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首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Delayed Extubation to Nasal Continuous Positive Airway Pressure in the Immature Baboon Model of Bronchopulmonary Dysplasia: Lung Clinical and Pathological Findings
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Delayed Extubation to Nasal Continuous Positive Airway Pressure in the Immature Baboon Model of Bronchopulmonary Dysplasia: Lung Clinical and Pathological Findings

机译:支气管肺发育不良的不成熟狒狒模型中延迟拔管至鼻腔持续气道正压的肺临床和病理学发现

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OBJECTIVE. Using the 125-day baboon model of bronchopulmonary dysplasia treated with prenatal steroid and exogenous surfactant, we hypothesized that a delay of extubation from low tidal volume positive pressure ventilation to nasal continuous positive airway pressure at 5 days (delayed nasal continuous positive airway pressure group) would not induce more lung injury when compared with baboons aggressively weaned to nasal continuous positive airway pressure at 24 hours (early nasal continuous positive airway pressure group), because both received positive pressure ventilation.METHODS AND RESULTS. After delivery by cesarean section at 125 days (term: 185 days), infants received 2 doses of Curosurf (Chiesi Farmaceutica S.p.A., Parma, Italy) and daily caffeine citrate. The delay in extubation to 5 days resulted in baboons in the delayed nasal continuous positive airway pressure group having a lower arterial to alveolar oxygen ratio, high Paco2, and worse respiratory function. The animals in the delayed nasal continuous positive airway pressure group exhibited a poor respiratory drive that contributed to more reintubations and time on mechanical ventilation. A few animals in both groups developed necrotizing enterocolitis and/or sepsis, but infectious pneumonias were not documented. Cellular bronchiolitis and peribronchiolar alveolar wall thickening were more frequently seen in the delayed nasal continuous positive airway pressure group. Bronchoalveolar lavage levels of interleukin-6, interleukin-8, monocyte chemotactic protein-1, macrophage inflammatory protein-1 α, and growth-regulated oncogene-α were significantly increased in the delayed nasal continuous positive airway pressure group. Standard and digital morphometric analyses showed no significant differences in internal surface area and nodal measurements between the groups. Platelet endothelial cell adhesion molecule vascular staining was not significantly different between the 2 nasal continuous positive airway pressure groups.CONCLUSIONS. Volutrauma and/or low-grade colonization of airways secondary to increased reintubations and ventilation times are speculated to play causative roles in the delayed nasal continuous positive airway pressure group findings.
机译:目的。使用产前类固醇和外源性表面活性剂治疗的125天狒狒狒狒模型,我们假设在5天时从低潮气量正压通气到鼻持续气道正压延迟拔管(延迟的鼻持续气道正压组)与狒狒在24小时主动断奶至鼻持续气道正压通气(早期鼻持续气道正压通气组)相比,它不会引起更多的肺损伤,因为它们都接受了正压通气。方法和结果。在125天(足月:185天)通过剖宫产分娩后,婴儿接受了2剂Curosurf(意大利帕尔马的Chiesi Farmaceutica S.p.A.)和柠檬酸咖啡因。拔管延迟至5天导致狒狒鼻延迟持续气道正压通气组具有较低的动脉与肺泡氧比,较高的Paco2和较差的呼吸功能。延迟鼻持续气道正压通气组的动物表现出较差的呼吸驱动力,这导致更多的再次插管和机械通气时间。两组中的一些动物都发展为坏死性小肠结肠炎和/或败血症,但未记录到感染性肺炎。在延迟的鼻持续气道正压通气组中,细胞性细支气管炎和支气管周围肺泡壁增厚更为常见。在延迟鼻持续气道正压通气组中,白细胞介素6,白细胞介素8,单核细胞趋化蛋白-1,巨噬细胞炎性蛋白-1α和生长调节癌基因α的支气管肺泡灌洗水平显着增加。标准形态和数字形态分析表明,两组之间的内表面积和淋巴结测量值无显着差异。两组鼻腔持续气道正压通气组之间的血小板内皮细胞粘附分子血管染色无明显差异。据推测,由于重新插管和通气时间增加,继发于气道的轻度定植和/或低度定植在延迟持续的鼻持续气道正压组发现中起着致病作用。

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