Abstract
Purpose of Review
To summarize recommendations and common practices for long-term surveillance after hepatitis C cure.
Recent Findings
Patients with advanced fibrosis and cirrhosis have continued risk of the complications of portal hypertension and hepatocellular carcinoma after hepatitis C cure. While improvement in fibrosis has been noted, the clinical implications are not fully understood. Guidelines recommend no alteration in surveillance strategies based upon fibrosis measurements after hepatitis C cure.
Summary
Liver wellness approaches and strategies to avoid reinfection are recommended for all patients after hepatitis C cure. Patients with early stage fibrosis after hepatitis C cure can be discharged from specialty care unless a co-existing liver disease is present, including nonalcoholic fatty liver disease. Patients with advanced fibrosis or cirrhosis are recommended to have indefinite surveillance for the complications of portal hypertension and hepatocellular carcinoma. Further investigation is needed to understand fibrosis regression and thresholds when surveillance can be discontinued.
Similar content being viewed by others
Availability of Data and Material
Not applicable.
Code Availability
Not applicable.
References
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
Cooper CL, et al. HCV-infected individuals have higher prevalence of comorbidity and multimorbidity: a retrospective cohort study. BMC Infect Dis. 2019;19(1):712.
Abubakar I, et al. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2015;385(9963):117–71.
Falade-Nwulia O, et al. Oral direct-acting agent therapy for hepatitis C virus infection: a systematic review. Ann Intern Med. 2017;166(9):637–48.
Asselah T, Marcellin P, Schinazi RF. Treatment of hepatitis C virus infection with direct-acting antiviral agents: 100% cure? Liver Int. 2018;38(Suppl 1):7–13.
Backus LI, et al. A sustained virologic response reduces risk of all-cause mortality in patients with hepatitis C. Clin Gastroenterol Hepatol. 2011;9(6):509-516.e1.
Dieperink E, et al. All-cause mortality and liver-related outcomes following successful antiviral treatment for chronic hepatitis C. Dig Dis Sci. 2014;59(4):872–80.
Lens S, et al. Association between severe portal hypertension and risk of liver decompensation in patients with hepatitis C, regardless of response to antiviral therapy. Clin Gastroenterol Hepatol. 2015;13(10):1846-1853.e1.
Conti F, et al. Early occurrence and recurrence of hepatocellular carcinoma in HCV-related cirrhosis treated with direct-acting antivirals. J Hepatol. 2016;65(4):727–33.
Kanwal F, et al. Risk of hepatocellular cancer in HCV patients treated with direct-acting antiviral agents. Gastroenterology. 2017;153(4):996-1005.e1.
Pawlotsky J-M, et al. EASL recommendations on treatment of hepatitis C 2018. J Hepatol. 2018;69(2):461–511.
EASL clinical practice guidelines: management of hepatocellular carcinoma. J Hepatol, 2018. 69(1): 182-236.
Schillie S, et al. CDC recommendations for hepatitis C screening among adults—United States, 2020. MMWR Recommendations and Reports. 2020;69(2):1.
•• Verna EC, et al. DAA therapy and long-term hepatic function in advanced/decompensated cirrhosis: Real-world experience from HCV-TARGET cohort. J Hepatol. 2020;73(3):540–8. (An important cohort study showing that in patients with advanced/decompensated cirrhosis, few patients had improvement in MELD score and other markers of liver function.)
Ioannou GN, Green PK, Berry K. HCV eradication induced by direct-acting antiviral agents reduces the risk of hepatocellular carcinoma. J Hepatol. 2017;68(1):25–32.
Waziry R, et al. Hepatocellular carcinoma risk following direct-acting antiviral HCV therapy: a systematic review, meta-analyses, and meta-regression. J Hepatol. 2017;67(6):1204–12.
Lack of evidence of an effect of direct-acting antivirals on the recurrence of hepatocellular carcinoma: data from three ANRS cohorts. J Hepatol, 2016. 65(4): p. 734–740.
Kim D, et al. Decline in Annual Mortality of Hepatitis C Virus-Related Hepatocellular Carcinoma in the United States, From 2009 to 2018. Gastroenterology. 2020;159(4):1558–60.
•• Kanwal F, et al. Long-term risk of hepatocellular carcinoma in HCV patients treated with direct acting antiviral agents. Hepatology. 2020;71(1):44–55. (Retrospective cohort study from the Veterans Administration of HCV patients with cirrhosis who achieved SVR with DAAs showing that long-term HCC risk remains above thresholds for surveillance.)
Omata M, et al. Asia-Pacific clinical practice guidelines on the management of hepatocellular carcinoma: a 2017 update. Hepatol Int. 2017;11(4):317–70.
Monitoring patients who are starting HCV treatment, are on treatment, or have completed therapy. Available from: https://www.hcvguidelines.org/evaluate/monitoring.
Jakab SS, Garcia-Tsao G. Screening and surveillance of varices in patients with cirrhosis. Clin Gastroenterol Hepatol. 2019;17(1):26–9.
Garcia-Tsao G, et al. Portal hypertensive bleeding in cirrhosis: risk stratification, diagnosis, and management: 2016 practice guidance by the American Association for the Study of Liver Diseases. Hepatology. 2017;65(1):310–35.
•• Mandorfer M, et al. Changes in hepatic venous pressure gradient predict hepatic decompensation in patients who achieved sustained virologic response to interferon-free therapy. Hepatology. 2020;71(3):1023–36. (Prospective cohort study finding that patients with pretreatment clinically significant portal hypertension who experience an immediate decrease in hepatic venous pressure gradient have a decreased rate of hepatic decompensation.)
Jacobson I, et al. Course of cirrhosis regression: lessons from patients with HCV cirrhosis following successful sofosbuvir‐based treatment. Hepatology. 2019;70(339A).
Berzigotti A, et al. Obesity is an independent risk factor for clinical decompensation in patients with cirrhosis. Hepatology. 2011;54(2):555–61.
Everhart JE, et al. Weight-related effects on disease progression in the hepatitis C antiviral long-term treatment against cirrhosis trial. Gastroenterology. 2009;137(2):549–57.
Jamal MM, Saadi Z, Morgan TR. Alcohol and hepatitis C. Dig Dis. 2005;23(3–4):285–96.
Bhattacharya R, Shuhart MC. Hepatitis C and alcohol: interactions, outcomes, and implications. J Clin Gastroenterol. 2003;36(3):242–52.
Ganesan M, et al. Human immunodeficiency virus and hepatotropic viruses co-morbidities as the inducers of liver injury progression. World J Gastroenterol. 2019;25(4):398–410.
• Chalouni M et al. Increased mortality in HIV/HCV-coinfected compared to HCV-monoinfected patients in the DAA era due to non-liver-related death. J Hepatol. 2020;74(1):37–47. (After DAA treatment, HIV/HCV co-infected patients with SVR have similar risk of liver-related deaths and liverrelated events but higher risk of all-cause and non-liver-related deaths compared to those monoinfected with HCV.)
Evon DM, et al. A comprehensive assessment of patient reported symptom burden, medical comorbidities, and functional well being in patients initiating direct acting antiviral therapy for chronic hepatitis C: results from a large US multi-center observational study. PLoS One. 2018;13(8):e0196908.
Ioannou GN, Feld JJ. What are the benefits of a sustained virologic response to direct-acting antiviral therapy for hepatitis C virus infection? Gastroenterology. 2019;156(2):446-460.e2.
• Younossi ZM, et al. Long-term benefits of sustained virologic response for patient-reported outcomes in patients with chronic hepatitis C virus infection. Clin Gastroenterol Hepatol. 2020;18(2):468-476.e11. (Registry study found that patient-reported outcomes improved post-treatment in those with HCV achieving SVR and decreased in patients who did not achieve SVR.)
Simmons B, et al. Risk of late relapse or reinfection with hepatitis C virus after achieving a sustained virological response: a systematic review and meta-analysis. Clin Infect Dis. 2016;62(6):683–94.
Young J, et al. Risk factors for hepatitis C virus reinfection after sustained virologic response in patients coinfected with HIV. Clin Infect Dis. 2017;64(9):1154–62.
Martinello M, et al. Strategies to reduce hepatitis C virus reinfection in people who inject drugs. Infect Dis Clin North Am. 2018;32(2):371–93.
Islam N, et al. Incidence, risk factors, and prevention of hepatitis C reinfection: a population-based cohort study. Lancet Gastroenterol Hepatol. 2017;2(3):200–10.
Hepatitis C. guidance: AASLD-IDSA recommendations for testing, managing, and treating adults infected with hepatitis C virus. Hepatology. 2015;62(3):932–54.
Olshansky SJ, et al. A potential decline in life expectancy in the United States in the 21st century. N Engl J Med. 2005;352(11):1138–45.
Jantaratnotai N, et al. The interface of depression and obesity. Obes Res Clin Pract. 2017;11(1):1–10.
Chan JS, Yan JH, Payne VG. The impact of obesity and exercise on cognitive aging. Front Aging Neurosci. 2013;5:97.
Elkrief L, et al. Diabetes mellitus is an independent prognostic factor for major liver-related outcomes in patients with cirrhosis and chronic hepatitis C. Hepatology. 2014;60(3):823–31.
Hézode C, et al. Daily cannabis smoking as a risk factor for progression of fibrosis in chronic hepatitis C. Hepatology. 2005;42(1):63–71.
Ishida JH, et al. Influence of cannabis use on severity of hepatitis C disease. Clin Gastroenterol Hepatol. 2008;6(1):69–75.
Hutchinson SJ, Bird SM, Goldberg DJ. Influence of alcohol on the progression of hepatitis C virus infection: a meta-analysis. Clin Gastroenterol Hepatol. 2005;3(11):1150–9.
2015–2020 dietary guidelines for Americans 2020 [cited 2020 9/21/2020]; 8th Edition:[Available from: https://health.gov/sites/default/files/2019-09/2015-2020_Dietary_Guidelines.pdf.
Sims OT, et al. Quality of Life, Functioning, and Coping in HCV Patients Continuing Versus Ceasing Alcohol Use. Health Promot Pract. 2019;21(6):1012–7.
Bravi F, et al. Coffee reduces risk for hepatocellular carcinoma: an updated meta-analysis. Clin Gastroenterol Hepatol. 2013;11(11):1413-1421.e1.
Bhurwal A, et al. Inverse association of coffee with liver cancer development: an updated systematic review and meta-analysis. J Gastrointestin Liver Dis. 2020;29(3):421–9.
Bravi F, et al. Coffee drinking and hepatocellular carcinoma risk: a meta-analysis. Hepatology. 2007;46(2):430–5.
Larsson SC, Wolk A. Coffee consumption and risk of liver cancer: a meta-analysis. Gastroenterology. 2007;132(5):1740–5.
Ohfuji S, et al. Coffee consumption and reduced risk of hepatocellular carcinoma among patients with chronic type C liver disease: a case–control study. Hepatol Res. 2006;36(3):201–8.
Author information
Authors and Affiliations
Contributions
Mr. Morris and Dr. Muir both conducted the research for this review. Mr. Morris wrote the first draft, and Dr. Muir edited the manuscript.
Corresponding author
Ethics declarations
Conflict of Interest
Dr. Muir has received research grants and served on advisory boards for AbbVie, Gilead, and Merck.
Human and Animal Rights and Informed Consent
This article does not contain any studies with human or animal subjects performed by any of the authors.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
This article is part of the Topical Collection on Hepatitis C
Rights and permissions
About this article
Cite this article
Morris, K.E., Muir, A.J. Care After Cure: Long-term Follow-up in Hepatitis C. Curr Hepatology Rep 20, 183–190 (2021). https://doi.org/10.1007/s11901-021-00579-5
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11901-021-00579-5