Table 3.
Surveillance activities needed to describe the epidemiology of viral hepatitis, including hepatitis B and hepatitis C.
Parameter | Activities that contribute to surveillance for viral hepatitis | ||||
Surveillance for acute hepatitis that reflect new infections | Surveillance for chronic, prevalent hepatitis | Surveillance for sequelae | |||
Activities | Syndromic surveillance in the general population; Event-based surveillancea | Enhanced case reporting (with in vitro diagnosis and collection of information on risk factors) countrywide or in sentinel sitesb | Case reporting from laboratories or health care facilities | Regular biomarker surveys | Combination of data from cancer registries, death certificates, and testing of cirrhosis and HCCc patients for HBVd and HCVe infection |
Population under surveillance | Persons presenting with acute hepatitis in health care facilities (discrete onset of symptoms) | Persons presenting with acute hepatitis in health care facilities (discrete onset of symptoms) | Persons without acute symptoms tested in health care facilities/laboratories | Person without acute symptoms tested during population surveys | Persons diagnosed with cirrhosis and HCC |
Usual implementer | Communicable disease surveillance | Communicable disease surveillance (if countrywide); hepatitis program (if sentinel sites) | Communicable disease surveillance and/or hepatitis program | Hepatitis program in coordination with the other actors implementing biomarker surveys | Hepatitis program collating data from various different sources, including vital registration |
Case definitions to use (see Table 4) | Presumptive case of acute hepatitis | Confirmed case of acute hepatitis (by type) | Chronic HBV and HCV infection; serological evidence of past or present HCV infection | Chronic HBV and HCV infection; serological evidence of past or present HCV infection | Cases of HCC or cirrhosis with chronic HBV or HCV infection |
Objective of the surveillance activity | Detect outbreaks | Describe trends in type-specific acute hepatitisf and identify risk factors | Estimate the proportion of chronically infected persons who have been identified | Estimate the burden of chronic infections; model incidence trends | Estimate the incidence of HCC and cirrhosis |
aIn vitro diagnosis needs to be organized on a sample of cases when an outbreak is reported.
bHigh-quality data (ie, reliable in vitro diagnosis and good information on risk factors) from a smaller number of tertiary centers is preferable and more efficient than poor-quality data from many sites.
cHCC: hepatocellular carcinoma.
dHBV: hepatitis B virus.
eHCV: hepatitis C virus.
fSurveillance for acute hepatitis cannot be used directly to quantify new infections. The reported number of cases of acute hepatitis needs to be adjusted for the large proportion of asymptomatic cases and underreporting.