Urinary tract

Published on 12/06/2015 by admin

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Last modified 22/04/2025

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Urinary tract

Methods of imaging the urinary tract

1. Plain film radiography

2. Excretion urography (IVU)

3. Ultrasound (US)

4. Computed tomography (CT):

5. Magnetic resonance imaging (MRI):

6. Micturating cystography and cystourethrography

7. Ascending urethrography

8. Retrograde pyeloureterography

9. Percutaneous renal procedures:

10. Arteriography

11. Venography

12. Conduitogram

13. Radionuclide imaging:

Intravenous excretion urography (IVU)

The technique is less frequently used than in the past and is now largely replaced by CT, MRI or US.

Contraindications

See Chapter 2 – general contraindications to intravenous (i.v.) water-soluble contrast media and ionizing radiation. In patients with contrast medium allergies alternative modalities such as ultrasound or MR can be considered. Patients with impaired renal function, particularly those with diabetes should be prepared with oral or intravenous hydration, or an alternative imaging modality considered. See Chapter 2.

Images

1. Immediate film. AP of the renal areas. This film is exposed 10–14 s after the injection (approximate ‘arm-to-kidney’ time). It aims to show the nephrogram at its most dense, i.e. the renal parenchyma opacified by contrast medium in the renal tubules. Tomography may assist in evaluation of the renal outline or possible masses (or ultrasound if subsequently available).

2. 5-min film. AP of the renal areas. This film gives an initial assessment of pathology – specifically the presence or absence of obstruction before administering compression.

    A compression band is then applied positioned midway between the anterior superior iliac spines, i.e. precisely over the ureters as they cross the pelvic brim. The aim is to produce pelvicalyceal distension. Compression is contraindicated:

3. 10-min film. AP of the renal areas. There is usually adequate distension of the pelvicalyceal systems with opaque urine by this time. Compression is released when satisfactory demonstration of the pelvicalyceal system has been achieved. If the compression film is inadequate the compression should be checked and repositioned if necessary and a further 50 ml of contrast medium administered and the film after 5 minutes.

4. Release film. Supine AP abdomen taken immediately after release of compression. This film is taken to show the ureters. If this film is satisfactory, the patient is asked to empty their bladder.

5. After micturition film. Full-length supine AP abdomen. The aims of this film are to assess bladder emptying, to demonstrate drainage of the upper tracts, to aid the diagnosis of bladder tumours, to confirm ureterovesical junction calculi and, uncommonly, to demonstrate a urethral diverticulum in females.

Ultrasound of the urinary tract

Technique

1. Patient supine, right (RAO) and left anterior oblique (LAO) positions or lateral for kidneys. The kidneys are scanned longitudinally in an oblique coronal plane supplemented by transverse sections perpendicular to the axis. The right kidney may be scanned through the liver and posteriorly in the right loin. The left kidney is harder to visualize anteriorly, but can be visualized from a lateral approach. In difficult cases the patient should lie on their side with a pillow under the left loin to widen the space between the rib cage and pelvis.

2. The length of the kidney measured by US is 1–2 cm smaller than that measured at excretion urography because there is no geometric magnification. With US measurement, care must be taken to ensure that the true longitudinal lengthwise measurement is obtained. The range of lengths of the normal kidneys is 9–12 cm, and the difference between each kidney should be less than 1–2 cm.

3. The bladder is scanned suprapubically in transverse and longitudinal planes. Measurements taken of the three orthogonal diameters before and after micturition enable an approximate volume to be calculated by multiplying the three diameters and applying a conversion factor. (A conversion factor is usually pre-programmed into modern ultrasound machines.)

4. Renal transplants are usually located in the right or left iliac fossa. These usually lie fairly superficially and are easy to evaluate using oblique planes and gentle pressure to displace overlying bowel loops.

5. The native or transplant kidneys can be evaluated for vascular pathology using Doppler techniques.

• Renal artery stenosis is diagnosed by direct Doppler interrogation of the main renal arteries from a transabdominal approach. Elevated peak systolic velocities greater than 200 cm s–1 are suggestive of a >50% stenosis. Alternatively, as the main renal arteries in the native kidneys are often hard to visualize, the intrarenal arteries can be evaluated from a flank approach for downstream changes in waveform – the tardusparvus pattern;1 a slow rise (tardus) to a reduced peak (parvus) producing a prolonged acceleration time (a value >70 ms is indicative of a severe stenosis).

• Renal vein thrombosis is diagnosed by absent colour Doppler venous flow, direct visualization of thrombus within the distended vein, and a raised resistive index with reversal of arterial diastolic flow within the intrarenal arteries.

Computed tomography of the urinary tract

Techniques

CT KUB

Plain CT (commonly referred to as CT KUB – kidneys, ureters, bladder) is useful to assess possible stone disease. It is used in many centres as the primary investigation of renal colic (replacing plain KUB radiograph):

CT urogram (CTU)

This technique uses a combination of unenhanced, nephrographic and delayed scans following i.v. contrast to sequentially allow examination of renal parenchyma and collecting systems.

Suggested protocol:

1. An oral water load of 500–1000 ml 30–60 minutes before injection is recommended to ensure a diuresis and collecting system dilatation. No positive oral contrast

2. Patient supine

3. Initial low-dose unenhanced scans of urinary tract (CT KUB) to determine if renal tract calculus disease is present

4. Low osmolar contrast material (LOCM) 300 mg I ml–1 100 ml is given as bolus intravenously

5. Thin-section (usually 1 mm) scans are obtained from diaphragm to lower poles of kidneys during nephrographic/parenchymal enhancement phase (100 s following start of bolus injection). Alternatively, scan may instead be acquired during the portal venous phase (70 s) but normal corticomedullary differentiation may make small tumours difficult to appreciate

6. Delayed thin-section (1 mm) scans are acquired from upper pole of kidneys to bladder base 20 min after contrast injection, to examine collecting systems and ureters

7. Source images are reviewed along with multiplanar reconstructions. Post-processing with maximum-intensity projections and surface-shaded displays may be helpful, especially for demonstration.

CT angiography

Magnetic resonance imaging of the urinary tract

Magnetic resonance imaging of the prostate

Technique/example protocol

1. Patient supine. Phased array body coil. The best images will be obtained with an endorectal coil, but many authorities do not use these. 1.5T or 3T scanners are both used. 3T scanners afford better signal-to-noise ratio but may be subject to more artefacts, notably susceptibility

2. Antiperistaltic drugs (hyoscine butyl-bromide or glucagon are recommended)

3. T1W and T2W axial scans whole pelvis

4. Thin-section (3–4 mm) small field of view T1-weighted spin echo (SE) scans in axial plane orthogonal to the axis of the prostate to evaluate for post-biopsy haemorrhage

5. Thin-section (3–4 mm) small field of view T2-weighted spin echo (SE) scans in transverse, sagittal and coronal planes orthogonal to the axis of the prostate

6. Multiparametric MRI – there is increasing use of the following functional studies:

Magnetic resonance urography

Technique

The two most common MR urographic techniques are:

1. Patient supine with an empty bladder for comfort. If the bladder is of interest, a moderately full bladder may be preferred.

2. Scout views are obtained.

3. Static MR urography may be performed prior to excretory urography. Thick-slab, single-shot, fast-spin echo or a similar thin-section technique, e.g. half-Fourier rapid acquisition with relaxation enhancement; single-shot, fast-spin echo; single-shot, turbo-spin echo. 3D respiratory triggered sequences may be used to obtain thin-section data sets that may be further post-processed.

4. Oral or intravenous hydration, compression or diuretics may be used to enhance collecting system distension.

5. Excretory MR urography: a gadolinium-based contrast agent is administered i.v. using a dose of 0.1 mmol gadolinium kg–1 body weight. The collecting systems are imaged during the excretory phase (10–20 min) using a breath-hold, three-dimensional gradient echo, T1-weighted sequence. Fat suppression will improve the conspicuity of the ureters. T2* effects from a high concentration of contrast agent may reduce the signal intensity of urine and potentially obscure small masses within the collecting system. This can be overcome by using a lower volume of i.v. contrast but may compromise soft-tissue imaging.

Magnetic resonance renal angiography

Micturating cystourethrography

Technique

To demonstrate vesico-ureteric reflux (this indication is almost exclusively confined to children):

1. Using aseptic technique the bladder is catheterized. Residual urine is drained.

2. Contrast medium (LOCM 150 mg I ml–1) is slowly injected or dripped in with the patient supine and bladder filling is observed by intermittent fluoroscopy. It is important that early filling is monitored by fluoroscopy in case the catheter is malpositioned, e.g. in the distal ureter or vagina.

3. Intermittent monitoring is also necessary to identify transient reflux. Any reflux should be recorded.

4. The catheter should not be removed until the radiologist is confident that the patient will be able to micturate, the patient does not tolerate further infusion or until no more contrast medium will drip into the bladder.

5. Older children and adults are given a urine receiver but smaller children should be allowed to pass urine onto absorbent pads on which they can lie. Children can lie on the table but adults will probably find it easier to micturate while standing erect. In infants and children with a neuropathic bladder, micturition may be accomplished by suprapubic pressure.

6. Spot images are taken during micturition and any reflux recorded. A video recording may be useful. The lower ureter is best seen in the anterior oblique position of that side. Boys should micturate in an oblique or lateral projection, so that spot films can be taken of the entire urethra.

7. Finally, a full-length view of the abdomen is taken to demonstrate any undetected reflux of contrast medium that might have occurred into the kidneys and to record the post-micturition residue.

8. Lateral views are helpful when fistulation into the rectum or vagina are suspected.

9. Oblique views are needed when evaluating for leaks.

10. Stress views are used for urodynamic studies.

Ascending urethrography in the male

Technique

Depending on the clinical indication, ascending urethrography may be followed by descending micturating cystourethrography to demonstrate the proximal urethra and bladder, assuming there is no contraindication to bladder catheterization, e.g. false passage, stricture. It may be possible to fill the bladder retrogradely via the urethral catheter if the patient is able to relax the bladder neck (and thus avoid bladder catheterization).

Retrograde pyeloureterography

Technique

Conduitogram

Technique

1. The patient should be advised to bring a spare stoma bag or one should be available.

2. A urinary catheter is chosen tailored to the size of the stoma. (Although larger catheters may pass more easily, a smaller catheter may be needed.)

3. The catheter is flushed with contrast medium and a syringe or giving set with contrast medium is connected. It is very important to exclude air bubbles which can be confused for upper tract tumours.

4. The conduit is then catheterized using a sterile technique.

5. The catheter balloon is inflated and minimal traction applied to the catheter to occlude the stoma.

6. Contrast is instilled under fluoroscopic control into the lumen of the conduit.

7. AP and oblique views are taken as appropriate, of sufficient number to demonstrate the whole pelvicalyceal systems and ureters.

Percutaneous renal cyst puncture and biopsy

Technique

Insertion of the needle can be controlled by either ultrasonography or CT:

1. The patient is placed in the prone position, or as appropriate depending on patient habitus and position of lesion.

2. The kidney, mass or cyst is located directly with US or CT or indirectly, after opacification of the kidneys with i.v. contrast medium. The optimum site for puncture is marked on the skin. For renal biopsy in the investigation of parenchyma disease the lower pole of the left kidney is often preferred.

3. The skin and subcutaneous tissues are infiltrated with 1% lidocaine.

4. The needle is passed directly into the lesion during suspended respiration. US or CT are used to monitor the path of the needle. For cyst puncture the stilette is removed and the cyst contents are aspirated and examined.

5. For biopsy, the biopsy needle is deployed following confirmation of needle position with imaging.

Percutaneous antegrade pyelography and nephrostomy

This is the introduction of a drainage catheter into the collecting system of the kidney.

Technique

Techniques of puncture, catheterization

The skin and soft tissues are infiltrated with local anaesthetic using a spinal needle.

Puncture may then be made using one of the following systems (depending on preference):

1. An 18G sheathed needle, or Kellett needle, using the Seldinger technique for catheterization. Contrast injection is used to confirm successful siting of the needle and for preliminary demonstration of the pelvicalyceal system. On occasion air is used as a negative contrast medium to enable targeting of a posterior non-dependent calyx. Upon successful puncture a J-guidewire is inserted and coiled within the collecting system; the sheath is then pushed over the wire, which may be exchanged for a stiffer wire. Dilatation is then performed to the size of the drainage catheter, which is then inserted. Care must be taken not to kink the guidewire within the soft tissues. Sufficient guidewire should be maintained within the collecting system, ideally with the wire in the upper ureter to maintain position and, if kinking does occur, the kinked portion of the wire can be withdrawn outside the skin.

2. Coaxial needle puncture systems using a 22/21G puncturing needle that takes a 0.018 guidewire. This affords a single puncture with a fine needle, with insertion of a three-part coaxial system to allow insertion of 0.035 guidewire and then proceed as in (1) above.

3. The trocar-cannula system, in which direct puncture of the collecting system is made with the drainage catheter already assembled over a trocar. On removal of the trocar the drainage catheter is advanced further into the collecting system.

Having successfully introduced the catheter, it is securely fixed to the skin and drainage commenced.

Antegrade pyelography is rarely performed as an isolated procedure; usually it is undertaken following placement of, and via, a nephrostomy catheter as above. Oblique and AP images are taken with gentle introduction of water-soluble contrast medium. Semi-erect films may be necessary to encourage contrast medium down the ureters to show the site and nature of obstruction. Post nephrostomy studies are best performed after a delay of 1–2 days to allow the patient to recover and be able to cooperate, blood clot to resolve, and infected systems to be drained.

Percutaneous nephrolithotomy

This is the removal of renal calculi through a nephrostomy track. It is often reserved for large complicated calculi which are unsuitable for extracorporeal shock-wave lithotripsy.

Technique

Pre-procedure planning may include a CT KUB and CTU to localize stones and to choose most appropriate access.

Puncture of the collecting system

A lower pole posterior calyx is ideally chosen if the calculus is situated in the renal pelvis. Otherwise the calyx in which the calculus is situated is usually punctured. Special care must be taken if puncturing above the twelfth rib because of the risk of perforating the diaphragm and pleura. Puncture is in an oblique plane from the posterior axillary line through the renal parenchyma. Puncture of the selected calyx is made using a combination of US and a rotating C-arm fluoroscopic facility. On successful puncture a guidewire is inserted through the cannula and as much wire as possible is guided into the collecting system. The cannula is then exchanged for an angled catheter and the wire and catheter are manipulated into the distal ureter. At this stage full dilatation may be performed (single-stage) or a nephrostomy tube left in situ with dilatation later (two-stage procedure).

Renal arteriography

Technique

The catheter is placed proximal to the renal vessels (i.e. approximately T12) and AP and oblique runs are performed (the oblique run demonstrating the renal origins). Selective catheterization as required is used for optimal demonstration of intrarenal vessels, and prior to interventional procedures.

Static renal radionuclide scintigraphy

Dynamic renal radionuclide scintigraphy

Radiopharmaceuticals

1. 99mTc-MAG-3 (mercaptoacetyltriglycine), 100 MBq max (0.7 mSv ED); (200 MBq max (1 mSv ED) for first-pass blood flow imaging). Highly protein-bound, it is mainly cleared by tubular secretion (80%), but with around 20% glomerular filtration. It is now the radiopharmaceutical of choice owing to better image quality, particularly in patients with impaired renal function (compared with 99mTc-diethylene triaminepentacetic acid (DTPA)).

2. 99mTc-DTPA, 150 MBq typical (1 mSv ED), 300 MBq max (2 mSv ED); (800 MBq max (5 mSv ED) for first-pass blood flow imaging). This is cleared by glomerular filtration. There is a lower kidney/background ratio than MAG-3 resulting in poorer image quality and noisier clearance curves.

3. 123I-orthoiodohippurate (hippuran). This is almost entirely cleared by tubular secretion. It is not in common clinical use now.

Technique

1. The patient lies supine or sits reclining with their back against the camera.

2. The radiopharmaceutical is injected i.v. and image acquisition is started simultaneously.

3. Perform dynamic acquisition with 10–15 s frames for 30–40 min. (For quantitative perfusion studies, e.g. in the transplanted kidney, 1–2 s frames over the first minute are acquired.)

4. If poor drainage is seen from one or both kidneys after 10–20 min, a diuretic (furosemide 40 mg) is administered slowly during imaging. Imaging should be continued for at least a further 15 min. Since maximum diuresis does not occur until 15 min after administration of furosemide, as an alternative it may be given 15 min before the radiopharmaceutical (the so-called ‘F – 15’ renogram), which can be useful after equivocal standard ‘F + 20’ studies.

5. If significant retention in the kidneys is apparent at the end of the imaging period, the patient is asked to void and walk around for a minute, then a further short image is taken.

Additional techniques

1. Pre- and 1 h post-captopril (25–50 mg) study for diagnosis of renal artery stenosis (RAS). Radionuclide techniques have the advantage of showing the functional effect of a stenotic renal artery, as opposed to the anatomical demonstration as provided by angiographic techniques. This, therefore, helps identify patients in whom RAS is the cause of hypertension (renovascular). The patient should, ideally, stop diuretic and ACE inhibitor medication 3–5 days prior to the test. The renogram curves post-captopril are compared with the baseline study to look for a deterioration.

2. In direct micturating cystography following renography to demonstrate vesicoureteric reflux. The bladder must not have been emptied and the kidneys should be reasonably clear of activity. Continuous dynamic 5-s images are acquired for 2 min before and up to 3 min after micturition, with generation of bladder and kidney time–activity curves.

3. Glomerular filtration rate (GFR) measurement and individual kidney GFR can be performed with DTPA studies by taking blood samples for counting. GFR is measured using a non-imaging technique with 51Cr EDTA.

Direct radionuclide micturating cystography