HIV / AIDS Flashcards

1
Q

How is HIV transmitted?

A
  1. unprotected sex with infected person
  2. sharing infected needles with infected person
  3. mother to child during pregnancy, birth, and breastfeeding
  4. receiving contaminated blood / blood products
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2
Q

How is HIV diagnosed?

A
  • serum antibody detection
  • HIV RNA detection / quantification (viral load) - PCR
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3
Q

What are the goals of HIV treatment?

A
  1. decrease HIV-associated mortality
  2. restore and preserve immune functions
  3. increase duration and quality of survival
  4. prevent HIV transmission
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4
Q

What are the surrogate markers for HIV?

A

CD4+ cell count and HIV viral load

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5
Q

How is CD4+ cell count used?

A
  1. determine urgency to treat
  2. assess response to ART (at baseline, then 3-6m upon initiation and every 12m if stable; adequate response = CD4 increase by 50 -150 cells/mm3 in 1st year)
  3. assess need for initiating / discontinuing prophylaxis
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6
Q

How is HIV viral load used?

A
  • indicator of response to therapy
  • measure before initiation, 2-4w after, then every 4-8w until suppression, then every 3-6m after suppression
  • suppression usually takes 8-24w
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7
Q

What are the benefits of early ART initiation?

A
  • maintain higher CD4 count, prevent irreversible damage
  • decrease risk of HIV associated complications
  • decrease risk of opportunistic infections
  • decrease transmission risk
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8
Q

What are the limitations of early ART initiation?

A
  • side effects and toxicity
  • risk of drug resistance if incomplete suppression
  • transmission of drug resistant virus
  • less time for education
  • increased total time on medications, increased treatment fatigue
  • increased costs
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9
Q

What is the definition of AIDS?

A

CD4 < 200 cells / mm3 or opportunistic infections

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10
Q

What are the recommended ART combinations for ART naive HIV patients?

A

2 NRTI + 1 INSTI
- tenofovir + emtricitabine + bictagravir
- tenofovir + emtricitabine + dolutegravir
- abacavir + lamivudine + dolutegravir
1 NRTI + 1 INSTI
- emtricitabine + dolutegravir (only for HIV RNA < 500,000, no HBV coinfection, ART not started prior to genotypic resistance test / HBV test)

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11
Q

What are the available classes of drugs for HIV ART?

A

NRTI, NNRTI, PI, INSTI, fusion inhibitors, CCR5 antogonist

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12
Q

What are the NRTIs?

A

tenofovir, abacavir, emtricitabine, lamivudine, zidovudine

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13
Q

What are the adverse effects of NRTIs?

A
  • mitochondrial toxicity
  • N/V/D
  • tenofovir: renal impairment, decrease bone mineral density
  • abacavir: hypersensitivity, do not rechallenge
  • zidovudine: bone marrow suppression, myopathy
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14
Q

How to identify an INSTI?

A

-gravir

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15
Q

What are the drug-drug / drug-food interactions for INSTI?

A

reduced bioavailability with polyvalent cations
B, D, E are CYP3A4 substrates

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16
Q

What are the adverse effects of INSTIs?

A

weight gain, N/D, headache
B, D: increase SCr
R: pyretic, increase creatinine kinase

17
Q

What are the NNRTIs?

A

efavirenz, rilpivirine

18
Q

Which NNRTI cannot be administered with PPI?

A

rilpivirine

19
Q

How to identify a protease inhibitor?

A

-navir

20
Q

What is the fusion inhibitor?

A

enfuvirtide
(SC injection 2x a day, injection site reactions, and increase risk of bacterial pneumonia)

21
Q

What is a CCR5 antagonist?

A

maraviroc
(used only in pt whose strain of HIV uses CCR5)
is CPY3A4 substrate