Prevalence of fluconazole-resistant strains of Candida albicans in otherwise healthy outpatients

被引:14
作者
Haberland-Carrodeguas, C
Allen, CM
Beck, FM
Buesching, WJ
Koletar, SL
Sundstrom, P
机构
[1] Temple Univ, Sch Dent, Sect Oral & Maxillofacial Pathol, Philadelphia, PA 19140 USA
[2] Ohio State Univ, Coll Dent, Sect Oral Maxillofacial & Pathol, Columbus, OH 43210 USA
[3] Ohio State Univ, Coll Dent, Sect Hlth Sci Res, Columbus, OH 43210 USA
[4] Ohio State Univ, Ctr Med, Div Clin Microbiol, Dept Pathol, Columbus, OH 43210 USA
[5] Ohio State Univ, Ctr Med, Div Infect Dis, Dept Internal Med, Columbus, OH 43210 USA
[6] Ohio State Univ, Coll Med, Dept Med Microbiol Immunol, Columbus, OH 43210 USA
关键词
fluconazole; oral candidiasis; in vitro susceptibility testing; Candida albicans; antifungal treatment; yeast strain differentiation;
D O I
10.1034/j.1600-0714.2002.310207.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: In contrast to the immunosupressed patient population, the prevalence of fluconazole-resistant strains of Candida albicans among healthy individuals has not been extensively studied. Methods: Candida species were cultured form 50 healthy outpatients with clinical signs of oral candidiasis. Following one week of the recommended fluconazole regimen, post-treatment cultures were obtained. Both pre- and post-treatment yeasts were identified and in vitro susceptibility testing was performed using the NCCLS M-27A method. Strains were further differentiated using established cDNA probes. Results: Forty-four patients (88%) had positive C.albicans cultures prior to treatment. Antifungal susceptibility testing of these strains demonstrated no in vitro resistance to fluconazole. At post-treatment evaluation, eight patients (18%) had persistent signs of infection and 10 patients (23%) had positive Candida sp. cultures despite no clinical signs of infection. DNA analysis confirmed that the same C. albicans strain was present both in the pre-treatment and the post-treatment cultures. Conclusions: Our results showed that the presence of fluconazole-resistant strains of C.albicans does not appear to be prevalent among healthy outpatients furthermore, in vitro antifungal susceptibility testing does not always predict successful therapy in these patients.
引用
收藏
页码:99 / 105
页数:7
相关论文
共 39 条
[1]   DIAGNOSING AND MANAGING ORAL CANDIDIASIS [J].
ALLEN, CM .
JOURNAL OF THE AMERICAN DENTAL ASSOCIATION, 1992, 123 (01) :77-&
[2]   FLUCONAZOLE-RESISTANT CANDIDA-ALBICANS [J].
BOKEN, DJ ;
SWINDELLS, S ;
RINALDI, MG .
CLINICAL INFECTIOUS DISEASES, 1993, 17 (06) :1018-1021
[3]   ETIOLOGY, PATHOGENESIS, THERAPY, AND PROPHYLAXIS OF ORAL YEAST INFECTIONS [J].
BUDTZJORGENSEN, E .
ACTA ODONTOLOGICA SCANDINAVICA, 1990, 48 (01) :61-69
[4]   CORRELATION OF IN-VITRO FLUCONAZOLE RESISTANCE OF CANDIDA ISOLATES IN RELATION TO THERAPY AND SYMPTOMS OF INDIVIDUALS SEROPOSITIVE FOR HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 [J].
CAMERON, ML ;
SCHELL, WA ;
BRUCH, S ;
BARTLETT, JA ;
WASKIN, HA ;
PERFECT, JR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (11) :2449-2453
[5]   Non-albicans oral candidosis in HIV-positive patients [J].
Cartledge, JD ;
Midgley, J ;
Gazzard, BG .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 43 (03) :419-422
[6]  
DABROWA N, 1970, Sabouraudia, V8, P163
[7]  
DIOZ PD, 1995, ORAL SURG ORAL MED O, V79, P170
[8]   Mixed oropharyngeal candidiasis due to Candida albicans and non-albicans Candida strains in HIV-infected patients [J].
Dronda, F ;
AlonsoSanz, M ;
Laguna, F ;
Chaves, F ;
MartinezSuarez, JV ;
RodriguezTudela, JL ;
GonzalezLopez, A ;
Valencia, E .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1996, 15 (06) :446-452
[9]   DEVELOPMENT OF RESISTANCE IN CANDIDA ISOLATES FROM PATIENTS RECEIVING PROLONGED ANTIFUNGAL THERAPY [J].
FANHAVARD, P ;
CAPANO, D ;
SMITH, SM ;
MANGIA, A ;
ENG, RHK .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (11) :2302-2305
[10]   Refractory mucosal candidiasis in advanced human immunodeficiency virus infection [J].
Fichtenbaum, CJ ;
Koletar, S ;
Yiannoutsos, C ;
Holland, F ;
Pottage, J ;
Cohn, SE ;
Walawander, A ;
Frame, P ;
Feinberg, J ;
Saag, M ;
Van der Horst, C ;
Powderly, WG .
CLINICAL INFECTIOUS DISEASES, 2000, 30 (05) :749-756