Literature DB >> 19563489

Susceptibility profile of vaginal isolates of Candida albicans prior to and following fluconazole introduction - impact of two decades.

C C Bulik1, J D Sobel, M D Nailor.   

Abstract

Current treatment options for vulvovaginal candidiasis due to Candida albicans include over-the-counter and prescription antifungal agents. Fluconazole has been used extensively with an unknown impact on susceptibility. To investigate antifungal susceptibility trends in clinical vaginal isolates of C. albicans from 1986 to 2008, microdilution susceptibility was performed on randomly selected single isolates. Minimum inhibitory concentrations (MICs) were determined for: fluconazole, clotrimazole, miconazole, ketoconazole, itraconazole, voriconazole, flucytosine and amphotericin B. The MIC(90) for each drug was then calculated for the time periods: 1986-1989, 1992-1996 and 2005-2007. A total of 250 C. albicans vaginal isolates were included. The MIC(90) (mcg ml(-1) ) for fluconazole was 0.25, 0.5 and 0.5 mcg ml(-1) for each grouping, respectively. The corresponding MIC(90) for flucytosine was 1, 2 and 8 mcg ml(-1) , respectively. The MIC(90) for the remaining agents remained unchanged across time periods mentioned. Of note, the percentage of isolates with MIC ≥1 and ≥2 mcg ml(-1) for fluconazole increased from 3% to 9% over the study period. Although the C. albicans MIC(90) to fluconazole in vaginal isolates has not shown a clinically significant increase since 1986, there is an increasing number of isolates with elevated MICs. The implications of this increase are unknown, but given the achievable vaginal concentrations of fluconazole, reduced susceptibility may have clinical relevance.
© 2009 Blackwell Verlag GmbH.

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Year:  2011        PMID: 19563489     DOI: 10.1111/j.1439-0507.2009.01752.x

Source DB:  PubMed          Journal:  Mycoses        ISSN: 0933-7407            Impact factor:   4.377


  4 in total

1.  Clotrimazole as a potent agent for treating the oomycete fish pathogen Saprolegnia parasitica through inhibition of sterol 14α-demethylase (CYP51).

Authors:  Andrew G S Warrilow; Claire M Hull; Nicola J Rolley; Josie E Parker; W David Nes; Stephen N Smith; Diane E Kelly; Steven L Kelly
Journal:  Appl Environ Microbiol       Date:  2014-08-01       Impact factor: 4.792

Review 2.  Antifungal agents commonly used in the superficial and mucosal candidiasis treatment: mode of action and resistance development.

Authors:  Małgorzata Bondaryk; Wiesław Kurzątkowski; Monika Staniszewska
Journal:  Postepy Dermatol Alergol       Date:  2013-10-30       Impact factor: 1.837

3.  In vitro activity of econazole in comparison with three common antifungal agents against clinical Candida strains isolated from superficial infections.

Authors:  M Abastabar; T Shokohi; R Rouhi Kord; H Badali; S J Hashemi; Z Ghasemi; A Ghojoghi; N Baghi; M Abdollahi; S Hosseinpoor; N Rahimi; Z Seifi; S Gholami; I Haghani; M R Jabari; A Pagheh
Journal:  Curr Med Mycol       Date:  2015-12

4.  Antifungal (oral and vaginal) therapy for recurrent vulvovaginal candidiasis: a systematic review protocol.

Authors:  Juliana Lírio; Paulo Cesar Giraldo; Rose Luce Amaral; Ayane Cristine Alves Sarmento; Ana Paula Ferreira Costa; Ana Katherine Gonçalves
Journal:  BMJ Open       Date:  2019-05-22       Impact factor: 2.692

  4 in total

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