Blood Borne Viruses: HIV and Viral Hepatitis Flashcards

1
Q

The global total of people with a HIV infection is 37 million, with 107,800 in the U.K. Where is there a high prevalence?

A

Subsaharan Africa.

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2
Q

How can a HIV infection present?

A

Immunocompromised, so recurrent infections of varying types and weight
loss. May present with: Oral candidiasis, Kaposi’s sarcoma (skin lesions/rashes) and PCP (pneumocytic pneumonia - consolidation). Anyone with HIV may be infected by any pathogen, but commonly: reactivation of latent viral infections (including EBV), fungi (yeasts and mounds) and Protozoa (parasites).

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3
Q

What is the outcome of HIV?

A

Chronic infection, with or without disability and death is probable if it’s diagnosed late and untreated.

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4
Q

In the U.K., 67% of HIV cases are men, so 33% female, but globally this is higher due to ________ _____________. Globally 43% of cases are MSM and 57% _____________, but in the U.K. there are more _______ diagnoses. Half of these are _______ ____________. IV drug users make up __/1000 cases.

A
Gender inequalities 
Heterosexual
MSM
Black African
2
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5
Q

The rate of sexual transmissions of HIV being MSM are increasing, but what danger is seen is diagnosed heterosexuals?

A

The average are of diagnosis of a heterosexual wit HIV in the U.K. is 40. Over 50% are diagnosed at a late stage.

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6
Q

Infection of HIV acquired in the U.K. _________ that acquired abroad. There are hotspots within the country, including the ___________. ___% of people living with HIV, do not know that they have it.

A

Exceeds
Midlands
17

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7
Q

Describe the genome of the HIV virus

A

Genome - RNA or DNA (never both), single or double stranded.

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8
Q

What is the capsid of the HIV virus and what is its shape?

A

The capsid is the protein shell that protects the genome; it’s helical (rod shaped/coiled) or icosahedral (spherical/symmetric).

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9
Q

Does the HIV virus have a lipid envelope?

A

The lipid envelope is either present or absent. If present, it is derived from the host cell’s membrane and contains virus specific proteins (antigens).

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10
Q

Name 4 viral structure and behaviour components of HIV.

A

Genome, capsid, lipid envelope, replication strategy.

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11
Q

What does it mean that the Human Immunodeficiency Virus is a retro virus?

A

ssRNA–>DNA–>ssRNA

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12
Q

How does HIV infect cells?

A

It infects cells with a CD4 cell surface receptor: T helper lymphocytes (monocytes/macrophages) - replicates inside cells and destroys it, causes inflammation then spreads to infect more cells.

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13
Q

At a cellular level, what does HIV do? Include the following enzymes in the description: integrase, reverse transcriptase and protease.

A
  1. Free virus binds and fuses to CD4 molecule and coreceptor. 2. Injection - penetrates cell and contents emptied into. 3. Reverse transcription. 4. Integration of viral DNA into cell’s own (integrase). 5. Transcription. 6. Assembly - sets of viral protein chains come together. 7. Budding - immature virus pushes out of cell, taking some membrane with it and breaking free. 8. Protease enzyme cuts chain, so individual proteins can combine to form a working virus.
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14
Q

How is HIV transmitted?

A

Contact of infected bodily fluids with mucosal tissue/blood/broken tissue: sexual contact, transfusion, contaminated needles, perinatal/vertical transmission.

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15
Q

Explain the different stages of a HIV infection.

A

Primary infection/seroconversion - in months, CD4 dips and viral load is very high (infectious).
Latent infection - viral load rises from dropped viral ‘set point’ steadily and the CD4 count starts to drop again.
Symptomatic infection - after years, contamination with CD4 count= 350 cells/microL.
Severe infection/AIDS with CD4<200, maybe cancer.

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16
Q

As their CD4 count drops, people with HIV are more vulnerable infection and varying pathologies, list some factors affecting transmission.

A

Type of exposure, viral load in blood, condom use, breaks in skin/exposure.

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17
Q

Risk of HIV (not usually high) guides the use of ____________. Living with HIV: ______ ___________ and quality of life are now excellent in the general population. The general life expectancy of the population is 77yrs, which is the same as if you were HIV positive and had early ___________, there was treatment ___________ and healthy living. Late detection leads to a worse ____________. If a region has a high prevalence, ___-_____ testing is suggested.

A
Prophylaxis 
Life expectancy
Detection
Adherence
Prognosis
Opt-out
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18
Q

What diagnostic tests can be used for HIV?

A

Blood tests/serology, PCR and ‘rapid’ tests.

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19
Q

Explain the blood test for HIV.

A

Blood tests - serology, for HIV antigen and Ab, current test detects both on same day (false negative if test too early - before 4 weeks).

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20
Q

Explain the PCR test for HIV.

A

PCR - detects HIV nucleic acid, highly sensitive, detects very early infection (up to 1 week), not used for initial testing, but follow up/treatment response.

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21
Q

Explain the ‘Rapid’ test for HIV.

A

‘Rapid’ tests - low cost and under an hour, may be done at home and posted, usually detects HIV Ab with finger prick/saliva - if negative, then accurate, but false positive needs conformation with serology.

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22
Q

How is it decided who is tested for HIV?

A

If the rate is over 2/1000, then it’s recommended that everyone be tested. Also, otherwise unexplained multi-infection presenting to the GP: repspiratory - bacterial pneumonia/TB, neurological - meningitis/dementia, dermatological - severe psoriasis/recurrent or multi-dermal shingles, gastrological - chronic diarrhoea/weight loss, haematological - any unexplained abnormality, oncology - lymphoma/anal cancer, gynaecology - CIN, any STI/Hep B/C.

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23
Q

What is the aim of HIV treatment?

A

To get an undetectable HIV viral load, reconstitute the CD4 count (immune system), reduce general inflammation and the risk of transmission. Get a good quality of life and normalise the life span.

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24
Q

Who gets treated for their HIV infection?

A

Until recently, only those with a CD4<350, or if there were other illnesses, but now everyone is treated ASAP.

25
Q

What is the treatment for HIV?

A

Anti-retro viral drugs (ARVs), which antagonise key enzymes to stop binding and fusion, reverse transcription and maturation.
3 ARVs are given - nucleoside reverse transcriptase inhibitor x 2 + non-nucleoside (NNRTI) OR protease inhibitor OR integrase inhibitor.

26
Q

Why are 3 ARVs given to treat HIV?

A

There are millions of rounds of viral replication a day and the virus mutates every 2-3 rounds. Using 3 ARVs, makes it harder for the virus to develop resistance. The patient must keep taking the drugs or it will develop within days.

27
Q

Which strategies are employed to treat and reduce HIV prevalence?

A

Increased condom usage, prevent mother-child transmission, ARV treatment as prevention, medical circumcision, post-exposure prophylaxis (PEP) and pre-exposure prophylaxis (PrEP), all in combination.

28
Q

What hope is there for future HIV treatment?

A

There may be future stem cell treatment from those who are naturally resistant; they have no increased viral load or decreased CD4 (cases where lack of treatment does not lead to AIDS).

29
Q

What are some ethical dilemmas involving the HIV infection?

A

Psychological impact of diagnosis, dealing with stigma, patient confidentiality vs her health, children, sexual partners, patients/staff at workplace.

30
Q

The risk of acquiring HIV from a needle stick injury involving a HIV positive person, is 1:_____, compared to 1:3 for Hep B and 1:30 for Hep C. In the U.K., HIV treatment is ______ to anyone, including those who come from abroad.

A

300 (lower if on ARVs/VL is undetectable)

Free

31
Q

5-8% of the global population have Hepatitis ___ (4 million in the U.K.) and 3% globally have Hepatitis ___ - unknown _____________ in the U.K., as most remain untested.

A

B
C
Prevalence

32
Q

What are Hepatitis are Hepatitis viruses?

A

Hepatitis means inflammation of the liver and although many system viruses can cause collateral liver damage (EBV, CMV, VZV), hepatitis viruses are hepatotrophic and so replicate specifically in hepatocytes, destroying them.

33
Q

What may untreated hepatitis B and C lead to?

A

Liver cirrhosis (10% hep B and 80% hep C) and hepatocellular carcinoma.

34
Q

The family of hepatitis viruses includes A, B, C, D and E; how are they all transmitted, what are their incubation periods and what is the eventual result of infection? (There’s a certain symmetry)

A

A: faecal oral, with an incubation of 2-6 weeks (from acquiring to having symptoms), not chronic.
B: blood/sex/vertical, 6wks-6months, leads to chronic illness.
C: blood (sex), 6-12wks, chronic infection.
D: blood/sex/vertical, 6wks-6months, chronic with hep B.
E: faeco-oral, 2-6wks, uncommonly chronic.

35
Q

What are the genomes and envelopes like for hepatitis viruses?

A

Hepatitis B has double stranded DNA and is enveloped.
The others are single stranded RNA.
Hepatitis C has a icosahedral envelope and Heps A, D and E are non-enveloped icosahedral.

36
Q

What is the typical presentation of someone with a hepatitis infection?

A

Abnormal LFTs, 2 weeks of fatigue, loss of appetite, abdominal pain, nausea, yellow tinge to the eyes, admits to unprotected sex and drug taking when recently away in Thailand.

37
Q

Why might someone with Hepatitis be jaundiced?

A

High bilirubin (breakdown molecule of haem), hence the jaundice - coagulation in the liver usually makes it soluble for urine/faeces, but it can be toxic to the brain if there’s too much built up.

38
Q

What are the different types of jaundice?

A

(Excessive) haemolytic/prehepatic, cholestatic - intrahepatic (including viral hepatitis) or extrahepatic.

39
Q

When considering viral hepatitis, what are tests for liver transaminases looking for?

A

Enzymes are raised if there is hepatocyte damage / loss of cellular integrity.
ALT/alanine transaminase and AST/asparate amino transferase.

40
Q

Aside from bilirubin and liver transaminase tests, when suspecting viral hepatitis, what other liver function tests may be performed?

A

ALP/alkaline phosphatase is raised if there’s biliary tract cell damage/cholestasis.
Albumin is a protein synthesised in the liver.
Tests for coagulation, as clotting factors are made in the liver - INR (international normalised ratio) and PT.

41
Q

Which set of results from liver function tests would suggest intrahepatic jaundice?

A

High bilirubin, very high ALT, slightly raised ALP and normal haemoglobin.

42
Q

How is hepatitis B transmitted?

A

75% of cases globally are vertically transmitted (perinatal from highly endemic areas), sexual contact, those who inject drugs, close household contacts (significant blood exposure), healthcare workers via a needle stick injury.

43
Q

What are the symptoms of an acute Hepatitis B infection?

A

Jaundice, fatigue, abdominal pain, anorexia/nausea/vomiting, arthralgia.

44
Q

The incubation period for a hep B infection is 6 weeks to ___ _________. _____/ALT will be in their 1000s. Up to ___% of infections will have no/vague symptoms. There will be a clear infection within 6 months. Less than 1% will go on to have fulminant __________ failure. Less than 10% of cases in infected adults become _________ - 90% if infected in __________.

A
6 months
AST
50
Hepatic
Chronic
Infancy
45
Q

Explain the Hepatitis B serology and PCR results over time.

A

First seen is the HbsAg - surface antigen, followed by the HbeAg - high infectious e antigen, then the core antibody IgM, which is the first to appear, followed by HbeAb - shows the disappear of the e antibody and infectivity, HbsAb is the last to appear, showing clearance of the virus/recovery. IgG is another core antibody - it persists for life.
PCR will show HBV DNA - find viral load.

46
Q

What constitutes a chronic hepatitis B infection and what can come as a result of it?

A

Persistence of HbsAg, surface antigen for over 6 months. 25% lead to cirrhosis (chronic inflammation) and 5% to hepatocellular carcinoma.

47
Q

What can be done to stop/treat Hepatitis B infection?

A

The is no cure, but an infection may be treated with antivirals to suppress replication (as with HIV), which are not required for everyone (e.g. ‘Inactive carrier’ with a low VL, normal LFTs and no liver damage).
Vaccination: genetically engineered HbsAg - 3 doses and boosters if required. Effective in most - produces Ab response > 10 is adequate and > 100 is long term protection.

48
Q

Transmission:
90% of those with Hepatitis C in the U.K., had transmission through _________, but many are ________________. Sexual contact makes up <1% of transmission, but this is higher if HIV _____________. Infants born to HCV positive mothers are

A
IVDU
Undiagnosed
Co-infected
5
Transfusions
Needle stick
49
Q

What are the symptoms of a Hepatitis C infection?

A

80% of those infected have no symptoms (acute/chronic) and 20% will have vague symptoms of: fatigue, anorexia, nausea, abdominal pain (RUQ).

50
Q

Disease progression:
After HCV transmission, 80% of people become _____________ infected - some develop ________/chronic liver disease, leading to decompensated liver disease, hepatocellular carcinoma, a transplant or ________.

A

Chronically
Cirrhosis
Death

51
Q

What does the Hepatitis C serology show and what else needs to be done, test wise?

A

The anti HepC antibody only, which remains positive for life, even after clearance/cure. It is not protective and reinfection is possible, so check VL with PCR (if the positive confirms current or chronic infection).

52
Q

Can Hepatitis C be treated or vaccinated against?

A

Hepatitis C can be cured with a directly acting antiviral drugs combination. There is no vaccine.

53
Q

PEP stands for post-exposure prophylaxis and may be used in an instance of a needle stick injury. What is the risk of transmission in this case for Hepatitises B and C?

A

Hep B is 1/3 (lower if the recipient is vaccinated) and Hep C is 1/30.

54
Q

What measure are taken after a needle stick injury?

A

Immediately: first aid (bleed and wash), collect blood from both involved, inform occupational health, check Hep B vaccination status, access risk and need for immediate HIV PEP. Early initiation of ARVs reduces dissemination and replication of HIV in tissue and bodily fluids, so give 3x ARVs for 28 days - start ASAP, as useless after 72 hours - HIV test at baseline (if they’ve already had it, a short course would be bad), after 1 and 3 months.

55
Q

Compare the presentation of an acute infection of HIV, Hep B and Hep C.

A

HIV- flu like symptoms/nil.
Hep B - jaundice, nausea, abdominal pain/anorexia.
Hep C- usually nil.

56
Q

Compare the prevention of HIV, Hep B and Hep C.

A

HIV- condoms, PEP.
Hep B - vaccination.
Hep C - risk avoidance only.

57
Q

Compare the outcome of untreated infection for HIV, Hep B and Hep C.

A

HIV- AIDS.
Hep B - minority will lead to chronic inflammation and cure for the majority.
Hep C - chronic inflammation (majority).

58
Q

Compare the treatment of HIV, Hep B and Hep C.

A

HIV - lifelong ARVs.
Hep B - nil/lifelong antiviral drugs.
Hep C - 8-12 weeks of antiviral drugs.