What is the recommended dose of glutathione (glutathione) for a patient with acute viral hepatitis?

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Glutathione Dosing in Acute Viral Hepatitis

Glutathione is not a standard or guideline-recommended treatment for acute viral hepatitis, and no established dosing regimen exists in major hepatology guidelines.

Evidence-Based Treatment Recommendations

The major international hepatology guidelines (EASL, AASLD) do not include glutathione as a recommended therapy for acute viral hepatitis. The standard approach focuses on:

For Acute Hepatitis C

  • Pegylated interferon-α monotherapy (pegylated IFN-α2a 180 µg/week or pegylated IFN-α2b 1.5 µg/kg/week for 24 weeks) achieves viral eradication in >90% of patients 1
  • Treatment should be considered in patients not convalescing 2-4 months after disease onset 1

For Acute Hepatitis B

  • Most patients (>95%) recover spontaneously without specific treatment 1
  • Only patients with severe acute hepatitis B (characterized by coagulopathy with INR ≥1.5 or protracted course) should receive nucleoside analogue therapy 1

Supportive Care Remains the Cornerstone

  • Bedrest if symptomatic, high-calorie diet, avoidance of hepatotoxic medications, and alcohol abstinence are the mainstays of management 2
  • Hospitalization is indicated for severe nausea/vomiting preventing oral intake, INR ≥1.5 with any mental alteration, or signs of acute liver failure 3, 4
  • Balanced crystalloid solutions (Ringer's lactate, Plasmalyte) are preferred over normal saline for IV rehydration 5

Glutathione Research Data (Not Guideline-Supported)

While glutathione is not recommended in guidelines, limited research exists:

Study in Chronic Hepatitis B (Not Acute)

  • One small study (n=104) used 1200 mg glutathione IV daily for 8 weeks in chronic hepatitis B patients, showing improvements in liver enzymes and inflammatory markers 6
  • This was studied in chronic, not acute hepatitis B, and was an adjunct to standard therapy

Physiologic Observations

  • Acute viral hepatitis causes marked depletion of reduced glutathione in erythrocytes (0.79 ± 0.43 mmol/L vs normal 2.45 ± 0.15 mmol/L) during the acute phase 7
  • Glutathione system enzymes show altered activity patterns during acute hepatitis B 8
  • These are observational findings, not treatment recommendations

Critical Clinical Caveats

The absence of glutathione from all major hepatology guidelines (EASL 2011-2017, AASLD) is significant 1. When guidelines extensively detail supportive care measures but omit a therapy entirely, this suggests insufficient evidence for its use.

If considering glutathione despite lack of guideline support:

  • The only published dosing is 1200 mg IV daily, studied only in chronic (not acute) hepatitis B 6
  • No safety or efficacy data exist for acute viral hepatitis specifically
  • This should never replace standard antiviral therapy when indicated (acute HCV, severe acute HBV) 1

Focus clinical efforts on:

  • Early identification of patients requiring antiviral therapy 1
  • Recognition of acute liver failure indicators (INR ≥1.5, encephalopathy) requiring immediate hospitalization 3, 4
  • Ensuring adequate supportive care and monitoring 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Acute Viral Hepatitis.

Current treatment options in gastroenterology, 2000

Guideline

Indications for Hospital Admission in Patients with Acute Hepatitis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Hospitalization Criteria for Hepatitis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Fluid Management in Acute Viral Hepatitis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Effects of reduced glutathione therapy on chronic hepatitis B.

Central-European journal of immunology, 2017

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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.

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