Single-dose versus multidose cardioplegia in neonatal hearts
We designed an experiment to compare single-dose versus multidose cardioplegia (calcium 0.3 mmol/L) in neonatal rabbit hearts 1, 4 and 6 weeks of age at 25 degrees C and 32 degrees C. Isolated hearts had a stabilization period of retrograde perfusion, a working period, a period of ischemia with sing...
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Veröffentlicht in: | The Journal of thoracic and cardiovascular surgery 1994-06, Vol.107 (6), p.1512-1518 |
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description | We designed an experiment to compare single-dose versus multidose cardioplegia (calcium 0.3 mmol/L) in neonatal rabbit hearts 1, 4 and 6 weeks of age at 25 degrees C and 32 degrees C. Isolated hearts had a stabilization period of retrograde perfusion, a working period, a period of ischemia with single or multidose cardioplegia, reperfusion, and a final working period. We measured hemodynamic recovery, creatine kinase during reperfusion, and coronary vascular resistance during administration of the cardioplegic solution. One-week and 4-week-old hearts exhibited better recovery with single-dose than with multidose cardioplegia. Six-week-old hearts, on the other hand, showed better recovery with multidose cardioplegia. Four-week-old hearts at 25 degrees C showed increased creatine kinase release with multidose cardioplegia. The 6-week-old hearts tended toward lower creatine kinase release with multidose cardioplegia. Coronary vascular resistance rose with subsequent administrations in 1-week and 4-week-old hearts at 25 degrees C but did not rise in 1- and 4-week-old hearts at 32 degrees C or in 6-week-old hearts at either temperature. On the basis of hemodynamic recovery, single-dose cardioplegia appears to provide better protection than multidose cardioplegia to 1- and 4-week-old isolated rabbit hearts. Once the rabbit has reached 6 weeks of age, multidose cardioplegia has some advantage over single-dose cardioplegia, similar to the findings in adult hearts. Creatine kinase release and coronary vascular resistance data corroborate the hemodynamic findings. |
doi_str_mv | 10.1016/S0022-5223(12)70151-4 |
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Isolated hearts had a stabilization period of retrograde perfusion, a working period, a period of ischemia with single or multidose cardioplegia, reperfusion, and a final working period. We measured hemodynamic recovery, creatine kinase during reperfusion, and coronary vascular resistance during administration of the cardioplegic solution. One-week and 4-week-old hearts exhibited better recovery with single-dose than with multidose cardioplegia. Six-week-old hearts, on the other hand, showed better recovery with multidose cardioplegia. Four-week-old hearts at 25 degrees C showed increased creatine kinase release with multidose cardioplegia. The 6-week-old hearts tended toward lower creatine kinase release with multidose cardioplegia. Coronary vascular resistance rose with subsequent administrations in 1-week and 4-week-old hearts at 25 degrees C but did not rise in 1- and 4-week-old hearts at 32 degrees C or in 6-week-old hearts at either temperature. On the basis of hemodynamic recovery, single-dose cardioplegia appears to provide better protection than multidose cardioplegia to 1- and 4-week-old isolated rabbit hearts. Once the rabbit has reached 6 weeks of age, multidose cardioplegia has some advantage over single-dose cardioplegia, similar to the findings in adult hearts. Creatine kinase release and coronary vascular resistance data corroborate the hemodynamic findings.</description><identifier>ISSN: 0022-5223</identifier><identifier>EISSN: 1097-685X</identifier><identifier>DOI: 10.1016/S0022-5223(12)70151-4</identifier><identifier>PMID: 8196397</identifier><identifier>CODEN: JTCSAQ</identifier><language>eng</language><publisher>Philadelphia, PA: AATS/WTSA</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. 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Isolated hearts had a stabilization period of retrograde perfusion, a working period, a period of ischemia with single or multidose cardioplegia, reperfusion, and a final working period. We measured hemodynamic recovery, creatine kinase during reperfusion, and coronary vascular resistance during administration of the cardioplegic solution. One-week and 4-week-old hearts exhibited better recovery with single-dose than with multidose cardioplegia. Six-week-old hearts, on the other hand, showed better recovery with multidose cardioplegia. Four-week-old hearts at 25 degrees C showed increased creatine kinase release with multidose cardioplegia. The 6-week-old hearts tended toward lower creatine kinase release with multidose cardioplegia. Coronary vascular resistance rose with subsequent administrations in 1-week and 4-week-old hearts at 25 degrees C but did not rise in 1- and 4-week-old hearts at 32 degrees C or in 6-week-old hearts at either temperature. On the basis of hemodynamic recovery, single-dose cardioplegia appears to provide better protection than multidose cardioplegia to 1- and 4-week-old isolated rabbit hearts. Once the rabbit has reached 6 weeks of age, multidose cardioplegia has some advantage over single-dose cardioplegia, similar to the findings in adult hearts. Creatine kinase release and coronary vascular resistance data corroborate the hemodynamic findings.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biological and medical sciences</subject><subject>Cardioplegic Solutions - administration & dosage</subject><subject>Coronary Vessels - physiology</subject><subject>Creatine Kinase - analysis</subject><subject>Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care</subject><subject>Heart - physiology</subject><subject>Heart Arrest, Induced - methods</subject><subject>Hemodynamics</subject><subject>In Vitro Techniques</subject><subject>Intensive care medicine</subject><subject>Medical sciences</subject><subject>Myocardium - enzymology</subject><subject>Rabbits</subject><subject>Random Allocation</subject><subject>Vascular Resistance</subject><issn>0022-5223</issn><issn>1097-685X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1LAzEQhoMoWqs_obAHkXpYzSSbZANepPgFggcVvIU0ybYp2d2a7Cr-e9e29DQw87wzw4PQBPA1YOA3bxgTkjNC6BTIlcDAIC8O0AiwFDkv2echGu2RE3Sa0gpjPHDyGB2XIDmVYoRu33yzCC63bXLZt4upT1ndh85vGkZH69t1cAuvM99kjWsb3emQLZ2OXTpDR5UOyZ3v6hh9PNy_z57yl9fH59ndS24KoF1OLQVpqeSVlqIsrJkzy4m0WPA5E66ohDVUMqfBFcAYSEZ0xUvpCGUaS0rH6HK7dx3br96lTtU-GReCHh7qkxKcQUFKMYBsC5rYphRdpdbR1zr-KsDq35raWFP_ShQQtbGmiiE32R3o57Wz-9RO0zC_2M11MjpUUTfGpz1WAOFcsgGbbrGlXyx_fHQq1TqEYSmoVWcSYKG4Gk4S-gcMgYGw</recordid><startdate>19940601</startdate><enddate>19940601</enddate><creator>Kohman, Leslie J</creator><creator>Veit, Linda J</creator><general>AATS/WTSA</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>19940601</creationdate><title>Single-dose versus multidose cardioplegia in neonatal hearts</title><author>Kohman, Leslie J ; Veit, Linda J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-3d319d396fa9784dcb5d629d076b57e4f7dc395ea1e41551952af689e235a0933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biological and medical sciences</topic><topic>Cardioplegic Solutions - administration & dosage</topic><topic>Coronary Vessels - physiology</topic><topic>Creatine Kinase - analysis</topic><topic>Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care</topic><topic>Heart - physiology</topic><topic>Heart Arrest, Induced - methods</topic><topic>Hemodynamics</topic><topic>In Vitro Techniques</topic><topic>Intensive care medicine</topic><topic>Medical sciences</topic><topic>Myocardium - enzymology</topic><topic>Rabbits</topic><topic>Random Allocation</topic><topic>Vascular Resistance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kohman, Leslie J</creatorcontrib><creatorcontrib>Veit, Linda J</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 Journal of thoracic and cardiovascular surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kohman, Leslie J</au><au>Veit, Linda J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single-dose versus multidose cardioplegia in neonatal hearts</atitle><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle><addtitle>J Thorac Cardiovasc Surg</addtitle><date>1994-06-01</date><risdate>1994</risdate><volume>107</volume><issue>6</issue><spage>1512</spage><epage>1518</epage><pages>1512-1518</pages><issn>0022-5223</issn><eissn>1097-685X</eissn><coden>JTCSAQ</coden><abstract>We designed an experiment to compare single-dose versus multidose cardioplegia (calcium 0.3 mmol/L) in neonatal rabbit hearts 1, 4 and 6 weeks of age at 25 degrees C and 32 degrees C. Isolated hearts had a stabilization period of retrograde perfusion, a working period, a period of ischemia with single or multidose cardioplegia, reperfusion, and a final working period. We measured hemodynamic recovery, creatine kinase during reperfusion, and coronary vascular resistance during administration of the cardioplegic solution. One-week and 4-week-old hearts exhibited better recovery with single-dose than with multidose cardioplegia. Six-week-old hearts, on the other hand, showed better recovery with multidose cardioplegia. Four-week-old hearts at 25 degrees C showed increased creatine kinase release with multidose cardioplegia. The 6-week-old hearts tended toward lower creatine kinase release with multidose cardioplegia. Coronary vascular resistance rose with subsequent administrations in 1-week and 4-week-old hearts at 25 degrees C but did not rise in 1- and 4-week-old hearts at 32 degrees C or in 6-week-old hearts at either temperature. On the basis of hemodynamic recovery, single-dose cardioplegia appears to provide better protection than multidose cardioplegia to 1- and 4-week-old isolated rabbit hearts. Once the rabbit has reached 6 weeks of age, multidose cardioplegia has some advantage over single-dose cardioplegia, similar to the findings in adult hearts. Creatine kinase release and coronary vascular resistance data corroborate the hemodynamic findings.</abstract><cop>Philadelphia, PA</cop><pub>AATS/WTSA</pub><pmid>8196397</pmid><doi>10.1016/S0022-5223(12)70151-4</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Animals, Newborn Biological and medical sciences Cardioplegic Solutions - administration & dosage Coronary Vessels - physiology Creatine Kinase - analysis Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care Heart - physiology Heart Arrest, Induced - methods Hemodynamics In Vitro Techniques Intensive care medicine Medical sciences Myocardium - enzymology Rabbits Random Allocation Vascular Resistance |
title | Single-dose versus multidose cardioplegia in neonatal hearts |
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