Viral Hepatitis Flashcards

1
Q

hepatitis A - transmission

A
faecal-oral spread
poor hygiene/overcrowding
cases imported
gay men 
IV drug users
importance declined in UK
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2
Q

hep a - clinical

A

acute hepatitis, no chronic infection

peak incidence of symptomatic disease in older children/young adults

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3
Q

hep a - diagnosis

A

laboratory confirmation of acute infection
clotted blood for serology
hepatitis A IgM

control - hygiene, vaccine prophylaxis

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4
Q

hepatitis E

A

more common in tropics
clinically like hep A
more common than hep A

faecal-oral transmission

evidence of chronic infection in pigs - common cause in UK

no vaccine available

some immunocompromised humans can get chronic infection

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5
Q

hepatitis D

A

only found with hep B virus

parasite of a parasite

exacerbates hep B
co-infection or syperinfection

rare in scotland

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6
Q

hepatitis B - transmission

A

sex
mother to child
blood

chronic infection more likely to result if first exposure is in childhood

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7
Q

hep B - at risk groups

A

people born in areas of intermediate/high prevalence
multiple sexual partners
people who inject drugs
children of infected mothers

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8
Q

hep B - diagnosis

A

laboratory confirmation
hep B surface antigen (HBsAg) present in blood of all infectious individuals
present for more than 6 months in chronic infection
highly infected = HBeAg

hep B IgM most likely to be present in recently infected cases
anti-HBs present in immunity

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9
Q

hep B - control

A

minimise exposure - safe blood, safe sex, needle exchange, prevention of needle sticks, screening of pregnant women

two pre-exposure vaccination strategies in use in UK

post-exposure prophylaxis - vaccine, plus HBIG

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10
Q

hepatitis C - transmission

A

similar to hep B
no vaccine available

infection results in chronic infection in about 75% of cases
natural history does not seem to be dependent on age at time of infection

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11
Q

chronic infection

A

6 months of infection

time from infection to cirrhosis typically >20years

infection to hepatocellular carcinoma typically >30years

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12
Q

chronic infection - Hep B

A

spontaneous cure not uncommon

even after many years of infection

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13
Q

chronic infection - Hep C

A

once chronic infection established, spontaneous cure is not seen

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14
Q

most common cause of viral acute hepatitis

A

hep E

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15
Q

management of acute viral hepatitis

A
symptomatic
no antivirals given
monitor for encephalopathy
monitor for resolution
notify public health
immunisation of contacts
test for other infections if at risk
vaccinate against other infections if at risk
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16
Q

management of chronic viral hepatitis

A

ANTIVIRALS

VACCINATION
other hepatitis viruses
if cirrhotic - influenza and pneumococcal

INFECTION CONTROL

ALCOHOL
drink as little as possible

HEPATOCELLUALR CARINOMA SCREENING
most important for patients with cirrhosis

17
Q

antiviral treatment of chronic viral hepatitis - who

A

CHRONIC INFECTION
HCV - RNA present and genotype known

RISK OF COMPLICATIONS
evidence of inflammation (mostly in Hep B)

FIT FOR TREATMENT
established cirrhosis more difficult to treat - priority
liver cancer = contraindication

patients may have other priorities

18
Q

antiviral treatment of chronic viral hepatitis - when

A

before complications

evidence of inflammation

when patient ready and clinical priority

19
Q

interferon alfa

A

not used in hep C
sometimes in hep B

Many side effects

given my injection as peginterferon
flu-like symptoms, chills, sore muscles, malaise
thyroid disease, autoimmune disease, psychiatric disease

20
Q

ribavirin

A

anaemia

21
Q

therapy for chronic hep B

A

SUPPRESSIVE ANTIVIRAL DRUG
safer, increasing range available
suppression not cure, resistance can develop

PEGINTERFERON
sustained cure possible
side effects, injections, only minority gain benefit

22
Q

benefits of chronic hep B therapy

A
virological
improved liver biochemistry
improved histopathology
reduced infectivity
reduced progression to cirrhosis and primary hepatocellular carcinoma
reduced mortality
23
Q

benefits of chronic hep C therapy

A

response defined by loss of HCV RNA in blood sustained to 6 months after end of therapy

sustained virological response 
improved liver biochemist 
improved histopahtology
reduced infectivity
reduced incidence of primary liver cancer
reduced mortality