- •Hematuria II: causes and investigation
- •Hematospermia
- •Lower urinary tract symptoms (LUTS)
- •Nocturia and nocturnal polyuria
- •Flank pain
- •Urinary incontinence in adults
- •Genital symptoms
- •Abdominal examination in urological disease
- •Digital rectal examination (DRE)
- •Lumps in the groin
- •Lumps in the scrotum
- •2 Urological investigations
- •Urine examination
- •Urine cytology
- •Radiological imaging of the urinary tract
- •Uses of plain abdominal radiography (KUB X-ray—kidneys, ureters, bladder)
- •Intravenous pyelography (IVP)
- •Other urological contrast studies
- •Computed tomography (CT) and magnetic resonance imaging (MRI)
- •Radioisotope imaging
- •Post-void residual urine volume measurement
- •3 Bladder outlet obstruction
- •Regulation of prostate growth and development of benign prostatic hyperplasia (BPH)
- •Pathophysiology and causes of bladder outlet obstruction (BOO) and BPH
- •Benign prostatic obstruction (BPO): symptoms and signs
- •Diagnostic tests in men with LUTS thought to be due to BPH
- •Why do men seek treatment for their symptoms?
- •Watchful waiting for uncomplicated BPH
- •Medical management of BPH: combination therapy
- •Medical management of BPH: alternative drug therapy
- •Minimally invasive management of BPH: surgical alternatives to TURP
- •Invasive surgical alternatives to TURP
- •TURP and open prostatectomy
- •Indications for and technique of urethral catheterization
- •Indications for and technique of suprapubic catheterization
- •Management of nocturia and nocturnal polyuria
- •High-pressure chronic retention (HPCR)
- •Bladder outlet obstruction and retention in women
- •Urethral stricture disease
- •4 Incontinence
- •Causes and pathophysiology
- •Evaluation
- •Treatment of sphincter weakness incontinence: injection therapy
- •Treatment of sphincter weakness incontinence: retropubic suspension
- •Treatment of sphincter weakness incontinence: pubovaginal slings
- •Overactive bladder: conventional treatment
- •Overactive bladder: options for failed conventional therapy
- •“Mixed” incontinence
- •Post-prostatectomy incontinence
- •Incontinence in the elderly patient
- •Urinary tract infection: microbiology
- •Lower urinary tract infection
- •Recurrent urinary tract infection
- •Urinary tract infection: treatment
- •Acute pyelonephritis
- •Pyonephrosis and perinephric abscess
- •Other forms of pyelonephritis
- •Chronic pyelonephritis
- •Septicemia and urosepsis
- •Fournier gangrene
- •Epididymitis and orchitis
- •Periurethral abscess
- •Prostatitis: presentation, evaluation, and treatment
- •Other prostate infections
- •Interstitial cystitis
- •Tuberculosis
- •Parasitic infections
- •HIV in urological surgery
- •6 Urological neoplasia
- •Pathology and molecular biology
- •Prostate cancer: epidemiology and etiology
- •Prostate cancer: incidence, prevalence, and mortality
- •Prostate cancer pathology: premalignant lesions
- •Counseling before prostate cancer screening
- •Prostate cancer: clinical presentation
- •PSA and prostate cancer
- •PSA derivatives: free-to-total ratio, density, and velocity
- •Prostate cancer: transrectal ultrasonography and biopsies
- •Prostate cancer staging
- •Prostate cancer grading
- •General principles of management of localized prostate cancer
- •Management of localized prostate cancer: watchful waiting and active surveillance
- •Management of localized prostate cancer: radical prostatectomy
- •Postoperative course after radical prostatectomy
- •Prostate cancer control with radical prostatectomy
- •Management of localized prostate cancer: radical external beam radiotherapy (EBRT)
- •Management of localized prostate cancer: brachytherapy (BT)
- •Management of localized and radiorecurrent prostate cancer: cryotherapy and HIFU
- •Management of locally advanced nonmetastatic prostate cancer (T3–4 N0M0)
- •Management of advanced prostate cancer: hormone therapy I
- •Management of advanced prostate cancer: hormone therapy II
- •Management of advanced prostate cancer: hormone therapy III
- •Management of advanced prostate cancer: androgen-independent/ castration-resistant disease
- •Palliative management of prostate cancer
- •Prostate cancer: prevention; complementary and alternative therapies
- •Bladder cancer: epidemiology and etiology
- •Bladder cancer: pathology and staging
- •Bladder cancer: presentation
- •Bladder cancer: diagnosis and staging
- •Muscle-invasive bladder cancer: surgical management of localized (pT2/3a) disease
- •Muscle-invasive bladder cancer: radical and palliative radiotherapy
- •Muscle-invasive bladder cancer: management of locally advanced and metastatic disease
- •Bladder cancer: urinary diversion after cystectomy
- •Transitional cell carcinoma (UC) of the renal pelvis and ureter
- •Radiological assessment of renal masses
- •Benign renal masses
- •Renal cell carcinoma: epidemiology and etiology
- •Renal cell carcinoma: pathology, staging, and prognosis
- •Renal cell carcinoma: presentation and investigations
- •Renal cell carcinoma: active surveillance
- •Renal cell carcinoma: surgical treatment I
- •Renal cell carcinoma: surgical treatment II
- •Renal cell carcinoma: management of metastatic disease
- •Testicular cancer: epidemiology and etiology
- •Testicular cancer: clinical presentation
- •Testicular cancer: serum markers
- •Testicular cancer: pathology and staging
- •Testicular cancer: prognostic staging system for metastatic germ cell cancer
- •Testicular cancer: management of non-seminomatous germ cell tumors (NSGCT)
- •Testicular cancer: management of seminoma, IGCN, and lymphoma
- •Penile neoplasia: benign, viral-related, and premalignant lesions
- •Penile cancer: epidemiology, risk factors, and pathology
- •Squamous cell carcinoma of the penis: clinical management
- •Carcinoma of the scrotum
- •Tumors of the testicular adnexa
- •Urethral cancer
- •Wilms tumor and neuroblastoma
- •7 Miscellaneous urological diseases of the kidney
- •Cystic renal disease: simple cysts
- •Cystic renal disease: calyceal diverticulum
- •Cystic renal disease: medullary sponge kidney (MSK)
- •Acquired renal cystic disease (ARCD)
- •Autosomal dominant (adult) polycystic kidney disease (ADPKD)
- •Ureteropelvic junction (UPJ) obstruction in adults
- •Anomalies of renal ascent and fusion: horseshoe kidney, pelvic kidney, malrotation
- •Renal duplications
- •8 Stone disease
- •Kidney stones: epidemiology
- •Kidney stones: types and predisposing factors
- •Kidney stones: mechanisms of formation
- •Evaluation of the stone former
- •Kidney stones: presentation and diagnosis
- •Kidney stone treatment options: watchful waiting
- •Stone fragmentation techniques: extracorporeal lithotripsy (ESWL)
- •Intracorporeal techniques of stone fragmentation (fragmentation within the body)
- •Kidney stone treatment: percutaneous nephrolithotomy (PCNL)
- •Kidney stones: open stone surgery
- •Kidney stones: medical therapy (dissolution therapy)
- •Ureteric stones: presentation
- •Ureteric stones: diagnostic radiological imaging
- •Ureteric stones: acute management
- •Ureteric stones: indications for intervention to relieve obstruction and/or remove the stone
- •Ureteric stone treatment
- •Treatment options for ureteric stones
- •Prevention of calcium oxalate stone formation
- •Bladder stones
- •Management of ureteric stones in pregnancy
- •Hydronephrosis
- •Management of ureteric strictures (other than UPJ obstruction)
- •Pathophysiology of urinary tract obstruction
- •Ureter innervation
- •10 Trauma to the urinary tract and other urological emergencies
- •Renal trauma: clinical and radiological assessment
- •Renal trauma: treatment
- •Ureteral injuries: mechanisms and diagnosis
- •Ureteral injuries: management
- •Bladder and urethral injuries associated with pelvic fractures
- •Bladder injuries
- •Posterior urethral injuries in males and urethral injuries in females
- •Anterior urethral injuries
- •Testicular injuries
- •Penile injuries
- •Torsion of the testis and testicular appendages
- •Paraphimosis
- •Malignant ureteral obstruction
- •Spinal cord and cauda equina compression
- •11 Infertility
- •Male reproductive physiology
- •Etiology and evaluation of male infertility
- •Lab investigation of male infertility
- •Oligospermia and azoospermia
- •Varicocele
- •Treatment options for male factor infertility
- •12 Disorders of erectile function, ejaculation, and seminal vesicles
- •Physiology of erection and ejaculation
- •Impotence: evaluation
- •Impotence: treatment
- •Retrograde ejaculation
- •Peyronie’s disease
- •Priapism
- •13 Neuropathic bladder
- •Innervation of the lower urinary tract (LUT)
- •Physiology of urine storage and micturition
- •Bladder and sphincter behavior in the patient with neurological disease
- •The neuropathic lower urinary tract: clinical consequences of storage and emptying problems
- •Bladder management techniques for the neuropathic patient
- •Catheters and sheaths and the neuropathic patient
- •Management of incontinence in the neuropathic patient
- •Management of recurrent urinary tract infections (UTIs) in the neuropathic patient
- •Management of hydronephrosis in the neuropathic patient
- •Bladder dysfunction in multiple sclerosis, in Parkinson disease, after stroke, and in other neurological disease
- •Neuromodulation in lower urinary tract dysfunction
- •14 Urological problems in pregnancy
- •Physiological and anatomical changes in the urinary tract
- •Urinary tract infection (UTI)
- •Hydronephrosis
- •15 Pediatric urology
- •Embryology: urinary tract
- •Undescended testes
- •Urinary tract infection (UTI)
- •Ectopic ureter
- •Ureterocele
- •Ureteropelvic junction (UPJ) obstruction
- •Hypospadias
- •Normal sexual differentiation
- •Abnormal sexual differentiation
- •Cystic kidney disease
- •Exstrophy
- •Epispadias
- •Posterior urethral valves
- •Non-neurogenic voiding dysfunction
- •Nocturnal enuresis
- •16 Urological surgery and equipment
- •Preparation of the patient for urological surgery
- •Antibiotic prophylaxis in urological surgery
- •Complications of surgery in general: DVT and PE
- •Fluid balance and management of shock in the surgical patient
- •Patient safety in the operating room
- •Transurethral resection (TUR) syndrome
- •Catheters and drains in urological surgery
- •Guide wires
- •JJ stents
- •Lasers in urological surgery
- •Diathermy
- •Sterilization of urological equipment
- •Telescopes and light sources in urological endoscopy
- •Consent: general principles
- •Cystoscopy
- •Transurethral resection of the prostate (TURP)
- •Transurethral resection of bladder tumor (TURBT)
- •Optical urethrotomy
- •Circumcision
- •Hydrocele and epididymal cyst removal
- •Nesbit procedure
- •Vasectomy and vasovasostomy
- •Orchiectomy
- •Urological incisions
- •JJ stent insertion
- •Nephrectomy and nephroureterectomy
- •Radical prostatectomy
- •Radical cystectomy
- •Ileal conduit
- •Percutaneous nephrolithotomy (PCNL)
- •Ureteroscopes and ureteroscopy
- •Pyeloplasty
- •Laparoscopic surgery
- •Endoscopic cystolitholapaxy and (open) cystolithotomy
- •Scrotal exploration for torsion and orchiopexy
- •17 Basic science of relevance to urological practice
- •Physiology of bladder and urethra
- •Renal anatomy: renal blood flow and renal function
- •Renal physiology: regulation of water balance
- •Renal physiology: regulation of sodium and potassium excretion
- •Renal physiology: acid–base balance
- •18 Urological eponyms
- •Index
52 CHAPTER 2 Urological investigations
Radioisotope imaging
A variety of organic compounds can be labeled with a radioactive isotope that emits gamma rays, allowing the radiation to penetrate through tissues and reach a gamma camera placed adjacent to the patient. The most commonly used radioisotope is technetium—99mTc (half-life 6 hours, gamma-ray emission energy 0.14 MeV). The excretion characteristics of the organic compound to which the 99mTc is bound determine the clinical use.
MAG3 renogram
99mTc is bound to mercapto-acetyl-triglycine. Over 90% of MAG3 becomes bound to plasma proteins following intravenous injection. It is excreted from the kidneys principally by tubular secretion (glomerular filtration is minimal).
Following intravenous injection, MAG3 is very rapidly excreted (appearing in the kidney within 15 seconds of the injection and starting to appear in the bladder within about 3 minutes). Approximately two-thirds of the injected dose of MAG3 is taken up by the kidneys with each passage of blood through the kidney. The radioactivity over each kidney thus increases rapidly.
The peak of radioactivity represents the point at which delivery of MAG3 to the kidney from the renal artery is equivalent to excretion of MAG3. The radioactivity starts to decline as excretion outstrips supply. Thus, a time–activity curve can be recorded for each kidney. This time– activity curve is known as a renogram.
Images are collected onto a film at 30-second intervals for the first 3 minutes and then at 5-minute intervals for the remainder of the study (usually a total of 30 minutes).
A normal renogram has 3 phases
•First phase: a steeply rising curve lasting 20–30 seconds
•Second phase: a more slowly rising curve, rising to a peak. If the curve does not reach a peak, the second phase is said to rise continually.
A normal second phase ends with a sharp peak.
•Third phase: a curve that descends after the peak. There can be no third phase if there is no peak.
Description of the renogram
No comment is made about the first phase. The second phase is described as being absent, impaired, or normal. The third phase is described as being absent, impaired, or normal.
The time to the peak depends on urine flow and level of hydration and is a crude measure of the time it takes the tracer to travel through the parenchyma of the kidney and through the renal pelvis. The time to the peak of the renogram normally varies between 2 and 4.5 minutes.
If the renogram continues beyond the time at which the peak should normally occur, then there may be a distal obstruction (e.g., at the PUJ or lower down the ureter). In this situation, an injection of 40 mg of Lasix is given (at about 18 minutes) and if the curves start to fall rapidly, this is taken as proof that there is no obstruction. If it continues to rise, there is
RADIOISOTOPE IMAGING 53
obstruction. If it remains flat (neither rising nor falling), this is described as an “equivocal” result.
Parenchymal transit time can also be measured (parenchymal transit time index [PTTI]). The normal range for PTTI is 40–140 seconds, and averages 70 seconds. PTTI is prolonged (to >156 seconds) in obstruction and in renal ischemia. A normal PTTI excludes obstruction.
Uses
•“Split” renal function (i.e., the % function contributed by each kidney)
•Determine presence of renal obstruction—based on shape of renogram curve and PTTI
•Determine presence of renal obstruction in response to IV Lasix injection
DMSA scanning
Dimercaptosuccinic acid (DMSA) is labeled with 99mTc. It is taken up by the proximal tubules and retained there, with very little being excreted in the urine. A “static” image of the kidneys is thus obtained (at about 3–4 hours after intravenous injection of radioisotope). It demonstrates whether a lesion contains functioning nephrons or not.
Uses
•“Split” renal function (i.e., the % function contributed by each kidney)
•Detection of scars in the kidney (these appear as defects in the cortical outline, representing areas in which the radioisotope is not taken up)
Radioisotope bone imaging
99mTc-labeled methylene-disphosphonate (MDP) is taken up by areas of bone where there is increased blood supply and increased osteoblastic activity. There are many causes of a focal increase in isotope uptake— bone metastases, site of fractures, osteomyelitis, TB, benign bone lesions (e.g., osteoma).
Metastases from urological cancers are characterized by their predilection for the spine and the fact that they are multiple (single foci of metastasis are rare). Prostate cancer classically metastasizes in this way.
54 CHAPTER 2 Urological investigations
Uroflowmetry
Uroflowmetry is the measurement of flow rate (Fig. 2.13). It provides a visual image of the “strength” of a patient’s urinary stream. Urine flow rate is measured in mL/s and is determined using commercially available electronic flowmeters (Fig. 2.14).
These flowmeters are able to provide a printout recording the voided volume, maximum flow rate, and time taken to complete the void, together with a record of the flow pattern. Maximum flow rate, Qmax, is influenced by the volume of urine voided, by the contractility of the patient’s bladder, and by the conductivity (resistance) of their urethra.
A number of nomograms are available that relate voided volume to flow rate (Fig. 2.15).
Interpretation and misinterpretation of urine flow rate
The “wag” artifact (see Fig. 2.13b) is seen as a sudden, rapid increase in flow rate on the uroflow tracing and is due to the urine flow suddenly being directed at the center of the flowmeter, producing a sudden artifactual surge in flow rate.
In men with prostatic symptoms, for the same voided volume, flow rate varies substantially on a given day (by as much as 5 mL/s if four flows are done1). Most guidelines recommend measuring at least two flow rates, and using the highest as representing the patient’s best effort.
What does a low flow mean?
Uroflowmetry alone cannot tell you why the flow is abnormal. It cannot distinguish between low flow due to bladder outlet obstruction and that due to a poorly contractile bladder.
(a) 25ml/s flow rate
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Results of uroflowmetry |
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Voiding time |
T100 |
13s |
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Flow time |
TQ |
13s |
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Time to max flow |
TQmax |
8s |
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Max flow rate |
Qmax |
18.1ml/s |
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Average flow rate |
Qave |
11.7ml/s |
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Voided volume |
Vcomp |
151ml |
0 |
10 |
20 |
30 seconds |
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(b) 25ml/s flow rate
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Results of uroflowmetry |
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Voiding time |
T100 |
34s |
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Flow time |
TQ |
34s |
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Time to max flow |
TQmax |
9s |
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Max flow rate |
Qmax |
23.5ml/s |
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Average flow rate |
Qave |
10.2ml/s |
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Voided volume |
Vcomp |
354ml |
0 |
10 |
20 |
30 |
40 |
50 |
seconds |
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Figure 2.13 a) A uroflow trace; b) a uroflow trace with a “wag” artifact. The true Qmax is not 23.5mL/s as the readout suggests but is nearer 18 mL/s.
1 Reynard JM, Peters TJ, Lim C, Abrams P (1996). The value of multiple free-flow studies in men with lower urinary tract symptoms. Br J Urol 77:813–818.
UROFLOWMETRY 55
Figure 2.14 Dantec flowmeter. |
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(ml/s) |
24 |
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–1 s.d. |
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Voided volume (ml)
Figure 2.15 The Bristol flow rate nomogram for men over 50 years. This figure was published in Fitzpatrick J, Societe Internationale D’Urologie Reports. Non-surgical Treatment of BPH, p. 39. Copyright Elsevier 1992.
56 CHAPTER 2 Urological investigations
The principal use of urine flow rate measurement is in the assessment of elderly men with suspected prostatic obstruction (LUTS/BPH), although there is debate about its usefulness as a test for predicting outcome of various treatments.
Some studies suggest that men with poor outcomes are more likely to have had higher flows preoperatively compared with those with good outcomes, whereas other studies report equivalent improvements in symptoms regardless of whether the preoperative flow rate is high or low. A recent Veterans Administration trial comparing transurethral resection of the prostate (TURP) with watchful waiting in men with LUTS/BPH found that flow rate could not predict the likelihood of a good symptomatic outcome after TURP.2
As a consequence, different guidelines give different guidance with regard to performing uroflowmetry in men with LUTS/BPH. It is regarded as an optional test by the American Urological Association (AUA)3 and is recommended by the Fourth International Consultation on BPH.4 The European Association of Urology (EAU) BPH Guidelines state that it “is obligatory prior to undertaking surgical treatment.”5
Generally speaking, urine flow rate measurement is regarded as having insufficient diagnostic accuracy for it to be useful in the assessment of female lower urinary tract dysfunction. Although urine flow measurement can be used to assess voiding function in men with urethral strictures, it has limited value in younger men because in this age group the bladder can compensate for a marked degree of obstruction by contracting more forcefully. Thus, a young man may have a normal flow rate despite having a significant urethral stricture.
2 Bruskewitz RC, Reda DJ, Wasson JH, et al. (1997). Testing to predict outcome after transurethral resection of the prostate. J Urol 157:1304–1308.
3 McConnell JD, Barry MJ, Bruskewitz RC, et al. (1994). Benign prostatic hyperplasia: diagnosis and treatment. Clinical practice guideline. Rockville, MD: Agency for Health Care Policy and Research.
4 Denis L (Ed.) (1997). Fourth International Consultation on Benign Prostatic Hyperplasis (BPH), Paris 1997.
5 EAU guidelines for diagnosis of BPH (2001). Eur Urol 40:256–263.
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