What is the treatment for nephritic syndrome?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: September 18, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

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:

  1. Post-infectious glomerulonephritis:

    • Antimicrobial therapy for the underlying infection 1
    • Supportive care for symptoms
  2. IgA nephropathy:

    • ACE inhibitors or ARBs for proteinuria control
    • Consider corticosteroids for persistent proteinuria 1
  3. ANCA-associated vasculitis:

    • Cyclophosphamide or rituximab plus corticosteroids 1
  4. 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
  5. Non-genetic, non-infectious causes:

    • Consider kidney biopsy if screening is negative
    • Trial of immunosuppressant therapy based on biopsy findings 2

Supportive Treatment

  1. Fluid management:

    • Restrict sodium and fluid intake based on volume status assessment 2
    • Avoid intravenous fluids and saline when possible 2
  2. Blood pressure control:

    • ACE inhibitors or ARBs are preferred agents 1
    • Target blood pressure to age-appropriate goals
  3. Edema management:

    • Diuretics: Furosemide 0.5-2 mg/kg per dose intravenously or orally up to six times daily (maximum 10 mg/kg per day) 2, 1
    • For severe cases, consider combination therapy with thiazide or potassium-sparing diuretics 2
    • Monitor electrolytes, blood pressure, and kidney function during diuretic therapy
  4. Antiproteinuric therapy:

    • ACE inhibitors or ARBs to reduce proteinuria 2, 1
    • Dose-dependent mechanism to reduce glomerular protein loss
  5. Thromboprophylaxis:

    • Consider prophylactic anticoagulation in high-risk patients 1
    • Especially important if central venous access is required 2

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

  1. Pediatric patients:

    • Monitor growth velocity, especially with prolonged corticosteroid treatment 1
    • Consider growth hormone substitution in children with growth issues 1
  2. Ambulatory management:

    • Preferred when possible to improve quality of life and reduce infection risk 1
  3. Severe cases:

    • Consider nephrectomy in patients with persistent severe symptoms despite optimal conservative treatment 1
    • Early referral to transplant unit when appropriate 2

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.

References

Guideline

Nephrotic and Nephritic Syndromes

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.