubble up or down.
Stacking Images
Stacking enables you to move quickly and easily through the images of a stacked series.
2. Choose one of the following options to define how you want the images to be sorted:
3. Select how you want to sort the images in the stack. You can sort by Image Number,
Slice Location, Reverse Slice Location, Acquisition Time, or Image Time. Position the
mouse pointer over the series, and click and drag it up or down within the pane.
NOTE: The image number displayed for an image in eFilm may not be sequential as it
depends on the image number present in the DICOM instance.
NOTE: Stacking becomes faster once you have loaded all images in a series into memory
by viewing them. To automate this, you might consider using the Cine tool (see
“Using the Cine Tool” on page 41).
40
• Click .
• Loop repeatedly displays the sequence from the first to the last image in a series.
• Shuffle moves back and forth through the images between the first and last one in a
series.
41
NOTE: You can also right-click on any image to open a menu from which you can select
the required series.
• Click .
• Click .
• Click .
• Click .
42
Synchronizing Series
The Synchronizing tool enables you to bring all series in the same plane into alignment. This
tool uses the series slice location to line up image navigation for these series in panes. With
synchronization, you can navigate through the images of one series (scroll, cine), and all other
series with images in the same plane navigate accordingly.
1. Select the image/plane with which you want all others to synchronize.
• Click .
If you detect an offset in the images, you can manually synchronize the images (see
“Synchronizing Series Manually” on page 43).
43
1. Scroll through each series and display the images you want to synchronize.
• Click .
• Click .
2. Right-click on any displayed 2D image. This same point is indicated on all other 2D
images, regardless of the plane, by a +. In order to find the point in another series, eFilm
Lite may need to display different slices in those series. Not all points in the current
images necessarily exist on other series. In this case, the + sign is not displayed.
3. You can drag the point around the image and the corresponding points in the other images
move accordingly. You can navigate through the images (stack, cine) and you see the
point in 3D space.
44
• Adjust window/level settings for images (see “Setting Window/Level Values” on page 45).
• Overlay reference lines on an image (see “Overlaying Reference Lines” on page 50).
• Adjust your view of an image (see “Adjusting Image Viewing Options” on page 53).
• Reset image settings (see “Resetting the Original Image Settings” on page 57).
• Adjust your view of a series (see “Adjusting Series Viewing Options” on page 57).
• Split multi-phase series into separate series (see “Splitting a Series” on page 69).
• Use non-linear window leveling (see “Using Non-Linear (Sigmoidal) Window Leveling”
on page 49).
45
Adjusting Brightness
• Click .
2. Position the cursor over the image to be adjusted, and right-click and drag the cursor up or
down over the image.
3. Release the mouse button to apply the new values to all images within the series. These
values are displayed on the lower left corner of each image (for example, W:33/L:777).
Adjusting Contrast
• Click .
2. Position the cursor over the image to be adjusted, and right-click and drag the cursor left
or right over the image.
3. Release the mouse button to apply the new values to all images within the series. These
values are displayed on the lower left corner of each image (for example, W:33/L:777).
46
NOTE: To achieve a finer resolution with window leveling, use the arrow cursor keys (up
and down to adjust brightness, and right and left to adjust contrast). To
compensate for any inherent non-linearities in an image, use non-linear window
leveling (see “Using Non-Linear (Sigmoidal) Window Leveling” on page 49).
The sensitivity of the manual adjustment is set by a relative number. If the change between
window levels is too sensitive and changes too much while you are moving the cursor over the
image, then lower the sensitivity value. If the change between window levels is not sensitive
enough, then increase the sensitivity value.
2. Adjust the sensitivity value either by using the up or down arrows, or by entering the
specification manually. The specification is a relative number that you define.
3. Click OK.
NOTE: When you change the sensitivity, the new value becomes the default and is
applied to all images and studies until it is changed again.
NOTE: Avoid pressing the window/level key presets repeatedly while viewing 3D images,
unless you are viewing these images using DirectX 9.0.
47
2. Click the arrow to the immediate right of . The Window/Level menu opens.
3. Select a preset from the menu. Alternatively, you can use the Function keys (as specified
in the menu) at the top of the keyboard, or press F2 to scroll through all the window/level
presets.
Code Description
You can specify custom window level values using the following procedure.
1. Select a series.
4. Adjust the Window and Level values by using the spin arrows, or by entering the values
manually. These specifications appear in the lower left hand corner of each pane (for
example, W:50/L:100).
5. Click Apply to save the changes, or click Cancel to exit without saving any changes.
48
1. Select a series.
3. Select Sigmoidal. The non-linear window leveling function is applied to the image and
is automatically activated.
2. Position the cursor over the image to be adjusted, and click and drag the cursor left or
right over the image to adjust its coherence (Alpha).
3. Position the cursor over the image to be adjusted, and click and drag the cursor left or
right over the image to adjust its black/white bias (Beta).
4. Release the mouse button to apply the new value to all images within the series. This
value is displayed on the lower left corner of each image (for example, A:4.00 B:5.00).
49
Inverting Images
Inverting enables you to invert the sense in which the brightness of displayed pixels is
calculated. By default, low intensity pixels are dark on the screen, and high intensity pixels are
bright. Using the Invert tool changes the intensity so that low intensity pixels are bright and
high intensity pixels are dark. Applying this tool again restores the previous pixel intensity
setting.
• Click .
You can show any or all of the following with this function:
• Location of all image slices of the selected series on all intersecting planes
50
1. Select an image.
• Click .
NOTE: The number at the end of each line is the image number. The image number
displayed for an image in eFilm may not be sequential as it depends on the image
number present in the DICOM instance.
1. Select an image.
• Click .
51
1. Select an image.
• Click
NOTE: As you scroll through the images of a series, the current reference line on other
images changes accordingly. You can view the first and last reference lines and
current reference line at the same time.
52
Tools > Flip Horizontal Flips an image 180° on the horizontal axis
Tools > Flip Vertical Flips an image 180° on the vertical axis
NOTE: These functions are applied to all selected series and images in the selected
series.
53
Panning
Panning enables you to position images within the pane. This feature is especially useful when
the image is larger than the pane, as it usually is after zooming.
• Click .
2. Position the cursor over the image you want to move, and click and drag the cursor
around the pane to move the image.
3. Release the mouse button to drop the image in its new position.
NOTE: To restore the original image display value (except window/level), click .
54
Magnifying
Magnifying enables you to magnify an area of interest within a small, separate magnification
window that moves in conjunction with the cursor.
2. Select one of the following percent magnification values: 200%, 400%, 600%, or 800%.
3. Click and drag the mouse over the area of the image you want to magnify. The magnifying
window opens and follows the cursor as it magnifies the selected area.
55
Zooming
There are three methods of performing zooming: manual, preset, and custom zooming. Pixel-
for-pixel mode, which treats each pixel in the DICOM image as one pixel on your monitor, is
also available in this section.
NOTE: Images with a 1:1 pixel aspect ratio look normal when pixel-for-pixel mode is
applied; however, images with a different pixel aspect ratio look compressed in
one direction, as this feature represents actual pixels, but not presentation intent.
In these cases, you must exit pixel-for-pixel mode by selecting another zoom
value.
• Click .
2. Position the cursor over the image, and right-click and drag. Dragging up increases the
image zoom and dragging down decreases it.
3. Release the mouse button to keep the image at the new zoom setting.
NOTE: You can select one of the preset zoom values or create a custom value.
3. Adjust the zoom value either by using the spin arrows, or by entering the value manually.
56
NOTE: To restore the original image display value (except window/level), click .
• Click .
• Increase or decrease the size of the image panes used to display a series (see
“Exploding Series” on page 58).
• Apply or remove the modality shutter (see “Toggling the Shutter” on page 59).
• Match series in the same plane to scale (see “Matching Field of View” on page 60).
57
Exploding Series
The explode mode changes the layout of a selected series so that it fills the entire main
window, while the survey mode reverts to the original series display. This function is especially
useful for skeletal surveys or any study that has multiple series.
• Click .
58
The same functionality can be achieved for images within a series. Select an image and
double-click it so that it fills the entire series pane. Double-click it again to return to the survey
mode.
• Click .
59
• Click .
1. Select a series.
• Click .
60
3. Using the slider, adjust the Mask value to correspond with the slice number of the image
that is to be subtracted from all other images.
NOTE: The mask is usually the first image in a series; however, in certain cases, it may
not be the first one.
4. Adjust the Integration value using the slider. This adjustment corresponds to how many
images you want to integrate.
NOTE: Integration allows a representation of how the dye flows through the vessel over
time. You cannot integrate more images than are in the current series.
5. Using the slider, adjust the Bone value to the required value. This value adjusts the
intensity of the image.
NOTE: Alignment is a manual control used for greater image clarity. This feature aligns
the image in relation to the selected mask.
8. Click X in the top right corner to close the Digital Subtraction Angiography dialog box. Your
changes are applied to the selected series.
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Using Filters
You can manipulate displayed images in a number of ways, using image operations that you
can define by programming compatible custom image manipulation plug-ins for eFilm Lite.
The capacity to use an infinite range of custom imaging effects greatly extends eFilm Lite’s
image manipulation abilities. Consult the following notes:
• Two sample filters are included in eFilm Lite: the Contrast Enhancement Filter and
Sharpening Filter. Both filters operate on any type of modality, pixel representation, and
photometric interpretation supported by eFilm Lite. The Contrast Enhancement Filter
improves image contrast, while the Sharpening Filter enhances edges by subtractive
smoothing.
• Both of the sample filters provided with eFilm Lite are Dynamic Link Library (DLL) files and
may be used as plug-ins for eFilm Lite or any other imaging program.
• A proper interface between eFilm Lite and any custom DLL is needed for successful
operation of the plug-in.
• Source code is only available for the Contrast Enhancement Filter. This code is intended
to assist in custom filter development. Please consult our Web site at www.merge.com
for more information on developing custom image manipulation plug-ins, or contact a
Merge Healthcare service engineer.
• Add a filter to eFilm Lite (see “Adding Filters to eFilm Lite” on page 62).
NOTE: Changes to pixel values are temporary and are not seen if the study is closed and
reopened. Changed images can be added to the scrapbook but are not saved as
part of key image description.
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• Click .
3. Select the filter you want to use from the menu of currently added filters, either
eFilmClaheFilter or eFilmSharpening.
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• Click .
In the case of the CLAHE (Contrast Limited Adaptive Histogram Equalization) Filter, the
CLAHE Filter Settings dialog box opens.
2. Adjust the Clip Limit Value (1-10 000). Increased clip limits correspond to increased
image contrast. The default value is 1, which indicates no filtering.
3. Adjust the Number of Contextual Regions (2-16). The Horizontal value determines the
width of the image, and the Vertical value determines the height of the image. The default
value of each of these parameters is 2. A higher valued is usually optimal. Both sample
filters require some user experimentation in order to achieve the optimal values for each
parameter.
NOTE: The only parameter provided in the Sharpening Filter Settings dialog box is Mask
Size. This parameter is expressed in pixels and is restricted to four options. A
higher Mask Size requires a longer processing time; however, the parameter
option chosen must be appropriate for the size of the image being manipulated.
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NOTE: If you change the filter settings and want the settings to be applied to the selected
image, you must either click Apply Image Filter on the Tools menu or click
. Image filter settings are not applied automatically.
• Fuse images from a two-modality image series together (see “Fusing Images from Two-
Modality Image Series” on page 65).
• Adjust the Alpha setting (see “Adjusting the Alpha Setting” on page 67).
• Configure the image fusion pipeline (see “Configuring the Image Fusion Pipeline” on
page 67).
• Click .
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The Fusion Series Generator dialog box opens, which indicates the progress of the image
fusion stage.
3. When generated, the fused series opens in the right-hand pane of the main window, while
the background series opens in the left-hand pane and the foreground series opens in the
middle pane.
NOTE: The default settings of image fusion are that the PT images appear in the
foreground and CT images appear in the background.
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• Click the arrow to the immediate right of and Select Alpha Blend. The Alpha
control bar opens.
NOTE: Any Alpha setting greater than 50% means more of the foreground image than the
background is contributed to the fused image; whereas any Alpha setting less
than 50% means more of the background image is contributed to the fused image
than the foreground. The blend value is saved in the current user’s profile.
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• Click the arrow to the immediate right of and select Image Fusion Pipeline.
The Image Fusion Pipeline dialog box opens.
• Color: displays the color range of the foreground as varying shades of the color
specified by clicking Select Color and selecting a color from the Color dialog box.
• Color Mapping: displays the color range of the foreground as varying shades of the
color specified by selecting a mapping from the drop-down list (for example,
Rainbow).
NOTE: The colored bar on the right offers a preview of the blend that is applied to the
fused series. All settings are saved in the current user’s profile.
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5. The following table shows the default color mappings and corresponding colored bar that
can be applied to the foreground image.
HotMetal
Rainbow
Rainbow16
Rainbow65
Bronson
6. Click OK.
NOTE: Advanced users can add new color mappings or modify existing ones from the
ColourMapping.txt file in the installation folder. We recommend that you save a
backup copy before editing this file.
Splitting a Series
eFilm Lite can split a series that has overlapping images (such as a multi-phase series) into
multiple series, one series per phase. You can set eFilm Lite to do this automatically (see
“Customizing Advanced User Settings for a Modality” on page 20) or split a multi-phase
series manually. The only difference between the two is that manual mode enables you to
select which series are split and when, and automatic mode splits all multi-phase series when
the study is loaded.
NOTE: The original series may or may not be included in the right-click menu following
the split, depending on how the advanced settings for that modality are
configured.
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• Click .
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• Measure the angle between two lines on an image (see “Displaying Angle
Measurements” on page 78).
• Determine the pixel or Hounsfield value of a point on an image (see “Probing Images”
on page 82).
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Overlaying Text
Toggling the overlay hides or shows the displayed study information for a series and the scale
marker.
1. Select a series.
• Click .
3. To display the written information again, select the series and click again.
NOTE: If you applied lossy compression to the image, its identifier and compression ratio
is not hidden, even when this tool is off. Lossy compression information, where
relevant, is always visible.
Annotating Images
The annotation tool enables you to add text to images, and then edit or delete the text.
Annotations can be added to an image to describe certain features in more detail. You can
copy your annotations and measurements to other images in the study.
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To add an annotation
1. Select an image.
• Click .
3. Click the area in the image where you want to add the annotation. A text field opens.
5. When completed, press Enter, or click again. The annotation is set in the image.
NOTE: Loading a different series into the series window after adding an annotation
causes the annotation to be lost unless you have saved the image to a scrapbook
or as a key image.
To edit an annotation
You can edit an annotation by selecting it and then editing the text as necessary. You can drag
and drop the annotation anywhere on the image.
Annotations can be removed from an image if it is affecting the clarity of the image.
To delete an annotation
NOTE: To remove an annotation from all images in a series to which it was copied, select
Delete All instead.
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(0018,1114) is used to adjust the Imager Pixel Spacing value (0018,1164) to account for
geometric magnification. In this scenario, the application appends the calibrated label to the
measurement. The application also displays the ERMF value in the DICOM Overlay.
• Click .
2. Position the cursor at the starting location, and right-click and drag the cursor to the
ending location.
3. Release the mouse button. A line with a distance measurement appears in green.
You can stretch the line or move it to a new location. You can also move the measurement
caption to a new location.
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Left-click anywhere on the line except at the ends and drag it to a new location.
NOTE: A line that appears in blue indicates that the line is selected and can be
manipulated. An unselected line appears in orange.
• Click .
2. Position the cursor at the starting location, and right-click and drag the cursor to the
ending location.
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3. Release the mouse button. An ellipse with Area, Mean, and Standard Deviation
measurements appears.
You can stretch or move the ellipse to a new location. You can also move the measurement
caption to a new location.
Left-click one of the corner markers (+) and drag-and-drop it to a new location.
Left-click anywhere on the ellipse and drag-and-drop it to a new location. The ellipse turns
blue and the cursor changes to a four-pointed arrow when the mouse is in position to move the
ellipse.
NOTE: An ellipse that appears in blue indicates that the ellipse is selected and can be
manipulated. An unselected ellipse appears in orange. If the measurement
caption has been moved independent of the ellipse, moving the ellipse no longer
moves the measurement caption as well.
Drawing Arrows
You can draw arrows to point to an area of interest on the image.
To draw an arrow
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• Click
2. Position the cursor at the source (the arrow tail), and right-click and drag the cursor to the
destination (the arrow head).
3. Release the mouse button. An arrow appears in green with an annotation box, in which
you can type notes.
NOTE: An arrow that appears in green indicates that the arrow is selected and can be
manipulated. An unselected arrow appears in orange. When moving the arrow,
the annotation box does not move with it. To move the annotation box, click and
drag the annotation to a new position on the image.
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• Click .
1. Right-click the annotation or measurement and select Copy. A copy of the selected
annotation or measurement appears on the current image.
1. Mouse over the annotation or measurement you want to copy. The annotation turns blue
once you can select it.
2. Right-click and select Copy To All. The annotation or measurement should now appear
on all images in the series.
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Calibrating Images
Calibrating enables you to manually specify the image pixel size for images which are not
automatically calibrated or which you want to recalibrate due to magnification errors. Only
Computed Tomography (CT) and Magnetic Resonance (MR) studies are automatically
calibrated accurately; all other studies should be calibrated manually.
To calibrate an image
1. Select the image you want to calibrate, and follow the procedure outlined in “Making
Linear Measurements” on page 74 to create a line overlaying a bit of the scale to the
right of the image.
2. Count how long the line is according to the scale (in this example, the line is 4 hashmarks
long).
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3. Select the line by right-clicking anywhere on it. The line appears in blue.
• Click .
5. Specify the length in centimeters of the line you drew, as measured by the scale on the
image, and click OK.
NOTE: Due to variable scaling per image, each image must be calibrated individually.
7. When an image is calibrated, you can change its measurement units back to pixels by
entering 0 as the length value in the Measurement Calibration control bar.
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Probing Images
Probing enables you to query the image intensity values.
• Click .
2. Click anywhere on the image and hold the mouse button down to view the value at that
point. The Hounsfield value (for CT) or pixel value (for all other modalities) is displayed.
NOTE: If the units of measure are present in the DICOM information, they are displayed
after the Pixel Value.
Labeling a Spine
You can label the vertebrae of a spine using predefined annotations. You can use text
annotations, or text annotations with adjustable arrows. The predefined annotations refer to
the spinal column as follows:
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• C1 to C7 — Cervical vertebrae 1 to 7
• L1 to L5 — Lumbar vertebrae 1 to 5
• S1 to S5 — Sacrum vertebrae 1 to 5
To label a spine
1. Select a series.
• Click .
4. In the Scope section, select how the application should apply the labels:
• One Image — Select this option if you want the application to only apply the labels to
the current image.
• All Images — Select this option if you want the application to apply the labels to all
images within the series.
• Select the Enable Scroll Wheel check box if you do not want to preselect the labels.
This option enables you to access all labels by scrolling the mouse wheel. After you
select this check box, click C1 and click Go.
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NOTE: If you select this option, you cannot scroll through the images in the series using
the mouse wheel.
• Click the desired labels to select them. When you are finished, click Go.
Selected labels
6. If you selected Text Only in step 3, click in the image to insert the text label in the desired
location. If you selected Text and Arrow in step 3, position the arrow head by the desired
location, then click in the image.
NOTE: If the viewport is not currently displaying the desired image, you can roll the
mouse wheel to scroll to the desired image before inserting the label.
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NOTE: If you selected Enable Scroll Wheel in Step 5, scrolling the mouse wheel only
changes the label attached to your cursor. Scroll the mouse wheel until it displays
the desired label, then insert the label in the image.
7. After you have inserted one label in the image, the application attaches the next label to
your cursor. Repeat step 6 until you have inserted all the selected labels.
NOTE: The application attaches the labels to your cursor in sequential order (for
example, T 9, then T10, then T11 and so on).
NOTE: If you selected Enable Scroll Wheel in Step 5, double-click to insert your last label.
• Change the angle of the arrow (see “To change the angle of an arrow” on
page 85).
• To change the angle of an arrow, click and either endpoints of the arrow its new
position.
• To insert and change the angle of the arrow at the same time, position the arrow head
at the desired location, then click and drag to draw the angle of the arrow.
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To reposition a label
You can reposition both the location of the arrow and the text annotation.
2. When your cursor changes to , click and drag the item to its new location.
To edit a label
2. When the background of the text annotation changes from black to white, and the cursor is
a blinking I-beam in the text annotation, type the new annotation.
Clearing Measurements
If you do not want any measurements on the images of a series, you can remove them all at
once.
1. Select a series.
• Click .
NOTE: To remove the measurement from all images in a series, select Delete All.
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• About the volume rendering techniques supported by eFilm Lite (see “3D Modes” on
page 87).
• How to create MPR images (see “Creating MPR Views” on page 103).
3D Modes
eFilm Lite includes several 3D imaging techniques:
NOTE: MPR views are normally created from a 2D dataset; however, if volume rendering
is not available (see below), you can create an MPR view from a 3D volume.
• Maximum Intensity Projection (MIP) – An interpolation technique that passes rays through
a data set, that finds and displays the maximum intensity pixel value along each ray. This
value is used as the final pixel value for the ray. You can rotate, crop, and window/level an
MIP.
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• Volume Rendering – This technique projects a volume onto a screen image pane,
assigning colors based on an opacity map. The opacity map determines how opaque each
intensity value should be rendered, and which color the value contributes to the resulting
image.
NOTE: Volume rendering is only available on computers that have compatible video
cards. If volume rendering is not available, you can create an MPR view from a 3D
volume.
• Simgram™ Image – A mode that uses Holorad’s patented Simgram algorithm to simulate
the appearance of a holographic 3D Voxgram® image on your 2D screen. You can rotate,
crop, and window/level a Simgram image. eFilm Lite provides a simple way to send the
data to Holorad for production of a real holograph. Simgram images simulate the
transparency of Voxgram images and retain grayscale information.
NOTE: 3D functionality is only supported for CT and MR studies, because only these
types of studies contain orientation information on slices.
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Using 3D Images
This section describes how to create, configure, and manipulate Maximum Intensity Projection
(MIP), volume rendered, and Simgram images. This section describes how to do the following:
• Adjust the loading parameters for 3D images (see “Adjusting Loading Parameters for
3D Volumes” on page 92).
• View 3D images in stereo display mode (see “Viewing 3D Images in Stereo Display
Mode” on page 96).
• Set all pixels outside the conventional window to black (see “Using the Black Outside
Window Setting” on page 97).
• Adjust mapping settings for volume rendered images (see “Adjusting Mapping Settings
for 3D Volumes” on page 97).
• Order a hard-copy Voxgram image matching a Simgram image (see “Ordering Voxgram
Images” on page 102).
Creating 3D Images
This method enables you to create an MIP, volume rendered, or Simgram image as a 3D
volume.
To create a 3D image
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3. Select either MIP, Volume, or Simgram Image as the 3D mode. The Advanced Volume
Loading dialog box opens.
NOTE: The selected 3D mode becomes the default mode until you choose another. This
means you can access the Advanced Volume Loading dialog box directly by
clicking the View 3D button.
4. Adjust the loading parameters (see “Adjusting Loading Parameters for 3D Volumes”
on page 92), and click Create Volume. The 3D image appears in the main window.
5. (Optional) Export the 3D volume in AVI format (see “Exporting Volumes to AVI Files” on
page 118).
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NOTE: If you are creating a volume rendered image, you may want to adjust the color or
grayscale opacity mappings and recreate the volume. See “Adjusting Mapping
Settings for 3D Volumes” on page 97 for information on working with opacity
maps.
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The top left window provides a graphical representation of the slice distribution of the series
and indicates which slices are available for inclusion in the volume. White slices are included,
red slices are excluded, and the green slice is the currently selected slice in the thumbnail
display.
The top right window displays thumbnails of the slices in the series. You can drag the slider to
browse through all available slices. As you adjust the slider to browse through the slices, the
thumbnail, Slice Info, and which slice is highlighted in green are updated to correspond with
the selected slice.
1. In the Series Subset area, use the From and To spinners to narrow the range of images
that are used to create the volume.
2. To exclude only a particular slice instead of a range, browse through the available slices
until you reach the one you want to exclude. Under Slice Info, clear the Include in
Volume check box.
3. Click Reset Selection to return to the default setting of including all the slices in the
volume.
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NOTE: The following parameters can optionally be adjusted to improve the result.
3. By default, Auto is selected. This option automatically selects the best interpolation pixel
spacing that can be handled by your current memory availability.
NOTE: The Memory Required box displays the memory required to load the volume with
the currently selected slices and interpolation settings. Compare this value to the
Memory Available box, which displays the total memory currently available on
your system. If the Memory Required exceeds the Memory Available, you
cannot load the volume using the current settings. In this case, you must reduce
the number of slices you are attempting to use.
Cropping 3D Volumes
Cropping enables you to crop a volume in all three dimensions. This feature enables you to
identify a volume-of-interest and remove the other parts of the volume from the display.
To crop a volume
• Click .
2. Using the sides of the blue volume cube as your cropping planes, position the cursor over
the edge of the cube you want to crop. Click and drag the cursor in the direction you want
to crop.
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3. Release the mouse button to set the new boundary of the cropped volume cube.
4. The following notes pertain to both the 3D rotating and cropping tools:
• The left mouse button is used for 3D rotating and cropping. Rotating is the default
active tool. As you move the cursor over the edge a cropping plane, the cursor shape
changes to the cropping symbol, indicating that the cropping tool is now the active
tool.
• When in crop mode, the highlighted plane indicates the side of the cube that is resized
when you click and drag the mouse.
• You can combine cropping, rotating and windowing in any order. At first, you may find
it easier to crop in one of the preset rotations: Anterior, Posterior, Left, Right,
Superior, or Inferior, which are outlined in “Rotating 3D Volumes” on page 95.
• While cropping, all parts of the volume outside of the cropped volume are displayed at
a reduced brightness to help you understand the context of what is in and what is out.
Once you have finished cropping, toggle the crop icon to display only the cropped-in
volume.
5. Since the cropped volume is smaller, it can be rendered faster. To improve rendering
speed, once you have cropped your volume, click to display only the cropped
volume.
NOTE: You can reset the crop by clicking Reset on the Crop Volume menu.
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Rotating 3D Volumes
There are two ways to rotate a volume: manually or preset selection.
• Click .
2. Position the cursor over the volume, left-click and drag the cursor over the volume. The
volume rotates in the direction of the mouse movement.
3. Release the left mouse button to set the volume at the new rotation.
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3. Select either Anterior, Posterior, Left, Right, Superior or Inferior to rotate the volume to
one of the standard anatomical orientations.
4. The cube in the bottom right corner of the image pane shows the current rotation of the
volume.
NOTE: You can also use the Flip Horizontal/Vertical and Rotate 90 Degrees Clockwise/
Counter Clockwise tools to change the orientation of the image (see “Changing
Image Orientation” on page 52).
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NOTE: You cannot rely on this mode when making clinical decisions. Stereo effect has
significant limitations, depending on your position relative to the screen. As you
move left or right, up or down, the stereo volume warps. As you move closer or
further away, the stereo volume shrinks or expands respectively. If you turn your
head so one eye is above the other, the stereo effect vanishes.
• Click .
2. To change the strength of the stereo effect, adjust the stereo display settings.
NOTE: You cannot activate the volume MPR tool while in stereo mode (see “Creating
MPRs from 3D Volumes” on page 106).
• Click the arrow to the immediate right of and select Black Outside Window.
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NOTE: These settings only apply to volume rendered 3D images, not MIP or Simgram
images.
The Opacity Settings tool enables you to assign color mappings to ranges within a CT or MR
study. This feature is only available for volume rendering; it does not function with Simgram or
MIP images.
• Click .
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3. Click the + or – buttons to zoom in or out on the graph, and the < or > buttons to pan left or
right.
NOTE: The Pan options become available once you zoom in.
4. Select the number of bands for the series. Bands define the range of values in a data set
to which specific colors can be assigned. This is useful in highlighting different types of
tissue for diagnostic purposes. The number of bands is limited to 20.
5. Select a band range between the blue dashed lines. The current range bounds appear in
white.
7. Select a basic color or create your own custom color to use as the new color mapping.
8. To create a custom color, use the color selector on the right, or adjust the RGB values
directly, and then click Add to Custom Colors.
9. Click OK to save your changes, or click Cancel to exit without saving any changes.
10. Adjust the Left Bound and Right Bound values. These values define the boundaries for
each band range.
11. Adjust the Opacity and Sharpness values. Opacity illustrates the intensity of the color
value. Sharpness illustrates the clarity of the color value.
12. Click the X in the upper right-hand corner to close the Color/Opacity Settings dialog box.
The image is updated according to the new color mapping.
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NOTE: To save these settings to the Preset menu, follow the procedure described in
“Editing Color/Grayscale Mappings” on page 102.
The Opacity Settings tool enables you to assign grayscale mappings to ranges within a CT or
MR study. This feature is only available for volume rendering; it does not function with
Simgram or MIP images.
• Click .
3. Click B/W Setting. The Grayscale Opacity Settings dialog box opens.
4. Click the + or – buttons to zoom in or out, and the < or > buttons to pan left or right.
NOTE: The Pan options become available once you zoom in.
5. Adjust the Sensitivity value. The Sensitivity value specifies the increment by which the
Window/Level and Opacity values change when adjusted. You can also set this value by
following the procedure outlined in “Adjusting Manual Window/Level Control
Sensitivity” on page 47.
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6. Adjust the Window and Level values. Select the Invert check box to switch the Window
value from white to black. Clear the Invert check box to switch this value from black to
white.
7. Adjust the Opacity Slope and Position values. Select the Invert check box to switch the
Slope value from white to black. Clear the Invert check box to switch this value from black
to white.
8. Click Auto Opacity Setting to automatically create a straight opacity angle, or DICOM
Setting to revert to the Window/Level settings defined in “Specifying Custom Window/
Level Values” on page 48.
NOTE: To save these settings to the Preset menu, follow the procedure described in
“Editing Color/Grayscale Mappings” on page 102.
9. Click the X in the upper right-hand corner to close the Grayscale Opacity Settings dialog
box. The image is updated according to the new grayscale mapping.
A number of predefined color and grayscale mappings (grouped by anatomical regions) are
available, which you can load from the Preset menu.
• Click .
2. Select the color mapping name from the drop-down list, and click Load Presets.
NOTE: If you are using B/W Setting, the presets displayed produce grayscale images
(see “Assigning Grayscale Mappings to 3D Volumes” on page 100).
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1. Load the color or grayscale mapping that you want to edit (see “Loading Color/
Grayscale Mappings” on page 101).
NOTE: To remove a color or grayscale mapping, select it and click Delete Preset.
• Click the arrow to the immediate right of and select Order Voxgram. The
Voxgram Image Preview pane opens.
NOTE: You can open the Voxgram Image Preview pane from an interactive Simgram
image by pressing Alt+V.
NOTE: Do not burn entire studies to a CD or send entire studies to Holorad for Voxgram
image production. Hologram production requires additional information which is
assembled during the process of ordering a Voxgram image.
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3. For help ordering a Voxgram image, click Help in the Voxgram Image Preview pane.
You can create MPR views of an existing data set from either 2D images or 3D volumes. From
a 2D image, the MPR view you generate creates a viewing plane that is perpendicular to the
image plane. From a 3D volume, the MPR view you generate creates a viewing plane that can
be rotated to any angle relative to the original image plane.
NOTE: You can only generate MPR views of a 3D volume if your system does not meet
the hardware requirements to support volume rendering.
Once created, an MPR series behaves the same as a regular eFilm Lite image series. You can
use most of the eFilm Lite tools, such as window/level, stack, zoom, pan, measurements, and
reference lines, on the MPR series. However, you cannot apply any 3D image tools to the
MPR series until it is saved to the database.
NOTE: Once an MPR series has been saved and closed, you can reopen it and apply 3D
image tools to it (see “Saving and Deleting MPR Views” on page 113).
• Create MPRs of the two orthogonal viewing planes from a 2D image (see “Creating
Orthogonal MPR Viewing Planes” on page 104).
• Create MPRs of an arbitrary perpendicular viewing plane from a 2D image (see “Creating
MPRs from 2D Images” on page 105).
• Create MPRs of an arbitrary viewing plane through a 3D volume (see “Creating MPRs
from 3D Volumes” on page 106).
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• Interact with the MPR series you have created (see “Interacting with MPR Series” on
page 107).
• Adjust your view of the MPR (see “Adjusting the MPR View” on page 108).
• Create a slab from the MPR view (see “Creating MPR Slabs” on page 113).
• Save or delete the MPR view (see “Saving and Deleting MPR Views” on page 113).
NOTE: The oblique view is optional; you can set eFilm Lite to create or omit this view in
the Edit Properties window (see “Customizing Volume Settings” on page 25).
• Click .
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3. The MPR views are generated and the screen layout is automatically adjusted to 2 x 2
(unless four viewports are already configured), displaying the original series in the top left
corner and the three MPR series in adjacent viewports. The oblique view, if generated, is
shown in the lower right viewport.
NOTE: You can adjust your MPR view by manipulating the MPR lines (see “Adjusting
the MPR View” on page 108).
4. With the original series selected, click again to remove these lines and corresponding
views.
• Click .
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3. Position the cursor at the starting location, and right-click and drag the cursor to define the
viewing plane.
4. Release the mouse button. A line appears in green, which represents a perpendicular
plane passing through the data set to create the MPR viewing plane.
NOTE: You can only generate MPR views of a 3D volume if your system does not meet
the hardware requirements to support volume rendering.
NOTE: You cannot enter stereo mode while the volume MPR tool is active (see “Viewing
3D Images in Stereo Display Mode” on page 96).
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• Click .
NOTE: With the original series selected, click again to remove the MPR plane and
the corresponding MPR view. If you want to save the MPR view, remove the MPR
plane.
• The MPR series that you created are added to the right-click menu for the selected study.
To view an MPR series, right-click in an open pane and select the MPR series.
• If you right-click on the series that contains the MPR line and select a different series to
load into that pane, you are prompted to save or delete the corresponding MPR as a
series view.
• If you close the study prior to saving the MPR series, the MPR series are lost and must be
recreated when you reopen the study.
• You can adjust your MPR view by manipulating the MPR lines (for 2D images) or by
manually rotating the plane independent of the volume, by highlighting the plane to select
which item you want to rotate (for 3D volumes). For details, see “Adjusting the MPR
View” on page 108.
• You can adjust the slice separation used to create your MPR view on the Volume Settings
tab of the Edit Properties window (see “Customizing Volume Settings” on page 25).
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• Rotate and resize the MPR line: this adjusts the size and angle of the MPR view, allowing
you to focus on a particular area of the screen.
• Adjust the range lines to restrict the number of images in the MPR view.
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1. Left- or right-click either end of the MPR line. The cursor changes to a + and the line
changes color from orange to green.
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1. Left- or right-click anywhere on the MPR line. The cursor changes to a four-headed arrow
and the line changes color from orange to green.
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1. Left- or right-click anywhere on one of the range lines (the dotted lines on either size of the
MPR line). The line changes from orange to green.
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You can also move the MPR line by stacking through the slices on the MPR view. As you stack
through the slices, the MPR line is dynamically updated to reflect the new viewing plane on the
original image.
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1. Left- or right-click one of the circular nodes on an MPR line. The line changes from orange
to green.
2. Drag and drop the node to the new location. This specifies the thickness of the slab.
NOTE: As you are changing the thickness of the slab that defines the MPR plane, the
corresponding MPR view is dynamically updated. The MPR view is now an MIP of
the portion of the stack defined by the slab.
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1. Select the MPR line and press Delete. A message box opens.
NOTE: You can delete all MPR lines and views from a series by selecting the series and
clicking . You are prompted to delete each MPR view; you can click No to all
in the message box that opens to avoid multiple prompts.
• Click Yes to save the series. For local exams, the Store MPR Series box opens in a
new pane.
3. Type a series description for the MPR view and click OK.
NOTE: If you right-click a series that contains an MPR line and select a different series to
load into that pane, you are prompted, as described above, to save or delete the
corresponding MPR view.
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• Export images as JPEG files (see “Exporting Images as Graphic Files” on page 116).
• Export images as AVI files (see “Exporting Images to AVI Files” on page 116).
• Export volumes as AVI files (see “Exporting Volumes to AVI Files” on page 118).
4. In a new document for the application, press Ctrl+V to paste the copied image.
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1. Select the images that you want to export by clicking the image marker in the lower right
corner of each image, or by selecting a series and clicking to select all images in the
series. The marker located at the bottom of each selected image fills in orange.
2. Select File > Export > as Image(s). The Save As dialog box opens.
4. Select the Windows directory in which to save the images and type a filename. If multiple
images are selected, the series and image number are appended to the filename of each
image file.
5. Click Save.
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1. Select the images to be exported by clicking the image marker in the lower right corner of
each image, or by selecting a series and clicking to select all images in the series.
The markers located at the bottom of the selected images fills in orange.
2. Select File > Export > as AVI Video. The Create AVI dialog box opens.
4. Specify the Image Width and Image Height dimensions (the size of the AVI image in
screen pixels).
5. Select the frame rate preferences (the number of images or frames that display per
second).
NOTE: The Total Running Time value is calculated according to the frame rate.
If a DICOM frame rate has been encoded in the DICOM header, the Use DICOM Frame
Rate check box is activated. If you select this option, the Frames Per Second value is set
according to the frame rate.
6. After you have set all of your preferences, click Create. The Save As dialog box opens.
7. Select the destination directory and type a filename. The new AVI file is saved to this
location.
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8. If you wish to view the AVI image at this point, click View.
NOTE: When you open the AVI file in Windows, the movie plays automatically on your
computer’s default media player.
• Click .
The Cine Control Bar dialog box opens. The controls in this dialog box enable you to
preview and fine-tune the settings for the video file before exporting the volume.
5. Specify the Sweep Angle (degree of rotation) and Step Size (degrees per frame).
118
NOTE: Select the Tumble check box if you want the sweep angle to be 360°.
6. Select one or more of the Rotation Axis check boxes to rotate the volume about the
corresponding axes.
7. Click Export to AVI. The Volume AVI Creation dialog box opens.
9. Specify the Image Width and Image Height dimensions (size of the AVI image in screen
pixels).
10. Select a frame rate (the number of images/frames that display per second).
NOTE: The Total Running Time value is calculated according to the frame rate.
12. After all of your preferences are set, click Create. The Save As dialog box opens.
13. Select the destination directory and type a filename. The new AVI file is saved to this
location.
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14. If you wish to view the AVI volume at this point, click View.
NOTE: When you open the AVI file in Windows, the volume plays automatically on your
computer’s default media player.
Printing Images
Images can be printed from either a regular printer.
NOTE: Before changing any of the configuration settings for your DICOM printer, refer to
your printer’s DICOM Conformance Statement to confirm that these settings are
supported by the printer. Setting the resolution too high results in a very large
image. 100 DPI is usually satisfactory.
1. Select the images you want to print by clicking the image marker in the lower right corner
of the image. The marker fills in orange.
NOTE: You can preview the print job by clicking Print Preview on the File menu.
120
NOTE: You must have the ability to create a properly formatted DICOMDIR file set in
order to create an eFilm Lite CD. In other words, your process or software must
be able to act as a File Set Creator in the General Purpose CD-R Interchange
profile (STD-GEN-CD) for both the Basic Directory and Composite Storage &
Stand-alone Storage categories. For more information, refer to the DICOM
Standard, version 3, Part 11.
1. Create the DICOMDIR file set, including the DICOMDIR Basic Directory file, and place
them into a temporary directory. See “DICOMDIR Directory Structure” on page 122 for
details on the directory structure of the file set.
2. Copy the Autorun.inf file into the root of the temporary directory.
3. In the temporary directory, create a folder called “eFilmLite” and copy all of the eFilm Lite
runtime files into that folder. See “eFilm Lite Runtime Files” on page 122 for details on
the runtime files.
4. If required, in the temporary directory, create a folder called “Other Files” and place any
additional files you want copied into that folder.
5. Write the entire temporary directory contents to the root directory of the CD-R.
121
NOTE: Ensure that the Autorun.inf file is in the root directory of the CD <ROOTDIR>.
122
123
124
125
A colors
assigning mappings 98
accessing. See opening editing mappings 102
adding inverting 50
annotations 72 loading mappings 101
filters 62 mapping 67, 97
MPR slabs 113 common tools. See tools
MPR views 103 configuring
advanced user settings 20 advanced user settings 20
alpha setting 67 alpha setting 67
angle measurements 78 color maps 97
annotations 72 hanging protocol preferences 22
applying image brightness 46
filters 63 image contrast 46
arranging studies in panes 31 image orientation 52
arrows 77 image view 53
assigning images with DSA 60
color mappings 98 loading parameters 92
grayscale mappings 100 modality layouts 19
automatic series synchronization 43 MPR view 108
AVI video files screen layout 33
exporting images 116 series view 57
exporting volumes 118 system preferences 22
toolbar 11
viewer 28
volume settings 25
B contrast 46
background 67 creating. See adding
black outside window 97 cropping volumes 93
brightness 46
D
C deleting
calibrating images 80 annotations 72
canceling. See deleting MPR view 113
cine tool 41 drawing arrows 77
clearing measurements 86 DSA 60
closing
studies 37
coherence 49
126
E hiding
toolbar 11
editing histogram analysis 20
annotations 72 Hounsfield units 82
color mappings 102
filters 64
grayscale mappings 102
passwords 33 I
eFilm Lite
images
configuring viewer 28
annotating 72
opening viewer 28
brightness 46
overview 8
calibrating 80
workspace 10
coherence 49
elliptical measurements 76
color inversion 50
encryption password 33
configuring with DSA 60
exiting. See closing
contrast 46
exploding series 58
exporting as AVI files 116
exporting
exporting as JPEG files 116
images as AVI files 116
flipping 52
images as JPEG files 116
fusing 65
volumes as AVI files 118
magnifying 55
MIP 89
moving through 38
F orienting 52
panning 54
field of view 60 printing 120
filters 62 probing 82
finding. See searching resetting 57
flipping retrieving 28
images 52 rotating 52
foreground 67 scaling 120
fusing images 65 scrolling through 39
selecting 35
Sigmoidal 49
Simgram 89
G stacking 40
grayscale mappings toggling shutter 59
assigning 100 tools. See tools
editing 102 viewing in stereo 96
loading 101 viewing options 53
toolbar 11 zooming 56
inserting. See adding
interacting with MPR series 107
interpolation 20
H inverting image color 50
hanging protocols
preferences 22
hardware requirements 9, 10
127
J MPRs
adding views 103
JPEG image files 116 configuring view 108
creating from 2D images 105
creating from 3D volumes 106
creating slabs 113
L deleting view 113
layouts interacting with series 107
modality 19 orthogonal viewing planes 104
screen 33 saving view 113
linear measurements 74 multiplanar tools. See tools
loading multiple
color mappings 101 image fusion 65
grayscale mappings 101
locating 3D points 44
N
navigating. See moving
M next tools. See tools
magnifying images 55 non-linear window levelling 49
main tools. See tools
manual
series synchronization 43
volume rotation 95 O
window/level settings 46 opening
mapping colors 97 mini bar 12
marking viewer 28
images 23 operating system 9
matching field of view 60 orienting
measurements images 52
angle 78 orthogonal viewing planes 104
clearing 86 overlaying
elliptical 76 reference lines 50
linear 74 overview
moving caption 74, 76 eFilm Lite 8
tools. See tools filters 62
mini bar 12 3D modes 87
MIP images 89 toolbar 11
modality tools 13
CT/PT fusion 65
layouts 19
mode, pixel-for-pixel 56
moving P
image markers 23
panes, arranging 31
measurement caption 74, 76
panning images 54
MPR line 108
passwords
through images 38
encryption 33
through series 42
pipeline, image fusion 67
through studies 42
128
129
tools viewing
3D cursor 44 image options 53
angle 78 images in stereo 96
annotate 72 matching fields 60
arrow 77 MPRs 103
calibrate 80 orthogonal MPR planes 104
cine 41 reference lines 50
clear all 86 series options 57
common 14 stacked images 41
ellipse 76 studies 29
explode 58 study information 32
filters 62 volumes
image manipulation 16 creating MPRs 106
line 74 cropping 93
magnify 55 exporting as AVI files 118
main 13 loading parameters 92
measurement 15 rendering 87
MPR 105 rotating 95
multiplanar 16 settings 25
next 15, 39 stereo display mode 96
overview 13 tools. See tools
pan 54
previous 15, 39
probe 82
reset 57 W
shutter 59 window levelling
volume 17, 106 manual settings 46
zoom 56 non-linear 49
true size printing 120 presets 47
settings 45
workspace 10
U
users
advanced settings 20 Z
zooming images 56
V
viewer
configuring 28
opening 28
130