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首页> 外文期刊>Clinical Infectious Diseases >Microbial Etiologies of Hospital-Acquired Bacterial Pneumonia and Ventilator-Associated Bacterial Pneumonia
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Microbial Etiologies of Hospital-Acquired Bacterial Pneumonia and Ventilator-Associated Bacterial Pneumonia

机译:医院获得性细菌性肺炎和呼吸机相关细菌性肺炎的微生物病因

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Hospital-acquired bacterial pneumonia (HABP) and ventilator-associated bacterial pneumonia (VABP) can be caused by a wide variety of bacteria that originate from the patient flora or the health care environment. We review the medical and microbiology literature and the results of the SENTRY Antimicrobial Surveillance Program (1997-2008) to establish the pathogens most likely to cause HABP or VABP. In all studies, a consistent 6 organisms (Staphylococcus aureus [28.0%], Pseudomonas aeruginosa [21.8%], Klebsiella species [9.8%], Escherichia coli [6.9%], Acinetobacter species [6.8%], and Enterobacter species [6.3%]) caused ∼80% of episodes, with lower prevalences of Serratia species, Stenotrophomonas maltophilia, and community-acquired pathogens, such as pneumococci and Haemophilus influenzae. Slight changes in the pathogen order were noted among geographic regions; Latin America had an increased incidence of nonfermentative gram-negative bacilli. In addition, VABP isolates of the same species had a mean of 5%-10% less susceptibility to frequently used extended-spectrum antimicrobials, and the rate of drug resistance among HABP and VABP pathogens has been increasing by 1% per year (2004-2008). In conclusion, the empirical treatment of HABP and VABP due to prevailing bacterial causes and emerging drug resistance has become more challenging and requires use of multidrug empirical treatment regimens for routine clinical practice. These facts have profound impact on the choices of comparison therapies to be applied in contemporary new drug clinical trials for pneumonia.
机译:医院获得性细菌性肺炎(HABP)和呼吸机相关细菌性肺炎(VABP)可能是由源自患者菌群或医疗环境的多种细菌引起的。我们回顾了医学和微生物学文献以及SENTRY抗菌监测计划(1997-2008年)的结果,以确定最可能引起HABP或VABP的病原体。在所有研究中,一致的6种生物体(金黄色葡萄球菌[28.0%],铜绿假单胞菌[21.8%],克雷伯菌属[9.8%],大肠杆菌[6.9%],不动杆菌属[6.8%]和肠杆菌属[6.3%] ])引起约80%的发作,沙雷氏菌,嗜麦芽单胞菌和嗜肺菌和流感嗜血杆菌等社区获得性病原体的患病率较低。注意到地理区域之间病原体顺序略有变化。拉丁美洲的非发酵革兰氏阴性菌发病率增加。此外,同一物种的VABP分离株对常用的广谱抗菌剂的敏感性降低了5%-10%,而且HABP和VABP病原体之间的耐药率每年以1%的速度增长(2004-2004年2008)。总之,由于主要的细菌病因和新出现的耐药性导致的HABP和VABP的经验治疗变得更具挑战性,并且需要在常规临床实践中使用多药经验治疗方案。这些事实对肺炎的当代新药临床试验中采用的比较疗法的选择产生了深远的影响。

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