Long-term efficacy of mexiletine alone and in combination with class Ia antiarrhythmic drugs for refractory ventricular arrhythmias
The efficacy of mexiletine used alone, and in combination with a class Ia antiarrhythmic drug, was assessed in 159 previously drug-refractory patients with ventricular tachycardia (VT) during serial electrophysiologic studies and during long-term (5-year) clinical follow-up. Electrically-inducible v...
Gespeichert in:
Veröffentlicht in: | The American heart journal 1988-02, Vol.115 (2), p.360-366 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 366 |
---|---|
container_issue | 2 |
container_start_page | 360 |
container_title | The American heart journal |
container_volume | 115 |
creator | WHITFORD, E. G MCGOVERN, B SCHOENFELD, M. H GARAN, H NEWELL, J. B MCELROY, M RUSKIN, J. N |
description | The efficacy of mexiletine used alone, and in combination with a class Ia antiarrhythmic drug, was assessed in 159 previously drug-refractory patients with ventricular tachycardia (VT) during serial electrophysiologic studies and during long-term (5-year) clinical follow-up. Electrically-inducible ventricular tachycardia was suppressed by mexiletine alone in 23% of patients tested, and a combined antiarrhythmic drug regimen was effective in 29% of the trials performed. Mexiletine was much more likely to be effective in patients presenting with nonsustained VT or ventricular fibrillation than in patients with sustained VT (p less than 0.005). After 1 and 4 years of treatment, 18% and 42% of the patients treated with mexiletine alone had died suddenly or suffered recurrent symptomatic VT, compared to 11% and 25% of patients treated with the combined antiarrhythmic drug regimens (p = NS). Mexiletine therapy was associated with frequent, though readily reversible, adverse reactions. However, mexiletine treatment had to be discontinued permanently in 8 of 92 patients (9%) because of intolerable side effects. We conclude that the added efficacy and possible improved arrhythmia-free survival associated with combining mexiletine with a class Ia agent should be further investigated. |
doi_str_mv | 10.1016/0002-8703(88)90482-6 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_78104958</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>78104958</sourcerecordid><originalsourceid>FETCH-LOGICAL-p199t-dd432051719e26e700fabe7747c53f95616926c67665167eb21a4c8fadbccb2e3</originalsourceid><addsrcrecordid>eNo90EtLAzEQAOAgitbqP1DIQUQPq8k-ks1Rii8oeNFzmc1O2shuUpOs2rN_3BVLLzMM8zHMDCFnnN1wxsUtYyzPasmKq7q-Vqys80zskQlnSmZCluU-mezIETmO8X0sRV6LQ3JYFCXnkk3Iz9y7ZZYw9BSNsRr0hnpDe_y2HSbrkELn_6JrqXVU-76xDpL1jn7ZtKK6gxjpM4wgWQhhtUmr3mrahmEZqfGBBjQBdPJhQz_RpWD10EGgOwvxhBwY6CKebvOUvD3cv86esvnL4_Psbp6tuVIpa9uyyFnFJVeYC5SMGWhQylLqqjCqElyoXGghhai4kNjkHEpdG2gbrZsciym5_J-7Dv5jwJgWvY0auw4c-iEuZM1Zqap6hOdbODQ9tot1sD2EzWL7tbF_se1D1NCN9zlt447JSo0LFMUvK0h-3w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>78104958</pqid></control><display><type>article</type><title>Long-term efficacy of mexiletine alone and in combination with class Ia antiarrhythmic drugs for refractory ventricular arrhythmias</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>WHITFORD, E. G ; MCGOVERN, B ; SCHOENFELD, M. H ; GARAN, H ; NEWELL, J. B ; MCELROY, M ; RUSKIN, J. N</creator><creatorcontrib>WHITFORD, E. G ; MCGOVERN, B ; SCHOENFELD, M. H ; GARAN, H ; NEWELL, J. B ; MCELROY, M ; RUSKIN, J. N</creatorcontrib><description>The efficacy of mexiletine used alone, and in combination with a class Ia antiarrhythmic drug, was assessed in 159 previously drug-refractory patients with ventricular tachycardia (VT) during serial electrophysiologic studies and during long-term (5-year) clinical follow-up. Electrically-inducible ventricular tachycardia was suppressed by mexiletine alone in 23% of patients tested, and a combined antiarrhythmic drug regimen was effective in 29% of the trials performed. Mexiletine was much more likely to be effective in patients presenting with nonsustained VT or ventricular fibrillation than in patients with sustained VT (p less than 0.005). After 1 and 4 years of treatment, 18% and 42% of the patients treated with mexiletine alone had died suddenly or suffered recurrent symptomatic VT, compared to 11% and 25% of patients treated with the combined antiarrhythmic drug regimens (p = NS). Mexiletine therapy was associated with frequent, though readily reversible, adverse reactions. However, mexiletine treatment had to be discontinued permanently in 8 of 92 patients (9%) because of intolerable side effects. We conclude that the added efficacy and possible improved arrhythmia-free survival associated with combining mexiletine with a class Ia agent should be further investigated.</description><identifier>ISSN: 0002-8703</identifier><identifier>EISSN: 1097-6744</identifier><identifier>DOI: 10.1016/0002-8703(88)90482-6</identifier><identifier>PMID: 3341170</identifier><identifier>CODEN: AHJOA2</identifier><language>eng</language><publisher>New York, NY: Elsevier</publisher><subject>Anti-Arrhythmia Agents - therapeutic use ; Antiarythmic agents ; Biological and medical sciences ; Cardiac Pacing, Artificial ; Cardiovascular system ; Disopyramide - therapeutic use ; Drug Therapy, Combination ; Female ; Follow-Up Studies ; Humans ; Male ; Medical sciences ; Mexiletine - therapeutic use ; Middle Aged ; Pharmacology. Drug treatments ; Procainamide - therapeutic use ; Quinidine - therapeutic use ; Tachycardia - drug therapy ; Time Factors</subject><ispartof>The American heart journal, 1988-02, Vol.115 (2), p.360-366</ispartof><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7595163$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3341170$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WHITFORD, E. G</creatorcontrib><creatorcontrib>MCGOVERN, B</creatorcontrib><creatorcontrib>SCHOENFELD, M. H</creatorcontrib><creatorcontrib>GARAN, H</creatorcontrib><creatorcontrib>NEWELL, J. B</creatorcontrib><creatorcontrib>MCELROY, M</creatorcontrib><creatorcontrib>RUSKIN, J. N</creatorcontrib><title>Long-term efficacy of mexiletine alone and in combination with class Ia antiarrhythmic drugs for refractory ventricular arrhythmias</title><title>The American heart journal</title><addtitle>Am Heart J</addtitle><description>The efficacy of mexiletine used alone, and in combination with a class Ia antiarrhythmic drug, was assessed in 159 previously drug-refractory patients with ventricular tachycardia (VT) during serial electrophysiologic studies and during long-term (5-year) clinical follow-up. Electrically-inducible ventricular tachycardia was suppressed by mexiletine alone in 23% of patients tested, and a combined antiarrhythmic drug regimen was effective in 29% of the trials performed. Mexiletine was much more likely to be effective in patients presenting with nonsustained VT or ventricular fibrillation than in patients with sustained VT (p less than 0.005). After 1 and 4 years of treatment, 18% and 42% of the patients treated with mexiletine alone had died suddenly or suffered recurrent symptomatic VT, compared to 11% and 25% of patients treated with the combined antiarrhythmic drug regimens (p = NS). Mexiletine therapy was associated with frequent, though readily reversible, adverse reactions. However, mexiletine treatment had to be discontinued permanently in 8 of 92 patients (9%) because of intolerable side effects. We conclude that the added efficacy and possible improved arrhythmia-free survival associated with combining mexiletine with a class Ia agent should be further investigated.</description><subject>Anti-Arrhythmia Agents - therapeutic use</subject><subject>Antiarythmic agents</subject><subject>Biological and medical sciences</subject><subject>Cardiac Pacing, Artificial</subject><subject>Cardiovascular system</subject><subject>Disopyramide - therapeutic use</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mexiletine - therapeutic use</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Procainamide - therapeutic use</subject><subject>Quinidine - therapeutic use</subject><subject>Tachycardia - drug therapy</subject><subject>Time Factors</subject><issn>0002-8703</issn><issn>1097-6744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo90EtLAzEQAOAgitbqP1DIQUQPq8k-ks1Rii8oeNFzmc1O2shuUpOs2rN_3BVLLzMM8zHMDCFnnN1wxsUtYyzPasmKq7q-Vqys80zskQlnSmZCluU-mezIETmO8X0sRV6LQ3JYFCXnkk3Iz9y7ZZYw9BSNsRr0hnpDe_y2HSbrkELn_6JrqXVU-76xDpL1jn7ZtKK6gxjpM4wgWQhhtUmr3mrahmEZqfGBBjQBdPJhQz_RpWD10EGgOwvxhBwY6CKebvOUvD3cv86esvnL4_Psbp6tuVIpa9uyyFnFJVeYC5SMGWhQylLqqjCqElyoXGghhai4kNjkHEpdG2gbrZsciym5_J-7Dv5jwJgWvY0auw4c-iEuZM1Zqap6hOdbODQ9tot1sD2EzWL7tbF_se1D1NCN9zlt447JSo0LFMUvK0h-3w</recordid><startdate>19880201</startdate><enddate>19880201</enddate><creator>WHITFORD, E. G</creator><creator>MCGOVERN, B</creator><creator>SCHOENFELD, M. H</creator><creator>GARAN, H</creator><creator>NEWELL, J. B</creator><creator>MCELROY, M</creator><creator>RUSKIN, J. N</creator><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19880201</creationdate><title>Long-term efficacy of mexiletine alone and in combination with class Ia antiarrhythmic drugs for refractory ventricular arrhythmias</title><author>WHITFORD, E. G ; MCGOVERN, B ; SCHOENFELD, M. H ; GARAN, H ; NEWELL, J. B ; MCELROY, M ; RUSKIN, J. N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p199t-dd432051719e26e700fabe7747c53f95616926c67665167eb21a4c8fadbccb2e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Anti-Arrhythmia Agents - therapeutic use</topic><topic>Antiarythmic agents</topic><topic>Biological and medical sciences</topic><topic>Cardiac Pacing, Artificial</topic><topic>Cardiovascular system</topic><topic>Disopyramide - therapeutic use</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mexiletine - therapeutic use</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Procainamide - therapeutic use</topic><topic>Quinidine - therapeutic use</topic><topic>Tachycardia - drug therapy</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WHITFORD, E. G</creatorcontrib><creatorcontrib>MCGOVERN, B</creatorcontrib><creatorcontrib>SCHOENFELD, M. H</creatorcontrib><creatorcontrib>GARAN, H</creatorcontrib><creatorcontrib>NEWELL, J. B</creatorcontrib><creatorcontrib>MCELROY, M</creatorcontrib><creatorcontrib>RUSKIN, J. N</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The American heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WHITFORD, E. G</au><au>MCGOVERN, B</au><au>SCHOENFELD, M. H</au><au>GARAN, H</au><au>NEWELL, J. B</au><au>MCELROY, M</au><au>RUSKIN, J. N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term efficacy of mexiletine alone and in combination with class Ia antiarrhythmic drugs for refractory ventricular arrhythmias</atitle><jtitle>The American heart journal</jtitle><addtitle>Am Heart J</addtitle><date>1988-02-01</date><risdate>1988</risdate><volume>115</volume><issue>2</issue><spage>360</spage><epage>366</epage><pages>360-366</pages><issn>0002-8703</issn><eissn>1097-6744</eissn><coden>AHJOA2</coden><abstract>The efficacy of mexiletine used alone, and in combination with a class Ia antiarrhythmic drug, was assessed in 159 previously drug-refractory patients with ventricular tachycardia (VT) during serial electrophysiologic studies and during long-term (5-year) clinical follow-up. Electrically-inducible ventricular tachycardia was suppressed by mexiletine alone in 23% of patients tested, and a combined antiarrhythmic drug regimen was effective in 29% of the trials performed. Mexiletine was much more likely to be effective in patients presenting with nonsustained VT or ventricular fibrillation than in patients with sustained VT (p less than 0.005). After 1 and 4 years of treatment, 18% and 42% of the patients treated with mexiletine alone had died suddenly or suffered recurrent symptomatic VT, compared to 11% and 25% of patients treated with the combined antiarrhythmic drug regimens (p = NS). Mexiletine therapy was associated with frequent, though readily reversible, adverse reactions. However, mexiletine treatment had to be discontinued permanently in 8 of 92 patients (9%) because of intolerable side effects. We conclude that the added efficacy and possible improved arrhythmia-free survival associated with combining mexiletine with a class Ia agent should be further investigated.</abstract><cop>New York, NY</cop><pub>Elsevier</pub><pmid>3341170</pmid><doi>10.1016/0002-8703(88)90482-6</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0002-8703 |
ispartof | The American heart journal, 1988-02, Vol.115 (2), p.360-366 |
issn | 0002-8703 1097-6744 |
language | eng |
recordid | cdi_proquest_miscellaneous_78104958 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Anti-Arrhythmia Agents - therapeutic use Antiarythmic agents Biological and medical sciences Cardiac Pacing, Artificial Cardiovascular system Disopyramide - therapeutic use Drug Therapy, Combination Female Follow-Up Studies Humans Male Medical sciences Mexiletine - therapeutic use Middle Aged Pharmacology. Drug treatments Procainamide - therapeutic use Quinidine - therapeutic use Tachycardia - drug therapy Time Factors |
title | Long-term efficacy of mexiletine alone and in combination with class Ia antiarrhythmic drugs for refractory ventricular arrhythmias |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T09%3A04%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Long-term%20efficacy%20of%20mexiletine%20alone%20and%20in%20combination%20with%20class%20Ia%20antiarrhythmic%20drugs%20for%20refractory%20ventricular%20arrhythmias&rft.jtitle=The%20American%20heart%20journal&rft.au=WHITFORD,%20E.%20G&rft.date=1988-02-01&rft.volume=115&rft.issue=2&rft.spage=360&rft.epage=366&rft.pages=360-366&rft.issn=0002-8703&rft.eissn=1097-6744&rft.coden=AHJOA2&rft_id=info:doi/10.1016/0002-8703(88)90482-6&rft_dat=%3Cproquest_pubme%3E78104958%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=78104958&rft_id=info:pmid/3341170&rfr_iscdi=true |