<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2(11)</volume><submitter>Mark PB</submitter><funding>Vifor Fresenius Medical Care Renal Pharma</funding><funding>Kidney Research UK</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>People with kidney failure treated with hemodialysis (HD) are at increased risk of stroke compared with similarly aged people with normal kidney function. One concern is that treatment of renal anemia might increase stroke risk. We studied risk factors for stroke in a prespecified secondary analysis of a randomized, controlled trial of intravenous iron treatment strategies in HD.&lt;h4>Methods&lt;/h4>We analyzed data from the Proactive IV Iron Therapy in Haemodialysis Patients (PIVOTAL) trial, focusing on variables associated with risk of stroke. The trial randomized 2141 adults who had started HD &lt;12 months earlier and who were receiving an erythropoiesis-stimulating agent (ESA) to high-dose IV iron administered proactively or low-dose IV iron administered reactively in a 1:1</pubmed_abstract><journal>Kidney360</journal><pagination>1761-1769</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8785850</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Stroke in Hemodialysis Patients Randomized to Different Intravenous Iron Strategies: A Prespecified Analysis from the PIVOTAL Trial.</pubmed_title><pmcid>PMC8785850</pmcid><pubmed_authors>Ford I</pubmed_authors><pubmed_authors>Akbani H</pubmed_authors><pubmed_authors>Brown A</pubmed_authors><pubmed_authors>Khwaja A</pubmed_authors><pubmed_authors>Ramadoss S</pubmed_authors><pubmed_authors>Solomon L</pubmed_authors><pubmed_authors>Severn A</pubmed_authors><pubmed_authors>Wheeler DC</pubmed_authors><pubmed_authors>Ayub W</pubmed_authors><pubmed_authors>Neary J</pubmed_authors><pubmed_authors>Walters MR</pubmed_authors><pubmed_authors>Barratt J</pubmed_authors><pubmed_authors>Winnett G</pubmed_authors><pubmed_authors>Lawman S</pubmed_authors><pubmed_authors>Hall M</pubmed_authors><pubmed_authors>Nicholas J</pubmed_authors><pubmed_authors>Dasgupta I</pubmed_authors><pubmed_authors>Moriarty J</pubmed_authors><pubmed_authors>McMurray JJV</pubmed_authors><pubmed_authors>Basanyake K</pubmed_authors><pubmed_authors>Connor A</pubmed_authors><pubmed_authors>Vilar E</pubmed_authors><pubmed_authors>Harty J</pubmed_authors><pubmed_authors>Petrie MC</pubmed_authors><pubmed_authors>Wellberry-Smith M</pubmed_authors><pubmed_authors>Jhund PS</pubmed_authors><pubmed_authors>Mark PB</pubmed_authors><pubmed_authors>Connolly E</pubmed_authors><pubmed_authors>Macdougall IC</pubmed_authors><pubmed_authors>Benzimra R</pubmed_authors><pubmed_authors>Alchi B</pubmed_authors><pubmed_authors>Winearls CG</pubmed_authors><pubmed_authors>McCafferty K</pubmed_authors><pubmed_authors>Bolton S</pubmed_authors><pubmed_authors>PIVOTAL Investigators</pubmed_authors><pubmed_authors>Griffiths M</pubmed_authors><pubmed_authors>Mikhail A</pubmed_authors><pubmed_authors>Wessels J</pubmed_authors><pubmed_authors>Chowdury P</pubmed_authors><pubmed_authors>Swift P</pubmed_authors><pubmed_authors>Balasubramaniam G</pubmed_authors><pubmed_authors>Banerjee D</pubmed_authors><pubmed_authors>Anker SD</pubmed_authors><pubmed_authors>Bhandari S</pubmed_authors><pubmed_authors>White C</pubmed_authors><pubmed_authors>Thomson P</pubmed_authors><pubmed_authors>Shivashankar G</pubmed_authors><pubmed_authors>Power A</pubmed_authors><pubmed_authors>Tomson CRV</pubmed_authors><pubmed_authors>Mitra S</pubmed_authors><pubmed_authors>Ross C</pubmed_authors><pubmed_authors>Kirk A</pubmed_authors><pubmed_authors>Ledson T</pubmed_authors><pubmed_authors>Walsh S</pubmed_authors><pubmed_authors>Goldsmith C</pubmed_authors><pubmed_authors>Stratton J</pubmed_authors><pubmed_authors>Doyle A</pubmed_authors><pubmed_authors>Maxwell P</pubmed_authors><pubmed_authors>Quinn M</pubmed_authors><pubmed_authors>Doulton T</pubmed_authors><pubmed_authors>Clarke H</pubmed_authors><pubmed_authors>Day C</pubmed_authors><pubmed_authors>Smith S</pubmed_authors><pubmed_authors>Bell S</pubmed_authors><pubmed_authors>Farrington K</pubmed_authors><pubmed_authors>Ramakrishna B</pubmed_authors><pubmed_authors>Robertson M</pubmed_authors><pubmed_authors>Jesky M</pubmed_authors><pubmed_authors>Kalra PA</pubmed_authors><pubmed_authors>Brown R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Stroke in Hemodialysis Patients Randomized to Different Intravenous Iron Strategies: A Prespecified Analysis from the PIVOTAL Trial.</name><description>&lt;h4>Background&lt;/h4>People with kidney failure treated with hemodialysis (HD) are at increased risk of stroke compared with similarly aged people with normal kidney function. One concern is that treatment of renal anemia might increase stroke risk. We studied risk factors for stroke in a prespecified secondary analysis of a randomized, controlled trial of intravenous iron treatment strategies in HD.&lt;h4>Methods&lt;/h4>We analyzed data from the Proactive IV Iron Therapy in Haemodialysis Patients (PIVOTAL) trial, focusing on variables associated with risk of stroke. The trial randomized 2141 adults who had started HD &lt;12 months earlier and who were receiving an erythropoiesis-stimulating agent (ESA) to high-dose IV iron administered proactively or low-dose IV iron administered reactively in a 1:1</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2026-05-09T09:30:33.627Z</modification><creation>2025-04-04T22:04:17.602Z</creation></dates><accession>S-EPMC8785850</accession><cross_references><pubmed>35372992</pubmed><doi>10.34067/kid.0004272021</doi><doi>10.34067/KID.0004272021</doi></cross_references></HashMap>