Nephritic Syndrome (NMC Licensing Exams Note)

 

Nephritic Syndrome (Nursing Lecture Notes)

Nephritic Syndrome (Nursing Lecture Notes)

Definition

Nephritic syndrome is a renal disorder caused by inflammation of the glomeruli, resulting in leakage of red blood cells and proteins into the urine, reduction in glomerular filtration rate (GFR), and fluid retention. It is important to differentiate this condition from nephrotic syndrome, which is characterized by massive proteinuria and edema.

Key Point: Nephritic = “Inflammation & Blood” → Hematuria + Hypertension + Oliguria

Etiology (Causes)

Nephritic syndrome can occur after infections, autoimmune reactions, or systemic diseases.

  • Post-streptococcal glomerulonephritis (PSGN): follows throat or skin infection with group A beta-hemolytic streptococcus. Common in children.
  • IgA nephropathy (Berger’s disease): hematuria after respiratory or GI infection.
  • Rapidly progressive glomerulonephritis (RPGN): aggressive type with crescent-shaped lesions on biopsy.
  • Systemic diseases: Lupus nephritis, Goodpasture’s syndrome, Vasculitis.

Pathophysiology

Nephritic syndrome results from immune-mediated glomerular injury. Antigen-antibody complexes deposit in the glomerular basement membrane (GBM), activating the complement system. This leads to:

  • Inflammation of glomerular capillaries
  • Damage to GBM → leakage of RBCs and proteins
  • Reduced filtration → oliguria and azotemia
  • Salt and water retention → hypertension and edema

Clinical Features

Nephritic syndrome typically presents with:

  • Hematuria: cola or tea-colored urine due to RBCs
  • Oliguria: urine output less than 400 ml/day in adults
  • Hypertension: from sodium and water retention
  • Edema: often periorbital, may be mild to moderate
  • Proteinuria: present but < 3.5 g/day (not as severe as nephrotic)
  • Systemic symptoms: malaise, headache, flank pain
📌 Mnemonic for Features of Nephritic Syndrome → "PHAROAH"
P – Proteinuria (mild)
H – Hematuria
A – Azotemia
R – RBC casts in urine
O – Oliguria
A – Anti-streptococcal antibodies (PSGN)
H – Hypertension

Investigations

  • Urinalysis: hematuria, RBC casts, mild proteinuria
  • Blood tests: ↑ BUN and creatinine, ↓ GFR
  • Serology: ASO titer (post-strep), ANA (lupus), ANCA (vasculitis)
  • Complement levels: often decreased (especially C3 in PSGN)
  • Renal biopsy: confirms diagnosis and underlying cause

Complications

  • Acute kidney injury (AKI)
  • Chronic kidney disease (CKD) if progressive
  • Hypertensive encephalopathy
  • Heart failure (from severe fluid overload)

Management

Management is both supportive and cause-specific.

  • Blood pressure control: ACE inhibitors, ARBs, diuretics
  • Edema: salt and fluid restriction, diuretics
  • Treat underlying infection: antibiotics for streptococcal infection
  • Immunosuppressive therapy: corticosteroids, cyclophosphamide in lupus or vasculitis
  • Dialysis: in cases of severe renal failure
Exam Tip: Differentiate Nephritic from Nephrotic Syndrome
• Nephritic: Hematuria, mild proteinuria, hypertension, oliguria.
• Nephrotic: Massive proteinuria, severe edema, hypoalbuminemia, hyperlipidemia.
📝 Nursing Considerations:
- Monitor fluid balance strictly (intake/output, daily weight)
- Monitor blood pressure regularly
- Restrict fluids and sodium as ordered
- Provide patient education: importance of follow-up, adherence to medications, diet restrictions
- Emotional support: especially in children and families, as prognosis is generally good in post-streptococcal cases
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