Crouch Brewer S, Wunderink R G, Jones C B, Leeper K V
Department of Medicine, University of Tennessee, Memphis, USA.
Chest. 1996 Apr;109(4):1019-29. doi: 10.1378/chest.109.4.1019.
Ventilator-associated pneumonia (VAP) caused by Pseudomonas aeruginosa has been associated with higher case fatality rates than VAP caused by other bacterial etiologies. The causes of this excess mortality are unclear.
Retrospective review of 38 consecutive ventilated patients with Pseudomonas pneumonia, documented by highly reliable methods. Charts of five additional patients were unavailable for review.
Medical ICUs of a university-affiliated Veterans Affairs Medical Center and a university-affiliated municipal hospital.
Prospectively collected hospital admission acute physiologic and chronic health examination (APACHE) II scores and cause of ICU admission. Retrospectively calculated organ failure and APACHE scores, VAP score. Clinical and microbiologic variables. Antibiotic treatment and outcome. Direct cause of death by standard definitions.
Overall mortality was 69% (26/38), significantly higher than the APACHE II predicted mortality of 42.6% (p=0.037). At least 38% (10/26) of deaths were directly attributable to Pseudomonas VAP. Multivariate analysis of factors associated with death found infectious cause for ICU admission (odds ratio [OR]=8.67; 95% confidence interval [CI], 0.86 to 85.94) and number of organ dysfunctions on the day of diagnosis (OR=1.73, 95% CI, 1.02 to 2.92) were significant. Septic shock from Pseudomonas VAP, septic shock from subsequent infection, and multiple organ dysfunction syndrome were the most common immediate causes of death. Mortality increased linearly with increasing APACHE III score on the day of diagnosis. Of initial antibiotic regimens, 67% (26/36) were considered failures. Persistent pneumonia occurred in 35% of patients while recurrent pneumonia was unusual (1/38).
Development of Pseudomonas pneumonia results in a mortality rate in excess of that due to the presenting illness. The attributable mortality determined by several means appears to approach 40%. The excess mortality appears to be related to the host defense response to the pneumonia rather than any characteristic of the pneumonia. Even standard antibiotic regimens fail frequently and do not prevent the excess mortality. Since at least 38% of deaths can be directly attributable to the Pseudomonas pneumonia, improvement in therapy is needed.
由铜绿假单胞菌引起的呼吸机相关性肺炎(VAP)的病死率高于其他细菌病因所致的VAP。这种额外死亡率的原因尚不清楚。
对38例连续的经可靠方法确诊为假单胞菌肺炎的机械通气患者进行回顾性研究。另外5例患者的病历无法查阅。
一所大学附属医院的退伍军人事务医疗中心和一所大学附属医院的市级医院的内科重症监护病房。
前瞻性收集患者入院时的急性生理与慢性健康状况评估(APACHE)II评分及入住重症监护病房的原因。回顾性计算器官功能衰竭和APACHE评分、VAP评分。临床和微生物学变量。抗生素治疗及结局。按照标准定义确定直接死因。
总体死亡率为69%(26/38),显著高于APACHE II预测的死亡率42.6%(p = 0.037)。至少38%(10/26)的死亡直接归因于铜绿假单胞菌VAP。对与死亡相关因素的多变量分析发现,入住重症监护病房的感染原因(比值比[OR]=8.67;95%置信区间[CI],0.86至85.94)以及诊断当天器官功能障碍的数量(OR = 1.73,95% CI,1.02至2.92)具有显著意义。铜绿假单胞菌VAP所致的感染性休克、继发感染所致的感染性休克以及多器官功能障碍综合征是最常见的直接死因。死亡率随诊断当天APACHE III评分的增加呈线性上升。在初始抗生素治疗方案中,67%(26/36)被认为治疗失败。35%的患者发生持续性肺炎,而复发性肺炎并不常见(1/38)。
铜绿假单胞菌肺炎的发生导致的死亡率超过了因当前疾病所致的死亡率。通过多种方法确定的可归因死亡率似乎接近40%。额外死亡率似乎与宿主对肺炎的防御反应有关,而非肺炎的任何特征。即使是标准的抗生素治疗方案也经常失败,无法预防额外死亡率。由于至少38%的死亡可直接归因于铜绿假单胞菌肺炎,因此需要改进治疗方法。