首页> 外文期刊>Journal of Infection >Incidence and clinical impact of extended-spectrum-beta-lactamase (ESBL) production and fluoroquinolone resistance in bloodstream infections caused by Escherichia coli in patients with hematological malignancies.
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Incidence and clinical impact of extended-spectrum-beta-lactamase (ESBL) production and fluoroquinolone resistance in bloodstream infections caused by Escherichia coli in patients with hematological malignancies.

机译:血液恶性肿瘤患者大肠埃希氏菌引起的血液感染中广谱β-内酰胺酶(ESBL)产生和氟喹诺酮耐药性的发生率和临床影响。

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OBJECTIVES: To identify risk factors for mortality in patients suffering from hematological malignancies with concurrent bacteremia caused by Escherichia coli. Particular attention was focused on defining the impact of extended-spectrum-beta-lactamase (ESBL) production and fluoroquinolone resistance by the bacterial isolates on mortality. MATERIALS AND METHODS: A retrospective eight-year cohort study design was employed. The outcome measured was death within 30 days of the first positive blood culture. Survivor and non-survivor subgroups were compared to identify predictors of mortality. RESULTS: A total of 62 episodes of bacteremia caused by E. coli were analyzed. The overall incidences of ESBL production and fluoroquinolone resistance were 41.9% and 62.9%, respectively. The overall 30-day mortality rate was 20.9% (13/62). In a multivariate analysis, significant predictors of mortality were inadequate initial antimicrobial therapy (OR=14.96, 95% CI 1.95-114.51; P=0.009), infection caused by ESBL-producing isolates (OR=8.84, 95% CI 1.48-52.91; P=0.01), and prolonged neutropenia (OR=8.10, 95% CI 1.29-50.57; P=0.02). CONCLUSIONS: Sound knowledge of the local distribution of pathogens and their susceptibility patterns and prompt initiation of effective antimicrobial treatment are essential in patients suffering from hematological malignancies with BSIs caused by E. coli.
机译:目的:确定患有血液恶性肿瘤并由大肠杆菌引起的同时菌血症的患者死亡的危险因素。特别关注的是确定细菌分离株对广谱β-内酰胺酶(ESBL)产生和氟喹诺酮耐药性的影响。材料与方法:采用回顾性八年队列研究设计。测得的结果是首次阳性血液培养后30天内死亡。比较幸存者和非幸存者亚组,以确定死亡率的预测因子。结果:共分析了62例由大肠杆菌引起的菌血症。 ESBL产生和氟喹诺酮耐药性的总发生率分别为41.9%和62.9%。 30天总死亡率为20.9%(13/62)。在多变量分析中,死亡率的重要预测因素是初始抗微生物治疗不充分(OR = 14.96,95%CI 1.95-114.51; P = 0.009),是由产生ESBL的分离株引起的感染(OR = 8.84,95%CI 1.48-52.91; P = 0.01)和中性粒细胞减少症延长(OR = 8.10,95%CI 1.29-50.57; P = 0.02)。结论:对于由大肠杆菌引起的BSI血液系统恶性肿瘤患者,掌握病原体的局部分布及其易感性模式以及迅速启动有效的抗菌治疗的知识非常重要。

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