This article discusses the use of high concentration CT contrast in CT Angiography applications. Contrast administration and protocols are included.
Dennis Foley, MD
Director, Section of Digital Imaging, Medical College of
Wisconsin, Milwaukee, WI
CT angiography (CTA) of the extremities has proven to be
extremely useful for evaluating vascular anatomy and patency,
demonstrating the source of limb ischemia, and aiding in
endovascular and surgical planning. One reason for the success of
CT angiography is that, unlike other imaging techniques, it is
capable of demonstrating arteries, including lumen, thrombus, and
calcification; skeletal tissue, and soft tissue in detail, and in
relation to one another.
Figure 1 provides an example of the remarkable detail that can
be achieved with CTA, in this case, in an upper-extremity study.
The 3-dimensional volume rendering in Figure 1A demonstrates the
thoracic outlet in a young person who has had a cervical rib
resection, with bone detail provided as background. Figures 1B and
1C show the right subclavian artery in a curved planar reformation
of the data, with the patient in the neutral position and the Adson
maneuver, respectively. Not only do these CT images together
demonstrate the vascular, skeletal and soft tissues in detail; they
do so relatively dynamically.
Like other CT applications, extremity arteriography has
benefited from impressive advances in multidetector helical scanner
technology. The introduction of first 4-, and now 8- and
16-detector channels, along with improvements in scan rotation
speeds, have made it possible to image the vasculature more quickly
and with thinner slices, thus improving both temporal and spatial
resolution.
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Taking advantage of the advanced capabilities of new, faster
scanners requires that adjustments be made in scanning parameters
and contrast administration. This article will provide a brief
overview of some of the ways that contrast injection protocols and
scanning methods can be modified to achieve high-quality extremity
CTA.
The protocols described here represent projections only, rather
than protocols that we use in everyday practice. They are designed
to conform to a basic principle that holds true of angiographic
imaging in general, that of maintaining high intra-arterial iodine
concentrations, so that attenuation is maintained at about 300 HU
from the distal aorta all the way through to the feet.
Lower-Extremity CTA
The lower extremities can be evaluated well with a detector
collimation of 2.5 mm. Figure 2 is an example of lower-extremity
CTA covering the length of the femoral arteries to the popliteal
arteries at the knee. Figure 3 shows a subsequent lower-extremity
CTA in another patient, who was scheduled to undergo surgery to
donate a fibula as part of mandibular reconstruction for head and
neck cancer. This 3-dimensional volume rendering demonstrates the
circulation below the knee, with bone detail present. It is
possible to identify the tibioperoneal vessels and the pedal arches
to the level of the intermetatarsal vessels.
While it is easy to perform CTA below the knee and retain the
bone in the image, lower-extremity CTA presents other, more
sophisticated technical challenges. General acceptance of
lower-extremity CTA may hinge on the efficiency of accomplishing 3
tasks: bone segmentation below the knee, vessel tracking, and
stenosis sizing throughout the lower-extremity circulation.
Certain automated techniques may help in accomplishing that
goal. Automated vessel analysis, for example, uses center-line
tracking and edge detection, and can do a superb job of stenosis
sizing. It excels not only in determining the diameter of the
vessel but also area reduction. This technology can be effectively
applied throughout the vascular system, particularly in the lower
extremities.
Contrast Administration
In extremity CTA, the issues of injection rate, injection
duration, and acquisition interval are the same as for CTA in other
parts of the body. It is important that image acquisition be timed
to correspond with the first circulation of contrast; that the
duration of the acquisition interval match that of the injection
interval; and that the intra-arterial iodine concentration produce
an arterial attenuation of approximately 300 HU throughout the full
sequence of the acquisition.
Vascular coverage depends on several factors, including the
number of detectors, detector collimation, beam width, pitch, and
scan rotation speed. In general, CT angiography is optimized by
coupling the thinnest possible image slices with the table speed
needed to cover the targeted cephalocaudad dimension during the
first circulation of a bolus of contrast media.
Table 1 demonstrates how the details of contrast injection and
scanning may vary with scanner configuration. Starting with the
assumption of a cephalocaudad coverage of 120 cm, the schematic
provides examples of how that coverage could be accomplished using
a 4-channel scanner with a 0.8-second scan rotation speed; a
4-channel scanner with a 0.5-second scan rotation speed; and an
8-channel scanner with a 0.5-second scan rotation speed.
Consider a modern 4-channel scanner. At a scan rotation speed of
0.5 sec, a table speed of 15 mm per rotation produces a coverage
speed of 3 cm/sec. Combined with a coverage requirement of 120 cm,
this results in an acquisition interval of 40 seconds. As a result,
the injection rate at which 160 mL of contrast is delivered must
drop from the standard 5 mL/sec to 4 mL/sec in order to lengthen
the injection interval in accordance with the relatively long
acquisition interval.
When scanning on an 8-channel system, detector collimation can
be reduced by half, from 2.5 mm to 1.25 mm, which will increase
z-axis resolution. Because the beam width remains the same as with
a 4-detector system, the acquisition interval remains the same, as
does the injection interval. An alternative in using an 8-channel
system that is not shown in Table 1 involves maintaining detector
collimation at 2.5 mm. By doubling imaging speed in this way, it
may be possible to perform lower-extremity CTA with less than 100
mL of contrast material, while at the same time covering all the
way from the renal vascular pedicle to the feet.
Higher-concentration contrast media with an iodine concentration
of 370 mg/mL is useful in achieving higher intra-arterial iodine
concentrations and thereby improving the definition of stenoses. I
anticipate that the use of higher-concentration contrast will prove
superior for lower-extremity arteriography because it should
maintain a high intra-arterial iodine concentration throughout the
study. *