<HashMap><database>biostudies-literature</database><scores/><additional><submitter>During J</submitter><funding>Thelma Zoega Foundation</funding><funding>European Clinical Research Infrastructures Network</funding><funding>Hans-Gabriel and Alice Trolle-Wachtmeister Foundation for Medical Research</funding><funding>Swedish Heart Lung Foundation</funding><funding>The Torsten Söderberg foundation at the Royal Swedish Academy of Sciences</funding><funding>The Swedish Brain Foundation</funding><funding>Lions Research fund Skåne</funding><funding>Swedish Research Council</funding><funding>Lundbeck Foundation</funding><funding>The Koch Foundation</funding><funding>TrygFonden</funding><funding>Arbetsmarknadens Försäkringsaktiebolag</funding><funding>The County Council of Skåne</funding><funding>Stig and Ragna Gorthon Foundation</funding><funding>Skåne University Hospital Foundations, the Gyllenstierna-Krapperup Foundation, and governmental funding of clinical research within the Swedish National Health System</funding><funding>Thure Carlsson Foundation</funding><funding>Lundbeckfonden</funding><funding>The Swedish Society of Medicine</funding><funding>South Swedish Hospital Region Research Funds</funding><pagination>185</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7189642</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Arginine vasopressin has complex actions in critically ill patients, involving vasoregulatory status, plasma volume, and cortisol levels. Copeptin, a surrogate marker for arginine vasopressin, has shown promising prognostic features in small observational studies and is used clinically for early rule out of acute coronary syndrome. The objective of this study was to explore the association between early measurements of copeptin, circulatory status, and short-term survival after out-of-hospital cardiac arrest.&lt;h4>Methods&lt;/h4>Serial blood samples were collected at 24, 48, and 72 h as part of the target temperature management at 33 °C versus 36 °C after cardiac arrest trial, an international multicenter randomized trial where unconscious survivors after out-of-hospital card</pubmed_abstract><journal>Critical care (London, England)</journal><pubmed_title>Copeptin as a marker of outcome after cardiac arrest: a sub-study of the TTM trial.</pubmed_title><pmcid>PMC7189642</pmcid><funding_grant_id>R186-2015-2132</funding_grant_id><funding_grant_id>NA</funding_grant_id><funding_grant_id>134281, 296161, 286321</funding_grant_id><funding_grant_id>M2010/1837, M2010/1641, 353301</funding_grant_id><funding_grant_id>100001</funding_grant_id><funding_grant_id>20090275</funding_grant_id><pubmed_authors>Wise M</pubmed_authors><pubmed_authors>Horn J</pubmed_authors><pubmed_authors>Wanscher MJ</pubmed_authors><pubmed_authors>Hassager C</pubmed_authors><pubmed_authors>During J</pubmed_authors><pubmed_authors>Devaux Y</pubmed_authors><pubmed_authors>Unden J</pubmed_authors><pubmed_authors>Annborn M</pubmed_authors><pubmed_authors>Dankiewicz J</pubmed_authors><pubmed_authors>Nielsen N</pubmed_authors><pubmed_authors>Friberg H</pubmed_authors><pubmed_authors>Cronberg T</pubmed_authors><pubmed_authors>Stammet P</pubmed_authors><pubmed_authors>Kuiper M</pubmed_authors><pubmed_authors>Kjaergaard J</pubmed_authors><pubmed_authors>Nikoukhah HR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Copeptin as a marker of outcome after cardiac arrest: a sub-study of the TTM trial.</name><description>&lt;h4>Background&lt;/h4>Arginine vasopressin has complex actions in critically ill patients, involving vasoregulatory status, plasma volume, and cortisol levels. Copeptin, a surrogate marker for arginine vasopressin, has shown promising prognostic features in small observational studies and is used clinically for early rule out of acute coronary syndrome. The objective of this study was to explore the association between early measurements of copeptin, circulatory status, and short-term survival after out-of-hospital cardiac arrest.&lt;h4>Methods&lt;/h4>Serial blood samples were collected at 24, 48, and 72 h as part of the target temperature management at 33 °C versus 36 °C after cardiac arrest trial, an international multicenter randomized trial where unconscious survivors after out-of-hospital card</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2026-05-01T03:24:36.801Z</modification><creation>2020-05-22T19:10:45Z</creation></dates><accession>S-EPMC7189642</accession><cross_references><pubmed>32345356</pubmed><doi>10.1186/s13054-020-02904-8</doi></cross_references></HashMap>