Cook D J, Walter S D, Cook R J, Griffith L E, Guyatt G H, Leasa D, Jaeschke R Z, Brun-Buisson C
McMaster University, Hamilton, Ontario, Canada.
Ann Intern Med. 1998 Sep 15;129(6):433-40. doi: 10.7326/0003-4819-129-6-199809150-00002.
Understanding the risk factors for ventilator-associated pneumonia can help to assess prognosis and devise and test preventive strategies.
To examine the baseline and time-dependent risk factors for ventilator-associated pneumonia and to determine the conditional probability and cumulative risk over the duration of stay in the intensive care unit.
Prospective cohort study.
16 intensive care units in Canada.
1014 mechanically ventilated patients.
Demographic and time-dependent variables reflecting illness severity, ventilation, nutrition, and drug exposure. Pneumonia was classified by using five methods: adjudication committee, bedside clinician's diagnosis, Centers for Disease Control and Prevention definition, Clinical Pulmonary Infection score, and positive culture from bronchoalveolar lavage or protected specimen brush.
177 of 1014 patients (17.5%) developed ventilator-associated pneumonia 9.0 +/- 5.9 days (median, 7 days [interquartile range, 5 to 10 days]) after admission to the intensive care unit. Although the cumulative risk increased over time, the daily hazard rate decreased after day 5 (3.3% at day 5, 2.3% at day 10, and 1.3% at day 15). Independent predictors of ventilator-associated pneumonia in multivariable analysis were a primary admitting diagnosis of burns (risk ratio, 5.09 [95% CI, 1.52 to 17.03]), trauma (risk ratio, 5.00 [CI, 1.91 to 13.11]), central nervous system disease (risk ratio, 3.40 [CI, 1.31 to 8.81]), respiratory disease (risk ratio, 2.79 [CI, 1.04 to 7.51]), cardiac disease (risk ratio, 2.72 [CI, 1.05 to 7.01]), mechanical ventilation in the previous 24 hours (risk ratio, 2.28 [CI, 1.11 to 4.68]), witnessed aspiration (risk ratio, 3.25 [CI, 1.62 to 6.50]), and paralytic agents (risk ratio, 1.57 [CI, 1.03 to 2.39]). Exposure to antibiotics conferred protection (risk ratio, 0.37 [CI, 0.27 to 0.51]). Independent risk factors were the same regardless of the pneumonia definition used.
The daily risk for pneumonia decreases with increasing duration of stay in the intensive care unit. Witnessed aspiration and exposure to paralytic agents are potentially modifiable independent risk factors. Exposure to antibiotics was associated with low rates of early ventilator-associated pneumonia, but this effect attenuates over time.
了解呼吸机相关性肺炎的危险因素有助于评估预后,并制定和测试预防策略。
研究呼吸机相关性肺炎的基线和时间依赖性危险因素,并确定重症监护病房住院期间的条件概率和累积风险。
前瞻性队列研究。
加拿大的16个重症监护病房。
1014例机械通气患者。
反映疾病严重程度、通气、营养和药物暴露情况的人口统计学和时间依赖性变量。肺炎采用五种方法分类:判定委员会、床边临床医生诊断、疾病控制和预防中心定义、临床肺部感染评分以及支气管肺泡灌洗或保护性标本刷检的阳性培养结果。
1014例患者中有177例(17.5%)在入住重症监护病房9.0±5.9天(中位数,7天[四分位间距,5至10天])后发生呼吸机相关性肺炎。尽管累积风险随时间增加,但第5天后每日危险率下降(第5天为3.3%,第10天为2.3%,第15天为1.3%)。多变量分析中,呼吸机相关性肺炎的独立预测因素包括主要入院诊断为烧伤(风险比,5.09[95%CI,1.52至17.03])、创伤(风险比,5.00[CI,1.91至13.11])、中枢神经系统疾病(风险比,3.40[CI,1.31至8.81])、呼吸系统疾病(风险比,2.79[CI,1.04至7.51])、心脏病(风险比,2.72[CI,1.05至7.01])、前24小时内进行机械通气(风险比,2.28[CI,1.11至4.68])、目睹误吸(风险比,3.25[CI,1.62至6.50])以及使用麻痹剂(风险比,1.57[CI,1.03至2.39])。使用抗生素有保护作用(风险比,0.37[CI,0.27至0.51])。无论采用何种肺炎定义,独立危险因素均相同。
重症监护病房住院时间越长,肺炎的每日风险越低。目睹误吸和使用麻痹剂是潜在可改变的独立危险因素。使用抗生素与早期呼吸机相关性肺炎的低发生率相关,但这种效应会随时间减弱。