Voriconazole: A new triazole antifungal

被引:112
作者
Sabo, JA
Abdel-Rahman, SM
机构
[1] Childrens Mercy Hosp, Clin Pharmacol Sect, Kansas City, MO 64108 USA
[2] Univ Missouri, Kansas City, MO 64110 USA
关键词
voriconazole; UK-109,496; triazole; antifungal;
D O I
10.1345/aph.19237
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To review the currently available information on the pharmacology, pharmacokinetics, efficacy, adverse effects, drug interactions,and dosage guidelines of voriconazole. Comparative data for voriconazole and other azole antifungal agents are described where available. DATA SOURCES: A MEDLINE search restricted to English-language articles (1966 to September 1999) was conducted, and an extensive review of journals and meeting abstracts was performed. MeSH headings included itraconazole, itraconazole, voriconazole, UK-109,496, and amphotericin B. DATA EXTRACTION: The data on pharmacokinetics, adverse effects, and drug interactions were obtained from open-label and controlled studies and case reports. Controlled studies and case reports were evaluated to demonstrate the efficacy of voriconazole in treatment of various fungal infections. DATA SYNTHESIS: Voriconazole is a derivative of fluconazole that demonstrates enhanced in vitro activity against existent and emerging fungal pathogens. Limited data have revealed a favorable pharmacokinetic and safety profile for the agent. Moreover, select clinical trials and case studies of voriconazole suggest good in vivo efficacy against several fungal pathogens including Candida, Aspergillus, and Scedosporium. CONCLUSIONS: Voriconazole has shown promise in the treatment of superficial and systemic mycoses. While several unresolved issues remain, voriconazole may be a viable therapeutic alternative for fluconazole-resistant mucocutaneous candidiasis and in cases of mild to moderate systemic mycoses requiring chronic treatment or that are refractory to currently available agents.
引用
收藏
页码:1032 / 1043
页数:12
相关论文
共 97 条
[1]   Emerging applications of recombinant human granulocyte-macrophage colony-stimulating factor [J].
Armitage, JO .
BLOOD, 1998, 92 (12) :4491-4508
[2]  
BAILEY EM, 1990, PHARMACOTHERAPY, V10, P146
[3]  
BARCHIESI F, 1995, 35 INT C ANT AG CHEM
[4]  
Barone JA, 1998, PHARMACOTHERAPY, V18, P295
[5]   In vitro studies of two triazole antifungal agents (Voriconazole [UK-109,496] and fluconazole) against Candida species [J].
Barry, AL ;
Brown, SD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (08) :1948-1949
[6]   Voriconazole (UK-109,496) inhibits the growth and alters the morphology of fluconazole-susceptible and -resistant Candida species [J].
Belanger, P ;
Nast, CC ;
Fratti, R ;
Sanati, H ;
Ghannoum, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (08) :1840-1842
[7]   Deep infections caused by Scedosporium prolificans - A report on 16 cases in Spain and a review of the literature [J].
Berenguer, J ;
RodriguezTudela, JL ;
Richard, C ;
Alvarez, M ;
Sanz, MA ;
Gaztelurrutia, L ;
Ayats, J ;
MartinezSuarez, JV .
MEDICINE, 1997, 76 (04) :256-265
[8]   Clinical resolution of Scedosporium prolificans fungemia associated with reversal of neutropenia following administration of granulocyte colony-stimulating factor [J].
Bouza, E ;
Munoz, P ;
Vega, L ;
RodriguezCreixems, M ;
Berenguer, J ;
Escudero, A .
CLINICAL INFECTIOUS DISEASES, 1996, 23 (01) :192-193
[9]   Damage to yeast cells of Cryptococcus neoformans by voriconazole and fluconazole: a culture and microscopic study [J].
Brummer, E ;
Kamei, K ;
Miyaji, M .
MEDICAL MYCOLOGY, 1998, 36 (04) :227-233
[10]   Improved management of invasive pulmonary aspergillosis in neutropenic patients using early thoracic computed tomographic scan and surgery [J].
Caillot, D ;
Casasnovas, O ;
Bernard, A ;
Couaillier, JF ;
Durand, C ;
Cuisenier, B ;
Solary, E ;
Piard, F ;
Petrella, T ;
Bonnin, A ;
Couillault, G ;
Dumas, M ;
Guy, H .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (01) :139-147