The Global and Tropical Health Division, Menzies School of Health Research, Charles Darwin University; Department of Infectious Diseases, Royal Darwin Hospital, Darwin, NT, Australia.
The Global and Tropical Health Division, Menzies School of Health Research, Charles Darwin University.
Chest. 2014 Oct;146(4):1038-1045. doi: 10.1378/chest.13-3065.
The genus Acinetobacter, well known as a nosocomial pathogen, can also cause severe community-onset pneumonia. Previous small case series have suggested fulminant disease and a pooled hospital mortality of > 60%.
We conducted a prospective observational study of all episodes of bacteremic, community-onset, and radiologically confirmed pneumonia due to Acinetobacter species at a tertiary referral hospital in tropical Australia from 1997 to 2012 following the introduction of routine empirical treatment protocols covering Acinetobacter. Demographic, clinical, microbiologic, and outcome data were collected.
There were 41 episodes of bacteremic community-onset Acinetobacter pneumonia, of which 36 had no indicators suggesting health-care-associated infection. Of these, 38 (93%) were Indigenous Australians, one-half were men, the average age was 44.1 years, and 36 episodes (88%) occurred during the rainy season. All patients had at least one risk factor, with hazardous alcohol intake in 82%. Of the 37 isolates available for molecular speciation, 35 were Acinetobacter baumannii and two were Acinetobacter nosocomialis. All isolates were susceptible in vitro to gentamicin, meropenem, and ciprofloxacin, but only one was fully susceptible to ceftriaxone. ICU admission was required in 80%. All 41 patients received appropriate antibiotics within the first 24 h of admission, and 28- and 90-day mortality were both low at 11%.
Community-acquired Acinetobacter pneumonia is a severe disease, with the majority of patients requiring ICU admission. Most patients have risk factors, particularly hazardous alcohol use. Despite this severity, correct initial empirical antibiotic therapy in all patients was associated with low mortality.
不动杆菌属,众所周知是一种医院获得性病原体,也可引起严重的社区获得性肺炎。之前的小病例系列研究表明,该病可能迅速恶化,医院病死率>60%。
我们对 1997 年至 2012 年期间,在澳大利亚热带地区的一家三级转诊医院中,所有血源性、社区获得性和放射学确诊的不动杆菌属引起的肺炎进行了前瞻性观察性研究。纳入标准为采用常规经验性治疗方案覆盖不动杆菌属的情况下,符合血源性、社区获得性和放射学确诊的肺炎。收集人口统计学、临床、微生物学和结局数据。
共发生 41 例血源性社区获得性不动杆菌肺炎,其中 36 例无提示医源性感染的指标。其中,38 例(93%)为澳大利亚原住民,半数为男性,平均年龄 44.1 岁,36 例(88%)发生在雨季。所有患者均存在至少一个危险因素,82%的患者有危险的饮酒史。37 株可供分子种属鉴定的分离株中,35 株为鲍曼不动杆菌,2 株为鲍氏不动杆菌。所有分离株体外均对庆大霉素、美罗培南和环丙沙星敏感,但仅有 1 株对头孢曲松完全敏感。80%的患者需要入住 ICU。所有 41 例患者均在入院后 24 小时内接受了适当的抗生素治疗,28 天和 90 天的死亡率均较低,分别为 11%。
社区获得性不动杆菌肺炎是一种严重疾病,大多数患者需要入住 ICU。大多数患者存在危险因素,特别是危险的饮酒史。尽管病情严重,但所有患者的初始经验性抗生素治疗正确,死亡率均较低。