IN-VITRO ACTIVITY OF ITRACONAZOLE AGAINST FLUCONAZOLE-SUSCEPTIBLE ANDFLUCONAZOLE-RESISTANT CANDIDA-ALBICANS ISOLATES FROM ORAL CAVITIES OFPATIENTS INFECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS
F. Barchiesi et al., IN-VITRO ACTIVITY OF ITRACONAZOLE AGAINST FLUCONAZOLE-SUSCEPTIBLE ANDFLUCONAZOLE-RESISTANT CANDIDA-ALBICANS ISOLATES FROM ORAL CAVITIES OFPATIENTS INFECTED WITH HUMAN-IMMUNODEFICIENCY-VIRUS, Antimicrobial agents and chemotherapy, 38(7), 1994, pp. 1530-1533
A broth macrodilution technique, which was performed by following the
recommendations provided by the National Committee for Clinical Labora
tory Standards (document M27-P), was applied to study the in vitro act
ivity of itraconazole against fluconazole-susceptible and -resistant C
andida albicans isolates from the oral cavities of 100 patients infect
ed with human immunodeficiency virus. The in vitro data demonstrated t
hat itraconazole had good activity against the tested isolates; for 90
% of all strains of C. albicans, MICs were 1 mu g/ml, and only one iso
late was highly resistant to this triazole (MIC, >16 mu g/ml). However
, the itraconazole MICs for the fluconazole-susceptible isolates were
significantly lower than those for the fluconazole-resistant isolates;
the MICs for 50 and 90% of the isolates tested were less than or equa
l to 0.03 and 0.25 mu g/ml, respectively, for the fluconazole-suscepti
ble isolates and 0.5 and 1 mu g/ml, respectively, for the fluconazole-
resistant isolates (P = 0.00001). Our findings could be of clinical re
levance because human immunodeficiency virus-infected patients who fai
l fluconazole therapy for oral and/or esophageal candidiasis may requi
re itraconazole at doses higher than those used in standard therapy.