Hep B/C + BBVs - 29-31 Flashcards

1
Q

Describe the global epidemiology of HBV

A

Around 550 m people chronically infected w/ viral hepatitis worldwide
China, India, SSA + Amazonian basin has high Hep B prevalence - increased risk of perinatal infection in Asia

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2
Q

What is the mode of transmission for HBV?

A

Vertical - mother to baby; blood to blood
Horizontal - children/siblings
Sexual transmission

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3
Q

What are the risk factors for HepB?

A

MTCT - 90% chronicity
IVDU
Sex workers
Unsafe medical practices

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4
Q

What is the relationship between risk of developing chronic infection and age?

A
Inversely related
Higher risk at younger age
Perinatally 90%
Childhood 30-50%
Adult 5%
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5
Q

What are the interventions available for prevention of HBV?

A

Safe + 95% effective vaccine
1st dose at 4 weeks but this is too late to prevent perinatal transmission - should ideally be given straight away
3rd dose coverage is poor
If vaccination maintained, 1.3m deaths averted by 2030

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6
Q

Give a case study of a successful national HBV vaccination programme

A

Taiwan 1984
Earliest nationwide HepB mass vaccination
Good strategy, good uptake of vacc + good antenatal programme - NOT representative of all countries
Prevalence of HBV in younger age groups reduced to < 1%

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7
Q

Why won’t vaccination address HBV worldwide?

A

Immunisation coverage is suboptimal
Infant vaccination doesn’t eliminate risk of perinatal transmission
Large pool of chronically infected carriers still remains for decades

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8
Q

What % of blood supply in Africa is screened for HBsAg?

A

< 50% (WHO)

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9
Q

What treatment is available for HBV?

A

Interferon
Nucleos(t)ide analogue drugs e.g. tenofovir (also Tx for HIV) + entecavir (high potency + high barrier to resistance) BUT cost + access still remains an issue
Tx reduces risk of progression to cirrhosis + HCC
AIM IS VIRAL SUPPRESSION - persistence of viral cccDNA in host cells (HBV) whereas in HIV there is latency in CD4 memory cells

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10
Q

How does treatment for HBV differ from HCV?

A
HBV= Long term viral suppression like HIV
HCV = Sustained virological response as HCV has entirely cytoplasmic lifecycle; < 1% relapse - CURE like TB
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11
Q

Why isn’t hepatitis treated in resource poor settings?

A

Not on global health agenda - lack of political will
Complex diagnostics - needs to be accessible + simplified
Drug cost + availability - global fund can get generic prices for some drugs incl tenofovir but only for HIV Tx or if co-infection w/ HIV/HBV
Skills + education - management + screening

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12
Q

What can be done to improve hepatitis treatment that is related to HIV treatment?

A

Integrate with HIV services - there is an obvious overlap and infrastructure is already in place for HIVW
Benefits: trained staff; lab facilities; drug supply (tenofovir); management of co-infection
Problem: potential for stigmatisation

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13
Q

What study shows the cost-effectiveness of Tenofovir?

A

PROLIFICA study in Gambia, Howell et al., 2016

Also showed that barriers still exist

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14
Q

What needs to be done in the future to improve health outcomes for hepatitis?

A
R&amp;D to improve data collection
Strengthen laboratory capacity
Build clinical capacity
Build clinical expertise
Integration w/ HIV services
Drug pricing
Education
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15
Q

What is the epidemiology of HCV?

A

Viral hepatitis is 7th leading cause of death - most in India, China + SE Asia
Approx 170 m infected - high prevalence in UK, USA + Central Europe

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16
Q

Is there a vaccine for HCV?

A

NO - only one out of all the types of hepatitis w/o vaccine

17
Q

Why is there no vaccine for HCV?

A

Technically difficult to develop attenuated vaccine and not enough funding

18
Q

What are the factors contributing to ongoing transmission? (x4)

A

Unsafe medical practices e.g. transfusion, medical care
IVDU
Sexual transmission
MTCT

19
Q

What are the prevention methods for HCV? (X3)

A

Screening of blood products for BBV
Provision of disposable medical needles
Needle exchange + OST Tx for those IDU

20
Q

What are the Tx options for HCV?

A

Pegylated interferon - directly hinders replication of virus
Ribavirin - inhibits viral growth
Direct Acting Antiviral (DAA) - 95% Cure rate

21
Q

What are the barriers to HCV treatment? (x3)

A

3 C’s
Costs
Cure rates - Hep C most likely to become chronic + outcomes in HIC v similar to LIC
Complexity

22
Q

What study shows the length of time to achieve SVR for Hep C?

A

Ford et al.

Showed 12 weeks of treatment needed to achieve SVR + therefore < 1% relapse

23
Q

Name and describe a Global Strategy to tackle viral hepatitis

A

Global Viral Hepatitis Strategy 2016-21
Approved by WHA 2016
Elimination of viral hepatitis as a public health threat
80% eligible patients treated for HBV + HCV by 2030
Task shifting + simplification
Scale up diagnosis + Tx

24
Q

What are the barriers to viral hepatitis treatment?

A
Research + surveillance
Simplification
Cost of care
Patient + community engagement
Access to services
Task shifting
Integration with other services e.g. HIV
Human rights 
Political will + financing
25
Q

What does the Lancet Commission on Viral Hepatitis Elimination aim to achieve? (x4)

A

National focus + hold countries accountable
Ensure affordable pangenotypic drugs - different immunology
Harm reduction + decriminalization of drug use + sex work
Fiscal space for investment

26
Q

What policy focuses on holding countries accountable for hepatitis?

A

Lancet Commission on Viral Hepatitis Elimination

27
Q

What are the risk factors for MTCT?

A

Prolonged rupture of membranes >6 hours
Exposure to maternal blood during vaginal delivery
Invasive monitoring of fetus with scalp electrodes/intrauterine pressure catheter placement

28
Q

What are the prevention interventions for MTCT? (x3)

A

Mode of delivery - C section?
Formula feeding
Novel anti-HCV therapies