We thank Dr. Procianoy and Dr. Silveira for their interest in our paper (1).
They suggested that our study probably underestimated the burden of candidemia in Brazil because of the study design (laboratory-based survey). They cited a study in which they reported that the rates of candidemia in their neonatal intensive care unit varied widely according to different standards of clinical suspicion (4). It is important to highlight that the mentioned papers are examples of different studies with different objectives and designs.
Surveillance studies of candidemia can be categorized into population-based and sentinel surveillance programs. Of note, both sentinel and population-based studies use a laboratory-based methodology for the identification of patients with candidemia, since an incident case of candidemia starts with the growth of Candida species from blood cultures. Laboratory-based sentinel surveillance studies may be criticized because they potentially miss data from patients with hematogenous candidiasis, from which positive blood cultures will never be obtained, thus underestimating the burden of disease. Nevertheless, their approach represents the most reliable and accurate methodology for conducting surveillance studies of candidemia (2). On the other hand, close monitoring of patients at risk, as in the study by Procianoy et al., is feasible only if performed with selected high-risk populations, such as premature neonates. It is hard to imagine such a strategy applied in a large hospital. Furthermore, as shown in our study, a substantial number of candidemic patients have coexisting exposures that are risk factors for candidemia, including prior colonization, the use of central venous catheters, the use of broad-spectrum antimicrobials, mucosal surface disruption, and neutropenia. While the exposure to multiple risk factors may occur in a large proportion of hospitalized patients, the vast majority will never develop candidemia. For example, in a study of 2,890 critically ill adults patients admitted to intensive care units of nine hospitals in the United States and Brazil, among 303 patients at high risk for candidemia identified by a prediction rule, only 9.9% developed invasive candidiasis (3). Invasive candidiasis presents a major challenge to clinicians, and the conductance of epidemiologic studies with different designs that may help to understand its epidemiology, risk factors, natural history, and predictors of outcome is very useful and welcome.
REFERENCES
-
1.Colombo, A. L., M. Nucci, B. J. Park, S. A. Nouér, B. Arthington-Skaggs, D. A. da Matta, D. Warnock, and J. Morgan for the Brazilian Network Candidemia Study. 2006. Epidemiology of candidemia in Brazil: a nationwide sentinel surveillance of candidemia in eleven medical centers. J. Clin. Microbiol. 44:2816-2823. [DOI] [PMC free article] [PubMed] [Google Scholar]
-
2.Morgan, J. 2005. Global trends in candidemia: review of reports from 1995-2005. Curr. Infect. Dis. Rep. 7:429-439. [DOI] [PubMed] [Google Scholar]
-
3.Ostrosky-Zeichner, L., C. Sable, J. Sobel, B. D. Alexander, G. Donowitz, V. Kan, C. A. Kauffman, D. Kett, R. A. Larsen, V. Morrison, M. Nucci, P. G. Pappas, M. E. Bradley, S. Major, L. Zimmer, D. Wallace, W. E. Dismukes, and J. H. Rex. 2007. Multicenter retrospective development and validation of a clinical prediction rule for nosocomial invasive candidiasis in the intensive care setting. Eur. J. Clin. Microbiol. Infect. Dis. 26:271-276. [DOI] [PubMed] [Google Scholar]
-
4.Procianoy, R. S., M. V. Enéas, and R. C. Silveira. 2006. Empiric guidelines for treatment of Candida infection in high-risk neonates. Eur. J. Pediatr. 165:422-423. [DOI] [PubMed] [Google Scholar]