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Electrocortical brain activity, cerebral haemodynamics and oxygenation during progressive hypotension in newborn piglets
Objective: To investigate the relationships between systemic and cerebral haemodynamics and oxygenation, and electroencephalogram (EEG) amplitude and frequency analysis studied by the cerebral function analyzing monitor (CFAM) during progressive hypovolemic hypotension. Methods: Six piglets of 1 wee...
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Published in: | Clinical neurophysiology 2001, Vol.112 (1), p.52-59 |
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creator | Gavilanes, A.W.D Vles, J.S.H von Siebenthal, K Reulen, J.P Nieman, F.H van Sprundel, R Blanco, C.E |
description | Objective: To investigate the relationships between systemic and cerebral haemodynamics and oxygenation, and electroencephalogram (EEG) amplitude and frequency analysis studied by the cerebral function analyzing monitor (CFAM) during progressive hypovolemic hypotension.
Methods: Six piglets of 1 week of age, weighing 1.9–3.4 kg were mechanically ventilated under 1–1.5% halothane anaesthesia. After 1 h stabilization, blood was withdrawn in aliquots of 10 ml/kg over 15 min up to a total of 40–60 ml/kg. Arterial oxygenation was maintained at normal levels. Thereafter, the total blood volume previously withdrawn, was reinfused. Changes in near infrared spectroscopy (NIRS) parameters [cerebral oxidized cytochrome aa3 (Cytaa3), cerebral blood volume (CBV) or total haemoglobin (tHb: oxy- + deoxyhaemoglobin)], carotid blood flow (Q
car), maximal EEG amplitude and EEG frequency percentages were analyzed continuously.
Results: The EEG amplitude remained stable until the mean arterial blood pressure (MAP), Q
car and tHb dropped below 30 mmHg (41% of baseline), 20 ml/min (33% of baseline) and 82% of baseline, respectively. Delta (δ) wave frequency percentage of the CFAM increased significantly at MAP below 30 mmHg. EEG amplitude remained depressed after blood reinfusion and haemodynamic recovery. Cytaa3 changes were not statistically significant, reflecting sufficient neuronal oxygenation.
Conclusion: Our results show that electrocortical function is affected only by profound systemic hypotension. This occurred at a higher level of cerebral oxygen delivery than the level associated with neuronal hypoxia and secondary cell damage. |
doi_str_mv | 10.1016/S1388-2457(00)00499-5 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70575043</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1388245700004995</els_id><sourcerecordid>70575043</sourcerecordid><originalsourceid>FETCH-LOGICAL-c456t-f2250750fa0245abc2f711a10f1378df97b041c994601a8747fc65e85b57c28a3</originalsourceid><addsrcrecordid>eNqFkUFvFCEUx4mxsbX6ETQcjNGko49ZGJiTMU3VJk08qGfCMI8tZgZWYNfOt5ftrtFbTxD4vT_v_SDkBYN3DFj3_htbKdW0XMg3AG8BeN834hE5Y0q2jepF-7ju_yKn5GnOPwFAAm-fkFPG2Ep2HTsjd1cT2pKijal4ayY6JOMDNbb4nS_LBbWYsJ5N9NbgHMclmNnbTE0Yabxb1hhM8THQcZt8WNNNiuuEOfsd0ttlEwuGvL-ukQF_DzEFuvHrCUt-Rk6cmTI-P67n5Menq--XX5qbr5-vLz_eNJaLrjSubQVIAc5AHcQMtnWSMcPA1QnU6Ho5AGe273kHzCjJpbOdQCUGIW2rzOqcvD7k1tZ-bTEXPftscZpMwLjNWoKo8XxVQXEAbYo5J3R6k_xs0qIZ6L1yfa9c731qAH2vXIta9_L4wHaYcfxXdXRcgVdHwORq2CUTrM__pfNOqr5iHw4YVhs7j0ln6zFYHH2qX6TH6B_o5A-7eZ_4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70575043</pqid></control><display><type>article</type><title>Electrocortical brain activity, cerebral haemodynamics and oxygenation during progressive hypotension in newborn piglets</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Gavilanes, A.W.D ; Vles, J.S.H ; von Siebenthal, K ; Reulen, J.P ; Nieman, F.H ; van Sprundel, R ; Blanco, C.E</creator><creatorcontrib>Gavilanes, A.W.D ; Vles, J.S.H ; von Siebenthal, K ; Reulen, J.P ; Nieman, F.H ; van Sprundel, R ; Blanco, C.E</creatorcontrib><description>Objective: To investigate the relationships between systemic and cerebral haemodynamics and oxygenation, and electroencephalogram (EEG) amplitude and frequency analysis studied by the cerebral function analyzing monitor (CFAM) during progressive hypovolemic hypotension.
Methods: Six piglets of 1 week of age, weighing 1.9–3.4 kg were mechanically ventilated under 1–1.5% halothane anaesthesia. After 1 h stabilization, blood was withdrawn in aliquots of 10 ml/kg over 15 min up to a total of 40–60 ml/kg. Arterial oxygenation was maintained at normal levels. Thereafter, the total blood volume previously withdrawn, was reinfused. Changes in near infrared spectroscopy (NIRS) parameters [cerebral oxidized cytochrome aa3 (Cytaa3), cerebral blood volume (CBV) or total haemoglobin (tHb: oxy- + deoxyhaemoglobin)], carotid blood flow (Q
car), maximal EEG amplitude and EEG frequency percentages were analyzed continuously.
Results: The EEG amplitude remained stable until the mean arterial blood pressure (MAP), Q
car and tHb dropped below 30 mmHg (41% of baseline), 20 ml/min (33% of baseline) and 82% of baseline, respectively. Delta (δ) wave frequency percentage of the CFAM increased significantly at MAP below 30 mmHg. EEG amplitude remained depressed after blood reinfusion and haemodynamic recovery. Cytaa3 changes were not statistically significant, reflecting sufficient neuronal oxygenation.
Conclusion: Our results show that electrocortical function is affected only by profound systemic hypotension. This occurred at a higher level of cerebral oxygen delivery than the level associated with neuronal hypoxia and secondary cell damage.</description><identifier>ISSN: 1388-2457</identifier><identifier>EISSN: 1872-8952</identifier><identifier>DOI: 10.1016/S1388-2457(00)00499-5</identifier><identifier>PMID: 11137661</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Animals ; Animals, Newborn - physiology ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood Gas Analysis ; Blood Glucose - metabolism ; Cardiology. Vascular system ; Cerebral Cortex - cytology ; Cerebral Cortex - physiology ; Cerebral function analyzing monitor ; Cerebrovascular Circulation - physiology ; Electroencephalography ; Experimental diseases ; Female ; Hypotension - physiopathology ; Hypoxic-ischemic encephalopathy ; Male ; Medical sciences ; Near infrared spectroscopy ; Neurons - physiology ; Newborn ; Oxygen Consumption - physiology ; Piglet ; Reperfusion Injury - physiopathology ; Swine</subject><ispartof>Clinical neurophysiology, 2001, Vol.112 (1), p.52-59</ispartof><rights>2001 Elsevier Science Ireland Ltd</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-f2250750fa0245abc2f711a10f1378df97b041c994601a8747fc65e85b57c28a3</citedby><cites>FETCH-LOGICAL-c456t-f2250750fa0245abc2f711a10f1378df97b041c994601a8747fc65e85b57c28a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1046789$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11137661$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gavilanes, A.W.D</creatorcontrib><creatorcontrib>Vles, J.S.H</creatorcontrib><creatorcontrib>von Siebenthal, K</creatorcontrib><creatorcontrib>Reulen, J.P</creatorcontrib><creatorcontrib>Nieman, F.H</creatorcontrib><creatorcontrib>van Sprundel, R</creatorcontrib><creatorcontrib>Blanco, C.E</creatorcontrib><title>Electrocortical brain activity, cerebral haemodynamics and oxygenation during progressive hypotension in newborn piglets</title><title>Clinical neurophysiology</title><addtitle>Clin Neurophysiol</addtitle><description>Objective: To investigate the relationships between systemic and cerebral haemodynamics and oxygenation, and electroencephalogram (EEG) amplitude and frequency analysis studied by the cerebral function analyzing monitor (CFAM) during progressive hypovolemic hypotension.
Methods: Six piglets of 1 week of age, weighing 1.9–3.4 kg were mechanically ventilated under 1–1.5% halothane anaesthesia. After 1 h stabilization, blood was withdrawn in aliquots of 10 ml/kg over 15 min up to a total of 40–60 ml/kg. Arterial oxygenation was maintained at normal levels. Thereafter, the total blood volume previously withdrawn, was reinfused. Changes in near infrared spectroscopy (NIRS) parameters [cerebral oxidized cytochrome aa3 (Cytaa3), cerebral blood volume (CBV) or total haemoglobin (tHb: oxy- + deoxyhaemoglobin)], carotid blood flow (Q
car), maximal EEG amplitude and EEG frequency percentages were analyzed continuously.
Results: The EEG amplitude remained stable until the mean arterial blood pressure (MAP), Q
car and tHb dropped below 30 mmHg (41% of baseline), 20 ml/min (33% of baseline) and 82% of baseline, respectively. Delta (δ) wave frequency percentage of the CFAM increased significantly at MAP below 30 mmHg. EEG amplitude remained depressed after blood reinfusion and haemodynamic recovery. Cytaa3 changes were not statistically significant, reflecting sufficient neuronal oxygenation.
Conclusion: Our results show that electrocortical function is affected only by profound systemic hypotension. This occurred at a higher level of cerebral oxygen delivery than the level associated with neuronal hypoxia and secondary cell damage.</description><subject>Animals</subject><subject>Animals, Newborn - physiology</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Gas Analysis</subject><subject>Blood Glucose - metabolism</subject><subject>Cardiology. Vascular system</subject><subject>Cerebral Cortex - cytology</subject><subject>Cerebral Cortex - physiology</subject><subject>Cerebral function analyzing monitor</subject><subject>Cerebrovascular Circulation - physiology</subject><subject>Electroencephalography</subject><subject>Experimental diseases</subject><subject>Female</subject><subject>Hypotension - physiopathology</subject><subject>Hypoxic-ischemic encephalopathy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Near infrared spectroscopy</subject><subject>Neurons - physiology</subject><subject>Newborn</subject><subject>Oxygen Consumption - physiology</subject><subject>Piglet</subject><subject>Reperfusion Injury - physiopathology</subject><subject>Swine</subject><issn>1388-2457</issn><issn>1872-8952</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqFkUFvFCEUx4mxsbX6ETQcjNGko49ZGJiTMU3VJk08qGfCMI8tZgZWYNfOt5ftrtFbTxD4vT_v_SDkBYN3DFj3_htbKdW0XMg3AG8BeN834hE5Y0q2jepF-7ju_yKn5GnOPwFAAm-fkFPG2Ep2HTsjd1cT2pKijal4ayY6JOMDNbb4nS_LBbWYsJ5N9NbgHMclmNnbTE0Yabxb1hhM8THQcZt8WNNNiuuEOfsd0ttlEwuGvL-ukQF_DzEFuvHrCUt-Rk6cmTI-P67n5Menq--XX5qbr5-vLz_eNJaLrjSubQVIAc5AHcQMtnWSMcPA1QnU6Ho5AGe273kHzCjJpbOdQCUGIW2rzOqcvD7k1tZ-bTEXPftscZpMwLjNWoKo8XxVQXEAbYo5J3R6k_xs0qIZ6L1yfa9c731qAH2vXIta9_L4wHaYcfxXdXRcgVdHwORq2CUTrM__pfNOqr5iHw4YVhs7j0ln6zFYHH2qX6TH6B_o5A-7eZ_4</recordid><startdate>2001</startdate><enddate>2001</enddate><creator>Gavilanes, A.W.D</creator><creator>Vles, J.S.H</creator><creator>von Siebenthal, K</creator><creator>Reulen, J.P</creator><creator>Nieman, F.H</creator><creator>van Sprundel, R</creator><creator>Blanco, C.E</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2001</creationdate><title>Electrocortical brain activity, cerebral haemodynamics and oxygenation during progressive hypotension in newborn piglets</title><author>Gavilanes, A.W.D ; Vles, J.S.H ; von Siebenthal, K ; Reulen, J.P ; Nieman, F.H ; van Sprundel, R ; Blanco, C.E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-f2250750fa0245abc2f711a10f1378df97b041c994601a8747fc65e85b57c28a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Animals, Newborn - physiology</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Gas Analysis</topic><topic>Blood Glucose - metabolism</topic><topic>Cardiology. Vascular system</topic><topic>Cerebral Cortex - cytology</topic><topic>Cerebral Cortex - physiology</topic><topic>Cerebral function analyzing monitor</topic><topic>Cerebrovascular Circulation - physiology</topic><topic>Electroencephalography</topic><topic>Experimental diseases</topic><topic>Female</topic><topic>Hypotension - physiopathology</topic><topic>Hypoxic-ischemic encephalopathy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Near infrared spectroscopy</topic><topic>Neurons - physiology</topic><topic>Newborn</topic><topic>Oxygen Consumption - physiology</topic><topic>Piglet</topic><topic>Reperfusion Injury - physiopathology</topic><topic>Swine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gavilanes, A.W.D</creatorcontrib><creatorcontrib>Vles, J.S.H</creatorcontrib><creatorcontrib>von Siebenthal, K</creatorcontrib><creatorcontrib>Reulen, J.P</creatorcontrib><creatorcontrib>Nieman, F.H</creatorcontrib><creatorcontrib>van Sprundel, R</creatorcontrib><creatorcontrib>Blanco, C.E</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical neurophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gavilanes, A.W.D</au><au>Vles, J.S.H</au><au>von Siebenthal, K</au><au>Reulen, J.P</au><au>Nieman, F.H</au><au>van Sprundel, R</au><au>Blanco, C.E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrocortical brain activity, cerebral haemodynamics and oxygenation during progressive hypotension in newborn piglets</atitle><jtitle>Clinical neurophysiology</jtitle><addtitle>Clin Neurophysiol</addtitle><date>2001</date><risdate>2001</risdate><volume>112</volume><issue>1</issue><spage>52</spage><epage>59</epage><pages>52-59</pages><issn>1388-2457</issn><eissn>1872-8952</eissn><abstract>Objective: To investigate the relationships between systemic and cerebral haemodynamics and oxygenation, and electroencephalogram (EEG) amplitude and frequency analysis studied by the cerebral function analyzing monitor (CFAM) during progressive hypovolemic hypotension.
Methods: Six piglets of 1 week of age, weighing 1.9–3.4 kg were mechanically ventilated under 1–1.5% halothane anaesthesia. After 1 h stabilization, blood was withdrawn in aliquots of 10 ml/kg over 15 min up to a total of 40–60 ml/kg. Arterial oxygenation was maintained at normal levels. Thereafter, the total blood volume previously withdrawn, was reinfused. Changes in near infrared spectroscopy (NIRS) parameters [cerebral oxidized cytochrome aa3 (Cytaa3), cerebral blood volume (CBV) or total haemoglobin (tHb: oxy- + deoxyhaemoglobin)], carotid blood flow (Q
car), maximal EEG amplitude and EEG frequency percentages were analyzed continuously.
Results: The EEG amplitude remained stable until the mean arterial blood pressure (MAP), Q
car and tHb dropped below 30 mmHg (41% of baseline), 20 ml/min (33% of baseline) and 82% of baseline, respectively. Delta (δ) wave frequency percentage of the CFAM increased significantly at MAP below 30 mmHg. EEG amplitude remained depressed after blood reinfusion and haemodynamic recovery. Cytaa3 changes were not statistically significant, reflecting sufficient neuronal oxygenation.
Conclusion: Our results show that electrocortical function is affected only by profound systemic hypotension. This occurred at a higher level of cerebral oxygen delivery than the level associated with neuronal hypoxia and secondary cell damage.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>11137661</pmid><doi>10.1016/S1388-2457(00)00499-5</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Animals, Newborn - physiology Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels Blood Gas Analysis Blood Glucose - metabolism Cardiology. Vascular system Cerebral Cortex - cytology Cerebral Cortex - physiology Cerebral function analyzing monitor Cerebrovascular Circulation - physiology Electroencephalography Experimental diseases Female Hypotension - physiopathology Hypoxic-ischemic encephalopathy Male Medical sciences Near infrared spectroscopy Neurons - physiology Newborn Oxygen Consumption - physiology Piglet Reperfusion Injury - physiopathology Swine |
title | Electrocortical brain activity, cerebral haemodynamics and oxygenation during progressive hypotension in newborn piglets |
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