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. 2020 Nov 3;38(1):423–440. doi: 10.1007/s12325-020-01535-3

Estimating the Year Each State in the United States Will Achieve the World Health Organization’s Elimination Targets for Hepatitis C

Mark Sulkowski 1, Wei-Han Cheng 2, Steven Marx 2, Yuri Sanchez Gonzalez 2, John Strezewski 2, Nancy Reau 3,
PMCID: PMC7609357  PMID: 33145648

Abstract

Introduction

Although hepatitis C virus (HCV) infection remains a major clinical, economic, and societal burden, the development of curative antiviral therapy may accelerate the path toward elimination. This analysis assessed the progress of United States (US) states towards achieving the World Health Organization’s (WHO) 2030 HCV elimination targets for incidence, mortality, diagnosis, and treatment.

Methods

A previously published Markov model was used to simulate HCV progression over time to estimate the path to HCV elimination in each state based on prevalence, annual treatment, and diagnosis inputs from two large US laboratory datasets from January 2013 to December 2017. State-specific fibrosis stage restrictions on treatment in 2017 were included. The model estimated the year individual states would meet the WHO targets for diagnosing 90% of the HCV-infected population, treating 80% of the eligible population, reducing new HCV infections by 80%, and reducing HCV-related deaths by 65%. The minimum number of annual treatments needed between 2020 and 2030 to achieve the WHO treatment target was also calculated.

Results

Overall, the USA is projected to achieve HCV elimination by 2037, with individual targets related to mortality, diagnosis, treatment, and incidence being achieved by 2020, 2027, 2033, and 2037, respectively. Three states (Connecticut, South Carolina, and Washington) are on track to meet all four elimination targets by 2030, and 18 states are not expected to meet these targets before 2040. The estimated annual number of treatments required during 2020–2030 nationally to reach the WHO treatment target is 173,514.

Conclusion

With the exception of three states, the USA is not on target to meet the WHO 2030 elimination targets and 35% are off track by 10 years or more. Strategies must be implemented to reduce overall prevalence by preventing new infections, increasing rates of screening, improving linkage to care, and implementing unfettered access to curative therapy.

Electronic supplementary material

The online version of this article (10.1007/s12325-020-01535-3) contains supplementary material, which is available to authorized users.

Keywords: Elimination, Epidemiology, Hepatitis C, Infectious disease, Prevalence

Digital Features

This article is published with digital features, including a summary slide and infographic, to facilitate understanding of the article. To view digital features for this article go to https://doi.org/10.6084/m9.figshare.13042667.graphic file with name 12325_2020_1535_Figa_HTML.jpggraphic file with name 12325_2020_1535_Figb_HTML.jpggraphic file with name 12325_2020_1535_Figc_HTML.jpg

Introduction

Viral hepatitis C is one of the most common blood-borne infectious diseases and is associated with a substantial clinical, societal, and economic burden with over 70 million individuals affected globally [1, 2], including an estimated 2.4 million people living with chronic hepatitis C virus (HCV) infection in the USA [3]. This burden is especially high among younger people who inject drugs, with up to 70% of new HCV infections occurring among people who inject drugs in the USA [4]. The number of new cases of HCV infection among this demographic has increased from 10,000 annually in 2005 to 40,000 annually in 2016 [5]. Owing to these increases in HCV infections among younger individuals, the Centers for Disease Control and Prevention (CDC), the US Preventive Services Task Force (USPTF), and the American Association for the Study of Liver Diseases–Infectious Diseases Society of America (AASLD–IDSA) have all endorsed universal screening for HCV in adults (≥18 years of age) [68]. Chronic HCV infection is characterized by progressive liver fibrosis and the potential development of cirrhosis and hepatocellular carcinoma (HCC) [9, 10]. In addition to advanced liver disease, chronic HCV infection has been associated with many extrahepatic manifestations that involve several organ systems [9, 11]. As a result, untreated HCV infection is a leading cause of morbidity and mortality [10]. While mortality from other top infectious diseases including human immunodeficiency virus (HIV), malaria, and tuberculosis is declining, mortality caused by viral hepatitis is increasing. The number of global deaths from hepatitis was 1.34 million in 2015 [10] which exceeds the number of HIV-related annual deaths in 2017 (0.95 million) [12]. Recently approved pangenotypic direct-acting antiviral (DAA) regimens have demonstrated high rates of sustained virologic response and good tolerability compared with former interferon-based therapies, and have substantially shortened treatment durations to 8 to 12 weeks of oral therapy [13]. Therefore, with access and linkage to care, HCV can be successfully treated and cured in most individuals, which is expected to yield substantial reductions in estimated future healthcare costs ($3.3 billion), morbidity, and mortality (an estimated 320,000 lives saved) in the USA [14].

The World Health Organization (WHO), through the Global Health Sector Strategy on Viral Hepatitis 2016–2021, has called for the elimination of viral hepatitis as a significant public health threat by 2030 [15]. To achieve the goal of HCV elimination, the WHO has established a series of HCV elimination targets related to increases in diagnosis and treatment and reduction in incidence and HCV-related death [15]. With the WHO target year of elimination only 10 years away, global progress towards HCV elimination has been limited. A recent study has shown that many high-income countries are not expected to achieve elimination before 2050, including the USA [16]. The identification of states not on track to meet elimination targets allows for modification of screening, assessment, and linkage of care; therefore, the objective of this study was to assess the progress and timeline of US states towards achieving the 2030 HCV elimination targets set by the WHO.

Methods

Markov Model

A previously published Markov disease progression model [1, 16] was used and expanded to simulate HCV progression over time in all 50 US states, Washington, DC, and Puerto Rico (which will be referred to as “states” henceforward). The model was used to forecast the annual HCV-infected population, HCV-related deaths, and disease burden by HCV sequelae, including fibrosis, cirrhosis, decompensated cirrhosis, HCC, and liver-related deaths as a means of estimating the path to the elimination of HCV in each state. The annual disease progression rates and mortality rates for each disease state in the model were obtained from published literature and validation of modelled outcomes was previously published [17]. The model has been widely adopted for this purpose in multiple global countries and three individual US states to forecast HCV prevalence, and the details have been described in the literature [16, 1823]. The disease progression model tracks the sex- and age-structured HCV-infected population from incidence through all stages of liver disease [fibrosis (F0–F3 on the METAVIR scale), compensated cirrhosis, decompensated cirrhosis, HCC, and liver transplantation] to eventual death (all-cause or HCV-liver-related). The Markov model calculated the disease progression among the HCV-infected population by age and sex beginning in 1950, accounting for the inflows of incidence cases, and the outflows of mortality and patients who were treated and cured year over year to 2050.

Key HCV epidemiology data were generated as inputs for the model, including the historical prevalence of viremic HCV infection, the annual diagnosed cases among the HCV-infected population, and the antiviral treatment regimen (number of annual treatments). HCV prevalence data and number of treated patients in each state (Table S1 in the supplementary material) were estimated on the basis of the combined de-identified data from the two large US laboratory datasets. Identical datasets were requested from both laboratories over the period of 2013–2017. All individuals who had an HCV antibody test (used for HCV screening to assess exposure to HCV) and an HCV-RNA viral-load test (used to confirm current HCV infection) between January 1, 2013 and December 31, 2017 were included in this analysis. In this dataset, the HCV RNA+ population was defined as the total number of patients with a positive HCV RNA test in the selected year. A longitudinal methodology was applied to define the prevalence of chronic HCV infection based on continuous laboratory tests to assess eligibility and carry HCV-related results forward. A machine learning methodology was applied to predict the proportion of patients with active HCV (RNA+) who were treated and cured in each year [24]. The total number of unique HCV RNA+ individuals from 2013 to 2017 who were not cured was calculated to represent the total number of patients with diagnosed HCV in the USA [25].

To estimate the real-world number of HCV viremic patients in the US population, a geographic area-specific utilization of the data from the laboratory companies was used to extrapolate the number of HCV RNA+ patients in our dataset. The overall HCV viremic population was defined as the total number of unique patients with a positive HCV RNA test recorded during 2013–2017. The total number of unique HCV RNA+ individuals from 2013 to 2017 who had not been cured was calculated to represent the noninstitutionalized population of HCV-infected persons similar to the national representative sample from the published literature (National Health and Nutrition Examination Survey, NHANES) [26]. The extrapolated HCV RNA+ estimates can be interpreted as the total number of diagnosed HCV viremic patients in the USA. A 48% undiagnosed rate was assumed in the estimation of the overall number of HCV-infected patients in the USA up to 2017 [27]. The proportion of patients with active HCV (RNA+) who were treated in 2017 as estimated by the machine learning algorithm was then applied to calculate the annual number of treated patients among all diagnosed HCV viremic patients.

Incident HCV infections were calculated separately into historical and future years. Previously described calibration procedures were used to calibrate historical incident cases to match the reported total viremic HCV prevalence for the overall population, as well as by sex and age group [1, 16]. Afterwards, the sex and age distribution of new infections was back-calculated to match reported prevalence by sex and age, assuming that the sex and age distributions of the general and HCV-infected populations were the same on the state level as on the national level. Future incident cases of HCV infection were assumed to change at the same annual rate as chronic prevalent cases (F0 or overall), relative to 2017 benchmark levels. In states with treatment or reimbursement restrictions based on fibrosis stage, the annual rate of change in incident cases was linked to the annual rate of change in modeled F0 prevalence. In states without treatment or reimbursement restrictions by fibrosis stage, the rate of change in HCV infection incident cases was based on the rate of change in all chronic prevalent cases [16].

The data on the annual number of treatments from 2015 to 2017 estimated from the two large laboratory datasets demonstrated a trending decrease in the number of patients treated each year. During this period, an approximate decrease of 4% in the annual number of treated patients was observed at the US national level. To reflect the trend in which the number of treated patients decreased between 2015 and 2017 in the actual observed data, we assumed the annual number of treated patients will continue to decrease at a 4% rate from 2020. State Medicaid restrictions on treatment in 2017 based on fibrosis stage were also considered to assess their role in delaying HCV elimination [28].

The primary clinical outcome of the model was the annual HCV-infected population by stage of liver disease, sex, and age, as well as the HCV-related deaths in the population. These outputs were used to estimate the path toward the elimination of HCV as a public health threat as per the WHO targets for 2030.

WHO Elimination Targets

The WHO has identified four targets that need to be achieved to eliminate HCV as a public health threat by 2030 (relative to 2015 benchmark levels): (1) diagnosing 90% of the HCV-infected population; (2) treating 80% of the eligible population; (3) reducing new HCV infections by 80%; and (4) reducing HCV-related deaths by 65% [15]. Modeled forecasts on the annual HCV-infected population and the number of HCV-related deaths were used to estimate the year in which individual states would meet these four WHO elimination targets, assuming levels of HCV diagnosis and treatment in 2017 would remain constant through 2030 [15]. The projected year in which all four WHO elimination targets were collectively met was considered the year of HCV elimination. States that met all four goals before 2030 were considered on track for meeting the WHO elimination goal.

The study also estimated HCV prevalence for each state. On the basis of this information, the average minimum number of annual treatments necessary to achieve the WHO’s treatment target over the course of 2020–2030 was calculated for every state to establish policy benchmarks for monitoring progress towards elimination annually. In line with the diagnosis coverage target, 90% of the chronic prevalent population was considered treatment eligible. The number of annual treatments necessary to meet the treatment target for elimination by 2030 was calculated by dividing 80% of the treatment-eligible population by 11 (the number of years between 2020 and 2030), net of cumulative treatments during the years 2015–2019.

Compliance with Ethics Guidelines

With permission, this modeling study utilized de-identified data from two US laboratory datasets. Because the data were de-identified, no ethics committee approval was required.

Results

Estimated Prevalence of Patients with HCV (HCV RNA+) in 2017

The estimated prevalence of patients who are HCV RNA+ in 2017 is illustrated in Fig. S1 in the supplementary material. Overall, we estimated a total of 3,063,343 patients with HCV in the USA in 2017 with prevalence varying by state. The state with the highest prevalence of HCV infection was California (507,181), and the state with the lowest prevalence was Hawaii (854).

WHO Elimination Targets: Overall Year of Elimination

The projected year for achieving all four WHO elimination targets (i.e., overall year of elimination) in individual states in the USA is shown in Fig. 1 and Table 1. The projected year of overall elimination was soonest in Connecticut (2028) and latest in Hawaii, North Dakota, Ohio, Oregon, Puerto Rico, Rhode Island, South Dakota, and West Virginia (all beyond 2050). According to the national-level data, overall HCV elimination in the USA is projected to be achieved by 2037. Only three states (Connecticut, South Carolina, and Washington) are on track to meet all four elimination targets by 2030, and 18 states are not expected to meet these targets before 2040.

Fig. 1.

Fig. 1

Year of elimination. a The estimation may be less accurate owing to the small number of patients with HCV in the area. HCV hepatitis C virus

Table 1.

Annual number needed to treat between 2020 and 2030 to achieve elimination by 2030

State Year in which individual WHO elimination targets will be metb Year of HCV elimination Annual number of treatments from 2020–2030 to achieve 2030 target Treatment restrictions by fibrosis stage in 2017c NVHR 2020 medicaid access graded
Incidence Liver-related death Diagnosis Treatment
AK 2033 2020 2024 2029 2033 380 None A−
AL 2034 2020 2025 2031 2034 1922 F2 D+
AR 2039 2020 2025 2032 2039 2078 F3 F
AZ 2037 2020 2028 2034 2037 6322 None C+
CA 2039 2020 2030 2035 2039 29,147 None A−
CO 2042 2021 2028 2039 2042 3551 None A−
CT 2028 2019 2026 2026 2028 1639 None A+
DC 2039 2020 2043 2032 2043 749 None B−
DE 2038 2021 2026 2034 2038 733 None A−
FL 2031 2019 2028 2028 2031 13,350 None B+
GA 2039 2019 2026 2030 2039 3608 None C
HIa  > 2050 2049 2045  > 2050  > 2050 51 None B
IA 2036 2020 2026 2032 2036 443 F2 C
ID 2034 2020 2025 2030 2034 313 None A−
IL 2044 2022 2027 2042 2044 3905 None B−
IN 2040 2021 2025 2037 2040 2264 None A−
KS 2031 2019 2027 2028 2031 766 None B
KY 2045 2025 2026 2045 2045 4505 None B
LA 2041 2021 2024 2038 2041 2469 None A
MA 2032 2019 2026 2029 2032 4760 None A
MD 2034 2020 2028 2031 2034 3648 F1 B
ME 2037 2021 2031 2034 2037 629 None A−
MI 2042 2023 2026 2041 2042 7113 None A−
MN 2032 2019 2025 2027 2032 930 F3 D+
MO 2037 2020 2025 2034 2037 2584 None A
MS 2031 2019 2025 2028 2031 943 None D+
MT 2040 2021 2025 2035 2040 428 F3 A−
NC 2032 2019 2026 2029 2032 4564 None B
NDa  > 2050 2045 2028  > 2050  > 2050 122 None C+
NE 2047 2025 2024 2047 2047 430 F2 C−
NH 2036 2020 2025 2032 2036 393 None B+
NJ 2033 2020 2031 2030 2033 3880 None A−
NM 2040 2021 2022 2036 2040 1347 None A
NV 2031 2019 2029 2028 2031 1124 None A−
NY 2034 2020 2035 2031 2035 7268 None A−
OH  > 2050 2040 2026  > 2050  > 2050 13,521 None A−
OK 2032 2019 2026 2029 2032 1957 None C
OR  > 2050 2027 2025  > 2050  > 2050 2322 None A−
PA 2035 2020 2029 2032 2035 7931 None A−
PRa  > 2050  > 2050  > 2050  > 2050  > 2050 205 None B
RIa  > 2050 2042 2025  > 2050  > 2050 166 None A−
SC 2030 2019 2026 2027 2030 1538 None B+
SD  > 2050 2034 2026  > 2050  > 2050 210 F3 F
TN 2040 2021 2026 2037 2040 3284 None C
TX 2039 2020 2027 2032 2039 13,621 F3 D+
UT 2042 2022 2026 2039 2042 585 None C−
VA 2033 2020 2028 2030 2033 3160 None B+
VT 2047 2025 2032 2043 2047 144 None A−
WA 2030 2019 2025 2027 2030 3133 None A
WI 2039 2021 2025 2035 2039 1171 None A
WV  > 2050 2029 2028  > 2050  > 2050 1774 None B−
WYa 2041 2022 2028 2036 2041 148 None B

HCV hepatitis C virus, NVHR National Viral Hepatitis Roundtable, WHO World Health Organization

aThe estimation may be less accurate owing to the small number of patients with HCV in the area

bElimination target thresholds: 80% reduction in incidence, 65% reduction in liver-related deaths, diagnosis of 90% of the HCV-infected population, and treating 80% of the eligible population

cPatients must reach a certain stage of fibrosis/liver disease prior to becoming eligible for treatment

d2020 Medicaid Access Grades are provided by the National Viral Hepatitis Roundtable and based on discriminatory state Medicaid restrictions (i.e., fibrosis/liver disease treatment restrictions, sobriety treatment restrictions, and prescriber restrictions) [28]

Year of Achieving Individual WHO Elimination Targets

The years in which individual states are estimated to meet each of the four elimination targets related to incidence, liver-related death, diagnosis, and treatment are shown in Table 1. Of the four targets, reducing new HCV infections by 80% by the year 2030 is least likely to be achieved in individual states. Specifically, only three states (6%; Connecticut, South Carolina, and Washington) are on track to reduce new HCV infections by 80% by 2030. Less than one-third of states [16 states (31%)] are on track to meet the goal of treating 80% of the eligible population by 2030. On the other hand, states are more likely to meet the WHO goals of diagnosing 90% of HCV infections by 2030 [45 states (87%) are on track] and reducing HCV mortality by 65% by 2030 [47 states (90%) are on track].

Similar trends for achieving the four individual goals were observed for the USA as a whole, with the estimated year of achieving each goal being 2020 for reducing HCV mortality by 65%, 2027 for diagnosing more than 90% of the HCV population, 2033 for treating more than 80% of the eligible HCV population, and 2037 for reducing new HCV infections by 80%.

Nine states (17%) had treatment restrictions based on liver fibrosis severity in 2017 (Table 1) according to the reported state Medicaid restriction policy [28]. This included five states with restrictions based on F3 disease (Arkansas, Minnesota, Montana, South Dakota, and Texas), three states with restrictions by F2 disease (Alabama, Iowa, and Nebraska), and one state with restrictions based on F1 disease (Maryland). None of these states were expected to achieve HCV elimination by 2030.

Annual Number Needed to Treat to Meet 2030 Elimination Targets

The estimated annual number of treatments required nationally during 2020–2030 to reach the treatment target for HCV elimination by 2030 is 173,514. The estimated number needed to treat in each individual state is illustrated in Fig. 2 and listed for each state in Table 1. The estimated annual number of treatments ranged from 51 to 29,147 across the 52 states, with Hawaii having the lowest number needed to treat (51) and California (29,147) having the highest number needed to treat. Other states requiring at least 5000 patients to be treated to reach 2030 targets are (in decreasing order) Texas, Ohio, Florida, Pennsylvania, New York, Michigan, and Arizona. Thirteen states require at most 500 treatments between 2020 and 2030 to reach 2030 targets. These include (in decreasing order) Iowa, Nebraska, Montana, New Hampshire, Alaska, Idaho, South Dakota, Puerto Rico, Rhode Island, Wyoming, Vermont, North Dakota, and Hawaii.

Fig. 2.

Fig. 2

Annual number needed to treat between 2020 and 2030. a The estimation may be less accurate owing to the small number of patients with HCV in the area. HCV hepatitis C virus

Discussion

Our study, which assessed the progress and timeline for US states to achieve the 2030 WHO HCV elimination targets, suggests that the USA is not on track to meet these targets, as it is projected to achieve HCV elimination by 2037. Our analysis of states that are not projected to meet elimination targets allows for modifications in screening, assessment, and linkage to care. Comprehensive data similar to those used in this study that are regularly updated can be accessed by healthcare providers, policymakers, and payers to view the progress towards elimination in their states (accessed at MappingHepC.com) [25].

In a previous study that utilized similar methodologies and models to project the year of elimination, the estimated year of elimination in the USA was beyond 2050 [16]. The present analysis estimates an earlier year of HCV elimination based on the availability of prevalence, diagnosis, and treatment inputs from two large laboratory datasets. In contrast, the previous study was based on data derived from the Polaris Observatory, which relied on the best available published sources at the time of the study [16]. In the present study, we identified substantial differences between states for the estimated time to HCV elimination; these differences were driven by heterogeneous progress toward meeting the targets set by the WHO for HCV diagnosis, treatment, incidence, and mortality. When assessed at the state level, only 6% of states are on track to achieve overall HCV elimination by 2030 and 35% of states are not expected to meet these targets before 2040. Additionally, we estimated the overall prevalence of patients with active HCV infection (RNA+ patients) in the USA to be approximately 3,063,343, which is a higher estimate than previously reported from the NHANES data (2.3–2.4 million) [3, 26, 29]. The present study utilizes a dataset that combines two large de-identified US laboratory datasets from January 2013 through December 2017, while the NHANES data included data from 2013 to 2016 based on surveys extrapolated to the US population.

Among the individual WHO targets, the goal of reducing new incidences of HCV by 80% appears to be the most difficult to achieve. Only three states (6%) are on track to meet this goal by 2030, while 18 states (35%) are estimated to achieve this goal in 2040 or later. These data indicate that increased efforts are needed to prioritize treatment for all patients with active HCV infection, particularly those at risk of transmitting HCV to others, including those who inject drugs and prisoners [3]. Meeting the WHO treatment target by 2030 is also behind schedule in most states (69%) and the USA as a whole. The annual number needed to treat to meet the treatment target is 173,514 between 2020 and 2030. In five of eight states not projected to achieve elimination before 2050 (Hawaii, North Dakota, Rhode Island, Puerto Rico, and South Dakota), the annual number needed to treat is less than 500, suggesting the annual treatment benchmark in many of these states is low and achievable.

This study highlights the disparity between treatment targets and restrictions and offers an opportunity for states to reconsider barriers to treatment. The National Viral Hepatitis Roundtable (NVHR) report cards provide Medicaid access grades based on restrictions that still exist in each state which may be prohibitive to states meeting 2030 elimination targets [28]. Meeting the treatment target may be hampered by the persistence of treatment restrictions based on liver fibrosis severity in nine states (17%); most of these states had Medicaid access grades of C to F, apart from Maryland (B) and Montana (A−) [28]. Additional restrictions that may impact access to treatment, especially among high-risk groups, include sobriety restrictions in some states with 18 states requiring abstinence for at least 6 months, as well as limited access to healthcare and health insurance among the HCV-infected population [28]. Meeting the incidence and treatment targets will require the removal of these restrictions along with improved linkage to care efforts, especially among those with substance abuse disorders and poor social determinants of health. In support of increased screening, treatment, and improved linkage to care, the CDC, USPTF, and AASLD–IDSA have all provided updated guidance that supports universal screening recommendations. The universal screening guidelines indicate that all adults over the age of 18 years should be screened for HCV [68]. Additionally, AASLD–IDSA recommends that all patients with HCV infection should be treated, regardless of sobriety [7].

In contrast, the WHO elimination targets relating to diagnosis and reduction in mortality are on track for achievement in 2030 or earlier overall in the USA as well as in at least 87% of states. The 2019 National Virus Progress Report estimates the USA has met the 2020 goal to reduce the rate of HCV-related deaths [30]. While it is hard to compare different data sources, the model projections in our study align with that report as the model estimated the USA to meet the mortality reduction target in 2020. Mortality may be the easiest metric to meet by prioritizing (through restrictions) those patients with more advanced fibrosis, in which it would be the easiest to measure a decrease in mortality. Mortality may also be reduced in those patients with more comorbid conditions that are improved by viral eradication. However, it should be noted that the reductions in mortality cannot capture all-cause mortality (i.e., extrahepatic manifestations such as type 2 diabetes, end-stage renal disease, cardiovascular disease, or malignancy) that are also drivers of mortality but are not directly linked to HCV.

There are key barriers that directly contribute to the limited progress in achieving HCV elimination targets. In particular, political will is considered crucial for providing sustained commitment and funding of HCV elimination strategies [16]. An example of a country in which political will exists is Australia, which has an estimated elimination target of 2026, which is earlier than the 2030 WHO elimination target [16]. In the USA there is growing political will as evidenced by recent universal screening guidelines issued by the CDC and USPTF [6, 8] and the CDC has designated May as Hepatitis C Awareness Month to encourage screening of high-risk populations [31]. Sustained political will and policy changes at the federal and state level as well as funding for efforts to reduce HCV incidence and prevalence are required for HCV elimination. Examples of ways the USA could increase public health infrastructure to support elimination efforts include increased federal funding of national surveillance systems, expansion of access to and funding for syringe exchange programs and opioid agonist therapy, and removal of all restrictions to HCV treatment [31]. Treatment restrictions play a role since, in an effort to limit costs, some states have restricted access to treatment based on stage of liver disease [32]. The NVHR report cards highlight the states in which there is the greatest need to reduce treatment restrictions [28]. Stigma and discrimination against people with HCV can also impact access to HCV care [15]. Some states limit access to treatment for those with a history of illicit drug use or alcohol abuse [33]. This is compounded by the high lack of awareness of HCV status among those who inject drugs and the criminalization of drug use in most states [34]. The link between substance abuse and HCV is highlighted by the sharp increase in HCV infections among subgroups of the population who abuse or inject opioids [35]. Syringe exchange programs were previously shown to reduce the rates of HCV infection in New York City [36]. Limited public health and healthcare system resources, especially from government health insurance programs (i.e., Medicare, Medicaid) for screening and diagnosis and treatment, are also a significant barrier to treatment [14, 32]. Despite these barriers, there is evidence suggesting that full access strategies result in cost-savings and are associated with a reduction in the number of patients who progress to more advanced fibrosis or cirrhosis compared with more restrictive strategies [32, 37]. The overall long-term social value generated from increasing access broadly is estimated to be substantial despite the increased short-term costs [38]. However, lifting treatment restrictions based on fibrosis staging or sobriety alone will not allow elimination targets to be met and may require improved linkage to care efforts to cure marginalized and disengaged patient populations.

There are several limitations to this analysis. First, the model assumes that every patient with HCV infection is at constant risk of transmitting HCV, even though HCV transmission patterns and risk factors may vary regionally and depend on the size of the at-risk population in each state [39]. The size of the at-risk population in each state may depend on many factors, including the number of injection drug users, incarcerated individuals, and migrants from areas of high HCV prevalence. Another limitation is that HCV prevalence data prior to 2013 were not captured in our study. Therefore, information is not available for individuals with an HCV RNA+ test prior to this date without subsequent viral load tests. The model also assumes annual rates of treatment and diagnosis remain constant in the future, which may require increased efforts in screening and linkage to care to maintain. However, increased efforts in screening and linkage to care and initiating treatment in new patients may be hampered by the recent COVID-19 global pandemic. In light of the pandemic, HCV treaters have seen a reduction in face-to-face interactions and increases in telehealth visits in the USA and many healthcare providers have seen reductions in new prescriptions, which may be due to patients’ unwillingness to initiate new therapy remotely and a lack of diagnostic testing that prevent diagnosis of new conditions, such as HCV infections [40]. It is anticipated that there may be a long-term impact of COVID-19 on healthcare provider engagement. Despite these challenges that healthcare providers face amid the COVID-19 pandemic, several major liver and hepatology societies recommend that providers should continue treatment of HCV-infected patients with COVID-19 and proceed with treatment in HCV-infected patients without COVID-19 as clinically warranted [4146]. Additionally, if there is an indication of a flare-up or reactivation of disease, therapy should be initiated in patients with COVID-19 and chronic HCV who are not already receiving treatment [4143, 45, 46]. In patients with COVID-19 and elevated serum liver levels, other etiologies such as HCV should be considered, and these patients should be screened for viral hepatitis, which may highlight a need for increased screening and diagnosis in the USA [41, 43]. Further, the model does not account for risk reduction due to harm-reduction programs or from the prioritized treatment of high-risk groups. The model also does not account for the impact of new treatment options or shortened treatment durations that may become available after 2017. Finally, as with any forecast, the model results and the estimated year of elimination provide directional guidance on potential shortfalls in efforts to achieve HCV elimination and therefore may not exactly match the future trajectories observed in the real world.

Conclusion

This study highlights the limited progress towards HCV elimination in the USA and the need to increase HCV awareness. The estimates in this analysis suggest that the USA and most (94%) of the individual states are not on track to achieve the WHO goal of HCV elimination by 2030. With 10 years remaining to meet these targets, it is important that strategies are implemented to increase rates of screening, linkage to care, and unfettered access to curative therapy.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Acknowledgements

We would like to acknowledge technical support provided by Homie Razavi and Ivane Gamkrelidze, employees of Center for Disease Analysis. AbbVie provided funding for this technical support.

Funding

Financial support for this study and the journal’s Rapid Service Fee was provided by AbbVie. AbbVie participated in the interpretation of data, review, and approval of the publication. All authors contributed to the development of the publication and maintained control over the final content.

Medical Writing, Editorial, and Other Assistance

Medical writing services were provided by Brandy Menges of JK Associates, Inc. (a member of the Fishawack Group of Companies) and funded by AbbVie.

Authorship

All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published. No honoraria or payments were made for authorship.

Authorship Contributions

AbbVie participated in the interpretation of data, review, and approval of the publication. All authors contributed to the development of the publication and maintained control over the final content.

Prior Presentation

Data were presented in part at the European Association for the Study of the Liver’s Digital International Liver Congress, August 27–29, 2020 and the Digestive Disease Week (DDW) 2020 digital platform.

Disclosures

Mark Sulkowski is an employee of Johns Hopkins University School of Medicine and reports grants from AbbVie, Gilead, Janssen, and the National Institutes of Health and personal fees from AbbVie, Gilead, Janssen, and Trek. Wei-Han Cheng, Steven Marx, Yuri Sanchez Gonzalez, and John Strezewski are employees of AbbVie and may own stocks and/or stock options of the company. Nancy Reau is an employee of Rush University Medical Center and is a consultant for AbbVie, Gilead Sciences, Merck and Co, and Abbott. Her institution has received research support from Abbott, AbbVie, and Gilead Sciences.

Compliance with Ethics Guidelines

With permission, this modeling study utilized de-identified data from two US laboratory datasets. Because the data were de-identified, no ethics committee approval was required.

Data Availability

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.


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