Economic evaluations of the primary prevention programs for viral hepatitis-related liver disease and liver cancer: a systematic literature review.
Viral hepatitis, including hepatitis B virus (HBV) and hepatitis C virus (HCV), significantly contributes to the global burden of liver disease and hepatocellular carcinoma. This systematic review evaluates the cost-effectiveness of primary prevention strategies for viral hepatitis-related liver disease and liver cancer in high-income countries. We systematically searched electronic databases (January 2013 to June 2024) for economic evaluations of HBV/HCV prevention strategies. Quality assessment used Consolidated Health Economic Evaluation Reporting Standards (CHEERS) guidelines. Analysis included model structures, assumptions, outcome measures, and cost-effectiveness findings. Twenty-one economic evaluations were included (13 USA, 8 Europe/ Canada). Most used Markov models with time horizons ranging from five years to lifetime. Universal screening was cost-effective across different populations, with Incremental Cost-Effectiveness Ratios (ICERs) ranging from $11,378-$28,000 per Quality-Adjusted Life Years (QALY) for universal HCV screening. Early HCV treatment (F0-F2) was cost-effective compared to delayed treatment. Universal HBV vaccination showed substantial economic benefits. Most interventions were cost-effective according to country-specific willingness-to-pay thresholds, though treatment costs remained a significant barrier to implementation. Primary prevention strategies for viral hepatitis-related liver disease are generally cost-effective, particularly in high-risk populations. Universal screening and early treatment were associated with improved health outcomes, including reductions in hepatocellular carcinoma, cirrhosis, and liver-related mortality. However, significant variations in methodological approaches limit direct comparability across studies and across countries.
- Discussion
16
- 10.1016/s2214-109x(21)00547-7
- Jan 18, 2022
- The Lancet Global Health
Expanded screening for chronic hepatitis B virus infection in China
- Research Article
3309
- 10.1053/j.gastro.2011.12.061
- Apr 23, 2012
- Gastroenterology
Most cases of hepatocellular carcinoma (HCC) are associated with cirrhosis related to chronic hepatitis B virus (HBV) or hepatitis C virus (HCV) infection. Changes in the time trends of HCC and most variations in its age-, sex-, and race-specific rates among different regions are likely to be related to differences in hepatitis viruses that are most prevalent in a population, the timing of their spread, and the ages of the individuals the viruses infect. Environmental, host genetic, and viral factors can affect the risk of HCC in individuals with HBV or HCV infection. This review summarizes the risk factors for HCC among HBV- or HCV-infected individuals, based on findings from epidemiologic studies and meta-analyses, as well as determinants of patient outcome and the HCC disease burden, globally and in the United States.
- Research Article
108
- 10.1016/s2214-109x(21)00517-9
- Jan 18, 2022
- The Lancet. Global Health
SummaryBackgroundChina has the highest prevalence of hepatitis B virus (HBV) infection worldwide. Universal HBV screening might enable China to reach the WHO 2030 target of 90% diagnostics, 80% treatment, and 65% HBV-related death reduction, and eventually elimination of viral hepatitis. We evaluated the cost-effectiveness of implementing universal HBV screening in China and identified optimal screening strategies.MethodsWe used a Markov cohort model, inputting parameters based on data from previous studies and public databases, to assess the cost-effectiveness of four HBV serological screening strategies in China in different screening scenarios. We simulated universal screening scenarios in 15 adult age groups between 18 and 70 years, with different years of screening implementation (2021, 2026, and 2031) and compared to the status quo (ie, no universal screening); in total, we investigated 180 different screening scenarios. We calculated the incremental cost-effectiveness ratio (ICER) between the different screening strategies and the status quo (current screening strategy). We performed probabilistic and one-way deterministic sensitivity analyses to assess the robustness of our findings.FindingsWith a willingness-to-pay level of three times the Chinese gross domestic product (GDP) per capita (US$30 828), all universal screening scenarios in 2021 were cost-effective compared with the status quo. The serum HBsAg/HBsAb/HBeAg/HBeAb/HBcAb (five-test) screening strategy in people aged 18–70 years was the most cost-effective strategy in 2021 (ICER $18 295/quality-adjusted life-years [QALY] gained). This strategy remained the most cost-effective, when the willingness-to-pay threshold was reduced to 2 times GDP per capita. The two-test strategy for people aged 18–70 years became more cost-effective at lower willingness-to-pay levels. The five-test strategy could prevent 3·46 million liver-related deaths in China over the lifetime of the cohort. It remained the most cost-effective strategy when implementation was delayed until 2026 (ICER $20 183/QALY) and 2031 (ICER $23 123/QALY). Screening young people (18–30 years) will no longer be cost-effective in delayed scenarios.InterpretationThe five-test universal screening strategy in people aged 18–70 years, implemented within the next 10 years, is the optimal HBV screening strategy for China. Other screening strategies could be cost-effective alternatives, if budget is limited in rural areas. Delaying strategy implementation reduces overall cost-effectiveness. Early screening initiation will aid global efforts in achieving viral hepatitis elimination.FundingNational Natural Science Foundation of China.
- Research Article
22
- 10.1097/00005176-200208002-00002
- Aug 1, 2002
- Journal of pediatric gastroenterology and nutrition
Acute and chronic hepatitis: Working Group Report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition.
- Research Article
28
- 10.1016/j.jhep.2004.05.001
- May 18, 2004
- Journal of Hepatology
Hepatitis viruses and human immunodeficiency virus co-infection: pathogenisis and treatment
- Research Article
23
- 10.1053/j.gastro.2012.03.013
- Mar 26, 2012
- Gastroenterology
Identifying Hepatitis B Carriers at Low Risk for Hepatocellular Carcinoma
- Research Article
350
- 10.1016/s0168-8278(03)00141-7
- Jan 1, 2003
- Journal of Hepatology
Epidemiology of hepatitis B in Europe and worldwide.
- Research Article
147
- 10.1002/ijc.23937
- Oct 30, 2008
- International journal of cancer
Liver cancers are strongly linked to hepatitis B virus (HBV) and hepatitis C virus (HCV). Egypt has the highest prevalence of HCV worldwide and has rising rates of hepatocellular carcinoma (HCC). Egypt's unique nature of liver disease presents questions regarding the distribution of HBV and HCV in the etiology of HCC. Accordingly, a systematic search of MEDLINE, ISI Web of Science, ScienceDirect and World Health Organisation databases was undertaken for relevant articles regarding HBV and HCV prevalence in Egypt among healthy populations and HCC cases. We calculated weighted mean prevalences for HBV and HCV among the populations of interest and examined differences in prevalence by descriptive features, including age, year and geographic region. Prevalences for HBV and HCV were 6.7% and 13.9% among healthy populations, and 25.9% and 78.5% among HCC cases. Adults had higher prevalences of both infections (Adult HBV=8.0%, Child HBV=1.6%; Adult HCV=15.7%, Child HCV=4.0%). Geographically, HBV was higher in the south, whereas HCV was greater in the north (North HBV=4.6%, South HBV=11.7%; North HCV=15.8%, South HCV=6.7%). Among HCC cases, HBV significantly decreased over time (p=0.001) while HCV did not, suggesting a shift in the relative influences of these viruses in HCC etiology in Egypt. Our results highlight large amounts of heterogeneity among the epidemiological factors associated with liver disease in Egypt and underscore the necessity of an integrated strategy for the successful prevention of viral hepatitis infections and chronic liver disease.
- Research Article
121
- 10.1016/j.cgh.2010.06.032
- Aug 14, 2010
- Clinical Gastroenterology and Hepatology
Hepatitis C virus (HCV) infections pose a growing challenge to health care systems. Although chronic HCV infection begins as an asymptomatic condition with few short-term effects, it can progress to cirrhosis, hepatic decompensation, hepatocellular carcinoma (HCC), and death. The rate of new HCV infections is decreasing, yet the number of infected people with complications of the disease is increasing. In the United States, people born between 1945 and 1964 (baby boomers) are developing more complications of infection. Men and African Americans have a higher prevalence of HCV infection. Progression of fibrosis can be accelerated by factors such as older age, duration of HCV infection, sex, and alcohol intake. Furthermore, insulin resistance can cause hepatic steatosis and is associated with fibrosis progression and inflammation. If more effective therapies are not adopted for HCV, more than 1 million patients could develop HCV-related cirrhosis, hepatic decompensation, or HCC by 2020, which will impact the US health care system. It is important to recognize the impact of HCV on liver disease progression and apply new therapeutic strategies.
- Research Article
76
- 10.1016/j.jceh.2014.04.003
- May 22, 2014
- Journal of Clinical and Experimental Hepatology
Hepatocellular carcinoma (HCC) is one of the major causes of morbidity, mortality and healthcare expenditure in patients with chronic liver disease. There are no consensus guidelines on diagnosis and management of HCC in India. The Indian National Association for Study of the Liver (INASL) set up a Task-Force on HCC in 2011, with a mandate to develop consensus guidelines for diagnosis and management of HCC, relevant to disease patterns and clinical practices in India. The Task-Force first identified various contentious issues on various aspects of HCC and these issues were allotted to individual members of the Task-Force who reviewed them in detail. The Task-Force used the Oxford Center for Evidence Based Medicine-Levels of Evidence of 2009 for developing an evidence-based approach. A 2-day round table discussion was held on 9th and 10th February, 2013 at Puri, Odisha, to discuss, debate, and finalize the consensus statements. The members of the Task-Force reviewed and discussed the existing literature at this meeting and formulated the INASL consensus statements for each of the issues. We present here the INASL consensus guidelines (The Puri Recommendations) on prevention, diagnosis and management of HCC in India.
- Research Article
442
- 10.1053/j.gastro.2019.02.049
- Apr 12, 2019
- Gastroenterology
Surveillance for Hepatocellular Carcinoma: Current Best Practice and Future Direction.
- Research Article
10
- 10.1111/j.1872-034x.2010.00655.x
- May 19, 2010
- Hepatology Research
Is the measurement of tumor marker levels effective for monitoring patients after the treatment of hepatocellular carcinoma? RECOMMENDATIONFor patients in whom tumor marker levels were elevated before treatment, tumor markers measured after treatment may serve as useful indices of the effects of treatment.(grade C1) 30
- Research Article
88
- 10.1053/j.gastro.2012.02.012
- Apr 23, 2012
- Gastroenterology
With the development of effective therapies against human immunodeficiency virus (HIV), hepatitis C virus (HCV) infection has become a major cause of morbidity and mortality among patients with both infections (coinfection). In addition to the high prevalence of chronic HCV, particularly among HIV-infected injection drug users, the rate of incident HIV infections is increasing among HIV-infected men who have sex with men, leading to recommendations for education and screening for HCV in this population. Liver disease is the second leading and, in some cases, a preventable cause of death among coinfected patients. Those at risk for liver disease progression are usually treated with a combination of interferon (IFN) and ribavirin (RBV), which is not highly effective; it has low rates of sustained virologic response (SVR), especially for coinfected patients with HCV genotype 1 and those of African descent. Direct-acting antivirals might overcome factors such as immunodeficiency that can reduce the efficacy of IFN. However, for now it remains challenging to treat coinfected patients due to interactions among drugs, additive drug toxicities, and the continued need for combination therapies that include pegylated IFN. Recently developed HCV protease inhibitors such as telaprevir and boceprevir, given in combination with pegylated IFN and RBV, could increase the rate of SVR with manageable toxicity and drug interactions. We review the latest developments and obstacles to treating coinfected patients.
- Research Article
39
- 10.1016/j.cgh.2011.06.004
- Jun 13, 2011
- Clinical Gastroenterology and Hepatology
Surveillance for Hepatocellular Carcinoma in Patients With Cirrhosis
- Discussion
8
- 10.1053/j.gastro.2003.05.011
- Dec 1, 2003
- Gastroenterology
Occult HBV infection—both hidden and mysterious