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chapter 33 Anti-CMV Agents 213<br />

Ganciclovir dose 5 50 kg 3 5 mg/kg 5 250 mg<br />

ganciclovir<br />

Valganciclovir dose 5 900 mg 3 0.60 bioavailability<br />

5 540 mg of active ganciclovir<br />

This patient would receive more than double<br />

the amount of active ganciclovir if 900 mg<br />

BID of valganciclovir were used. It thus may<br />

be worth considering dose reduction in underweight<br />

patients, particularly if they are at high<br />

risk of toxicity.<br />

• Foscarnet has significant nephrotoxicity. This<br />

can be somewhat attenuated through hydration<br />

with normal saline. Cidofovir is also<br />

nephrotoxic.<br />

• Even if a patient’s isolate of CMV is resistant<br />

to both ganciclovir and foscarnet, it may still be<br />

susceptible to the combination.<br />

What They’re Good For<br />

Ganciclovir and valganciclovir are first-line drugs<br />

for the treatment and prevention of CMV infections.<br />

Valganciclovir is often given to prevent CMV<br />

infection after transplant. Foscarnet is a secondline<br />

agent for CMV that can also be used for severe<br />

or resistant HSV infections. Cidofovir is a secondline<br />

agent for CMV.<br />

Don’t Forget!<br />

Although valganciclovir is oral, it is highly bioavailable<br />

and has adverse effects similar to those<br />

of ganciclovir. Valganciclovir use requires monitoring<br />

for toxicity that is just as rigorous as that for<br />

ganciclovir.

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