Umbilical artery eucapnic pH to assess fetal well being.

Neonatal metabolic acidosis cord gas eucapnic pH hypoxic-ischemic encephalopathy newborn

Journal

American journal of obstetrics and gynecology
ISSN: 1097-6868
Titre abrégé: Am J Obstet Gynecol
Pays: United States
ID NLM: 0370476

Informations de publication

Date de publication:
03 Apr 2024
Historique:
received: 16 10 2022
revised: 19 03 2024
accepted: 31 03 2024
medline: 6 4 2024
pubmed: 6 4 2024
entrez: 5 4 2024
Statut: aheadofprint

Résumé

Umbilical artery gas results help obstetricians to assess fetal well being during the course of labor and guide screening decisions on eligibility for therapeutic hypothermia or also know as whole body or head cooling. The accuracy of results, especially base deficit on arterial cord gas analysis, in predicting brain injury is questioned. A novel biomarker specifically calculated for fetal acid-base physiology and response to asphyxia-neonatal eucapnic pH as a marker of neonatal metabolic acidosis-has the potential to be an accurate predictor of hypoxic-ischemic encephalopathy. We aimed to compare false-negative rates of hypoxic-ischemic encephalopathy for umbilical artery pH, base deficit, and neonatal eucapnic pH in assessing fetal acid-base balance as a marker of fetal well being and predicting acute brain injury. This is a retrospective single-center cohort study of newborns ≥ 35 weeks' gestation diagnosed with hypoxic-ischemic encephalopathy. We compared false-negative rates for any grade of hypoxic-ischemic encephalopathy using unilateral paired χ We included 113 newborns. False-negative rate for hypoxic-ischemic encephalopathy was significantly higher for base deficit < 16 mmol/ (n=78/113; 69.0%) compared to base deficit < 12 mmol/L (n=46/113; 40.7%), pH > 7.00 (n=41/113; 36.3%) or neonatal eucpanic pH > 7.14 (n=35/113; 31.0%) (p<0.0001). All true positive cases were identified using only umbilical artery pH and neonatal eucapnic pH. Base deficit ≥16 or ≥12 mmol/L did not add any value in identifying newborns with hypoxic-ischemic encephalopathy when using umbilical artery pH and neonatal eucapnic pH. No association emerged between any marker and hypoxic-ischemic encephalopathy severity grading. Our findings support the accuracy of neonatal eucapnic pH to assess fetal well being during labor and to improve predictive performance for acute brain injury. Neonatal eucpanic pH, in addition to umbilical artery pH, may be a viable alternative in identifying newborns at risk for hypoxic-ischemic encephalopathy.

Sections du résumé

BACKGROUND BACKGROUND
Umbilical artery gas results help obstetricians to assess fetal well being during the course of labor and guide screening decisions on eligibility for therapeutic hypothermia or also know as whole body or head cooling. The accuracy of results, especially base deficit on arterial cord gas analysis, in predicting brain injury is questioned. A novel biomarker specifically calculated for fetal acid-base physiology and response to asphyxia-neonatal eucapnic pH as a marker of neonatal metabolic acidosis-has the potential to be an accurate predictor of hypoxic-ischemic encephalopathy.
OBJECTIVES OBJECTIVE
We aimed to compare false-negative rates of hypoxic-ischemic encephalopathy for umbilical artery pH, base deficit, and neonatal eucapnic pH in assessing fetal acid-base balance as a marker of fetal well being and predicting acute brain injury.
STUDY DESIGN METHODS
This is a retrospective single-center cohort study of newborns ≥ 35 weeks' gestation diagnosed with hypoxic-ischemic encephalopathy. We compared false-negative rates for any grade of hypoxic-ischemic encephalopathy using unilateral paired χ
RESULTS RESULTS
We included 113 newborns. False-negative rate for hypoxic-ischemic encephalopathy was significantly higher for base deficit < 16 mmol/ (n=78/113; 69.0%) compared to base deficit < 12 mmol/L (n=46/113; 40.7%), pH > 7.00 (n=41/113; 36.3%) or neonatal eucpanic pH > 7.14 (n=35/113; 31.0%) (p<0.0001). All true positive cases were identified using only umbilical artery pH and neonatal eucapnic pH. Base deficit ≥16 or ≥12 mmol/L did not add any value in identifying newborns with hypoxic-ischemic encephalopathy when using umbilical artery pH and neonatal eucapnic pH. No association emerged between any marker and hypoxic-ischemic encephalopathy severity grading.
CONCLUSION CONCLUSIONS
Our findings support the accuracy of neonatal eucapnic pH to assess fetal well being during labor and to improve predictive performance for acute brain injury. Neonatal eucpanic pH, in addition to umbilical artery pH, may be a viable alternative in identifying newborns at risk for hypoxic-ischemic encephalopathy.

Identifiants

pubmed: 38580045
pii: S0002-9378(24)00479-4
doi: 10.1016/j.ajog.2024.03.042
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Auteurs

Thierry Daboval (T)

Professor of Pediatrics, University of Ottawa, Children's Hospital of Eastern Ontario. The Ottawa Hospital, General Campus 401 Smyth Road, Ottawa ON K1H 8L6. Electronic address: thierrydaboval@montfort.on.ca.

Paul Ouellet (P)

Adjunct Professor (Ret.) Department of Surgery, University of Sherbrooke, Clinical consultant, Vitality Health Network, North West Zone, Edmundston, NB, Canada Paul Ouellet.

Amr El Shahed (AE)

Assistant Professor of Pediatrics - University of Toronto, Staff Neonatologist - The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8.

Linh Ly (L)

Medical director of the neonatal neurodevelopmental follow-up clinic, Assistant Professor of Pediatrics - University of Toronto, Staff Neonatologist - The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8.

Caroline Ahearne (C)

Fellow in Neonatal Neurology - University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8.

Claude Racinet (C)

Professor Emeritus, University of Grenoble-Alpes, 621 Av. Centrale, 38400 Saint-Martin-d'Hères, Grenoble, France, Childhood Disabilities and Perinatal Data Register, 23 Avenue Albert 1er de Belgique, 38000 Grenoble, France.

Classifications MeSH