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Viral Hepatitis A A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E E NANB B B D D C C
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Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Dec 24, 2015

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Neil Summers
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Page 1: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Viral Hepatitis

AA“Infectious”

“Serum”

Viral hepatitis

Entericallytransmitted

Parenterallytransmitted

F, G,? other

EE

NANB

BB DD CC

Page 2: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Hepatitis A Virus

• Naked RNA virus• Related to enteroviruses, formerly known as

enterovirus 72, now put in its own family: hepatovirus • One stable serotype only• Difficult to grow in cell culture: primary marmoset cell

culture and also in vivo in chimpanzees and marmosets

• 4 genotypes exist, but in practice most of them are group 1

Page 3: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.
Page 4: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Incubation period: Average 30 days

Range 15-50 days Jaundice by <6 yrs, <10%

age group: 6-14 yrs, 40%-50%>14 yrs, 70%-80%

Complications: Fulminant hepatitisCholestatic hepatitisRelapsing hepatitis

Chronic sequelae: None

Page 5: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

FecalHAV

Symptoms

0 1 2 3 4 5 6 12

24

Hepatitis A Infection

Total anti-HAV

Titre ALT

IgM anti-HAV

Months after exposure

Typical Serological Course

Page 6: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

• Close personal contact

(e.g., household contact, sex contact, child day care centers)

• Contaminated food, water(e.g., infected food handlers, raw shellfish)

• Blood exposure (rare)(e.g., injecting drug use, transfusion)

Transmission

Page 7: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

EndemicityDisease

RatePeak Age

of Infection Transmission Patterns

High Low to High

Early childhood

Person to person;outbreaks uncommon

Moderate High Late childhood/

young adults

Person to person;food and waterborne outbreaks

Low Low Young adults Person to person;food and waterborne outbreaks

Very low Very low Adults Travelers; outbreaks uncommon

Global Patterns of Hepatitis A Virus Transmission

Page 8: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.
Page 9: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Diagnosis

• Acute infection is diagnosed by the detection of HAV-IgM in serum by EIA.

• Past Infection i.e. immunity is determined by the detection of HAV-IgG by EIA.

• Cell culture – difficult and take up to 4 weeks, not routinely performed

• Direct Detection – EM, RT-PCR of faeces. Can detect illness earlier than serology but rarely performed.

Page 10: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.
Page 11: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Hepatitis E virus

Hepeviridae Hepevirus

Page 12: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Hepatitis E Virus

• unenveloped RNA virus, 32-34nm in diameter

• +ve stranded RNA genome, 7.6 kb in size.

• very labile and sensitive

• Can only be cultured recently

Page 13: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Incubation period: Average 40 days

Range 15-60 days Case-fatality rate: Overall, 1%-3%

Pregnant women, 15%-25%

Illness severity: Increased with age

Chronic sequelae: None identified

Hepatitis E - Clinical Features

Page 14: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Symptoms

ALT IgG anti-HEV

IgM anti-HEV

Virus in stool

0 1 2 3 4 5 6 7 8 9 10

11

12

13

Hepatitis E Virus InfectionTypical Serologic Course

Titer

Weeks after Exposure

Page 15: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.
Page 16: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.
Page 17: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.
Page 18: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Most outbreaks associated with faecally contaminated drinking water.

Several other large epidemics have occurred since in the Indian subcontinent and the USSR, China, Africa and Mexico.

In the United States and other nonendemic areas, where outbreaks of hepatitis E have not been documented to occur, a low prevalence of anti-HEV (<2%) has been found in healthy populations. The source of infection for these persons is unknown.

Minimal person-to-person transmission. Risk groups for severe course: Pregnancy, DM, obesity,

hypertension, ischemic heart disease

Hepatitis E - Epidemiologic

Features

Page 19: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Genotype 1

(Burma)

Genotype 2

(Mexico)

Genoytpe 3

(USA-swine)

Genotype 4

(China)

-causes epidemies

- subtropical regions

-Transmitted with contaminated water

- ın Europe travel associated

-Reservoir: Human

-Sporadic cases

- worldwide distributed (except Africa)

-Zoonotic

-In Europe: autochton

-Reservoir: wild boar

Page 20: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

Epidemiological features of hepatitis E in disease-endemic areas

Large outbreaks involving several hundred to several thousandpersons in developing countries

Sporadic hepatitis cases frequent

Fecal–oral transmission (usually through contaminated water) is thepredominant route of transmission

Insignificant person-to-person transmission

Parenteral transmission known but appears to contribute to only aminority of cases

Page 21: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

• Mother-to-newborn (transplacental) transmission known

• Highest attack rate among young adults aged 15–40 years, with• relative sparing of children

• High attack rate and mortality among pregnant women, particularlythose in second and third trimesters

• Low overall case fatality rate

• Chronic infection ? Immunosuppression?

• Superinfection can occur among persons with chronic liver disease

• Overall attack rates during hepatitis E outbreaks have rangedfrom 1% to 15%.

Page 22: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.
Page 23: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

• Diagnosis

Detection of anti-HEV IgM and IgG

Detection of virus RNA (rarely applied)

Page 24: Viral Hepatitis A “Infectious” “Serum” Viral hepatitis Enterically transmitted Parenterally transmitted F, G, ? other E NANB BD C.

• PreventionPossibly contaminated drinking water should be avoided as should uncooked food in endemic areas.

• Immune globulin is not effective if it comes from donors in western countries.

• There is no vaccine.