#9 HIV CLinical case Flashcards

1
Q

Guidelines for monitoring AIDS

A

Screen any pts, aged 13-64 once at any healtcare setting
Any pregant person at initial visit and in the 3rd treimester
Annually if : IVDU, commercial sex, more then one sex partner since last HIV test

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2
Q

Statistics show: testing reduces transmission:

A

54% of infections are caused by 25% of people unaware they are infected vs… 75% are aware of infection and cause only 46% of transmission

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3
Q

What are the Benefits of Testing

A
  1. diagnosis allows indi to get antiretroviral tx = decreased mortality
  2. 32% of new HIV cases also diagnosed w/in 1 year
  3. missed opportuniteis is don’t test in clinic~~~ most HIV+ have had previous visits to clinic
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4
Q

Acute retroviral syndrome

______wks post infection see primary response to infection

A

2-6

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5
Q
  1. Symptoms seen in 80% for acute retroviral syndrome:
A

a. fever (80%)
b. Arthralgia/myalgia (54%)
c. anorexia/weight loss (54%)
d. rash and lympadenopathy
e. fatigue and malaise
f. pharygitis and oral ulcers

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6
Q

1% of ind tested for infectious mono were + for acute HIV!!! Not mono (did a test of blood samples)

A

when we did a blood test for mono

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7
Q

Comon symptoms of acute retroviral syndrome

A

anrthalgia/anorexia/rash

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8
Q

During acute retroviral syndrome we see: High levels of _______

A

viremia

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9
Q

During viremia of acute retroviral syndrome we see what in regard to viral load and infectious aspect?

A

widespread seeding of other lymph tissues w/ high viral lode and really infectious
22xs more infectious to others than in chronic HIV phase

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10
Q

What do we see happen to CD4 cells or HIV CD8-T cells?

A

Decreased CD4 cells circulating
HIV specific CD8-T cell reponse contains infection
~~during acute retroviral syndrome

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11
Q

The Antibody test shows up:

A

negative until 4-6 wks post infection

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12
Q

For the AntiB test we use ELISA, its affordable and fast and we can detect IgM in the blood from

A

(detect IgM for HIV from week 3 until 24 weeks)

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13
Q

If an ELISA comes back +… what do we do

A

follow up with Western Blot

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14
Q

Benefits of antigent test:

A

Antigen test: detect infection after 10-14 days but very expensive

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15
Q

What are we ‘looking for’ in the antigen test

the specific antiG and timeframe

A

looks for HIV viral load/RNA

p24 antigen detection (only detected week 2-4)

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16
Q

Whats a fast and cheap way to do HIV RNA testing?

A

Pooled HIV RNA testing: samples of 20-90 pts: cheaper and faster and increases yield of HIV testing by 10% compared to antiB testing alone

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17
Q

Resistance of HIV prior to tx:

A

d/t inhereted strain mutation from person you got it from

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18
Q

Goals of HIV tx

A

a. undetectable viral lode (less then 20 copies/uL)
Increase CD4T cells
eliminate HIV-related symptoms

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19
Q

HIV tx follow Tcell counts every ___ months

Current consensus: start tx if CD4 is below ______ cells/mm3 or you can offer tx at any CD4 level

A

3 months

500 cells/mm3

20
Q

Antiretroviral tx recommendation

A
  1. 3 meds and 2 classes of drugs
    1. Classes
      a. Nucleoside reverse transctiptase inhibitors (NRTIs)~~ most commonly chosen
      b. Nonnucleoside reverse transcriptase inhibitor (NNRTI)
      c. Protease inhibitor (PI)
      d. Integrase inhibitor or fusion inhibitor or CCR5 R antagonist
21
Q

Integrase inhibitor or fusion inhibitor or ______R antagonist

22
Q

Preferred guidelines: use 2 NRTI’s and then another based on

A

genetics of virus and pt response

23
Q

We didn’t see a decline in death age d/t HIV until we had

A

the 3 drug tx regimen in 1996

24
Q

Perinatal transmission

1. HIV infected pregnant woman: has \_\_\_\_\_chance she would infect her baby
2. Mom on AZT orally, IV during labor and the baby receiving it orally—\_\_\_\_\_ chance
25
Standard of care for pregnant women: HAART to mother –_______ + IV AZT at labor and AZT to baby X6 wks and formula feed~~~ see 0-1%
2nd trimester
26
HIV viral loads | Determines liki-hood of transmission:
as viral load increases, so does the likilhood of transmission: especially male to female
27
When people go off meds......
their viral loads increase as does their chance for transmitting the virus
28
Saw NO transmission when viral load is less then _______
1500
29
Test and tx strategy: 1. Universal HIV testing and immediate ARVs Expected results:
see 1/1000 in in 10 yrs with a prevalance of under 1% in under 50 yrs → goal is put on immediate HAART once HIV + → this would reduce 8 million deaths d/t AIDS
30
HIV exposure | Main modes Transmission
Needle sharing (67%), receptive anal sex, percutaneous needle stick, receptive penile vaginal intercourse, insertive anal intercourse, instertive penile-vaginal intercourse (6.5%), receptive oral an instertive oral
31
Largest cause of HIV transmission
needle sharing receptive anal sex percutaneous needle stick
32
rule of 3’s
Hep B = 30% Hep C = 3% HIV = .3% | for transmission per 1 exposure
33
Pecuratnous injury (needlestick or cut) OR contact of mucous membrane or non-intact skin WITH
a. blood and tissue (other potentially fluids---CSF, synovial, vaginal, pericardial, amnionic, semen or vag)
34
What will NOT cause transmission
NOT infectious for HIV unless bloody: feces, nasal secreations, urine, sweat, tears, vomit, saliva
35
factors associated with injury more likely to cause transmission:
deep injury, visible blood on device, intravascular devic,e terminally ill
36
ARBs for post-exposure prophylaxsis (PEP) | 1. started in health care settins d/t 400,000 needlesticks/yr
- -started in healthcare setting - -initiate 2-3 drug therapy within 72 hours - -saw that HIV seroconverters were 80% less likely to have taken PEP
37
Post-exposure prophy in non health-care related is applicable for:
for sexual exposure to HIV (nonoccupational, nPEP) | ~~feasible, especially dedicated prograoma and its timely ARVs and expensive
38
Pre-exposure prophylaxsis (PrEP):
1. an HIV uninfected ind uses antiretroviral meds ahead of HIV exposure 2. presence of HIV antiretrovirals in blood/tissue, makes difficult for HIV to establish infection
39
1. an HIV uninfected ind uses antiretroviral meds ahead of HIV exposure 2. presence of HIV antiretrovirals in blood/tissue, makes difficult for HIV to establish infection
use PrEP
40
Prescribing PrEP | a. Before:
assess sexual risk/ Screen for HIV and STIs
41
Inination or PrEP:
reinforce adherence, discuss additional risk reduction methods
42
On PrEP how do we monitor our patients
Every 3 months: HIV testing and STI testing and assess medication adherence every 6 moths: monitor kidney fnx and assess sexual risk
43
Every 3 months: | every 6 moths:
- HIV testing and STI testing and assess medication adherence - monitor kidney fnx and assess sexual risk
44
3 RCTs of PEP
a. iPrEx in men-men saw 44% protection with iPrEx b. Partners that PrEP in hetorsexual couples saw 75% HIV protection c. TDF2 in male and femal saw 56% HIV protection
45
Adherence and efficacy in PrEP trials
a. saw a clear dose response between evidence of PrEP use and efficacy b. higher the tenofovir levels, the lower the incidence of spread c. if you take tenofovir you see 90% reduction in transmission