A. K. Sığ, Diğdem Özer Yıldırım, Başak Göl Serin, Mustafa Güney
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Results: A total of 6047 BC sets were obtained and randomly chosen 1040+122 negative sets (A and B groups, respectively) were included. In group A, none of them had fungal growth. In B (ongoing empiric antifungal ≤48h), only 2 sets showed significant fungal growth, which were observed in 7±2 days, and all strains were identified as C.glabrata complex and these patients were on empiric fluconazole (200 mg/day). One isolate was susceptible dose dependent, the other one was resistant for fluconazole. Latter sets of these fungemia patients showed positive signals in routine incubation period. Conclusion: Invasive fungal infections are increasingly encountered and isolation capacity and optimization of BCs are crucial. In this study, it was obviously observed that standard incubation period is satisfactory in order to detect almost all fungemia.","PeriodicalId":247163,"journal":{"name":"Balıkesır Health Sciences Journal","volume":"66 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Can Prolonged Incubation of Negative Blood Cultures Show Fungal Positivity?\",\"authors\":\"A. K. Sığ, Diğdem Özer Yıldırım, Başak Göl Serin, Mustafa Güney\",\"doi\":\"10.53424/balikesirsbd.1205875\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective: Standard duration of one set blood culture (BC) is a maximum of 5-7 days. The aim of this study was to evaluate “culture-negative” vials with a prolonged incubation (max 30 days) time and to observe any mycological growth. 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One isolate was susceptible dose dependent, the other one was resistant for fluconazole. Latter sets of these fungemia patients showed positive signals in routine incubation period. Conclusion: Invasive fungal infections are increasingly encountered and isolation capacity and optimization of BCs are crucial. 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引用次数: 0
摘要
目的:一组血培养(BC)的标准时间最长为5-7天。本研究的目的是通过延长孵育时间(最多30天)来评估“培养阴性”小瓶,并观察任何真菌学生长。材料和方法:纳入Balıkesir atatat rk市医院成人患者一年的常规bc。使用Render BC System BC128 (Render Biotech Co. Ltd, Shenzhen, China)。随机选择的小瓶按常规方法再孵育3周。如果有任何生长,用phoenix™100系统(Becton Dickinson, MA, USA)和玉米粉间80琼脂(RTA实验室,Kocaeli,土耳其)进行鉴定。采用CLSI盘片扩散法进行药敏试验。结果:共获得6047个BC组,随机抽取1040+122个阴性组(A组和B组)。A组均无真菌生长。在B组(持续经验性抗真菌≤48h)中,仅有2组真菌明显生长,观察时间为7±2天,所有菌株均鉴定为C.glabrata复合体,并给予经验性氟康唑(200mg /d)治疗。一株对氟康唑有剂量依赖性,另一株对氟康唑有耐药性。这些真菌血症患者的后几组在常规潜伏期显示阳性信号。结论:侵袭性真菌感染日益增多,bc的分离能力和优化至关重要。在本研究中,明显地观察到标准的潜伏期是令人满意的,以检测几乎所有的真菌病。
Can Prolonged Incubation of Negative Blood Cultures Show Fungal Positivity?
Objective: Standard duration of one set blood culture (BC) is a maximum of 5-7 days. The aim of this study was to evaluate “culture-negative” vials with a prolonged incubation (max 30 days) time and to observe any mycological growth. Materials and Methods: Routine BCs optained from adult patients of Balıkesir Atatürk City Hospital for a year period were included. Render BC System BC128 (Render Biotech Co. Ltd., Shenzhen, China) were used. Randomly selected vials were re-incubated for additional three weeks by conventional methods. In case of any growth, identifications were done by PhoenixTM 100 system (Becton Dickinson, MA, USA) with cornmeal tween 80 agar (RTA Laboratories, Kocaeli, Turkey). Antifungal susceptibility testing was applied with CLSI disk diffusion method. Results: A total of 6047 BC sets were obtained and randomly chosen 1040+122 negative sets (A and B groups, respectively) were included. In group A, none of them had fungal growth. In B (ongoing empiric antifungal ≤48h), only 2 sets showed significant fungal growth, which were observed in 7±2 days, and all strains were identified as C.glabrata complex and these patients were on empiric fluconazole (200 mg/day). One isolate was susceptible dose dependent, the other one was resistant for fluconazole. Latter sets of these fungemia patients showed positive signals in routine incubation period. Conclusion: Invasive fungal infections are increasingly encountered and isolation capacity and optimization of BCs are crucial. In this study, it was obviously observed that standard incubation period is satisfactory in order to detect almost all fungemia.