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Continuous versus intermittent warm blood cardioplegia: Functional and energetics changes

Identifieur interne : 000A15 ( Istex/Corpus ); précédent : 000A14; suivant : 000A16

Continuous versus intermittent warm blood cardioplegia: Functional and energetics changes

Auteurs : Lucia Torracca ; Evasio Pasini ; Salvatore Curello ; Claudio Ceconi ; Giuseppe Coletti ; Ottavio Alfieri ; Roberto Solfrini ; Roberto Ferrari

Source :

RBID : ISTEX:8C01E83916A3B4556425FCC51D981C54CB81E6D0

Abstract

Background.The aim of this study was to compare the protective effects of continuous warm blood cardioplegia (CWBC) and intermittent warm blood cardioplegia (IWBC) in an experimental model of blood-perfused, isolated rabbit heart.Methods.In the CWBC group, cardiac arrest was induced by continuous infusion of blood cardioplegia (10 mEq/L KCI) followed by 30 minutes of reperfusion with blood. In the IWBC group, after 5 minutes of perfusion with blood cardioplegia (10 mEq/L KCl), coronary flow was abolished for 10 minutes, followed by reperfusion with blood cardioplegia for 5 minutes. This sequence was repeated three times for a total period of 45 minutes. Finally the hearts were reperfused for 30 minutes with blood.Results.Infusion of potassium induced a marked increase in coronary perfusion pressure (from 50 ± 3 to 98 ± 1 mm Hg; p < 0.01), which remained elevated throughout in the CWBC group, whereas in the IWBC group, it dropped to 0 during each no-flow period. In both groups, cardioplegia resulted in a significant reduction in oxygen consumption (from 5.5 ± 0.2 to 0.6 ± 0.03 mL O2 · min−1 · 100 g−1 wet wt; p < 0.01). During CWBC, glucose extraction was significantly reduced (from 152 ± 10 to 64 ± 18 μg · min−1 · g−1 wet wt; p < 0.01). Free fatty acid uptake and creatine kinase and lactate release were not affected. During IWBC, in contrast, a transient but significant release of creatine kinase (from 643 ± 254 to 2,234 ± 296 mU · min−1 · g−1 wet wt; p < 0.01) and lactate (from 63 ± 22 to 374 ± 32 μg · min−1 wet wt; p < 0.01) occurred after each period of ischemia. Despite these metabolic differences, both cardioplegic procedures allowed a prompt and complete recovery of mechanical function and tissue content of high-energy phosphates.Conclusions.Both CWBC and IWBC exert optimal protection in the isolated blood perfused rabbit heart. Thus, IWBC can be safely used to improve visualization of the surgical field.

Url:
DOI: 10.1016/0003-4975(96)00598-X

Links to Exploration step

ISTEX:8C01E83916A3B4556425FCC51D981C54CB81E6D0

Le document en format XML

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<name sortKey="Coletti, Giuseppe" sort="Coletti, Giuseppe" uniqKey="Coletti G" first="Giuseppe" last="Coletti">Giuseppe Coletti</name>
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<name sortKey="Alfieri, Ottavio" sort="Alfieri, Ottavio" uniqKey="Alfieri O" first="Ottavio" last="Alfieri">Ottavio Alfieri</name>
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<name sortKey="Ferrari, Roberto" sort="Ferrari, Roberto" uniqKey="Ferrari R" first="Roberto" last="Ferrari">Roberto Ferrari</name>
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<mods:affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</mods:affiliation>
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<mods:affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</mods:affiliation>
</affiliation>
<affiliation>
<mods:affiliation>Address reprint requests to Dr Ferrari, Cattedra di Cardiologia, Università degli Studi di Brescia, c/o Spedali Civili, P.le Spedali Civili, 1, 25123 Brescia, Italy</mods:affiliation>
</affiliation>
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<mods:affiliation>E-mail: ferrari@master.cci.unibs.it</mods:affiliation>
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<title level="j">The Annals of Thoracic Surgery</title>
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<div type="abstract" xml:lang="en">Background.The aim of this study was to compare the protective effects of continuous warm blood cardioplegia (CWBC) and intermittent warm blood cardioplegia (IWBC) in an experimental model of blood-perfused, isolated rabbit heart.Methods.In the CWBC group, cardiac arrest was induced by continuous infusion of blood cardioplegia (10 mEq/L KCI) followed by 30 minutes of reperfusion with blood. In the IWBC group, after 5 minutes of perfusion with blood cardioplegia (10 mEq/L KCl), coronary flow was abolished for 10 minutes, followed by reperfusion with blood cardioplegia for 5 minutes. This sequence was repeated three times for a total period of 45 minutes. Finally the hearts were reperfused for 30 minutes with blood.Results.Infusion of potassium induced a marked increase in coronary perfusion pressure (from 50 ± 3 to 98 ± 1 mm Hg; p < 0.01), which remained elevated throughout in the CWBC group, whereas in the IWBC group, it dropped to 0 during each no-flow period. In both groups, cardioplegia resulted in a significant reduction in oxygen consumption (from 5.5 ± 0.2 to 0.6 ± 0.03 mL O2 · min−1 · 100 g−1 wet wt; p < 0.01). During CWBC, glucose extraction was significantly reduced (from 152 ± 10 to 64 ± 18 μg · min−1 · g−1 wet wt; p < 0.01). Free fatty acid uptake and creatine kinase and lactate release were not affected. During IWBC, in contrast, a transient but significant release of creatine kinase (from 643 ± 254 to 2,234 ± 296 mU · min−1 · g−1 wet wt; p < 0.01) and lactate (from 63 ± 22 to 374 ± 32 μg · min−1 wet wt; p < 0.01) occurred after each period of ischemia. Despite these metabolic differences, both cardioplegic procedures allowed a prompt and complete recovery of mechanical function and tissue content of high-energy phosphates.Conclusions.Both CWBC and IWBC exert optimal protection in the isolated blood perfused rabbit heart. Thus, IWBC can be safely used to improve visualization of the surgical field.</div>
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<name>Claudio Ceconi</name>
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<name>Giuseppe Coletti MD</name>
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<name>Ottavio Alfieri MD</name>
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<json:string>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</json:string>
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<name>Roberto Solfrini MD</name>
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<json:string>Divisione di Cardiochirurgia, Spedali Civili, Italy</json:string>
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<name>Roberto Ferrari MD, PhD</name>
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<json:string>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</json:string>
<json:string>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</json:string>
<json:string>Address reprint requests to Dr Ferrari, Cattedra di Cardiologia, Università degli Studi di Brescia, c/o Spedali Civili, P.le Spedali Civili, 1, 25123 Brescia, Italy</json:string>
<json:string>E-mail: ferrari@master.cci.unibs.it</json:string>
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<abstract>Background.The aim of this study was to compare the protective effects of continuous warm blood cardioplegia (CWBC) and intermittent warm blood cardioplegia (IWBC) in an experimental model of blood-perfused, isolated rabbit heart.Methods.In the CWBC group, cardiac arrest was induced by continuous infusion of blood cardioplegia (10 mEq/L KCI) followed by 30 minutes of reperfusion with blood. In the IWBC group, after 5 minutes of perfusion with blood cardioplegia (10 mEq/L KCl), coronary flow was abolished for 10 minutes, followed by reperfusion with blood cardioplegia for 5 minutes. This sequence was repeated three times for a total period of 45 minutes. Finally the hearts were reperfused for 30 minutes with blood.Results.Infusion of potassium induced a marked increase in coronary perfusion pressure (from 50 ± 3 to 98 ± 1 mm Hg; p > 0.01), which remained elevated throughout in the CWBC group, whereas in the IWBC group, it dropped to 0 during each no-flow period. In both groups, cardioplegia resulted in a significant reduction in oxygen consumption (from 5.5 ± 0.2 to 0.6 ± 0.03 mL O2 · min−1 · 100 g−1 wet wt; p > 0.01). During CWBC, glucose extraction was significantly reduced (from 152 ± 10 to 64 ± 18 μg · min−1 · g−1 wet wt; p > 0.01). Free fatty acid uptake and creatine kinase and lactate release were not affected. During IWBC, in contrast, a transient but significant release of creatine kinase (from 643 ± 254 to 2,234 ± 296 mU · min−1 · g−1 wet wt; p > 0.01) and lactate (from 63 ± 22 to 374 ± 32 μg · min−1 wet wt; p > 0.01) occurred after each period of ischemia. Despite these metabolic differences, both cardioplegic procedures allowed a prompt and complete recovery of mechanical function and tissue content of high-energy phosphates.Conclusions.Both CWBC and IWBC exert optimal protection in the isolated blood perfused rabbit heart. Thus, IWBC can be safely used to improve visualization of the surgical field.</abstract>
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<title level="a" type="main" xml:lang="en">Continuous versus intermittent warm blood cardioplegia: Functional and energetics changes</title>
<author>
<persName>
<forename type="first">Lucia</forename>
<surname>Torracca</surname>
</persName>
<roleName type="degree">MD</roleName>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
</author>
<author>
<persName>
<forename type="first">Evasio</forename>
<surname>Pasini</surname>
</persName>
<roleName type="degree">MD</roleName>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
</author>
<author>
<persName>
<forename type="first">Salvatore</forename>
<surname>Curello</surname>
</persName>
<roleName type="degree">MD</roleName>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
</author>
<author>
<persName>
<forename type="first">Claudio</forename>
<surname>Ceconi</surname>
</persName>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
</author>
<author>
<persName>
<forename type="first">Giuseppe</forename>
<surname>Coletti</surname>
</persName>
<roleName type="degree">MD</roleName>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
</author>
<author>
<persName>
<forename type="first">Ottavio</forename>
<surname>Alfieri</surname>
</persName>
<roleName type="degree">MD</roleName>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
</author>
<author>
<persName>
<forename type="first">Roberto</forename>
<surname>Solfrini</surname>
</persName>
<roleName type="degree">MD</roleName>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
</author>
<author>
<persName>
<forename type="first">Roberto</forename>
<surname>Ferrari</surname>
</persName>
<roleName type="degree">MD, PhD</roleName>
<email>ferrari@master.cci.unibs.it</email>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
<affiliation>Address reprint requests to Dr Ferrari, Cattedra di Cardiologia, Università degli Studi di Brescia, c/o Spedali Civili, P.le Spedali Civili, 1, 25123 Brescia, Italy</affiliation>
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<p>Background.The aim of this study was to compare the protective effects of continuous warm blood cardioplegia (CWBC) and intermittent warm blood cardioplegia (IWBC) in an experimental model of blood-perfused, isolated rabbit heart.Methods.In the CWBC group, cardiac arrest was induced by continuous infusion of blood cardioplegia (10 mEq/L KCI) followed by 30 minutes of reperfusion with blood. In the IWBC group, after 5 minutes of perfusion with blood cardioplegia (10 mEq/L KCl), coronary flow was abolished for 10 minutes, followed by reperfusion with blood cardioplegia for 5 minutes. This sequence was repeated three times for a total period of 45 minutes. Finally the hearts were reperfused for 30 minutes with blood.Results.Infusion of potassium induced a marked increase in coronary perfusion pressure (from 50 ± 3 to 98 ± 1 mm Hg; p < 0.01), which remained elevated throughout in the CWBC group, whereas in the IWBC group, it dropped to 0 during each no-flow period. In both groups, cardioplegia resulted in a significant reduction in oxygen consumption (from 5.5 ± 0.2 to 0.6 ± 0.03 mL O2 · min−1 · 100 g−1 wet wt; p < 0.01). During CWBC, glucose extraction was significantly reduced (from 152 ± 10 to 64 ± 18 μg · min−1 · g−1 wet wt; p < 0.01). Free fatty acid uptake and creatine kinase and lactate release were not affected. During IWBC, in contrast, a transient but significant release of creatine kinase (from 643 ± 254 to 2,234 ± 296 mU · min−1 · g−1 wet wt; p < 0.01) and lactate (from 63 ± 22 to 374 ± 32 μg · min−1 wet wt; p < 0.01) occurred after each period of ischemia. Despite these metabolic differences, both cardioplegic procedures allowed a prompt and complete recovery of mechanical function and tissue content of high-energy phosphates.Conclusions.Both CWBC and IWBC exert optimal protection in the isolated blood perfused rabbit heart. Thus, IWBC can be safely used to improve visualization of the surgical field.</p>
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<ce:copyright type="unknown" year="1996">The Society of Thoracic Surgeons</ce:copyright>
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<head>
<ce:article-footnote>
<ce:note-para>This study was supported by the target project G179038C FATMA of the National Council of Research (CNR), Rome, Italy.</ce:note-para>
</ce:article-footnote>
<ce:dochead>
<ce:textfn>Original article: Cardiovascular</ce:textfn>
</ce:dochead>
<ce:title>Continuous versus intermittent warm blood cardioplegia: Functional and energetics changes</ce:title>
<ce:author-group>
<ce:author>
<ce:degrees>MD</ce:degrees>
<ce:given-name>Lucia</ce:given-name>
<ce:surname>Torracca</ce:surname>
<ce:cross-ref refid="aff1">
<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff3">
<ce:sup loc="post">c</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff4">
<ce:sup loc="post">d</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:degrees>MD</ce:degrees>
<ce:given-name>Evasio</ce:given-name>
<ce:surname>Pasini</ce:surname>
<ce:cross-ref refid="aff1">
<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff3">
<ce:sup loc="post">c</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff4">
<ce:sup loc="post">d</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:degrees>MD</ce:degrees>
<ce:given-name>Salvatore</ce:given-name>
<ce:surname>Curello</ce:surname>
<ce:cross-ref refid="aff1">
<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff3">
<ce:sup loc="post">c</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff4">
<ce:sup loc="post">d</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:given-name>Claudio</ce:given-name>
<ce:surname>Ceconi</ce:surname>
<ce:cross-ref refid="aff1">
<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff3">
<ce:sup loc="post">c</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff4">
<ce:sup loc="post">d</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:degrees>MD</ce:degrees>
<ce:given-name>Giuseppe</ce:given-name>
<ce:surname>Coletti</ce:surname>
<ce:cross-ref refid="aff1">
<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff3">
<ce:sup loc="post">c</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff4">
<ce:sup loc="post">d</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:degrees>MD</ce:degrees>
<ce:given-name>Ottavio</ce:given-name>
<ce:surname>Alfieri</ce:surname>
<ce:cross-ref refid="aff1">
<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff3">
<ce:sup loc="post">c</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff4">
<ce:sup loc="post">d</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:degrees>MD</ce:degrees>
<ce:given-name>Roberto</ce:given-name>
<ce:surname>Solfrini</ce:surname>
<ce:cross-ref refid="aff1">
<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff3">
<ce:sup loc="post">c</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff4">
<ce:sup loc="post">d</ce:sup>
</ce:cross-ref>
</ce:author>
<ce:author>
<ce:degrees>MD, PhD</ce:degrees>
<ce:given-name>Roberto</ce:given-name>
<ce:surname>Ferrari</ce:surname>
<ce:cross-ref refid="aff1">
<ce:sup loc="post">a</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff2">
<ce:sup loc="post">b</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff3">
<ce:sup loc="post">c</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="aff4">
<ce:sup loc="post">d</ce:sup>
</ce:cross-ref>
<ce:cross-ref refid="cor1">
<ce:sup loc="post">*</ce:sup>
</ce:cross-ref>
<ce:e-address type="email">ferrari@master.cci.unibs.it</ce:e-address>
</ce:author>
<ce:affiliation id="aff1">
<ce:label>a</ce:label>
<ce:textfn>Divisione di Cardiochirurgia, Spedali Civili, Italy</ce:textfn>
</ce:affiliation>
<ce:affiliation id="aff2">
<ce:label>b</ce:label>
<ce:textfn>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</ce:textfn>
</ce:affiliation>
<ce:affiliation id="aff3">
<ce:label>c</ce:label>
<ce:textfn>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</ce:textfn>
</ce:affiliation>
<ce:affiliation id="aff4">
<ce:label>d</ce:label>
<ce:textfn>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</ce:textfn>
</ce:affiliation>
<ce:correspondence id="cor1">
<ce:label>*</ce:label>
<ce:text>Address reprint requests to Dr Ferrari, Cattedra di Cardiologia, Università degli Studi di Brescia, c/o Spedali Civili, P.le Spedali Civili, 1, 25123 Brescia, Italy</ce:text>
</ce:correspondence>
</ce:author-group>
<ce:date-accepted day="30" month="5" year="1996"></ce:date-accepted>
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<ce:abstract-sec>
<ce:section-title>Background.</ce:section-title>
<ce:simple-para view="all" id="simple-para.0010">The aim of this study was to compare the protective effects of continuous warm blood cardioplegia (CWBC) and intermittent warm blood cardioplegia (IWBC) in an experimental model of blood-perfused, isolated rabbit heart.</ce:simple-para>
</ce:abstract-sec>
<ce:abstract-sec>
<ce:section-title>Methods.</ce:section-title>
<ce:simple-para view="all" id="simple-para.0015">In the CWBC group, cardiac arrest was induced by continuous infusion of blood cardioplegia (10 mEq/L KCI) followed by 30 minutes of reperfusion with blood. In the IWBC group, after 5 minutes of perfusion with blood cardioplegia (10 mEq/L KCl), coronary flow was abolished for 10 minutes, followed by reperfusion with blood cardioplegia for 5 minutes. This sequence was repeated three times for a total period of 45 minutes. Finally the hearts were reperfused for 30 minutes with blood.</ce:simple-para>
</ce:abstract-sec>
<ce:abstract-sec>
<ce:section-title>Results.</ce:section-title>
<ce:simple-para view="all" id="simple-para.0020">Infusion of potassium induced a marked increase in coronary perfusion pressure (from 50 ± 3 to 98 ± 1 mm Hg;
<ce:italic>p</ce:italic>
< 0.01), which remained elevated throughout in the CWBC group, whereas in the IWBC group, it dropped to 0 during each no-flow period. In both groups, cardioplegia resulted in a significant reduction in oxygen consumption (from 5.5 ± 0.2 to 0.6 ± 0.03 mL O
<ce:inf loc="post">2</ce:inf>
· min
<ce:sup loc="post">−1</ce:sup>
· 100 g
<ce:sup loc="post">−1</ce:sup>
wet wt;
<ce:italic>p</ce:italic>
< 0.01). During CWBC, glucose extraction was significantly reduced (from 152 ± 10 to 64 ± 18
<ce:italic>μ</ce:italic>
g · min
<ce:sup loc="post">−1</ce:sup>
· g
<ce:sup loc="post">−1</ce:sup>
wet wt;
<ce:italic>p</ce:italic>
< 0.01). Free fatty acid uptake and creatine kinase and lactate release were not affected. During IWBC, in contrast, a transient but significant release of creatine kinase (from 643 ± 254 to 2,234 ± 296 mU · min
<ce:sup loc="post">−1</ce:sup>
· g
<ce:sup loc="post">−1</ce:sup>
wet wt;
<ce:italic>p</ce:italic>
< 0.01) and lactate (from 63 ± 22 to 374 ± 32
<ce:italic>μ</ce:italic>
g · min
<ce:sup loc="post">−1</ce:sup>
wet wt;
<ce:italic>p</ce:italic>
< 0.01) occurred after each period of ischemia. Despite these metabolic differences, both cardioplegic procedures allowed a prompt and complete recovery of mechanical function and tissue content of high-energy phosphates.</ce:simple-para>
</ce:abstract-sec>
<ce:abstract-sec>
<ce:section-title>Conclusions.</ce:section-title>
<ce:simple-para view="all" id="simple-para.0025">Both CWBC and IWBC exert optimal protection in the isolated blood perfused rabbit heart. Thus, IWBC can be safely used to improve visualization of the surgical field.</ce:simple-para>
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<ce:label>1.</ce:label>
<sb:reference>
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<sb:author>
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<title>Continuous versus intermittent warm blood cardioplegia: Functional and energetics changes</title>
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<title>Continuous versus intermittent warm blood cardioplegia: Functional and energetics changes</title>
</titleInfo>
<name type="personal">
<namePart type="given">Lucia</namePart>
<namePart type="family">Torracca</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
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<name type="personal">
<namePart type="given">Evasio</namePart>
<namePart type="family">Pasini</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
<role>
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</name>
<name type="personal">
<namePart type="given">Salvatore</namePart>
<namePart type="family">Curello</namePart>
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<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Claudio</namePart>
<namePart type="family">Ceconi</namePart>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Giuseppe</namePart>
<namePart type="family">Coletti</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
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<roleTerm type="text">author</roleTerm>
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</name>
<name type="personal">
<namePart type="given">Ottavio</namePart>
<namePart type="family">Alfieri</namePart>
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<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
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<name type="personal">
<namePart type="given">Roberto</namePart>
<namePart type="family">Solfrini</namePart>
<namePart type="termsOfAddress">MD</namePart>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Roberto</namePart>
<namePart type="family">Ferrari</namePart>
<namePart type="termsOfAddress">MD, PhD</namePart>
<affiliation>Divisione di Cardiochirurgia, Spedali Civili, Italy</affiliation>
<affiliation>Salvatore Maugeri Foundation, IRCCS, Cardiovascular Pathophysiology Research Centre, Gussago, Italy</affiliation>
<affiliation>Cattedra di Cardiologia, Università degli Studi di Brescia, Italy</affiliation>
<affiliation>Laboratorio Analisi, Opera Pia Paolo Richiedei, Gussago, Brescia, Italy</affiliation>
<affiliation>Address reprint requests to Dr Ferrari, Cattedra di Cardiologia, Università degli Studi di Brescia, c/o Spedali Civili, P.le Spedali Civili, 1, 25123 Brescia, Italy</affiliation>
<affiliation>E-mail: ferrari@master.cci.unibs.it</affiliation>
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<abstract lang="en">Background.The aim of this study was to compare the protective effects of continuous warm blood cardioplegia (CWBC) and intermittent warm blood cardioplegia (IWBC) in an experimental model of blood-perfused, isolated rabbit heart.Methods.In the CWBC group, cardiac arrest was induced by continuous infusion of blood cardioplegia (10 mEq/L KCI) followed by 30 minutes of reperfusion with blood. In the IWBC group, after 5 minutes of perfusion with blood cardioplegia (10 mEq/L KCl), coronary flow was abolished for 10 minutes, followed by reperfusion with blood cardioplegia for 5 minutes. This sequence was repeated three times for a total period of 45 minutes. Finally the hearts were reperfused for 30 minutes with blood.Results.Infusion of potassium induced a marked increase in coronary perfusion pressure (from 50 ± 3 to 98 ± 1 mm Hg; p < 0.01), which remained elevated throughout in the CWBC group, whereas in the IWBC group, it dropped to 0 during each no-flow period. In both groups, cardioplegia resulted in a significant reduction in oxygen consumption (from 5.5 ± 0.2 to 0.6 ± 0.03 mL O2 · min−1 · 100 g−1 wet wt; p < 0.01). During CWBC, glucose extraction was significantly reduced (from 152 ± 10 to 64 ± 18 μg · min−1 · g−1 wet wt; p < 0.01). Free fatty acid uptake and creatine kinase and lactate release were not affected. During IWBC, in contrast, a transient but significant release of creatine kinase (from 643 ± 254 to 2,234 ± 296 mU · min−1 · g−1 wet wt; p < 0.01) and lactate (from 63 ± 22 to 374 ± 32 μg · min−1 wet wt; p < 0.01) occurred after each period of ischemia. Despite these metabolic differences, both cardioplegic procedures allowed a prompt and complete recovery of mechanical function and tissue content of high-energy phosphates.Conclusions.Both CWBC and IWBC exert optimal protection in the isolated blood perfused rabbit heart. Thus, IWBC can be safely used to improve visualization of the surgical field.</abstract>
<note>This study was supported by the target project G179038C FATMA of the National Council of Research (CNR), Rome, Italy.</note>
<note type="content">Section title: Original article: Cardiovascular</note>
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