HIV & AIDS Flashcards
progression of HIV to Aids
HIV destroy CD4+ -> hard for immune system to fight infection -> AIDS
who should be tested for HIV
1) IV drug user
2) unprotected sex w multiple partner
3) gay sex
4) person treated from STD
5) recipient of multiple blood transfusion
6) person who have been SAed
7) pregnant (prevent mother to child)
how to test for hIV
1) serum antibody detection
- HIV EIA test
2) HIV RNA detection/quantification
- PCR
stages of HIV infection
1) acute (primary) HIV infection
2) asymptomatic
3) persistent generalised lymphadenopathy
4) AIDs & related conditions
clinical presentation of acute HIV
- soon after contracting
- flu-like illness, swollen lymph nodes, fever, malaise, rash
- 2-3 wk
clinical presentation of persistent ggeneralised lymphadenopathy
persistent unexplained lymph nodes enlargement in neck, underarm, groin > 3 months
clinical presentation of AIDS
1) CD4 < 200/mm^3, presence of AIDS-defining disease
2) advanced stage succumb to infections
3) GLENS (GI, lung, eye, nervous system, skin)
4) systemic symptom
5) rare cancer, candidiasis
monitoring parameters for anti-retroviral therapy (ART) - CD4
- healthy: 500-1200 cells/mm^3
- baseline, every 3-6 month after initiation, every 12 month after adequate response (increase by 50-100 cells/mm^3 during first year)
- start prophylaxis for opportunistic infection when CD4 < certain number
monitoring parameter for ART - viral load
- before initiation
- within 2-4 wks after initiation/modification
- 4-8 wks until viral load suppressed
- 3-6 month after viral load suppression
- ideally suppression by 8-24 wks
types of ART combination
1) 2 NRTI + 1 INSTI
- tenofovir + emtricitabine + bictegravir
- tenofovir + emtricitabine + dolutegravir
- abacavir + lamivudine + dolutegravir
2) 1 NRTI + 1 INSTI
- newly started on ART
- emtricitabine + dolutegravir
- X for individuals who
** HIV RNA > 500k copies/mL
** Hep B virus coinfection
** ART started before genotypic testing/HBV testing results
nucleoside reverse transcriptase inhibitor (NRTI) - AE
1) lamivudine
- minimal tox
- N/V/D
2) emtricitabine
- minimal tox
- hyperpigmentation, N/D
3) tenofovir
- N/V/D
- renal impairment
- decrease in bone mineral density
4) abacavir
- N/V/D
- X use if high cardiovascular risk cuz of MI
- hypersensitivity in pt w HLA-B*5701
** rash, fever, malaise/fatigue, loss of appetite, sore throat, cough, SOB
** fatal: discontinue
advantages and disadvantages of NRTI
advantage: renal elimination
disadvantage
- mitochondrial toxicity
** lactic acidosis, hepatic steatosis
** lipoatrophy - require dose adjustment
advantages of non-nucleoside reverse transcriptase inhibitor (NNRTIs)
- long t1/2
- less metabolic tox (hyperlipidemia, insulin resistance)
disadvantages of non-nucleoside reverse transcriptase inhibitors (NNRTIs)
- potential CYP450 DI
- QTC prolongation
- skin rash, SJS (rilpivirine > efavirenz)
- efavirenz: neuropysch, increase LDL-C & TG, hepatotox
- riflvipirine: depression, headache
INSTI advantages
- bictegravir, dolutegravir good virologic effectiveness
- higher genetic barrier to resistance
- well tolerated