IADR Abstract Archives

Fluconazole Resistance Against Oral Candida in Patients Taking Antipsychotic Drugs

Objective: To determine the Candida species present and colonisation level of the oral mucosa in people taking antipsychotic drugs relative to healthy individuals and other xerostomic patients.  To investigate Candida resistance to fluconazole and antispsychotics, as the antipsychotic fluphenazine is known to induce fluphenazine resistance in Candida albicans.

Method: Consented participants aged between 20 to 70, who were on antipsychotic drugs were enrolled.  Xerostomia symptoms were determined from the Xerostomia Inventory (XI) and from clinical examinations.  Saliva rinses were collected and smears were taken from the buccal mucosae and tongue, and other suspicious mucosa.  Smears were examined for candida hyphae and yeast identification.  Saliva samples were plated onto Chromagar Candida agar plates, and incubated at 37°C for 48 hours. The colony-forming units (CFU) and species (from the colony colour) were recorded. The susceptibility of C. albicans isolates towards fluconazole was measured using the E-test according to the manufacturer's instructions

Result: Current findings showed that although 75% of participants had evidence of dry mouth clinically, they did not neccessarily have symptoms (only a third had high XI scores).  More than 60% were positive for oral candida hyphae and candida colonies.  Susceptibility testing is currently being undertaken.

Conclusion:   Many antipsychotic drugs are known to cause xerostomia and lead to increased incidence of candida infections.  Investigating the resistance of Candida isolates from patiensts taking antipsychotic medications to fluconazole may lead to more appropriate treatment.

Division: Australian/New Zealand Division Meeting
Meeting: 2014 Australian/New Zealand Division Meeting (Brisbane, Australia)
Location: Brisbane, Australia
Year: 2014
Final Presentation ID:
Abstract Category|Abstract Category(s): Scientific Groups
Authors
  • Mohamed Thani, Wan Syasliza  ( Sir John Walsh Research Institute, University of Otago, Dunedin, , New Zealand )
  • Macfadyen, Eithne  ( Sir John Walsh Research Institute, University of Otago, Dunedin, , New Zealand )
  • Rich, Alison  ( Sir John Walsh Research Institute, University of Otago, Dunedin, , New Zealand )
  • Cannon, Richard  ( Sir John Walsh Research Institute, University of Otago, Dunedin, , New Zealand )
  • SESSION INFORMATION
    Pharmacology/Therapeutics/Toxicology