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氟康唑、伊曲康唑和伏立康唑活性评估:一项病例对照研究。

Evaluation of fluconazole, itraconazole, and voriconazole activity on : A case control study.

作者信息

Partha Agung Dewi Sekar Langit, Widodo Agung Dwi Wahyu, Endraswari Pepy Dwi

机构信息

Study Program of Clinical Microbiology, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.

Department of Clinical Microbiology, Faculty of Medicine, Universitas Airlangga - Dr. Soetomo General Academic Hospital, Surabaya, Indonesia.

出版信息

Ann Med Surg (Lond). 2022 Nov 11;84:104882. doi: 10.1016/j.amsu.2022.104882. eCollection 2022 Dec.

Abstract

BACKGROUND

Azole antifungals are the most commonly used antifungals. The high use of azoles for long-term therapy and prophylaxis is prone to cause resistance. Thus, it is necessary to evaluate the antifungal activity against .

OBJECTIVES

Analyzing the comparison of antifungal exposure on the time-kill curve to .

METHOD

A case-control study was conducted with a posttest control group design. This study used clinical and ATCC isolates exposed to antifungal solutions with 1 ×, 4 ×, and 16 × minimum inhibitory concentrations (MIC). Antibiotics used included fluconazole, itraconazole, and voriconazole. isolates were incubated with MIC, and the number of colonies was counted at 0, 2, 4, 8, 12, 24, and 48 h. The number of colonies that grew every hour of observation was included in the time-kill curve. The data were then analyzed using an ANOVA test with  <0.05.

RESULTS

The antifungals (fluconazole, itraconazole, and voriconazole) showed fungistatic activity against clinical and ATCC isolates. There was a significant comparison between the antifungal group and the control group at 12, 24, and 48 h. The most significant difference between antifungal and control group was found at 24 h where fluconazole had 95% CI = 0.807-2.061 ( <0.001), itraconazole 95% CI = 0.722-1.976 ( <0.001), and voriconazole CI 95% = 0.807-2.062 ( <0.001).

CONCLUSION

Fluconazole, itraconazole, and voriconazole were effective in inhibiting the growth of . Maximum inhibition in vitro occurs after 12 h of antifungal exposure.

摘要

背景

唑类抗真菌药是最常用的抗真菌药。长期用于治疗和预防的唑类药物使用频率高,容易产生耐药性。因此,有必要评估其对……的抗真菌活性。

目的

分析抗真菌暴露在时间 - 杀菌曲线上对……的比较。

方法

采用后测对照组设计进行病例对照研究。本研究使用了临床和美国典型培养物保藏中心(ATCC)的分离株,使其暴露于1×、4×和16×最低抑菌浓度(MIC)的抗真菌溶液中。使用的抗生素包括氟康唑、伊曲康唑和伏立康唑。将分离株与MIC一起孵育,并在0、2、4、8、12、24和48小时计数菌落数。观察的每小时生长的菌落数纳入时间 - 杀菌曲线。然后使用方差分析检验分析数据,P<0.05。

结果

抗真菌药(氟康唑、伊曲康唑和伏立康唑)对临床和ATCC分离株显示出抑菌活性。在12、24和48小时,抗真菌组与对照组之间存在显著差异。抗真菌组与对照组之间最显著的差异出现在24小时,其中氟康唑的95%置信区间为0.807 - 2.061(P<0.001),伊曲康唑的95%置信区间为0.722 - 1.976(P<0.001),伏立康唑的95%置信区间为0.807 - 2.062(P<0.001)。

结论

氟康唑、伊曲康唑和伏立康唑可有效抑制……的生长。抗真菌暴露12小时后在体外出现最大抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d932/9758354/8e99d4bf633d/gr1.jpg

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