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Continuous Monitoring of Cerebral Autoregulation in Children Supported by Extracorporeal Membrane Oxygenation: A Pilot Study

Objective Cerebral autoregulation (CA) impairment may pose a risk factor for neurological complications among children supported by extracorporeal membrane oxygenation (ECMO). Our first objective was to investigate the feasibility of CA continuous monitoring during ECMO treatment and to describe its...

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Published in:Neurocritical care 2021-06, Vol.34 (3), p.935-945
Main Authors: Joram, Nicolas, Beqiri, Erta, Pezzato, Stefano, Moscatelli, Andrea, Robba, Chiara, Liet, Jean-Michel, Chenouard, Alexis, Bourgoin, Pierre, Czosnyka, Marek, Léger, Pierre-Louis, Smielewski, Peter
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container_title Neurocritical care
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creator Joram, Nicolas
Beqiri, Erta
Pezzato, Stefano
Moscatelli, Andrea
Robba, Chiara
Liet, Jean-Michel
Chenouard, Alexis
Bourgoin, Pierre
Czosnyka, Marek
Léger, Pierre-Louis
Smielewski, Peter
description Objective Cerebral autoregulation (CA) impairment may pose a risk factor for neurological complications among children supported by extracorporeal membrane oxygenation (ECMO). Our first objective was to investigate the feasibility of CA continuous monitoring during ECMO treatment and to describe its evolution over time. The second objective was to analyze the association between CA impairment and neurological outcome. Design Observational prospective study. Patients and Setting Twenty-nine children treated with veno-arterial or veno-venous ECMO in the PICU of Nantes University Hospital, France, and the PICU of the IRCCS Giannina Gaslini Institute in Genoa, Italy. Measurements A correlation coefficient between the variations of regional cerebral oxygen saturation and the variations of mean arterial blood pressure (MAP) was calculated as an index of CA (cerebral oxygenation reactivity index, COx). A COx > 0.3 was considered as indicative of autoregulation impairment. COx—MAP plots were investigated allowing determining optimal MAP (MAPopt) and limits of autoregulation: lower (LLA) and upper (ULA). Neurological outcome was assessed by the onset of an acute neurological event (ANE) after ECMO start. Results We included 29 children (median age 84 days, weight 4.8 kg). MAPopt, LLA, and ULA were detected in 90.8% (84.3–93.3) of monitoring time. Mean COx was significantly higher during day 1 of ECMO compared to day 2 [0.1 (0.02–0.15) vs. 0.01 (− 0.05 to 0.1), p  = 0.002]. Twelve children experienced ANE (34.5%). The mean COx and the percentage of time spent with a COx > 0.3 were significantly higher among ANE+ compared to ANE− patients [0.09 (0.01–0.23) vs. 0.04 (− 0.02 to 0.06), p  = 0.04 and 33.3% (24.8–62.1) vs. 20.8% (17.3–23.7) p  = 0.001]. ANE+ patients spent significantly more time with MAP below LLA [17.2% (6.5–32.9) vs. 5.6% (3.6–9.9), p  = 0.02] and above ULA [13% (5.3–38.4) vs. 4.2% (2.7–7.4), p  = 0.004], respectively. Conclusion CA assessment is feasible in pediatric ECMO. The first 24 h following ECMO represents the most critical period regarding CA. Impaired autoregulation is significantly more severe among patients who experience ANE.
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Our first objective was to investigate the feasibility of CA continuous monitoring during ECMO treatment and to describe its evolution over time. The second objective was to analyze the association between CA impairment and neurological outcome. Design Observational prospective study. Patients and Setting Twenty-nine children treated with veno-arterial or veno-venous ECMO in the PICU of Nantes University Hospital, France, and the PICU of the IRCCS Giannina Gaslini Institute in Genoa, Italy. Measurements A correlation coefficient between the variations of regional cerebral oxygen saturation and the variations of mean arterial blood pressure (MAP) was calculated as an index of CA (cerebral oxygenation reactivity index, COx). A COx &gt; 0.3 was considered as indicative of autoregulation impairment. COx—MAP plots were investigated allowing determining optimal MAP (MAPopt) and limits of autoregulation: lower (LLA) and upper (ULA). Neurological outcome was assessed by the onset of an acute neurological event (ANE) after ECMO start. Results We included 29 children (median age 84 days, weight 4.8 kg). MAPopt, LLA, and ULA were detected in 90.8% (84.3–93.3) of monitoring time. Mean COx was significantly higher during day 1 of ECMO compared to day 2 [0.1 (0.02–0.15) vs. 0.01 (− 0.05 to 0.1), p  = 0.002]. Twelve children experienced ANE (34.5%). The mean COx and the percentage of time spent with a COx &gt; 0.3 were significantly higher among ANE+ compared to ANE− patients [0.09 (0.01–0.23) vs. 0.04 (− 0.02 to 0.06), p  = 0.04 and 33.3% (24.8–62.1) vs. 20.8% (17.3–23.7) p  = 0.001]. ANE+ patients spent significantly more time with MAP below LLA [17.2% (6.5–32.9) vs. 5.6% (3.6–9.9), p  = 0.02] and above ULA [13% (5.3–38.4) vs. 4.2% (2.7–7.4), p  = 0.004], respectively. Conclusion CA assessment is feasible in pediatric ECMO. The first 24 h following ECMO represents the most critical period regarding CA. Impaired autoregulation is significantly more severe among patients who experience ANE.</description><identifier>ISSN: 1541-6933</identifier><identifier>EISSN: 1556-0961</identifier><identifier>DOI: 10.1007/s12028-020-01111-1</identifier><identifier>PMID: 33029743</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Aged, 80 and over ; Blood pressure ; Brain death ; Cardiac arrest ; Cerebrovascular Circulation ; Child ; Critical Care Medicine ; Extracorporeal membrane oxygenation ; Extracorporeal Membrane Oxygenation - adverse effects ; Hemodynamics ; Homeostasis ; Humans ; Intensive ; Internal Medicine ; Medicine ; Medicine &amp; Public Health ; NCT ; NCT04282525 ; Neurology ; Neurosurgery ; Original Work ; Patients ; Pediatrics ; Pilot Projects ; Prospective Studies ; Software ; Traumatic brain injury ; Veins &amp; arteries</subject><ispartof>Neurocritical care, 2021-06, Vol.34 (3), p.935-945</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2020. corrected publication 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-a240f045c0facfcffab38dadb6f2b2f8c2159d8530db055711e74b8d401e096c3</citedby><cites>FETCH-LOGICAL-c419t-a240f045c0facfcffab38dadb6f2b2f8c2159d8530db055711e74b8d401e096c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33029743$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Joram, Nicolas</creatorcontrib><creatorcontrib>Beqiri, Erta</creatorcontrib><creatorcontrib>Pezzato, Stefano</creatorcontrib><creatorcontrib>Moscatelli, Andrea</creatorcontrib><creatorcontrib>Robba, Chiara</creatorcontrib><creatorcontrib>Liet, Jean-Michel</creatorcontrib><creatorcontrib>Chenouard, Alexis</creatorcontrib><creatorcontrib>Bourgoin, Pierre</creatorcontrib><creatorcontrib>Czosnyka, Marek</creatorcontrib><creatorcontrib>Léger, Pierre-Louis</creatorcontrib><creatorcontrib>Smielewski, Peter</creatorcontrib><title>Continuous Monitoring of Cerebral Autoregulation in Children Supported by Extracorporeal Membrane Oxygenation: A Pilot Study</title><title>Neurocritical care</title><addtitle>Neurocrit Care</addtitle><addtitle>Neurocrit Care</addtitle><description>Objective Cerebral autoregulation (CA) impairment may pose a risk factor for neurological complications among children supported by extracorporeal membrane oxygenation (ECMO). Our first objective was to investigate the feasibility of CA continuous monitoring during ECMO treatment and to describe its evolution over time. The second objective was to analyze the association between CA impairment and neurological outcome. Design Observational prospective study. Patients and Setting Twenty-nine children treated with veno-arterial or veno-venous ECMO in the PICU of Nantes University Hospital, France, and the PICU of the IRCCS Giannina Gaslini Institute in Genoa, Italy. Measurements A correlation coefficient between the variations of regional cerebral oxygen saturation and the variations of mean arterial blood pressure (MAP) was calculated as an index of CA (cerebral oxygenation reactivity index, COx). A COx &gt; 0.3 was considered as indicative of autoregulation impairment. COx—MAP plots were investigated allowing determining optimal MAP (MAPopt) and limits of autoregulation: lower (LLA) and upper (ULA). Neurological outcome was assessed by the onset of an acute neurological event (ANE) after ECMO start. Results We included 29 children (median age 84 days, weight 4.8 kg). MAPopt, LLA, and ULA were detected in 90.8% (84.3–93.3) of monitoring time. Mean COx was significantly higher during day 1 of ECMO compared to day 2 [0.1 (0.02–0.15) vs. 0.01 (− 0.05 to 0.1), p  = 0.002]. Twelve children experienced ANE (34.5%). The mean COx and the percentage of time spent with a COx &gt; 0.3 were significantly higher among ANE+ compared to ANE− patients [0.09 (0.01–0.23) vs. 0.04 (− 0.02 to 0.06), p  = 0.04 and 33.3% (24.8–62.1) vs. 20.8% (17.3–23.7) p  = 0.001]. ANE+ patients spent significantly more time with MAP below LLA [17.2% (6.5–32.9) vs. 5.6% (3.6–9.9), p  = 0.02] and above ULA [13% (5.3–38.4) vs. 4.2% (2.7–7.4), p  = 0.004], respectively. Conclusion CA assessment is feasible in pediatric ECMO. The first 24 h following ECMO represents the most critical period regarding CA. 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Our first objective was to investigate the feasibility of CA continuous monitoring during ECMO treatment and to describe its evolution over time. The second objective was to analyze the association between CA impairment and neurological outcome. Design Observational prospective study. Patients and Setting Twenty-nine children treated with veno-arterial or veno-venous ECMO in the PICU of Nantes University Hospital, France, and the PICU of the IRCCS Giannina Gaslini Institute in Genoa, Italy. Measurements A correlation coefficient between the variations of regional cerebral oxygen saturation and the variations of mean arterial blood pressure (MAP) was calculated as an index of CA (cerebral oxygenation reactivity index, COx). A COx &gt; 0.3 was considered as indicative of autoregulation impairment. COx—MAP plots were investigated allowing determining optimal MAP (MAPopt) and limits of autoregulation: lower (LLA) and upper (ULA). Neurological outcome was assessed by the onset of an acute neurological event (ANE) after ECMO start. Results We included 29 children (median age 84 days, weight 4.8 kg). MAPopt, LLA, and ULA were detected in 90.8% (84.3–93.3) of monitoring time. Mean COx was significantly higher during day 1 of ECMO compared to day 2 [0.1 (0.02–0.15) vs. 0.01 (− 0.05 to 0.1), p  = 0.002]. Twelve children experienced ANE (34.5%). The mean COx and the percentage of time spent with a COx &gt; 0.3 were significantly higher among ANE+ compared to ANE− patients [0.09 (0.01–0.23) vs. 0.04 (− 0.02 to 0.06), p  = 0.04 and 33.3% (24.8–62.1) vs. 20.8% (17.3–23.7) p  = 0.001]. ANE+ patients spent significantly more time with MAP below LLA [17.2% (6.5–32.9) vs. 5.6% (3.6–9.9), p  = 0.02] and above ULA [13% (5.3–38.4) vs. 4.2% (2.7–7.4), p  = 0.004], respectively. Conclusion CA assessment is feasible in pediatric ECMO. The first 24 h following ECMO represents the most critical period regarding CA. Impaired autoregulation is significantly more severe among patients who experience ANE.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>33029743</pmid><doi>10.1007/s12028-020-01111-1</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged, 80 and over
Blood pressure
Brain death
Cardiac arrest
Cerebrovascular Circulation
Child
Critical Care Medicine
Extracorporeal membrane oxygenation
Extracorporeal Membrane Oxygenation - adverse effects
Hemodynamics
Homeostasis
Humans
Intensive
Internal Medicine
Medicine
Medicine & Public Health
NCT
NCT04282525
Neurology
Neurosurgery
Original Work
Patients
Pediatrics
Pilot Projects
Prospective Studies
Software
Traumatic brain injury
Veins & arteries
title Continuous Monitoring of Cerebral Autoregulation in Children Supported by Extracorporeal Membrane Oxygenation: A Pilot Study
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