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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_3860_Библиотеки_им_академика_М_И_Перельмана

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34 J. A. Kaufman
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A B
C
FIGURE 5-6. Three-dimensional phase contrast (3-D PC)
magnetic resonance angiogram of the renal arteries of a normal volunteer illustrating the directional information pro­duced by PC imaging. Velocity encoding was 100 cm/sec for this study, and flow in all three directions was imaged. A: Axial maximum intensity projection (MIP) of the speed images (all flow is white). Notice the anterior-to-posterior course of the renal arteries ( (IVC) (
small straight arrow
The superior mesenteric artery (SMA) ( and the superior mesenteric vein (SMV) ( are anterior to the aorta. The splenic vein can be seen anterior to the SMA. Note also the absence of any anatomic detail in the background. B: Coronal MIP of the same images. Notice the slightly caudal course of the right renal artery and the
E
right-to-left flow. The flow in the left renal artery is white (blood flows from the aorta to the left), whereas flow in the right renal artery is black (blood flows from the aorta to the right). Notice how the aorta and SMA are not well visualized. Why is flow in
arrow
the splenic vein ( because flow is posterior toward the kidneys (refer to A). The SMV ( trajectory toward the portal vein. Again, notice how the aorta and SMA are not well seen. E: Axial image showing superior to inferior flow. Using the preceding four images, explain why the aorta ( proximal right renal artery (
curved arrow
), and IVC (
) black? D: Axial image showing anterior-to-posterior flow. The renal arteries (
long straight arrow
open curved arrow
) are white, whereas the distal left renal artery (
) are black.
cranial course of the left renal artery. The tapered appearance of the distal aorta is due to loss of signal from saturation of spins within the 3-D imaging volume. C: Axial image showing
small arrow
short straight arrow
large straight arrows
) is anterior to the right renal artery.
) is also white because it has a slighly posterior
), SMA (
). The inferior vena cava
solid curved arrow
open curved arrow
large arrows
) are white
open straight arrow
curved arrow
), SMV (
D
) )
), and
tightly
FIGURE 5-8. Aliasing artifact in a gated two-dimensional
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phase contrast magnetic resonance angiogram of the de­scending thoracic aorta. Velocity encoding was 40 cm/sec, flow in the superior to inferior direction was imaged, and phase-dif­ference signal processing was used. When flow in the superior to inferior direction exceeded 40 cm/sec, it abruptly changed color from white to black, with a sharp interface ( interface changed considerably throughout the cardiac cycle, an important clue to the nature of the artifact.
arrows
). This
CT/CT angiography
Principles of CT
CT imaging revolutionized diagnostic and interventional radiology because it allowed physicians to view the body in a way that had been previously restricted to the gross anatomy laboratory. Developed by Sir Gregory Houns­field, the technique is based on computerized reconstruc­tion of data acquired by rotating a narrow radiographic source (mounted in a circular gantry) around a patient in an axial plane. An axial image is created that looks as though the body has been bisected at that point. This technology has had a tremendous impact on diagnostic visceral angiography, as pathology such as solid liver le-
MR and CT Angiography 35
FIGURE 5-7. Schematic diagram of phase differ-
ence signal processing in phase contrast magnetic resonance angiography. Phase shifts are assigned a pixel intensity that increases as the velocity in­creases. When the phase shift exceeds the maxi­mum value of the velocity encoding ( color abruptly changes; this is termed Choosing an appropriate est will result in improved visualization of flow and avoid aliasing.
V
enc
V
), the pixel
enc
aliasing.
for the vessel of inter-
sions now can be visualized and characterized with greater accuracy and without the need for an invasive procedure.
The core principle of CT imaging is identical to that of flouroscopy: variable absorption of ionizing radiation by different tissues. Using sophisticated data processing, CT is more sensitive to subtle differences in tissue density than most conventional radiographic techniques. Con­ventional gastrointestinal and vascular contrast agents can be used during scanning to enhance these differences or aid in the identification or evaluation of structures. The radiographic density of a structure can be measured and is described in Hounsfield units (HU). Air, fat, mus­cle, fresh hematoma, bone, and contrast-enhanced blood all have characteristic densities that permit confident identification.
CT technology
The construction of conventional CT scanners permits acquisition of only one image at a time, because the gantry makes one rotation per slice. Regardless of how quickly this rotation can occur, the gantry must return (unwind) to a start position before the next image can be acquired. Patients are imaged by lying on a table that is fed incrementally through the gantry, with the table mov­ing a predetermined distance between slice acquisitions. Scanners with this type of gantry are well suited for body interventions such as drainage or biopsy, in which indi­vidual slices are used for planning approaches and moni­toring progress. Unlike ultrasound guided procedures, however, there is limited capability for monitoring the actual manipulation of needles or tubes, because most CT scanners require too much time to acquire and pro­cess the necessary data to construct an image.
Regardless of how quickly an image can be acquired, scanning on a slice-by-slice basis unavoidably results in a time penalty related to the gantry and the table feed. Certain dynamic processes, such as blood flow, cannot be studied using this type of equipment. The application of slip-ring technology to CT scan gantry construction allows
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continuous rotation of the tube, without the need to stop and “unwind” (Fig. 5-9). Usually, each rotation requires 1 sec; therefore, the rate of acquisition is 1 slice/sec. Helical (or spiral) CT scanners image continuously as the patient is moved through the gantr y. In addition to the usual parameters of thickness of the x-ray beam (collimation), such as peak kilovolt (KvP) and milliampere second (MaS), the operator must also choose a rate of table feed (pitch, which is the ratio of the distance of table movement to collimation assuming a 1 sec. tube rotation per slice). Data are acquired as a volume rather than as individual slices; so large anatomic areas can be scanned completely in 20 to 30 sec. (a single breath-hold). In practical terms, this means image acquisition time is limited by the heat capacity of the equipment and the patient’s ability to sus­pend respiration. Because scanning is faster than image reconstruction, image processing can be the longest por­tion of the study. The volumetrically acquired data can be displayed in any plane, but most manufacturers display the data as axial slices. The greatly reduced scan time of helical scanners allows CT imaging of physiologic proc­esses formerly beyond the capability of this technology, such as tracking of a bolus of vascular contrast. The latter process is CTA. This technique has been applied to a wide range of vascular structures within the body, including the carotid arteries, the aorta and its branches, the lower ex­tremity arteries, the peripheral and central veins, and the pulmonary arteries.
16–26
The basic principle of CTA is a carefully timed helical acquisition of data during the rapid peripheral infusion of large amounts of iodinated contrast. The amount of anatomic coverage required and the size of the blood vessel of interest determine the collimation, pitch, and contrast injection. Typically, the collimation varies from 1 to 7 mm in thickness, and from 1 to 2, in pitch. For example, a study of the iliac arteries might be performed with a collimation of 5 mm and a pitch of 2, whereas a study of the circle of Willis might use a collimation of 1 mm and a pitch of 1. In general, the thinner the collima­tion or greater the pitch, the lower the ratio of signal to noise in the image.
Unlike MRA, CTA is entirely dependent on the imag­ing of an intravascular contrast agent; suppression of information from background tissues is not possible. Three factors regarding intravascular contrast agents in CTA are important: rate of injection, volume of contrast, and concentration of iodine. Visualization of vessels im­proves as the concentration of contrast in the blood in­creases. Therefore, rapid injection of a large amount of contrast is necessary to maintain a density of intravascular contrast that permits indentification of small vascular structures. Most CTA studies require injection rates of 3 to 5 mL/sec for a total volume of 100 to 150 mL. The concentration of iodine is as important as the rate and volume of contrast injection, as dilute contrast will result
in inadequate opacification because of further dilution in the bloodstream. For most applications, contrast contain­ing 60% iodine (such as Renografin 60 or Ominpaque
300) provides the best results. Intravenous lines used for CTA should be checked carefully for patency before con­trast injection, because large subcutaneous extravasations may result if the catheter is in a small vein or is partially dislodged. Keep in mind that the volume of contrast used for CTA is comparable to, and in some cases may actually exceed, that used in conventional angiography.
Timing of imaging in relation to contrast injection is critical in CTA (Fig. 5-10). A sufficient delay must be used to allow contrast to reach the vascular bed of interest be­fore commencing the scan. Furthermore, the duration of contrast injection must be long enough to ensure ade­quate vascular opacification for the entire time image ac­quisition. For example, a delay of 20 to 30 sec. is typical for most abdominal applications,whereas a delay of only 10 to 15 sec. may be necessary for the carotid arteries. The ideal approach is to perform a test bolus of contrast injected at the planned rate, with acquisition of images at a fixed point at the top of the helical volume every 1 to 2 secs. following a 5- to 10-sec. delay. A time/density curve then can be plotted from a region of interest placed in the vessel of interest. The peak of the curve then determines the delay for the helical scan. The only disadvantage to this approach is the tube heating, which may delay the helical acquisition. Some scanners can automatically detect the arrival of the bolus of contrast in the vessel of interest.
Suspended respiration is important for many abdomi­nal and thoracic applications of CTA. Motion during the scan will result in blurring and partial volume averaging. The duration of the scan thus may be determined by the patient’s ability to hold his or her breath; patients on respirators or with severe tachypnia may not be suitable candidates for this technique. Certain types of motion cannot be avoided during a scan; in particular, cardiac pulsation can distort the appearance of the adjacent aorta and other structures (Fig. 5-11).
By convention, CTA images are displayed on the scan­ning console as sequential images (i.e., no overlap) in the axial plane. To provide the smoothest angiographic im­ages during subsequent image postprocessing, the de­gree of overlap of adjacent slices should be close to 50%. For this reason, a second set of overlapping images is reconstructed from the source data set from which an­giographic images will be created. The degree of overlap must be specified by the operator; for example, an acqui­sition of the renal arteries with a collimation of 3 mm and a pitch of 2 might be reconstructed as 3-mm slices at
1.5-mm intervals. In this case, data from two sequential source images in the center of the acquisition would be included in five overlapping reconstructed slices. Obvi­ously, reconstructed data image sets are usually much larger than source image sets.
FIGURE 5-9. Schematic diagram of the difference between helical computed tomography (CT) and conventional CT. With helical acquisition of data, a spiral of
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contiguous data is acquired as the patient moves through the gantry. Slices then are reconstructed from this volume of data. With conventional scanners, one discrete slice is obtained during one rotation of the gantry while the patient remains stationary. While the gantry unwinds, the patient is repositioned for the next slice. IGD-ISD-(Diagram courtesy of GE Medical Systems, Milwaukee, WI.)
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FIGURE 5-10. Axial image from a computed tomographic angiogram of a patient with abdominal aortic aneurysm and severe tricuspid regurgitation. Although a 30-sec. delay be­tween initiation of contrast injection and initiation of scanning was used, poor aortic opacification is present ( Note the intense opacification of the inferior vena cava and right hepatic vein ( from the right atrium. Contrast was injected in a peripheral vein in the left upper extremity.
black arrows
) caused by reflux of contrast
white arrow
One of the major advantages of CTA is that the source images are simply slices from a CT scan with intense vascu­lar opacification. In other words, all the information that one would normally expect regarding the background tis­sues on a CT scan is also present, allowing more compre­hensive evaluation of the vessel wall and adjacent struc­tures than with MRA. For example, CTA of the pulmonary arteries performed to look for pulmonary emboli also permits evaluation of the lung parenchyma, pleural cavity, and mediastinum for coexistent pathology or alternative diagnoses.
Limitations
CTA is a quick, readily available technique, but it has certain important limitations. Patients who have contrast allergies or renal failure (serum creatinine⬎ 1.5 mg/dL) are not suitable, nor are those who have contraindica­tions to exposure to ionizing radiation (e.g., patients in the first trimester of pregnancy). Heavily calcified vessels can be difficult to evaluate, as dense mural calcium can obscure the vessel lumen. As with MRA, patients must be able to cooperate during the study to avoid detrimental motion or respiratory artifacts.
Image postprocessing
To view the data from MRA and CTA studies as angio­grams, postprocessing of source images is usually neces­sary. This crucial step occurs after the study has been
).
FIGURE 5-11. Pulsatility artifact due to cardiac motion in com­puted tomographic angiography of the thoracic aorta in a pa­tient with a type I aortic dissection. This image is an oblique sagittal slice created retrospectively from a contrast-enhanced helical scan. Note the serrated appearance of the mobile intra­cardiac portion of the aortic root ( parison to the smooth contour of the fixed descending thoracic aorta (
open white arrows
tially to motion of the aortic root with cardiac activity during imaging as well as to slice thickness (7 mm) and the curved contour of the vessel wall. The dissection flap ( seen as a dark line within the vessel lumen. The serrated appearance of the flap is due to movement of the flap during the cardiac cycle.
) at the same level. This is due par-
solid white arrows
black arrows
completed, usually after the patient has been removed from the scanner. Thus, a thorough understanding and familiarity with this technique is important to ensure proper interpretation of the images. A variety of post­processing options are available, ranging from simple reformating of data into different planes (i.e., coronal slices from axially acquired data) to 3-D renderings that permit an endoscopic viewpoint of the vascular lumen. Excellent postprocessed images can be created only from excellent source data. Even the most sophisticated post­processing techniques cannot recover useful information from a poor study (the old computer science dictum “garbage in, garbage out”).
The source data for MRA and CTA are composed of discrete elements termed voxels. Each element has only one value. This concept is important because postproc­essing is essentially manipulation of these elements. For example, in 3-D imaging, if a voxel contains two struc­tures with similar but differing values, it will be assigned
) in com-
)is
MR and CT Angiography 39
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a value that is an average of both. There is no way to separate these two structures retrospectively using cur­rent postprocessing techniques.
A major determinant of the value assigned to a voxel are its dimensions. If an image is constructed of voxels that are too large, small objects may get “lost” (partial volume averaging). The dimensions of voxels are deter­mined by the field of view of an image, the slice thickness, and the matrix size. For example, in a 3-D MRA with a 20-cm field of view, a slice thickness of 2 mm, and a 256 ⫻ 256 matrix, the effective voxel size will be 0.8 ⫻ 0.8 ⫻
2.0 mm. Because these voxels are rectangular, the highest resolution images will be obtained when viewing the data set from the angle that presents the voxels on end. When voxels are true cubes, they are considered isotropic and can be viewed with equal resolution from any angle. One of the objectives in MRA and CTA is to create source images that are composed of the smallest pixels and voxels possible while maintaining adequate signal-to­noise ratios (the smaller the voxel, the greater the impact of background noise). Matrices of 512 ⫻ 512 are rou­tinely available with CTA, whereas 256 ⫻ 256 is more typical for MRA.
The most common technique for image postprocess­ing is maximum intensity projection (MIP), in which the highest value voxels within a stack of 2-D images or a 3-D volume are projected as a single image in any plane (Fig. 5-12). Multiple images can be created with incremental degrees of rotation around any axis. Restricted MIPs can be created easily by limiting the amount of the source data set to be projected. The chief advantage of this technique is that the low-intensity background structures are not projected, which results in images that are pleas­ing to view because of a very high signal-to-noise ratio. This is also the chief disadvantage of the technique, be­cause subtle abnormalities present on source images may not appear on the final projection.
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A simple postprocessing technique that retains all the data present in source images is reformatting, a technique that essentially reslices the source data in different planes from the original acquisition. For example, a stack of axial images can be reformatted into images in the coro­nal or sagittal plane, or a curved reformat can be used to trace the path of a renal artery as it arises from the aorta and travels through the retroperitoneum (Fig. 5-13). The integrity of the source data is preserved while the struc­ture of interest is depicted from the most advantageous angle. A major limitation of this technique is the extreme dependence on operator input to maintain accuracy: Ap­propriate selection of viewing planes or curves is essential for accurate diagnosis. Furthermore, reformatted images can only be one pixel or voxel thick, thus limiting the amount of data that can be displayed.
Segmentation techniques divide the image data sets into flow and nonflow groups, or “segments,” using a
number of different strategies. In thresholding, one of the most widely available methods of segmentation, an opera­tor can set a threshold value below which all data are discarded. Other techniques include region-growing (seed) algorithms, in which the user defines a starting point within a vessel, and adjacent voxels are tested auto­matically for inclusion or exclusion. Segmentation tech­niques permit modification of large data sets to include only pertinent information. As with MIPs, insensitivity to subtle abnormalities is a major limitation unless these techniques are performed carefully.
3-D rendering techniques provide the most dramatic displays of MRA and CTA data. This form of postprocess­ing imparts a “real” appearance to the vessels in that they seem to have both volume and depth (Fig. 5-14). Spatial relationships are self-evident, rather than deduced. Col­orization schemes can be superimposed on the images to emphasize various structures. The two most common dis­plays are surface or volume rendering. The former is a repre­sentation of the vascular data as a shell, and the latter presents the data as a solid object. These post-processing techniques usually are performed on independent work­stations equipped with fast processors using proprietary software. Data sets must be edited heavily when using seg­mentation techniques and excision of unwanted portions
28
of the images to produce satisfactory 3-D renderings.
In addition, the actual source images must have good con­trast between vascular structures and background tissues. For these reasons, all 3-D renderings must be viewed with care before rendering a diagnosis, because important in­formation can be omitted at several stages during creation of the final images. A fundamental rule of MRA and CTA is that the source images always must be reviewed when­ever a questionable finding is present on any type of post­processed image.
■ Specific Applications
Lower-extremity arteries
Peripheral arterial occlusive disease is a common prob­lem in developed countries. The evaluation of patients with claudication, rest pain, or tissue loss begins with an accurate history, a careful physical examination, and non­invasive tests, such as pulse-volume recordings. Before any intervention, accurate morphologic information about the lower-extremity arteries is required. Conventional angiography is the “gold standard” method for acquiring these data, despite its invasive nature. Among the nonin­vasive techniques, MRA is particularly suited to evaluation of lower-extremity occlusive disease. In some centers, MRA has become the primary means of imaging these patients.
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A B
C
FIGURE 5-12. Maximum intensity projection (MIP) display of a two-dimensional time-of-flight magnetic resonance (MR) veno-
gram of the pelvis. A: Axial slice from the source MR venogram shows the external iliac veins ( the external iliac veins ( stack of axial slices. The vague area of increased signal in the upper right of the image is due to bowel motion. C: Coronal projection of a MIP of the entire stack of slices creates a display of the data that looks like a venogram. D: Right posterior oblique projection of the MIP of the entire stack of slices shows the 3-dimensional relationships that can be demonstrated with this technique. (
Continued
MRA
Flow in the normal peripheral muscular arteries is pulsa­tile, with a triphasic wave form (rapid for ward flow with systole, a brief period of retrograde flow as the aortic valve closes, and then slow forward flow during diastole). In the presence of occlusive disease, flow becomes slow and nonpulsatile. This type of flow is ideal for imaging
small arrows
)
large arrows
). Note the excellent background signal suppression. B: Axial projection of a MIP of the entire
) and branches of
with 2-D TOF sequences. Most lower-extremity MRA pro­tocols are based in part on 2-D TOF techniques, with image acquisition in the axial plane, and an inferior satu­ration band to mask venous flow. Imaging acquisition in the axial plane is used because flow in most of the periph­eral arterial segments will be perpendicular to the slice and thus have maximal flow-related enhancement. Two
D
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A
E
FIGURE 5-12. (
central 4 cm of each slice improves the appearance of the final image by eliminating much of the background noise. Note that the internal iliac veins are truncated because they are excluded from the MIP.
Continued
)E:Restricted coronal MIP of the
areas where this is not true, and thus where in-plane saturation is difficult, are tortuous iliac arteries in the pelvis and the origin of the anterior tibial artery. Typical slice thicknesses are 1.5 to 3.0 mm, with the highest-reso­lution images obtained when imaging with thin slices, high matrices, and small fields of view. Recently, gadolin­ium-enhanced 3-D acquisitions of the aorta, pelvis, and thighs have replaced 2-D TOF as the primary imaging technique. 2-D TOF remains important for imaging the tibial and pedal vessels. The pelvis and thigh usually can be imaged in the body coil, but the lower extremities must be imaged in either the extremity or the head coil to achieve consistent diagnostic results (Fig. 5-15). The average study requires 1 to 2 hours to image from the toes to the aortic bifurcation.
One of the chief advantages of MRA in imaging distal vessels is that extremely slow flow beyond occlusions is detected easily using this technique, but it is sometimes difficult to demonstrate with conventional angiography if collateral formation is poor (Fig. 5-16). Although results
FIGURE 5-13. Curved coronal reformation of the renal arter­ies from a computed tomographic angiogram of a patient with an aortic dissection. A: This coronal image, which is 1 pixel thick, was created by tracing the course of the renal arteries through the retroperitoneum from the axial source images. This explains why the aorta appears truncated at the top of the image. B: Schematic showing how the curved coronal reformat is proscribed from the axial source image.
vary among institutions, depending on the specifics of both the MR and the conventional angiographic tech­niques, thereis no doubt that MRA is an excellent method for imaging the pedal vessels in the presence of extensive proximal occlusive disease.
5
A major disadvantage of MRA is that it is sometimes difficult to determine the quality of the vessel, as calcium is not seen on these im­ages. Retrograde flow below an occlusion is frequently saturated by the inferior saturation band in 2-D TOF im­aging, thus making an occlusion appear longer than it actually is.
The pelvic arteries can be difficult to image accurately by using 2-D TOF techniques if the vessels are tortuous or aneurysmal. Contrast-enhanced MRA using rapid injec­tion of gadolinium chelates during acquisition of a 3-D TOF sequence has largely resolved this issue (Fig. 5-17). Pitfalls of this technique include difficulty with timing of contrast injections when ultrafast acquisitions are used.
B
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FIGURE 5-14. Shaded surface display of the two-dimensional time-of-flight pelvic magnetic resonance venogram from Figure 5-12. Note that the three-dimensional display allows apprecia­tion of such details as the impression on the inferior vena cava and iliac veins by the common iliac arteries (
arrows
).
In addition to occlusive disease, other uses of lower-ex­tremity MRA include evaluation of tibial vessels before plastic reconstructive procedures, staging of vascular mal­formations and tumors, and diagnosis of popliteal artery entrapment by anomalous muscular or tendonous struc­tures.
Limitations
There are many limitations of MRA of the lower extremi­ties; careful patient selection is therefore important to avoid unnecessary examinations. Patients who are unco­operative, subject to frequent involuntary movements, or claustrophobic, or who have metallic joint prostheses in the extremity of interest should not undergo MRA be­cause the studies undoubtedly will be inadequate or in­complete. MRA does not have the image resolution to detect subtle intimal irregularities or to distinguish be­tween atherosclerosis and other types of occlusive disease such as arteritis. Patients who will clearly require a cathe-
FIGURE 5-15. Coronal maximum intensity projection of a two­dimensional time-of-flight magnetic resonance angiogram of the tibial arteries in a patient with occlusion of the external iliac, femoral, and popliteal arteries bilaterally. Performed in the head coil, both legs were imaged at the same time. On the patient’s right, the peroneal ( (
open arrow
peroneal ( ies are patent. Multiple small collateral vessels are present in the medial calf bilaterally.
) arteries are patent. On the patient’s left, the
solid arrow
) and anterior tibial (
solid arrow
) and posterior tibial
curved arrow
) arter-
ter-based intervention based on history, physical exami­nation, and noninvasive studies, should proceed directly to angiography if access to MR scanners is limited. Lastly, patients with traumatized or acutely ischemic, threatened limbs should not be studied with MRA because valuable time may be lost if the study is inadequate or a catheter­based intervention is needed.
CTA
The role of CTA in the evaluation of peripheral vascular occlusive disease is dependent on the anatomic area that must be imaged. CTA of the infrainguinal runoff is sub­ject to the same limitations as conventional contrast an­giography: Vessels distal to severe proximal occlusive dis­ease are difficult to opacify with contrast. In general, this is not a good modality for studying diseased infrapop­liteal and pedal arteries. CTA is an excellent modality for evaluation of the pelvic and femoropopliteal arteries, be­cause there is no degradation of the images as a result of tortuousity or the presence of aneur ysms. In addition, there is little movement of retroperitoneal structures in the pelvis with respiration compared with the abdomen, so breath-holding is less of an issue. In many cases, pelvic CTA is combined with a study of the abdominal aorta.
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High-quality pelvic CT angiograms can be obtained us­ing injection of contrast (60% iodine) at 3 to 5 mL/sec, 5 mm collimation, and a pitch of 1 to 2. An appropriate delay should be used, preferably calculated from a test bolus of 20 mL and sequential acquisition of slices at the aortic bifurcation over20 to30 secs.Bowel contrast should be avoided, as high density barium or gastrografin inter­feres with subsequent image postprocessing. Diagnostic lower-extremity studies from the inguinal ligament to the midcalf can be acquired using a 5-mm collimation, a pitch of 1,200 mL of contrast injected at 2 to 3 mL/sec, and two 60-sec. spirals.
21
It should be kept in mind that the average conventional bilateral lower-extremity angiogram re­quires 70 to 100 mL of contrast.
An advantage of CTA over MRA in the peripheral ves­sels is that the study is always performed with contrast, so that pulsatility, turbulence, and retrograde or in-plane flow do not degrade image quality. For example, cross­femoral grafts are imaged easily by CTA.
Limitations
Major limitations of CTA are the large amount of iodi­nated contrast required, and the difficulty of grading the degree of stenosis in the presence of heavy vascular calci­fication.
Lower-extremity veins and the inferior vena cava
MR venography
Blood flow in veins is, as a rule, slower and less pulsatile than flow in adjacent arteries. Most MRA techniques fa­vor blood flow with these exact characteristics. Indeed, MR venography has proved a highly accurate means of evaluation of the lower-extremity and pelvic veins and the inferior vena cava. In most studies, the sensitivity and specificity for detection of lower-extremity deep venous thrombosis with MR venography exceed 90%.
The indications for MR venography include detection of thrombus; evaluation of anomalous lower-extremity venous drainage, such as Klippel-Trenauny disease; and presurgical evaluation of venous anatomy in patients with suspected intracaval extension of renal cell carci­noma. In most institutions, lower-extremity ultrasound is the study of choice (on both the basis of cost and availability) for detection of infrainguinal deep venous thrombosis, and MR venography is useful for document­ing pelvic extent or origin of thrombus, as this anatomic region is an important “blind spot” for ultrasound (Fig. 5-18).
The most commonly applied technique for MR venog­raphy is 2-D TOF, because of its sensitivity to slow flow and its ability to cover large anatomic areas. flow, the saturation band is placed over the arterial inflow (superior if axial slices are used). Thicker slices are used
8
8
To select venous
with MR venography than with MRA, because the detec­tion of thrombus does not require the same resolution in all planes as grading of stenoses. The thicker slices also permit more anatomic coverage in less time. Other than increased slice thickness and repositioning the saturation band, little modification is required of arterial 2-D TOF sequences; however, anatomic T1-weighted images are an important part of pelvic and abdominal MR venography with which to exclude the presence of extrinsic compres­sion of venous structures by masses.
CT venography
The indications for CT evaluation of the lower extremity and pelvic veins, and the inferior vena cava are the same as MR venography. CT is a highly accurate means of evaluating the pelvic veins and inferior vena cava for patency and involvement by masses. An advantage of CT of the veins in the pelvis and abdomen is the acquisition of useful cross-sectional anatomic information about ex­travascular structures. A major limitation is the demand placed on the tube by the large area (ankles to inferior vena cava) that must be covered in patients with sus­pected thromboembolic disease.
Lower-extremity CT venography can be performed by direct injection of contrast into the extremity under eval­uation. Dilute contrast injected at a low rate (Omni 300 or equivalent diluted 1:5 with normal saline and injected at 2 mL/sec), with a 35-sec. delay, 10-mm collimation, and a pitch of 2 will permit examination of the lower extremity from the ankle to the inferior vena cava (17). Although initial results are promising, the indications for extremity CT venography have yet to be determined. In certain situations, the cross-sectional images obtained with CT venography may be essential to resolve complex anatomic relationships, an extrinsic lesion with mass effect on a vein, or to characterize an intravascular process.
The pelvic veins and inferior vena cava also can be imaged by infusion of contrast into a peripheral upper extremity vein. Contrast is injected at a lower rate than for CTA (2–3 mL/sec), and a delay sufficient to allow venous enhancement is used. Scanning too soon will re­sult in differential opacification of the vena cava at the level of the renal veins, which may lead to interpretive errors. The thickness of the collimation will vary with the desired degree of coverage, but 5 mm should be ade­quate for most cases. Similarly, the pitch will vary from 1 to 2 based on the amount of coverage required. Breath­holding is necessary for optimal helical CT studies of the inferior vena cava.
Abdominal aorta and visceral branches
The primary indications for MRA and CTA of the ab­dominal aorta and its visceral branches are preoperative staging of aortic aneurysms or occlusions, diagnosis of