Τόμος 18 (2004) – Τεύχος 1 – Άρθρο 37 – Επιθεώρηση Κλινικής Φαρμακολογίας και Φαρμακοκινητικής-Διεθνής Έκδοση – Volume 18 (2004) – Issue 1 – Article 37 – Epitheorese Klinikes Farmakologias και Farmakokinetikes-International Edition

Title In vitro susceptibility of oral candida species to antifungal agents in renal transplant recipients
Author M. Belazi1, A. Velegraki2, Th. Koussidou-Eremondi3, D. Andreadis1, F. Solonaki4, S. Hini2 and D. Antoniades1

1Dept.of Oral Medicine/Maxillofacial Pathology, School of Dentistry, Aristotle University of Thessaloniki, Greece.

2Mycology Reference Laboratory (KEEL), Dept, of Microbiology, School of Medicine, University of Athens, Greece.

3State Hospital of Skin and venereal Diseases, Mycology Laboratory, Thessaloniki, Greece.

4Dept.of Solid Organ Transplantation, Hippokration Hospital of Thessaloniki, Greece

Citation Belazi, M., Velegraki, A., Koussidou-Eremondi, T., Andreadis, D., Solonaki, F., et al.: In vitro susceptibility of oral candida species to antifungal agents in renal transplant recipients, Epitheorese Klin. Farmakol. Farmakokinet. 18(1): 94-97 (2004)
Publication Date Accepted for publication: 2004
Full Text Language English
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Keywords Oral Candida Species, Antifungal Agents, renal transplant patients
Other Terms review article
Summary Fungal infections are considered as a factor implicated in morbidity and mortality of immunocompromising, renal transplant recipients. Although, systemic antifungal prophylaxis is given, resistant strains of Candida and non-Candida species have been isolated. The aim of the present study was to determine the fluconazole, itraconazole, voriconazole, and amphotericin B susceptibility profiles of Candida species isolated from the oral cavity of renal transplant patients. Methods: 124 renal transplant recipients (RTRs) (56 females and 68 males, mean age 46+6 years with a range of 24 to 61 years) and 78 healthy control (HC) subjects, age-and sex-matched were examined. Isolation and presumptive identification followed by a definitive identification of Candida species using an API 32 ID system. All species were also screened by indirect immunofluorescence (IFA) and furthermore PCR test for differentiation between C. albicans and C. dubliniensis isolates was also performed. Susceptibility testing of oral Candida species to antifungal agents (Itraconazole, fluconazole, voriconazole and amphotericin B) included of both Broth microdilution method (BMD) and Quality control (QC). Results: 38 (31%) of the patients had positive cultures with confluent yeast growth. Cultures of clinical material from six patients revealed multiple Candida species in the lesions. C. krusei and C. glabrata fluconazole MIC90 were found increased (range 16->64 pg/ml), whereas no elevated amphotericin B, itraconazole and voriconazole MICs were recorded for the other Candida and Saccharomyces species. Conclusions: MIC testing is indicated for immunocompromised patients at high risk for colonization and infection of Candida species with primary resistance to fluezole, such as C. krusei or C. glabrata, Furthermore, screening mucosal isolates for phenotypic traits such as susceptibility to antifungals, allows the identification of resistant Candida species subpopulations selected during prophylactic or empirical therapy in cases of renal transplant recipients.
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