Hepatitis Flashcards

1
Q

Positive strand RNA genome with open reading frame encoding for structural and non-structural proteins

A

Hepatitis C

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2
Q

Hepacivirus genus; Flaviviridae family (yellow fever, dengue, etc.)

A

Hep C

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3
Q

What are the structural proteins of Hep C?

A

Core, and Envelope E1 and E2

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4
Q

Very high replication rate

Half-life = few hours

A

Hep C

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5
Q

Like HIV, Hep C has a high

A

Genetic variability

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6
Q

Hep C has lack of proof-reading function of viral

A

RNA polymerase

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7
Q

The most common genotype of Hep C ion the US is

A

Genotype 1

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8
Q

Principal cause of death from liver disease and leading indication for liver transplant in U.S.

A

Hep C

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9
Q

Often asymptomatic; if clinical illness, infant, young women, more likely to clear virus

A

Acute Hep C infection

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10
Q

With acute infection, anti-HCV can be negative for

A

Months

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11
Q

Characterized by asymptomatic fatigue, normal ALT/AST

A

Chronic Hep C

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12
Q

What percentage of chronic Hep C patients progress to advanced liver disease?

A

25%

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13
Q

Type II mixed cryoglobulinemia, glomerulonephritis, lymphoma, and neuropathy are all complications of

A

Hep C infection

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14
Q

If you received clotting factors made before 1987, you should be screened for

A

Hep C

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15
Q

Increases linearly with Hep C infection?

A

Hepatocellular carcinoma

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16
Q

To eradicate HCV as reflected in a sustained virologic response (SVR) to therapy

A

Treatment goals in chronic HCV

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17
Q

Absence of HCV RNA (by PCR) 12 weeks after completion of treatment course

A

SVR

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18
Q

Is associated with 99% chance of being HCV RNA negative in long-term follow up

A

SVR

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19
Q

What is the standard treatment for the HCV genotype 1?

A

Alpha 2a/2b pegylated interferon + ribavirin

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20
Q

With completion of a full course of alpha 2a/2b pegylated interferon + ribavirin, the SVR is

A

40-50%

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21
Q

Response to genotype 1 therapy is lower in

A

African Americans

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22
Q

NS3/4 protease inhibitor used to treat HCV genotype 1

A

Simeprevir

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23
Q

Nucleotide polymerase inhibitor used to treat HCV genotype 1

A

Sofosbuvir

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24
Q

An NS5A inhibitor used to treat HCV genotype 1

A

Ledipasvir

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25
A protease inhibitor used to treat HCV genotype 1
Paritaprevir/ritonavir
26
An NS5B inhibitor used to treat HCV genotype 1
Dasabuvir
27
Self-limited, with or without symptoms
Acute Hep B infection
28
Characterized by persistence of HBsAg in serum
Chronic HBV infection
29
Advanced liver disease; cirrhosis hepatocellular carcinoma, and co-infection with HIV, hepatitis C are complications of
HBV
30
HBV infection is most prevalent in
Africa and Asia
31
What are 3 serologic markers of HBV infection?
HBsAg, Anti-HBs, and HBcoreAg
32
The best correlation of immunity is
Anti HBs
33
Not measurable; structural component of nucleocapsid
HBcoreAg
34
Appears early during acute infection and during flares of chronic hepatitis
Anti-HBcore IgM
35
Lifelong marker of HBV infection, no correlate of activity or immunity
Anti-HBcore IgG/total
36
Soluble nucleocapsid protein which strongly correlates with level of viral replication
HBeAg (Hep B e antigen)
37
Important correlate of reduced viral replication and necroinflammatory activity in some patients
Anti-HBe
38
Lower in chronic HBV infection
Anti-HBs and Anti-HBe
39
Higher in chronic HBV infection than acute
HBeAg and HBsAg
40
Characterized by a Replicative phase with acute liver disease (immune clearance), and a non-replicative phase with remission of liver disease
Chronic HBV
41
What are the three phases of Chronic HBV?
1. ) Immune tolerance phase 2. ) Replicative phase 3. ) Non-replicative phase
42
Characterized by normal ALT, asymptomatic, high HBV DNA levels, and HBeAG (+)
Immune tolerance phase
43
What is the characteristic of HBeAg for the immune tolerance phase?
HBeAg (+)
44
There is a high rate of maternal-fetal transmission for the
Immune-tolerance phase
45
AST/ALT may be elevated intermittently or constantly during the
Immune clearance phase of HBV
46
During the immune clearance phase of HBV, severe hepatitis may occur leading to more rapid progression to
Cirrhosis
47
What is a major serological characteristic of the non-replicative phase?
HBeAg (-) > Anti-HBe (+)
48
During the non-replicative phase of HBV, we also see
HBsAg (+)
49
HBV DNA is low or undetectable, and ALT is normal/mildly elevated during the
Non-replicative phase of HBV
50
There is a reduced inflammation score on biopsy during the
Non-replicative phase
51
The biochemical response to therapy in chronic HBV is normal/reduction of
ALT/AST
52
Serologically, when treating chronic HBV, we expect to see conversion of
HBeAG and HBsAg to Anti-HBe and HBs respectively
53
Lamivudine, Adefovir , Entecavir, Tenofovir, and Interferon are all
Anti-virals for HBV infection
54
First nucleoside/tide agent for HBV infection -Low cost but high resistance risk limits long-term benefit
Lamivudine
55
The resistance rate to lamivudine is up to 20% at one year, however at 5 years, it is at
70%
56
Second antiviral developed for HBV -Slower antiviral response than other agents: HBV DNA fall
Adefovir
57
The dose of adefovir is 10 mg. Higher doses are associated with
Creatinine elevations
58
Not recommended for primary therapy when tenofoviris available -Used for tenofovir-resistant patients
Adefovir
59
At 5 years, the resistance to adefovir is
30%
60
Recommended for 12 months post HBeAg conversion indefinite for Anti-HBe patients
Adefovir
61
Adefovir-resistant mutants have diminished susceptibility to
Tenofovir
62
Cyclopental guanosine analogue -Not recommended for pts. with lamivudine-resistant mutants because of lesser antiviral effect and ↑ risk of resistance
Entecavir
63
Dose is 0.5 mg; may be increased to 1.0 mg in cirrhosis or very high HBV DNA levels
Entecavir
64
Nucleotide reverse transcriptase inhibitor -Comparable viral suppression to entecavir
Tenofovir
65
No resistance mutations detected for HBV (0/585 pts. at 6 yrs.) -Treatment of choice for pts. with prior exposure to other nucleoside analogues (lamivudine)
Tenofovir
66
Can cause decreased bone density -Not for use in children
Tenofovir
67
Target –global eradication of chronic infection -Prevention of hepatocellular carcinoma
HBV vaccine
68
What are the two yeast derived vaccines for HBV in the US?
Engerix and Recombivax
69
What are the 3 dose regimens for HBV vaccine
0, 1, and 6 months
70
An adequate response to the HBV vaccine is defined as Anti-HBs serum level of
Greater than 10 mIU/ml
71
Causes acute hepatitis with no chronic infection -Transmitted by fecal to oral route
Hepatitis A virus
72
Most adults from low income countries are immune to
Hepatitis A virus
73
Hep A has no association with
Liver Cancer
74
In the hepatovirus family, but with only a single serotype
HAV
75
The highest prevalence of HAV is in
Africa and the middle east
76
What is the incubation period for HAV?
15-50 days
77
The replication site for HAV seems to be limited to the
Liver
78
HAV is diagnosed by serology via
Anti-HAV IgM
79
Contagious during the incubation period and for a week after jaundice appears
HAV
80
Humans are the only known reservoir for
HAV
81
Alum-adjuvanted vaccine for HAV prepared from cell culture
HAVRIX
82
What are the protective anti-body levels for HAV vaccine?
10-20 mIU/ml
83
The seroconversion to protective HAV antibodies takes
2-4 weeks
84
Incorporated into the routine childhood immunization schedule in 2006 (given at ~ 12 months)
HAV vaccine
85
Men who have sex with men, persons traveling to high/intermediate endemicity, HIV infection, and chronic liver disease (especially HCV) are indications for
HAV vaccine
86
The current gold standard for the treatment of HCV genotype 1 is a triple drug therapy including
Peginterferon, ribavirin, and a protease inhibitor
87
What are the two available protease inhibitors?
Telaprevir and boceprevir
88
What is the anti-viral drug choice for pre-emptive therapy for HBV?
lamivudine or tenofovir/entecavir
89
Asian patients moving from immune tolerance phase to immune clearance show progression to
Chronic liver diseae
90
Any adult with chronic HBV can show progression to chronic
Liver disease
91
Progression to chronic liver disease is also caused by co-infection of
HCV and HIV
92
Patients who are HBeAg positive with increased HBV DNA may require
Longer courses of treatment
93
Patients who are HBsAg and anti-HBs negative, but antiHBc positive, indicating prior infection, may also -Follow closely but without treatment
Reactivate
94
For HBsAg negative patients, we want to give a high dose of
HBV vaccine