Preventable Deaths During Widespread Community Hepatitis A Outbreaks — United States, 2016–2022

Megan G. Hofmeister, MD1; Neil Gupta, MD1; Hepatitis A Mortality Investigators (View author affiliations)

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Summary

What is already known about this topic?

Hepatitis A is a vaccine-preventable disease that typically causes mild, self-limited illness. Serious complications, including death, are rare, but are more frequent among older adults. Hepatitis A outbreaks associated with person-to-person transmission have been widespread in the United States since 2016.

What is added by this report?

During August 1, 2016–October 31, 2022, 27 U.S. states reported 315 hepatitis A outbreak–related deaths. Deaths peaked in 2019 and then decreased annually through 2022. Overall, 63% of decedents had at least one documented preexisting indication for hepatitis A vaccination.

What are the implications for public health practice?

Increased hepatitis A vaccination coverage, particularly among adults at increased risk for infection with hepatitis A virus or for severe disease from infection, is critical to preventing future hepatitis A deaths.

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Abstract

Hepatitis A is acquired through the fecal-oral route and is preventable by a safe and effective vaccine. Although hepatitis A is generally mild and self-limited, serious complications, including death, can occur. Since 2016, widespread hepatitis A outbreaks have been reported in 37 U.S. states, primarily among persons who use drugs and those experiencing homelessness. Nearly twice as many hepatitis A–related deaths were reported during 2016–2022 compared with 2009–2015. CDC analyzed data from 27 hepatitis A outbreak-affected states* that contributed data during August 1, 2016–October 31, 2022, to characterize demographic, risk factor, clinical, and cause-of-death data among 315 outbreak-related hepatitis A deaths from those states. Hepatitis A was documented as an underlying or contributing cause of death on 60% of available death certificates. Outbreak-related deaths peaked in 2019, and then decreased annually through 2022. The median age at death was 55 years; most deaths occurred among males (73%) and non-Hispanic White persons (84%). Nearly two thirds (63%) of decedents had at least one documented indication for hepatitis A vaccination, including drug use (41%), homelessness (16%), or coinfection with hepatitis B (12%) or hepatitis C (31%); only 12 (4%) had evidence of previous hepatitis A vaccination. Increasing vaccination coverage among adults at increased risk for infection with hepatitis A virus or for severe disease from infection is critical to preventing future hepatitis A–related deaths.

Introduction

Hepatitis A virus (HAV) infections are acquired through fecal-oral transmission. Although hepatitis A is generally mild and self-limited, serious complications, including death, can occur (1,2). Hepatitis A is preventable by a highly effective and safe vaccine (3). Since 2016, hepatitis A outbreaks associated with person-to-person transmission have been reported in 37 states, involving approximately 44,900 cases, 27,450 hospitalizations, and 423 deaths as of October 6, 2023 (4,5). These outbreaks have disproportionately affected persons who use drugs and persons experiencing homelessness, who might be at increased risk for HAV infection because of poor hygiene practices, lack of access to sanitation, or crowded living conditions (3). Nearly twice as many deaths involving hepatitis A in the United States occurred during 2016–2022 compared with 2009–2015 (6).

Methods

Deidentified demographic, risk factor, and clinical data from state outbreak databases, along with place and cause of death data from death certificates, were requested for all hepatitis A outbreak–related deaths from the 32 state health departments that publicly reported at least one outbreak-related death during August 1, 2016–October 31, 2022. All hepatitis A cases met the Council of State and Territorial Epidemiologists’ hepatitis A surveillance case definition (7). Risk factors were self-reported during the exposure period (15–50 days before symptom onset). Outbreak-related deaths were defined as deaths that state health departments determined were attributable to hepatitis A. Death certificate data were reviewed to determine if hepatitis A was listed as 1) a cause of death (listed anywhere in the chain of events that directly caused death) or 2) a significant condition contributing to death. The analysis was conducted using SAS software (version 9.4; SAS Institute). This activity was reviewed by CDC, deemed not research, and conducted consistent with applicable federal law and CDC policy.

Results

CDC analyzed data from 27 (84%) states contributing data, among the 32 outbreak-affected states that had publicly reported at least one hepatitis A outbreak-related death. These 27 states accounted for 315 outbreak-related deaths, approximately 75% of publicly reported hepatitis A outbreak-related deaths (approximately 71% of publicly reported hepatitis A outbreak-related cases) at the time of the request for data. Deaths occurred during September 13, 2016–June 20, 2022 (Figure), most among males (73%) and non-Hispanic White persons (84%); the median age at death was 55 years (Table 1). Outbreak-related deaths peaked in 2019, and then decreased annually through 2022. The median interval between symptom onset and date of death was 17 days. Among decedents, 91% were hospitalized, 77% had jaundice, and one (<1%) underwent liver transplantation; among the 218 hospitalized decedents with available information, the median length of hospitalization was 7 days (IQR = 4–14 days). Drug use was the most commonly reported risk factor for HAV infection (41%), followed by homelessness or unstable housing (16%). Coinfection with hepatitis C (31%) was more prevalent than was coinfection with hepatitis B (12%). Only 12 decedents (4%) had evidence of previous hepatitis A vaccination; 63% had at least one documented indication for vaccination according to recommendations of the Advisory Committee on Immunization Practices (3).

Death certificate data were provided by 25 (93%) of 27 states for 272 (86%) decedents (Table 2). Hepatitis A was not listed on 108 (40%) of the death certificates. Among the 164 (60%) death certificates with hepatitis A documented, hepatitis A was listed as a cause of death on 142 (87%) and as a significant condition contributing to death on 26 (16%).

Discussion

Data from 27 states were analyzed to characterize the epidemiology of 315 hepatitis A outbreak–related deaths during August 1, 2016–October 31, 2022. Deaths occurred predominantly among males, non-Hispanic White persons, and persons aged ≥50 years. Nearly two thirds of decedents had at least one documented indication for hepatitis A vaccination, including drug use, homelessness, or coinfection with hepatitis B virus or hepatitis C virus; however, only 12 decedents had evidence of previous hepatitis A vaccination, indicating substantial missed opportunities to prevent hepatitis A deaths. Lack of stable housing and substance use disorder are commonly associated with viral hepatitides (3,4) and interact to increase disease incidence and health disparities. Although hepatitis A is usually a self-limited and preventable disease, it can have lethal consequences when introduced into populations with limited access to preventive care, unstable housing situations, inadequate access to sanitary services, or coexisting liver disease. These findings underscore the importance of integrated, comprehensive services, including vaccination, harm reduction, substance use disorder treatment, and hygiene and sanitation, to improve the health of medically underserved populations.

Among 272 outbreak-related decedents with available death certificate data, hepatitis A was listed as a cause of death or significant condition contributing to death on only 60% of death certificates, suggesting a substantial underestimation of hepatitis A mortality related to the outbreaks associated with person-to-person transmission in U.S. national vital statistics data. The 60% reporting rate for hepatitis A outbreak–related deaths is substantially higher than reporting rates for hepatitis B and hepatitis C; in previous death certificate analyses of cohorts of patients with chronic hepatitis B and chronic hepatitis C, only 19% of decedents had hepatitis B or hepatitis C reported on their death certificates (8,9).

Limitations

The findings in this report are subject to at least five limitations. First, states did not use a standardized hepatitis A–related death definition, which might have resulted in differential classification of deaths as being related to hepatitis A. Second, death from hepatitis A is not a reportable condition and health departments might not have identified all outbreak-related hepatitis A deaths. Third, risk factor data were self-reported and subject to social desirability and recall biases and missingness. Consequently, information about additional decedents with indications for hepatitis A vaccination was unavailable. Fourth, vaccination information was missing for nearly one half of decedents; however, HAV infection after vaccination or appropriately timed postexposure prophylaxis is rare given the documented high immunogenicity of the vaccine (3). Finally, although the analysis captured nearly three quarters of publicly reported outbreak-related deaths, the results might not be generalizable to all outbreak-related deaths in the United States.

Implications for Public Health Practice

Hepatitis A is a vaccine-preventable disease; safe and highly effective vaccines have been available for decades (3). Substantial progress has been made in controlling the recent outbreaks through intensive efforts by health departments, including outreach through mobile vans and foot teams, nontraditional vaccination clinics in jails and homeless shelters, and partnerships with sheriffs’ associations and other community-based partners to expand vaccination coverage. As of October 2023, 34 states have declared ends to their outbreaks; however, many susceptible adults, particularly among persons who use drugs, persons experiencing homelessness, and persons with chronic liver disease, remain at increased risk for HAV infection or severe disease from HAV infection (5,10). Increased hepatitis A vaccination coverage is critical to maintain the progress that has been made and prevent future hepatitis A deaths.

Acknowledgments

Local and state health department staff members who responded to hepatitis A outbreaks in their jurisdictions; vital records staff members.

Hepatitis A Mortality Investigators

Priscilla Lauro, Arizona Department of Health Services; E. Marilea Brock, Arkansas Department of Health; Alan May, Arkansas Department of Health; Cherie Smith, Arkansas Department of Health; Olivia Arizmendi, California Department of Public Health; Kerri Brown, Colorado Department of Public Health & Environment; Rachel H. Jervis, Colorado Department of Public Health & Environment; Ann Q. Shen, Colorado Department of Public Health & Environment; Ami P. Gandhi, Georgia Department of Public Health; Dawn Nims, Illinois Department of Public Health; Nicole Stone, Indiana Department of Health; Lauren Maxwell, Kansas Department of Health and Environment; Jennifer A. Khoury, Kentucky Department for Public Health; Amanda K. Odegård, Kentucky Department for Public Health; Douglas A. Thoroughman, CDC and Kentucky Department for Public Health; Raychel N. Berkheimer, Louisiana Department of Health; Jenna V. Iberg Johnson, Louisiana Department of Health; Sean H. Simonson, Louisiana Department of Health; Kompan Ngamsnga, Maryland Department of Health; Lindsay Bouton, Massachusetts Department of Public Health; Shauna Onofrey, Massachusetts Department of Public Health; Sharon Pagnano, Massachusetts Department of Public Health; Cole Burkholder, Michigan Department of Health & Human Services; Theresa S. Kittle, Mississippi State Department of Health; John Bos, Missouri Department of Health and Senior Services; Kate Cleavinger, Missouri Department of Health and Senior Services; Nathan Koffarnus, Missouri Department of Health and Senior Services; Salena Savarda, Nevada Department of Health and Human Services; Zuwen Qiu-Shultz, Southern Nevada Health District; Devin Raman, Southern Nevada Health District; Hannah Bowen, New Hampshire Division of Public Health Services; John J. Dreisig, New Hampshire Division of Public Health Services; Katrina E. Hansen, New Hampshire Division of Public Health Services; Patricia Amarilla, New Jersey Department of Health; Troy Brancard, New Jersey Department of Health; Mojisola Ojo, New Jersey Department of Health; Marla M. Sievers, New Mexico Department of Health; Justin P. Albertson, North Carolina Department of Health and Human Services; Susan M. Sullivan, North Carolina Department of Health and Human Services; Abdoulaye Diedhiou, South Carolina Department of Health and Environmental Control; LaKita D. Johnson, South Carolina Department of Health and Environmental Control; Jun Tang, South Carolina Department of Health and Environmental Control; Jane M. Brittingham, Tennessee Department of Health; Danita C. Crear, Tennessee Department of Health; Robb L. Garman, Tennessee Department of Health; Elise M. Huebner, Texas Department of State Health Services; Binoj Peter, Texas Department of State Health Services; Marc Williamson, Dallas County Health and Human Services; Bree Barbeau, Utah Department of Health and Human Services; MaryBeth DeMarco, Virginia Department of Health; Kelsey Holloman, Virginia Department of Health; Mary Chan, Washington State Department of Health; Hilary Armstrong, , Public Health – Seattle & King County; Jean-Jacques Kayembe Kashondo, Public Health – Seattle & King County; Alana G. Hudson, West Virginia Department of Health and Human Resources; Shannon McBee, West Virginia Department of Health and Human Resources; Melissa A. Scott, West Virginia Department of Health and Human Resources.

Corresponding author: Megan G. Hofmeister, lxn7@cdc.gov.


1Division of Viral Hepatitis, National Center for HIV, Viral Hepatitis, STD, and TB Prevention, CDC.

All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. No potential conflicts of interest were disclosed.


* The following 27 states contributed data for the analysis: Arizona, Arkansas, California, Colorado, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Mississippi, Missouri, Nevada, New Hampshire, New Jersey, New Mexico, North Carolina, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, and West Virginia.

45 C.F.R. part 46, 21 C.F.R. part 56; 42 U.S.C. Sect. 241(d); 5 U.S.C. Sect. 552a; 44 U.S.C. Sect. 3501 et seq.

References

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Return to your place in the textFIGURE. Date of hepatitis A outbreak–related deaths* ― 27 U.S. states, August 1, 2016–October 31, 2022
The figure is a histogram showing the date of hepatitis A outbreak-related deaths in 27 U.S. states during August 1, 2016–October 31, 2022.

* Among 306 outbreak-related deaths for which the date of death was known.

TABLE 1. Characteristics of persons whose death was related to a hepatitis A outbreak — 27 U.S. states,* August 1, 2016–October 31, 2022Return to your place in the text
Characteristic (no. with available data) No. (%)
Total no. of reported hepatitis A outbreak–related deaths 315
Death date range (306) Sep 13, 2016–Jun 20, 2022
Year of death (306)
2016 4 (1.3)
2017 39 (12.7)
2018 86 (28.1)
2019 94 (30.7)
2020 53 (17.3)
2021 24 (7.8)
2022 6 (2.0)
Interval between symptom onset and death, days, median (IQR) (306)§ 17.0 (9.0–33.0)
Sex
Female 85 (27.0)
Male 230 (73.0)
Age group at death, yrs (314)
0–19 0 (—)
20–29 12 (3.8)
30–39 27 (8.6)
40–49 62 (19.8)
50–59 97 (30.9)
≥60 116 (36.9)
Median age at death, yrs (range) (314) 55 (24–96)
Race and ethnicity
American Indian or Alaska Native, non-Hispanic 3 (1.0)
Black or African American, non-Hispanic 15 (4.8)
White, non-Hispanic 265 (84.1)
Hispanic or Latino 13 (4.1)
Multiple races, non-Hispanic 2 (0.6)
Unknown 17 (5.4)
Jaundice or scleral icterus
Yes 242 (76.8)
No 52 (16.5)
Unknown 21 (6.7)
Hospitalized
Yes 288 (91.4)
Length of hospitalization, days, median (IQR) (218) 7.0 (4.0–14.0)
No 24 (7.6)
Unknown 3 (1.0)
Liver transplant
Yes 1 (0.3)
No 134 (42.5)
Unknown 180 (57.1)
Hepatitis A vaccination status
Ever vaccinated (≥1 dose) 12 (3.8)
Unvaccinated 146 (46.4)
Unknown 157 (49.8)
Risk factors**
Any drug use
Yes 128 (40.6)
No 113 (35.9)
Unknown 74 (23.5)
Injection drug use
Yes 76 (24.1)
No 140 (44.4)
Unknown 99 (31.4)
Noninjection drug use
Yes 77 (24.4)
No 123 (39.1)
Unknown 115 (36.5)
Experiencing homelessness or unstable housing
Yes 50 (15.9)
No 217 (68.9)
Unknown 48 (15.2)
Male-to-male sexual contact (230)††
Yes 7 (3.0)
No 91 (39.6)
Unknown 132 (57.4)
International travel
Yes 2 (0.6)
No 200 (63.5)
Unknown 113 (35.9)
Incarcerated
Yes 9 (2.9)
No 160 (50.8)
Unknown 146 (46.4)
Epidemiologically linked§§
Yes 30 (9.5)
No 99 (31.4)
Unknown 186 (59.1)
Coinfection
Hepatitis B
Yes 37 (11.7)
No 231 (73.3)
Unknown 47 (14.9)
Hepatitis C
Yes 97 (30.8)
No 179 (56.8)
Unknown 39 (12.4)
HIV
Yes 0 (—)
No 140 (44.4)
Unknown 175 (55.6)

* The following 27 states contributed data for the analysis: Arizona, Arkansas, California, Colorado, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Mississippi, Missouri, Nevada, New Hampshire, New Jersey, New Mexico, North Carolina, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, and West Virginia.
Missing data were categorized as unknown for the purpose of the analysis.
§ When symptom onset date was not available, date of collection of the specimen that tested positive for hepatitis A virus immunoglobulin M antibodies was used as a proxy for symptom onset date.
Characteristics related to hepatitis A vaccination status of those reported as “ever vaccinated” were not available (the number of hepatitis A vaccine doses received, whether the hepatitis A vaccine doses were self-reported or confirmed in a state immunization information system, and the timing of doses). These do not necessarily represent instances of hepatitis A vaccine failure (e.g., they could represent instances of postexposure prophylaxis having been administered outside the recommended 14-day window when it is effective).
** Risk factors were ascertained during the exposure period (15–50 days before symptom onset).
†† Restricted to males.
§§ Contact (e.g., household or sexual) with a laboratory-confirmed hepatitis A case 15–50 days before symptom onset.

TABLE 2. Death certificate analysis of hepatitis A outbreak–related deaths — 25 U.S. states,* August 1, 2016–October 31, 2022Return to your place in the text
Characteristic (no. with available data) No. (%)
Death certificate available (315)
Yes 272 (86.3)
No 22 (7.0)
Unknown 21 (6.7)
Hepatitis A status when death certificate was available (272)§
Hepatitis A not listed on death certificate 108 (39.7)
Hepatitis A listed on death certificate 164 (60.3)
Hepatitis A listed as a cause of death (164) 142 (86.6)
Hepatitis A listed as a significant condition contributing to death (164) 26 (15.9)
Place of death (272)§
Inpatient facility 226 (83.1)
Hospice facility 16 (5.9)
Decedent’s home 13 (4.8)
Other 8 (2.9)
Emergency department or outpatient facility 6 (2.2)
Nursing home or long-term care facility 3 (1.1)

* The following 25 states contributed death certificate data for the analysis: Arizona, Arkansas, California, Colorado, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Michigan, Mississippi, Missouri, Nevada, New Hampshire, New Jersey, New Mexico, North Carolina, South Carolina, Tennessee, Texas, Utah, Washington (Seattle-King County only), and West Virginia.
Calculated among all 315 hepatitis A outbreak–related deaths from 27 states.
§ Calculated among 272 hepatitis A outbreak–related decedents from 25 states for whom death certificate data was available.
Categories are not mutually exclusive.


Suggested citation for this article: Hofmeister MG, Gupta N. Preventable Deaths During Widespread Community Hepatitis A Outbreaks — United States, 2016–2022. MMWR Morb Mortal Wkly Rep 2023;72:1128–1133. DOI: http://dx.doi.org/10.15585/mmwr.mm7242a1.

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