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
What does the Lancet Commission on Viral Hepatitis Elimination aim to achieve? (x4)
National focus + hold countries accountable Ensure affordable pangenotypic drugs - different immunology Harm reduction + decriminalization of drug use + sex work Fiscal space for investment
26
What policy focuses on holding countries accountable for hepatitis?
Lancet Commission on Viral Hepatitis Elimination
27
What are the risk factors for MTCT?
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
What are the prevention interventions for MTCT? (x3)
Mode of delivery - C section? Formula feeding Novel anti-HCV therapies