M. Mallie et Jm. Bastide, IN-VITRO SUSCEPTIBILITY OF 115 ISOLATES OF CANDIDA TO AMPHOTERICIN-B,FLUCONAZOLE AND ITRACONAZOLE, Drugs under experimental and clinical research, 22(6), 1996, pp. 301-307
Opportunistic fungal infections are an increasingly important cause of
morbidity and mortality particularly due to Candida species (1). Ther
e is also an increase of candidosis especially ascribed to acquired or
induced immunodeficiency syndromes or in the event of long-term antib
iotic, immunosuppressor or cytotoxic therapies. Consequently there has
been an increase in the use of systemic antifungal agents responsible
for the emergence of new opportunistic fungi (2) and resistant specie
s (3, 4). Oropharyngeal candidiasis caused by various species of Candi
da is one of the most common opportunistic infections in AIDS. In rece
nt years there has been an increasing number of yeast isolates resista
nt to fluconazole (4, 5) or to amphotericin B (6). The aim of the pres
ent study was to examine the susceptibility in vitro of itraconazole,
a newly introduced antifungal agent in the local or systemic therapy o
f oropharyngeal candidiosis, vs well-known agents such as amphotericin
B and fluconazole, against various Candida clinical isolates. The pre
sent results, in agreement with other studies, show strong in vitro ac
tivity of itraconazole against Candida spp. and particularly against l
ess susceptible species C. glabrata, C. tropicalis or C. krusei.