Antiretrovirals (Only ARVs) Flashcards

1
Q

When should someone start ARV treatment?

A

As soon as they are diagnosed, except few cases(ART deferral)

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2
Q

Describe ART Deferral

there’s four reasons for ART deferral

A
  1. Drug-sensitive TB
    (CD4<50 cells per muL- initiate ART 2 weeks after TB treatment)
    (CD4>=50 cells- initiate ART 8 weeks after TB treatment)
  2. Cryptococcal Meningitis (defer ART until 4-6 weks of antifungal treatment is complete)
    1. TB meningitis (Defer ART until 4-8 weeks of TB treatment)
  3. Pneumocystis Jirovecci Pneumonia (Defer ART for 1-2 weeks after commencing treatment for the infenction)
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3
Q

ARV classes

1.Name all NRTIs
2. Describe MOA and Adverse Effects of NRTIs.

there’s 5 drugs that are NRTIs.

A
  1. (Z-LATE) Zidovudine, Lamivudine, Abacavir, Tenofovir, Emtricitabine.
  2. MOA- Competrd with Nucleoside Triphosphate

Adverse Effects- Nucleoside Analogues(Nausea, headach, lactic acidosis…) and Nucleotide Analogues(Nephrotoxicity, Fanconi syndrome and Bone Mineralization disorder)

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4
Q

ARV classes

1.List all NNRTIs
2.Describe the MOA and Side Effects of NNRTIs.

A
  1. (RENE)- Rilpvirine, Efavirenz, Nevarapine and Etravirine.
  2. MOA- Inhibit the HIV reverse transcriptase
    A/E-
    (EFV)Abnormal dreams, Psychosis(lost contact with reality), Gynaecomastia, Maculopapular rash.
    (NVP)-Rash and Hepatitis
    (FTR)-Rash and Triglyceridaemia (presence of too many glycerides(fats) in bloodstream, Increasing risk of heart disease and atherosclerosis)
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5
Q

ARV classes

Describe side effects of each drug under Protein Inhibitors.

There are 4 drugs under PIs.

(LADS) for PIs

A
  1. Lopinavir (Hyperglycemia, Diarrhea, Dyslipidemia, Atherosclerosis)
  2. Atazanavir (Used if Lopinavir is not well tolerated, A/E: Jaundice and Abdominal Pain)
  3. Darunavir( A/E: Abdominal Pain, Fatigue, Headache)
  4. Saquinavir (A/E: Prolonged QT and PR intervals–Alters heart rhythm)

all these drugs are taken with RITONAVIR

[lads] for PIs

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6
Q

ARV classes

Name all 3 drugs under Integrase Inhibitors.
[Focus on Dolutegravir and Raltegravir] Describe their DI, A/E

A

[Carbotegravir, Dolutegravir, Raltegravir]
1.Dolutegravir
DI- Rifampicin
A/E- well tolerated though (Headache, Nausea, Fatigue, Myopathy and Rhabdomyolysis)

rhbdomyolysis occurs when damaged muscle tissue releases its proteins

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7
Q

NRTIs Pharmacokinetics

Name CI, DI and AE of Abacavir

A

CI- hypersensitivity and sever liver impairment
DI- Nothing significant
AE- Fatal Hypersensitivity, Hepatitis

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8
Q

NRTIs

Describe CI, DI and AE for Lamivudine

A

CI- Anemia and Neutropenia(abnormal low count of WBCs)
DI- Nothing significant
AE- Peripheral Neuropathy, Pancreatitis.

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9
Q

NRTIs

Describe CI, DI and AE for Emtricitabine

A

CI- Renal Failure
DI- Nothing significant
AE- Headache, Diarrhoea, Rash

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10
Q

NRTIs

Describe CI, DI and AE for Tenofovir

A

CI- Renal Failure
DI- Increases levels of ddl
AE- Nephrotoxicity

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11
Q

NRTIs

Describe CI, AE and DI for Zidovudine

A

CI- Anaemia and Neutropenia
DI-
AE- Anemia and Myelosuppression

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12
Q

NNRIs

Describe CI, DI and AE for Efavirenz

A

CI- Severe Liver disease
DI-
AE- CNS effects(its a psychoactive drug), Gynecomastia

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13
Q

NNRTIs

Describe CI, DI and AE Nevirapine

A

CI- Caution in liver insufficiency
DI- Oral Contraceptives reducued efficacy and with Rifampicin
AE- Rash and Hepatitis

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14
Q

Antiretroviral Regimens

Pre-Exposure Prophylaxis (PrEP)
which drugs(ARVs) does it have?

A

2 NRTIs
(Tenofovir/Emtricitabine) or (Tenofovir/Emtricitabine)

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15
Q

Antiretroviral Regimen

Which ARVs do PEP have and when must they be given?

A

Must be given to HIV negative patients 72 hours(at latest) after possible exposure to HIV.

3ARV

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16
Q

PMTCT

Categorise the infant risk based on mother’s viral load results.

don’t confuse viral load with CD4 count,

A

VL<1000c/ml=low risk
VL>1000c/ml=high risk
No VL results is interpreted as high risk

17
Q

How is HIV treated?

Describe what drug classes Highly Active Antiretroviral Therapy entails, and describe the drugs in the first and seocnd line regimens.

A

HAART= 2NRTIs+1NNRTI or 1InSTI

First Line Regimens
Tenofovir(TDF)+ Emtricitabine(FTC)+Lamivudine(3TC)+Efacirenz(EFV)
or replace EFV with DTG
or use ABC+3TC(when there is renal imparement)

Second Line Regimens
(NRTI combinations)
Zidovudine(AZT)+ 3TC OR Tenofovir(TDF)+ Emtricitabine(FTC)

18
Q

PEP Drugs

What drugs does HIV PEP have?

A

TDF+3TC+DTG

OR

AZT instead of DTG