24 Non-Glomerular Hematuria Flashcards

(33 cards)

1
Q

Non-Glomerular Causes of Hematuria:
DDx & Work-up

A
  • DDx
    • Cancer – until proven otherwise
    • Trauma
    • Stones
    • Infection
    • Iatrogenic
    • Miscellaneous
  • Work-up
    • Urinalysis
      • Upper vs. lower tract
    • CT scan
      • (-) Contrast or (+/-) contrast
      • [Historical: Intravenous pyelogram (IVP)]
    • Cystoscopy
    • Retrograde urethrogram and cystogram
    • 90% of work up will be negative
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2
Q

Hematuria of Cancer

A
  • Gross hematuria common
  • Work-up as indicated and urine cytology
  • Bladder cancer- Transitional cell –Urothelial cell
  • Renal carcinoma
    • Detected incidentally, not usually from hematuria
  • Prostate cancer
    • Dectected by PSA and rectal exam, not hematuria
  • Urethral cancer
    • Only GU cancer more common in females
    • Urothelial cancer in proximal urethra
    • Squamous cancer in distal
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3
Q

Hematuria from Trauma

A
  • Blunt and penetrating renal trauma
  • Ureteral trauma
  • Blunt and penetrating bladder trauma
  • Rupture of the membranous urethra
  • Straddle trauma to the bulbar urethra
  • Injury to the penile urethra
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4
Q

Blunt Renal Trauma

  • Etiology
  • Grade
  • W/ microscopic hematuria
  • CT
  • Treatment
A
  • Etiology
    • Motor vehicle accident’s
    • Falls
    • Contact sports
  • Graded I - V
  • W/ microscopic hematuria
    • Work-up not necessary if hemodynamically stable
    • Except children or clinical suspicion
  • CT usually done for other injuries
  • Treatment
    • Observation
      • Until urine clear
    • Surgery
      • Grade V
      • Thrombosis of the main renal artery
      • Multiple major lacerations
      • Avulsion of the main renal artery and/or vein
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5
Q

Penetrating Renal & Bladder Trauma

A
  • Both
    • Stab or gun shot wound
  • Renal
    • 88% associated with other organ injury
    • After stabilization, surgical exploration
      • Rare to study
  • Bladder
    • Diagnostic studies only if stable
    • Surgical repair
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6
Q

Ureteral Trauma

A
  • Rare
  • Deceleration injury or penetrating trauma
  • Iatrogenic causes
  • Incidental congenital anomalies
    • Uretero-pelvic junction obstruction
  • Surgical repair
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7
Q

Blunt Bladder Trauma

A
  • Motor vehicle accident’s, deceleration injuries
  • Gross hematuria typically present
  • Types
    • Contusion
    • Extraperitoneal rupture
      • 10% of pelvic fracture
      • Treatment: bladder drainage
    • Intraperitoneal rupture
      • Surgical repair
  • Retrograde urethrogram first
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8
Q

Rupture of the Membranous Urethra

A
  • 10% pelvic fractures in males
  • GROSS BLOOD AT MEATUS
  • Retrograde urethrogram
  • Operative realignment
    • Open or endoscopic
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9
Q

Straddle Trauma to the Bulbar Urethra

A
  • Butterfly hematoma
  • Treatment: extended drainage
  • Long term: stricture disease
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10
Q

Injury to the Penile Urethra

A
  • Penetrating trauma or sexual activity
    • Fractured penis
  • Gross blood
  • Retrograde urethrogram
  • Open surgical repair
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11
Q

Kidney Stones:
Calculus Disease

A
  • One of the most common renal diseases of the Western World
  • Present in Egyptian mummies dated to 4800 B.C.
  • 2 to 4% of the American population are at risk of at least one stone episode
    during his/her life time
  • 50% of those will experience at least one further episode of stone formation over the ensuing 10 years
  • Stone disease accounts for 1 of every 1000 hospitalizations
    • 200,000 hospitalizations per year
    • Exceeding $400 million dollars annually
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12
Q

Kidney Stones:
3 Theories of Stone Formation

A
  • Matrix Theory
    • Organic matrix compounds present in all stones are causally related to stone formation
  • Inhibitor Theory
    • Deficiency in the urine of substrates which normally inhibit crystallization and growth
  • Crystalloid or Precipitation-Crystallization Theory
    • Supersaturation with respect to the stone-forming constituents
  • Reality: likely due to a combination of these theories
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13
Q

Kidney Stones:
Calcium Oxalate Monohydrate or Dihydrate:
Pathogenesis / Risk Factors

A
  • Idiopathic
  • Metabolic defects
    • Alkaline urine pH
    • Hypercalciuria
    • Hyperoxaluria
    • Hyperuricosuria
  • Family history
  • Dehydration
  • Diet or medications
    • Vitamins A, D, C
    • Acetazolamide
    • Antacid abuse
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14
Q

Kidney Stones:
CaOx Features

A
  • Accounts for about 85% of all stones
  • Male to female ratio is 3-4:1
  • High incidence of stones in the South Eastern United States = Stone Belt [Texas to Virginia and south]
  • Hypercalciuria
    • > 300 mg/24 hr in males
    • > 250 mg/24 hr in females
  • Calcium homeostasis requires
    • Hormones: 1,25 vitamin D, PTH
    • Organs: bone, kidney, gut
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15
Q

Kidney Stones:
Hypercalciuria

A
  • Increased gut absorption of calcium
    • Increased 1,25 vit D (sarcoid, primary hyperparathyroidism)
    • Dietary calcium excess
    • Idiopathic
  • Increased bone reabsorption
    • Primary hyperparathyroidism
    • Distal RTA
    • Idiopathic
  • Increased renal excretion
    • Hypercalcemia of any cause
    • Distal RTA
    • Dietary sodium or protein excess
    • Idiopathic hypercalciuria
    • Renal leak
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16
Q

Kidney Stones:
Other Hypers

  • Hyperuricosuria
  • Hyperoxaluria
A
  • Hyperuricosuria
    • Uric acid crystals may serve as a nucleus for calcium salt precipitation
  • Hyperoxaluria
    • > 40 mg/24 hours
    • End product of metabolism
    • Forms an insoluble complex with calcium
    • NOT pH dependent
    • Causes:
      • Increased production
        • Congenital
        • Vitamic C (2 gm/day)
        • Ethylene glycol
      • Increased intestinal absorption
        • Dietary excess
        • Enteric hyperoxaluria
        • Dietary calcium restriction
17
Q

Kidney Stones:
Enteric Hyperoxaluria

A
  • Malabsorption syndromes
    • Crohn’s disease
    • Intestinal bypass
  • Pathophysiology
    • Fatty acid soaps bind calcium in the gut
    • Calcium prevented from complexing with oxalate
    • Oxalate then “free” to be absorbed in large quantities
  • Paradoxical treatment
    • Calcium or magnesium supplementation
    • Treat the underlying condition
18
Q

Kidney Stones:
Calcium Oxalate Diagnosis & Treatment

A
  • Diagnosis
    • Stone analysis
    • Calcium oxalate crystals NOT diagnostic
    • 24 hour urine studies
  • Treatment
    • Decrease urinary calcium/sodium/oxalate/uric acid
    • Inhibitors
    • Fluids, treat underlying defect, education
19
Q

Kidney Stones:
Calcium Phosphate

  • Pathogenesis/risk factors
  • Clinical features
  • Diagnosis
  • Treatment
A
  • Pathogenesis/risk factors
    • Hypercalciuria
      • Vitamin D intoxication
      • Hyperparathyroidism
      • Sarcoid
    • Alkaline urine
      • Urinary acidification defect
        • Distal, Type I RTA
      • Acetazolamide
      • Milk-alkali syndrome
        • Excessive intake of milk/antacids to control dyspepsia: results in hypercalcemia
  • Clinical features
    • Common minor constituent of garden variety calcium stones
    • Pure calcium phosphate stones are rare
  • Diagnosis
    • Stone analysis; crystals NOT diagnostic
    • 24 hour urine studies: hypercalciuria
    • Identify other causative risk factors
  • Treatment
    • Decrease calcium excretion
    • Fluids, Rx underlying defect, education
20
Q

Kidney Stones:
Urate Nephropathy

A
  • Uric acid stones
    • Most common form of uric acid disposition in the urinary tract
  • Acute uric acid nephropathy
    • Particularly malignant form of uric acid precipitation
    • Chemotherapy for a lymphoma or leukemia
    • May obstruct of the urinary tubules by sludging
    • True crystals, or stones do not form
  • Chronic urate nephropathy
    • Unrelated to stone disease
    • Progressive disease occurring in a minority of gout patients
    • Precipitates in the interstitium and pyramids
      • Interstitial nephritis
21
Q

Kidney Stones:
Uric Acid Calculi

  • Pathogenesis
  • Clinical features
  • Diagnosis
  • Treatment
A
  • Pathogenesis
    • Hyperuricosuria
      • gout
      • psoriasis
      • Lesch Nyhan syndrome
        • Juvenile gout: x-linked recessive deficiency in enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT): resulting in elevated uric acid
      • obesity
      • Status post chemotx
    • Persistently acid, concentrated urine (pH < 5.5)
      • chronic diarrheal disease, esp. via ileostomy
    • Uric acid solubility decreases 10-20x when urine pH falls 7 to 5
  • Clinical features
    • 5-10% of all stones
    • Only truly radiolucent stone
  • Diagnosis
    • Stone analysis
    • Uric acid crystals in the urine NOT diagnostic
    • 24 hour urine studies: hyperuricosuria
  • Treatment
    • Very susceptible to solubility conditions
    • Alkalinization to reach urinary pH 6.5-7.0 (solubility product)
    • Fluids, treat underlying condition, education
22
Q

Kidney Stones:
Struvite Stones

  • Pathogenesis / risk factors
  • Clinical features
  • Diagnosis
  • Treatment
A
  • Pathogenesis / risk factors
    • Urinary tract infection with urea-splitting organism
      • Proteus - most common
      • Klebsiella
      • Serratia
      • Enterobacter
    • Markedly alkaline urine (pH 7.5-8.0)
    • Supersaturation with magnesium-ammonium phosphate
  • Clinical features
    • Accounts for about 20% of stones
    • Most common cause of staghorn calculi
    • Most common stone in women and paraplegics
    • Recurrent UTIs
      • Bacteria reside in stone (i.e. coral)
    • 40% of struvite stones are mixed calculi
    • Sequela
      • Progressive renal insufficiency
      • Urosepsis or perinephric abscesses
      • Obstruction
  • Diagnosis
    • Stone analysis
    • Struvite crystals diagnostic of UTI with urea splitting organism
      • NOT necessarily struvite stone
    • Urinary pH 8 suspect struvite stones
  • Treatment
    • Antibiotics
    • Percutaneous surgery/lithotripsy
    • Fluids, treat underlying disease, education
23
Q

Kidney Stones:
Cystine Calculi

  • Pathogenesis / risk factors
  • Clinical features
  • Diagnosis
  • Treatment
  • Drugs
A
  • Pathogenesis / risk factors
    • Cystinuria
      • Autosomal recessive genetic defect in dibasic amino acid transport in renal tubule and gastric mucosa
        • COLA = cystine, ornithine, lysine, arginine
      • Only amino acid to cause clinical disease
    • 1% of all stones
  • Clinical features
    • Onset often in childhood or early adolescence
    • Family history
    • Staghorn calculi can form, mildly radio-opaque
    • Progression to renal failure
      • Renal parenchymal damage
  • Diagnosis
    • Stone analysis
    • Cystine crystalluria
      • Hexagonal crystals
    • Cyanide-nitroprusside test
      • Qualitative
    • 24 hour urine studies
      • Quantitative
      • Homozygous vs. heterozygous
  • Treatment
    • High fluid intake (4L/d)
    • Patient education- compliance
    • Resistant to ESWL
    • Meds
  • Drugs
    • Alkali therapy – Potassium Citrate
      • Increase in cystine solubility at urine pH > 7.5
    • d-Penicillamine
      • Covalently bonds to cystine, making a soluble complex
      • Toxic – glomerulonephritis, Lupus syndrome, marrow depression
    • Tiopronin (Thiola)—similar action to penicillamine but better tolerated
24
Q

Kidney Stones:
Inhibitors

A
  • Deficient in urine of stone-former
  • Citrate
    • Forms a soluble Ca+2-citrate complex
    • Increases urinary pH
    • Hypocitraturia occurs in states of chronic metabolic acidosis (distal RTA, chronic real failure, acetazolamide therapy), K+ depletion and idiopathic cases
    • Presumably raises the formation product of all types of calcium stones
25
Kidney Stones: Clinical Features & Treatment Options
* Dull ache in the loin from distention of the renal capsule * Renal "colic" from acute or transient obstruction * Lumbar area and radiates around and down into groin, testis, labia or thigh * Pain changes as calculus moves * Patient cannot get comfortable * Nausea, vomiting, abdominal distention * Hematuria - gross or microscopic—does not have to be present * Frequency and urgency * Fever/chills
26
Kidney Stones: Acute Management * Diagnostic Procedures * Treatment * Surgery
* Diagnostic Procedures * History and physical examination * Risk factors, associated medical conditions, medications * Urinalysis: pH, rbc, wbc, culture, crystals * Not all crystals are diagnostic of stone disease * Spiral CT without contrast * Current diagnostic test of choice * Patients unable to have contrast agents * Treatment * 90% of stones less than 5 mm in diameter will pass spontaneously * Increase fluid intake * Strain all urine to catch stone for analysis * Steroid, alpha-blocker, antibiotic * Indications for surgical intervention * Infected system * Obstruction persists \>4 weeks * Intractable pain or nausea * Stone unlikely to pass due to size * Surgery * If small calculus in the lower or middle third of the ureter * Ureteroscopy with basket or ESWL * May need to be fragmented to remove * Laser, pneumatic, or electrohydraulic * If large calculus and/or in the pelvis of the kidney, or upper third of the ureter * Ureteroscopy, percutaneous removal or ESWL
27
Kidney Stones: Diagnostic Procedures * CT Scan without contrast * More Diagnostic Procedures
* CT Scan without contrast * “Renal colic CT” * “Kidney stone protocol CT” * CT abd/pelvis without contrast, low dose protocol * Rapid and specific * More Diagnostic Procedures * IVP = intravenous pyelogram * Previously best first test * Evaluation for obstruction and location * Ultrasound * May diagnose obstruction * Locate radio-opaque calculi * Limited in ureteral calculi * KUB = x-ray of the abdomen with pelvis * Kidney, Ureter, Bladder
28
Bladder Stone Surgery * Extracorporeal Shock Wave Lithotripsy - ESWL * Staghorn Calculi
* Extracorporeal Shock Wave Lithotripsy - ESWL * Effective and safe procedure * Revolutionized the treatment of all types of stone disease * Typically first line therapy * Minimal anesthesia * Outpatient * Staghorn Calculi * Percutaneous surgery alone or with ESWL * Recurrence reported at 10-40%
29
Percutaneous Nephrolithotomy: Chronic Management * Metabolic Work Up * Treatment
* Metabolic Work Up * Blood chemistry: calcium, phosphate, bicarbonate, uric acid, BUN, creatinine * 24 hour urine collections on "normal" diet * calcium nl to 300 mg in M, 250 mg in F * uric acid nl to 800 mg in M, 750 mg in F * sodium desired 100-125 mEq * volume desired \>2000 ml * citrate nl 300-900 mg * oxalate nl \< 40 mg * cystine nl \< 100 mg * Stone analysis * Treatment * Fluid intake 24 hours/day \> 2-3 L/day * Dietary modification * Regulate urinary pH * Alkalinization: uric acid and cystine stones * Acidification almost never indicated * Cranberry juice NOT indicated
30
Percutaneous Nephrolithotomy: Drug Therapy
* Citrate * Alkalinization also for calcium phosphate stones * Thiazide diuretic * Decreases urinary calcium for calcium stones * Sodium cellulose phosphate * Binds calcium in the gut for absorptive hypercalciuria * Allopurinol * Decreases urinary uric acid for uric acid and calcium stones * Antibiotics * D-penicillamine * Thiola
31
Percutaneous Nephrolithotomy: Prostate * Benign Prostatic Hyperplasia * Photovaporization of the Prostate
* Benign Prostatic Hyperplasia * Common cause hematuria: turbulent flow * Symptoms determine therapy, not size! * Meds: alpha blockers, 5-alpha reductase inhibitors * Surgery * Minimally invasive * Microwave, laser, radiofrequency * Endoscopic Resection – transurethral resection of prostate (TURP) * Open surgery * Photovaporization of the Prostate * Equivalent results to TURP * Less side effects
32
Renal Cystic Disease * Simple Renal Cysts * Adult Polycystic Renal Disease
* Simple Renal Cysts * Not cause of hematuria * Definition * Homogeneous throughout * Smooth walls * Posterior enhancement (Ultrasound) * Adult Polycystic Renal Disease * 1 in 500 * Cause end-stage renal disease * Autosomal dominant * Involves nephron * Other organs * Pancreas, spleen, lungs * Hypertension common * Flank pain * No treatment necessary to cure, treatment symptoms
33
Renal Cystic Disease * Infectious Causes * Miscellaneous Rare Causes
* Infectious Causes * Cystitis * Urethritis * Prostatitis * Pyelonephritis * Examine urinalysis & culture * White blood cell’s, nitrate positive, leukocyte esterase positive * Miscellaneous Rare Causes * Instrumentation * Foreign body * Anticoagulation * Remember: something is bleeding * Chemotherapy * Cyclophosphamide