Infectious Diseases - HIV + MRSA Flashcards

1
Q

Women commencing on cART in pregnancy, when should CD4 cell count be performed?

A

At initiation of cART and at delivery.

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2
Q

Women commencing on cART in pregnancy, when should a HIV viral load be preformed?

A
  • 2-4 weeks after commencing cART,
  • at least once in every trimester
  • 36 weeks
  • At delivery
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3
Q

Women commencing on cART in pregnancy, when should LFTs be checked?

A

At invitation of cART
At same time as viral load - each trimester, 36 weeks and delivery

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4
Q

If cART and viral load >50 HIV RNA copies/mL, what interventions are recommended?

A

Review adherence (including a full exploration of potential impacting factors) and concomitant medication

Perform resistance test if appropriate

Consider therapeutic drug monitoring (TDM)

Optimise to best regimen
Consider intensification.

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5
Q

Women on cART should continue in pregnancy the effective regime except in which cases?

A
  1. Non standard regimes for example on protease inhibitor (PI) mono therapy
  2. Regime’s that have lower pharomokinestics in pregnancy e.g. darunavir/cobicistat and elvitegravir/cobicistat or if absence of data e.g. altegravir 1200 mg once daily (od)
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6
Q

What impact can dolutegravir have on pregnancy? What can be done to minimise this risk?

A

Neural tube defect
Folic acid 5mg

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7
Q

All pregnant women with HIV should commence ART and continue lifelong treatment.

When should cART be commenced?

A

Depends on viral load

  1. <30,000 - as soon as able to in 2nd trimester
  2. 30,000-100,000 - Immediately 2nd trimester
  3. > 100,000 +/- CD4 < 200 - 1st trimster

All by 24 weeks

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8
Q

What cART should be started

A

Tenofovir DF or abacavir
with
emtricitabine or lamivudine
with
efavirenz or atazanavir / ritonavir,

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9
Q

If a women presents late in pregnancy >28 weeks with HIV, what should happen?

A

Commence cART without delay

If the viral load is unknown or over 100,000 HIV RNA copies/mL, a three- or four-drug regimen that includes raltegravir 400 mg bd or dolutegravir 50 mg od is suggested.

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10
Q

If a women presents in labour without HIV result, what should happen?

A

Urgent HIV test, if reactive/positive must be acted on to avoid vertical transmission of HIV.

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11
Q

If invasive testing required in pregnancy in HIV patient?

A

Should not be performed until viral load <50 RNA copies/mL (same with ECV)

If not on cART and testing required and cannot be delayed, commence cART raltegravir and nevirapine 2-4 hrs before procedure

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12
Q

How to decide on mode of delivery for patient with HIV?

A

Check plasma viral load at 36 weeks

  1. <50 - planned vaginal delivery
  2. 50-399 - consider pre-labour CS, consider vital load, trajectory, length of time of Tx, adherence issues, obstetric factors and woman views
  3. > 400 ELCS

If CS required for HIV 38-39weeks
VD with low viral load, no different but shorted time of SROM

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13
Q

How to manage SROM in HIV +ve woman?

A

If after >34 weeks deliver within 24hrs

Viral load < 50
- Immediate IOL, low threshold for Tx IP pyrexia

50-399 - consider CS
>400 CS

Give IV Ben Pen if 34-37 weeks

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14
Q

How to manage SROM in HIV women < 34weeks?

A

Im steroids
Optimise HIV viral load
MDT discussed re timing of delivery

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15
Q

When is IV zidovudine recommended?

A
  1. Viral load >1000, who present in labour/SROM or admitted for ELCS
  2. Untreated women where viral load is not known

Consider if viral load 50-1000 and in labour

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16
Q

For infant post exposure prophylaxis - how is very low risk defined and what is the management?

A

Very low risk - 2 weeks zidovudine monnotherpay

  • cART > 10 weeks
  • 2 x viral load < 50, 4 weeks apart
  • Viral load < at or after 36 weeks
17
Q

For infant post exposure prophylaxis - how is low risk defined and what is the management?

A

Low risk - 4 weeks zidovudine mono therapy

  • If very low risk not fulfilled but viral load <50 at or after 36 weeks
  • Preterm but most recent viral load < 50
18
Q

For infant post exposure prophylaxis - how is high risk defined and what is the management?

A

High risk, viral load no known or likely >50

Neonatal PEP within 4 hours

19
Q

If baby born preterm with mother with poorly controlled HIV, what additional medication can be given

A

In preterm labour, if the infant is unlikely to be able to absorb oral medications consider the addition of double-dose tenofovir to further load the baby

20
Q

Is breastfeeding advised? If mother does breatfeed how should vertical transmission be minimised?

A

Should not breastfeed (can give cabergoline to suppress lactation)

Maternal cART (rather than infant PrEP)

21
Q

In non-breast fed babies when should molecular diagnostics be performed fro HIV infection?

A
  1. 1st 48hrs & before discharge
  2. 6 weeks (or 2 weeks after stopping prophylaxis)
  3. 12 weeks (or 8 weeks after stopping prophylaxis)
  4. Other occasions if additional risk at at 2 weeks if high risk delivery
22
Q

When should antibody testing in neonate occur in non breast fed infants?

A

1st sample of blood if maternal antibody status not known
22-24 months

23
Q

In breast fed babies when should molecular diagnostics be performed fro HIV infection?

A
  1. 1st 48hrs and before discharge
  2. At 2 weeks
  3. Monthly throughout breastfeeding
  4. 4 & 8 weeks after stopping breast feeding
24
Q

When should antibody testing in neonate occur in breast fed infants?

A

1st sample of blood if maternal antibody status not known
22-24 months or 8 weeks after stopping breast feeding

25
Q

How should HIV +ve women be managed postpartum?

A

Continue cART
Review 4-6 weeks
Consider mental health referral
Contraception (may need to change ART)
Test partner and children

26
Q

What % of people admitted to hospital are colonised with MRSA?

A

1-5%

27
Q

How to eradicate colonisation MRSA

A

Intranasal or topical mupirocin ointment TDS 5 days
Skin/hair wash with chlorhexadine

28
Q

What main agents are used in the treatment of MRSA infections?

A

Vancomycin and teicoplanin

If resistant to those consider linezolid

29
Q

Why mos vancomycin be given by slow IV infusion?

A

Red man syndrome