Attenuation of the negative inotropic effects of metoprolol at short cycle lengths in humans : Comparison with sotalol and verapamil
This study sought to compare the influence of changes in systolic interval on the negative inotropic effects of metoprolol, sotalol, and verapamil in patients with ischemic heart disease. The long-term symptomatic and prognostic effects of antiarrhythmic agents are not easily predicted on the basis...
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Veröffentlicht in: | Journal of the American College of Cardiology 2006-09, Vol.48 (6), p.1234-1241 |
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creator | RITCHIE, Rebecca H ZEITZ, Christopher J WUTTKE, Ronald D HII, John T. Y HOROWITZ, John D |
description | This study sought to compare the influence of changes in systolic interval on the negative inotropic effects of metoprolol, sotalol, and verapamil in patients with ischemic heart disease.
The long-term symptomatic and prognostic effects of antiarrhythmic agents are not easily predicted on the basis of acute hemodynamic actions at rest, but may be unmasked during tachycardia. However, this has not been studied extensively in vivo.
The force-interval relationship of the intact human left ventricle was examined before and 10 min after intravenous bolus administration of the negatively inotropic agents metoprolol, sotalol, or verapamil in patients undergoing diagnostic cardiac catheterization.
All three drugs similarly reduced maximal rate of increase of left ventricular pressures (LV+dP/dt(max)) by approximately 10%, but diversely modified the force-interval relationship. The parameter c (the reduction in LV+dP/dt(max) of a fixed premature stimulus on mechanical restitution) was significantly reduced by metoprolol (by 9+/- 4%, p < 0.05), was increased by verapamil (by 6 +/- 2%, p < 0.05), and was not significantly changed by sotalol. Similarly, metoprolol had a minimal effect on the extent of frequency potentiation, whereas sotalol and verapamil attenuated frequency potentiation (the relative response to 10 s of rapid pacing was 1.19 +/- 0.58-fold, 0.07 +/- 0.35-fold, and 0.03 +/- 0.17-fold of the baseline response after 10 min of metoprolol, sotalol, or verapamil, respectively).
These results show that the negative inotropic effects of metoprolol are attenuated and those of verapamil are accentuated at short cycle lengths; sotalol is intermediate between the two. These properties may contribute to the relative safety of these agents in patients prone to hemodynamic deterioration during sustained tachycardia. |
doi_str_mv | 10.1016/j.jacc.2006.04.092 |
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The long-term symptomatic and prognostic effects of antiarrhythmic agents are not easily predicted on the basis of acute hemodynamic actions at rest, but may be unmasked during tachycardia. However, this has not been studied extensively in vivo.
The force-interval relationship of the intact human left ventricle was examined before and 10 min after intravenous bolus administration of the negatively inotropic agents metoprolol, sotalol, or verapamil in patients undergoing diagnostic cardiac catheterization.
All three drugs similarly reduced maximal rate of increase of left ventricular pressures (LV+dP/dt(max)) by approximately 10%, but diversely modified the force-interval relationship. The parameter c (the reduction in LV+dP/dt(max) of a fixed premature stimulus on mechanical restitution) was significantly reduced by metoprolol (by 9+/- 4%, p < 0.05), was increased by verapamil (by 6 +/- 2%, p < 0.05), and was not significantly changed by sotalol. Similarly, metoprolol had a minimal effect on the extent of frequency potentiation, whereas sotalol and verapamil attenuated frequency potentiation (the relative response to 10 s of rapid pacing was 1.19 +/- 0.58-fold, 0.07 +/- 0.35-fold, and 0.03 +/- 0.17-fold of the baseline response after 10 min of metoprolol, sotalol, or verapamil, respectively).
These results show that the negative inotropic effects of metoprolol are attenuated and those of verapamil are accentuated at short cycle lengths; sotalol is intermediate between the two. These properties may contribute to the relative safety of these agents in patients prone to hemodynamic deterioration during sustained tachycardia.</description><identifier>ISSN: 0735-1097</identifier><identifier>EISSN: 1558-3597</identifier><identifier>DOI: 10.1016/j.jacc.2006.04.092</identifier><identifier>PMID: 16979012</identifier><identifier>CODEN: JACCDI</identifier><language>eng</language><publisher>New York, NY: Elsevier Science</publisher><subject>Aged ; Angina pectoris ; Anti-Arrhythmia Agents - therapeutic use ; Biological and medical sciences ; Cardiac arrhythmia ; Cardiac Catheterization ; Cardiac Pacing, Artificial ; Cardiology ; Cardiology. Vascular system ; Cardiovascular disease ; Catheters ; Female ; Heart ; Heart attacks ; Heart rate ; Hemodynamics ; Humans ; Intubation ; Ischemia ; Male ; Mathematical models ; Medical sciences ; Metoprolol - therapeutic use ; Middle Aged ; Mortality ; Myocardial Contraction - drug effects ; Myocardial Ischemia - drug therapy ; Myocardial Ischemia - physiopathology ; Pressure ; Pulmonary arteries ; Restitution ; Rodents ; Sotalol - therapeutic use ; Studies ; Systole - drug effects ; Time Factors ; Veins & arteries ; Ventricular Function, Left - drug effects ; Verapamil - therapeutic use</subject><ispartof>Journal of the American College of Cardiology, 2006-09, Vol.48 (6), p.1234-1241</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright Elsevier Limited Sep 19, 2006</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=18123800$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16979012$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RITCHIE, Rebecca H</creatorcontrib><creatorcontrib>ZEITZ, Christopher J</creatorcontrib><creatorcontrib>WUTTKE, Ronald D</creatorcontrib><creatorcontrib>HII, John T. Y</creatorcontrib><creatorcontrib>HOROWITZ, John D</creatorcontrib><title>Attenuation of the negative inotropic effects of metoprolol at short cycle lengths in humans : Comparison with sotalol and verapamil</title><title>Journal of the American College of Cardiology</title><addtitle>J Am Coll Cardiol</addtitle><description>This study sought to compare the influence of changes in systolic interval on the negative inotropic effects of metoprolol, sotalol, and verapamil in patients with ischemic heart disease.
The long-term symptomatic and prognostic effects of antiarrhythmic agents are not easily predicted on the basis of acute hemodynamic actions at rest, but may be unmasked during tachycardia. However, this has not been studied extensively in vivo.
The force-interval relationship of the intact human left ventricle was examined before and 10 min after intravenous bolus administration of the negatively inotropic agents metoprolol, sotalol, or verapamil in patients undergoing diagnostic cardiac catheterization.
All three drugs similarly reduced maximal rate of increase of left ventricular pressures (LV+dP/dt(max)) by approximately 10%, but diversely modified the force-interval relationship. The parameter c (the reduction in LV+dP/dt(max) of a fixed premature stimulus on mechanical restitution) was significantly reduced by metoprolol (by 9+/- 4%, p < 0.05), was increased by verapamil (by 6 +/- 2%, p < 0.05), and was not significantly changed by sotalol. Similarly, metoprolol had a minimal effect on the extent of frequency potentiation, whereas sotalol and verapamil attenuated frequency potentiation (the relative response to 10 s of rapid pacing was 1.19 +/- 0.58-fold, 0.07 +/- 0.35-fold, and 0.03 +/- 0.17-fold of the baseline response after 10 min of metoprolol, sotalol, or verapamil, respectively).
These results show that the negative inotropic effects of metoprolol are attenuated and those of verapamil are accentuated at short cycle lengths; sotalol is intermediate between the two. These properties may contribute to the relative safety of these agents in patients prone to hemodynamic deterioration during sustained tachycardia.</description><subject>Aged</subject><subject>Angina pectoris</subject><subject>Anti-Arrhythmia Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cardiac arrhythmia</subject><subject>Cardiac Catheterization</subject><subject>Cardiac Pacing, Artificial</subject><subject>Cardiology</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular disease</subject><subject>Catheters</subject><subject>Female</subject><subject>Heart</subject><subject>Heart attacks</subject><subject>Heart rate</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>Intubation</subject><subject>Ischemia</subject><subject>Male</subject><subject>Mathematical models</subject><subject>Medical sciences</subject><subject>Metoprolol - therapeutic use</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Myocardial Contraction - drug effects</subject><subject>Myocardial Ischemia - drug therapy</subject><subject>Myocardial Ischemia - physiopathology</subject><subject>Pressure</subject><subject>Pulmonary arteries</subject><subject>Restitution</subject><subject>Rodents</subject><subject>Sotalol - therapeutic use</subject><subject>Studies</subject><subject>Systole - drug effects</subject><subject>Time Factors</subject><subject>Veins & arteries</subject><subject>Ventricular Function, Left - drug effects</subject><subject>Verapamil - therapeutic use</subject><issn>0735-1097</issn><issn>1558-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0M-L1TAQB_Agivtc_Qc8SED01jppm6Txtjz8BQte9FymabLNo01qku6yd_9ws_pE8DQMfObLzBDykkHNgIl3p_qEWtcNgKihq0E1j8iBcd5XLVfyMTmAbHnFQMkL8iylExTYM_WUXDChpALWHMjPq5yN3zG74GmwNM-GenNT-ltDnQ85hs1paqw1OqcHsZocthiWsFDMNM0hZqrv9WLoYvxNnlMZo_O-ok_0PT2GdcPoUkm_c3mmKWT8Peonemsibri65Tl5YnFJ5sW5XpLvHz98O36urr9--nK8uq7mFppcSdSI0DUWWmknbrtR9cCZUuUwOXbKCN52XFohRC_HBsau6XAql9qp7VrU7SV5-ye37P9jNykPq0vaLAt6E_Y0iL4XD3EFvv4PnsIefdltYBwEkwJ4U9Srs9rH1UzDFt2K8X74-90C3pwBJo2Ljei1S_9cX0wP0P4CStyK_g</recordid><startdate>20060919</startdate><enddate>20060919</enddate><creator>RITCHIE, Rebecca H</creator><creator>ZEITZ, Christopher J</creator><creator>WUTTKE, Ronald D</creator><creator>HII, John T. Y</creator><creator>HOROWITZ, John D</creator><general>Elsevier Science</general><general>Elsevier Limited</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20060919</creationdate><title>Attenuation of the negative inotropic effects of metoprolol at short cycle lengths in humans : Comparison with sotalol and verapamil</title><author>RITCHIE, Rebecca H ; ZEITZ, Christopher J ; WUTTKE, Ronald D ; HII, John T. Y ; HOROWITZ, John D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h302t-7acaa042f037fd5f4b98051990007b49e653457f66687b20b424ad979fd343ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aged</topic><topic>Angina pectoris</topic><topic>Anti-Arrhythmia Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Cardiac arrhythmia</topic><topic>Cardiac Catheterization</topic><topic>Cardiac Pacing, Artificial</topic><topic>Cardiology</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular disease</topic><topic>Catheters</topic><topic>Female</topic><topic>Heart</topic><topic>Heart attacks</topic><topic>Heart rate</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>Intubation</topic><topic>Ischemia</topic><topic>Male</topic><topic>Mathematical models</topic><topic>Medical sciences</topic><topic>Metoprolol - therapeutic use</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Myocardial Contraction - drug effects</topic><topic>Myocardial Ischemia - drug therapy</topic><topic>Myocardial Ischemia - physiopathology</topic><topic>Pressure</topic><topic>Pulmonary arteries</topic><topic>Restitution</topic><topic>Rodents</topic><topic>Sotalol - therapeutic use</topic><topic>Studies</topic><topic>Systole - drug effects</topic><topic>Time Factors</topic><topic>Veins & arteries</topic><topic>Ventricular Function, Left - drug effects</topic><topic>Verapamil - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RITCHIE, Rebecca H</creatorcontrib><creatorcontrib>ZEITZ, Christopher J</creatorcontrib><creatorcontrib>WUTTKE, Ronald D</creatorcontrib><creatorcontrib>HII, John T. Y</creatorcontrib><creatorcontrib>HOROWITZ, John D</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>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American College of Cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RITCHIE, Rebecca H</au><au>ZEITZ, Christopher J</au><au>WUTTKE, Ronald D</au><au>HII, John T. Y</au><au>HOROWITZ, John D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Attenuation of the negative inotropic effects of metoprolol at short cycle lengths in humans : Comparison with sotalol and verapamil</atitle><jtitle>Journal of the American College of Cardiology</jtitle><addtitle>J Am Coll Cardiol</addtitle><date>2006-09-19</date><risdate>2006</risdate><volume>48</volume><issue>6</issue><spage>1234</spage><epage>1241</epage><pages>1234-1241</pages><issn>0735-1097</issn><eissn>1558-3597</eissn><coden>JACCDI</coden><abstract>This study sought to compare the influence of changes in systolic interval on the negative inotropic effects of metoprolol, sotalol, and verapamil in patients with ischemic heart disease.
The long-term symptomatic and prognostic effects of antiarrhythmic agents are not easily predicted on the basis of acute hemodynamic actions at rest, but may be unmasked during tachycardia. However, this has not been studied extensively in vivo.
The force-interval relationship of the intact human left ventricle was examined before and 10 min after intravenous bolus administration of the negatively inotropic agents metoprolol, sotalol, or verapamil in patients undergoing diagnostic cardiac catheterization.
All three drugs similarly reduced maximal rate of increase of left ventricular pressures (LV+dP/dt(max)) by approximately 10%, but diversely modified the force-interval relationship. The parameter c (the reduction in LV+dP/dt(max) of a fixed premature stimulus on mechanical restitution) was significantly reduced by metoprolol (by 9+/- 4%, p < 0.05), was increased by verapamil (by 6 +/- 2%, p < 0.05), and was not significantly changed by sotalol. Similarly, metoprolol had a minimal effect on the extent of frequency potentiation, whereas sotalol and verapamil attenuated frequency potentiation (the relative response to 10 s of rapid pacing was 1.19 +/- 0.58-fold, 0.07 +/- 0.35-fold, and 0.03 +/- 0.17-fold of the baseline response after 10 min of metoprolol, sotalol, or verapamil, respectively).
These results show that the negative inotropic effects of metoprolol are attenuated and those of verapamil are accentuated at short cycle lengths; sotalol is intermediate between the two. These properties may contribute to the relative safety of these agents in patients prone to hemodynamic deterioration during sustained tachycardia.</abstract><cop>New York, NY</cop><pub>Elsevier Science</pub><pmid>16979012</pmid><doi>10.1016/j.jacc.2006.04.092</doi><tpages>8</tpages></addata></record> |
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subjects | Aged Angina pectoris Anti-Arrhythmia Agents - therapeutic use Biological and medical sciences Cardiac arrhythmia Cardiac Catheterization Cardiac Pacing, Artificial Cardiology Cardiology. Vascular system Cardiovascular disease Catheters Female Heart Heart attacks Heart rate Hemodynamics Humans Intubation Ischemia Male Mathematical models Medical sciences Metoprolol - therapeutic use Middle Aged Mortality Myocardial Contraction - drug effects Myocardial Ischemia - drug therapy Myocardial Ischemia - physiopathology Pressure Pulmonary arteries Restitution Rodents Sotalol - therapeutic use Studies Systole - drug effects Time Factors Veins & arteries Ventricular Function, Left - drug effects Verapamil - therapeutic use |
title | Attenuation of the negative inotropic effects of metoprolol at short cycle lengths in humans : Comparison with sotalol and verapamil |
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