TY - JOUR
T1 - Influence of PCO2 Control on Clinical and Neurodevelopmental Outcomes of Extremely Low Birth Weight Infants
AU - For the PHELBI Study Group
AU - Thome, Ulrich H.
AU - Dreyhaupt, Jens
AU - Genzel-Boroviczeny, Orsolya
AU - Bohnhorst, Bettina
AU - Schmid, Manuel
AU - Fuchs, Hans
AU - Rohde, Oliver
AU - Avenarius, Stefan
AU - Topf, Hans Georg
AU - Zimmermann, Andrea
AU - Faas, Dirk
AU - Timme, Katharina
AU - Kleinlein, Barbara
AU - Buxmann, Horst
AU - Schenk, Wilfried
AU - Segerer, Hugo
AU - Teig, Norbert
AU - Ackermann, Benjamin
AU - Hentschel, Roland
AU - Heckmann, Matthias
AU - Schlösser, Rolf
AU - Peters, Jochen
AU - Rossi, Rainer
AU - Rascher, Wolfgang
AU - Böttger, Ralf
AU - Seidenberg, Jürgen
AU - Hansen, Gesine
AU - Bode, Harald
AU - Zernickel, Maria
AU - Muche, Rainer
AU - Hummler, Helmut D.
N1 - Publisher Copyright:
© 2018 S. Karger AG, Basel.
PY - 2018/3/1
Y1 - 2018/3/1
N2 - 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 χ2 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 × 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). Conclusions: 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.
AB - 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 χ2 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 × 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). Conclusions: 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.
KW - Bayley scales
KW - Bronchopulmonary dysplasia
KW - Intraventricular hemorrhage
KW - Neurodevelopmental outcome
KW - Permissive hypercapnia
UR - http://www.scopus.com/inward/record.url?scp=85040041305&partnerID=8YFLogxK
U2 - 10.1159/000485828
DO - 10.1159/000485828
M3 - Article
C2 - 29298438
AN - SCOPUS:85040041305
SN - 1661-7800
VL - 113
SP - 221
EP - 230
JO - Neonatology
JF - Neonatology
IS - 3
ER -