<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Campbell NG</submitter><funding>British Heart Foundation</funding><pagination>618</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5745783</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Atrial fibrillation (AF) occurs in approximately one in three patients after cardiac surgery, and is associated with increased short-term and long-term mortality, intensive care unit (ICU) and hospital stay, and increased cost of care. In an attempt to reduce AF incidence in these patients, serum potassium (K+) levels are commonly maintained at the high end of normal (4.5-5.5 mEq/L). However, such potassium supplementation is without proven benefit, and is not without negative consequences. It carries clinical risk, negatively impacts patient experience and is both time-consuming and costly. This protocol describes a randomised controlled pilot trial to assess the feasibility of a proposed randomised non-inferiority trial to investigate the impact of maintaining serum po</pubmed_abstract><journal>Trials</journal><pubmed_title>The impact of maintaining serum potassium ≥3.6 mEq/L vs ≥4.5 mEq/L on the incidence of new-onset atrial fibrillation in the first 120 hours after isolated elective coronary artery bypass grafting - study protocol for a randomised feasibility trial for the proposed Tight K randomized non-inferiority trial.</pubmed_title><pmcid>PMC5745783</pmcid><funding_grant_id>PG/16/15/32050</funding_grant_id><pubmed_authors>Campbell NG</pubmed_authors><pubmed_authors>Sanders J</pubmed_authors><pubmed_authors>O'Brien B</pubmed_authors><pubmed_authors>Swinson R</pubmed_authors><pubmed_authors>Sturgess J</pubmed_authors><pubmed_authors>Montgomery H</pubmed_authors><pubmed_authors>Allen E</pubmed_authors><pubmed_authors>Birch S</pubmed_authors><pubmed_authors>Elbourne D</pubmed_authors><pubmed_authors>Al-Subaie N</pubmed_authors></additional><is_claimable>false</is_claimable><name>The impact of maintaining serum potassium ≥3.6 mEq/L vs ≥4.5 mEq/L on the incidence of new-onset atrial fibrillation in the first 120 hours after isolated elective coronary artery bypass grafting - study protocol for a randomised feasibility trial for the proposed Tight K randomized non-inferiority trial.</name><description>&lt;h4>Background&lt;/h4>Atrial fibrillation (AF) occurs in approximately one in three patients after cardiac surgery, and is associated with increased short-term and long-term mortality, intensive care unit (ICU) and hospital stay, and increased cost of care. In an attempt to reduce AF incidence in these patients, serum potassium (K+) levels are commonly maintained at the high end of normal (4.5-5.5 mEq/L). However, such potassium supplementation is without proven benefit, and is not without negative consequences. It carries clinical risk, negatively impacts patient experience and is both time-consuming and costly. This protocol describes a randomised controlled pilot trial to assess the feasibility of a proposed randomised non-inferiority trial to investigate the impact of maintaining serum po</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Dec</publication><modification>2026-06-09T06:39:41.107Z</modification><creation>2019-03-27T03:05:53Z</creation></dates><accession>S-EPMC5745783</accession><cross_references><pubmed>29282098</pubmed><doi>10.1186/s13063-017-2349-x</doi></cross_references></HashMap>