Content on this page:
Content on this page:
Clinical Presentation
Most acute viral hepatitis infections
are asymptomatic, or they can cause an anicteric illness that may not be
diagnosed as hepatitis.
Hepatitis A generally causes minor
illness in childhood with >80% of infections being asymptomatic. Adults are
more likely to produce clinical symptoms. Symptoms usually last for <2
months, however, some patients may suffer from prolonged infection or may
experience disease relapse.
Hepatitis B, C, and D may also be
asymptomatic. Symptomatic hepatitis B will depend on the mode and time of
transmission. Vertical transmission from mother to child is almost always
asymptomatic while other routes of transmission are more likely to produce
symptomatic disease (30% of cases transmitted by intravenous [IV] drug use are icteric).
Hepatitis E is usually asymptomatic and patients with
symptoms are usually older adolescents or young adults. The extrahepatic
manifestations such as Guillain-Barré syndrome, Parsonage-Turner syndrome,
neuralgic amyotrophy, bilateral brachial neuritis, peripheral neuropathy,
encephalitis, membranoproliferative glomerulonephritis with or without
cryoglobulinemia, membranous glomerulonephritis, acute pancreatitis, other
autoimmune manifestations (eg myocarditis, arthritis, thyroiditis), and
thrombocytopenia have been observed. Some patients may experience persistent
hepatitis E virus replication and immunocompromised patients or those with
chronic liver disease are at risk for chronic hepatitis E virus infection with prolonged
viremia (>6 months).
During the preicteric phase,
patients may manifest with nonspecific systemic symptoms (eg myalgia, nausea,
vomiting, fatigue, malaise with discomfort in the right upper quadrant of the
abdomen), altered sense of smell or taste, coryza, photophobia, headache,
cough, diarrhea, dark urine, and serum sickness-like syndrome. Hepatomegaly,
splenomegaly, and lymphadenopathy may be seen during physical examination. During
the icteric phase, jaundice is usually noted after the onset of the fever or
upon lysis of the fever.
If fulminant hepatitis
ensues, the development of symptoms of hepatic encephalopathy (eg confusion,
drowsiness within 8 weeks of symptoms or within 2 weeks of the onset of
jaundice). Hypoglycemia and prolonged prothrombin time (PT) may also occur.
The routes of transmission
of hepatitis differ according to type. Hepatitis A may be transmitted via the oral-fecal
(eg ingestion of contaminated food or water) route, person-to-person contact, or
sexual contact. Hepatitis B may be transmitted via the perinatal route,
percutaneous route, sexual contact, or close person-to-person contact (ie by
open cuts and sores). Hepatitis C may be transmitted via blood transfusions,
organ transplants, percutaneous (especially intravenous drug use) route, sexual
contact, or perinatal route. Hepatitis D is transmitted via sexual contact,
percutaneous route especially intravenous drug use, or mucous membrane contact
with infectious blood or body fluids. They may be found only in patients with hepatitis
B since it requires the hepatitis B outer coat. Hepatitis E is transmitted via
the oral-fecal route (ingestion of contaminated food or water), or by blood
transfusion in endemic areas.

The incubation period of hepatitis likewise differs according to type. Hepatitis A has an incubation period of 15 to 50 days. Hepatitis B has an incubation period of 30 to 180 days. Hepatitis C has an incubation period of 14 to 180 days. Hepatitis D has an incubation period of 30 to 180 days. Hepatitis E has an incubation period of 15 to 60 days.
Hepatitis B virus contains DNA nucleic acid while A, C, and E viruses have RNA nucleic acid. Hepatitis D has an incomplete RNA and needs the B virus to replicate. Hepatitis A and E viruses cause epidemics while Hepatitis B, C, and D viruses may predispose an individual to chronic disease and hepatic malignancy.

History
The following are important points in the clinical history of patients with suspected viral hepatitis:
- Contacts with jaundiced patients
- Intravenous drug use
- History of blood transfusion
- Surgery or hospitalizations
- Family history of chronic liver disease
- Occupation
- Food and water sources
- Alcohol use
- Migration from a country with high hepatitis B or hepatitis D virus prevalence rates
Screening
Screening for chronic hepatitis B virus infection is recommended for household members, sex partners, and drug-sharing partners of a person with chronic hepatitis B virus infection, men who have sex with men (MSM), HIV-positive individuals, pregnant women, blood or plasma or organ or tissue or semen donors, infants born to HBsAg-positive mothers, patients on hemodialysis, chemotherapy, or immunosuppressive therapy, patients with elevated AST/ALT of unknown etiology, correctional facility inmates, and individuals born in countries with hepatitis B virus prevalence of ≥2%.