Invasive and disseminated Candida infections have become a major sourc
e of morbidity and mortality in the modern surgical intensive care uni
t. The most common risks for invasion and dissemination are the use of
antibiotics, central venous lines, total parenteral nutrition, burns,
immunosuppression, and other markers for severity of illness (APACHE
> 10, ventilatory use for > 48 hours). Data suggest that colonization
can be a late predictor of invasive disease in today's critically ill
surgical patient and that prophylaxis or early treatment in high risk
patients is warranted, particularly before invasive/disseminated disea
se becomes life-threatening. When advanced disease is present, the dia
gnosis of invasive or disseminated Candida infection is often prompted
by clinical suspicion and supported by consistent clinical data; labo
ratory tests alone lack sufficient sensitivity and specificity to dire
ct therapeutic decision-making. Once the diagnosis of invasive or diss
eminated Candida infection is ascertained, early systemic treatment, a
long with treatment of localized infection, is as fundamental as dth a
ny other serious infectious disease. Reported toxicity and efficacy su
pports the use of fluconazole for most patients with invasive/dissemin
ated Candida infections. For the most critically ill surgical patient
amphotericin B remains the treatment of choice. Prophylaxis and early
treatment strategies with minimally toxic agents may diminish the need
to use more toxic therapy in the most severely ill patients.