潜伏期对坦桑尼亚姆万扎Sekou Toure地区转诊医院儿童血液培养结果和引起血液感染的细菌病原体的影响

Access microbiology Pub Date : 2025-03-19 eCollection Date: 2025-01-01 DOI:10.1099/acmi.0.000942.v3
James Thomas, Albert Wasira, Darus Maarafu, Faustin Igogo, Eunice Emmanuel, Roza Ernest, Martha F Mushi, Stephen E Mshana
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引用次数: 0

摘要

背景。延迟一小时才开始适当的抗微生物治疗会使血液感染患者的死亡率增加2%。这突出了手工血液培养方法的风险,因为它们往往需要较长的周转时间,初始潜伏期为18-24小时,导致获得诊断结果的延迟。本研究检查了孵育时间对血液培养结果的影响,并分析了在坦桑尼亚姆万扎Sekou Toure地区转诊医院(SRRH)就诊的儿童中引起血液感染的病原体模式。2024年5月至7月在SRRH进行了一项以医院为基础的描述性横断面研究。采用常规血培养方法,在盲代培养初始时间(8、24和120 h)稍作修改后,使用自制的脑心灌注肉汤,分离引起bsi的病原体。描述性数据分析采用STATA软件版本15。结果。该研究招募了302名临床诊断为BSIs的儿童。其中160例(53%)为男性,年龄中位数为6岁,四分位数间距[IQR]为1-7岁。发热是259例(85.8%)患儿的主要临床症状。在90例(29.8%)儿童中检测到微生物学证实的bsi。初孵育8 h后,盲传代检出率为51.1%(46/90)。孵育24 h和120 h后分别检出31例(34.4%)和13例(14.4%)。检出最多的病原菌为肺炎克雷伯菌(25.6%,23/90)和金黄色葡萄球菌(24.4%,22/90)。革兰氏阴性菌(GNB)占多数(71.1%,64/90),其中62.5%(40/64)对第三代头孢菌素(3GC)耐药。45.5%(10/22)的金黄色葡萄球菌为耐甲氧西林金黄色葡萄球菌。结论。初始孵育8小时后的盲传代培养正确检测出超过一半的微生物学证实的bsi患儿。在mcconkey琼脂上添加2µg ml-1头孢噻肟(MCA-C)进行盲代培养,培养8小时后,半数GNB引起的bsi患儿在24小时内得到了正确的治疗。在3GC耐药高发地区,8 h内盲代培养应包括MCA-C,以便在24 h内进行适当处理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of the incubation time on blood culture results and bacterial pathogens causing bloodstream infections among children attending Sekou Toure Regional Referral Hospital in Mwanza, Tanzania.

Background. A one hour delay in initiating appropriate antimicrobial treatment increases the mortality rate of patients with bloodstream infections by 2%. This highlights the risk associated with manual blood culture methods, as they tend to have long turnaround time, with an initial incubation period of 18-24 h, leading to delays in obtaining diagnostic results. This study examined the impact of incubation time on blood culture results and analysed the patterns of the pathogens causing bloodstream infections (BSIs) among children attending Sekou Toure Regional Referral Hospital (SRRH), Mwanza, Tanzania Methodology. A hospital-based, descriptive cross-sectional study was conducted at SRRH from May to July 2024. The conventional blood culture method, using in-house prepared brain heart infusion broth with slight modifications on the initial time of the blind subculture (at 8, 24 and 120 h) was done to isolate the pathogens causing BSIs. Descriptive data analysis was performed using STATA software version 15. Results. The study enrolled 302 children with clinical diagnosis of BSIs. Of these, 160 (53%) were male, with a median age of 6 years interquartile range [IQR] 1-7 years. Fever was the predominant clinical sign reported in 259 (85.8%) children. Microbiologically confirmed BSIs were detected in 90 (29.8%) children. Among them, 51.1% (46/90) were detected through blind subculture after 8 h of initial incubation. An additional 31 (34.4%) and 13 (14.4%) were detected after 24 h and 120 h of incubation, respectively. The most frequently isolated pathogens were Klebsiella pneumoniae (25.6%, 23/90) and Staphylococcus aureus (24.4%, 22/90). Gram-negative bacteria (GNB) formed the majority (71.1%, 64/90) of the isolated pathogens, with 62.5% (40/64) showing resistance to third-generation cephalosporin (3GC). Additionally, 45.5% (10/22) of the S. aureus strains were methicillin-resistant S. aureus. Conclusion. Blind subculture after 8 h of initial incubation correctly detected more than half of the children with microbiologically confirmed BSIs. Incorporating blind subculture on MacConkey agar supplemented with 2 µg ml-1 cefotaxime (MCA-C) after 8 h of incubation resulted in the correct treatment of half of the children with BSIs caused by GNB within 24 h. In areas with high prevalence of 3GC resistance, blind subculture within 8 h should include MCA-C for appropriate treatment within 24 h.

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