Caspofungin in the treatment of Candida auris candiduria in Hemato-oncological Patients: An observational retrospective cohort study.

IF 1.2 4区 医学 Q4 MICROBIOLOGY
New Microbiologica Pub Date : 2025-07-01
Umran Elbahr, Amira Khairy, Farouq Dayyab, Clark Steven Delos Reyes, Jennie Pastrana, Chithra Vineeth, Ahmed Qaedi, Suha Hejres, Shruti Prem Sudha, Ozge Keskin, Shiv Pratap Singh Rana, Elias Fadel, Hakan Erdem, Oguz Resat Sipahi
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Abstract

Candiduria is a common problem especially in advanced stage oncology/hematology cases. Herein, we aimed to analyze the efficacy of caspofungin treatment in Candida auris isolated from urine culture. We conducted an observational retrospective study in a tertiary-care educational hemato-oncology hospital from October 2021 to November 2022. The patients hospitalized in our center and having at least two consecutive urine cultures that yielded C. auris with significant pyuria were included in the study. The effectiveness of caspofungin was evaluated based on clinical and microbiological outcomes. In total, 10 patients (two female, aged 55.3 ± 15) were included in the study. Four (40%) patients had urinary tract infections, and six (60%) patients had asymptomatic C. auris candiduria which required antifungal therapy. Nine cases had urinary instrumentation: two nephrostomy, one suprapubic catheter, and six urinary catheters. The 10 cases received a mean of 13.4 ± 3.5 days of caspofungin. Four of 10 cases (40%) had at least 1 negative culture between day 1 and the end of caspofungin treatment. Relapse and re-infection rates 30 days after the end of therapy in microbiologically successful cases were 3/4 and 2/4. Caspofungin resistance developed in three cases (30%) within 30 days after treatment. Overall day-30 mortality was 3/10 (30%) while overall success (microbiological success + no relapse/reinfection during 30 days follow up after end of therapy) was 10%. Caspofungin demonstrated limited efficacy in treating C. auris-related urinary tract infection/colonization in hospitalized cancer patients.

卡泊芬净治疗血液肿瘤患者耳念珠菌:一项观察性回顾性队列研究。
念珠菌是一个常见的问题,特别是在晚期肿瘤/血液学病例。本研究旨在分析卡泊真菌素对尿培养的耳念珠菌的治疗效果。我们于2021年10月至2022年11月在一家三级教育血液肿瘤医院进行了一项观察性回顾性研究。本研究纳入了在本中心住院且至少连续两次尿培养产生伴有明显脓尿的耳念珠菌的患者。根据临床和微生物学结果评估卡泊芬净的有效性。共纳入10例患者,其中女性2例,年龄55.3±15岁。4例(40%)患者有尿路感染,6例(60%)患者有无症状耳念珠菌,需要抗真菌治疗。9例行尿路置管:2例肾造口术,1例耻骨上置管,6例导尿管。10例患者平均用药时间为13.4±3.5 d。10例患者中有4例(40%)在卡泊芬净治疗第1天至治疗结束期间至少有1次阴性培养。微生物学治疗成功的患者治疗结束后30天的复发率为3/4,再感染率为2/4。3例(30%)在治疗后30天内出现卡泊芬金耐药性。总体第30天死亡率为3/10(30%),而总体成功率(微生物学成功+治疗结束后30天随访无复发/再感染)为10%。Caspofungin在治疗住院癌症患者C. auris相关尿路感染/定植方面的疗效有限。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
New Microbiologica
New Microbiologica 生物-微生物学
CiteScore
2.20
自引率
5.60%
发文量
40
审稿时长
6-12 weeks
期刊介绍: The publication, diffusion and furtherance of research and study on all aspects of basic and clinical Microbiology and related fields are the chief aims of the journal.
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