Table 2.
IFI parameters | N | % |
---|---|---|
IFI profile during induction | ||
Possible | 16/46 | 32.6 |
Probable | 4/46 | 8.6 |
Proven | Zero | Zero |
IFI site | 20/46 | 43.4 |
Pulmonary (HRCT chest) | 19 | 41.3 |
PNS (CT PNS) | 1 | 2.1 |
Total no. of GM done during the induction phase | 20/46 | 43.4 |
Positive | 4 | 20 |
Serum | 3 | 15 |
BAL | 1 | 5 |
Negative | 16 | 80 |
Day of onset of IFI | ||
Median (range) | 13(4–24) | |
IFI on different antifungal prophylaxis | ||
Posaconazole (n = 41) | 19 | 46.3 |
Amphotericin-B (n = 4) | 1 | 25 |
Voriconazole (n = 1) | Zero | Zero |
IFI treatment and outcome | ||
IFI treatment (possible + probable) | 20 | 43.4 |
Empirical antifungal treatment | 10 | 21.7 |
Drugs used to treat fungal infection (n = 30) | ||
Monotherapy | 22 | 73.3 |
Voriconazole | 4 | 18.1 |
Amphotericin-B | 14 | 63.6 |
Caspofungin | 4 | 18.1 |
Double antifungal therapy | 8 | 26.6 |
Duration of antifungal treatment (in days) | ||
Median (range) | 12.5 (6–84) | |
Outcome of fungal infection (n = 20) | ||
Resolved | 12 | 60 |
Not resolved | 4 | 20 |
Death | 4 | 20 |
IFI invasive fungal infection, HRCT high resolution computed tomography, PNS para-nasal sinus, GM galactomannan, BAL broncho-alveolar lavage