Influence of PCO2 Control on Clinical and Neurodevelopmental Outcomes of Extremely Low Birth Weight Infants

被引:15
|
作者
Thome, Ulrich H. [1 ]
Dreyhaupt, Jens
Genzel-Boroviczeny, Orsolya [2 ]
Bohnhorst, Bettina [3 ]
Schmid, Manuel [4 ]
Fuchs, Hans [5 ]
Rohde, Oliver [6 ]
Avenarius, Stefan [7 ]
Topf, Hans-Georg [8 ]
Zimmermann, Andrea [9 ]
Faas, Dirk [10 ]
Timme, Katharina [11 ]
Kleinlein, Barbara [12 ]
Buxmann, Horst [13 ]
Schenk, Wilfried [14 ]
Segerer, Hugo [15 ]
Teig, Norbert [16 ]
Ackermann, Benjamin [17 ]
Hentschel, Roland
Heckmann, Matthias
Schloesser, Rolf
Peters, Jochen
Rossi, Rainer
Rascher, Wolfgang [8 ,17 ]
Boettger, Ralf [4 ,7 ]
Seidenberg, Juergen [6 ]
Hansen, Gesine [3 ]
Bode, Harald [18 ]
Zernickel, Maria
Muches, Rainer [19 ]
Hummler, Helmut D. [4 ]
机构
[1] Univ Leipzig, Univ Hosp Children & Adolescents, Div Neonatol, Leipzig, Germany
[2] Ludwig Maximilian Univ Munich, IS Dr Hauner Univ Childrens Hosp, Div Neonatol, Munich, Germany
[3] Hannover Med Sch, Div Pediat Pneumol Allergol & Neonatol, Hannover, Germany
[4] Univ Ulm, Univ Hosp Children & Adolescents, Div Neonatol & Pediat Crit Care, Ulm, Germany
[5] Albert Ludwigs Univ Freiburg, Univ Hosp Children & Adolescents, Div Neonatol & Pediat Crit Care, Freiburg, Germany
[6] Carl von Ossietzky Univ Oldenburg, Elisabeth Childrens Hosp, Div Neonatol & Pediat Crit Care, Klinikum Oldenburg, Med Campus, Oldenburg, Germany
[7] Otto von Guericke Univ, Hosp Gen Pediat & Neonatol, Magdeburg, Germany
[8] Friedrich Alexander Univ Erlangen, Univ Hosp Children & Adolescents, Div Neonatol, Erlangen, Germany
[9] Tech Univ Munich, Klinikum Rechts Isar, Mutter Kind Zentrum, Munich, Germany
[10] Justus Liebig Univ Giessen, Univ Hosp Gen Pediat & Neonatol, Giessen, Germany
[11] Vivantes Hosp Neukolln, Hosp Children & Adolescents, Div Neonatol, Berlin, Germany
[12] Childrens Hosp Third Order, Hosp Children & Adolescents, Munich, Germany
[13] Goethe Univ Frankfurt Main, Univ Hosp Children & Adolescents JW, Div Neonatol, Frankfurt, Germany
[14] Cent Hosp Augsburg, Hosp Children & Adolescents, Augsburg, Germany
[15] Univ Regensburg, St Hedwig Hosp, Regensburg, Germany
[16] Ruhr Univ Bochum, Kathol Klinikum, Dept Neonatol & Pediat Intens Care, Bochum, Germany
[17] Ernst Moritz Arndt Univ Greifswald, Univ Hosp Children & Adolescents, Div Neonatol & Pediat Crit Care, Greifswald, Germany
[18] Univ Ulm, Univ Hosp Children & Adolescents, Div Neuropediatr, Ulm, Germany
[19] Univ Ulm, Inst Epidemiol & Med Biometry, Ulm, Germany
关键词
Neurodevelopmental outcome; Permissive hypercapnia; Bayley scales; Bronchopulmonary dysplasia; Intraventricular hemorrhage; EXTREMELY PRETERM INFANTS; SEVERE INTRAVENTRICULAR HEMORRHAGE; BRONCHOPULMONARY DYSPLASIA; HYPERCAPNIC ACIDOSIS; PRESSURE; FLUCTUATIONS; OXYGENATION; SURFACTANT; TARGETS; PHELBI;
D O I
10.1159/000485828
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Levels or fluctuations in the partial pressure of CO2 (PCO2) may affect outcomes for extremely low birth weight infants. Objectives: In an exploratory analysis of a randomized trial, we hypothesized that the PCO2 values achieved could be related to significant outcomes. Methods: 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 X-2 test, and the Fisher exact test as well as by multiple logistic regression. Results: 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 x FiO(2)). 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 x FiO(2) (p < 0.01). The incidence of adverse neurodevelopment was associated with birth weight (p < 0.001) and intraventricular hemorrhage (IVH; p < 0.01). Conclusions: Birth weight and respiratory morbidity, as measured by MAP x FiO(2), 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. (C) 2018 S. Karger AG, Basel
引用
收藏
页码:221 / 230
页数:10
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