Nephritic Syndrome (NMC Licensing Exams Note)
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.
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
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
• Nephritic: Hematuria, mild proteinuria, hypertension, oliguria.
• Nephrotic: Massive proteinuria, severe edema, hypoalbuminemia, hyperlipidemia.
- 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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