Please use the following request forms as appropriate for submitting isolates and clinical samples:
Y1 Mycology identification/susceptibility testing form (PDF, 312 KB) when referring isolates of yeast or mould for identification and/or susceptibility testing
Y2 Diagnostic mycology testing form (PDF, 320 KB) when referring clinical samples for diagnostic mycology testingAll samples should be securely packaged conforming to current postal regulations.
| Oral flucytosine | pre-dose and 2 hours post-dose |
| IV flucytosine | pre-dose and 30 mins. post-dose |
| Oral or IV itraconazole | pre-dose after 7 days |
| Oral posaconazole | pre-dose after 5 days |
| Oral voriconazole | pre-dose after 5 days |
| IV voriconazole | pre-dose after 5 days |
| Amphotericin | 1 – 2 hours post-dose |
| Oral fluconazole | 2 hours post-dose |
| IV fluconazole | 30 mins. post-dose |
Please ensure all high risk samples are clearly labelled.
FLUCYTOSINE
Serum samples should be taken just before a dose of flucytosine, and 2 hours after an oral dose or 30 min after an intravenous dose. The dose and interval should be adjusted in order to produce peak serum concentrations of about 70-90 mg/L and trough concentrations of 20-40 mg/L. Levels >100 mg/L are toxic.
ITRACONAZOLE
The trough level should be maintained above 0.5 mg/L.
Less than 0.5mg/L is a low concentration.
There may be toxicity issues at higher concentrations (>4 mg/L). Liver function tests should be monitored during prolonged courses.
POSACONAZOLE
The absorption and metabolism of posaconazole will vary from patient to patient and although there are no established recommendations, better therapeutic responses have been documented in patients with levels above 0.7 mg/L.
VORICONAZOLE
The absorption and metabolism of voriconazole will vary from patient to patient and although there are no established recommendations, better therapeutic responses have been documented in patients with levels above 1.3 mg/L.
Levels above 6.0 mg/L are more likely to lead to liver toxicity and levels above 10.0 mg/L should be avoided.
AMPHOTERICIN B
Monitoring of blood concentrations of amphotericin B during treatment is seldom indicated. The optimum serum concentrations of the drug for particular fungal infections have not been determined. Toxicity is assessed by monitoring renal function. Although amphotericin B is nephrotoxic, high blood concentrations do not lead to greater impairment of renal function, nor does renal failure result in higher blood concentrations.
Last reviewed: 11 January 2012