Blood Borne Viruses Flashcards

1
Q

What are our current treatment capabilities for HIV?

A

No cure but can supress the infection leading to just a chronic infection without any progression or disability.

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2
Q

What’s the difference between world wide and UK risk of catching HIV?

A

Globally young women are much more at risk of catching HIV

In the UK, there is still a tendency for higher risk in MSM.

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3
Q

Are IVDU at a high risk of catching HIV from needles?

A

IVDU (intravenous drug users) have quite a low risk of contracting HIV.

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4
Q

What results in the illness in patients with HIV

A

Generally, people who have HIV will acquire infections from opportunistic pathogens that wouldn’t normally be able to cause an infection such as: a fungal infection in the mouth from candida albicans causing white patches all over the buccal cavity, small red rashes may appear on the skin due to malignancies caused by Herpes virus and another common infection is TB.

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5
Q

Which microorganisms are you particualry at risk from when you have HIV?

A

Because HIV causes immunosuppression you are much more at risk of infections from yeasts, moulds and protozoal infections.

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6
Q

How do HIV viruses replicate?

A

Retrovirus RNA  DNA  RNA before transcription takes place
Infects and replicated in mostly in T immune cells – CD4.
HIV replicates inside the cell utilising its machinery and destroys the cell as all the new viruses leave, many more viruses the go on to infect more cells.

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7
Q

How does the HIV gain entrance to the CD4+ cells?

A

Enveloped proteins bind to the CD4 receptors (CCR5 and CXCR4). Once bound it spills all its contents into the cytoplasm of the lymphocyte where the retrovirus replication takes place. DNA integrates into the cell’s DNA. All this is replicated and then the virus buds out and kills the cell in the process.

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8
Q

What are some of the important proteins for HIV to be successful in its host?

A

Integrase (into the cell DNA) reverse transcriptase and Viral protease enzyme are some of the important enzymes present in the viral RNA.

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9
Q

How does a HIV infection progress from initial infection?

A

Initially the body’s immune system manages to recover but doesn’t manage to kill it completely. Over the next few years you have latent infection and slowly CD4 count decreases whilst the viral load increases. Some people never progress from this stage but that is very rare. When CD4 becomes too low you begin to get serious infections (less than 200) at this point you have AIDS.

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10
Q

What effect does the viral load have on the host in general?

A

Can just get a generalised wasting syndrome due to the viral load.

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11
Q

What are the names of the different stages to infection from HIV?

A

The first phase is called the acute infection or seroconversion, after this the next stage is latent infection, stage 3 is symptomatic infection and finally severe infection/AIDS.

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12
Q

How is HIV transmitted?

A

Sexual transmission – vaginal, anal or oral. Sharing of injecting equipment. Vertical transmission when giving birth or feeding.

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13
Q

What factors effect HIV transmission?

A

Type of exposure, viral level, other STIs, whether the person they’re in contact with is on medication for the HIV as the risk of transferring HIV becomes negligible, condom use and breaks in skin or mucosa.

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14
Q

What is the prognosis for someone who is diagnosed with a HIV infection in the UK?

A

General life expectancy in the UK is about 77 years. Only if early detection, treatment, adherence, health living such as smoking, alcohol drugs and exercise. Late detection means worse prognosis.

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15
Q

What tests can be done for HIV?

A

Blood tests – HIV antigen and HIV antibody – result can come on the same day, must be after 4-6 weeks of infection, may get a false negative result if done too early.

Rapid tests – low cost and less than an hour before result. Blood test, oral, saliva. In home tests and postal testing. If negative quite accurate. May get false positive results so need to confirm.

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16
Q

How does testing for HIV vary between different places?

A

In some areas because of the high prevelance of HIV it is important to test everyone that you can. Other than that it forms part of a standard STD tests, certain infections such as TB, meningeal infections, unexplained low blood cell counts etc.

17
Q

When should antiviral drugs be started?

A

The earlier you start the better the prognosis so as soon as you have a definite diagnosis or a strong suspicion.

18
Q

What should HIV treatment achieve?

A

HIV treatment should be used so that the virus is undetectable in the blood, allowing the immune system to reconstruct, have a good quality of life and allows a normalised lifespan. Some people will require counselling beforehand because it is a very high impact diagnosis.

19
Q

How do HIV drugs work?

A

How they work
Prevent attachment
Prevent integration
Prevent maturation

Always use 3 drugs together to prevent resistance.

20
Q

Briefly discuss Hep A, E and D

A

Hep A and E are self-limiting viruses that are not a long-term problem. Hep D usually occurs with Hep B but is relatively rare.

21
Q

How is Hepatitis transmitted between people?

A

Vertical transmission – mother to child.
IVDU
Sexual contact
Long term close household contacts
Health Care Worker via needle stick injuries - much higher rate of transmission that in HIV.

22
Q

How does acute Hep B infection present?

A

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

AST/ALT in 1000s
Up to 50% have no or vague symptoms

23
Q

What is the incubation period for Hep B

A

Incubation is 6 weeks – 6 months

24
Q

How does acute Hep B effect people differently in terms of outcome?

A

Majority of people clear infection after 6 months and then have long lasting immunity.
1% fulminant (severe and sudden in onset) hepatic failure
Becomes chronic in approx. 6-10% of infected adults (more if from infancy).

25
Q

Discuss the different antigens and antibodies you will see in the blood with Hep B?

A

3 main antigens and 3 main antibodies
HBsAg – HbsAb
HBeAg – HbeAb
HBcAg – HbcAb both IgM and IgG (only found in the liver not present in the blood)

IgM means probably acute phase of infection
IgG probably means chronic

26
Q

How do we test the viral load of Hep B?

A

HepB Virus DNA PCR

27
Q

What order do antibodies and antigens of Hep B appear

A

Surface antigen first followed by e-antigen which shows that the patient is highly infectious.
Core antibody IgM is the first antibody to appear
Followed by the e-antibody meaning no longer that infectious as e-antigen is disappearing
Surface antibody is the last antibody to appear and show clearance of the virus/recovery.
When core antibody IgG is present this shows immunity for life.

28
Q

What is a chronic Hep B infection?

A

Persistence of HBsAg after 6 months. 25% chronic infection leads to cirrhosis and 5% will develop hepatocellular carcinoma. (liver cancer.)

29
Q

How is chronic Hep B infection managed?

A

No cure for chronic infection but can take lifelong anti-viral to suppress viral replication.

Not required for everyone as some people can be inactive carriers. Low VL/normal LFTs/mild fibrosis

30
Q

What vaccinations are available for Hep B?

A

Genetically engineered surface antigen 3 doses + boosters if required, effective in most people produces surface antibody response >10 = adequate and > 100 = long term protection.

31
Q

How can people be infected with Hep C?

A

IVDU/Crack or heroin smokers
Blood transfusion prior to 1991 but as we test now
Infants born to HCV positive mothers (<5%)
Sexual contact (<1% but higher if HIV co-infected)
Needle stick injuries to HCW etc.

32
Q

How does Hep C progress?

A

Disease progression – 80% become chronically infected. Of these some will develop chronic liver disease – cirrhosis resulting in decompensated liver disease, hepatoma, transplant and death.

33
Q

What symptoms are there with Hep C infection?

A

80% have no symptoms, 20% have vague symptoms – fatigue, anorexia, dark urine, nausea and abdominal pain (Right upper quadrant).

34
Q

How is Hep C infection managed?

A

Can now be cured by a directly acting antiviral drug combo. 8-12 weeks >90% change of cure but are very expensive. Can get re-infected once rid of it as there is not lifelong immunity.

35
Q

Is there a vaccine for Hep C

A

No