Department of Epidemiology, Colorado School of Public Health, University of Colorado Denver, Aurora, CO.
Department of Anesthesiology, Section of Pediatric Critical Care Medicine, Wake Forest University School of Medicine, Winston-Salem, NC.
Crit Care Med. 2019 Jul;47(7):e547-e554. doi: 10.1097/CCM.0000000000003766.
We sought to compare the performance of the 2008 Centers for Disease Control and Prevention Pediatric criteria for ventilator-associated pneumonia, the 2013 Adult Ventilator-Associated Condition criteria, the new Draft Pediatric Ventilator-Associated Condition criteria, and physician-diagnosed ventilator-associated pneumonia in a cohort of PICU patients.
Secondary analysis of a previously conducted prospective observational study.
PICU within a tertiary care children's hospital between April 1, 2010, and April 1, 2011.
Patients between 31 days and 18 years old, mechanically ventilated via endotracheal tube for more than 72 hours and no limitations of care.
None.
Ventilator-associated pneumonia criteria applied in real time and ventilator-associated condition criteria applied retrospectively. Outcomes assessed between cases and noncases within criteria. Of the 133 eligible participants, 24 (18%) had ventilator-associated pneumonia by 2008 Pediatric criteria and 27 (20%) by physician diagnosis. Sixteen (12%) and 10 (8%) had ventilator-associated condition by 2013 Adult and Draft Pediatric criteria, respectively. We found significant overlap between cases identified with 2008 Pediatric criteria and physician diagnosis (p = 0.549), but comparisons between the other definitions revealed that the newer criteria identify different patients than previous Centers for Disease Control and Prevention ventilator-associated pneumonia criteria and physician diagnosis (p < 0.01). Although 20 participants were diagnosed with ventilator-associated pneumonia by 2008 Pediatric criteria and physician diagnosis, only three participants were identified by all four criteria. Three subjects uniquely identified by the Draft Pediatric criteria were noninfectious in etiology. Cases identified by all criteria except Draft Pediatric had higher ratios of actual ICU length of stay to Pediatric Risk of Mortality III-adjusted expected length of stay compared with noncases.
The Draft Pediatric criteria identify fewer and different patients than previous ventilator-associated pneumonia criteria or physician diagnosis, potentially missing patients with preventable harms, but also identified patients with potentially preventable noninfectious respiratory deteriorations. Further investigations are required to maximize the identification of patients with preventable harms from mechanical ventilation.
我们旨在比较 2008 年美国疾病控制与预防中心儿科呼吸机相关性肺炎标准、2013 年成人呼吸机相关性条件标准、新的草案儿科呼吸机相关性条件标准以及在儿科重症监护病房(PICU)患者队列中由医生诊断的呼吸机相关性肺炎之间的性能。
对先前进行的前瞻性观察研究进行二次分析。
2010 年 4 月 1 日至 2011 年 4 月 1 日期间,三级儿童保健医院内的 PICU。
年龄在 31 天至 18 岁之间,通过气管内插管机械通气超过 72 小时且无护理限制的患者。
无。
实时应用呼吸机相关性肺炎标准和回顾性应用呼吸机相关性条件标准。在标准内评估病例和非病例之间的结果。在 133 名合格参与者中,24 名(18%)根据 2008 年儿科标准和 27 名(20%)由医生诊断患有呼吸机相关性肺炎。16 名(12%)和 10 名(8%)根据 2013 年成人和草案儿科标准患有呼吸机相关性条件。我们发现使用 2008 年儿科标准和医生诊断识别的病例之间存在显著重叠(p = 0.549),但对其他定义的比较表明,较新的标准确定的患者与以前的疾病控制与预防中心呼吸机相关性肺炎标准和医生诊断不同(p < 0.01)。尽管有 20 名参与者根据 2008 年儿科标准和医生诊断诊断为呼吸机相关性肺炎,但只有 3 名参与者根据所有 4 项标准被识别。根据草案儿科标准唯一确定的 3 名受试者在病因上是非传染性的。除草案儿科标准外,根据所有标准确定的病例的实际 ICU 住院时间与儿科风险死亡率 III 调整后的预期住院时间的比例高于非病例。
草案儿科标准确定的患者数量较少,与以前的呼吸机相关性肺炎标准或医生诊断不同,可能会错过可预防危害的患者,但也确定了可能有预防措施的非传染性呼吸恶化的患者。需要进一步研究以最大限度地识别可从机械通气中受益的患者。