Atovaquone Flashcards
Atovaquone
Activity against several important protozoans
Activity against malaria parasite enhanced when given with proguanil (Malarone)
Tends to be better tolerated than comparator drugs but limited by lack of IV form (for severe disease), high cost, and somewhat lower efficacy (for Pneumocystis)
Atovaquone MOA
Appears to interfere with electron transport in the parasitic mitochondria
Atovaquone Spectrum
Like a parasite but technically a fungus
P. jirovecii
Protozoa
Plasmodium species
T. gondii
Babesia species
Atovaquone Adverse Effects
Very well tolerated
Most common GI (N/V/D, abdominal pain)
Atovaquone Important Facts
Atovaquone available as suspension
Malarone as tablet
Bioavailability low for both, but enhanced substantially with food (especially high fat meals)
Both should be taken with food
Clinical trials in treating mild to moderate Pneumocystis pneumonia in patients intolerant of T/S- atovaquone slightly less effective than its comparators (dapsone or pentamidine) but better tolerated (leading to similar overall success rates); do not use in severe disease or in patients whose GI absorption is thought to be poor
Malarone favorable for malaria prophylaxis for travelers; but cost is high
Highly effective, well tolerated, active against chloroquine resistant Plasmodium, requires administration only 1-2 days prior to travel, while in malaria endemic area, and for 7 days after return
Many other agents require beginning 2 weeks before travel and continuing for 4 weeks afterward
Make sure to take with food (at very least a glass of milk)
Bioavailability increased approximately 5-fold
Atovaquone Good For
Atovaquone:
Treatment mild moderate Pneumocystis pneumonia
Prophylaxis against Pneumocystis in patients intolerant of 1st line therapy
Atovaquone/proguanil:
Treatment of uncomplicated malaria and prophylaxis against malaria