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Updated: Aug 14, 2026

"Liver-on-a-Chip" Cultures of Primary Hepatocytes and Kupffer Cells for Hepatitis B Virus Infection
Published on: February 19, 2019
[Monitoring patients with chronic hepatitis during and after therapy]
1Zavod za gastroenterologzju, Klinika za unutrasnje bolesti, Klinicka bolnica "Merkur", Zagreb, Hrvatska. vesnacoliccvrlje@yahoo.com
Insights
Hepatitis C and B screening should target at-risk groups, not general populations. Monitoring viral markers and liver function aids treatment response assessment and early detection of liver cancer in patients with chronic hepatitis.
Area of Science:
- Hepatology
- Virology
- Public Health
Context:
- Hepatitis C (HCV) and Hepatitis B (HBV) are significant global health concerns.
- Chronic HBV infection is a primary cause of liver cancer and mortality.
- Coinfection with HIV is common and increases liver disease progression risk.
Purpose:
- To outline appropriate screening and monitoring strategies for Hepatitis C and B.
- To emphasize the importance of assessing disease severity and treatment response.
- To highlight the need for early hepatocellular carcinoma (HCC) detection in at-risk populations.
Summary:
- Liver biopsy is the gold standard for assessing Hepatitis C severity, but AST, ALT, and HCV RNA levels are crucial for monitoring treatment response.
- HCV screening should be limited to high-risk individuals; general screening is not advised.
- For chronic HBV, monitoring viral markers (HBsAg, HBeAg, HBV DNA) is essential before and after antiviral therapy. PCR is used for HBV DNA monitoring, and YMDD mutation testing is vital for lamivudine-treated patients.
- Hepatocellular carcinoma (HCC) surveillance in cirrhotic patients involves alpha-fetoprotein (AFP) and liver sonography every six months, with upper GI endoscopy recommended periodically.
- While ultrasound and AFP aid HCC detection, their reliability is limited.
Impact:
- Provides evidence-based guidelines for managing chronic viral hepatitis.
- Aims to improve patient outcomes by optimizing screening, treatment monitoring, and early cancer detection.
- Highlights the critical role of viral load and genotype testing in guiding therapy and assessing response.
- Emphasizes the need for tailored monitoring protocols for different hepatitis viral infections and coinfections.
Abstract:
Hepatitis C is a major public health problem. General screening is not advisable and should be limited to risk groups. The gold standard for the assessment of disease severity is liver biopsy. AST and ALT do not correlate with histology. Serum HCV RNA by qualitative assay and HCV genotype should be determined prior to therapy. Response to antiviral therapy should be assessed by testing AST, ALT and qualitative HCV RNA. Repeat liver biopsy is not necessary. The incidence of HCC related to HCV infection is rising. Early detection by a cost effective screening program is essential. In patients with liver cirrhosis caused by hepatitis C, alpha fetoprotein and liver sonography should be done every 6 months. Upper GI endoscopy is recommended every 1-4 years in cirrhotic patients. Over 350 000 000 people are infected with HBV worldwide, and chronic HBV infection is the leading cause of liver cancer and tenth leading cause of death. HBs Ag, HBeAg and HBV DNA positive patients should be monitored for 6 months before treatment. Patients treated with antiviral therapy should be tested for HBAg, HBeAg and HBV DNA at the end of treatment and every 6 months thereafter to assess virologic response. Monitoring of serum HBV DNA is done by PCR. Patients treated with lamivudine should be tested for YMDD mutation. Ultrasound and AFP monitoring are recommended for detection of HCC, but results are not always reliable. Approximately 40% -70% of HIV infected patients have coinfection with HCV, HBV and HDV. HIV/HCV coinfected patients have an increased risk of progressive liver disease and should be treated accordingly.
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