HIV Flashcards

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1
Q

What are the four stages of untreated HIV infection?

A
  • Flu-like
  • Feeling fine
  • Falling count
  • Final crisis
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3
Q

What do ring-enhancing lesions on a head CT in HIV suggest? What do the other images show?

A
  • Head - Toxoplasma gondii (parasite from cat faeces)
  • Lungs - reticulonodular shadowing - pneumocystic pneumonia
  • Retinal -

HIV also causes hairy leukoplakia - cannot be scraped off unlike candidiasis

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4
Q

Which herpes virus causes Kaposi’s sarcoma?

A

HHV8

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5
Q

What is the mode of transmission of HIV?

A

The virus is transmitted via blood, sexual fluids, and breast milk

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7
Q

Define HIV.

A

HIV is a retrovirus which infects and replicates in human lymphocytes (CD4 +ve T cells) and macrophages

This leads to immune system dysfunction, opportunistic infection, and malignancy = AIDS (acquired immunodeficiency syndrome)

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9
Q

What are the subtypes of HIV?

A

Virus subtypes include HIV1 (global epidemic) and HIV2 (↓ pathogenic, predominantly West Africa).

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10
Q

How common is HIV? What prevalence in UK? What % is unaware of their infection?

A
  • ~37 million affected worldwide; 1.2 million deaths/yr.
  • Africa has most of the disease and mortality
  • UK has ~100 000 living with HIV (~1/500)
  • 5% of MSM
  • ~17% in UK are unaware
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11
Q

What is the pathophysiology of HIV?

A
  • HIV binds via GP120 envelope glycoprotein to CD4 receptors on T helper cells, monocytes, and macrophages
  • CD4 cells migrate to lymphoid tissue when the virus replicates, producing millions of new virons
  • These are released and in turn infect new CD4 cells
  • As infection progresses, depletion or impaired function of CD4 cells leads to low immune function
  • HIV is a retrovirus - encodes reverse transcriptase, allowing DNA copies to be produced from viral RNA. This is error prone –> significant mutation rate –> treatment resistance
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12
Q

How does HIV present?

A

Primary HIV infection

  • Symptomatic in 80% - 2-4 weeks after infection - seroconversion illness, acute retroviral syndrome
  • Flu-like illness and erythematous/maculopapular rash, fever, myalgia, pharyngitis, mucosal ulceration, headache/aseptic meningitis
  • Persistent generalised lymphadenopathy (>1cm in two or more non-contiguous sites but not inguinal for >3 months)

Latent phase - asymptomatic - in latent phase of chronic HIV infection

Late - complications of immune system dysfunction/malignancy

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13
Q

What are the available tests for HIV?

A
  1. ELISA for HIV antibody and antigen testing - 4th generation assay test; this reduces “window period” to average ~10days.
  2. Rapid point-of-care testing -immunoassay kit which gives a rapid result from a finger prick or mouth swab. Only CE-marked kits should be used. Needs serological confirmation.
  3. Viral load - quantifies HIV RNA. Monitors response to ART. But not diagnostic due to possibility of false positive result. Confirmation of seroconversion is still required in symptomatic primary HIV.
  4. Nucleic acid testing/viral PCR - tests HIV RNA levels- high in early infection when antibodies might be negative. Used to test vertical transmission.
  5. CD4 count - not for diagnosis. Monitors immune system function and disease progression. <200cells/microlitre is the defining criteria for AIDS.
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14
Q

Which HIV test is used for testing vertical transmission?

A

Nucleic acid testing/viral PCR - used to test vertical transmission in neonates as placental transfer of maternal antibodies can affect ELISA antibody testing up to 18months of age.

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15
Q

What can be detected first: antigen or antibody?

A

Usually antigen

Antibody takes time to make

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16
Q

Why is diagnosis of primary HIV a unique opportunity to prevent transmission?

A

There is increased viral load and genital shedding - even though HIV antibody testing may be negative, HIV RNA levels are high

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17
Q

What defines AIDS?

A

CD4 count <200cells/microlitre

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18
Q

What are the three categories of main HIV complications?

A

Complications:

  1. complications of immune dysfunction (opportunistic infection/malignancy)
  2. complicating comorbidity
  3. complications of treatment i.e. adverse drug events
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19
Q

List 5 different opportunistic diseases associated with HIV.

A

<500

  • Tuberculosis
  • Candidiasis - oral/oesophageal
  • Kaposi’s sarcoma- tumour defining AIDS and HIV (HHV8)

<200

  • Pneumocystis jirovecii →perihilar infiltrates on CXR
  • Lymphoma - non-Hodgkin’s

<100

  • Cryptococcus neoformans - systemic fungal infection; molluscum like papules
  • Cryptosporidium - chronic diarrhoea in pre-ART HIV
  • PML

<50

  • CMV - causes retinitis, GI ulceration with “owl’s eye” inclusions on biopsy
  • MAC
  • Toxoplasma gondii - intracranial abscesses especially in AIDS
20
Q

Summarise the treatment of HIV.

A

Anti-Retroviral Treatment (ART) - recommended to everyone with HIV regardless of CD4 count

Aims - to reduce viral load to an undetectable level

Consists of two nucleoside reverse transcriptase inhibitors (NRTI e.g. tenofovir and emtricitabine) plus one of

  • ritonavir-boosted protease inhibitor - atazanavir
  • non-nucleoside reverse transcriptase inhibitor- (NNRTI e.g. efavirenz)
  • integrase inhibitor - raltegravir
21
Q

What are the methods of prevention of HIV infection? (4)

A

Sexual transmission - use of condoms reduce transmission by 90%; even if both parters are HIV positive this does not protect from treatment resistance, other STIs, hepatitis so serosortic is unreliable.

PEP - post-exposure prophylaxis - short term ART used after potential HIV exposure; can be given up to 72hrs after exposure. First line in UK is Truvada (tenofovir/emtricitabine) and raltegravir for 28 days. Test after 8-12 weeks.

PrEP - pre-exposure prophylaxis - in those at high risk e.g. serodifferent relationships, condomless anal sex in MSM

Vertical transmission - all pregnant women with HIV should have commenced ART by 24 weeks gestation. Caesarean indicated if >50copies/mL viral load. Neonatal PEP given from birth to 4 weeks with formula feeding.

22
Q

What is the first line PEP regimen? (BASH)

A

Truvada (tenofovir/emtricitabine) and raltegravir for 28 days. Test after 8-12 weeks.

In order of drugs by mechanism: NRTI/NRTI + II (TDF/FTC + RAL)

23
Q

How effective is PEP for HIV prevention?

A

Reduces likelihood of HIV conversion by approximately 80%

Should be initiated within 2 hours and preferably within 24hours

Most efficacious if taken in first 72hrs

24
Q

What is PrEP? What are the indications?

A

Pre-exposure prophylaxis:

  • MSM
  • HIV partner
  • IV drug user
  • high risk e.g. sex worker
25
Q

What is the first line PrEP regimen?(BASH)

A

Daily oral tenofovir/emtricitabine (Truvada)

26
Q

What is the preferred HIV regimen?

A

2 NRTI + 3rd drug (NNRTI/boosted PI/integrase)

  • e.g. truvada + bictegravir
  • OR abacavir + lamivudine + dolutegravir

Quadruple therapy is no more effective than triple therapy.

Sometimes now a two drug regimen of dolutegravir and lamivudine is recommended.

27
Q

What drug classes for HIV are currently in use?

A

NRTI- nucleoside reverse transcriptase inhibitors

NNRTI - non-nucleoside reverse tanscriptase inhibitors

Boosted PI - protease inhibitors

INSTI/II - integrase strand transfer inhibitors

Boosters require lower doses of the drug to be required.

28
Q

Give examples of each class of HIV drugs in use currently.

A

NRTI - “T**h**en** S_it_ _Bac_k **Lady!” - HIV treatment backbone is usually either:

  • Ten**ofovir + Emtri**citabine
  • OR A_bac_avir + _L_amivudine

NNRTI - “vir”

  • Efavirenz
  • Rilpivirine

Boosted protease inhibitors - “navir”

Darunavir

Atazanavir

Ritonavir

Integrase inhibitors

  • Dolutegravir
  • Raltegravir

Truvada = tenofovir + emtricitabine

Atripla = tenofovir + emtricitabine + efavirenz

29
Q

What are the complications of HIV treatment?

A
30
Q

What kind of investigations are recommended for monitoring in HIV?

A

CD4 - every 3-6m initially then after 2yrs every year.

HIV viral load - 2-8weeks after ART changes/start, until <200copies/mL then every 3-6m

Resistance testing - only in treatment failure

Other:

  • FBC, LFTs, U&Es - every 2-8weeks initially then 6monthly
  • HBV/HCV - yearly
  • Urinalysis - yearly
  • Fasting glucose - yearly
  • Lipids - yearly
31
Q

What are the adverse effects of ART?

A

Short term:

  • Nausea
  • Fatigue
  • Insomnia
  • Rash
  • Diarrhoea
  • Headache

Long term:

  • High cholesterol (TDF)
  • Renal damage (TDF)
  • Bone damage (TFD) - osteoporosis, osteopenia
  • Hepatic damage (NNRTI)
32
Q

What are the complications of HIV?

A
  • Acute seroconversion - 50% of those with flu-like symptoms after initial infection will develop HIV
  • Rapid progressors - some may develop AIDS in 1-2yrs
  • AIDS
  • Hypotestosteronism (70%)
  • CVD - cardiomyopathy, myositis, CCF
  • VTE
  • Cancer - Kaposi’s, NHL, cervical
  • Liver disease - usually due to hepatitis co-infection
  • Neurocognitive dysfunction - depression, cognitive and memory difficulties
  • Diabetes
  • Lung disease
  • Hearing impairment - unknown aetiology
  • Opportunistic infections
  • Immune suppression pre-AIDS
33
Q

What is the prognosis with HIV?

A

Untreated - many regulate viral replication for many years; may progress through the stages consecutively or move to a stage skipping one

Undetectable levels on ART - most achieve this in 3-6months

Poor adherence to ART may cause resistance

For patients aged 20 who started ART in 2008-10 have an estimated life expectancy of 63-67yrs

10% of deaths due to cancer

2 cases of remission - Berlin patient after SCT which had CCR5 mutation, and another NHL patient with similar transplant.

34
Q

Apart from medical treatment and monitoring what else is important in management of HIV?

A
  • Counselling and lifestyle advice
  • Prophylaxis, screening and vaccinations against infections
  • Micronutrient supplementation
  • Screening for co-morbidities