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Journal of Venomous Animals and Toxins including Tropical Diseases

On-line version ISSN 1678-9199

J. Venom. Anim. Toxins incl. Trop. Dis vol.18 no.2 Botucatu  2012

http://dx.doi.org/10.1590/S1678-91992012000200015 

ORIGINAL PAPER

 

Candidemia in a brazilian tertiary hospital: microbiological and clinical features over a six-year period

 

 

Mondelli ALI; Niéro-Melo LI; Bagagli EII; Camargo CHII; Bruder-Nascimento AII; Sugizaki MFII; Carneiro MVI; Villas Boas PJF I

IDepartment of Internal Medicine, Botucatu Medical School, São Paulo State University (UNESP - Univ Estadual Paulista), Botucatu, São Paulo State, Brazil
IIDepartment of Microbiology and Immunology, Botucatu Biosciences Institute, São Paulo State University (UNESP - Univ Estadual Paulista), Botucatu, São Paulo State, Brazil

Correspondence to

 

 


ABSTRACT

Yeasts are becoming a common cause of nosocomial fungal infections in immunocompromised patients. Such infections often develop into sepsis with high mortality rates. The aim of this study was to evaluate some of the numerous factors associated with the development of candidemia. Medical records were retrospectively analyzed of 98 Candida spp. patients. Results showed that the most prevalent risk factors for developing candidemia were: antibiotics and antifungal agents (93.9% and 79.6%, respectively); the use of central venous catheter (93.9%); mechanical ventilation (73.5%); and parenteral nutrition (60.2%). The main species of Candida found were: C. parapsilosis (37.76%), C. albicans (33.67%); and others (28.57%). C. glabrata showed the highest mortality rate (75%), followed by C. tropicalis (57.1%) and C. albicans (54.5%). The elevated mortality rate found in this study indicates that preventive measures against candidemia must be emphasized in hospitals.

Key words: candidemia, mortality, associated factors, Candida albicans.


 

 

INTRODUCTION

Several authors have reported a global increase in yeast infections over the past 20 years. Candida species can be found in the gastrointestinal tract of 20 to 80% of healthy adults, becoming pathogenic when host immune conditions are altered by offending factors (1). Of the invasive infections caused by Candida spp., blood infections, also known as candidemias, are the most clinically relevant (2). Candida spp. is currently one of the five main causes of blood infections in hospitals, and an increase in candidemia cases has been reported mainly in patients using antibiotics, under immunosuppressive therapy or parenteral nutrition, and in patients exposed to multiple invasive procedures (3, 4). Candidemia is one of the most common blood infections in tertiary hospitals; it has also been associated with long stay in hospitals and high mortality (5-8).

Although Candida albicans is the most frequent species isolated in patients with fungemia, cases of infections caused by other Candida species have increased (9-15). The frequency of C. albicans and other Candida species found in patients depends, among other factors, on the analyzed population and used therapy (16-19). The most commonly found species in Brazilian candidemia patients are C. albicans, Candida parapsilosis, and Candida tropicalis (20).

 

MATERIALS AND METHODS

We analyzed 98 yeast samples from different patients admitted to Botucatu Medical School University Hospital (HC-FMB) between 2000 and 2006 along with their medical records (obtained from the Statistical Medical Service - SAME, owned by HC-FMB). These patients developed symptoms of candidemia and samples were isolated from hemocultures (Bactec Aerobic, Peds or Myco/F BD - Becton Dickinson, USA) by the Microbiology Sector of the Clinical Analysis Laboratory. Samples included in the present study had records with all clinical data evaluated and legible; also, the yeast strain had to have been isolated between 2000 and 2006. Samples which did not meet the criteria were excluded, as were samples without records or with nonviable strains.

We analyzed the records and collected data on candidemia factors associated with development, including: gender; length of hospitalization; death and cause of death; use of antifungal agents; use of antibiotics; nosocomial infection; diabetes mellitus; liver disease; chronic bowel disease; neoplasia; kidney disease; neutropenia; immunosuppressive therapy; bowel surgery; central venous catheter; parenteral nutrition; positive HIV serology test; use of corticosteroids; prematurity; and mechanical ventilation.

Sample size was calculated using the Fisher and Belle formula, with a 95% confidence interval and 5% precision for expected prevalence of fungemia patients. Beck-Sagué and Jarvis (21) study was used as reference, which had 10.4% fungemia patients.

Samples employed in this study were stored in nutrient broth with crioprotective agent at -70ºC, in the Culture Collection of the Department of Microbiology and Immunology (Botucatu Biosciences Institute, UNESP). Yeast species were identified according to morphological and biochemical characteristics. Yeast samples were inoculated into plates with chromogenic growth medium Chromagar Candida (Difco, USA), for isolation and preliminary identification. Germ tube tests were then performed to assess filament and chlamydoconidia production and biochemical assays performed to check for carbohydrate production and assimilation. We used Vitek I (Durham, USA) for automated identification, which employs a plate with 40 different carbohydrate and amino acid tests, incubated at 35ºC for 24 to 48 hours.

Data were sorted into charts and frequency and association tables. Numeric variables were presented as mean and standard deviation, when variables presented symmetrical (normal) distribution, or median and percentiles, in cases of asymmetrical distribution. Categorical variables were expressed by number and rate of events and evaluated by the chi-squared test or Fisher's exact test (if n < 10). Normal distribution variables were evaluated by the Student's t test and non-normal variables by the Wilcoxon-Mann-Whitney test. ANOVA (analysis of variance) was used to compare the three groups. Results were considered significant if p < 0.05. The concordance test was used to analyze laboratory assays.

This study was approved by the Research Ethics Committee of Botucatu Medical School, UNESP, on October 2nd, 2006 (protocol number 490/2006).

 

RESULTS

Of the 98 evaluated candidemia cases, 33.67% were caused by C. albicans and 66.33% by other Candida species. C. parapsilosis had the highest percentage rate (37.7%). Only 12.2% of all samples were identified as Candida spp. due to technical difficulties in identification, even using different methods (Table 1).

When analyzing Candida species in relation to patient age, we can observe that other Candida species have a higher incidence in premature patients than C. albicans. Only 11.36% of patients aged less than one year presented candidemia caused by C. albicans, and C. parapsilosis was the most frequent cause of candidemia, affecting 56.8% of these patients (Table 2). Other Candida species were a little more frequent in younger patients whilst C. albicans infections prevailed in patients over 60 years (Figure 1).

Mortality rate in this study was 53.1% (Figure 2). Mortality distribution by species shows C. guilliermondii as the only species with less than 50% mortality rate; C. glabrata had the highest mortality rate (75%). However, both species had a small number of cases, compromising data analysis. C. albicans and C. parapsilosis had more adequate numbers of cases (54.2% and 58.4%) for analysis.

If age-specific mortality is analyzed, it is noticeable that the highest percentage of deaths was in patients aged more than 60 years (83.4%) (Table 3). Other age ranges did not present significant differences between the number of patients who died or lived.

Candidemia is one of the main causes of death provoked by infections in neonatal intensive care units (NICU), varying from 15 to 59%. Candida spp. is the third most common cause of late sepsis in NICU (22). In the present study we found a mortality rate of 50% in NICU patients (Table 3).

 

Factors Associated with Candidemia Development

Main factors

In the current study the most frequently factors associated with candidemia development were use of central venous catheter (93.9%); use of antibiotics (93.9%) and antifungal drugs (79.6%); mechanical ventilation (73.5%); and parenteral nutrition (60.2%) (Table 4). Transplant, HIV positive, and neutropenia were the factors least frequently associated with candidemia, which does not mean they were less significant, as there was no control group.

Candida albicans x other Candida species

In the present study, the main factors associated with candidemia caused by C. albicans were surgery, solid cancer, bowel disease, diabetes mellitus, immunosuppressant therapy, and higher age range. Other studies also showed that Candida infection is more frequent in adults (23, 24). The main factors associated with candidemia caused by other Candida species in the current work were age under one year, prematurity, use of antifungal drugs, and parenteral nutrition (Table 5). Such data are corroborated by other studies that indicate other Candida species as the leading causes of candidemia in patients born prematurely or under one year old (25).

Mortality-associated factors

Factors significantly connected with death (p < 0.05) were mechanical ventilation and solid cancer or chemotherapy; prevalence was higher among women. None of the other factors studied showed an association with patient mortality rate. As 70.8% of patients on mechanical ventilation died, it is suggested to avoid the use of mechanical ventilators or get patients off the ventilator at the earliest possible time (Table 6). Mechanical ventilation was also an important factor associated with candidemia development (Table 4)

Age-associated factors

Several factors associated with the development of candidemia were more common in some age ranges than others. In patients over 60 years of age, the most frequently associated factors were, once again, use of central venous catheter (100%) and antibiotics (88.9%) (Table 7).

In patients under one year old the most frequently associated factors were use of central venous catheter, parenteral nutrition, and use of antibiotics (Table 8). We found a 50% mortality rate in these patients, and prematurity alone can be considered an important associated factor.

 

DISCUSSION

An increase in invasive infections caused by Candida species other than C. albicans has been reported in recent years, which is corroborated by our findings (20, 26, 27). There are also significant geographical variations in the etiological pattern of invasive infections caused by Candida species other than C. albicans reported in different regions: in Latin America Candida tropicalis and Candida parapsilosis are more prevalent, whereas in the USA and many European countries the most frequent species is Candida glabrata (25, 28).

Candidemia caused by Candida species other than C. albicans is more common in children than adults; almost 60% of the affected patients were children. C. parapsilosis is also more common in children, mainly premature patients in NICU (29, 30). The present results agree with other studies that show C. parapsilosis as the most prevalent species in premature patients. This species provokes exogenous infections, since it colonizes the skin - especially the hands - of healthcare professionals, glycosylated solutions for hospital use, and central venous catheters, being associated with total parenteral nutrition (31).

The current study shows a different Candida spp. prevalence when compared to other research, even Brazilian studies. We observed that the incidence of C. parapsilosis (38%) was higher than other Candida species found, possibly due to the high number of studied patients under one year old and premature infants, in which C. parapsilosis frequency was over 50%.

Mortality rates in the present study are similar to those found by Colombo et al. (15). High mortality in patients over 60 years old could be explained by comorbidities found in this age range, such as kidney disease, bowel disease, diabetes mellitus, and solid cancer. Additionally, these patients had also been exposed to other predisposing factors for candidemia development, such as surgical procedures, mechanical ventilation, use of central venous catheter and antibiotics.

 

Factors Associated with Candidemia Development

Use of central venous catheter is one of the main factors associated with candidemia found in the present study (especially when combined with parenteral nutrition). Administration of multiple antibiotics for long periods is also an important variable. Both factors in addition to mechanical ventilation are also reported by Colombo et al. (15), who evaluated risk factors in four tertiary hospitals in São Paulo. In that same study, however, parenteral nutrition was only found in 30% of candidemia patients, while in our study it was found in 60.2%. This could be explained by the elevated number of premature and under one year old patients in our study, whereas Colombo only studied adults.

In Table 5, the greater incidence of Candida species other than C. albicans is evident, specifically in patients under one year old. It is important to notice that the risk factors associated with these patients - prematurity, parenteral nutrition and use of antifungal drugs - may explain the present findings. Infections by C. albicans are more frequent in adults, and the risk factors associated with them are: being older, surgery, solid tumors, bowel diseases, diabetes mellitus, and immunosuppressant therapy. Therefore, we must keep in mind the greater incidence of C. parapsilosis in patients under one year old and of C. albicans in adults.

Central venous catheter, antifungal treatment, and parenteral nutrition were the most frequent associated factors. However, they did not significantly affect patient mortality rate. Only the use of central venous catheter presented some significance, which could indicate the need for correct prophylactic measures concerning this condition. The same can be said about solid cancer, which presented statistical significance, requiring extra care. Higher mortality rates in women and elderly over 60 years can be explained by the comorbidities more frequently found in these patients, such as diabetes mellitus in women and impaired immune system in elderly patients.

Candidemia is a serious condition in the neonatal period, in which it is associated with high mortality rates, especially in very low birth weight newborns. Advances in intensive neonatal care have improved survival rates of newborns born under 1500 g or seriously ill, who are subjected to invasive procedures and thus at higher risk of nosocomial infections, including fungemia. Preventing hospital infection in this situation is challenging, since the immune system of these infants is immature and the skin barrier is ineffective and unprepared (32).

Based on present findings, it is suggested that invasive procedures such as use of central venous catheter, mechanical ventilation, and parenteral nutrition, as well as antibiotics and antifungal drugs should be administered with caution and removed as soon as clinical conditions allow (33). The use of antibiotics is also one of the factors which increases intestinal colonization by Candida species potentiating translocation. Therefore, they should be employed wisely as an effective candidemia preventive measure (33, 34).

 

CONCLUSION

The high mortality rate found in the current study allows us to conclude that preventive measures against candidemia must be emphasized in hospitals, mainly regarding the rational use of antibiotics and appropriateness of invasive therapeutic measures.

 

ACKNOWLEDGEMENTS

This work was supported by FAMESP; the Clinical Analysis Laboratory of Botucatu Medical School University Hospital; and the Department of Microbiology and Immunology of Botucatu Biosciences Institute, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.

 

REFERENCES

1. Garcia AL, Siqueira AM. Isolamento, identificação e sorotipagem de Candida albicans a partir de secreção vaginal. Rev Inst Med Trop São Paulo. 1988;30(4):270-3.         [ Links ]

2. Colombo AL, Guimarães T. Epidemiology of hematogenous infections due to Candida spp. Rev Soc Bras Med Trop. 2003;36(5):599-607.         [ Links ]

3. Nucci M, Colombo AL. Risk factors for breakthrough candidemia. Eur J Clin Microbiol Infect Dis. 2002;21(3):209-11.         [ Links ]

4. França JCB, Ribeiro CEL, Queiroz-Telles F. Candidemia em um hospital terciário brasileiro: incidência, frequência das diferentes espécies, fatores de risco e suscetibilidade aos antifúngicos. Rev Soc Bras Med Trop. 2008;41(1):23-8.         [ Links ]

5. Barberino MG, Silva N, Rebouças C, Barreiro K, Alcântara AP, Netto EM, et al. Evaluation of blood stream infections by Candida in three tertiary hospitals in Salvador, Brazil: a case-control study. Braz J Infect Dis. 2006;10(1):36-40.         [ Links ]

6. Edmond MB, Wallace SE, McClish DK, Pfaller MA, Jones RN, Wenzel RP. Nosocomial bloodstream infections in United States hospitals: a three-year analysis. Clin Infect Dis. 1999;29(2):239-44.         [ Links ]

7. Pittet D, Li N, Woolson R, Wenzel RP. Microbiological factors influencing the outcome of nosocomial bloodstream infections: a 6-year validated, populationbased model. Clin Infect Dis. 1997;24(6):1068-78.         [ Links ]

8. Wey SB, Mori M, Pfaller MA, Woolson RF, Wenzel RP. Hospital-acquired candidemia. The attributable mortality and excess length of stay. Arch Intern Med. 1988;148(12):2642-5.         [ Links ]

9. Pfaller MA, Jones RN, Doern GV, Sader HS, Hollis RJ, Messer SA. International surveillance of bloodstream infections due to candida species: frequency of occurrence and antifungal susceptibilities of isolates collected in 1997 in the United States, Canada, and South America for the SENTRY Program. J Clin Microbiol. 1998;36(7):1886-9.         [ Links ]

10. Pfaller MA, Jones RN, Messer SA, Edmond MB, Wenzel RP. National surveillance of nosocomial blood stream infection due to Candida albicans: frequency of occurrence and antifungal susceptibility in the SCOPE Program. Diagn Microbiol Infect Dis. 1998;31(1):327-32.         [ Links ]

11. Pfaller MA, Jones RN, Messer SA, Edmond MB, Wenzel RP. National surveillance of nosocomial blood stream infection due to species of candida other than Candida albicans: frequency of occurrence and antifungal susceptibility in the SCOPE Program. SCOPE Participant Group. Surveillance and control of pathogens of epidemiologic. Diagn Microbiol Infect Dis. 1998;30(2):121-9.         [ Links ]

12. Sandven P, Bevanger L, Digranes A, Gaustad P, Haukland HH, Steinbakk M, et al. Constant low rate of fungemia in norway, 1991 to 1996. J Clin Microbiol. 1998;36(12):3455-9.         [ Links ]

13. Krcméry V Jr, Kovacicová G. Longitudinal 10-year prospective survey of fungaemia in Slovak Republic: trends in etiology in 310 episodes. Diagn Microbiol Infect Dis. 2000;36(1):7-11.         [ Links ]

14. Lacaz CS, Porto E, Martins JEC, Heins-Vaccari EM, Takahashi de Melo N. Tratado de micologia médica. 9th ed. São Paulo: Sarvier; 2002. 1104 p.         [ Links ]

15. Colombo AL, Guimarães T, Silva LR, de Almeida Monfardini LP, Cunha AK, Rady P, et al. Prospective observational study of candidemia in São Paulo, Brazil: incidence rate, epidemiology, and predictors of mortality. Infect Control Hosp Epidemiol. 2007;28(5):570-6.         [ Links ]

16. Abi-Said D, Anaissie E, Uzun O, Raad I, Pinzcowski H, Vartivarian S. The epidemiology of hematogenous candidiasis caused by different Candida species. Clin Infect Dis. 1997;24(6):1122-8.         [ Links ]

17. Pfaller MA. Nosocomial candidiasis: emerging species, reservoirs, and modes of transmission. Clin Infect Dis. 1996;22(Suppl 2):S89-94.         [ Links ]

18. Nucci M, Colombo AL. Candidemia due to Candida tropicalis: clinical, epidemiologic, and microbiologic characteristics of 188 episodes occurring in tertiary care hospitals. Diagn Microbiol Infect Dis. 2007;58(1):77-82.         [ Links ]

19. Pfaller MA, Diekema DJ, Gibbs DL, Newell VA, Ng KP, Colombo A, et al. Geographic and temporal trends in isolation and antifungal susceptibility of Candida parapsilosis: a global assessment from the ARTEMIS DISK Antifungal Surveillance Program, 2001 to 2005. J Clin Microbiol. 2008;46(3):842-9.         [ Links ]

20. Colombo AL, Nucci M, Park BJ, Nouér SA, Arthington-Skaggs B, da Matta DA, et al. Epidemiology of candidemia in Brazil: a nationwide sentinel surveillance of candidemia in eleven medical centers. J Clin Microbiol. 2006;44(8):2816-23.         [ Links ]

21. Beck-Sagué C, Jarvis WR. Secular trends in the epidemiology of nosocomial fungal infections in the United States, 1980-1990. National Nosocomial Infections Surveillance System. J Infect Dis. 1993;167(5):1247-51.         [ Links ]

22. Rodriguez D, Almirante B, Park BJ, Cuenca-Estrella M, Planes AM, Sanchez F, et al. Candidemia in neonatal intensive care units: Barcelona, Spain. Pediatr Infect Dis J. 2006;25(3):224-9.         [ Links ]

23. Kao AS, Brandt ME, Pruitt WR, Conn LA, Perkins BA, Stephens DS, et al. The epidemiology of candidemia in two United States cities: results of a population-based active surveillance. Clin Infect Dis. 1999;29(5):1164-70.         [ Links ]

24. Almirante B, Rodríguez D, Park BJ, Cuenca-Estrella M, Planes AM, Almela M, et al. Epidemiology and predictors of mortality in cases of Candida bloodstream infection: results from population-based surveillance, Barcelona, Spain, from 2002 to 2003. J Clin Microbiol. 2005;43(4):1829-35.         [ Links ]

25. Matsumoto FE, Gandra RF, Ruiz LS, Auler ME, Marques SA, Pires MF, et al. Yeasts isolated from blood and catheter in children from a public hospital of São Paulo, Brazil. Mycopathologia. 2002;154(2):63-9.         [ Links ]

26. Morgan J. Global trends in candidemia: review of reports from 1995-2005. Curr Infect Dis Rep. 2005;7(6):429-39.         [ Links ]

27. Wisplinghoff H, Bischoff T, Tallent SM, Seifert H, Wenzel RP, Edmond MB. Nosocomial bloodstream infections in US hospitals: analysis of 24,179 cases from a prospective nationwide surveillance study. Clin Infect Dis. 2004;39(3):309-17.         [ Links ]

28. Colombo AL. Epidemiology and treatment of hematogenous candidiasis: a Brazilian perspective. Braz J Infect Dis. 2000;4(3):113-8.         [ Links ]

29. Wingard JR. Importance of Candida species other than C. albicans as pathogens in oncology patients. Clin Infect Dis. 1995;20(1):115-25.         [ Links ]

30. Colombo AL, Nakagawa Z, Valdetaro F, Branchini ML, Kussano EJ, Nucci M. Susceptibility profile of 200 bloodstream isolates of Candida spp. collected from Brazilian tertiary care hospitals. Med Mycol. 2003;41(3):235-9.         [ Links ]

31. Moreira ME. Controversies about the management of invasive fungal infections in very low birth weight infants. J Pediatr. 2005;81(1 Suppl):S52-8.         [ Links ]

32. Richtmann R, Takagi NB, Valciloto E, Kusano E, Marques MRM, Baltieri SR, et al. Candidemia em Unidade de Terapia Intensiva Neonatal: onde estamos? Rev Soc Paul Infectol. 2005;1(1):5-9.         [ Links ]

33. Wey S, Colombo A. Fungal infections of catheters. In: Seifert H, Jansen B, Farr BM, editors. New York: Catheter Related Infections; 1997. 139-56 p.         [ Links ]

34. Alexander JW, Boyce ST, Babcock GF, Gianotti L, Peck MD, Dunn DL, et al. The process of microbial translocation. Ann Surg. 1990;212(4):496-512.         [ Links ]

 

 

Correspondence to:
Alessandro Lia Mondelli
Departamento de Medicina Interna, Faculdade de Medicina de Botucatu, UNESP
Distrito de Rubião Júnior, s/n
18618-970, Botucatu, SP, Brazil
Tel: +55 14 3811 6213
Email: dralessandro@hotmail.com or alessandro@fmb.unesp.br

Received: January 20, 2012.
Accepted: March 5, 2012.
Abstract published online: March 6, 2012.
Full paper published online: May 31, 2012.
CONFLICTS OF INTEREST: The authors declare no conflicts of interest.
FINANCIAL SOURCE: The Medical and Hospital Development Foundation (FAMESP) of São Paulo State University (UNESP), Brazil, provided the financial grants.
ETHICS COMMITTEE APPROVAL: This study was approved by the Research Ethics Committee of Botucatu Medical School, UNESP, under protocol number 490/2006-CEP.

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