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chapter 29 Azoles 191<br />

■■<br />

Important Facts<br />

• Voriconazole is active against many fluconazoleresistant<br />

strains of Candida albicans, but it<br />

is less active against them than fluconazolesusceptible<br />

strains. An echinocandin is a better<br />

choice, but consider susceptibility testing if you<br />

need to use voriconazole for an oral option.<br />

• Voriconazole is a potent inhibitor and a substrate<br />

of the cytochrome P450 system. The list<br />

of drugs that interact with voriconazole is long<br />

and varied. Some of them are contraindicated,<br />

such as rifampin, while others, such as calcineurin<br />

inhibitors (e.g., cyclosporine), require<br />

dose adjustments. This is significant because<br />

many of the patients who require voriconazole<br />

are immunosuppressed.<br />

• The IV form of voriconazole contains a cyclodextrin<br />

vehicle that accumulates in renal<br />

dysfunction and may be nephrotoxic. It is contraindicated<br />

with a creatinine clearance of less<br />

than 50 ml/min. The oral formulations avoid<br />

this issue.<br />

• Voriconazole is eliminated hepatically and<br />

is unlikely to be useful in the treatment of<br />

candiduria.<br />

What It’s Good For<br />

Voriconazole is the drug of choice for invasive<br />

aspergillosis and is frequently used in the treatment<br />

of infections caused by other molds. It can be<br />

used for candidiasis as well, but fluconazole and<br />

echinocandins are more frequently used for these<br />

infections. Some clinicians use voriconazole in the<br />

empiric treatment of febrile neutropenia.

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