PEPSE Flashcards

1
Q

Once HIV crosses mucosal barrier, how long until it is detectable in lymph nodes?

A

48-72 hours

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2
Q

What benefit is the initiation of antiretroviral therapy following exposure to HIV?

A

Reduces dissemination and replication of virus in all tissues

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3
Q

What factors may result in PEP failure? (5)

A
Delayed initiation
Transmission of resistant virus
Variable genital tract drug penetration
Poor/non-adherence
Further high-risk sexual exposure
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4
Q

PEP completion rates are historically low, what are they?

A

42-82%

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5
Q

What factors increase the risk of HIV transmission? (6)

A
High plasma HIV viral load
Breaches in mucosal barrier - trauma or ulceration
Menstruation
STI (co infection)
Ejaculation
Non-circumcision
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6
Q

When should PEP be considered?

A

Transmission risk > 1 in 1000 - GIVE

Transmission risk 1 in 1000 - 1 in 10 000 - CONSIDER

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7
Q

If the source is HIV positive, when is PEP NOT recommended?

A

source on ART, >6 months, undetectable (VL <200)

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8
Q

When might PEP be considered if oral sex is the exposure type?

A

Primary HIV infection

Oropharyngeal trauma/ulceration

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9
Q

Once blood as dried, when does HIV become non-viable?

A

couple of hours

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10
Q

What is the HIV prevalence in female sex workers in Western, Central and Eastern Europe?

A

Western <1%
Central 1-2%
Eastern 2-8%

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11
Q

What is the IV prevalence in male sex workers?

A

14%

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12
Q

When should PEP be initiated?

A

As soon as possible
Preferably < 24 hours
Up to 72 hours

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13
Q

What is the recommended duration of PEP?

A

28 days

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14
Q

What is the recommended PEP of choice

A

Truvada and raltegravir

Recommend triple agent regimen

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15
Q

Truvada is the recommended NRTI back bone of PEP, why?

A

good genital tract and rectal tissue penetration
peak levels within 24h of dosing
maintaining high levels for up to seven days

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16
Q

Why not abacavir for PEP?

A

8% experience hypersensitivity reaction

17
Q

What is an reasonable alternative to raltegravir, if required, for PEP?

A

Dolutegravir, no PEP data though

18
Q

What is an alternative PEP regimen?

A

Combivir (zidovudine + lamivudine) with Protease inhibitor (lopinavir, darunavir, atazanavir with ritonavir) or Dolutegravir

19
Q

If a person has chronic hepatitis B what NRTI is preferred as PEP?

20
Q

Why is NNRTI PEP ie nevirapine not recommended?

A

10% experience grade 3 or 4 hepatotoxicity

21
Q

What are the limitations for PIs as PEP?

A

Frequent side effects

Risk of drug-drug interaction

22
Q

When should STI testing be performed in the setting of PEP?

A

At baseline

2 weeks after risk

23
Q

For people who get PEP, When should HIV testing take place?

A

8-12 weeks following exposure

24
Q

What other tests should be done at baseline before PEP?

A

HIV, Hep B surface antigen. creatinine, ALT, urinalysis, pregnancy test

25
What are the risks to pregnancy if HIV acquired during it?
High viraemia associated with primary infection results in high likelihood of INTRAUTERINE TRANSMISSION
26
Is pregnancy a contraindication to PEP?
No, but woman should be counselled that ARVs are unlicensed in pregnancy
27
If a further high risk sexual exposure occurs near the end of PEP course, what advice should be given?
extend PEP for further 48 hours after last exposure
28
If a person keeps re-attending for PEP, what should be considered/offer?
Review of safer sex strategies PREP (if available) Consider involvementof psychology
29
If a person is on PEP prior to a HIV positive result, what should be done?
Continue PEP Refer to HIV specialist Consider ongoing ART to avoid viral rebound and increased transmission risk
30
What follow up of the potential source should take place?
Attempt to establish their HIV risk and status, if establish contact could stop PEP early if drug resistance PEP should be altered
31
What hepatitis B vaccination schedule should be used for people presenting for PEP and non-immune to HBV?
Ultra-rapid hep B vaccination course
32
For women who present for PEP, what additional test should be performed?
pregnancy test