Arrindell Esmond L, Krishnan Ramesh, van der Merwe Marie, Caminita Frank, Howard Scott C, Zhang Jie, Buddington Randal K
Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee;
School of Health Studies, University of Memphis, Memphis, Tennessee;
Am J Physiol Lung Cell Mol Physiol. 2015 Nov 15;309(10):L1088-92. doi: 10.1152/ajplung.00292.2015. Epub 2015 Sep 25.
A translational preterm pig model analogous to infants born at 28 wk of gestation revealed that continuous positive airway pressure results in limited lung recruitment but does not prevent respiratory distress syndrome, whereas assist-control + volume guarantee (AC+VG) ventilation improves recruitment but can cause injury, highlighting the need for improved ventilation strategies. We determined whether airway pressure release ventilation (APRV) can be used to recruit the immature lungs of preterm pigs without injury. Spontaneously breathing pigs delivered at 89% of term (model for 28-wk infants) were randomized to 24 h of APRV (n = 9) vs. AC+VG with a tidal volume of 5 ml/kg (n = 10). Control pigs (n = 36) were provided with supplemental oxygen by an open mask. Nutrition and fluid support was provided throughout the 24-h period. All pigs supported with APRV and AC+VG survived 24 h, compared with 62% of control pigs. APRV resulted in improved lung volume recruitment compared with AC+VG based on radiographs, lower Pco2 levels (44 ± 2.9 vs. 53 ± 2.7 mmHg, P = 0.009) and lower inspired oxygen fraction requirements (36 ± 6 vs. 44 ± 11%, P < 0.001), and higher oxygenation index (5.1 ± 1.5 vs. 2.9 ± 1.1, P = 0.001). There were no differences between APRV and AC+VG pigs for heart rate, ratio of wet to dry lung mass, proinflammatory cytokines, or histopathological markers of lung injury. Lung protective ventilation with APRV improved recruitment of alveoli of preterm lungs, enhanced development and maintenance of functional residual capacity without injury, and improved clinical outcomes relative to AC+VG. Long-term consequences of lung volume recruitment by using APRV should be evaluated.
一种类似于孕28周出生婴儿的转化性早产猪模型显示,持续气道正压通气导致肺复张有限,但不能预防呼吸窘迫综合征,而辅助控制+容量保证(AC+VG)通气可改善肺复张,但可能导致损伤,这突出了改进通气策略的必要性。我们确定气道压力释放通气(APRV)是否可用于使早产猪未成熟的肺复张而不造成损伤。将孕89%(相当于28周婴儿的模型)时出生的自主呼吸猪随机分为接受24小时APRV组(n = 9)和潮气量为5 ml/kg的AC+VG组(n = 10)。对照组猪(n = 36)通过开放式面罩给予补充氧气。在整个24小时期间提供营养和液体支持。与62%的对照猪相比,所有接受APRV和AC+VG支持的猪均存活24小时。基于X线片,与AC+VG相比,APRV导致肺容量复张改善,Pco2水平更低(44±2.9 vs. 53±2.7 mmHg,P = 0.009),吸入氧分数需求更低(36±6 vs. 44±11%,P < 0.001),氧合指数更高(5.1±1.5 vs. 2.9±1.1,P = 0.001)。APRV组和AC+VG组猪在心率、肺湿重与干重之比、促炎细胞因子或肺损伤的组织病理学标志物方面无差异。与AC+VG相比,采用APRV的肺保护性通气改善了早产肺的肺泡复张,增强了功能残气量的发育和维持且无损伤,并改善了临床结局。应评估使用APRV进行肺容量复张的长期后果。