Hepatitis viruses - Heptatitis A, B, C, D and E, clinical features, epidemiology and lab diagnosis

6,738 views 38 slides May 01, 2014
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About This Presentation

This is a series of lectures on microbiology useful for undergraduate medical and paramedical students


Slide Content

HEPATITIS VIRUSES
Dr. Ashish V. Jawarkar
M.D. (Pathology)

Dr. Ashish JawarkarHepatitis viruses 2
Hepatitis
Infection of liver
Hepatitis viruses – A, B, C, D, E and G
B – DNA virus
All others – RNA viruses
Cause icteric jaundice
Type A and E – food borne, feco oral route
Type B and C – Blood borne, parenteral and
sexual routes

Dr. Ashish JawarkarHepatitis viruses 3
Hepatitis A
Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

Dr. Ashish JawarkarHepatitis viruses 4
Epidemiology
Common in children
Feco oral route – contaminated water
or milk
Over crowding and poor sanitation
Ingested, reaches intestine,
penetrates epithelium, reaches liver
through blood

Dr. Ashish JawarkarHepatitis viruses 5
Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

Dr. Ashish JawarkarHepatitis viruses 6
Clinical features
2-6 weeks incubation period –
asymptomatic
Clinical symptoms – malaise,
anorexia, nausea, vomitting and
abdominal pain
Yellow urine

Dr. Ashish JawarkarHepatitis viruses 7

Dr. Ashish JawarkarHepatitis viruses 8
Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

Dr. Ashish JawarkarHepatitis viruses 9
Lab diagnosis
Raised bilirubin in serum
(indirect>direct)
Yellow urine – bilirubin present
Demonstration of antibodies by ELISA
IgM – recent infection
IgG – remote infection

Dr. Ashish JawarkarHepatitis viruses 10
Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

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Prophylaxis
Improved sanitation
Vaccine is available
Natural infection leads to life long
immunity

Dr. Ashish JawarkarHepatitis viruses 12
Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

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Treatment
No antiviral drug available
Treatment is symptomatic

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TYPE B HEPATITIS
Over 350 million HBV carriers in the
world
One million die anually

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Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

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Epidemiology
Hepatitis B virus structure

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In the serum of Hep B patients we
can see – Australia antigen or

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Dane particle

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Developed countries
Adolscents and young adults
Infection occurs through
contaminated syringes and needles
Drug addicts
Homosexuals

Dr. Ashish JawarkarHepatitis viruses 20
Developing countries
Children
Vertical transmission from mother to
baby
Horizontal transmission among
infants and neonates

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Everywhere
Razors, nail clippers, acupuncture,
tatooing, circumscision, ear or nose
piercing
Barbers, dentists and doctors may
get infected

Dr. Ashish JawarkarHepatitis viruses 22
Carriers
Those who donot have symptoms but
are HbsAg positive

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Screening of blood donors
Compulsory

Dr. Ashish JawarkarHepatitis viruses 24
Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

Dr. Ashish JawarkarHepatitis viruses 25
Clinical features
No symptoms in carriers
Similar to HAV in acute phase

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Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

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Lab diagnosis
Demonstration of viral antibodies and
antigens in serum -

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HBsAg infection
IgM anti HBcAg recent infection
IgG anti HBcAg remote infection
HBeAg infective
Anti HBsAg immunity after
vaccination

Dr. Ashish JawarkarHepatitis viruses 30
Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

Dr. Ashish JawarkarHepatitis viruses 31
Prophylaxis
Avoid multiple partners
Avoid drug abuse
Use of disposable syringes and
needles
Screening of Blood, organ and semen
donors
Universal immunisation (vaccination)

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Immunisation - Passive
administer HBIG (Hepatitis B
immunoglobulin)
Administer soon after accidental
exposure
Can be administered to baby born to
a carrier mother

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Active immunisation - vaccine
Consists of HBsAg particles
Given as a routine to all babies

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Epidemiology
Clinical features
Lab diagnosis
Prophylaxis
Treatment

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Treatment
Acute phase – no treatment required,
patients recover
Chronic phase – become carriers, can
give antivirals like lamivudine and
adefovir to keep replication in check

Dr. Ashish JawarkarHepatitis viruses 36
Hepatitis C Virus
Also blood borne
Most common cause of post
transfusion hepatitis in developed
countries
Most common cause of post hepatitis
– hepatocellular carcinoma

Dr. Ashish JawarkarHepatitis viruses 37
Hepatitis E virus
Feco oral route
 Second common cause of hepatitis
after hepatitis A in developing
countries
Generally mild and self limiting illness
Unusually high mortality (20-40 %) in
pregnancy

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