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Hepatitis B
Definition
The term "hepatitis" refers to syndromes or
diseases causing liver inflammation, including
inflammation due to viruses and chronic alcohol
abuse. Viruses causing hepatitis include Hepatitis
A, B, C, E and the delta factor. Each virus
causes a distinct syndrome, though they share
some symptoms and consequences.
Most people who become infected with Hepatitis
B get rid of the virus within 6 months. A short
infection is known as an "acute" case of Hepatits
B.
Approximately 10% of people infected with the
Hepatitis B virus develop a chronic, life-long
infection. People with chronic infection may have
symptoms, but many of these patients never develop
symptoms. These patients are sometimes referred
to as "carriers" and can spread the disease to
others. Having chronic Hepatitis B increases your
chance of permanent liver damage, including cirrhosis
(scarring of the liver) and liver cancer.
Causes
and risks
Hepatitis B is transmitted via blood and other
body fluids. Infection can occur through:
- Contact with blood in healthcare settings
-- this puts physicians, nurses, dentists,
and other healthcare personnel at risk
- "Unsafe" sex with an infected person
- Blood transfusions
- Sharing needles during drug use
- Receiving a tattoo or acupuncture with contaminated
instruments
- Birth -- an infected mother can transmit
the virus to the baby during delivery or shortly
thereafter
People who are at higher risk, including people
who live with someone with hepatitis B and healthcare
workers, should get the hepatitis B vaccine.
In acute hepatitis, it takes about 1 to 6 months
from the time of infection until the disease
manifests itself. Early symptoms may include
nausea and vomiting, loss of appetite, fatigue,
and muscle and joint aches. Jaundice, together
with dark urine and light stools, follows. About
1 percent of patients infected with hepatitis
B die due to liver damage in this early stage.
The risk of becoming chronically infected depends
on the age at the time of infection: more than
90 percent of newborns, about 50 percent of
children, and less than 5 percent of adults
infected with hepatitis B develop chronic hepatitis.
Most damage from hepatitis B virus is caused
by the body’s response to the infection. The
body's immune response against the infected
liver cells (hepatocytes) damages the cells,
causing liver inflammation (hepatitis). As a
result, liver enzymes (transaminases) leak out
of the liver into the blood, causing transaminase
blood levels to be elevated. The virus impairs
the liver’s ability to produce the clotting
factor prothrombin, increasing the time required
for blood clot formation (prothrombin time).
Liver damage also impairs the body’s ability to
rid itself of bilirubin (a breakdown product of
old red blood cells), causing jaundice (yellow
discoloration of the eyes and body) and dark urine.
Prevention
Screening of all donated blood has reduced
the likelihood of contracting hepatitis B from
a blood transfusion. As an initial screen, blood
donors are now required to fill out a questionnaire
about their sexual and drug use activities.
The blood of those who are in high-risk groups
is not used. Also, serologic tests are used
to screen collected blood for the hepatitis
B virus.
Mandatory reporting of the disease allows state
health care workers to track people who have
been exposed and to immunize contacts that have
not yet developed the disease. Formerly, hepatitis
B vaccine was made from human blood products,
so it was not received well by the public. The
new hepatitis B vaccine is entirely artificial,
with no human products, and therefore cannot
transmit either hepatitis B or the AIDS virus.
The new vaccine is both safe and effective.
Those receiving the vaccine require three vaccinations
administered within a six month period to achieve
full immunity. Vaccination of babies has become
routine in pediatric care in the US.
Sexual contact with a person who has acute
or chronic hepatitis B should be avoided. Condoms,
if used consistently and properly, may also
reduce transmission through sexual contact.
However, immunization provides the only definitive
protection against the virus. Vaccination of
those at high risk has been of only limited
success. Therefore, the United States Public
Health Service has recommended universal vaccination
of all neonates and pre-pubertal teenagers.
Infants born of mothers who either currently
have acute hepatitis B or who have had the infection
receive a special immunization series to prevent
viral transmission. This includes administering
hepatitis B immune globulin and a hepatitis
B immunization within 12 hours of birth.
Symptoms
- Fatigue, malaise, joint aches (arthralgias)
and low grade fever
- Nausea, vomiting, loss of appetite and abdominal
pain
- Jaundice and dark urine due to increased
bilirubin
Signs
and tests
- Hepatitis B surface antigen (HBsAg) -- this
represents the first viral marker present
in blood tests after the patient is infected.
It usually disappears from the blood in 1-2
months.
- Hepatitis B core antibody (Anti-HBc) --
this is usually detected within 1-2 weeks
of the appearance of hepatitis B surface antigen.
- Hepatitis B surface antibody (Anti-HBs)
-- this is found both in those who have been
immunized and those who have recovered from
hepatitis infection.
- Both hepatitis B surface antibody and core
antibody persist indefinitely in the blood
of patients who have recovered from hepatitis
B.
- Liver enzyme (transaminase) blood levels
may be elevated due to liver damage.
- Albumin levels may be low and prothrombin
time may be prolonged due to severe liver
failure.
Treatment
Acute hepatitis needs no treatment other than
careful monitoring of liver function, by measuring
serum transaminases and prothrombin time.
In rare cases of liver failure, the patient
should be monitored in an intensive care unit.
Because damage to the liver decreases its ability
to degrade proteins, protein intake should be
restricted and oral lactulose or neomycin should
be administered (to limit protein production
by bacteria in the gut). Patients should be
supported and monitored until they recover or
until prognostic factors indicate a liver transplant
is necessary. Liver transplantation is the only
definitive cure in cases of liver failure.
Treatment of chronic hepatitis is geared towards
reducing inflammation, symptoms, and infectivity.
Recombinant alpha interferon, currently the
only approved antiviral agent for hepatitis,
converts 37 percent of patients from the replicative
phase to non-replicative phase. However, it
is ineffective in most patients, very expensive,
and causes some adverse effects. These include
a flu-like syndrome, fever, chills, malaise,
muscle aches, and rigors (’shakes’). Currently,
trials are underway in Europe for natural interferon,
which has fewer side effects and is more effective.
Liver transplantation is used to treat end-stage
chronic hepatitis B liver disease.
Support
groups
If you would like additional
support, a group where members share common experiences
and problems can help. See liver disease - support
group.
Prognosis
The acute illness usually
subsides after 2 to 3 weeks, and the liver returns
to normal within 16 weeks. 10% of people infected
may develop chronic hepatitis. There is a higher
incidence of hepatocellular carcinoma in those
who have had hepatitis B virus infection than
in the general population. Hepatitis B is fatal
in approximately 1% of cases of acute hepatitis
B.
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