Tuesday, November 25, 2025

Early Antiviral Therapy for Chronic Hepatitis B Patients Proves Cost-Effective

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Beneath the surface of stable alanine aminotransferase (ALT) levels in chronic hepatitis B patients, a silent threat may persist. Despite appearing clinically normal, a significant presence of the hepatitis B virus (HBV) in the bloodstream can result in severe long-term health issues. As revealed by an extensive study involving multiple institutions in South Korea and Taiwan, targeting early treatment with antivirals in such scenarios dramatically reduces the likelihood of developing liver cancer and other critical health events.

Study Overview and Key Findings

Dr. Lim Young-Seok of Seoul Asan Medical Center spearheaded an enlightening study from 2019 to 2023. By examining 734 chronic hepatitis B patients without liver cirrhosis across 22 medical institutions, the research assessed those with normal ALT levels but high HBV DNA loads (104-108 IU/mL). The results were striking: patients receiving early antiviral therapy showed a 79% decrease in major adverse clinical events, such as liver cancer and mortality, compared to a control group.

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Economic Implications of Early Therapy

From an economic standpoint, early treatment demonstrated significant long-term benefits. While the initial drug costs can be high, these are outweighed by substantial savings in preventing expensive complications like liver cancer and liver failure. This study thereby proves the superiority of early antiviral intervention not just medically but also economically.

– Early antiviral treatment reduces the risk of liver cancer by 79% in specific patients.

– High HBV DNA levels warrant immediate intervention regardless of ALT status.

– Current insurance limitations prevent many patients from receiving necessary treatment.

Chronic hepatitis B, particularly prevalent among those aged 30 to 60, poses significant socio-economic challenges. Although this condition frequently escalates to liver cancer, only 21% of patients currently receive necessary antiviral treatment. This gap stems from existing health insurance policies that solely rely on ALT levels to determine treatment eligibility, leaving a considerable number of patients underserved. The study’s findings advocate adopting HBV DNA levels rather than ALT as a decisive factor for treatment initiation in clinical practice. This approach could more effectively bridge the treatment gap, ensuring a broader patient demographic benefits from necessary medical interventions.

Experts suggest revising health insurance guidelines to incorporate viral load assessment, particularly for middle-aged patients with moderate HBV DNA levels. These adjustments could facilitate more extensive access to cost-effective, life-saving treatments, emphasizing patient-centered care. This narrative aligns with the overarching mission of the Patient-Centered Medical Technology Optimization Research Project and underscores the practical benefits of aligning policy with contemporary research insights.

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