2009
DOI: 10.1111/j.1469-0691.2009.02988.x
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Voriconazole-associated zygomycosis: a significant consequence of evolving antifungal prophylaxis and immunosuppression practices?

Abstract: Mucormycosis (zygomycosis) is an uncommon infection that afflicts severely immunocompromised patients and those with poorly controlled diabetes mellitus. A recent increase in the incidence of mucormycosis at many transplant centres has been linked to the introduction and widespread use of voriconazole prophylaxis in these high-risk populations. However, it is not known if this association reflects a true epidemiological link or represents a marker of changing immunosuppression occurring in parallel with the ev… Show more

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Cited by 112 publications
(86 citation statements)
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References 29 publications
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“…In experimental models, preexposure of Mucormycetes to voriconazole selectively enhanced their virulence in fly and murine infection models (179). Voriconazole-associated mucormycosis appears to have a poor outcome, perhaps reflecting the advanced immunosuppressive state of infected patients along with delayed diagnosis of the infection (264).…”
Section: Clinical Presentationmentioning
confidence: 99%
“…In experimental models, preexposure of Mucormycetes to voriconazole selectively enhanced their virulence in fly and murine infection models (179). Voriconazole-associated mucormycosis appears to have a poor outcome, perhaps reflecting the advanced immunosuppressive state of infected patients along with delayed diagnosis of the infection (264).…”
Section: Clinical Presentationmentioning
confidence: 99%
“…As with any antimicrobial class of drugs, widespread and prolonged use of triazoles may lead to the emergence of drug-resistant organisms [14]. Several reports have linked voriconazole use to a rising incidence of zygomycosis [15,16]. Moreover, unlike with fluconazole, many clinicians routinely obtain serum levels of these azoles in order to ensure efficacy and minimize toxicity.…”
Section: Chemoprophylaxismentioning
confidence: 99%
“…However, in most patients with hematologic diseases there is the potential for pharmacokinetic drug-drug interactions given that voriconazole is metabolized through the cytochrome P450 system [Pongas et al 2009]. For example, interactions between liver-metabolized chemotherapy agents (e.g.…”
Section: Monitoring Voriconazole Plasma Levelsmentioning
confidence: 99%