Nephrology Flashcards

1
Q

Discuss the management of hypernatremia

A

Oral free water intake

- 2mL/kg/hr of D5W increase Na by 12mEq/d

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2
Q

What are the characteristic ECG changes for hypokalemia

A
  • flattened or inverted T wave
  • u wave
  • ST depression
  • prolonged QT interval
  • severe: prolonged PR, wide QRS, heart block
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3
Q

Differentiate between nephrotic and nephritic syndrome

A
Nephrotic (associated with glomerular disease):
- proteinuria >40mg/m2/hr of albumin with 3+ urine dipstick
- edema
- hypoalbuminemia
- albuminuria
- hypercholesterolemia 
Nephritic:
- hematuria, gross 3+ on dipstick
- mild proteinuria <40
- hypertension
- azotemia
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4
Q

List the differential for proteinuria

A

Non-nephrotic range (<40, glomerual or tubular)
- postural proteinuria, secondary proteinuria
Nephrotic range
- minimal change nephrotic syndrome
- focal segmental glomerulosclerosis
- rare: IgA nephropathy, membrane glomerulonephropathy, membranoproliferative glomerulonephropathy

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5
Q

List the differential for hematuria

A

Vascular: renal vein thrombosis
Glomerular: post-streptococcal glomerulonephritis, henoch-schonlein purpura, IgA nephropathy
Tubulointerstitial: ATN, tubulointerstitial nephritis, polycystic kidney disease
Lower urinary tract: calculi, neoplasm, foreign body, trauma

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6
Q

Discuss the presentation and management of minimal change nephrotic syndrome

A
Demographics: 
- 2-6, Caucasian, Indian
Pathophysiology: 
- primary unknown
- secondary is rare and due to malignancy, infection, or collagen vascular disease
Presentation: 
- edema, possible pulmonary edema, 
Investigations: 
- proteinuria
- microscopic hematuria
- low albumin
- high cholesterol
- no evidence of renal pathology on biopsy 
Treatment: 
- 1st line is prednisone 60mg/m2/day divided TID for 6 weeks and then 40mg/m2/day divided q2 days for 6 weeks
- parents due daily urinalysis dipstick and have constant follow up for blood pressure and weight
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7
Q

List some of the complications of minimal change disease

A

Hypovolemia
Infection
- immune suppressive therapy plus loss of IgG increase risk of infection
- require broad spectrum antibiotics if infection is suspected or acyclovir and IVIG for VZV
Thrombosis
- decrease in intravascular volume and renal loss of anti-coagulant factors (anti-thrombin 3, protein C and S)
Hypercholesterolemia

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8
Q

Discuss the diagnosis and management of Post-streptococcal glomerulonephritis

A
Pathophysiology
- develop cross reactant antibodies against glomerular membrane
Presentation: 
- nephritic syndrome
- no proteinuria after 6 months and no hematuria after 12 months
Investigations: 
- high anti-streptococcal antibody titres
- low C3
- high creatine, high BUN
Treatment: 
- penicillin for strep infection
- address complications of AKI
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9
Q

Discuss the presentation and management of IgA nephropathy

A
Presentation: 
- gross hematuria following inciting event such as URTI or vaccine, 
- nephritic syndrome
Investigations: 
- tests to rule out other causes of nephritic syndrome (SLE, post-strep, kidney stone), 
- high IgA levels
- diagnosis with kidney biopsy
Treatment:
- hypertension with ACEi or ARB
- systemic steroid
- hypercholesterolemia with statin
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10
Q

What is postural proteinuria?

A

Epidemiology: Present in adolescent females

  • Have increased protein release during the day when upright, which decreases overnight
  • Benign disorder that disappears with age
  • <0.5g/day of protein lost
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11
Q

Discuss the red flags for minimal change disease requiring further evaluation with renal biopsy

A
Age <1
Age > 12 (membranous or SLE more likely)
Black (SLE)
Renal failure
Macro or microhematuria
No response within 4 weeks of initiating high dose steroids
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