Loading…
Acute hemodynamic effects of endogenous adenosine in patients with chronic heart failure
Objective The objective of this study was to assess the acute hemodynamic effects of endogenous adenosine accumulation in patients with chronic heart failure. Exogenously administered adenosine has been shown to reduce pulmonary vascular resistance and to increase cardiac index in normal subjects an...
Saved in:
Published in: | The American heart journal 1998-07, Vol.136 (1), p.37-42 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c389t-ce3495e5249f9747ff900f8940a285a2e2cba461cbc4cd705d5e9cc5a51072673 |
---|---|
cites | cdi_FETCH-LOGICAL-c389t-ce3495e5249f9747ff900f8940a285a2e2cba461cbc4cd705d5e9cc5a51072673 |
container_end_page | 42 |
container_issue | 1 |
container_start_page | 37 |
container_title | The American heart journal |
container_volume | 136 |
creator | Cortigiani, Lauro Baroni, Monica Picano, Eugenio Palmieri, Cataldo Boni, Andrea Ravani, Marcello Biagini, Andrea Nannini, Eugenio |
description | Objective The objective of this study was to assess the acute hemodynamic effects of endogenous adenosine accumulation in patients with chronic heart failure. Exogenously administered adenosine has been shown to reduce pulmonary vascular resistance and to increase cardiac index in normal subjects and in patients with pulmonary hypertension or end-stage biventricular heart failure. Endogenous adenosine accumulation can be provoked by dipyridamole.
Methods and Results Ultra-low-dose dipyridamole (0.07 mg/kg/min for 4 minutes) was administered in 20 patients with either symptomatic idiopathic (
n = 12) or ischemic (
n = 8) dilated cardiomyopathy and reduced left ventricular ejection fraction (mean 25% ± 5%). Hemodynamic variables were measured before and within 1 minute from the end of dipyridamole infusion. After dipyridamole administration, a mild but significant increase in heart rate (4.5%;
p = 0.03) and reduction in mean blood pressure (6.8%;
p < 0.001) without changes in right atrial pressure (
p = NS) were detected. Dipyridamole increased cardiac output by 26.6% (
p < 0.001), cardiac index by 24% (
p < 0.001), and stroke volume by 19.8% (
p < 0.001), with concomitant 24.6% reduction of systemic vascular resistance (
p < 0.001). Moreover, dipyridamole reduced mean pulmonary artery pressure by 8.3% (
p < 0.01) and pulmonary vascular resistance by 33.3% (
p = 0.001), without changes in pulmonary wedge pressure (
p = NS). A significant correlation between percent decrease from baseline in pulmonary and systemic vascular resistance (
r = 0.66;
p = 0.002) was found after administration of dipyridamole.
Conclusions Endogenous adenosine accumulation induced by ultra-low-dose dipyridamole infusion acutely improves the hemodynamic profile, decreasing pulmonary and, to a lower extent, systemic vascular resistance and increasing cardiac index in patients with severe chronic heart failure. (Am Heart J 1998;136:37-42.) |
doi_str_mv | 10.1016/S0002-8703(98)70179-6 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79999847</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0002870398701796</els_id><sourcerecordid>79999847</sourcerecordid><originalsourceid>FETCH-LOGICAL-c389t-ce3495e5249f9747ff900f8940a285a2e2cba461cbc4cd705d5e9cc5a51072673</originalsourceid><addsrcrecordid>eNqFkE1r3DAQhkVpSLdpf0JAh1LagxNJ1od1KiG0TSHQQ1voTWjHo6yCLW8luyH_PtrsstfoMoh53pnhIeScswvOuL78xRgTTWdY-8l2nw3jxjb6FVlxZk2jjZSvyeqIvCFvS7mvXy06fUpOrdZKcL0if69gmZFucJz6x-THCBRDQJgLnQLF1E93mKalUN_XWmJCGhPd-jliqsxDnDcUNnlKNbhBn2cafByWjO_ISfBDwfeHekb-fPv6-_qmuf35_cf11W0DbWfnBrCVVqES0gZrpAnBMhY6K5kXnfICBay91BzWIKE3TPUKLYDyijMjtGnPyMf93G2e_i1YZjfGAjgMPmG92xlbXyd3oNqDkKdSMga3zXH0-dFx5nZG3bNRt9PlbOeejTpdc-eHBct6xP6YOiis_Q-Hvi_gh5B9gliOmGi5EWKHfdljWGX8j5hdgeoQsI-56nb9FF845AnkXJMB</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>79999847</pqid></control><display><type>article</type><title>Acute hemodynamic effects of endogenous adenosine in patients with chronic heart failure</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Cortigiani, Lauro ; Baroni, Monica ; Picano, Eugenio ; Palmieri, Cataldo ; Boni, Andrea ; Ravani, Marcello ; Biagini, Andrea ; Nannini, Eugenio</creator><creatorcontrib>Cortigiani, Lauro ; Baroni, Monica ; Picano, Eugenio ; Palmieri, Cataldo ; Boni, Andrea ; Ravani, Marcello ; Biagini, Andrea ; Nannini, Eugenio</creatorcontrib><description><![CDATA[Objective The objective of this study was to assess the acute hemodynamic effects of endogenous adenosine accumulation in patients with chronic heart failure. Exogenously administered adenosine has been shown to reduce pulmonary vascular resistance and to increase cardiac index in normal subjects and in patients with pulmonary hypertension or end-stage biventricular heart failure. Endogenous adenosine accumulation can be provoked by dipyridamole.
Methods and Results Ultra-low-dose dipyridamole (0.07 mg/kg/min for 4 minutes) was administered in 20 patients with either symptomatic idiopathic (
n = 12) or ischemic (
n = 8) dilated cardiomyopathy and reduced left ventricular ejection fraction (mean 25% ± 5%). Hemodynamic variables were measured before and within 1 minute from the end of dipyridamole infusion. After dipyridamole administration, a mild but significant increase in heart rate (4.5%;
p = 0.03) and reduction in mean blood pressure (6.8%;
p < 0.001) without changes in right atrial pressure (
p = NS) were detected. Dipyridamole increased cardiac output by 26.6% (
p < 0.001), cardiac index by 24% (
p < 0.001), and stroke volume by 19.8% (
p < 0.001), with concomitant 24.6% reduction of systemic vascular resistance (
p < 0.001). Moreover, dipyridamole reduced mean pulmonary artery pressure by 8.3% (
p < 0.01) and pulmonary vascular resistance by 33.3% (
p = 0.001), without changes in pulmonary wedge pressure (
p = NS). A significant correlation between percent decrease from baseline in pulmonary and systemic vascular resistance (
r = 0.66;
p = 0.002) was found after administration of dipyridamole.
Conclusions Endogenous adenosine accumulation induced by ultra-low-dose dipyridamole infusion acutely improves the hemodynamic profile, decreasing pulmonary and, to a lower extent, systemic vascular resistance and increasing cardiac index in patients with severe chronic heart failure. (Am Heart J 1998;136:37-42.)]]></description><identifier>ISSN: 0002-8703</identifier><identifier>EISSN: 1097-6744</identifier><identifier>DOI: 10.1016/S0002-8703(98)70179-6</identifier><identifier>PMID: 9665216</identifier><identifier>CODEN: AHJOA2</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Adenosine - agonists ; Adenosine - blood ; Biological and medical sciences ; Cardiac Catheterization ; Cardiology. Vascular system ; Cardiomyopathy, Dilated - blood ; Cardiomyopathy, Dilated - drug therapy ; Cardiomyopathy, Dilated - physiopathology ; Chronic Disease ; Dipyridamole - administration & dosage ; Female ; Heart ; Heart failure, cardiogenic pulmonary edema, cardiac enlargement ; Hemodynamics - drug effects ; Hemodynamics - physiology ; Humans ; Infusions, Intravenous ; Male ; Medical sciences ; Middle Aged ; Vasodilator Agents - administration & dosage ; Ventricular Dysfunction, Left - blood ; Ventricular Dysfunction, Left - drug therapy ; Ventricular Dysfunction, Left - physiopathology</subject><ispartof>The American heart journal, 1998-07, Vol.136 (1), p.37-42</ispartof><rights>1998 Mosby, Inc.</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-ce3495e5249f9747ff900f8940a285a2e2cba461cbc4cd705d5e9cc5a51072673</citedby><cites>FETCH-LOGICAL-c389t-ce3495e5249f9747ff900f8940a285a2e2cba461cbc4cd705d5e9cc5a51072673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2317226$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9665216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cortigiani, Lauro</creatorcontrib><creatorcontrib>Baroni, Monica</creatorcontrib><creatorcontrib>Picano, Eugenio</creatorcontrib><creatorcontrib>Palmieri, Cataldo</creatorcontrib><creatorcontrib>Boni, Andrea</creatorcontrib><creatorcontrib>Ravani, Marcello</creatorcontrib><creatorcontrib>Biagini, Andrea</creatorcontrib><creatorcontrib>Nannini, Eugenio</creatorcontrib><title>Acute hemodynamic effects of endogenous adenosine in patients with chronic heart failure</title><title>The American heart journal</title><addtitle>Am Heart J</addtitle><description><![CDATA[Objective The objective of this study was to assess the acute hemodynamic effects of endogenous adenosine accumulation in patients with chronic heart failure. Exogenously administered adenosine has been shown to reduce pulmonary vascular resistance and to increase cardiac index in normal subjects and in patients with pulmonary hypertension or end-stage biventricular heart failure. Endogenous adenosine accumulation can be provoked by dipyridamole.
Methods and Results Ultra-low-dose dipyridamole (0.07 mg/kg/min for 4 minutes) was administered in 20 patients with either symptomatic idiopathic (
n = 12) or ischemic (
n = 8) dilated cardiomyopathy and reduced left ventricular ejection fraction (mean 25% ± 5%). Hemodynamic variables were measured before and within 1 minute from the end of dipyridamole infusion. After dipyridamole administration, a mild but significant increase in heart rate (4.5%;
p = 0.03) and reduction in mean blood pressure (6.8%;
p < 0.001) without changes in right atrial pressure (
p = NS) were detected. Dipyridamole increased cardiac output by 26.6% (
p < 0.001), cardiac index by 24% (
p < 0.001), and stroke volume by 19.8% (
p < 0.001), with concomitant 24.6% reduction of systemic vascular resistance (
p < 0.001). Moreover, dipyridamole reduced mean pulmonary artery pressure by 8.3% (
p < 0.01) and pulmonary vascular resistance by 33.3% (
p = 0.001), without changes in pulmonary wedge pressure (
p = NS). A significant correlation between percent decrease from baseline in pulmonary and systemic vascular resistance (
r = 0.66;
p = 0.002) was found after administration of dipyridamole.
Conclusions Endogenous adenosine accumulation induced by ultra-low-dose dipyridamole infusion acutely improves the hemodynamic profile, decreasing pulmonary and, to a lower extent, systemic vascular resistance and increasing cardiac index in patients with severe chronic heart failure. (Am Heart J 1998;136:37-42.)]]></description><subject>Adenosine - agonists</subject><subject>Adenosine - blood</subject><subject>Biological and medical sciences</subject><subject>Cardiac Catheterization</subject><subject>Cardiology. Vascular system</subject><subject>Cardiomyopathy, Dilated - blood</subject><subject>Cardiomyopathy, Dilated - drug therapy</subject><subject>Cardiomyopathy, Dilated - physiopathology</subject><subject>Chronic Disease</subject><subject>Dipyridamole - administration & dosage</subject><subject>Female</subject><subject>Heart</subject><subject>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</subject><subject>Hemodynamics - drug effects</subject><subject>Hemodynamics - physiology</subject><subject>Humans</subject><subject>Infusions, Intravenous</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Vasodilator Agents - administration & dosage</subject><subject>Ventricular Dysfunction, Left - blood</subject><subject>Ventricular Dysfunction, Left - drug therapy</subject><subject>Ventricular Dysfunction, Left - physiopathology</subject><issn>0002-8703</issn><issn>1097-6744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkE1r3DAQhkVpSLdpf0JAh1LagxNJ1od1KiG0TSHQQ1voTWjHo6yCLW8luyH_PtrsstfoMoh53pnhIeScswvOuL78xRgTTWdY-8l2nw3jxjb6FVlxZk2jjZSvyeqIvCFvS7mvXy06fUpOrdZKcL0if69gmZFucJz6x-THCBRDQJgLnQLF1E93mKalUN_XWmJCGhPd-jliqsxDnDcUNnlKNbhBn2cafByWjO_ISfBDwfeHekb-fPv6-_qmuf35_cf11W0DbWfnBrCVVqES0gZrpAnBMhY6K5kXnfICBay91BzWIKE3TPUKLYDyijMjtGnPyMf93G2e_i1YZjfGAjgMPmG92xlbXyd3oNqDkKdSMga3zXH0-dFx5nZG3bNRt9PlbOeejTpdc-eHBct6xP6YOiis_Q-Hvi_gh5B9gliOmGi5EWKHfdljWGX8j5hdgeoQsI-56nb9FF845AnkXJMB</recordid><startdate>19980701</startdate><enddate>19980701</enddate><creator>Cortigiani, Lauro</creator><creator>Baroni, Monica</creator><creator>Picano, Eugenio</creator><creator>Palmieri, Cataldo</creator><creator>Boni, Andrea</creator><creator>Ravani, Marcello</creator><creator>Biagini, Andrea</creator><creator>Nannini, Eugenio</creator><general>Mosby, Inc</general><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>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19980701</creationdate><title>Acute hemodynamic effects of endogenous adenosine in patients with chronic heart failure</title><author>Cortigiani, Lauro ; Baroni, Monica ; Picano, Eugenio ; Palmieri, Cataldo ; Boni, Andrea ; Ravani, Marcello ; Biagini, Andrea ; Nannini, Eugenio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-ce3495e5249f9747ff900f8940a285a2e2cba461cbc4cd705d5e9cc5a51072673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adenosine - agonists</topic><topic>Adenosine - blood</topic><topic>Biological and medical sciences</topic><topic>Cardiac Catheterization</topic><topic>Cardiology. Vascular system</topic><topic>Cardiomyopathy, Dilated - blood</topic><topic>Cardiomyopathy, Dilated - drug therapy</topic><topic>Cardiomyopathy, Dilated - physiopathology</topic><topic>Chronic Disease</topic><topic>Dipyridamole - administration & dosage</topic><topic>Female</topic><topic>Heart</topic><topic>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</topic><topic>Hemodynamics - drug effects</topic><topic>Hemodynamics - physiology</topic><topic>Humans</topic><topic>Infusions, Intravenous</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Vasodilator Agents - administration & dosage</topic><topic>Ventricular Dysfunction, Left - blood</topic><topic>Ventricular Dysfunction, Left - drug therapy</topic><topic>Ventricular Dysfunction, Left - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cortigiani, Lauro</creatorcontrib><creatorcontrib>Baroni, Monica</creatorcontrib><creatorcontrib>Picano, Eugenio</creatorcontrib><creatorcontrib>Palmieri, Cataldo</creatorcontrib><creatorcontrib>Boni, Andrea</creatorcontrib><creatorcontrib>Ravani, Marcello</creatorcontrib><creatorcontrib>Biagini, Andrea</creatorcontrib><creatorcontrib>Nannini, Eugenio</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>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The American heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cortigiani, Lauro</au><au>Baroni, Monica</au><au>Picano, Eugenio</au><au>Palmieri, Cataldo</au><au>Boni, Andrea</au><au>Ravani, Marcello</au><au>Biagini, Andrea</au><au>Nannini, Eugenio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute hemodynamic effects of endogenous adenosine in patients with chronic heart failure</atitle><jtitle>The American heart journal</jtitle><addtitle>Am Heart J</addtitle><date>1998-07-01</date><risdate>1998</risdate><volume>136</volume><issue>1</issue><spage>37</spage><epage>42</epage><pages>37-42</pages><issn>0002-8703</issn><eissn>1097-6744</eissn><coden>AHJOA2</coden><abstract><![CDATA[Objective The objective of this study was to assess the acute hemodynamic effects of endogenous adenosine accumulation in patients with chronic heart failure. Exogenously administered adenosine has been shown to reduce pulmonary vascular resistance and to increase cardiac index in normal subjects and in patients with pulmonary hypertension or end-stage biventricular heart failure. Endogenous adenosine accumulation can be provoked by dipyridamole.
Methods and Results Ultra-low-dose dipyridamole (0.07 mg/kg/min for 4 minutes) was administered in 20 patients with either symptomatic idiopathic (
n = 12) or ischemic (
n = 8) dilated cardiomyopathy and reduced left ventricular ejection fraction (mean 25% ± 5%). Hemodynamic variables were measured before and within 1 minute from the end of dipyridamole infusion. After dipyridamole administration, a mild but significant increase in heart rate (4.5%;
p = 0.03) and reduction in mean blood pressure (6.8%;
p < 0.001) without changes in right atrial pressure (
p = NS) were detected. Dipyridamole increased cardiac output by 26.6% (
p < 0.001), cardiac index by 24% (
p < 0.001), and stroke volume by 19.8% (
p < 0.001), with concomitant 24.6% reduction of systemic vascular resistance (
p < 0.001). Moreover, dipyridamole reduced mean pulmonary artery pressure by 8.3% (
p < 0.01) and pulmonary vascular resistance by 33.3% (
p = 0.001), without changes in pulmonary wedge pressure (
p = NS). A significant correlation between percent decrease from baseline in pulmonary and systemic vascular resistance (
r = 0.66;
p = 0.002) was found after administration of dipyridamole.
Conclusions Endogenous adenosine accumulation induced by ultra-low-dose dipyridamole infusion acutely improves the hemodynamic profile, decreasing pulmonary and, to a lower extent, systemic vascular resistance and increasing cardiac index in patients with severe chronic heart failure. (Am Heart J 1998;136:37-42.)]]></abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>9665216</pmid><doi>10.1016/S0002-8703(98)70179-6</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0002-8703 |
ispartof | The American heart journal, 1998-07, Vol.136 (1), p.37-42 |
issn | 0002-8703 1097-6744 |
language | eng |
recordid | cdi_proquest_miscellaneous_79999847 |
source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Adenosine - agonists Adenosine - blood Biological and medical sciences Cardiac Catheterization Cardiology. Vascular system Cardiomyopathy, Dilated - blood Cardiomyopathy, Dilated - drug therapy Cardiomyopathy, Dilated - physiopathology Chronic Disease Dipyridamole - administration & dosage Female Heart Heart failure, cardiogenic pulmonary edema, cardiac enlargement Hemodynamics - drug effects Hemodynamics - physiology Humans Infusions, Intravenous Male Medical sciences Middle Aged Vasodilator Agents - administration & dosage Ventricular Dysfunction, Left - blood Ventricular Dysfunction, Left - drug therapy Ventricular Dysfunction, Left - physiopathology |
title | Acute hemodynamic effects of endogenous adenosine in patients with chronic heart failure |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T08%3A13%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Acute%20hemodynamic%20effects%20of%20endogenous%20adenosine%20in%20patients%20with%20chronic%20heart%20failure&rft.jtitle=The%20American%20heart%20journal&rft.au=Cortigiani,%20Lauro&rft.date=1998-07-01&rft.volume=136&rft.issue=1&rft.spage=37&rft.epage=42&rft.pages=37-42&rft.issn=0002-8703&rft.eissn=1097-6744&rft.coden=AHJOA2&rft_id=info:doi/10.1016/S0002-8703(98)70179-6&rft_dat=%3Cproquest_cross%3E79999847%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c389t-ce3495e5249f9747ff900f8940a285a2e2cba461cbc4cd705d5e9cc5a51072673%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=79999847&rft_id=info:pmid/9665216&rfr_iscdi=true |