Hep A & B Flashcards

1
Q

Hep A Background

A
  • Enveloped RNA virus
  • Piornavirus
  • Causes acute infection only
  • Spread via fecal oral route
  • Can survive outside the body for months
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2
Q

Which antibodies are elevated in acute vs prior Hep A

A

-IgM = acute infection
(5 to 10 days)
-IgG = prior infection
(4 to 6mo)

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3
Q

Seroconversion rates for vaccine

A
  • 94% with first dose
  • Booster is still recommended
  • Most common vaccine preventable infection
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4
Q

Why are Hep A rates highest in rural areas

A

-Lack of access

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5
Q

How many shots are in the Hep A schedule?

A
  • Havrix and VAQTA are both a 2 shot series (0 and 6-12mo)

- Twinrix (HAV/HAB) is a 3 shot series (0, 1, 6mo)

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6
Q

Hep B background

A
  • DNA virus that becomes a part of human DNA (cccDNA)
  • Transmitted via percutaneous or mucosal contact with infected blood/ fluids
  • Can live outside of the body for about 7 days
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7
Q

Hep B surface antigen (HBsAg)

A
  • Protein found on the surface of HBV

- Detectable (+) in acute and chronic infections

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8
Q

Hep B surface antibody (anti-HBs)

A
  • Will be (+) following successful vaccination series
  • Antibody = made by us
  • Antigen = made by virus
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9
Q

Hep B core antibody (Anti-HBc)

A
  • (+) result indicates prior or ongoing infection
  • If positive Anti-HBc and positive HBsAg then there is an active infection
  • IgM = active infection
  • IgG = prior/ chronic infection
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10
Q

Hep B vaccination

A
-3 dose series (0, 1, 6mo) 
30 to 50% with 1st dose 
75% with 2nd dose
96% with 3rd dose 
-Most patients do NOT finish series
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11
Q

Heplisav B

A
  • 2 doses (0 and 1mo)
  • New adjuvant = more robust immune response
  • Pts are more likely to finish series
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12
Q

Immunoglobulins in Hep B

A
  • Passive protection
  • Used to prevent perinatal transmission
  • Give w/in 24hrs of birth from HBV positive mother
  • Not routinely used in adults
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13
Q

When to treat Hep B

A
  • HBV > 2000 IU/mL
  • ALT levels > ULN
  • Pts with cirrhosis (compensated or decompensated)
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14
Q

Preferred treatments for Hep B

A

1) Entecavir- inhibits HBV polymerase
2) Tenofovir
TDF- requires renal adjustment
-Safe in pts with cirrhosis

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15
Q

Why do we not use interferons anymore?

A
  • Lots of side effects

- Risk of decompensation

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16
Q

Non-preferred agents due to concerns for developing resistance

A

1) Adefovir
- Safe in cirrhosis
- Some activity against HIV
2) Lamivudine
- High rates of resistance by 5 years use of treatment
- Safe in cirrhosis and immunocompromised
3) Telbivudine
- Specific for HBV
- Safe in cirrhosis

17
Q

Management of Hep B in immunosuppressive therapies

A
  • Should be tested for Hep B
  • Vaccinate
  • Check HBsAg and AntiHBc
  • Start prophylaxis before immunosuppressive therapy
  • Pts on immunosuppressive therapy are at risk for reactivation
18
Q

HBV and pregnancy

A
  • High risk of transmission at delivery
  • Risk is minimized by using tenofovir or lamivudine for mom
  • Vaccinate and use immunoglobulin for active and passive protection for the new born
19
Q

HBV and HIV

A
  • All patients should be tested for HIV
  • Antivirals can be used in both HBV and HIV
  • Ok to use monotherapy in HBV but NOT in HIV