Nephrology Glomerular Diseases Intermediate
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Nephritic vs Nephrotic Syndrome Cheat Sheet

INFLAMMATION
vs
PODOCYTE
PODIUM
Core clinical and urinalysis distinctions between glomerular inflammation (Nephritic) and glomerular charge/barrier breakdown (Nephrotic).

Nephritic syndrome involves inflammatory damage that ruptures the glomerular capillary wall. Nephrotic syndrome represents podocyte effacement or basement membrane damage allowing massive albumin filtration.

Systematic Breakdown

Nephritic

CAPS: Casts, Azotemia, Pressure (HTN), Sedimentary blood

RBC casts with dysmorphic red cells; mild-to-moderate proteinuria (< 3.5 g/day); oliguria, azotemia; hypertension from salt retention.

Nephrotic

PEAL: Proteinuria (>3.5g), Edema, Albumin low, Lipids high

Massive proteinuria (> 3.5 g/24h); severe hypoalbuminemia (< 3.0 g/dL); generalized pitting edema; hyperlipidemia with fatty casts (Maltese cross under polarized light).

Thrombosis

Hypercoagulability in Nephrotic

Urinary loss of Antithrombin III and protein C/S predisposes to renal vein thrombosis and DVT.

Infection

Infection Susceptibility in Nephrotic

Urinary loss of immunoglobulins and complement factor B predisposes to encapsulated bacterial peritonitis (Streptococcus pneumoniae).

High-Yield Clinical Pearls & Exam Tips
  • Pathognomonic Urinalysis Findings: Dysmorphic RBCs and RBC casts = Glomerulonephritis (Nephritic); Oval fat bodies with Maltese cross pattern = Nephrotic syndrome.
  • Minimal Change Disease is the most common cause of nephrotic syndrome in children (exquisitely responsive to steroids); FSGS is most common in adults.
Related Pharmaceuticals
Prednisone ACE Inhibitors Furosemide Statins
Related Clinical Conditions
Poststreptococcal Glomerulonephritis Minimal Change Disease Focal Segmental Glomerulosclerosis
Authoritative Sources: Brenner and Rector's The Kidney 11e · Robbins & Cotran Pathologic Basis of Disease 10e

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