Atorvastatin for prevention of atrial fibrillation recurrence following pulmonary vein isolation: A double-blind, placebo-controlled, randomized trial
Background It is known that statins are effective in preventing atrial fibrillation (AF) in patients undergoing cardiac surgery. Objective The purpose of this study was to evaluate the efficacy of statins in preventing AF recurrence following left atrial ablation. Methods One hundred twenty-five pat...
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creator | Suleiman, Mahmoud, MD Koestler, Celeste, RN Lerman, Amir, MD Lopez-Jimenez, Francisco, MD Herges, Regina, BS Hodge, David, MS Bradley, David, MD, PhD Cha, Yong-Mei, MD Brady, Peter A., MD Munger, Thomas M., MD Asirvatham, Samuel J., MD, FHRS Packer, Douglas L., MD, FHRS Friedman, Paul A., MD, FHRS |
description | Background It is known that statins are effective in preventing atrial fibrillation (AF) in patients undergoing cardiac surgery. Objective The purpose of this study was to evaluate the efficacy of statins in preventing AF recurrence following left atrial ablation. Methods One hundred twenty-five patients who had no statin indication undergoing catheter ablation due to drug-refractory paroxysmal (n = 90) or persistent (n = 35) AF were randomized in a prospective, double-blind, placebo-controlled trial to receive 80 mg atorvastatin (n = 62) or placebo (n = 63) for 3 months. The primary endpoint was freedom from symptomatic AF at 3 months. Secondary endpoints included freedom from any atrial arrhythmia recurrence irrespective of symptoms, quality of life (QoL), and reduction in C-reactive protein (CRP). Results At 3 months, 95% of patients in the atorvastatin group were free of symptomatic AF compared with 93.5% in the placebo group ( P = .75). Similarly, 85% of patients treated in the atorvastatin group remained free of any recurrent atrial arrhythmia vs 88% of patients in the placebo group ( P = .37). Mean CRP levels decreased in the atorvastatin group (mean change −0.75 ± 3, P = .02) and increased in the placebo group (mean change 2.1 ± 19.9, P = .48). Mean QoL score improved significantly in both groups (mean change 13.14 ± 18.2 in the atorvastatin group and 11.10 ± 17.7 in the placebo group, P = .53). Conclusion In patients with no standard indication for statin therapy, treatment with atorvastatin 80 mg/day following AF ablation does not decrease the risk of AF recurrence in the first 3 months and should not be routinely administered to prevent periprocedural arrhythmias. |
doi_str_mv | 10.1016/j.hrthm.2011.09.016 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_918575136</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S154752711101071X</els_id><sourcerecordid>918575136</sourcerecordid><originalsourceid>FETCH-LOGICAL-c479t-4203ee99209881a0552c31b1367d715109d87b317e3c2d3c7c0d40b8c999253f3</originalsourceid><addsrcrecordid>eNqFUk2LFDEUbERx19VfIEhuXuw2r9M96QgKw-IXLHhQwVtIJ6_djOlkTNIj6w_x95qeWT148ZTwqKpHVb2qegy0AQqb57vmOubruWkpQENFU2Z3qnPo-03NBg5313_H677lcFY9SGlHaSs2lN2vzloQLe0GOK9-bXOIB5WyytaTKUSyj3hAn23wJExE5WiVI5Mdo3VOHccR9RIjeo2F4Fz4Yf1Xsl_cHLyKN-SARcmmcEK_IFtiwjI6rEdnvXlG9k5pHEOtg8-x8LHMovImzPYnGnJc-LC6NymX8NHte1F9fvP60-W7-urD2_eX26tad1zkumspQxTFjBgGULTvW81gBLbhhkMPVJiBjww4Mt0aprmmpqPjoEXh9GxiF9XTk-4-hu8LpixnmzQWpx7DkqSAoed90StIdkLqGFKKOMl9tHPxK4HKtQ-5k8c-5NqHpEKWWWE9udVfxhnNX86fAgrg5QmAxeXBYpRJ2zVaY0vMWZpg_7Pg1T98XVK2WrlveINpF5boS4ASZGollR_Xk1gvAooi5fCF_QbZV7Tj</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>918575136</pqid></control><display><type>article</type><title>Atorvastatin for prevention of atrial fibrillation recurrence following pulmonary vein isolation: A double-blind, placebo-controlled, randomized trial</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Suleiman, Mahmoud, MD ; Koestler, Celeste, RN ; Lerman, Amir, MD ; Lopez-Jimenez, Francisco, MD ; Herges, Regina, BS ; Hodge, David, MS ; Bradley, David, MD, PhD ; Cha, Yong-Mei, MD ; Brady, Peter A., MD ; Munger, Thomas M., MD ; Asirvatham, Samuel J., MD, FHRS ; Packer, Douglas L., MD, FHRS ; Friedman, Paul A., MD, FHRS</creator><creatorcontrib>Suleiman, Mahmoud, MD ; Koestler, Celeste, RN ; Lerman, Amir, MD ; Lopez-Jimenez, Francisco, MD ; Herges, Regina, BS ; Hodge, David, MS ; Bradley, David, MD, PhD ; Cha, Yong-Mei, MD ; Brady, Peter A., MD ; Munger, Thomas M., MD ; Asirvatham, Samuel J., MD, FHRS ; Packer, Douglas L., MD, FHRS ; Friedman, Paul A., MD, FHRS</creatorcontrib><description>Background It is known that statins are effective in preventing atrial fibrillation (AF) in patients undergoing cardiac surgery. Objective The purpose of this study was to evaluate the efficacy of statins in preventing AF recurrence following left atrial ablation. Methods One hundred twenty-five patients who had no statin indication undergoing catheter ablation due to drug-refractory paroxysmal (n = 90) or persistent (n = 35) AF were randomized in a prospective, double-blind, placebo-controlled trial to receive 80 mg atorvastatin (n = 62) or placebo (n = 63) for 3 months. The primary endpoint was freedom from symptomatic AF at 3 months. Secondary endpoints included freedom from any atrial arrhythmia recurrence irrespective of symptoms, quality of life (QoL), and reduction in C-reactive protein (CRP). Results At 3 months, 95% of patients in the atorvastatin group were free of symptomatic AF compared with 93.5% in the placebo group ( P = .75). Similarly, 85% of patients treated in the atorvastatin group remained free of any recurrent atrial arrhythmia vs 88% of patients in the placebo group ( P = .37). Mean CRP levels decreased in the atorvastatin group (mean change −0.75 ± 3, P = .02) and increased in the placebo group (mean change 2.1 ± 19.9, P = .48). Mean QoL score improved significantly in both groups (mean change 13.14 ± 18.2 in the atorvastatin group and 11.10 ± 17.7 in the placebo group, P = .53). Conclusion In patients with no standard indication for statin therapy, treatment with atorvastatin 80 mg/day following AF ablation does not decrease the risk of AF recurrence in the first 3 months and should not be routinely administered to prevent periprocedural arrhythmias.</description><identifier>ISSN: 1547-5271</identifier><identifier>EISSN: 1556-3871</identifier><identifier>DOI: 10.1016/j.hrthm.2011.09.016</identifier><identifier>PMID: 21920481</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Anticholesteremic Agents - therapeutic use ; Atorvastatin ; Atorvastatin Calcium ; Atrial Fibrillation - prevention & control ; Atrial Fibrillation - surgery ; Atrial fibrillation ablation ; Cardiovascular ; Catheter Ablation - adverse effects ; Double-Blind Method ; Female ; Heptanoic Acids - therapeutic use ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use ; Kaplan-Meier Estimate ; Male ; Middle Aged ; Postoperative Complications - prevention & control ; Pulmonary Veins - surgery ; Pyrroles - therapeutic use ; Quality of Life ; Randomized trial ; Recurrence ; Secondary Prevention ; Treatment Outcome</subject><ispartof>Heart rhythm, 2012-02, Vol.9 (2), p.172-178</ispartof><rights>Heart Rhythm Society</rights><rights>2012 Heart Rhythm Society</rights><rights>Copyright © 2012 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-4203ee99209881a0552c31b1367d715109d87b317e3c2d3c7c0d40b8c999253f3</citedby><cites>FETCH-LOGICAL-c479t-4203ee99209881a0552c31b1367d715109d87b317e3c2d3c7c0d40b8c999253f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.hrthm.2011.09.016$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21920481$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suleiman, Mahmoud, MD</creatorcontrib><creatorcontrib>Koestler, Celeste, RN</creatorcontrib><creatorcontrib>Lerman, Amir, MD</creatorcontrib><creatorcontrib>Lopez-Jimenez, Francisco, MD</creatorcontrib><creatorcontrib>Herges, Regina, BS</creatorcontrib><creatorcontrib>Hodge, David, MS</creatorcontrib><creatorcontrib>Bradley, David, MD, PhD</creatorcontrib><creatorcontrib>Cha, Yong-Mei, MD</creatorcontrib><creatorcontrib>Brady, Peter A., MD</creatorcontrib><creatorcontrib>Munger, Thomas M., MD</creatorcontrib><creatorcontrib>Asirvatham, Samuel J., MD, FHRS</creatorcontrib><creatorcontrib>Packer, Douglas L., MD, FHRS</creatorcontrib><creatorcontrib>Friedman, Paul A., MD, FHRS</creatorcontrib><title>Atorvastatin for prevention of atrial fibrillation recurrence following pulmonary vein isolation: A double-blind, placebo-controlled, randomized trial</title><title>Heart rhythm</title><addtitle>Heart Rhythm</addtitle><description>Background It is known that statins are effective in preventing atrial fibrillation (AF) in patients undergoing cardiac surgery. Objective The purpose of this study was to evaluate the efficacy of statins in preventing AF recurrence following left atrial ablation. Methods One hundred twenty-five patients who had no statin indication undergoing catheter ablation due to drug-refractory paroxysmal (n = 90) or persistent (n = 35) AF were randomized in a prospective, double-blind, placebo-controlled trial to receive 80 mg atorvastatin (n = 62) or placebo (n = 63) for 3 months. The primary endpoint was freedom from symptomatic AF at 3 months. Secondary endpoints included freedom from any atrial arrhythmia recurrence irrespective of symptoms, quality of life (QoL), and reduction in C-reactive protein (CRP). Results At 3 months, 95% of patients in the atorvastatin group were free of symptomatic AF compared with 93.5% in the placebo group ( P = .75). Similarly, 85% of patients treated in the atorvastatin group remained free of any recurrent atrial arrhythmia vs 88% of patients in the placebo group ( P = .37). Mean CRP levels decreased in the atorvastatin group (mean change −0.75 ± 3, P = .02) and increased in the placebo group (mean change 2.1 ± 19.9, P = .48). Mean QoL score improved significantly in both groups (mean change 13.14 ± 18.2 in the atorvastatin group and 11.10 ± 17.7 in the placebo group, P = .53). Conclusion In patients with no standard indication for statin therapy, treatment with atorvastatin 80 mg/day following AF ablation does not decrease the risk of AF recurrence in the first 3 months and should not be routinely administered to prevent periprocedural arrhythmias.</description><subject>Aged</subject><subject>Anticholesteremic Agents - therapeutic use</subject><subject>Atorvastatin</subject><subject>Atorvastatin Calcium</subject><subject>Atrial Fibrillation - prevention & control</subject><subject>Atrial Fibrillation - surgery</subject><subject>Atrial fibrillation ablation</subject><subject>Cardiovascular</subject><subject>Catheter Ablation - adverse effects</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Heptanoic Acids - therapeutic use</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Postoperative Complications - prevention & control</subject><subject>Pulmonary Veins - surgery</subject><subject>Pyrroles - therapeutic use</subject><subject>Quality of Life</subject><subject>Randomized trial</subject><subject>Recurrence</subject><subject>Secondary Prevention</subject><subject>Treatment Outcome</subject><issn>1547-5271</issn><issn>1556-3871</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUk2LFDEUbERx19VfIEhuXuw2r9M96QgKw-IXLHhQwVtIJ6_djOlkTNIj6w_x95qeWT148ZTwqKpHVb2qegy0AQqb57vmOubruWkpQENFU2Z3qnPo-03NBg5313_H677lcFY9SGlHaSs2lN2vzloQLe0GOK9-bXOIB5WyytaTKUSyj3hAn23wJExE5WiVI5Mdo3VOHccR9RIjeo2F4Fz4Yf1Xsl_cHLyKN-SARcmmcEK_IFtiwjI6rEdnvXlG9k5pHEOtg8-x8LHMovImzPYnGnJc-LC6NymX8NHte1F9fvP60-W7-urD2_eX26tad1zkumspQxTFjBgGULTvW81gBLbhhkMPVJiBjww4Mt0aprmmpqPjoEXh9GxiF9XTk-4-hu8LpixnmzQWpx7DkqSAoed90StIdkLqGFKKOMl9tHPxK4HKtQ-5k8c-5NqHpEKWWWE9udVfxhnNX86fAgrg5QmAxeXBYpRJ2zVaY0vMWZpg_7Pg1T98XVK2WrlveINpF5boS4ASZGollR_Xk1gvAooi5fCF_QbZV7Tj</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Suleiman, Mahmoud, MD</creator><creator>Koestler, Celeste, RN</creator><creator>Lerman, Amir, MD</creator><creator>Lopez-Jimenez, Francisco, MD</creator><creator>Herges, Regina, BS</creator><creator>Hodge, David, MS</creator><creator>Bradley, David, MD, PhD</creator><creator>Cha, Yong-Mei, MD</creator><creator>Brady, Peter A., MD</creator><creator>Munger, Thomas M., MD</creator><creator>Asirvatham, Samuel J., MD, FHRS</creator><creator>Packer, Douglas L., MD, FHRS</creator><creator>Friedman, Paul A., MD, FHRS</creator><general>Elsevier 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>20120201</creationdate><title>Atorvastatin for prevention of atrial fibrillation recurrence following pulmonary vein isolation: A double-blind, placebo-controlled, randomized trial</title><author>Suleiman, Mahmoud, MD ; Koestler, Celeste, RN ; Lerman, Amir, MD ; Lopez-Jimenez, Francisco, MD ; Herges, Regina, BS ; Hodge, David, MS ; Bradley, David, MD, PhD ; Cha, Yong-Mei, MD ; Brady, Peter A., MD ; Munger, Thomas M., MD ; Asirvatham, Samuel J., MD, FHRS ; Packer, Douglas L., MD, FHRS ; Friedman, Paul A., MD, FHRS</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-4203ee99209881a0552c31b1367d715109d87b317e3c2d3c7c0d40b8c999253f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Anticholesteremic Agents - therapeutic use</topic><topic>Atorvastatin</topic><topic>Atorvastatin Calcium</topic><topic>Atrial Fibrillation - prevention & control</topic><topic>Atrial Fibrillation - surgery</topic><topic>Atrial fibrillation ablation</topic><topic>Cardiovascular</topic><topic>Catheter Ablation - adverse effects</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Heptanoic Acids - therapeutic use</topic><topic>Humans</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Postoperative Complications - prevention & control</topic><topic>Pulmonary Veins - surgery</topic><topic>Pyrroles - therapeutic use</topic><topic>Quality of Life</topic><topic>Randomized trial</topic><topic>Recurrence</topic><topic>Secondary Prevention</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suleiman, Mahmoud, MD</creatorcontrib><creatorcontrib>Koestler, Celeste, RN</creatorcontrib><creatorcontrib>Lerman, Amir, MD</creatorcontrib><creatorcontrib>Lopez-Jimenez, Francisco, MD</creatorcontrib><creatorcontrib>Herges, Regina, BS</creatorcontrib><creatorcontrib>Hodge, David, MS</creatorcontrib><creatorcontrib>Bradley, David, MD, PhD</creatorcontrib><creatorcontrib>Cha, Yong-Mei, MD</creatorcontrib><creatorcontrib>Brady, Peter A., MD</creatorcontrib><creatorcontrib>Munger, Thomas M., MD</creatorcontrib><creatorcontrib>Asirvatham, Samuel J., MD, FHRS</creatorcontrib><creatorcontrib>Packer, Douglas L., MD, FHRS</creatorcontrib><creatorcontrib>Friedman, Paul A., MD, FHRS</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>Heart rhythm</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suleiman, Mahmoud, MD</au><au>Koestler, Celeste, RN</au><au>Lerman, Amir, MD</au><au>Lopez-Jimenez, Francisco, MD</au><au>Herges, Regina, BS</au><au>Hodge, David, MS</au><au>Bradley, David, MD, PhD</au><au>Cha, Yong-Mei, MD</au><au>Brady, Peter A., MD</au><au>Munger, Thomas M., MD</au><au>Asirvatham, Samuel J., MD, FHRS</au><au>Packer, Douglas L., MD, FHRS</au><au>Friedman, Paul A., MD, FHRS</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Atorvastatin for prevention of atrial fibrillation recurrence following pulmonary vein isolation: A double-blind, placebo-controlled, randomized trial</atitle><jtitle>Heart rhythm</jtitle><addtitle>Heart Rhythm</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>9</volume><issue>2</issue><spage>172</spage><epage>178</epage><pages>172-178</pages><issn>1547-5271</issn><eissn>1556-3871</eissn><abstract>Background It is known that statins are effective in preventing atrial fibrillation (AF) in patients undergoing cardiac surgery. Objective The purpose of this study was to evaluate the efficacy of statins in preventing AF recurrence following left atrial ablation. Methods One hundred twenty-five patients who had no statin indication undergoing catheter ablation due to drug-refractory paroxysmal (n = 90) or persistent (n = 35) AF were randomized in a prospective, double-blind, placebo-controlled trial to receive 80 mg atorvastatin (n = 62) or placebo (n = 63) for 3 months. The primary endpoint was freedom from symptomatic AF at 3 months. Secondary endpoints included freedom from any atrial arrhythmia recurrence irrespective of symptoms, quality of life (QoL), and reduction in C-reactive protein (CRP). Results At 3 months, 95% of patients in the atorvastatin group were free of symptomatic AF compared with 93.5% in the placebo group ( P = .75). Similarly, 85% of patients treated in the atorvastatin group remained free of any recurrent atrial arrhythmia vs 88% of patients in the placebo group ( P = .37). Mean CRP levels decreased in the atorvastatin group (mean change −0.75 ± 3, P = .02) and increased in the placebo group (mean change 2.1 ± 19.9, P = .48). Mean QoL score improved significantly in both groups (mean change 13.14 ± 18.2 in the atorvastatin group and 11.10 ± 17.7 in the placebo group, P = .53). Conclusion In patients with no standard indication for statin therapy, treatment with atorvastatin 80 mg/day following AF ablation does not decrease the risk of AF recurrence in the first 3 months and should not be routinely administered to prevent periprocedural arrhythmias.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21920481</pmid><doi>10.1016/j.hrthm.2011.09.016</doi><tpages>7</tpages></addata></record> |
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subjects | Aged Anticholesteremic Agents - therapeutic use Atorvastatin Atorvastatin Calcium Atrial Fibrillation - prevention & control Atrial Fibrillation - surgery Atrial fibrillation ablation Cardiovascular Catheter Ablation - adverse effects Double-Blind Method Female Heptanoic Acids - therapeutic use Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use Kaplan-Meier Estimate Male Middle Aged Postoperative Complications - prevention & control Pulmonary Veins - surgery Pyrroles - therapeutic use Quality of Life Randomized trial Recurrence Secondary Prevention Treatment Outcome |
title | Atorvastatin for prevention of atrial fibrillation recurrence following pulmonary vein isolation: A double-blind, placebo-controlled, randomized trial |
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