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The Kidneys
Therese M. Weber, Michelle L. Robbin and Mark E. Lockhart
Renal Vascular Doppler Ultrasound and interpretation of the study will reduce examina-
tion time, improve study quality, and optimise
Ultrasound is the imaging modality of choice for
diagnostic accuracy. A dedicated quality control pro-
evaluation of the kidneys, especially in patients with
gramme is an important mechanism to assess accuracy
borderline renal function, the incidence of which is
and to review cases in which an incorrect diagnosis
increasing. In comparison with other modalities,
was made. The goal of this review process should be
ultrasound has the distinct advantage of providing
to improve the quality of future studies.
clinically diagnostic information without the need
One common challenge in renal vascular ultra-
for ionising radiation or contrast agents. The combi-
sound is direct visualisation of the proximal renal
nation of spectral, colour, and/or power Doppler is
arteries. Overlying bowel gas may completely obscure
extremely helpful in renal vasculature evaluation.
the renal vascular origins and result in a non-
diagnostic study. To improve the likelihood of a diag-
CLINICAL CONSIDERATIONS nostic study, we request that patients be fasting for at
Common clinical indications for renal ultrasound least 6 to 8 hours, when possible, to decrease bowel
include renal insufficiency and renal failure. Specif- gas. Another limitation is the deep location of the
ically, the request to exclude renal obstruction as native renal vessels, especially in obese patients, and
the aetiology of acute renal failure leads the list. utilisation of appropriate sonographic windows may
Doppler ultrasound is not routinely performed to be helpful. Graded transducer pressure can bring
evaluate acute renal failure but may be prompted the transducer closer to the arteries and simulta-
by certain clinical indicators (Box 9-1) or greyscale neously displace overlying gas. However, the renal
findings. Colour and spectral Doppler is more com- arteries occasionally may not be directly visualised
monly used in the native kidneys for evaluation of despite optimal technique; in some of these technically
unexplained or uncontrolled hypertension caused difficult cases, the identification of segmental arterial
by renal artery stenosis (RAS) or for determination waveform abnormalities may still allow successful
of vessel patency. In hypertensive patients, some diagnosis of RAS.
authors suggest Doppler should be reserved for
those patients with a strong clinical suspicion for Main Renal Artery Evaluation
RAS who are likely to benefit from intervention.1
Doppler evaluation of the renal arteries should not
As will be shown, there are many other vascular
occur without a thorough greyscale examination of
abnormalities than can be demonstrated by Dopp-
the kidneys. Greyscale imaging can provide useful
ler, and these can present with a wide variety of
information about renal size and cortical thickness
symptoms or signs.
and should be part of the initial series of images.
For Doppler image acquisition, a preliminary scan of
TECHNICAL CONSIDERATIONS the abdominal aorta is performed with colour Doppler
Renal Doppler ultrasound can be one of the most in the transverse plane beginning at the level of the
challenging vascular ultrasound examinations. superior mesenteric artery (SMA) to locate the main
Extensive training and experience in performance renal arteries, which typically originate within 2 cm
193
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194 9 The Kidneys
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9 The Kidneys 195
Greyscale visualisation of the renal arteries should A posterior flank approach reduces the distance
be optimised prior to colour and spectral Doppler eval- from the transducer to the segmental arteries. Of note,
uation. Doppler gain should be adjusted for flow detec- the liver and spleen should not be used as a window to
tion by increasing the gain to a level just below the improve visualisation of the kidney, as the vessels are
appearance of colour artifact in adjacent structures. closer to a zero degree angle with the transducer posi-
Pulse repetition frequency, or velocity scale, is the tioned using a more posterior approach. The upper,
frequency of sampling, and under-sampling may interpolar, and lower pole segmental arteries are indi-
underestimate peak velocities. In newer systems, vidually studied. A heel–toe technique is commonly
built-in software can automatically optimise these applied in which one edge of the transducer is angled
parameters, with manual adjustment occasionally into the skin to align the targeted segmental artery flow
required by the sonographer. For spectral Doppler, the as close to the transducer angle of insonation (theta
Doppler gate should be set to include the entire arterial less than 20 degrees) as possible to enhance the signal
lumen and angled to the direction of flow. The angle of quality. This can enhance the definition of the early
insonation should be maintained at 60 degrees or less. systolic peaks. Electronic beam steering can also be
As angulation increases to 80–90 degrees, the confi- used to better align angulation of the insonating beam
dence in the measured velocity decreases, as the cosine to enhance waveform morphology.
of the angle of insonation approaches zero. This yields Characteristics of the spectral Doppler tracing
large differences in measured velocity for a small in normal segmental intrarenal arteries should include
variation in the relative angle of flow. rapid upstroke to an early systolic peak with gentle
decrease in flow velocity during late systole and dias-
Segmental Intrarenal Artery Evaluation tole (Fig. 9-3). Persistent antegrade flow throughout
When the main renal artery is not well seen in its the cardiac cycle should be present without return
entirety, evaluation of the segmental intrarenal arteries to baseline. The resistive index (RI), calculated as:
may allow a non-diagnostic direct examination to
Peak systolic velocity ðPSVÞ End diastolic velocity ðEDVÞ
become diagnostic for RAS.5,6 We always examine the
Peak systolic velocity ðPSVÞ
segmental arteries even when the main renal
arteries are well seen, because the segmental artery is a common parameter for characterisation of arterial
waveform morphology may be useful in detecting flow. The RI is inversely proportionate to the relative
concomitant renal parenchymal disease. amount of diastolic flow. For instance, an end diastolic
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196 9 The Kidneys
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9 The Kidneys 197
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198 9 The Kidneys
Renal Infection
Renal ultrasound examination is not routinely
requested in cases of renal infection and ultrasound
findings are quite variable in these cases. Renal paren-
chymal infection may be global or focal and the route
of spread may be ascending or blood-borne. More B
common ultrasound findings, not consistently seen, FIGURE 9-7 Renal calculus. (A). Greyscale ultrasound shows an
are enlargement or altered echogenicity of the affected echogenic focus in the calyceal region of the renal lower pole.
kidney. The presence of perinephric fluid would add However, there are other echogenic foci in this region, which may
represent additional stones. (B) Colour Doppler confirms presence
confidence. Demonstration of altered blood flow, with
of two calculi with visualisation of ‘twinkle’ artifact.
reduction of Doppler indices and perfusion in an
affected renal segment adds confidence to the diagno-
sis of focal pyelonephritis.
rather than bright echogenic renal hilar adipose tissue.
This technique should be used to demonstrate the
Nephrolithiasis presence of the stone, not to measure size of the stone.
This is an especially useful adjunct to evaluate for dis-
Colour Doppler evaluation should be a routine com-
tal ureteral stone with endovaginal technique when a
ponent of the renal ultrasound examination when
dilated upper renal collecting system is identified in
nephrolithiasis is suspected. Greyscale alone has poor
pregnancy (Fig. 9-8).
sensitivity for small renal stones. Using colour
Doppler, twinkle artifact19 can increase confidence
in the presence of renal, ureteral or bladder stones
Renal Tumours
(Fig. 9-7). The irregular surface of the calculus causes
a Doppler shift which manifests as a noisy colour and Greyscale ultrasound is the primary sonographic tech-
spectral signal. This helps confirm that a bright echo- nique for detection of a renal tumour, but colour
genic focus within the renal hilum is indeed a calculus, Doppler can provide additional information for
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9 The Kidneys 199
B
FIGURE 9-8 Ureteral calculus. (A) Longitudinal greyscale ultrasound with sepia colour encoding shows the linear anechoic distal ureter with
a shadowing echogenic focus. (B) Colour Doppler confirms the presence of a ureteral stone with ‘twinkle’ artifact.
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200 9 The Kidneys
A B
FIGURE 9-9 Renal tumour. (A) Longitudinal greyscale ultrasound demonstrates a solid exophytic mass arising from the renal lower pole.
(B) Colour Doppler clearly depicts the margins of the tumour and the presence of vessels along its periphery. This allows better definition of
the depth of invasion to aid in surgical planning.
A B
FIGURE 9-10 Renal tumour venous extension into the IVC. (A) Greyscale image shows expansion of the infrahepatic IVC by a solid lesion
(calipers). (B) The addition of colour Doppler helps delineate the cranial extent of the tumour thrombus.
uncommon disorder seen most frequently in younger no significant difference in two randomised cohorts
women, and unlike atherosclerotic lesions, generally of patients between medical management versus stent
responds well to angioplasty.20,21 The role of imaging therapy for the treatment of RAS. The long-standing
is influenced by the potential benefit of intervention.1 ischaemic insult to the renal parenchyma with
Although renal artery stenosis can be identified with associated cholesterol crystal embolisation causes
imaging, recent studies suggest that simply the iden- significant damage that does not benefit from reestab-
tification of stenosis does not justify invasive treat- lishment of more normal flow through the main renal
ment by stenting. Two recent randomised trials, artery. Evaluation of renal perfusion in the presence
including the ASTRAL study, have shown no benefit of stenosis may be more useful to select patients
to revascularisation of atherosclerotic lesions, with who will benefit from intervention. Some authors
regards to either blood pressure or renal func- have suggested Doppler measurement of resistive
tion.22,23 The ASTRAL study found that there was index, with high resistance behind a stenosis
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9 The Kidneys 201
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202 9 The Kidneys
FIGURE 9-12 Renal artery stenosis. Duplex Doppler shows a region of colour Doppler aliasing (Doppler gate), and the peak systolic velocity
measures 528 cm/s, which is above the 200 cm/s threshold.
thresholds differ in patients older versus younger than systolic peak. In blunted waveforms, this early peak
46 years. Other sonographic criteria were not sub- may be absent, and the measurement should extend
stantially affected by patient age in their study.33 from onset of systole to the first point of deflection.36
The indirect method of RAS assessment of segmen- The presence of the tardus–parvus waveform morphol-
tal renal artery waveforms becomes important when ogy is helpful in the diagnosis of severe RAS; however,
the entire length of the main renal artery cannot be its absence does not exclude RAS.37 The tardus–parvus
directly seen with ultrasound. Stavros et al.5,34 have spectral waveform is defined by the slow upstroke (the
suggested that normal intrarenal waveform morphol- tardus) and spectral broadening with blunting of the
ogy with early systolic peak in the upper, interpolar, systolic peak (the parvus) (Fig. 9-15). It is important
and lower pole segmental renal arteries may be used to note that in patients with atherosclerotic disease,
to adequately exclude significant RAS. This normal vessel compliance may be diminished, making the
compliance peak (Fig. 9-14) is not present when there tardus–parvus waveform morphology less obvious.38
is flow-limiting stenosis in the proximal artery, A less common criterion suggested for diagnosis of
although others have found this sign less sensitive.35 RAS is excessive difference in RI of the two kidneys
Another criterion of RAS is prolonged acceleration ( 0.07).5,39 For lesser degrees of stenosis, the abnor-
time of greater than 0.07 second. Acceleration time is mal kidney will show lower RIs beyond the point of
the time interval from onset of systole to the early stenosis due to post-stenotic dilatation. However, as
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9 The Kidneys 203
FIGURE 9-13 Renal artery stenosis. (A) Duplex Doppler of renal artery demonstrates borderline peak systolic velocity, 199 cm/s. (B) Spectral
Doppler waveform of the aorta shows peak velocity is 59 cm/s. The calculated renal artery-aortic peak systolic velocity ratio of 3.72 is above the
3.5 threshold, suggesting significant stenosis.
the stenosis becomes more flow limiting, there may patients without clinical suspicion of restenosis, 22
not be persistence of flow throughout the cardiac patients had elevated PSV of greater than 200 cm/s
cycle, resulting in a high RI. and had significantly worsened rate of renal function
Another potential application of Doppler is for decline than those patients with PSV of less than
follow-up to assess for restenosis in patients after stent 200 cm/s.40 In 6 of 11 of these patients with this
placement for RAS (Fig. 9-16). This may be ordered criterion who underwent angiography despite the lack
due to worsening renal function or even when clinical of clinical suspicion, all had restenosis of greater than
signs of restenosis are absent. In a study of 64 stented 70% at angiography.
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204 9 The Kidneys
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9 The Kidneys 205
FIGURE 9-16 Restenosis after stenting. (A) Duplex Doppler of right main renal artery in stented patient with recurrent hypertension shows
elevated PSV in region of colour aliasing. (B) Spectral Doppler of a segmental renal artery demonstrates tardus-parvus waveform.
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206 9 The Kidneys
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FIGURE 9-18 Renal artery aneurysm. (A) Split image shows anechoic round structure on greyscale with flow on colour Doppler. The circular flow
on colour Doppler (arrows), termed the ‘yin-yang’ sign, can be seen with aneurysm or pseudoaneurysm. (B) On angiography, the typical round
vascular structure of an aneurysm is confirmed.
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208 9 The Kidneys
FIGURE 9-20 Arteriovenous fistula. (A) Spectral Doppler demonstrates arterialised venous flow with high velocities and low resistance. (B) CT
angiography shows early enhancement of right renal vein (arrow), compared with the left renal vein.
Nutcracker Syndrome (Fig. 9-23) and high venous diameter ratio as described
The ‘nutcracker’ phenomenon results from compres- in recent literature.43 Due to the complexity of the
sion of the left renal vein between the superior mesen- potential surgical repair, measurement of a pressure gra-
teric artery and the aorta and may lead to left renal vein dient between the IVC and the left renal vein may be
hypertension, haematuria, and varix formation. It is needed as confirmation before clinically significant
important to remember that a distended left renal vein renal vein compression is diagnosed. Visualisation of
may be seen in some of the normal population by CT, blood from the ureteral orifice on retrograde uretero-
MR, or ultrasound. Therefore, other criteria should scopy may also be supportive. Colour flow Doppler
be applied, including a high Doppler velocity ratio may provide noninvasive evidence of renal vein
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9 The Kidneys 209
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210 9 The Kidneys
FIGURE 9-23 Renal vein nutcracker. In a patient with unexplained haematuria, spectral Doppler of the (A) preaortic left renal vein demonstrates
normal low-velocity flow, 8 cm/s. (B) As the vein crosses between the aorta and SMA (Doppler gate), there is visible narrowing with elevated peak
systolic velocity, 103 cm/s.
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9 The Kidneys 211
FIGURE 9-24 Varicocele. (A) Colour Doppler shows dilatation and increased flow within the vessels (arrows) of the spermatic cord and scrotum
during Valsalva measuring greater than 3 mm diameter. In the setting of borderline findings, standing position of the patient may accentuate the
finding. (B) CT in the same patient shows retroaortic left renal vein (black arrow).
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212 9 The Kidneys
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9 The Kidneys 213
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