25: Nephrolithiasis Flashcards

1
Q

Causes of hypercalciuria

A
  • Bone resorption (overactive osteoclasts)
    • Hyperparathyroidism
    • Hyperthyroidism
    • Cancer
    • Renal tubular acidosis
    • Corticosteroids (prednisone)
  • Vitamin D excess
    • Vitamin D25
    • Vitamin D1,25
    • Inflammatory conditions
      • Sarcoidosis
      • Lymphoma
  • Idiopathic
    • Gut (absorptive)
    • Bone (↑ turnover)
    • Kidney (renal leak)
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2
Q

Calcium oxalate stones

A
  • 70% of stones
  • Normally:
    • 10% of dietary oxalate absorbed in colon
    • 90% bound by Ca and passed via stool
  • Risk factors for CaOx stone formation
    • Hypercalciuria
    • Hyperuricosuria (“salt out” CaOx)
    • Hypocitraturia (**citrate **inhibits calcium crystal formation)
    • Hyperoxaluria
    • Low urine volume
    • Medical conditions
      • Malabsoprtion (IBD, gastric bypass –> ↑oxalate uptake in colon)
      • Obesity/gout
      • Genetic dz (hyperoxalosis)
  • Envelope appearance on UA/micro
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3
Q

Calcium phosphate stones

A
  • 10-15% of stones
  • Coffin lid appearance on UA/micro
  • Risk factors:
    • Hypercalciuria
    • Alkaline urine pH (>7) (CaP forms under basic conditions)
    • Medullary sponge kidney (cystic kidney dz)
  • CaP crystals in the form of:
    • **Apatite **(bones/teeth)
    • Brushite (Ca monohydrogen phosphate): large stone, requires surgical removal
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4
Q

Uric acid stones

A
  • 10-15% of stones
  • 2nd most common mineral type
  • Diamond shape on UA/micro
  • Risk factors:
    • Acidic urine
    • Gout
    • Hyperuricemia
    • Metabolic syndrome
    • Malignancies
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5
Q

Struvite stones

A
  • Staghorn” stones
  • MgNH4PO4 + CaCO3
  • From urease-producing bacteria
    • Proteus
    • Haemophilus
    • Klebsiella
    • Ureaplasma urealyticum
  • Risk factors:
    • Women
    • Chronic urinary obstruction
    • Neurologic dysfunction
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6
Q

Cystine stones

A
  • AutR defect in tubular transporters of dibasic AA’s
    • Cystine
    • Ornithine
    • Arginine
    • Lysine
  • Cystine insoluble in acidic urine
  • Hexagonal urine crystals (less commonly, Staghorns) on UA/micro
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7
Q

Drug-induced stones

A

Indinavir, bactrim, allopurinol

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8
Q

Stone inhibitors

A

Negatively charged molecules (ionic or macromolecular/protein-based) that inhibit crystal nucleation by adsorbing onto crystal surface and interfering with lattice formation.

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9
Q

Nephrolithiasis presentation

A
  • Acute, colicky flank pain radiating to groin
  • Exam: CVA tenderness may be present
  • Hematuria (90% of cases; absence does not rule out stones)
  • Less often presentations:
    • Silent ureteral obstruction
    • Unexplained persistent UTI
    • Painless hematuria
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10
Q

kidneys-ureters-bladder (KUB) radiograph

A
  • To detect obvious abnormalities of the urinary system, such as kidney stones
  • Sensitivity 45-85%
  • Use in treatment planning (stone localization, diameter)
  • Preferred method of follow-up for radio-opaque stones (visible)
  • Cannot detect small stones
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11
Q

Renal ultrasound

A
  • Can image both radiolucent and radiopaque stones
  • Low radiation exposure (can use in pregnant patients, children)
  • High specificity (82-100%)
  • Quantifying size for small stones (<5mm) poor
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12
Q

Helical non-contrast CT urogram

A
  • Study of choice (sens: 95-98%, spec: 98-100%)
  • Can visualize uric acid stones by gray-scale methods
  • Help dx UT abnormalities predisoposing to stones
  • R/o conditions which may masquerade as renal colic (abdominal pain commonly caused by kidney stones)
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13
Q

Likelihood of passage of ureteral stones

A
  • If <2mm, 8 days to pass. Intervention unnecessary.
  • If 4-6mm, 22 days to pass. Need for intervention in 50% of cases.
  • If >6mm, intervention necessary.
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14
Q

Main causes of stone formation

A
  • Hypercalciuria
  • Hyperoxalauria
  • Alkalitic urine pH
  • Hyperuricosuria
  • UTI
  • Low urine citrate
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15
Q

Management: First time stone

A
  • Risk factor assessment:
    • Occupation/environment
    • Family Hx
    • Diet: protein, purines, Na, fluid, Ca, oxalate
    • Rx: triamterene, sulfonamides, carbonic anhydrase inhibitors
  • Lab evaluation:
    • Creatinine, HCO3, Ca, Phos, PTH
    • Urine analysis, Cx
  • Referral to stone clinic if:
    • Children
    • Solitary kidney
    • Struvite stones
    • Abn renal funct
    • RTA
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16
Q

Management: Recurrent stones or high-risk pt

A
  • Urine (24 hour) collection for:
    • Ca
    • Oxalate
    • Citrate
    • Uric acid
    • pH
    • Cystine
  • Urine cx if struvite/staghorn
17
Q

Nephrolithiasis treatment

A
  • Decrease ionic concentrations
    • Urine calcium: thiazides
    • Urine oxalate: diet
    • Uric acid: diet, allopurinol
  • Alter urine characteristics
    • Primary hyperparathyroidism: parathyroidectomy
    • Distal RTA: NaHCO3 therapy
  • Alter urine supersaturation
    • ↑water (single most important therapeutic intervention)
    • ↑citrate: urocit K
18
Q

Urinary citrate

A

Forms strong complexes with Ca in urine –> decreased free Ca ion –> lowered urine CaOx and CaP saturation

19
Q

Risk factors for uric acid stones

A
  • Low urine pH
  • Obesity and metabolic syndrome
  • Hyperuricosuria (rx allopurinol)
20
Q

Captopril

A

Makes cystine complexes 200x more soluble in urine

21
Q

Extracorporeal Shock Wave Lithotripsy (ESWL)

A
  • For proximal stones <2cm
  • Contraindications: bleeding tendencies, pregnancy, uncontrolled HTN, UTI, morbid obesity
  • Long-term risks: renal insufficiency, HTN
22
Q

Ureteroscopic removal

A
  • Fragmentation of stone via laser, electrohydraulics or ultrasound
  • Most stones can be treated
23
Q

Percutaneous nephrolithotomy

A
  • Nephroscope inserted through kidney capsule
  • Indicated for large proximal stones