Hemodynamic effects of direct biventricular compression studied in isovolumic and ejecting isolated canine hearts
Biventricular direct cardiac compression (DCC) can potentially support the failing heart without the complications associated with a blood/device interface. The effect of uniform DCC on left and right ventricular performance was evaluated in 7 isolated canine heart preparations. A computer-controlle...
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Veröffentlicht in: | Circulation (New York, N.Y.) N.Y.), 1999-04, Vol.99 (16), p.2177-2184 |
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creator | ARTRIP, J. H JIE WANG LEVENTHAL, A. R TSITLIK, J. E LEVIN, H. R BURKHOFF, D |
description | Biventricular direct cardiac compression (DCC) can potentially support the failing heart without the complications associated with a blood/device interface. The effect of uniform DCC on left and right ventricular performance was evaluated in 7 isolated canine heart preparations.
A computer-controlled afterload system either constrained the isolated heart to contract isovolumically or simulated hemodynamic properties of physiological ejection. Biventricular DCC was provided by a chamber surrounding the heart that allowed adjustment of the compression pressure, onset time, and duration. Through a series of ventricular preloads, the effect of DCC on the end-systolic pressure-volume relationship (ESPVR) was evaluated under isovolumic and ejecting conditions. Under both conditions, DCC shifted the ESPVR of the left and right ventricles upward by an amount approximately equal to the compression pressure. The augmentation of end-systolic pressure for each initial preload tested, however, was less under ejecting conditions, because reductions in end-systolic and end-diastolic volumes occurred with ejection. Nevertheless, the net effect was to increase stroke volume. Measurement of M O2 demonstrated that at a given ventricular volume, M O2 did not change with DCC; however, peak ventricular pressure increased substantially, so that the effective pressure-volume area increased.
Biventricular DCC can augment end-systolic pressure with no added costs of M O2. Under ejecting conditions, this augmentation of ventricular contracting ability manifests as increases in stroke volume. Thus, DCC represents a feasible alternative form of ventricular assist, and devices that support the heart in this manner should be further explored. |
doi_str_mv | 10.1161/01.CIR.99.16.2177 |
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A computer-controlled afterload system either constrained the isolated heart to contract isovolumically or simulated hemodynamic properties of physiological ejection. Biventricular DCC was provided by a chamber surrounding the heart that allowed adjustment of the compression pressure, onset time, and duration. Through a series of ventricular preloads, the effect of DCC on the end-systolic pressure-volume relationship (ESPVR) was evaluated under isovolumic and ejecting conditions. Under both conditions, DCC shifted the ESPVR of the left and right ventricles upward by an amount approximately equal to the compression pressure. The augmentation of end-systolic pressure for each initial preload tested, however, was less under ejecting conditions, because reductions in end-systolic and end-diastolic volumes occurred with ejection. Nevertheless, the net effect was to increase stroke volume. Measurement of M O2 demonstrated that at a given ventricular volume, M O2 did not change with DCC; however, peak ventricular pressure increased substantially, so that the effective pressure-volume area increased.
Biventricular DCC can augment end-systolic pressure with no added costs of M O2. Under ejecting conditions, this augmentation of ventricular contracting ability manifests as increases in stroke volume. Thus, DCC represents a feasible alternative form of ventricular assist, and devices that support the heart in this manner should be further explored.</description><identifier>ISSN: 0009-7322</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/01.CIR.99.16.2177</identifier><identifier>PMID: 10217660</identifier><identifier>CODEN: CIRCAZ</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Animals ; Biological and medical sciences ; Blood Pressure ; Cardiology. Vascular system ; Dogs ; Heart ; Heart - physiology ; Heart failure, cardiogenic pulmonary edema, cardiac enlargement ; Hemodynamics - physiology ; In Vitro Techniques ; Male ; Medical sciences ; Myocardial Contraction - physiology ; Shock, Cardiogenic - physiopathology ; Stroke Volume - physiology ; Systole ; Ventricular Function ; Ventricular Function, Right - physiology</subject><ispartof>Circulation (New York, N.Y.), 1999-04, Vol.99 (16), p.2177-2184</ispartof><rights>1999 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. Apr 27, 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-bd7f37dae132b80279df53cfb099de1ab282712a9abac1ba1e8295fc0d8be12c3</citedby><cites>FETCH-LOGICAL-c395t-bd7f37dae132b80279df53cfb099de1ab282712a9abac1ba1e8295fc0d8be12c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3674,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1762324$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10217660$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ARTRIP, J. H</creatorcontrib><creatorcontrib>JIE WANG</creatorcontrib><creatorcontrib>LEVENTHAL, A. R</creatorcontrib><creatorcontrib>TSITLIK, J. E</creatorcontrib><creatorcontrib>LEVIN, H. R</creatorcontrib><creatorcontrib>BURKHOFF, D</creatorcontrib><title>Hemodynamic effects of direct biventricular compression studied in isovolumic and ejecting isolated canine hearts</title><title>Circulation (New York, N.Y.)</title><addtitle>Circulation</addtitle><description>Biventricular direct cardiac compression (DCC) can potentially support the failing heart without the complications associated with a blood/device interface. The effect of uniform DCC on left and right ventricular performance was evaluated in 7 isolated canine heart preparations.
A computer-controlled afterload system either constrained the isolated heart to contract isovolumically or simulated hemodynamic properties of physiological ejection. Biventricular DCC was provided by a chamber surrounding the heart that allowed adjustment of the compression pressure, onset time, and duration. Through a series of ventricular preloads, the effect of DCC on the end-systolic pressure-volume relationship (ESPVR) was evaluated under isovolumic and ejecting conditions. Under both conditions, DCC shifted the ESPVR of the left and right ventricles upward by an amount approximately equal to the compression pressure. The augmentation of end-systolic pressure for each initial preload tested, however, was less under ejecting conditions, because reductions in end-systolic and end-diastolic volumes occurred with ejection. Nevertheless, the net effect was to increase stroke volume. Measurement of M O2 demonstrated that at a given ventricular volume, M O2 did not change with DCC; however, peak ventricular pressure increased substantially, so that the effective pressure-volume area increased.
Biventricular DCC can augment end-systolic pressure with no added costs of M O2. Under ejecting conditions, this augmentation of ventricular contracting ability manifests as increases in stroke volume. Thus, DCC represents a feasible alternative form of ventricular assist, and devices that support the heart in this manner should be further explored.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure</subject><subject>Cardiology. Vascular system</subject><subject>Dogs</subject><subject>Heart</subject><subject>Heart - physiology</subject><subject>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</subject><subject>Hemodynamics - physiology</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Myocardial Contraction - physiology</subject><subject>Shock, Cardiogenic - physiopathology</subject><subject>Stroke Volume - physiology</subject><subject>Systole</subject><subject>Ventricular Function</subject><subject>Ventricular Function, Right - physiology</subject><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU-LFDEQxYMo7rj6AbxIEPHWbSqZTiZHGVZ3YUEQPYd0UtEM3cls0r2w394MM6B4qj_83qOoR8hbYD2AhE8M-v3d917rHmTPQalnZAMD33bbQejnZMMY050SnF-RV7Ue2iiFGl6SK2CNlpJtyMMtztk_JTtHRzEEdEulOVAfS2vpGB8xLSW6dbKFujwfC9Yac6J1WX1ET2OisebHPK0nB5s8xUNTxvTrtJ_s0hhnU0xIf6MtS31NXgQ7VXxzqdfk55ebH_vb7v7b17v95_vOCT0s3ehVEMpbBMHHHeNK-zAIF0amtUewI99xBdxqO1oHowXccT0Ex_xuROBOXJOPZ99jyQ8r1sXMsTqcJpswr9VIrUAqxhv4_j_wkNeS2m2GA5dKy51sEJwhV3KtBYM5ljjb8mSAmVMYhoFpYRitDUhzCqNp3l2M13FG_4_i_P0GfLgAtjo7hWKTi_UvpyQXfCv-AI4plHQ</recordid><startdate>19990427</startdate><enddate>19990427</enddate><creator>ARTRIP, J. H</creator><creator>JIE WANG</creator><creator>LEVENTHAL, A. R</creator><creator>TSITLIK, J. E</creator><creator>LEVIN, H. R</creator><creator>BURKHOFF, D</creator><general>Lippincott Williams & Wilkins</general><general>American Heart Association, Inc</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>K9.</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>19990427</creationdate><title>Hemodynamic effects of direct biventricular compression studied in isovolumic and ejecting isolated canine hearts</title><author>ARTRIP, J. H ; JIE WANG ; LEVENTHAL, A. R ; TSITLIK, J. E ; LEVIN, H. R ; BURKHOFF, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-bd7f37dae132b80279df53cfb099de1ab282712a9abac1ba1e8295fc0d8be12c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure</topic><topic>Cardiology. Vascular system</topic><topic>Dogs</topic><topic>Heart</topic><topic>Heart - physiology</topic><topic>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</topic><topic>Hemodynamics - physiology</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Myocardial Contraction - physiology</topic><topic>Shock, Cardiogenic - physiopathology</topic><topic>Stroke Volume - physiology</topic><topic>Systole</topic><topic>Ventricular Function</topic><topic>Ventricular Function, Right - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ARTRIP, J. H</creatorcontrib><creatorcontrib>JIE WANG</creatorcontrib><creatorcontrib>LEVENTHAL, A. R</creatorcontrib><creatorcontrib>TSITLIK, J. E</creatorcontrib><creatorcontrib>LEVIN, H. R</creatorcontrib><creatorcontrib>BURKHOFF, 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>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ARTRIP, J. H</au><au>JIE WANG</au><au>LEVENTHAL, A. R</au><au>TSITLIK, J. E</au><au>LEVIN, H. R</au><au>BURKHOFF, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hemodynamic effects of direct biventricular compression studied in isovolumic and ejecting isolated canine hearts</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><addtitle>Circulation</addtitle><date>1999-04-27</date><risdate>1999</risdate><volume>99</volume><issue>16</issue><spage>2177</spage><epage>2184</epage><pages>2177-2184</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><coden>CIRCAZ</coden><abstract>Biventricular direct cardiac compression (DCC) can potentially support the failing heart without the complications associated with a blood/device interface. The effect of uniform DCC on left and right ventricular performance was evaluated in 7 isolated canine heart preparations.
A computer-controlled afterload system either constrained the isolated heart to contract isovolumically or simulated hemodynamic properties of physiological ejection. Biventricular DCC was provided by a chamber surrounding the heart that allowed adjustment of the compression pressure, onset time, and duration. Through a series of ventricular preloads, the effect of DCC on the end-systolic pressure-volume relationship (ESPVR) was evaluated under isovolumic and ejecting conditions. Under both conditions, DCC shifted the ESPVR of the left and right ventricles upward by an amount approximately equal to the compression pressure. The augmentation of end-systolic pressure for each initial preload tested, however, was less under ejecting conditions, because reductions in end-systolic and end-diastolic volumes occurred with ejection. Nevertheless, the net effect was to increase stroke volume. Measurement of M O2 demonstrated that at a given ventricular volume, M O2 did not change with DCC; however, peak ventricular pressure increased substantially, so that the effective pressure-volume area increased.
Biventricular DCC can augment end-systolic pressure with no added costs of M O2. Under ejecting conditions, this augmentation of ventricular contracting ability manifests as increases in stroke volume. Thus, DCC represents a feasible alternative form of ventricular assist, and devices that support the heart in this manner should be further explored.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>10217660</pmid><doi>10.1161/01.CIR.99.16.2177</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Blood Pressure Cardiology. Vascular system Dogs Heart Heart - physiology Heart failure, cardiogenic pulmonary edema, cardiac enlargement Hemodynamics - physiology In Vitro Techniques Male Medical sciences Myocardial Contraction - physiology Shock, Cardiogenic - physiopathology Stroke Volume - physiology Systole Ventricular Function Ventricular Function, Right - physiology |
title | Hemodynamic effects of direct biventricular compression studied in isovolumic and ejecting isolated canine hearts |
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