Treatment for Nephritic Syndrome
The treatment of nephritic syndrome requires rapid referral to a specialized nephrology unit and includes disease-specific therapy targeting the underlying cause, along with supportive measures to manage symptoms and prevent complications. 1
Diagnosis and Classification
Before initiating treatment, proper diagnosis is essential:
- Clinical presentation: Hematuria, hypertension, variable proteinuria (typically non-nephrotic range), fluid retention, and edema 1
- Laboratory findings: Elevated serum creatinine, urinalysis showing RBCs and RBC casts, possible low complement levels (C3, C4) in certain causes 1
- Classification: Determine if the nephritic syndrome is:
- Post-infectious (most commonly post-streptococcal)
- IgA nephropathy
- ANCA-associated vasculitis
- Lupus nephritis
- Other causes
Disease-Specific Treatment
Treatment varies based on the underlying cause:
Post-infectious glomerulonephritis:
- Antimicrobial therapy for the underlying infection 1
- Supportive care for symptoms
IgA nephropathy:
- ACE inhibitors or ARBs for proteinuria control
- Consider corticosteroids for persistent proteinuria 1
ANCA-associated vasculitis:
- Cyclophosphamide or rituximab plus corticosteroids 1
Lupus nephritis (Class III/IV):
- Initial treatment with mycophenolate mofetil or cyclophosphamide, plus glucocorticoids
- Maintenance therapy with MMF or azathioprine and low-dose prednisone for at least 3 years 1
Non-genetic, non-infectious causes:
- Consider kidney biopsy if screening is negative
- Trial of immunosuppressant therapy based on biopsy findings 2
Supportive Treatment
Fluid management:
Blood pressure control:
- ACE inhibitors or ARBs are preferred agents 1
- Target blood pressure to age-appropriate goals
Edema management:
Antiproteinuric therapy:
Thromboprophylaxis:
Monitoring and Follow-up
Regular monitoring is essential:
- Body weight and blood pressure
- Renal function (serum creatinine, GFR)
- Proteinuria and urinary sediment
- Serum albumin and electrolytes
- Visits every 2-4 weeks during the first 2-4 months after diagnosis or flare 1
Response Assessment
- Complete response: Return of serum creatinine to baseline and decline in urine protein:creatinine ratio to <500-700 mg/g 1
- Partial response: Stabilization or improvement of serum creatinine but urine protein:creatinine ratio still >500-700 mg/g 1
- Consider repeat kidney biopsy in cases of worsening kidney function, non-responsiveness to treatment, or relapse 1
Special Considerations
Pediatric patients:
Ambulatory management:
- Preferred when possible to improve quality of life and reduce infection risk 1
Severe cases:
Common Pitfalls to Avoid
- Delaying specialist referral for complex cases
- Inadequate thromboprophylaxis in high-risk patients
- Failure to monitor for and prevent infections in immunosuppressed patients
- Overreliance on immunosuppression for genetic forms of nephrotic syndrome 1
- Inadequate monitoring of electrolytes during diuretic therapy
By following this structured approach to the treatment of nephritic syndrome, focusing on both disease-specific therapy and supportive care, outcomes related to morbidity, mortality, and quality of life can be optimized.