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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Clinical Features and Risk Factors for Development of Breakthrough Gram-Negative Bacteremia during Carbapenem Therapy
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Clinical Features and Risk Factors for Development of Breakthrough Gram-Negative Bacteremia during Carbapenem Therapy

机译:碳青霉烯治疗期间突破性革兰氏阴性菌血症发展的临床特征和危险因素

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摘要

With the increasing use of carbapenems, carbapenem-resistant Gram-negative bacteria have become a major concern in health care-associated infections. The present study was performed to evaluate the clinical and microbiological features of breakthrough Gram-negative bacteremia (GNB) during carbapenem therapy and to assess risk factors for development of breakthrough GNB. A case-control study was performed at a tertiary hospital from 2005 to 2014. Case patients were defined as individuals whose blood cultures grew Gram-negative bacteria while the patients were receiving carbapenems for at least 48 h before breakthrough GNB. Age-, sex-, and date-matched controls were selected from patients who received carbapenem for at least 48 h and did not develop breakthrough GNB during carbapenem treatment. A total of 101 cases of breakthrough GNB were identified and compared to 100 controls. The causative microorganisms for breakthrough GNB were Stenotrophomonas maltophilia ( n = 33), Acinetobacter baumannii (n = 32), Pseudomonas aeruginosa (n = 21), and others (n = 15). Approximately 90% of S. maltophilia isolates were susceptible to levofloxacin and trimethoprim-sulfamethoxazole. The most common infection types were primary bacteremia (38.6%) and respiratory infections (35.6%). More than half of the patients died within a week after bacteremia, and the 30-day mortality rate was 70.3%. In a multivariate analysis, a longer hospital stay, hematologic malignancy, persistent neutropenia, immunosuppressant use, and previous colonization by causative microorganisms were significantly associated with breakthrough GNB. Our data suggest that S. maltophilia, A. baumannii, and P. aeruginosa are the major pathogens of breakthrough GNB during carbapenem therapy, in association with a longer hospital stay, hematologic malignancy, persistent neutropenia, immunosuppressant use, and previous colonization.
机译:随着碳青霉烯类药物的使用增加,对碳青霉烯类药物具有耐药性的革兰氏阴性细菌已成为与卫生保健相关的感染的主要关注点。本研究旨在评估碳青霉烯类药物治疗期间突破性革兰氏阴性菌血症(GNB)的临床和微生物学特征,并评估突破性GNB发生的危险因素。 2005年至2014年在一家三级医院进行了病例对照研究。病例患者定义为血液培养中生长出革兰氏阴性细菌的患者,而患者在突破GNB之前接受碳青霉烯至少48小时。从接受碳青霉烯酮治疗至少48小时且在碳青霉烯酮治疗期间未出现突破性GNB的患者中选择年龄,性别和日期匹配的对照。总共鉴定出101例突破性GNB病例,并与100例对照进行了比较。导致突破性GNB的致病微生物为嗜麦芽嗜单胞菌(n = 33),鲍曼不动杆菌(n = 32),铜绿假单胞菌(n = 21)和其他微生物(n = 15)。大约90%的嗜麦芽孢杆菌分离株对左氧氟沙星和甲氧苄氨嘧啶-磺胺甲基异恶唑敏感。最常见的感染类型是原发菌血症(38.6%)和呼吸道感染(35.6%)。一半以上的患者在菌血症后一周内死亡,其30天死亡率为70.3%。在多变量分析中,更长的住院时间,血液系统恶性肿瘤,持续的中性粒细胞减少,免疫抑制剂的使用以及先前因病原微生物定植与突破性GNB显着相关。我们的数据表明,嗜碳链球菌,鲍曼不动杆菌和铜绿假单胞菌是碳青霉烯治疗期间突破性GNB的主要病原体,与住院时间更长,血液恶性肿瘤,持续中性粒细胞减少,免疫抑制剂的使用和先前的定植有关。

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