Fungal infections are a leading cause of mortality in patients with neutrop
enia. Candidiasis and aspergillosis account for most invasive fungal infect
ions.
General prophylactic measures include strict hygiene and environmental meas
ures. Haemopoietic growth factors shorten the duration of neutropenia and t
hus may reduce the incidence of fungal infections. Fluconazole is appropria
te for antifungal prophylaxis and should be offered to patients with prolon
ged neutropenia, such as high-risk patients with leukaemia undergoing remis
sion induction or consolidation therapy and high-risk stem cell transplant
recipients.
Empirical antifungal therapy is mandatory in patients with persistent febri
le neutropenia who fail to respond to broad-spectrum antibacterials. Intrav
enous amphotericin B at a daily dose of 0.6 to 1 mg/kg is preferred wheneve
r aspergillosis cannot be ruled out. Lipid formulations of amphotericin B h
ave demonstrated similar efficacy and are much better tolerated.
Fluconazole is the best choice for acute candidiasis in stable patients; am
photericin B should be used in patients with unstable disease. Use of fluco
nazole is restricted by the existence of resistant strains (Candida krusei
and, to a lesser extent, C. glabrata).
Amphotericin B still remains the gold standard for invasive aspergillosis.
Lipid formulations of amphotericin B are effective in aspergillosis and bec
ause they are less nephrotoxic are indicated in patients with poor renal fu
nction. Itraconazole is an alternative in patients who have good intestinal
function and are able to eat.
Mucormycosis, trichosporonosis, fusariosis and cryptococcosis are less comm
on but require specific management.
New antifungal agents, especially new azoles, are under development. Their
broad in vitro spectrum and preliminary clinical results are premising.