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      Cerebrovascular responses to a 90° tilt in healthy neonates

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          Abstract

          Background

          Tilts can induce alterations in cerebral hemodynamics in healthy neonates, but prior studies have only examined systemic parameters or used small tilt angles (<90°). The healthy neonatal population, however, are commonly subjected to large tilt angles (≥90°). We sought to characterize the cerebrovascular response to a 90° tilt in healthy term neonates.

          Methods

          We performed a secondary descriptive analysis on 44 healthy term neonates. We measured cerebral oxygen saturation (rcSO 2), oxygen saturation (SpO 2), heart rate (HR), breathing rate (BR), and cerebral fractional tissue oxygen extraction (cFTOE) over three consecutive 90° tilts. These parameters were measured for 2-min while neonates were in a supine (0°) position and 2-min while tilted to a sitting (90°) position. We measured oscillometric mean blood pressure (MBP) at the start of each tilt.

          Results

          rcSO 2 and BR decreased significantly in the sitting position, whereas cFTOE, SpO 2, and MBP increased significantly in the sitting position. We detected a significant position-by-time interaction for all physiological parameters.

          Conclusion

          A 90° tilt induces a decline in rcSO 2 and an increase in cFTOE in healthy term neonates. Understanding the normal cerebrovascular response to a 90° tilt in healthy neonates will help clinicians to recognize abnormal responses in high-risk infant populations.

          Impact

          • Healthy term neonates (≤14 days old) had decreased cerebral oxygen saturation (~1.1%) and increased cerebral oxygen extraction (~0.01) following a 90° tilt.

          • We detected a significant position-by-time interaction with all physiological parameters measured, suggesting the effect of position varied across consecutive tilts.

          • No prior study has characterized the cerebral oxygen saturation response to a 90° tilt in healthy term neonates.

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          Most cited references51

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          Use of tissue oxygenation index and fractional tissue oxygen extraction as non-invasive parameters for cerebral oxygenation. A validation study in piglets.

          To evaluate the relation between cerebral tissue oxygenation index (TOI), measured with spatially resolved spectroscopy (SRS), and the different oxygenation parameters. To evaluate the relation between a new parameter named fractional tissue oxygen extraction (FTOE) and the cerebral fractional oxygen extraction (FOE). Six newborn piglets were measured at 33, 35, and 37 degrees C and in hypocapnia. Mean arterial blood pressure (MABP), haemoglobin (Hb), peripheral oxygen saturation (S(a)O(2)) and P(a)CO(2) were measured at each step. Cerebral blood flow (CBF) was measured by injection of coloured microspheres into the left atrium. Jugular bulb oxygen saturation (JVS), cerebral arterial and venous oxygen content (C(a)O(2) and C(v)O(2)) and FOE were calculated. TOI of the brain was calculated and FTOE was introduced as (S(a)O(2) - TOI)/S(a)O(2). The correlation was calculated with an ANCOVA test. There was a positive correlation (R = 0.4 and p = 0.011) between TOI and JVS. No correlation was found with CBF, MABP or Hb. There was a positive correlation between P(a)CO(2) and cerebral TOI (R = 0.24 and p = 0.03). FTOE correlated well with FOE (R = 0.4 and p = 0.016) and there was a negative correlation between FTOE and P(a)CO(2) (R = 0.24, p = 0.03). The measurement of TOI and FTOE by SRS correlated well with the cerebral venous saturation and FOE, respectively.
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            Fetal Physiology and the Transition to Extrauterine Life.

            The physiology of the fetus is fundamentally different from the neonate, with both structural and functional distinctions. The fetus is well-adapted to the relatively hypoxemic intrauterine environment. The transition from intrauterine to extrauterine life requires rapid, complex, and well-orchestrated steps to ensure neonatal survival. This article explains the intrauterine physiology that allows the fetus to survive and then reviews the physiologic changes that occur during the transition to extrauterine life. Asphyxia fundamentally alters the physiology of transition and necessitates a thoughtful approach in the management of affected neonates.
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              Influence of changes in blood pressure on cerebral perfusion and oxygenation.

              Cerebral autoregulation (CA) is a critical process for the maintenance of cerebral blood flow and oxygenation. Assessment of CA is frequently used for experimental research and in the diagnosis, monitoring, or prognosis of cerebrovascular disease; however, despite the extensive use and reference to static CA, a valid quantification of "normal" CA has not been clearly identified. While controlling for the influence of arterial Pco(2), we provide the first clear examination of static CA in healthy humans over a wide range of blood pressure. In 11 healthy humans, beat-to-beat blood pressure (radial arterial), middle cerebral artery blood velocity (MCAv; transcranial Doppler ultrasound), end-tidal Pco(2), and cerebral oxygenation (near infrared spectroscopy) were recorded continuously during pharmacological-induced changes in mean blood pressure. In a randomized order, steady-state decreases and increases in mean blood pressure (8 to 14 levels; range: approximately 40 to approximately 125 mm Hg) were achieved using intravenous infusions of sodium nitroprusside or phenylephrine, respectively. MCAv(mean) was altered by 0.82+/-0.35% per millimeter of mercury change in mean blood pressure (R(2)=0.82). Changes in cortical oxygenation index were inversely related to changes in mean blood pressure (slope=-0.18%/mm Hg; R(2)=0.60) and MCAv(mean) (slope=-0.26%/cm . s(-1); R(2)=0.54). There was a progressive increase in MCAv pulsatility with hypotension. These findings indicate that cerebral blood flow closely follows pharmacological-induced changes in blood pressure in otherwise healthy humans. Thus, a finite slope of the plateau region does not necessarily imply a defective CA. Moreover, with progressive hypotension and hypertension there are differential changes in cerebral oxygenation and MCAv(mean).
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                Author and article information

                Contributors
                ntran@chla.usc.edu
                Journal
                Pediatr Res
                Pediatr Res
                Pediatric Research
                Nature Publishing Group US (New York )
                0031-3998
                1530-0447
                27 January 2024
                27 January 2024
                2024
                : 95
                : 7
                : 1851-1859
                Affiliations
                [1 ]Institute for the Developing Mind, The Saban Research Institute, Children’s Hospital Los Angeles, ( https://ror.org/00412ts95) Los Angeles, CA USA
                [2 ]Fetal and Neonatal Institute, Division of Neonatology, Children’s Hospital Los Angeles, ( https://ror.org/00412ts95) Los Angeles, CA USA
                [3 ]Department of Pediatrics, Keck School of Medicine, University of Southern California, ( https://ror.org/03taz7m60) Los Angeles, CA USA
                [4 ]Keck School of Medicine, University of Southern California, ( https://ror.org/03taz7m60) Los Angeles, CA USA
                [5 ]GRID grid.16753.36, ISNI 0000 0001 2299 3507, Lurie Children’s Hospital of Chicago, , Northwestern University Feinberg School of Medicine, ; Chicago, IL USA
                [6 ]GRID grid.19006.3e, ISNI 0000 0000 9632 6718, School of Nursing, , University of California, Los Angeles, ; Los Angeles, CA USA
                [7 ]Dornsife College of Letters, Arts and Sciences, University of Southern California, ( https://ror.org/03taz7m60) Los Angeles, CA USA
                [8 ]Department of Psychiatry, Keck School of Medicine, University of Southern California, ( https://ror.org/03taz7m60) Los Angeles, CA USA
                [9 ]Division of Cardiology, Children’s Hospital Los Angeles, ( https://ror.org/00412ts95) Los Angeles, CA USA
                Article
                3046
                10.1038/s41390-024-03046-1
                11245387
                38280952
                89ce8617-ab16-44b3-b72f-979f4fd131a3
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 21 August 2023
                : 30 November 2023
                : 7 January 2024
                Categories
                Clinical Research Article
                Custom metadata
                © International Pediatric Research Foundation, Inc 2024

                Pediatrics
                Pediatrics

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