<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Strippoli GF</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Anemia is a risk factor for death, adverse cardiovascular outcomes and poor quality of life in patients with chronic kidney disease (CKD). Erythropoietin Stimulating Agents (ESA) are commonly used to increase hemoglobin levels in this population. In observational studies, higher hemoglobin levels (around 11-13 g/dL) are associated with improved survival and quality of life compared to hemoglobin levels around 9-10 g/dL. A systematic review of randomized trials found that targeting higher hemoglobin levels with ESA causes an increased risk of adverse vascular outcomes. It is possible, but has never been formally tested in a randomized trial, that ESA dose rather than targeted hemoglobin concentration itself mediates the increased risk of adverse vascular outcomes. The Cli</pubmed_abstract><journal>Trials</journal><pagination>70</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2903576</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effects of the dose of erythropoiesis stimulating agents on cardiovascular events, quality of life, and health-related costs in hemodialysis patients: the clinical evaluation of the dose of erythropoietins (C.E. DOSE) trial protocol.</pubmed_title><pmcid>PMC2903576</pmcid><pubmed_authors>Maione A</pubmed_authors><pubmed_authors>Vernaglione L</pubmed_authors><pubmed_authors>Strippoli GF</pubmed_authors><pubmed_authors>Flammini A</pubmed_authors><pubmed_authors>Di Micco L</pubmed_authors><pubmed_authors>Amoroso L</pubmed_authors><pubmed_authors>Nicolucci A</pubmed_authors><pubmed_authors>Triolo G</pubmed_authors><pubmed_authors>Amaru S</pubmed_authors><pubmed_authors>D'Alonzo D</pubmed_authors><pubmed_authors>Giannoccaro G</pubmed_authors><pubmed_authors>Di Franco D</pubmed_authors><pubmed_authors>Di Toro Mammarella R</pubmed_authors><pubmed_authors>D'Ambrosio N</pubmed_authors><pubmed_authors>Procaccini DA</pubmed_authors><pubmed_authors>Falco M</pubmed_authors><pubmed_authors>Montalto G</pubmed_authors><pubmed_authors>Malaguti M</pubmed_authors><pubmed_authors>Di Giulio S</pubmed_authors><pubmed_authors>Johnson DW</pubmed_authors><pubmed_authors>Vecchio M</pubmed_authors><pubmed_authors>Pellegrini F</pubmed_authors><pubmed_authors>Navaneethan SD</pubmed_authors><pubmed_authors>Bonifati C</pubmed_authors><pubmed_authors>Gori E</pubmed_authors><pubmed_authors>Fici M</pubmed_authors><pubmed_authors>La Rosa S</pubmed_authors><pubmed_authors>Hegbrant J</pubmed_authors><pubmed_authors>Querques M</pubmed_authors><pubmed_authors>Casu D</pubmed_authors><pubmed_authors>Vischini G</pubmed_authors><pubmed_authors>Palmer S</pubmed_authors><pubmed_authors>Santoro A</pubmed_authors><pubmed_authors>Saglimbene V</pubmed_authors><pubmed_authors>Tedesco M</pubmed_authors><pubmed_authors>Murgo A</pubmed_authors><pubmed_authors>Sambati M</pubmed_authors><pubmed_authors>Dagostino F</pubmed_authors><pubmed_authors>Tognoni G</pubmed_authors><pubmed_authors>Mandreoli M</pubmed_authors><pubmed_authors>Palumbo R</pubmed_authors><pubmed_authors>Craig JC</pubmed_authors><pubmed_authors>Greco V</pubmed_authors><pubmed_authors>Clinical Evaluation of the DOse of Erythropoietins Study Group (C.E. DOSE)</pubmed_authors><pubmed_authors>Boccia E</pubmed_authors><pubmed_authors>Valentini M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effects of the dose of erythropoiesis stimulating agents on cardiovascular events, quality of life, and health-related costs in hemodialysis patients: the clinical evaluation of the dose of erythropoietins (C.E. DOSE) trial protocol.</name><description>&lt;h4>Background&lt;/h4>Anemia is a risk factor for death, adverse cardiovascular outcomes and poor quality of life in patients with chronic kidney disease (CKD). Erythropoietin Stimulating Agents (ESA) are commonly used to increase hemoglobin levels in this population. In observational studies, higher hemoglobin levels (around 11-13 g/dL) are associated with improved survival and quality of life compared to hemoglobin levels around 9-10 g/dL. A systematic review of randomized trials found that targeting higher hemoglobin levels with ESA causes an increased risk of adverse vascular outcomes. It is possible, but has never been formally tested in a randomized trial, that ESA dose rather than targeted hemoglobin concentration itself mediates the increased risk of adverse vascular outcomes. The Cli</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jun</publication><modification>2025-04-19T15:13:32.876Z</modification><creation>2019-03-27T00:32:24Z</creation></dates><accession>S-EPMC2903576</accession><cross_references><pubmed>20534124</pubmed><doi>10.1186/1745-6215-11-70</doi></cross_references></HashMap>