Antifungal Susceptibility of Bloodstream Candida Isolates in Pediatric Patients

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ISSN: 2319-7706 Volume 4 Number 3 (2015) pp. 716-720 http://www.ijcmas.com Original Research Article Antifungal Susceptibility of Bloodstream Candida Isolates in Pediatric Patients Deepak Kumar 1, Sayan Bhattacharyya 1*, Prashant Gupta 1, Gopa Banerjee 1, Mala Kumar 2 and Mastan Singh 1 1 Department of Microbiology, King George s Medical University (U.P.) Lucknow-226003, India 2 Department of Pediatrics, King George s Medical University (U.P.) Lucknow-226003, India *Corresponding author A B S T R A C T K e y w o r d s Candidemia, Candida spp., antifungal susceptibility Candidemia causes considerable attributable mortality and morbidity in children. However, data about susceptibility of Candida spp. isolated from pediatric blood samples are scant, and empirical therapy is often erroneously based on susceptibility pattern in adults. Hence we studied the species distribution and antifungal susceptibility of pediatric bloodstream Candida spp. isolates. Candida non-albicans were predominantly found to cause candidemia in our study. Introduction The incidence of bloodstream Candida infection, in adults and pediatric patients, has risen in the last decade (1, 2, 3, 4, 5, 6). Currently, Candida spp. have become the fourth most frequent causal microorganisms of nosocomial sepsis following infection due to coagulase-negative staphylococci, Staphylococcus aureus, and Enterococcus species (3, 6). Furthermore, monitoring programs have detected an increase in the prevalence of infections caused by non- Candida albicans (essentially Candida parapsilosis, Candida glabrata, and Candida krusei) and other yeast genera (7, 8, 9). Unfortunately, data about antifungal susceptibility pattern in pediatric patients with candidemia are scarce, and empirical treatment in children with suspicion of invasive Candidiasis frequently has to be instituted by extrapolating information from adult patients. The need to update the mycological profiles in pediatric patients with candidemia was one of the aims of this study. Materials and methods Study design: The study was a hospitalbased prospective observational study. The study population consisted of 150 patients from ICU s of Gandhi Memorial and Associated Hospitals Lucknow, with risk factors for invasive fungal infection. Period of study: The study was carried out over a 13-month period, from August 2011 to July 2012. 716

Case definitions: An episode of candidemia was defined as the isolation of a Candida species from blood culture in a patient with temporally related clinical signs and symptoms. Neonates were defined as those <1 month of age, infants were defined as those 1 to 12 months of age, and children were defined as those 1 to 15 years old. Sample processing: The biphasic Brain Heart Infusion (BHI, Oxoid )fungal blood culture bottle inoculated with blood sample was incubated at 37 0 C aerobically and subcultured on 2 nd and 7 th days on Sabouraud s dextrose agar (SDA) media (Emmon s modification), ph 7.0 with chloramphenicol to look for fungal isolation. Identification of organisms and antifungal susceptibility study Candida isolated from blood cultures were identified according to standard microbiological procedures (10).Speciation of Candida isolates were carried out by using germ tube test, cornmeal agar with Tween 20, carbohydrate assimilation and fermentation tests(10). Candida albicans was defined to be positive for germ tube production and terminal chlamydospore and pseudohyphae formation by Dalmau technique. Candia tropicalis produced no chlamydospores while glabrata showed no pseudohyphae using Dalmau technique.(10). Antifungal susceptibility testing was performed, by the Broth microdilution method in RPMI 1640 medium. The MICs of four antifungal agents: amphotericin B, fluconazole, voriconazole, and caspofungin were analysed. Breakpoints applied were as per the Clinical and Laboratory Standards Institute (CLSI) (11). Since no breakpoints have been published for amphotericin B, isolates inhibited by >1 mg/liter, were considered resistant to the drug. Result and Discussion A total of 44 episodes of candidemia in 44 patients <15 years of age were identified during the study period. tropicalis (55.9%), albicans (14.7%), glabrata (11.8%), kefyr (8.8 %), Candida lusitaniae (5.9 %), guilliermondii (2.9%), were the predominant species causing candidemia during the study period, in order of frequency of isolation. No mixed infection was found during the entire study period. The etiological agents of candidemia varied according to age, gender, or patients' location in the hospital (Table 1) Most episodes of candidemia occurred in males (65.9%) and patients less than 1 month old (77.3%), and more cases of candidemia occurred among those hospitalized in neonatal ICUs (NICUs) (75.0%) than in general wards (18.2%) or Pediatrics intensive care units (PICUs) (6.8%). (Table 1) Antifungal susceptibility pattern of blood stream Candida isolates by BMD method In vitro susceptibility testing of the 44 BSI of Candida species against amphotericin B, fluconazole, caspofungin, and voriconazole is shown in table 2. Overall, the rate of resistance was 4% for amphotericin B and 17% for fluconazole. glabrata was the species most resistant to antifungals; all 5 isolates were found resistant to fluconazole, while 2 isolates were resistant to amphotericin B. The percentages of isolates of Candida spp. in general in each category (S or susceptible, SDD or susceptible, dose dependent, and R or resistant) were 67%, 0%, and 17% and 100%, 0%, and 0% for fluconazole and voriconazole, respectively according to the breakpoints recommended by CLSI. For 717

amphotericin B and caspofungin, applying the breakpoints of previous studies the percentages of isolates of Candida spp. in each category (S, I, and R) were 57%, 39%, and 4% and 100%, 0%, and 0% respectively. Studies on susceptibility pattern of Candida spp. causing bloodstream infections are more often to be found from adult populations. Thus, pediatricians often have to rely on data from these studies when applying treatment. To our knowledge, this is one of the unique prospective series of candidemia reported in pediatric patients, having a total of 44 patients from a tertiary hospital of North India. Data were collected for a period of 12 months and incorporated with results of in- vitro susceptibility to four systemic antifungal agents. As in case of adults, candidemia was found to occur more frequently in males (60.6%) ( 12, 13,14). Among pediatric patients, candidemia was found to be more frequent in neonates (35.4%) and children over 1 year of age. As in other studies, a higher proportion (75.0%) of candidemia episodes occur in patients admitted to Neonatal Intensive Care Units (NICU) (15,16). Overall, the predominant fungal pathogen implicated in bloodstream infection in our study was tropicalis which caused 55.9% of episodes. In the present study, Non-albicans Candida species accounted for 81.8% of cases of neonatal candidemia, whereas albicans was responsible for only 18.2% of cases. This corroborates well with the results of other authors.[17,18,19,20]. Ther is one study from north India which mentions that tropicalis was most common in cases of candidemia(21). In their case also, candidemia was more prevalent in meales than females. In another report from Uttarakhand, India, it is mentioned that parapsilosis was the commonest Candida species associated with bloodstream infection.(22). Patients characteristic Table.1 Characteristics of Candidemia episodes and distribution of isolate No. (%) of episodes Total tropicalis albicans 718 glabrata kefyr lusitaniae Age <1 month 34(77.3) 19(55.9) 5(14.7) 4(11.8) 3(8.8) 2(5.9) 1(2.9) 1-12 month 0 0 0 0 0 0 0 1-18 years 10(22.7) 6(60.0) 3(30.0) 1(10.0) 0 0 0 Gender Male 29(65.9) 18(62.1) 5(17.2) 4(13.8) 0 2(6.9) 0 Female 15(34.1) 7(46.6) 3(20.0) 1(6.7) 3(20.0) 0 1(6.7) Location at the time of IFI NICU 33(75.0) 18(54.5) 5(15.2) 4(12.1) 3(9.1) 2(6.1) 1(308) PICU 3(6.8) 3(100) 0 0 0 0 0 Ward 8(18.2) 4(22.2) 3(37.5) 1(12.5) 0 0 0 TOTAL 44 25(56.8) 8(18.2) 5(11.4) 3(6.8) 2(4.5) 1(2.3) guilliermondii

Table.2 Categorical result of Antifungal Susceptibility Testing of 44 blood stream Candida isolates by BMD Method Isolate No AMB FLC CAS VRC S I R S SDD R S I R S SDD R C.tropicalis 25 14 11 0 25 0 0 25 0 0 25 0 0 albicans 8 6 2 0 8 0 0 8 0 0 8 0 0 glabrata 5 0 3 2 0 0 5 5 0 0 5 0 0 kefyr 3 3 0 0 3 0 0 3 0 0 3 0 0 lusitaniae 2 1 1 0 2 0 0 2 0 0 2 0 0 guilliermondii 1 1 0 0 1 0 0 1 0 0 1 0 0 Total (%) 44 25(57) 17 2 39 44 44 0 5(17) 0 0 (39) (4) (67) (100) (100) 0 0 References 1. Neofytos D., et al.2010. Epidemiology and outcome of invasive fungal infections in solid organ transplant recipients. Transpl. Infect. Dis. 12:220 229. 2. Neofytos D., et al.2009. Epidemiology and outcome of invasive fungal infection in adult hematopoietic stem cell transplant recipients: analysis of Multicenter Prospective Antifungal Therapy (PATH) Alliance registry. Clin. Infect. Dis. 48:265 273. 3. Pfaller M. A., Diekema D. J.2007. Epidemiology of invasive candidiasis: a persistent public health problem. Clin. Microbiol. Rev. 20:133 163. 4. Pfaller M. A., Diekema D. J.2010. Epidemiology of invasive mycoses in North America. Crit. Rev. Microbiol. 36:1 53. 5. Tortorano A. M.,et al.2004. Epidemiology of candidaemia in Europe: results of a 28-month European Confederation of Medical Mycology (ECMM) hospital-based surveillance study. Eur. J. Clin. Microbiol. Infect. Dis. 23:317 322. 6. Wisplinghoff H., et al.2004. Nosocomial bloodstream infections in US hospitals: analysis of 24,179 cases from a prospective nationwide surveillance study. Clin. Infect. Dis. 39:309 317. 7. Almirante B.,et al.2006. Epidemiology, risk factors, and prognosis of Candida parapsilosis bloodstream infections: case-control populationbased surveillance study of patients in Barcelona, Spain, from 2002 to 2003. J. Clin. Microbiol. 44:1681 1685. 8. Hachem R., Hanna H., Kontoyiannis D., Jiang Y., Raad I.2008. The changing epidemiology of invasive candidiasis: Candida glabrata and Candida krusei as the leading causes of candidemia in hematologic malignancy. Cancer 112:2493 2499. 9. Pfaller M. A., et al.2008. 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. 46:842 849 10. Raju SB, Rajappa S. Isolation and Identification of Candida from the Oral CavityInternational Scholarly Research Network(ISRN) Dentistry 2011, Article ID 487921, 1-7. 719

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