Moler F W, Palmisano J M, Custer J R, Meliones J N, Bartlett R H
Department of Pediatrics, University of Michigan Hospitals, Ann Arbor 48109-0718.
Crit Care Med. 1994 Apr;22(4):620-5. doi: 10.1097/00003246-199404000-00018.
Recent reports have described the usefulness of the alveolar-arterial oxygen tension difference (P[A-a]O2) in predicting mortality in children with acute respiratory failure managed with mechanical ventilation. We reviewed our experience with extracorporeal life support for acute pediatric respiratory failure and specifically examined P(A-a)O2 measurements during the 24 hrs before extracorporeal life support to determine if defined cutoffs established with conventional mechanical ventilation were applicable to extracorporeal life-support survival.
Retrospective, case-series chart review.
A university tertiary medical center.
Infants and children (n = 36), one month to 18 yrs of age, with severe life-threatening respiratory failure who were believed to have failed conventional mechanical ventilatory support.
Veno-venous or veno-arterial extracorporeal life support.
From 1982 to 1992, we managed 36 pediatric patients with severe respiratory failure using extracorporeal life support. We identified 28 patients who had P(A-a)O2 values of > 400 torr (> 53.3 kPa) for the 24-hr time period before placement on bypass. At the time of bypass initiation, all blood gas and mechanical ventilator parameters except PaCO2 showed trends of worsening pulmonary function, compared with measurements done 24 hrs before bypass initiation. Oxygenation-related variables showed statistically significant worsening trends when measured 24 hrs before bypass, compared with the time of bypass: P(A-a)O2 539 vs. 582 torr (71.9 vs. 77.6 kPa), p < .01; PaO2/FIO2 ratio 70 vs. 57 torr (9.3 vs. 7.6 kPa), p < .05; oxygenation index 32 vs. 47 cm H2O/torr, p < .01; and FIO2 0.94 vs. 0.98, p < .05. Sixty-one percent of extracorporeal life support-managed patients (17 of 28) survived their life-threatening respiratory illness to be discharged home.
Based on previous reports of the utility of P(A-a)O2 measurements to predict mortality, our preliminary evidence suggests that extracorporeal life support results in 62% survival for pediatric respiratory failure patients predicted to have no chance of survival using conventional mechanical ventilation. Prospective, randomized trials of children with severe acute respiratory failure managed with mechanical ventilation vs. extracorporeal life support may be indicated.
最近的报告描述了肺泡-动脉血氧分压差(P[A-a]O2)在预测接受机械通气治疗的急性呼吸衰竭儿童死亡率方面的作用。我们回顾了我们在小儿急性呼吸衰竭体外生命支持方面的经验,并特别检查了体外生命支持前24小时内的P(A-a)O2测量值,以确定常规机械通气所确定的特定临界值是否适用于体外生命支持下的生存情况。
回顾性病例系列图表审查。
一所大学三级医疗中心。
年龄1个月至18岁的婴儿和儿童(n = 36),患有严重危及生命的呼吸衰竭,被认为常规机械通气支持治疗失败。
静脉-静脉或静脉-动脉体外生命支持。
从1982年到1992年,我们使用体外生命支持治疗了36例小儿严重呼吸衰竭患者。我们确定了28例患者在接受体外循环前24小时内P(A-a)O2值> 400托(> 53.3 kPa)。在开始体外循环时,与体外循环开始前24小时的测量值相比,除PaCO2外,所有血气和机械通气参数均显示肺功能有恶化趋势。与体外循环时相比,在体外循环前24小时测量时,与氧合相关的变量显示出统计学上显著的恶化趋势:P(A-a)O2为539对582托(71.9对77.6 kPa),p <.01;PaO2/FIO2比值为70对57托(9.3对7.6 kPa),p <.05;氧合指数为32对47 cm H2O/托,p <.01;FIO2为0.94对0.98,p <.05。接受体外生命支持治疗的患者中有61%(28例中的17例)在危及生命的呼吸疾病中存活并出院回家。
基于先前关于P(A-a)O2测量值用于预测死亡率的效用的报告,我们的初步证据表明,对于预计使用常规机械通气没有生存机会的小儿呼吸衰竭患者,体外生命支持的生存率为62%。可能需要对接受机械通气与体外生命支持治疗的严重急性呼吸衰竭儿童进行前瞻性随机试验。