Omega-3 Fatty Acid Supplementation Does Not Reduce Risk of Atrial Fibrillation After Coronary Artery Bypass Surgery: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial

BACKGROUND—Omega-3 polyunsaturated fatty acids (n-3 PUFA) have been reported to reduce the risk of sudden cardiac death presumed to be due to fatal ventricular arrhythmias, but their effect on atrial arrhythmias is unclear. METHODS AND RESULTS—Patients (n=108) undergoing coronary artery bypass graft...

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Veröffentlicht in:Circulation. Arrhythmia and electrophysiology 2010-02, Vol.3 (1), p.46-53
Hauptverfasser: Saravanan, Palaniappan, Bridgewater, Ben, West, Annette L, OʼNeill, Stephen C, Calder, Philip C, Davidson, Neil C
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container_end_page 53
container_issue 1
container_start_page 46
container_title Circulation. Arrhythmia and electrophysiology
container_volume 3
creator Saravanan, Palaniappan
Bridgewater, Ben
West, Annette L
OʼNeill, Stephen C
Calder, Philip C
Davidson, Neil C
description BACKGROUND—Omega-3 polyunsaturated fatty acids (n-3 PUFA) have been reported to reduce the risk of sudden cardiac death presumed to be due to fatal ventricular arrhythmias, but their effect on atrial arrhythmias is unclear. METHODS AND RESULTS—Patients (n=108) undergoing coronary artery bypass graft surgery were randomly assigned to receive 2 g/d n-3 PUFA or placebo (olive oil) for at least 5 days before surgery (median, 16 days; range, 12 to 21 days). Phospholipid n-3 PUFA were measured in serum at study entry and at surgery and in right atrial appendage tissue at surgery. Echocardiography was used to assess left ventricular function and left atrial dimensions. Postoperative continuous ECG monitoring (Lifecard CF) for 5 days or until discharge, if earlier, was performed with a daily 12-lead ECG and clinical review if patients remained in the hospital beyond 5 days. Lifecard recordings were analyzed for episodes of atrial fibrillation (AF) ≥30 seconds (primary outcome). Clinical AF, AF burden (% time in AF), hospital stay, and intensive care/high dependency care stay were measured as secondary outcomes. One hundred three patients completed the study (51 in the placebo group and 52 in the n-3 PUFA group). There were no clinically relevant differences in baseline characteristics between groups. n-3 PUFA levels were higher in serum and right atrial tissue in the active treatment group. There was no significant difference between groups in the primary outcome of AF (95% confidence interval [CI], −6% to 30%, P=0.28) in any of the secondary outcomes or in AF-free survival. CONCLUSIONS—Omega-3 PUFA do not reduce the risk of AF after coronary artery bypass graft surgery. CLINICAL TRIAL REGISTRATION—www.ukcrn.org.uk. Identifier4437.
doi_str_mv 10.1161/CIRCEP.109.899633
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METHODS AND RESULTS—Patients (n=108) undergoing coronary artery bypass graft surgery were randomly assigned to receive 2 g/d n-3 PUFA or placebo (olive oil) for at least 5 days before surgery (median, 16 days; range, 12 to 21 days). Phospholipid n-3 PUFA were measured in serum at study entry and at surgery and in right atrial appendage tissue at surgery. Echocardiography was used to assess left ventricular function and left atrial dimensions. Postoperative continuous ECG monitoring (Lifecard CF) for 5 days or until discharge, if earlier, was performed with a daily 12-lead ECG and clinical review if patients remained in the hospital beyond 5 days. Lifecard recordings were analyzed for episodes of atrial fibrillation (AF) ≥30 seconds (primary outcome). Clinical AF, AF burden (% time in AF), hospital stay, and intensive care/high dependency care stay were measured as secondary outcomes. One hundred three patients completed the study (51 in the placebo group and 52 in the n-3 PUFA group). There were no clinically relevant differences in baseline characteristics between groups. n-3 PUFA levels were higher in serum and right atrial tissue in the active treatment group. There was no significant difference between groups in the primary outcome of AF (95% confidence interval [CI], −6% to 30%, P=0.28) in any of the secondary outcomes or in AF-free survival. CONCLUSIONS—Omega-3 PUFA do not reduce the risk of AF after coronary artery bypass graft surgery. CLINICAL TRIAL REGISTRATION—www.ukcrn.org.uk. Identifier4437.</description><identifier>ISSN: 1941-3149</identifier><identifier>EISSN: 1941-3084</identifier><identifier>DOI: 10.1161/CIRCEP.109.899633</identifier><identifier>PMID: 20042769</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Aged ; Atrial Fibrillation - etiology ; Atrial Fibrillation - prevention &amp; control ; C-Reactive Protein - analysis ; Coronary Artery Bypass - adverse effects ; Double-Blind Method ; Echocardiography ; Electrocardiography ; Fatty Acids, Omega-3 - analysis ; Fatty Acids, Omega-3 - blood ; Fatty Acids, Omega-3 - therapeutic use ; Female ; Heart Atria - metabolism ; Humans ; Male ; Middle Aged ; Preoperative Care</subject><ispartof>Circulation. 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Arrhythmia and electrophysiology</title><addtitle>Circ Arrhythm Electrophysiol</addtitle><description>BACKGROUND—Omega-3 polyunsaturated fatty acids (n-3 PUFA) have been reported to reduce the risk of sudden cardiac death presumed to be due to fatal ventricular arrhythmias, but their effect on atrial arrhythmias is unclear. METHODS AND RESULTS—Patients (n=108) undergoing coronary artery bypass graft surgery were randomly assigned to receive 2 g/d n-3 PUFA or placebo (olive oil) for at least 5 days before surgery (median, 16 days; range, 12 to 21 days). Phospholipid n-3 PUFA were measured in serum at study entry and at surgery and in right atrial appendage tissue at surgery. Echocardiography was used to assess left ventricular function and left atrial dimensions. Postoperative continuous ECG monitoring (Lifecard CF) for 5 days or until discharge, if earlier, was performed with a daily 12-lead ECG and clinical review if patients remained in the hospital beyond 5 days. Lifecard recordings were analyzed for episodes of atrial fibrillation (AF) ≥30 seconds (primary outcome). Clinical AF, AF burden (% time in AF), hospital stay, and intensive care/high dependency care stay were measured as secondary outcomes. One hundred three patients completed the study (51 in the placebo group and 52 in the n-3 PUFA group). There were no clinically relevant differences in baseline characteristics between groups. n-3 PUFA levels were higher in serum and right atrial tissue in the active treatment group. There was no significant difference between groups in the primary outcome of AF (95% confidence interval [CI], −6% to 30%, P=0.28) in any of the secondary outcomes or in AF-free survival. CONCLUSIONS—Omega-3 PUFA do not reduce the risk of AF after coronary artery bypass graft surgery. CLINICAL TRIAL REGISTRATION—www.ukcrn.org.uk. Identifier4437.</description><subject>Aged</subject><subject>Atrial Fibrillation - etiology</subject><subject>Atrial Fibrillation - prevention &amp; control</subject><subject>C-Reactive Protein - analysis</subject><subject>Coronary Artery Bypass - adverse effects</subject><subject>Double-Blind Method</subject><subject>Echocardiography</subject><subject>Electrocardiography</subject><subject>Fatty Acids, Omega-3 - analysis</subject><subject>Fatty Acids, Omega-3 - blood</subject><subject>Fatty Acids, Omega-3 - therapeutic use</subject><subject>Female</subject><subject>Heart Atria - metabolism</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Preoperative Care</subject><issn>1941-3149</issn><issn>1941-3084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UU1P3TAQjKpWhVJ-QC-Vb700r_6KE_cWUh4goYJe4Rw5zgZcnDjYjtDrz-ovrFGgh5V35JlZ7U6WfSJ4Q4gg35qLXXN6vSFYbiopBWNvskMiOckZrvjb155weZB9COE3xoJURLzPDijGnJZCHmZ_r0a4UzlDWxXjHtXa9OjXMs8WRpiiisZN6IeDgH66iHbQLxrQzoQH5AZUR2-URVvTeWPtyq2HCB41zrtJ-eTnE9yjk_2sQkjG_i7B76hGOzX1bjR_oP-a_JfOQn5izZTQtVUaOpc3boreWQs9atKP0WnUzfPAj9m7QdkAxy_vUXa7Pb1pzvPLq7OLpr7MNZWlzHsgMHRFqUWpKYVCloUCqQvBRCcqWuByYDBwoSqBqx4wHUpJKeNaJ02hODvKvqy-s3ePC4TYjiZoSJtO4JbQloyJikleJCZZmdq7EDwM7ezNmPZvCW6fk2rXpBKU7ZpU0nx-cV-6Efr_itdoEoGvhCdn0xHDg12ewLf3oGy8bzFhrOSS5RQTjJMI56mwZP8AN36gFQ</recordid><startdate>201002</startdate><enddate>201002</enddate><creator>Saravanan, Palaniappan</creator><creator>Bridgewater, Ben</creator><creator>West, Annette L</creator><creator>OʼNeill, Stephen C</creator><creator>Calder, Philip C</creator><creator>Davidson, Neil C</creator><general>American Heart Association, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201002</creationdate><title>Omega-3 Fatty Acid Supplementation Does Not Reduce Risk of Atrial Fibrillation After Coronary Artery Bypass Surgery: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial</title><author>Saravanan, Palaniappan ; Bridgewater, Ben ; West, Annette L ; OʼNeill, Stephen C ; Calder, Philip C ; Davidson, Neil C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2979-de1efb57c67c22e5975ae9c5636b682507f3ef46a8608de02f792234cc57c5a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Aged</topic><topic>Atrial Fibrillation - etiology</topic><topic>Atrial Fibrillation - prevention &amp; control</topic><topic>C-Reactive Protein - analysis</topic><topic>Coronary Artery Bypass - adverse effects</topic><topic>Double-Blind Method</topic><topic>Echocardiography</topic><topic>Electrocardiography</topic><topic>Fatty Acids, Omega-3 - analysis</topic><topic>Fatty Acids, Omega-3 - blood</topic><topic>Fatty Acids, Omega-3 - therapeutic use</topic><topic>Female</topic><topic>Heart Atria - metabolism</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Preoperative Care</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saravanan, Palaniappan</creatorcontrib><creatorcontrib>Bridgewater, Ben</creatorcontrib><creatorcontrib>West, Annette L</creatorcontrib><creatorcontrib>OʼNeill, Stephen C</creatorcontrib><creatorcontrib>Calder, Philip C</creatorcontrib><creatorcontrib>Davidson, Neil C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Circulation. Arrhythmia and electrophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saravanan, Palaniappan</au><au>Bridgewater, Ben</au><au>West, Annette L</au><au>OʼNeill, Stephen C</au><au>Calder, Philip C</au><au>Davidson, Neil C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Omega-3 Fatty Acid Supplementation Does Not Reduce Risk of Atrial Fibrillation After Coronary Artery Bypass Surgery: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial</atitle><jtitle>Circulation. Arrhythmia and electrophysiology</jtitle><addtitle>Circ Arrhythm Electrophysiol</addtitle><date>2010-02</date><risdate>2010</risdate><volume>3</volume><issue>1</issue><spage>46</spage><epage>53</epage><pages>46-53</pages><issn>1941-3149</issn><eissn>1941-3084</eissn><abstract>BACKGROUND—Omega-3 polyunsaturated fatty acids (n-3 PUFA) have been reported to reduce the risk of sudden cardiac death presumed to be due to fatal ventricular arrhythmias, but their effect on atrial arrhythmias is unclear. METHODS AND RESULTS—Patients (n=108) undergoing coronary artery bypass graft surgery were randomly assigned to receive 2 g/d n-3 PUFA or placebo (olive oil) for at least 5 days before surgery (median, 16 days; range, 12 to 21 days). Phospholipid n-3 PUFA were measured in serum at study entry and at surgery and in right atrial appendage tissue at surgery. Echocardiography was used to assess left ventricular function and left atrial dimensions. Postoperative continuous ECG monitoring (Lifecard CF) for 5 days or until discharge, if earlier, was performed with a daily 12-lead ECG and clinical review if patients remained in the hospital beyond 5 days. Lifecard recordings were analyzed for episodes of atrial fibrillation (AF) ≥30 seconds (primary outcome). Clinical AF, AF burden (% time in AF), hospital stay, and intensive care/high dependency care stay were measured as secondary outcomes. One hundred three patients completed the study (51 in the placebo group and 52 in the n-3 PUFA group). There were no clinically relevant differences in baseline characteristics between groups. n-3 PUFA levels were higher in serum and right atrial tissue in the active treatment group. There was no significant difference between groups in the primary outcome of AF (95% confidence interval [CI], −6% to 30%, P=0.28) in any of the secondary outcomes or in AF-free survival. CONCLUSIONS—Omega-3 PUFA do not reduce the risk of AF after coronary artery bypass graft surgery. CLINICAL TRIAL REGISTRATION—www.ukcrn.org.uk. Identifier4437.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>20042769</pmid><doi>10.1161/CIRCEP.109.899633</doi><tpages>8</tpages></addata></record>
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source MEDLINE; American Heart Association Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Aged
Atrial Fibrillation - etiology
Atrial Fibrillation - prevention & control
C-Reactive Protein - analysis
Coronary Artery Bypass - adverse effects
Double-Blind Method
Echocardiography
Electrocardiography
Fatty Acids, Omega-3 - analysis
Fatty Acids, Omega-3 - blood
Fatty Acids, Omega-3 - therapeutic use
Female
Heart Atria - metabolism
Humans
Male
Middle Aged
Preoperative Care
title Omega-3 Fatty Acid Supplementation Does Not Reduce Risk of Atrial Fibrillation After Coronary Artery Bypass Surgery: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial
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