Granulocyte sequestration and early failure in the autoperfused heart-lung preparation

We investigated the role of pulmonary granulocyte sequestration in the development of early failure of the autoperfused working heart-lung preparation. A significant decline in the total circulating leukocyte count in 21 preparations at 60 minutes of perfusion (5.0 to 1.4 × 10 3/μL; 28% of baseline;...

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Veröffentlicht in:The Annals of thoracic surgery 1992-02, Vol.53 (2), p.217-226
Hauptverfasser: Genco, Christopher M., Connolly, Raymond J., Peterson, Myron B., Bernstein, Eugene A., Ramberg, Karen, Zhang, Xi, Cleveland, Richard J., Diehl, James T.
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container_end_page 226
container_issue 2
container_start_page 217
container_title The Annals of thoracic surgery
container_volume 53
creator Genco, Christopher M.
Connolly, Raymond J.
Peterson, Myron B.
Bernstein, Eugene A.
Ramberg, Karen
Zhang, Xi
Cleveland, Richard J.
Diehl, James T.
description We investigated the role of pulmonary granulocyte sequestration in the development of early failure of the autoperfused working heart-lung preparation. A significant decline in the total circulating leukocyte count in 21 preparations at 60 minutes of perfusion (5.0 to 1.4 × 10 3/μL; 28% of baseline; p < 0.001) was observed. Differential cell counts in 14 of these preparations revealed a predominant decrease in granulocyte count (8.7% of baseline) and a moderate decline in lymphocyte count (46% of baseline). In study I, indium 111-labeled autologous granulocytes were injected intravenously into 10 adult New Zealand While rabbits. In group I (n = 5), an autoperfused working heart-lung preparation was harvested and perfused for 60 minutes. In group II (controls, n = 5), the heart-lung block was harvested following 60 minutes of in situ perfusion. Organ blocks were imaged before and after saline flush. There was a significant decline in granulocyte counts at 60 minutes of perfusion in group I versus no change in group II (I, 2.3 ± 0.4 to 0.3 ± 0.1; p < 0.01; II, 1.7 ± 0.2 to 2.3 ± 0.5; not significant; ×10 3/μL ± standard error of the mean). Postflush lung activity was significantly increased in group I versus group II (I, 3,751 ± 566; II, 1,867 ± 532; p < 0.05; counts ± standard error of the mean). In study II, 15 autoperfused preparations were divided into two groups. Group I (n = 10) preparations were controls. Group II (n = 5) animals were depleted of leukocytes by pretreating with nitrogen mustard. Group I (controls) produced a bimodal survival distribution (Ia, 8.2 ± 1.0) Ib, 26.4 ± 2.0; hours ± standard error of the mean). Group II survival was significantly longer than that of group Ia and similar to that of group Ib (II, 25.3 ± 2.2; p < 0.01 versus group Ia, not significant versus group Ib; hours ± standard error of the mean). Hemodynamic profiles for group II closely paralleled those of group Ib. In conclusion, pulmonary sequestration of granulocytes occurs early in the autoperfused working heart-lung preparation (within 60 minutes of autoperfusion), and preoperative leukocyte depletion prolongs survival of the autoperfused working heart-lung preparation by eliminating the subset group Ia (short survivors) seen in untreated preparations.
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A significant decline in the total circulating leukocyte count in 21 preparations at 60 minutes of perfusion (5.0 to 1.4 × 10 3/μL; 28% of baseline; p &lt; 0.001) was observed. Differential cell counts in 14 of these preparations revealed a predominant decrease in granulocyte count (8.7% of baseline) and a moderate decline in lymphocyte count (46% of baseline). In study I, indium 111-labeled autologous granulocytes were injected intravenously into 10 adult New Zealand While rabbits. In group I (n = 5), an autoperfused working heart-lung preparation was harvested and perfused for 60 minutes. In group II (controls, n = 5), the heart-lung block was harvested following 60 minutes of in situ perfusion. Organ blocks were imaged before and after saline flush. There was a significant decline in granulocyte counts at 60 minutes of perfusion in group I versus no change in group II (I, 2.3 ± 0.4 to 0.3 ± 0.1; p &lt; 0.01; II, 1.7 ± 0.2 to 2.3 ± 0.5; not significant; ×10 3/μL ± standard error of the mean). Postflush lung activity was significantly increased in group I versus group II (I, 3,751 ± 566; II, 1,867 ± 532; p &lt; 0.05; counts ± standard error of the mean). In study II, 15 autoperfused preparations were divided into two groups. Group I (n = 10) preparations were controls. Group II (n = 5) animals were depleted of leukocytes by pretreating with nitrogen mustard. Group I (controls) produced a bimodal survival distribution (Ia, 8.2 ± 1.0) Ib, 26.4 ± 2.0; hours ± standard error of the mean). Group II survival was significantly longer than that of group Ia and similar to that of group Ib (II, 25.3 ± 2.2; p &lt; 0.01 versus group Ia, not significant versus group Ib; hours ± standard error of the mean). Hemodynamic profiles for group II closely paralleled those of group Ib. In conclusion, pulmonary sequestration of granulocytes occurs early in the autoperfused working heart-lung preparation (within 60 minutes of autoperfusion), and preoperative leukocyte depletion prolongs survival of the autoperfused working heart-lung preparation by eliminating the subset group Ia (short survivors) seen in untreated preparations.</description><identifier>ISSN: 0003-4975</identifier><identifier>EISSN: 1552-6259</identifier><identifier>DOI: 10.1016/0003-4975(92)91322-Z</identifier><identifier>PMID: 1731660</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Animals ; Blood Gas Analysis ; Blood Pressure ; Cardiac Output ; Granulocytes - diagnostic imaging ; Granulocytes - physiology ; Heart ; Leukocyte Count ; Lung ; Lung Compliance ; Organ Preservation - methods ; Platelet Count ; Pulmonary Artery - physiology ; Rabbits ; Radionuclide Imaging ; Tissue Survival</subject><ispartof>The Annals of thoracic surgery, 1992-02, Vol.53 (2), p.217-226</ispartof><rights>1992 The Society of Thoracic Surgeons</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-cc1c3970af35101afc0da5d553b1cb74c59f74f60ed1dedda40eb6a0af71bd9d3</citedby><cites>FETCH-LOGICAL-c458t-cc1c3970af35101afc0da5d553b1cb74c59f74f60ed1dedda40eb6a0af71bd9d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1731660$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Genco, Christopher M.</creatorcontrib><creatorcontrib>Connolly, Raymond J.</creatorcontrib><creatorcontrib>Peterson, Myron B.</creatorcontrib><creatorcontrib>Bernstein, Eugene A.</creatorcontrib><creatorcontrib>Ramberg, Karen</creatorcontrib><creatorcontrib>Zhang, Xi</creatorcontrib><creatorcontrib>Cleveland, Richard J.</creatorcontrib><creatorcontrib>Diehl, James T.</creatorcontrib><title>Granulocyte sequestration and early failure in the autoperfused heart-lung preparation</title><title>The Annals of thoracic surgery</title><addtitle>Ann Thorac Surg</addtitle><description>We investigated the role of pulmonary granulocyte sequestration in the development of early failure of the autoperfused working heart-lung preparation. A significant decline in the total circulating leukocyte count in 21 preparations at 60 minutes of perfusion (5.0 to 1.4 × 10 3/μL; 28% of baseline; p &lt; 0.001) was observed. Differential cell counts in 14 of these preparations revealed a predominant decrease in granulocyte count (8.7% of baseline) and a moderate decline in lymphocyte count (46% of baseline). In study I, indium 111-labeled autologous granulocytes were injected intravenously into 10 adult New Zealand While rabbits. In group I (n = 5), an autoperfused working heart-lung preparation was harvested and perfused for 60 minutes. In group II (controls, n = 5), the heart-lung block was harvested following 60 minutes of in situ perfusion. Organ blocks were imaged before and after saline flush. There was a significant decline in granulocyte counts at 60 minutes of perfusion in group I versus no change in group II (I, 2.3 ± 0.4 to 0.3 ± 0.1; p &lt; 0.01; II, 1.7 ± 0.2 to 2.3 ± 0.5; not significant; ×10 3/μL ± standard error of the mean). Postflush lung activity was significantly increased in group I versus group II (I, 3,751 ± 566; II, 1,867 ± 532; p &lt; 0.05; counts ± standard error of the mean). In study II, 15 autoperfused preparations were divided into two groups. Group I (n = 10) preparations were controls. Group II (n = 5) animals were depleted of leukocytes by pretreating with nitrogen mustard. Group I (controls) produced a bimodal survival distribution (Ia, 8.2 ± 1.0) Ib, 26.4 ± 2.0; hours ± standard error of the mean). Group II survival was significantly longer than that of group Ia and similar to that of group Ib (II, 25.3 ± 2.2; p &lt; 0.01 versus group Ia, not significant versus group Ib; hours ± standard error of the mean). Hemodynamic profiles for group II closely paralleled those of group Ib. In conclusion, pulmonary sequestration of granulocytes occurs early in the autoperfused working heart-lung preparation (within 60 minutes of autoperfusion), and preoperative leukocyte depletion prolongs survival of the autoperfused working heart-lung preparation by eliminating the subset group Ia (short survivors) seen in untreated preparations.</description><subject>Animals</subject><subject>Blood Gas Analysis</subject><subject>Blood Pressure</subject><subject>Cardiac Output</subject><subject>Granulocytes - diagnostic imaging</subject><subject>Granulocytes - physiology</subject><subject>Heart</subject><subject>Leukocyte Count</subject><subject>Lung</subject><subject>Lung Compliance</subject><subject>Organ Preservation - methods</subject><subject>Platelet Count</subject><subject>Pulmonary Artery - physiology</subject><subject>Rabbits</subject><subject>Radionuclide Imaging</subject><subject>Tissue Survival</subject><issn>0003-4975</issn><issn>1552-6259</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFLwzAYhoMoc07_gUJOoodq0jTNchFk6BQGXtTDLiFNvrpI19akFfbvzdahN08hvM_7Jd-D0DklN5TQ_JYQwpJMCn4l02tJWZomywM0ppynSZ5yeYjGv8gxOgnhM17TGI_QiApG85yM0fvc67qvGrPpAAf46iF0XneuqbGuLQbtqw0utat6D9jVuFsB1n3XtODLPoDFq4h0SdXXH7j10OqhfIqOSl0FONufE_T2-PA6e0oWL_Pn2f0iMRmfdokx1DApiC4Zjzvp0hCrueWcFdQUIjNcliIrcwKWWrBWZwSKXEde0MJKyybocpjb-mb3d7V2wUBV6RqaPiiRCklYNo1gNoDGNyF4KFXr3Vr7jaJEbXWqrSu1daVkqnY61TLWLvbz-2IN9q80-Iv53ZBDXPLbgVfBOKgNWOfBdMo27v8HfgCifocd</recordid><startdate>19920201</startdate><enddate>19920201</enddate><creator>Genco, Christopher M.</creator><creator>Connolly, Raymond J.</creator><creator>Peterson, Myron B.</creator><creator>Bernstein, Eugene A.</creator><creator>Ramberg, Karen</creator><creator>Zhang, Xi</creator><creator>Cleveland, Richard J.</creator><creator>Diehl, James T.</creator><general>Elsevier Inc</general><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>19920201</creationdate><title>Granulocyte sequestration and early failure in the autoperfused heart-lung preparation</title><author>Genco, Christopher M. ; Connolly, Raymond J. ; Peterson, Myron B. ; Bernstein, Eugene A. ; Ramberg, Karen ; Zhang, Xi ; Cleveland, Richard J. ; Diehl, James T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-cc1c3970af35101afc0da5d553b1cb74c59f74f60ed1dedda40eb6a0af71bd9d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animals</topic><topic>Blood Gas Analysis</topic><topic>Blood Pressure</topic><topic>Cardiac Output</topic><topic>Granulocytes - diagnostic imaging</topic><topic>Granulocytes - physiology</topic><topic>Heart</topic><topic>Leukocyte Count</topic><topic>Lung</topic><topic>Lung Compliance</topic><topic>Organ Preservation - methods</topic><topic>Platelet Count</topic><topic>Pulmonary Artery - physiology</topic><topic>Rabbits</topic><topic>Radionuclide Imaging</topic><topic>Tissue Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Genco, Christopher M.</creatorcontrib><creatorcontrib>Connolly, Raymond J.</creatorcontrib><creatorcontrib>Peterson, Myron B.</creatorcontrib><creatorcontrib>Bernstein, Eugene A.</creatorcontrib><creatorcontrib>Ramberg, Karen</creatorcontrib><creatorcontrib>Zhang, Xi</creatorcontrib><creatorcontrib>Cleveland, Richard J.</creatorcontrib><creatorcontrib>Diehl, James T.</creatorcontrib><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 Annals of thoracic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Genco, Christopher M.</au><au>Connolly, Raymond J.</au><au>Peterson, Myron B.</au><au>Bernstein, Eugene A.</au><au>Ramberg, Karen</au><au>Zhang, Xi</au><au>Cleveland, Richard J.</au><au>Diehl, James T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Granulocyte sequestration and early failure in the autoperfused heart-lung preparation</atitle><jtitle>The Annals of thoracic surgery</jtitle><addtitle>Ann Thorac Surg</addtitle><date>1992-02-01</date><risdate>1992</risdate><volume>53</volume><issue>2</issue><spage>217</spage><epage>226</epage><pages>217-226</pages><issn>0003-4975</issn><eissn>1552-6259</eissn><abstract>We investigated the role of pulmonary granulocyte sequestration in the development of early failure of the autoperfused working heart-lung preparation. A significant decline in the total circulating leukocyte count in 21 preparations at 60 minutes of perfusion (5.0 to 1.4 × 10 3/μL; 28% of baseline; p &lt; 0.001) was observed. Differential cell counts in 14 of these preparations revealed a predominant decrease in granulocyte count (8.7% of baseline) and a moderate decline in lymphocyte count (46% of baseline). In study I, indium 111-labeled autologous granulocytes were injected intravenously into 10 adult New Zealand While rabbits. In group I (n = 5), an autoperfused working heart-lung preparation was harvested and perfused for 60 minutes. In group II (controls, n = 5), the heart-lung block was harvested following 60 minutes of in situ perfusion. Organ blocks were imaged before and after saline flush. There was a significant decline in granulocyte counts at 60 minutes of perfusion in group I versus no change in group II (I, 2.3 ± 0.4 to 0.3 ± 0.1; p &lt; 0.01; II, 1.7 ± 0.2 to 2.3 ± 0.5; not significant; ×10 3/μL ± standard error of the mean). Postflush lung activity was significantly increased in group I versus group II (I, 3,751 ± 566; II, 1,867 ± 532; p &lt; 0.05; counts ± standard error of the mean). In study II, 15 autoperfused preparations were divided into two groups. Group I (n = 10) preparations were controls. Group II (n = 5) animals were depleted of leukocytes by pretreating with nitrogen mustard. Group I (controls) produced a bimodal survival distribution (Ia, 8.2 ± 1.0) Ib, 26.4 ± 2.0; hours ± standard error of the mean). Group II survival was significantly longer than that of group Ia and similar to that of group Ib (II, 25.3 ± 2.2; p &lt; 0.01 versus group Ia, not significant versus group Ib; hours ± standard error of the mean). Hemodynamic profiles for group II closely paralleled those of group Ib. In conclusion, pulmonary sequestration of granulocytes occurs early in the autoperfused working heart-lung preparation (within 60 minutes of autoperfusion), and preoperative leukocyte depletion prolongs survival of the autoperfused working heart-lung preparation by eliminating the subset group Ia (short survivors) seen in untreated preparations.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>1731660</pmid><doi>10.1016/0003-4975(92)91322-Z</doi><tpages>10</tpages></addata></record>
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subjects Animals
Blood Gas Analysis
Blood Pressure
Cardiac Output
Granulocytes - diagnostic imaging
Granulocytes - physiology
Heart
Leukocyte Count
Lung
Lung Compliance
Organ Preservation - methods
Platelet Count
Pulmonary Artery - physiology
Rabbits
Radionuclide Imaging
Tissue Survival
title Granulocyte sequestration and early failure in the autoperfused heart-lung preparation
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