Thome Ulrich H, Dreyhaupt Jens, Genzel-Boroviczeny Orsolya, Bohnhorst Bettina, Schmid Manuel, Fuchs Hans, Rohde Oliver, Avenarius Stefan, Topf Hans-Georg, Zimmermann Andrea, Faas Dirk, Timme Katharina, Kleinlein Barbara, Buxmann Horst, Schenk Wilfried, Segerer Hugo, Teig Norbert, Ackermann Benjamin, Hentschel Roland, Heckmann Matthias, Schlösser Rolf, Peters Jochen, Rossi Rainer, Rascher Wolfgang, Böttger Ralf, Seidenberg Jürgen, Hansen Gesine, Bode Harald, Zernickel Maria, Muche Rainer, Hummler Helmut D
Division of Neonatology, University Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany.
Neonatology. 2018;113(3):221-230. doi: 10.1159/000485828. Epub 2018 Jan 4.
Levels or fluctuations in the partial pressure of CO2 (PCO2) may affect outcomes for extremely low birth weight infants.
In an exploratory analysis of a randomized trial, we hypothesized that the PCO2 values achieved could be related to significant outcomes.
On each treatment day, infants were divided into 4 groups: relative hypocapnia, normocapnia, hypercapnia, or fluctuating PCO2. Ultimate assignment to a group for the purpose of this analysis was made according to the group in which an infant spent the most days. Statistical analyses were performed with analysis of variance (ANOVA), the Kruskal-Wallis test, the χ2 test, and the Fisher exact test as well as by multiple logistic regression.
Of the 359 infants, 57 were classified as hypocapnic, 230 as normocapnic, 70 as hypercapnic, and 2 as fluctuating PCO2. Hypercapnic infants had a higher average product of mean airway pressure and fraction of inspired oxygen (MAP × FiO2). For this group, mortality was higher, as was the likelihood of having moderate/severe bronchopulmonary dysplasia (BPD), necrotizing enterocolitis (NEC), and poorer neurodevelopment. Multiple logistic regression analyses showed an increased risk for BPD or death associated with birth weight (p < 0.001) and MAP × FiO2 (p < 0.01). The incidence of adverse neurodevelopment was associated with birth weight (p < 0.001) and intraventricular hemorrhage (IVH; p < 0.01).
Birth weight and respiratory morbidity, as measured by MAP × FiO2, were the most predictive of death or BPD and NEC, whereas poor neurodevelopmental outcome was associated with low birth weight and IVH. Univariate models also identified PCO2. Thus, hypercapnia seems to reflect greater disease severity, a likely contributor to differences in outcomes.
二氧化碳分压(PCO₂)水平或波动可能会影响极低出生体重儿的预后。
在一项随机试验的探索性分析中,我们假设所达到的PCO₂值可能与重要预后相关。
在每个治疗日,将婴儿分为4组:相对低碳酸血症组、正常碳酸血症组、高碳酸血症组或PCO₂波动组。为进行本分析,最终分组是根据婴儿在其中度过天数最多的组来确定的。采用方差分析(ANOVA)、Kruskal-Wallis检验、χ²检验、Fisher精确检验以及多因素逻辑回归进行统计分析。
359例婴儿中,57例被归类为低碳酸血症,230例为正常碳酸血症,70例为高碳酸血症,2例为PCO₂波动。高碳酸血症婴儿的平均气道压与吸入氧分数的乘积(MAP×FiO₂)较高。对于该组,死亡率更高,发生中度/重度支气管肺发育不良(BPD)、坏死性小肠结肠炎(NEC)的可能性以及神经发育较差的情况也更高。多因素逻辑回归分析显示,与出生体重(p<0.001)和MAP×FiO₂(p<0.01)相关的BPD或死亡风险增加。不良神经发育的发生率与出生体重(p<0.001)和脑室内出血(IVH;p<0.01)相关。
出生体重和以MAP×FiO₂衡量的呼吸疾病是死亡或BPD及NEC的最有力预测因素,而不良神经发育结局与低出生体重和IVH相关。单因素模型也确定了PCO₂。因此,高碳酸血症似乎反映了更高的疾病严重程度,这可能是导致预后差异的一个因素。