<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18</volume><submitter>Karlsen H</submitter><funding>South-Eastern Norway Regional Health Authority</funding><funding>Laerdal Foundation For Acute Medicine</funding><funding>ZOLL Foundation</funding><pubmed_abstract>&lt;h4>Aim&lt;/h4>To determine whether targeting mild hypercapnia (PaCO&lt;sub>2&lt;/sub> 7 kPa) would yield improved cerebral blood flow and metabolism compared to normocapnia (PaCO&lt;sub>2&lt;/sub> 5 kPa) with and without targeted temperature management to 33 °C (TTM33) in a porcine post-cardiac arrest model.&lt;h4>Methods&lt;/h4>39 pigs were resuscitated after 10 minutes of cardiac arrest using cardiopulmonary bypass and randomised to TTM33 or no-TTM, and hypercapnia or normocapnia. TTM33 was managed with intravasal cooling. Animals were stabilized for 30 minutes followed by a two-hour intervention period. Hemodynamic parameters were measured continuously, and neuromonitoring included intracranial pressure (ICP), pressure reactivity index, cerebral blood flow, brain-tissue pCO&lt;sub>2&lt;/sub> and microdialysis. Measurements are reported as proportion of baseline, and areas under the curve during the 120 min intervention period were compared.&lt;h4>Results&lt;/h4>Hypercapnia increased cerebral flow in both TTM33 and no-TTM groups, but also increased ICP (199% vs. 183% of baseline, &lt;i>p&lt;/i> = 0.018) and reduced cerebral perfusion pressure (70% vs. 84% of baseline, &lt;i>p&lt;/i> &lt; 0.001) in no-TTM animals. Cerebral lactate (196% vs. 297% of baseline, &lt;i>p&lt;/i> &lt; 0.001), pyruvate (118% vs. 152% of baseline, &lt;i>p&lt;/i> &lt; 0.001), glycerol and lactate/pyruvate ratios were lower with hypercapnia in the TTM33 group, but only pyruvate (133% vs. 150% of baseline, &lt;i>p&lt;/i> = 0.002) was lower with hypercapnia among no-TTM animals.&lt;h4>Conclusion&lt;/h4>In this porcine post-arrest model, hypercapnia led to increased cerebral flow both with and without hypothermia, but also increased ICP and reduced cerebral perfusion pressure in no-TTM animals. The effects of hypercapnia were different with and without TTM.(Institutional protocol number: FOTS, id 14931).</pubmed_abstract><journal>Resuscitation plus</journal><pagination>100604</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10950799</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cerebral perfusion and metabolism with mild hypercapnia vs. normocapnia in a porcine post cardiac arrest model with and without targeted temperature management.</pubmed_title><pmcid>PMC10950799</pmcid><pubmed_authors>Karlsen H</pubmed_authors><pubmed_authors>Sunde K</pubmed_authors><pubmed_authors>Olasveengen TM</pubmed_authors><pubmed_authors>Skare C</pubmed_authors><pubmed_authors>Eriksen M</pubmed_authors><pubmed_authors>Strand-Amundsen RJ</pubmed_authors><pubmed_authors>Tonnessen TI</pubmed_authors><pubmed_authors>Skulberg VM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cerebral perfusion and metabolism with mild hypercapnia vs. normocapnia in a porcine post cardiac arrest model with and without targeted temperature management.</name><description>&lt;h4>Aim&lt;/h4>To determine whether targeting mild hypercapnia (PaCO&lt;sub>2&lt;/sub> 7 kPa) would yield improved cerebral blood flow and metabolism compared to normocapnia (PaCO&lt;sub>2&lt;/sub> 5 kPa) with and without targeted temperature management to 33 °C (TTM33) in a porcine post-cardiac arrest model.&lt;h4>Methods&lt;/h4>39 pigs were resuscitated after 10 minutes of cardiac arrest using cardiopulmonary bypass and randomised to TTM33 or no-TTM, and hypercapnia or normocapnia. TTM33 was managed with intravasal cooling. Animals were stabilized for 30 minutes followed by a two-hour intervention period. Hemodynamic parameters were measured continuously, and neuromonitoring included intracranial pressure (ICP), pressure reactivity index, cerebral blood flow, brain-tissue pCO&lt;sub>2&lt;/sub> and microdialysis. Measurements are reported as proportion of baseline, and areas under the curve during the 120 min intervention period were compared.&lt;h4>Results&lt;/h4>Hypercapnia increased cerebral flow in both TTM33 and no-TTM groups, but also increased ICP (199% vs. 183% of baseline, &lt;i>p&lt;/i> = 0.018) and reduced cerebral perfusion pressure (70% vs. 84% of baseline, &lt;i>p&lt;/i> &lt; 0.001) in no-TTM animals. Cerebral lactate (196% vs. 297% of baseline, &lt;i>p&lt;/i> &lt; 0.001), pyruvate (118% vs. 152% of baseline, &lt;i>p&lt;/i> &lt; 0.001), glycerol and lactate/pyruvate ratios were lower with hypercapnia in the TTM33 group, but only pyruvate (133% vs. 150% of baseline, &lt;i>p&lt;/i> = 0.002) was lower with hypercapnia among no-TTM animals.&lt;h4>Conclusion&lt;/h4>In this porcine post-arrest model, hypercapnia led to increased cerebral flow both with and without hypothermia, but also increased ICP and reduced cerebral perfusion pressure in no-TTM animals. The effects of hypercapnia were different with and without TTM.(Institutional protocol number: FOTS, id 14931).</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2025-04-04T20:07:03.569Z</modification><creation>2025-04-04T20:07:03.569Z</creation></dates><accession>S-EPMC10950799</accession><cross_references><pubmed>38510376</pubmed><doi>10.1016/j.resplu.2024.100604</doi></cross_references></HashMap>