Hepatitis C Flashcards

1
Q

acute hepatitis C

A

infection that develops during the first 6 months following the exposure

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2
Q

chronic hepatitis C

A

HCV infection that persists beyond 6 months following exposure

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3
Q

Hep C virus pathogen

A

Hepacivirus C
RNA virus
risk of chronic infection depends on hosts ability to clear infection through activation of innate pathway
6 genotypes
reinfection with another HCV genotype is possible

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4
Q

transmission methods

A

parenteral - needle shharing among IVDU, needlestick injury, blood transfusion, dialysis
organ transplantation
sexual - rare in contrast to HBV and HIV
perinatal (vertical)

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5
Q

risk factors for HCV infection

A

injection drug use
HBV or HIV
Hx of incarceration
recieved blood transfusion or organ transplant before 1992

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6
Q

incubation period

A

2 weeks to 6 months

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7
Q

acute course of disease

A

asymptomatic in 80% of cases
malaise, fever, myalgias, arthralgias
RUQ pain, tender hhepatomegaly
nausea, vomitng, diarrhoea
jaundice, possibly pruritis (due to elevated bilirubin)

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8
Q

chronic course of disease

A

seen especially in asymptomatic individuals as treatment may be delayed or not initiated
findings often mild and non specific eg. fatigue
liver cirrhosis
extrahepatic features

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9
Q

extrahepatic features of HCV

A

haem: mixed cryoglobulinaemia, lymphoma, immune tyhrombocytopaenic purpura, autoimmune hemolytic anaemia, monoclonal gammopathies
renal - membranoproliferative GN, membranous GN
rheum - polyarteritis nodosa, sjogren syndrome
dermatological - porphyria cutanea tarda, lichen planus
endocrine - T2DM, autoimmune thhyroiditis
vascular - leukocytoclastic vasculitis
other - sialadenitis

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10
Q

screening for HCV in people without risk factors

A

everyone at least once per lifestime age >18
once per pregnancy
the CDC recommends against universal screening in settings where HCV disease prevelance is <0.1%

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11
Q

screening for people with risk factors

A

one time:
- upon diagnosis with HIV
- individuals <18 years with risk factors
- infants born to HCV pos mothers
repeat screening
- after exposure to HCV within 48 hours and then >6 months
- annual for people who inject drugs, Men with HIV who have unprotected sex with men, Men who have sex with men taking HIV preexposure prophylaxis

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12
Q

Hepatitis C tests for people who are HCV naive

A

Anti-HCV antibodies (EIA/ELISA immunoassay): as initial test for immunocompetant individuals who are HCV naive

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13
Q

Hepatitis C tests for people with prior HCV infection or immunocompromise

A

HCV RNA qualitative PCR
after seroconversion from prior HCV infection, HCV antibodies wil;l remain positive for life and have no further diagnostic utility

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14
Q

why are antibody tests less effective in immunocompromise

A

immunocompromise may prevent people from being able to produce antibodies
seroconversion may be delayed or absent

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15
Q

interpretation of hepatitis C tests

A
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16
Q

how to tell between acute or chronic infection

A

in contrast to Hep A and Hep B infections, there is no serologic or virology assay for HCV that distinguishes between acute and chronic infection

17
Q

how long until antibodies are detectable on immunoassay

A

as long as 6 weeks

18
Q

how long until RNA HCV is detectable on qualitative PCR

A

as long as 2-3 weeks

19
Q

laboritory studies for workup

A

quantitative PCR for HCV RNA viral load
routine studies: FBC, UECs
hepatocellular enzymes
cholestasis parameters
liver synthetic function tests
HIV, HAV, HBV for coinfection
serum pregnancy test

20
Q

hepatocellular enzyme changes

A

transaminases (ALT and AST)
are involved in amino acid metabolism and used clinically as parameters of hepatocellular injury
will be normal or raised
fluctuating ALT peaks indicate acute HCV infection

21
Q

cholestasis parameters changes

A

raised GGT
raised alk phos
raised bilirubin

22
Q

liver synthetic function tests

A

alterations indicate cirrhosis
decreased albumin
decreased total protein
increased PT/INR

23
Q

liver biopsy

A

consider if aeitiology of hepatitis is unknown
consider if liver fibrosis staging would alter treatment

24
Q

acute phase pathology

A

focal areas of macrovesicular steatosis
bile duct injury
sinusoidal inflammation of hepatic cells
lobular involvement in the form of eosinophillic single cell necrosis

25
Q

chronic phase pathology

A

lymphoid follicles in portal triad
necroinflammation of periportal liver cells
variable degree of fibrosis
severe hepatocyte injury

26
Q

general principles of treatment

A

the goal of treatment is sustained virological response (SVR)
refer patients with end-stage liver disease for liver transplant evaluation

27
Q

antiviral therapy

A

always treated with multidrug approach (no antivirals approved for monotherapy)
- direct acting antvirals: antivirals target and inhibit HCV encoded proteins that are essential for the HCV replication cycle
- interferon plus ribavirin was the preferred treatment before the development of DAAs

acute and chronic infections are treated the same

28
Q

are DAAs or interferon or ribavirin based therapies preferred

A

DAAs have superior efficacy and safety profiles

29
Q

supportive care

A

in all individuals with HCV:
- avoid hepatotoxic drugs and alcohol
- counsel about HIV and hep B prevention
- counsel regarding adherance, reinfection prevention, and medication risks
offer Hep A and B vaccination for Hep A and B seronegative individuals
give harm reduction strategies and refer for treatment for substance abuse for IVDU

30
Q
A