First postnatal lactate blood levels on day 1 and outcome of preterm infants with gestational age <29 weeks.

all-cause mortality bronchopulmonary dysplasia extremely preterm infants intraventricular haemorrhage lactate levels small for gestational age

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2024
Historique:
received: 03 06 2024
accepted: 17 09 2024
medline: 18 10 2024
pubmed: 18 10 2024
entrez: 18 10 2024
Statut: epublish

Résumé

Serum lactate levels are used as biomarkers for perinatal asphyxia, while their value for outcome prediction in preterm infants is uncertain. It was the aim of this observational study to determine the association of the first postnatal serum-lactate levels on day 1 of life and short-term outcome in preterm infants less than 29 gestational weeks. We analysed data in a population-based cohort of German Neonatal Network (GNN) preterm infants with available first postnatal lactate levels enrolled at 22-28 weeks of gestational age (GA) between 1st of April 2009 and 31st December 2020. We hypothesized that high lactate levels as measured in mmol/L increase the risk of intraventricular haemorrhage (IVH) and bronchopulmonary dysplasia (BPD) in infants with VLBW regardless of small-for-gestational-age (SGA) status. Hypotheses were evaluated in univariate analyses and multiple logistic regression models. First postnatal lactate levels were available in 2499 infants. The study population had a median GA of 26.7 [IQR 25.2-27.9] weeks and birth weight of 840 g [IQR 665-995]. Infants with short-term complications such as IVH and BPD had higher initial lactate levels than non-affected infants. The positive predictive value of a lactate cut-off of 4 mmol/L was 0.28 for IVH and 0.30 for BPD. After adjustment for known confounding variables, each 1 mmol/L increase of day 1 lactate levels was associated with a modestly increased risk of IVH (OR 1.18; 95% CI 1.03-1.37; In our observational cohort study higher initial lactate levels were associated with adverse outcome regardless of SGA status. However, the predictive value of lactate cut-off levels such as 4 mmol/L is low.

Sections du résumé

Background UNASSIGNED
Serum lactate levels are used as biomarkers for perinatal asphyxia, while their value for outcome prediction in preterm infants is uncertain. It was the aim of this observational study to determine the association of the first postnatal serum-lactate levels on day 1 of life and short-term outcome in preterm infants less than 29 gestational weeks.
Methods UNASSIGNED
We analysed data in a population-based cohort of German Neonatal Network (GNN) preterm infants with available first postnatal lactate levels enrolled at 22-28 weeks of gestational age (GA) between 1st of April 2009 and 31st December 2020. We hypothesized that high lactate levels as measured in mmol/L increase the risk of intraventricular haemorrhage (IVH) and bronchopulmonary dysplasia (BPD) in infants with VLBW regardless of small-for-gestational-age (SGA) status. Hypotheses were evaluated in univariate analyses and multiple logistic regression models.
Results UNASSIGNED
First postnatal lactate levels were available in 2499 infants. The study population had a median GA of 26.7 [IQR 25.2-27.9] weeks and birth weight of 840 g [IQR 665-995]. Infants with short-term complications such as IVH and BPD had higher initial lactate levels than non-affected infants. The positive predictive value of a lactate cut-off of 4 mmol/L was 0.28 for IVH and 0.30 for BPD. After adjustment for known confounding variables, each 1 mmol/L increase of day 1 lactate levels was associated with a modestly increased risk of IVH (OR 1.18; 95% CI 1.03-1.37;
Conclusions UNASSIGNED
In our observational cohort study higher initial lactate levels were associated with adverse outcome regardless of SGA status. However, the predictive value of lactate cut-off levels such as 4 mmol/L is low.

Identifiants

pubmed: 39421035
doi: 10.3389/fped.2024.1443066
pmc: PMC11484003
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1443066

Informations de copyright

© 2024 Zipf, Fortmann, Härtel, Andres, Frieauff, Paul, Häfke, Reutter, Morhart, Weller, Welp, Kipke, Herting, Humberg, Göpel and Hanke.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Stephanie Zipf (S)

Department of Pediatrics, University of Würzburg, Würzburg, Germany.

Ingmar Fortmann (I)

Department of Pediatrics, University Hospital Schleswig-Holstein/ Campus Lübeck, Lübeck, Germany.

Christoph Härtel (C)

Department of Pediatrics, University of Würzburg, Würzburg, Germany.

Oliver Andres (O)

Department of Pediatrics, University of Würzburg, Würzburg, Germany.

Eric Frieauff (E)

Department of Pediatrics, University of Würzburg, Würzburg, Germany.

Pia Paul (P)

Department of Pediatrics, University of Würzburg, Würzburg, Germany.

Anna Häfke (A)

Department of Pediatrics, University of Würzburg, Würzburg, Germany.

Heiko Reutter (H)

Department of Pediatrics, and Adolescent Medicine, Devision of Neonatology and Pediatric Intensive Care, University Hospital Erlangen, Erlangen, Germany.

Patrick Morhart (P)

Department of Pediatrics, and Adolescent Medicine, Devision of Neonatology and Pediatric Intensive Care, University Hospital Erlangen, Erlangen, Germany.

Ursula Weller (U)

Department of Pediatrics, University of Bielefeld, Bielefeld, Germany.

Amrei Welp (A)

Department of Obstetrics and Gynaecology, University Hospital Schleswig-Holstein/Campus Lübeck, Lübeck, Germany.

Henry Kipke (H)

Department of Pediatrics, University Hospital Schleswig-Holstein/ Campus Lübeck, Lübeck, Germany.

Egbert Herting (E)

Department of Pediatrics, University Hospital Schleswig-Holstein/ Campus Lübeck, Lübeck, Germany.

Alexander Humberg (A)

Department of Pediatrics, University Hospital Münster, Münster, Germany.

Wolfgang Göpel (W)

Department of Pediatrics, University Hospital Schleswig-Holstein/ Campus Lübeck, Lübeck, Germany.

Kathrin Hanke (K)

Department of Pediatrics, University Hospital Schleswig-Holstein/ Campus Lübeck, Lübeck, Germany.

Classifications MeSH