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体外伊曲康唑和氟康唑敏感性与外阴阴道念珠菌病患者临床结局的相关性

Correlation of in vitro itraconazole and fluconazole susceptibility with clinical outcome for patients with vulvovaginal candidiasis.

作者信息

Costa Milce, Passos Xisto Sena, Miranda André Thiago Borges, de Araújo Rosane Silva Carneiro, Paula Claudete Rodrigues, Silva Maria do Rosário Rodrigues

机构信息

Instituto de Patologia Tropical e Saúde Pública da Universidade Federal de Goiás, Brasil.

出版信息

Mycopathologia. 2004 Jan;157(1):43-7. doi: 10.1023/b:myco.0000012220.09227.25.

Abstract

Between April 2001 and April 2002 were studied 106 women with a clinical diagnosis of vaginal candidiasis seen at the Gynecology and Obstetrics Ambulatory of the Hospital das Clínicas da Universidade Federal de Goiás. The patients were assessed on two occasions, before starting treatment with itraconazole or fluconazole (initial visit) and 14 days after treatment (return). At two visits the signs and symptoms were recorded and vaginal secretion was collected. According to the clinical evaluation, itraconazole was effective in 64.3%, while fluconazole was effective in 71.0% of the patients. The mycological cure rates (negative culture) in the return were 64.3% for the patients treated with itraconazole and 78.9% for the patients treated with fluconazole. The MICs of itraconazole and fluconazole for 80 Candida isolates were determined by Etest method. We investigated the correlation between in vitro susceptibility (Susceptible, Susceptibility Depending Dose and Resistant) to itraconazole and fluconazole with clinical outcome of the patients. The success rates were 63.9% for itraconazole and 90.6% for fluconazole in the susceptible category, 100.0% for both drugs in the susceptible dose dependent category, and 0.0% for both drugs in the resistant category. Our results showed there were a positive correlation between in vitro susceptibility test results with clinical outcome in vaginal Candida infections and that both drugs might be one choice in the treatment of vaginal candidiasis.

摘要

2001年4月至2002年4月期间,对在戈亚斯联邦大学临床医院妇产科门诊就诊的106例临床诊断为阴道念珠菌病的女性进行了研究。患者在接受伊曲康唑或氟康唑治疗前(初诊)和治疗后14天(复诊)接受了两次评估。在两次就诊时记录体征和症状,并收集阴道分泌物。根据临床评估,伊曲康唑对64.3%的患者有效,而氟康唑对71.0%的患者有效。复诊时,接受伊曲康唑治疗的患者真菌学治愈率(培养阴性)为64.3%,接受氟康唑治疗的患者为78.9%。采用Etest法测定了80株念珠菌分离株对伊曲康唑和氟康唑的最低抑菌浓度(MIC)。我们研究了伊曲康唑和氟康唑的体外药敏情况(敏感、剂量依赖性敏感和耐药)与患者临床结局之间的相关性。在敏感组中,伊曲康唑的成功率为63.9%,氟康唑为90.6%;在剂量依赖性敏感组中,两种药物的成功率均为100.0%;在耐药组中,两种药物的成功率均为0.0%。我们的结果表明,阴道念珠菌感染的体外药敏试验结果与临床结局之间存在正相关,这两种药物可能都是治疗阴道念珠菌病的选择之一。

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