Impact of Chronic Oral H2-Antagonist Therapy on Left Ventricular Systolic Function and Exercise Capacity

It has been suggested that H2‐antagonists may adversely affect left ventricular systolic junction. To assess the effects of cimetidine, famotidine, and ranitidine on exercise capacity and left ventricular systolic function, the authors conducted a randomized, double‐blind, four‐way crossover study i...

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Veröffentlicht in:Journal of clinical pharmacology 1992-11, Vol.32 (11), p.1033-1037
Hauptverfasser: Hilleman, Daniel E., Mohiuddin, Syed M., Williams, Mark A., Gannon, Joan M., Mathias, Richard J., Thalken, Lisa J.
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container_end_page 1037
container_issue 11
container_start_page 1033
container_title Journal of clinical pharmacology
container_volume 32
creator Hilleman, Daniel E.
Mohiuddin, Syed M.
Williams, Mark A.
Gannon, Joan M.
Mathias, Richard J.
Thalken, Lisa J.
description It has been suggested that H2‐antagonists may adversely affect left ventricular systolic junction. To assess the effects of cimetidine, famotidine, and ranitidine on exercise capacity and left ventricular systolic function, the authors conducted a randomized, double‐blind, four‐way crossover study in 15 healthy male volunteers with placebo control. Each subject underwent a maximal upright treadmill exercise test, aerobic metabolic assessment, and two‐dimensional stress echocardiography on six separate occasions. The initial two treadmill exercise tests with aerobic metabolic assessment and stress echocardiography were performed to minimize the learning effect. In the final four evaluations, subjects were randomized to receive 7 days of oral treatment with cimetidine 400 mg twice daily, famotidine 40 mg daily, ranitidine 150 mg twice daily, and placebo. A comparison of exercise tests, aerobic metabolic assessment, and stress echocardiography results found no significant differences between any of the H2‐antagonists and placebo. In addition, there were no significant differences in test results between cimetidine, famotidine, and ranitidine. Specifically, exercise treadmill time, maximal oxygen consumption, respiratory quotient, maximal exercise systolic and diastolic blood pressure, maximal exercise heart rate, left ventricular end‐diastolic dimension, left ventricular end‐systolic dimension, and ejection fraction were not different between treatments. The authors conclude that 7 days of oral treatment with cimetidine, famotidine, or ranitidine has no deleterious effect on exercise capacity or left ventricular systolic function in healthy subjects.
doi_str_mv 10.1002/j.1552-4604.1992.tb03807.x
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To assess the effects of cimetidine, famotidine, and ranitidine on exercise capacity and left ventricular systolic function, the authors conducted a randomized, double‐blind, four‐way crossover study in 15 healthy male volunteers with placebo control. Each subject underwent a maximal upright treadmill exercise test, aerobic metabolic assessment, and two‐dimensional stress echocardiography on six separate occasions. The initial two treadmill exercise tests with aerobic metabolic assessment and stress echocardiography were performed to minimize the learning effect. In the final four evaluations, subjects were randomized to receive 7 days of oral treatment with cimetidine 400 mg twice daily, famotidine 40 mg daily, ranitidine 150 mg twice daily, and placebo. A comparison of exercise tests, aerobic metabolic assessment, and stress echocardiography results found no significant differences between any of the H2‐antagonists and placebo. In addition, there were no significant differences in test results between cimetidine, famotidine, and ranitidine. Specifically, exercise treadmill time, maximal oxygen consumption, respiratory quotient, maximal exercise systolic and diastolic blood pressure, maximal exercise heart rate, left ventricular end‐diastolic dimension, left ventricular end‐systolic dimension, and ejection fraction were not different between treatments. 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To assess the effects of cimetidine, famotidine, and ranitidine on exercise capacity and left ventricular systolic function, the authors conducted a randomized, double‐blind, four‐way crossover study in 15 healthy male volunteers with placebo control. Each subject underwent a maximal upright treadmill exercise test, aerobic metabolic assessment, and two‐dimensional stress echocardiography on six separate occasions. The initial two treadmill exercise tests with aerobic metabolic assessment and stress echocardiography were performed to minimize the learning effect. In the final four evaluations, subjects were randomized to receive 7 days of oral treatment with cimetidine 400 mg twice daily, famotidine 40 mg daily, ranitidine 150 mg twice daily, and placebo. A comparison of exercise tests, aerobic metabolic assessment, and stress echocardiography results found no significant differences between any of the H2‐antagonists and placebo. In addition, there were no significant differences in test results between cimetidine, famotidine, and ranitidine. Specifically, exercise treadmill time, maximal oxygen consumption, respiratory quotient, maximal exercise systolic and diastolic blood pressure, maximal exercise heart rate, left ventricular end‐diastolic dimension, left ventricular end‐systolic dimension, and ejection fraction were not different between treatments. The authors conclude that 7 days of oral treatment with cimetidine, famotidine, or ranitidine has no deleterious effect on exercise capacity or left ventricular systolic function in healthy subjects.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Cimetidine - administration &amp; dosage</subject><subject>Cimetidine - pharmacology</subject><subject>Double-Blind Method</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Electrocardiography</subject><subject>Exercise Test - drug effects</subject><subject>Famotidine - administration &amp; dosage</subject><subject>Famotidine - pharmacology</subject><subject>Histamine H2 Antagonists - administration &amp; dosage</subject><subject>Histamine H2 Antagonists - pharmacology</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Oxygen Consumption</subject><subject>Pharmacology. Drug treatments</subject><subject>Ranitidine - administration &amp; dosage</subject><subject>Ranitidine - pharmacology</subject><subject>Systole</subject><subject>Time Factors</subject><subject>Toxicity: cardiovascular system</subject><subject>Ventricular Function, Left - drug effects</subject><issn>0091-2700</issn><issn>1552-4604</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkV1v2yAYRtG0qku7_YRJaJp2Z5cvG3y31mqaVlY7ad12iTCBxZljZ4DV-N8XK1Z6BeI5HMH7APAFoxQjRK62Kc4ykrAcsRQXBUlDjahAPD28A4tT9B4sECpwQjhCH8CF91uEcM4yfA7OMc1xQbMF2Nzv9koH2FtYblzfNRo-OdXCFUmuu6D-xhMf4PPGOLUfYd_BytgAf5suuEYPrXLw5-hD38Z7y6HToYmI6tbw9mCcbryBpYr-JowfwZlVrTef5vUS_FrePperpHq6uy-vq6ShFPGEkPj-TFtV2IyIghgiyFoIS6wVOaVWqBzXRaExV2ytLGGc2hobmvE6Q3kcwyX4dvTuXf9_MD7IXeO1aVvVmX7wklNGEUMT-HkGh3pn1nLvmp1yo5xHE_Ovc668Vq11qosfOmGMIUEIidj3I_bStGZ8syA5VSW3cupDTn3IqSo5VyUP8qH8sZq2UZEcFXHU5nBSKPdP5pzyTP55vJM34rFiZbWUD_QVnaeWvA</recordid><startdate>199211</startdate><enddate>199211</enddate><creator>Hilleman, Daniel E.</creator><creator>Mohiuddin, Syed M.</creator><creator>Williams, Mark A.</creator><creator>Gannon, Joan M.</creator><creator>Mathias, Richard J.</creator><creator>Thalken, Lisa J.</creator><general>Blackwell Publishing Ltd</general><general>Sage Science</general><scope>BSCLL</scope><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>199211</creationdate><title>Impact of Chronic Oral H2-Antagonist Therapy on Left Ventricular Systolic Function and Exercise Capacity</title><author>Hilleman, Daniel E. ; Mohiuddin, Syed M. ; Williams, Mark A. ; Gannon, Joan M. ; Mathias, Richard J. ; Thalken, Lisa J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3307-221555cfa9f52892e282d88f2ff8633f8a61b99c17a4daf2473fb1e357b506b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Cimetidine - administration &amp; dosage</topic><topic>Cimetidine - pharmacology</topic><topic>Double-Blind Method</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Electrocardiography</topic><topic>Exercise Test - drug effects</topic><topic>Famotidine - administration &amp; dosage</topic><topic>Famotidine - pharmacology</topic><topic>Histamine H2 Antagonists - administration &amp; dosage</topic><topic>Histamine H2 Antagonists - pharmacology</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Oxygen Consumption</topic><topic>Pharmacology. Drug treatments</topic><topic>Ranitidine - administration &amp; dosage</topic><topic>Ranitidine - pharmacology</topic><topic>Systole</topic><topic>Time Factors</topic><topic>Toxicity: cardiovascular system</topic><topic>Ventricular Function, Left - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hilleman, Daniel E.</creatorcontrib><creatorcontrib>Mohiuddin, Syed M.</creatorcontrib><creatorcontrib>Williams, Mark A.</creatorcontrib><creatorcontrib>Gannon, Joan M.</creatorcontrib><creatorcontrib>Mathias, Richard J.</creatorcontrib><creatorcontrib>Thalken, Lisa J.</creatorcontrib><collection>Istex</collection><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>Journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hilleman, Daniel E.</au><au>Mohiuddin, Syed M.</au><au>Williams, Mark A.</au><au>Gannon, Joan M.</au><au>Mathias, Richard J.</au><au>Thalken, Lisa J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Chronic Oral H2-Antagonist Therapy on Left Ventricular Systolic Function and Exercise Capacity</atitle><jtitle>Journal of clinical pharmacology</jtitle><addtitle>J Clin Pharmacol</addtitle><date>1992-11</date><risdate>1992</risdate><volume>32</volume><issue>11</issue><spage>1033</spage><epage>1037</epage><pages>1033-1037</pages><issn>0091-2700</issn><eissn>1552-4604</eissn><coden>JCPCBR</coden><abstract>It has been suggested that H2‐antagonists may adversely affect left ventricular systolic junction. To assess the effects of cimetidine, famotidine, and ranitidine on exercise capacity and left ventricular systolic function, the authors conducted a randomized, double‐blind, four‐way crossover study in 15 healthy male volunteers with placebo control. Each subject underwent a maximal upright treadmill exercise test, aerobic metabolic assessment, and two‐dimensional stress echocardiography on six separate occasions. The initial two treadmill exercise tests with aerobic metabolic assessment and stress echocardiography were performed to minimize the learning effect. In the final four evaluations, subjects were randomized to receive 7 days of oral treatment with cimetidine 400 mg twice daily, famotidine 40 mg daily, ranitidine 150 mg twice daily, and placebo. A comparison of exercise tests, aerobic metabolic assessment, and stress echocardiography results found no significant differences between any of the H2‐antagonists and placebo. In addition, there were no significant differences in test results between cimetidine, famotidine, and ranitidine. Specifically, exercise treadmill time, maximal oxygen consumption, respiratory quotient, maximal exercise systolic and diastolic blood pressure, maximal exercise heart rate, left ventricular end‐diastolic dimension, left ventricular end‐systolic dimension, and ejection fraction were not different between treatments. The authors conclude that 7 days of oral treatment with cimetidine, famotidine, or ranitidine has no deleterious effect on exercise capacity or left ventricular systolic function in healthy subjects.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1361935</pmid><doi>10.1002/j.1552-4604.1992.tb03807.x</doi><tpages>5</tpages></addata></record>
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subjects Administration, Oral
Adult
Biological and medical sciences
Cimetidine - administration & dosage
Cimetidine - pharmacology
Double-Blind Method
Drug toxicity and drugs side effects treatment
Electrocardiography
Exercise Test - drug effects
Famotidine - administration & dosage
Famotidine - pharmacology
Histamine H2 Antagonists - administration & dosage
Histamine H2 Antagonists - pharmacology
Humans
Male
Medical sciences
Oxygen Consumption
Pharmacology. Drug treatments
Ranitidine - administration & dosage
Ranitidine - pharmacology
Systole
Time Factors
Toxicity: cardiovascular system
Ventricular Function, Left - drug effects
title Impact of Chronic Oral H2-Antagonist Therapy on Left Ventricular Systolic Function and Exercise Capacity
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