Early arterial pressure monitoring and term-equivalent age MRI findings in very preterm infants.


Journal

Pediatric research
ISSN: 1530-0447
Titre abrégé: Pediatr Res
Pays: United States
ID NLM: 0100714

Informations de publication

Date de publication:
09 2022
Historique:
received: 19 05 2021
accepted: 28 10 2021
revised: 21 10 2021
pubmed: 21 11 2021
medline: 15 10 2022
entrez: 20 11 2021
Statut: ppublish

Résumé

Variability of arterial blood pressure (ABP) has been associated with intraventricular hemorrhage in very preterm neonates (VPT) and may predict other brain lesions assessed at term-equivalent of age (TEA). This was a prospective single-center study including VPT with early invasive continuous ABP monitoring and assessed at TEA using brain magnetic resonance imaging (TEA-MRI). The association between early mean ABP (MABP) and TEA-MRI findings was modeled by multivariate logistic regression analysis using covariates selected by the LASSO method. Among 99 VPT, the LASSO procedure selected consecutive periods of lowest MABP of 30 min on day 1 (d1) and 10 min on day 2 (d2) as the most relevant durations to predict TEA-MRI findings (OR [95% CI], 1.11 [1.02-1.23], p = 0.03 and 1.13 [1.01-1.27], p = 0.03, respectively). ROC curve analysis showed optimal thresholds at 30.25 mmHg on d1 and 33.25 mmHg on d2. This significant association persisted after adjustment with covariates including birthweight, gestational age, sex, and inotrope exposure. Final models selected by LASSO included the decile of the birthweight and lowest MABP for 30 min on d1 and 10 min on d2, for which the areas under the ROC curve were 74% and 75%, respectively. Early continuous ABP monitoring may predict brain TEA-MRI findings in VPT. Early arterial blood pressure monitoring may contribute to predicting brain damage upon MRI at term-equivalent of age for infants born very preterm. Careful blood pressure continuous monitoring in very preterm infants may identify infants at risk of long-term brain damage. Umbilical artery catheterization provides the best option for continuously monitoring arterial blood pressure in very preterm infants.

Identifiants

pubmed: 34799666
doi: 10.1038/s41390-021-01839-2
pii: 10.1038/s41390-021-01839-2
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

822-828

Informations de copyright

© 2021. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc.

Références

Pellicer, A., Valverde, E., Gaya, F., Quero, J. & Cabanas, F. Postnatal adaptation of brain circulation in preterm infants. Pediatr. Neurol. 24, 103–109 (2001).
doi: 10.1016/S0887-8994(00)00239-3
Miall-Allen, V. M., de Vries, L. S. & Whitelaw, A. G. Mean arterial blood pressure and neonatal cerebral lesions. Arch. Dis. Child. 62, 1068–1069 (1987).
doi: 10.1136/adc.62.10.1068
Watkins, A. M., West, C. R. & Cooke, R. W. Blood pressure and cerebral haemorrhage and ischaemia in very low birthweight infants. Early Hum. Dev. 19, 103–110 (1989).
doi: 10.1016/0378-3782(89)90120-5
Huvanandana, J. et al. Prediction of intraventricular haemorrhage in preterm infants using time series analysis of blood pressure and respiratory signals. Sci. Rep. 7, 46538 (2017).
doi: 10.1038/srep46538
Vesoulis, Z. A., Liao, S. M. & Mathur, A. M. Gestational age-dependent relationship between cerebral oxygen extraction and blood pressure. Pediatr. Res. 82, 934–939 (2017).
doi: 10.1038/pr.2017.196
Vesoulis, Z. A. et al. Blood pressure extremes and severe IVH in preterm infants. Pediatr. Res. 87, 69–73 (2020).
doi: 10.1038/s41390-019-0585-3
Faust, K. et al. Short-term outcome of very-low-birthweight infants with arterial hypotension in the first 24 h of life. Arch. Dis. Child Fetal Neonatal Ed. 100, F388–F392 (2015).
doi: 10.1136/archdischild-2014-306483
Batton, B. et al. Early blood pressure, antihypotensive therapy and outcomes at 18-22 months’ corrected age in extremely preterm infants. Arch. Dis. Child Fetal Neonatal Ed. 101, F201–F206 (2016).
doi: 10.1136/archdischild-2015-308899
Parodi, A. et al. Cranial ultrasound findings in preterm germinal matrix haemorrhage, sequelae and outcome. Pediatr. Res. 87, 13–24 (2020).
doi: 10.1038/s41390-020-0780-2
Volpe, J. J. The encephalopathy of prematurity–brain injury and impaired brain development inextricably intertwined. Semin. Pediatr. Neurol. 16, 167–178 (2009).
doi: 10.1016/j.spen.2009.09.005
Kidokoro, H., Neil, J. J. & Inder, T. E. New MR imaging assessment tool to define brain abnormalities in very preterm infants at term. AJNR Am. J. Neuroradiol. 34, 2208–2214 (2013).
doi: 10.3174/ajnr.A3521
Belloni, A., Chernozhukov, V. & Hansen, C. Inference on treatment effects after selection amongst high-dimensional controls. Rev. Econ. Stud. 81, 608–650 (2014).
doi: 10.1093/restud/rdt044
Natalucci, G. et al. Effect of early prophylactic high-dose recombinant human erythropoietin in very preterm infants on neurodevelopmental outcome at 2 years: a randomized clinical trial. JAMA 315, 2079–2085 (2016).
doi: 10.1001/jama.2016.5504
Vesoulis, Z. A., El Ters, N. M., Wallendorf, M. & Mathur, A. M. Empirical estimation of the normative blood pressure in infants <28 weeks gestation using a massive data approach. J. Perinatol. 36, 291–295 (2016).
doi: 10.1038/jp.2015.185
Inder, T. E., Wells, S. J., Mogridge, N. B., Spencer, C. & Volpe, J. J. Defining the nature of the cerebral abnormalities in the premature infant: a qualitative magnetic resonance imaging study. J. Pediatr. 143, 171–179 (2003).
doi: 10.1067/S0022-3476(03)00357-3
Miller, S. P. et al. Early brain injury in premature newborns detected with magnetic resonance imaging is associated with adverse early neurodevelopmental outcome. J. Pediatr. 147, 609–616 (2005).
doi: 10.1016/j.jpeds.2005.06.033
Pittet, M. P., Vasung, L., Huppi, P. S. & Merlini, L. Newborns and preterm infants at term equivalent age: a semi-quantitative assessment of cerebral maturity. Neuroimage Clin. 24, 102014 (2019).
doi: 10.1016/j.nicl.2019.102014
Bass, W. T. et al. Indices of hemodynamic and respiratory functions in premature infants at risk for the development of cerebral white matter injury. J. Perinatol. 22, 64–71 (2002).
doi: 10.1038/sj.jp.7210612
Giraud, A. et al. Perinatal inflammation is associated with social and motor impairments in preterm children without severe neonatal brain injury. Eur. J. Paediatr. Neurol. 28, 126–132 (2020).
doi: 10.1016/j.ejpn.2020.06.008
Dammann, O. & Leviton, A. Maternal intrauterine infection, cytokines, and brain damage in the preterm newborn. Pediatr. Res. 42, 1–8 (1997).
doi: 10.1203/00006450-199707000-00001
Hagberg, H. & Mallard, C. Effect of inflammation on central nervous system development and vulnerability. Curr. Opin. Neurol. 18, 117–123 (2005).
doi: 10.1097/01.wco.0000162851.44897.8f
Furukawa, S., Sameshima, H. & Ikenoue, T. Circulatory disturbances during the first postnatal 24h in extremely premature infants 25 weeks or less of gestation with histological fetal inflammation. J. Obstet. Gynaecol. Res. 34, 27–33 (2008).
pubmed: 18226125
Vesoulis, Z. A. & Mathur, A. M. Cerebral autoregulation, brain injury, and the transitioning premature infant. Front. Pediatr. 5, 64 (2017).
doi: 10.3389/fped.2017.00064
Adams-Chapman, I. Long-term impact of infection on the preterm neonate. Semin. Perinatol. 36, 462–470 (2012).
doi: 10.1053/j.semperi.2012.06.009
Patra, A., Huang, H., Bauer, J. A. & Giannone, P. J. Neurological consequences of systemic inflammation in the premature neonate. Neural Regen. Res. 12, 890–896 (2017).
doi: 10.4103/1673-5374.208547
Prasad, J. D. et al. Coordinated microstructural disruptions of the developing neocortex and subcortical white matter after prolonged mild-to-moderate early postnatal systemic inflammation. Brain Behav Immun 94, 338–356 (2021).
doi: 10.1016/j.bbi.2020.12.006
Volpe, J. J. Systemic inflammation, oligodendroglial maturation, and the encephalopathy of prematurity. Ann. Neurol. 70, 525–529 (2011).
doi: 10.1002/ana.22533
Huning, B. et al. Relationship between brain function (AEEG) and brain structure (MRI) and their predictive value for neurodevelopmental outcome of preterm infants. Eur. J. Pediatr. 177, 1181–1189 (2018).
doi: 10.1007/s00431-018-3166-2
Durrmeyer, X. et al. Abstention or intervention for isolated hypotension in the first 3 days of life in extremely preterm infants: association with short-term outcomes in the Epipage 2 Cohort Study. Arch. Dis. Child Fetal Neonatal Ed. 102, 490–496 (2017).
doi: 10.1136/archdischild-2016-312104
Dempsey, E. M. et al. Hypotension in preterm infants (HIP) randomised trial. Arch. Dis. Child Fetal Neonatal Ed. 106, 398–403 (2021).
doi: 10.1136/archdischild-2020-320241

Auteurs

Roberta Butticci (R)

Division of Neonatology and Pediatric Intensive Care, Children's University Hospital of Geneva and University of Geneva, 1205, Geneva, Switzerland.

Céline Habre (C)

Pediatric Radiology Unit, Division of Radiology, Children's University Hospital of Geneva and University of Geneva, 1211, Geneva, Switzerland.

Alfredo Hernandez (A)

University of Rennes, CHU Rennes, Inserm, LTSI-UMR 1099, F-35000, Rennes, France.

Francisca Barcos-Munoz (F)

Division of Neonatology and Pediatric Intensive Care, Children's University Hospital of Geneva and University of Geneva, 1205, Geneva, Switzerland.

Riccardo Pfister (R)

Division of Neonatology and Pediatric Intensive Care, Children's University Hospital of Geneva and University of Geneva, 1205, Geneva, Switzerland.

Sylviane Hanquinet (S)

Pediatric Radiology Unit, Division of Radiology, Children's University Hospital of Geneva and University of Geneva, 1211, Geneva, Switzerland.

Alain Beuchée (A)

University of Rennes, CHU Rennes, Inserm, LTSI-UMR 1099, F-35000, Rennes, France.

Olivier Baud (O)

Division of Neonatology and Pediatric Intensive Care, Children's University Hospital of Geneva and University of Geneva, 1205, Geneva, Switzerland. olivier.baud@hcuge.ch.
NeuroDiderot, UMR 1141, Inserm, Université de Paris, Paris, France. olivier.baud@hcuge.ch.

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