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Disease Profile

Viral

Hepatitis A

甲型肝炎

Hepatitis A is a vaccine-preventable infection caused by hepatitis A virus (HAV), a positive-strand RNA virus [1][2]. It is an acute liver infection that usually resolves spontaneously without chronic sequelae, although prolonged or relapsed illness and acute liver failure can occur in a minority of cases [2]. The available source material emphasizes fecal-oral spread, outbreak association with sanitation-related exposures, and the public-health importance of vaccination and outbreak control [1][2].

Definition

Hepatitis A is a viral infection caused by hepatitis A virus (HAV), described in the source material as a positive-strand RNA virus [1][2]. The disease is characterized as a vaccine-preventable acute inflammatory illness of the liver [2]. Source-backed detail on genotype diversity, incubation period, or chronicity beyond the statement that it usually does not leave chronic sequelae is not yet available from the provided snippets [2].

Clinical features

The clinical picture is usually acute and self-limited, with the liver inflammation typically resolving spontaneously without chronic sequelae [2]. In children, infection is often asymptomatic, whereas adults may present with jaundice, abdominal pain, hepatitis, and hyperbilirubinemia [1]. The provided sources note that up to 20% of patients can have a prolonged or relapsed course, and fewer than 1% experience acute liver failure [2]. Host factors including immunological status, age, pregnancy, and underlying hepatic disease can influence severity [2].

Epidemiology

The source material reports that hepatitis A causes more than 150 million new infections annually [2]. Outbreaks are often linked to poor sanitation, overcrowding, or contamination of food and water, indicating a strong relationship with environmental and social conditions [1]. The available evidence also notes that more than 25 countries have implemented vaccination programmes, with a resulting reduction in incidence [2]. Source-backed detail on regional distribution beyond endemicity categories is not yet available from the provided snippets [2].

Transmission

HAV is transmitted feco-orally, and person-to-person contact is explicitly identified as a route of spread [1]. The source material also links outbreaks to food and water contamination, poor sanitation, and overcrowding, which are consistent with exposure settings that facilitate fecal-oral transmission [1][2]. Source-backed detail on persistence in the environment or specific high-risk exposures is not yet available from the provided snippets.

Risk groups

The supplied sources identify higher risk of severe disease in people with immunological compromise, older age, pregnancy, and underlying hepatic disease [2]. The WHO-linked prevention guidance also refers to individuals at higher risk of infection and/or severe disease, particularly in very low, low, and intermediate endemicity settings [2]. Source-backed detail on additional exposure-defined groups is not yet available from the provided snippets.

Prevention

Vaccination is described as the mainstay of prevention and should be given before exposure whenever possible [1]. The sources further state that the WHO recommends vaccination for individuals at higher risk of infection and/or severe disease in very low and low endemicity countries, and universal childhood vaccination in intermediate endemicity countries [2]. Improving hygiene and sanitation, together with rapid outbreak identification and prompt, accurate intervention, are presented as essential measures for reducing transmission [2].

Surveillance note

In surveillance terms, hepatitis A should be read as a vaccine-preventable fecal-oral infection whose burden is shaped by sanitation, crowding, and contamination of food and water [1][2]. The provided sources indicate that outbreaks can be identified through rapid recognition and control interventions, and that incidence has declined where vaccination programmes have been implemented [2]. Source-backed detail on case definitions, laboratory confirmation workflows, or routine reporting thresholds is not yet available from the provided snippets.

References
  1. 1 Abutaleb A et al. Hepatitis A: Epidemiology, Natural History, Unusual Clinical Manifestations, and Prevention. Gastroenterol Clin North Am. 2020 Jun. PMID: 32389358. doi: 10.1016/j.gtc.2020.01.002. PubMed: https://pubmed.ncbi.nlm.nih.gov/32389358/
  2. 2 Van Damme P et al. Hepatitis A virus infection. Nat Rev Dis Primers. 2023 Sep 28. PMID: 37770459. doi: 10.1038/s41572-023-00461-2. PubMed: https://pubmed.ncbi.nlm.nih.gov/37770459/
  3. 3 Kwo PY et al. ACG Clinical Guideline: Evaluation of Abnormal Liver Chemistries. Am J Gastroenterol. 2017 Jan. PMID: 27995906. doi: 10.1038/ajg.2016.517. PubMed: https://pubmed.ncbi.nlm.nih.gov/27995906/
  4. 4 Lupus Hepatitis and Autoimmune Hepatitis (Lupoid Hepatitis). The American Journal of the Medical Sciences. 2017. doi: 10.1016/j.amjms.2016.10.014. DOI: https://doi.org/10.1016/j.amjms.2016.10.014
  5. 5 Hepatitis Without Hepatitis? American Journal of Gastroenterology. 2012. doi: 10.1038/ajg.2012.16. DOI: https://doi.org/10.1038/ajg.2012.16
  6. 6 Hepatitis Viruses: Hepatitis B and Hepatitis D. Viral Infections of Humans. 2022. doi: 10.1007/978-1-4939-9544-8_32-1. DOI: https://doi.org/10.1007/978-1-4939-9544-8_32-1
Coding Register
ICD-10
B15
ICD-11
1E50.0
Key Statistics
Total cases
464K
Total deaths
140
Peak month
2019-01
Coverage
9 reporting countries · 2000-01-01 → 2023-12-30

Figure 1 | Full historical trajectories across all reporting countries.

Figure 2 | Year-over-year monthly comparison for seasonality and structural shifts.

Dataset Archive

Supplementary Data | Multi-country disease dataset

Machine-readable multi-country disease dataset (JSON/CSV) with source metadata.

Rows
2,620
Data Version
2026-06-20
Coverage
Included metadata
Source links, scope, cadence

Source Register

Official sources and update cadences used to construct the downloadable dataset.

AU
Australia NINDSSmonthlymicrosoft_bi

Australia

Australian national notifiable diseases surveillance dashboard.

Official source
CH
Switzerland FOPH IDDweeklyrest_api

Switzerland

Switzerland FOPH/BAG IDD mandatory reporting API normalized to national case rows. Monthly series may use the dashboard CHFL aggregate where CH-only monthly series are not exposed.

Official source
CN
China CDC WeeklyMONTHLYweb

China

Monthly notifiable infectious disease reports published by China CDC.

Official source
CN
National Disease Control and Prevention AdministrationMONTHLYweb

China

Official China public health bulletin and query portal.

Official source
CN
PubMedMONTHLYweb

China

Biomedical literature discovery feed used as supplementary context.

Official source
HK
Hong Kong, China CHP Notifiable Diseasesmonthlyopen_data_csv

Hong Kong, China

Hong Kong, China CHP annual notifiable infectious disease CSVs normalized to national monthly totals

Official source
JP
JP NIID Weeklyweeklyweb

Japan

Japan weekly infectious disease surveillance via NIID/JIHS.

Official source
KR
Korea KDCA EIDmonthlyopen_api_or_portal_download

South Korea

Korea KDCA notifiable infectious disease OpenAPI or portal/KOSIS downloads aggregated to national monthly notification counts.

Official source
NZ
phf_monthlymonthlyweb

New Zealand

PHF Science (formerly ESR) monthly notifiable disease surveillance data via internal globalID2 crawler

Official source
TW
Taiwan, China CDC NIDSSmonthlyopen_data_csv

Taiwan, China

Taiwan, China monthly notifiable infectious disease open-data CSV feed.

Official source
US
US CDC NNDSSweeklyapi

United States

CDC National Notifiable Diseases Surveillance System provisional data.

Official source
Suggested presentation pattern: cite the data version and coverage window when exporting charts or tables for publication.