<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lasocki S</submitter><funding>ministère de la santé</funding><funding>ministère de la santé (FR)</funding><pagination>62</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7885380</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Anemia is a significant problem in patients on ICU. Its commonest cause, iron deficiency (ID), is difficult to diagnose in the context of inflammation. Hepcidin is a new marker of ID. We aimed to assess whether hepcidin levels would accurately guide treatment of ID in critically ill anemic patients after a prolonged ICU stay and affect the post-ICU outcomes.&lt;h4>Methods&lt;/h4>In a controlled, single-blinded, multicenter study, anemic (WHO definition) critically ill patients with an ICU stay ≥ 5 days were randomized when discharge was expected to either intervention by hepcidin treatment protocol or control. In the intervention arm, patients were treated with intravenous iron (1 g of ferric carboxymaltose) when hepcidin was &lt; 20 μg/l and with intravenous iron and erythropoie</pubmed_abstract><journal>Critical care (London, England)</journal><pubmed_title>Impact of treating iron deficiency, diagnosed according to hepcidin quantification, on outcomes after a prolonged ICU stay compared to standard care: a multicenter, randomized, single-blinded trial.</pubmed_title><pmcid>PMC7885380</pmcid><funding_grant_id>STIC 2012 N° 2-12-0006</funding_grant_id><pubmed_authors>Puy H</pubmed_authors><pubmed_authors>Geneve C</pubmed_authors><pubmed_authors>Mercat A</pubmed_authors><pubmed_authors>Isslame S</pubmed_authors><pubmed_authors>Leger M</pubmed_authors><pubmed_authors>Asfar P</pubmed_authors><pubmed_authors>Seguin P</pubmed_authors><pubmed_authors>Hepcidane study group</pubmed_authors><pubmed_authors>Nagot N</pubmed_authors><pubmed_authors>Lehmann S</pubmed_authors><pubmed_authors>Barbaz M</pubmed_authors><pubmed_authors>Ferrandiere M</pubmed_authors><pubmed_authors>Chanques G</pubmed_authors><pubmed_authors>Kerforne T</pubmed_authors><pubmed_authors>Peoc'h K</pubmed_authors><pubmed_authors>Gaillard T</pubmed_authors><pubmed_authors>Lefebvre T</pubmed_authors><pubmed_authors>Montravers P</pubmed_authors><pubmed_authors>Launey Y</pubmed_authors><pubmed_authors>Asehnoune K</pubmed_authors><pubmed_authors>Delaby C</pubmed_authors><pubmed_authors>Beloncle F</pubmed_authors><pubmed_authors>Rineau E</pubmed_authors><pubmed_authors>Mimoz O</pubmed_authors><pubmed_authors>Jaber S</pubmed_authors><pubmed_authors>Mercier G</pubmed_authors><pubmed_authors>Hirtz C</pubmed_authors><pubmed_authors>Sargentini C</pubmed_authors><pubmed_authors>Roquilly A</pubmed_authors><pubmed_authors>Boisson M</pubmed_authors><pubmed_authors>Marin G</pubmed_authors><pubmed_authors>Gergaud S</pubmed_authors><pubmed_authors>Lasocki S</pubmed_authors><pubmed_authors>Dahyot-Fizelier C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of treating iron deficiency, diagnosed according to hepcidin quantification, on outcomes after a prolonged ICU stay compared to standard care: a multicenter, randomized, single-blinded trial.</name><description>&lt;h4>Background&lt;/h4>Anemia is a significant problem in patients on ICU. Its commonest cause, iron deficiency (ID), is difficult to diagnose in the context of inflammation. Hepcidin is a new marker of ID. We aimed to assess whether hepcidin levels would accurately guide treatment of ID in critically ill anemic patients after a prolonged ICU stay and affect the post-ICU outcomes.&lt;h4>Methods&lt;/h4>In a controlled, single-blinded, multicenter study, anemic (WHO definition) critically ill patients with an ICU stay ≥ 5 days were randomized when discharge was expected to either intervention by hepcidin treatment protocol or control. In the intervention arm, patients were treated with intravenous iron (1 g of ferric carboxymaltose) when hepcidin was &lt; 20 μg/l and with intravenous iron and erythropoie</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2026-05-09T09:51:27.07Z</modification><creation>2022-02-10T13:38:52.6Z</creation></dates><accession>S-EPMC7885380</accession><cross_references><pubmed>33588893</pubmed><doi>10.1186/s13054-020-03430-3</doi></cross_references></HashMap>