2011
DOI: 10.1007/s10156-010-0102-4
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Pharmacokinetic–pharmacodynamic study of itraconazole in patients with fungal infections in intensive care units

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Cited by 7 publications
(3 citation statements)
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“…More importantly, the dissemination was controlled much better by cross‐linked micelles, according to the histopathological analysis (Figure ). This result was in good agreement with the PK characteristics of cross‐linked or non‐cross‐linked micelles, owing to the antifungal effect of ITZ was dependent on its plasma concentration and AUC …”
Section: Resultssupporting
confidence: 84%
“…More importantly, the dissemination was controlled much better by cross‐linked micelles, according to the histopathological analysis (Figure ). This result was in good agreement with the PK characteristics of cross‐linked or non‐cross‐linked micelles, owing to the antifungal effect of ITZ was dependent on its plasma concentration and AUC …”
Section: Resultssupporting
confidence: 84%
“…The half-life of itraconazole is 24 hours, and the time to reach steady state for itraconazole and hydroxyitraconazole may take up to 1 to 2 weeks, delaying the time to early TDM intervention. Dose-dependent pharmacokinetics have been observed within the normal dosing range (100-400 mg/day) with significant intrapatient and interpatient variability recently reported within several patient cohorts [51][52][53].…”
Section: Itraconazolementioning
confidence: 96%
“…In a retrospective PK/PD analysis (10 patients receiving at least four doses), a total AUC 0-24 >30 mg h/L was associated with optimal antifungal efficacy [39]. However, in ca.…”
Section: Critically Ill Patients With Normal Renal Functionmentioning
confidence: 98%