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Identification of neonatal near miss by systematic screening for metabolic acidosis at birth

Aims: To evaluate the relevance of systematic screening for neonatal metabolic acidosis at birth as part of perinatal audit. Methods: For every baby, born in Ziekenhuis Oost Limburg, Genk Belgium between 1/1/2010 and 31/12/2010, cord blood was analysed to diagnose metabolic acidosis, defined as arte...

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Autores principales: Bonnaerens, A., Thaens, A., Mesens, T., Van Holsbeke, C., de Jonge, E.T.M., Gyselaers, W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Universa Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987470/
https://www.ncbi.nlm.nih.gov/pubmed/24753878
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author Bonnaerens, A.
Thaens, A.
Mesens, T.
Van Holsbeke, C.
de Jonge, E.T.M.
Gyselaers, W.
author_facet Bonnaerens, A.
Thaens, A.
Mesens, T.
Van Holsbeke, C.
de Jonge, E.T.M.
Gyselaers, W.
author_sort Bonnaerens, A.
collection PubMed
description Aims: To evaluate the relevance of systematic screening for neonatal metabolic acidosis at birth as part of perinatal audit. Methods: For every baby, born in Ziekenhuis Oost Limburg, Genk Belgium between 1/1/2010 and 31/12/2010, cord blood was analysed to diagnose metabolic acidosis, defined as arterial or venous pH ≤ 7.05 or 7.17 respectively, in association with base excess of ≤ -10 mmol/L. Three observers identified indicators for suboptimal peripartal care with likely contribution to metabolic acidosis. In a multidisciplinary consensus meeting, these indicators were classified into 5 categories : (a) fetal monitoring error (b) labour management error, (c) instrumental vaginal delivery for fetal distress within 2 h of second stage, (d) non-obstetric medical complications, (e) preterm births or accidental cases at term. Results: In a total of 2117 neonates, there were 11 intra-uterine, 1 intrapartum and 3 early neonatal deaths, bringing early perinatal mortality rate at 7.1‰. Metabolic acidosis was identified in 23 (1.1%) babies, of which 21 (91.3%) left hospital in good clinical condition. Two babies (0.9‰), born in category c, had chronic neurologic symptoms. Discussion: Systematic screening for neonatal metabolic acidosis caused a 2.5-fold increase of case identifications eligible for perinatal audit and opened perspectives towards rationalised improvement of perinatal care, in addition to the information obtained from cases of perinatal mortality. Next to indicators of perinatal mortality, perinatal audit programs should include neonatal metabolic acidosis as an extra parameter for quality assessment of perinatal care. Conclusion: Adding cases of near-miss neonatal morbidity to perinatal mortalities in perinatal audit programs increases opportunities for improvement of perinatal care.
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spelling pubmed-39874702014-04-21 Identification of neonatal near miss by systematic screening for metabolic acidosis at birth Bonnaerens, A. Thaens, A. Mesens, T. Van Holsbeke, C. de Jonge, E.T.M. Gyselaers, W. Facts Views Vis Obgyn Original Paper Aims: To evaluate the relevance of systematic screening for neonatal metabolic acidosis at birth as part of perinatal audit. Methods: For every baby, born in Ziekenhuis Oost Limburg, Genk Belgium between 1/1/2010 and 31/12/2010, cord blood was analysed to diagnose metabolic acidosis, defined as arterial or venous pH ≤ 7.05 or 7.17 respectively, in association with base excess of ≤ -10 mmol/L. Three observers identified indicators for suboptimal peripartal care with likely contribution to metabolic acidosis. In a multidisciplinary consensus meeting, these indicators were classified into 5 categories : (a) fetal monitoring error (b) labour management error, (c) instrumental vaginal delivery for fetal distress within 2 h of second stage, (d) non-obstetric medical complications, (e) preterm births or accidental cases at term. Results: In a total of 2117 neonates, there were 11 intra-uterine, 1 intrapartum and 3 early neonatal deaths, bringing early perinatal mortality rate at 7.1‰. Metabolic acidosis was identified in 23 (1.1%) babies, of which 21 (91.3%) left hospital in good clinical condition. Two babies (0.9‰), born in category c, had chronic neurologic symptoms. Discussion: Systematic screening for neonatal metabolic acidosis caused a 2.5-fold increase of case identifications eligible for perinatal audit and opened perspectives towards rationalised improvement of perinatal care, in addition to the information obtained from cases of perinatal mortality. Next to indicators of perinatal mortality, perinatal audit programs should include neonatal metabolic acidosis as an extra parameter for quality assessment of perinatal care. Conclusion: Adding cases of near-miss neonatal morbidity to perinatal mortalities in perinatal audit programs increases opportunities for improvement of perinatal care. Universa Press 2011 /pmc/articles/PMC3987470/ /pubmed/24753878 Text en Copyright: © 2011 Facts, Views & Vision http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Bonnaerens, A.
Thaens, A.
Mesens, T.
Van Holsbeke, C.
de Jonge, E.T.M.
Gyselaers, W.
Identification of neonatal near miss by systematic screening for metabolic acidosis at birth
title Identification of neonatal near miss by systematic screening for metabolic acidosis at birth
title_full Identification of neonatal near miss by systematic screening for metabolic acidosis at birth
title_fullStr Identification of neonatal near miss by systematic screening for metabolic acidosis at birth
title_full_unstemmed Identification of neonatal near miss by systematic screening for metabolic acidosis at birth
title_short Identification of neonatal near miss by systematic screening for metabolic acidosis at birth
title_sort identification of neonatal near miss by systematic screening for metabolic acidosis at birth
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987470/
https://www.ncbi.nlm.nih.gov/pubmed/24753878
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