Tubulointerstitial diseases Flashcards

1
Q

What are the causes of acute interstitial nephritis?

A
  • Drugs (RSVP)
  • infections
  • autoimmune disorders
  • acute obstructive disorders

RSVP

  • Rifampin
  • Sulpha drugs
  • Proton pump inhibitors
  • Pee pill (diuretics)
  • Penicillins
  • Pain killers (NSAIDs)
  • Phenytoin
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2
Q

What is the pathophysiology or acute interstitial nephritis?

A

tissue edema, tubular cell injury, & compromised tubular flow caused by

  • aggressive inflammatory infiltrates
  • frank obstruction of the tubules with casts, cellular debris, or crystals
  • drugs inducing type IV hypersensitivity reaction
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3
Q

What are the clinical features of acute interstitial nephritis?

A
  • AKI
  • eosinophilia
  • rash
  • fever
  • pyuria & hematuria
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4
Q

What are the diagnostics & management for acute interstitial nephritis?

A
  • elevated serum creatinine, eosinophilia
  • eosinophiluria
  • WBC cast, microscopic hematuria or mild proteinuria

stop offending drug & administer IV fluids
give glucocorticoids if function doesn’t improve

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5
Q

What are the causes of renal papillary necrosis?

A

POST CARDS

  • Pyelonephritis
  • Obstruction
  • Sickle cell disease
  • Tuberculosis
  • Cirrhosis
  • Analgesics (NSAIDs)
  • Rejection of renal transplant
  • Diabetes
  • Systemic vasculitis
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6
Q

What is the pathophysiology & clinical features of renal papillary necrosis?

A

necrosis & sloughing of papillae -> ureteral obstruction -> scarring

  • flank pain (colicky pain)
  • hematuria
  • proteinuria
  • fever, chills
  • AKI
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7
Q

How is renal papillary necrosis diagnosed & treated?

A
  • CT urography will show bilateral calcifications (ring shadows)

treat underlying cause

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8
Q

What are the types of renal tubular acidosis?

A

TYPE I -> inability to secrete H at distal tubule
TYPE II -> inability to reabsorb HCO3 at proximal tubule
TYPE IV -> aldosterone deficiency or resistance in collecting duct & distal convoluted tubules

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9
Q

What are the causes & clinical features of RTA type I?

A

caused by

  • congenital anomalies
  • multiple myeloma
  • nephrocalcinosis
  • amphotrecin B toxicity
  • autoimmune diseases

clinical features

  • urine PH > 5.5 (n=4.5-4.7)
  • hypokalemia & renal stones
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10
Q

How is RTA type I treated?

A
  • alkalinization therapy with oral sodium bicarbonate
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11
Q

What are the causes & clinical features of RTA type II?

A

caused by

  • Fanconi syndrome
  • multiple myeloma
  • carbonic anhydrase inhibitors

Clinical features

  • hypokalemia & Vitamin D-resistant hypophosphatemic osteomalacia
  • if serum HCO3 is higher than its reabsorption threshold pH >5.5
  • if serum HCO3 if depleted pH <5.5
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12
Q

How is RTA type II treated?

A

alkali therapy with orally administered potassium citrate

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13
Q

What are the causes & clinical features of RTA type IV?

A
  • increased aldosterone production -> DM, ACE-i, ARBs, adrenal insufficiency
  • aldosterone resistance -> K sparing diuretics, nephropathy due to obstruction, TMP-SMX

clinical features

  • urine pH <5.5
  • hyperkalemia
  • decreased urinary ammonium excretion
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14
Q

How is RTA type IV treated?

A
  • furosemide
  • mineralocorticoid replacement
  • low-potassium diet
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