The fate of circulating megakaryocytes during cardiopulmonary bypass

Megakaryocytes with intact cytoplasm normally leave the bone marrow, enter central venous blood, and are filtered in the lungs. During cardiopulmonary bypass, large megakaryocytes are not filtered by the lungs and may not be removed in the extracorporeal circuit by arterial line filters. In such cir...

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Veröffentlicht in:The Journal of thoracic and cardiovascular surgery 1993-10, Vol.106 (4), p.658-663
Hauptverfasser: Woods, M.J., Greaves, M., Smith, G.H., Trowbridge, E.A.
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container_title The Journal of thoracic and cardiovascular surgery
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creator Woods, M.J.
Greaves, M.
Smith, G.H.
Trowbridge, E.A.
description Megakaryocytes with intact cytoplasm normally leave the bone marrow, enter central venous blood, and are filtered in the lungs. During cardiopulmonary bypass, large megakaryocytes are not filtered by the lungs and may not be removed in the extracorporeal circuit by arterial line filters. In such circumstances, they could enter the systemic circulation and block smaller cerebral vessels, resulting in neurologic impairment. To investigate the fate of circulating megakaryocytes during cardiopulmonary bypass, central venous blood and oxygenated blood samples before and after arterial line filtration (40 µm polyester screen filter) were obtained from 10 patients undergoing cardiopulmonary bypass. Megakaryocytes were isolated by whole blood filtration and identified by their characteristic structure after May-Grunwald-Giemsa staining. In preliminary studies, megakaryocyte identification was verified by immunolabeling. All samples contained megakaryocytes with copious cytoplasm. Their frequencies in central venous blood and oxygenated blood before and after the arterial line filtration (corrected for hemodilution) were 23.4 ± 9.3 per milliliter (mean ± standard error of the mean, range 3.1 to 89.7 per milliliter), 21.0 ± 8.2 per milliliter (2.0 to 84.2 per milliliter) and 17.1 ± 7.4 per milliliter (3.1 to 80.4 per milliliter), respectively. Megakaryocytes with scant or no visible cytoplasm were also observed. The results confirm that circulating megakaryocytes are a normal physiologic component. During cardiopulmonary bypass, megakaryocytes with copious cytoplasm (mean diameter 42.7 µm, range 22 to 78 µm) can pass through the extracorporeal circuit. In the absence of filtration by the lungs, these large cells have access to the systemic circulation. This study supports a possible role for circulating megakaryocytes in the development of cerebral dysfunction after cardiopulmonary bypass. (J Thorac Cardiovasc Surg 1993;106:658-63)
doi_str_mv 10.1016/S0022-5223(19)33708-0
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Their frequencies in central venous blood and oxygenated blood before and after the arterial line filtration (corrected for hemodilution) were 23.4 ± 9.3 per milliliter (mean ± standard error of the mean, range 3.1 to 89.7 per milliliter), 21.0 ± 8.2 per milliliter (2.0 to 84.2 per milliliter) and 17.1 ± 7.4 per milliliter (3.1 to 80.4 per milliliter), respectively. Megakaryocytes with scant or no visible cytoplasm were also observed. The results confirm that circulating megakaryocytes are a normal physiologic component. During cardiopulmonary bypass, megakaryocytes with copious cytoplasm (mean diameter 42.7 µm, range 22 to 78 µm) can pass through the extracorporeal circuit. In the absence of filtration by the lungs, these large cells have access to the systemic circulation. This study supports a possible role for circulating megakaryocytes in the development of cerebral dysfunction after cardiopulmonary bypass. 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Coronary intensive care</subject><subject>Female</subject><subject>Hemofiltration</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Megakaryocytes - physiology</subject><subject>Megakaryocytes - ultrastructure</subject><subject>Middle Aged</subject><issn>0022-5223</issn><issn>1097-685X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtP3DAURq0KRAfan4CUBaJ0EXptJ3ayqipoCxISi1KpO8uxr2cMeUztBDT_HocZzZaVLX_nPnwIOaVwSYGKb38AGMtLxvgFrb9yLqHK4QNZUKhlLqry3wFZ7JGP5DjGRwCQQOsjclQVlDEBC3L9sMLM6RGzwWXGBzO1evT9MutwqZ902AxmM2LM7BTmV6OD9cN6aruhT2HWbNY6xk_k0Ok24ufdeUL-_vr5cHWT393_vr36cZebQlRjXgtwrJLOIAheCeSWIgNwDQorraUg9HzjJS0BCoQSG1PIQjvHua4bzU_I-bbvOgz_J4yj6nw02La6x2GKSgqAmjNIYLkFTRhiDOjUOvguLawoqNmeerOnZjWK1urNnprrTncDpqZDu6_a6Ur52S7X0ejWBd0bH_cYl1LWTCTsyxZb-eXqxQdUsdNtm5pS9TiamH6qCiXKKpHftyQmbc8eg4rGY2_QpiozKjv4d1Z-BbY2maU</recordid><startdate>19931001</startdate><enddate>19931001</enddate><creator>Woods, M.J.</creator><creator>Greaves, M.</creator><creator>Smith, G.H.</creator><creator>Trowbridge, E.A.</creator><general>Elsevier Inc</general><general>AATS/WTSA</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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>19931001</creationdate><title>The fate of circulating megakaryocytes during cardiopulmonary bypass</title><author>Woods, M.J. ; Greaves, M. ; Smith, G.H. ; Trowbridge, E.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-960f287fce06386e3d1e200fbe6d7dd106ae6d73515004e05ebc474aff33a9ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Cardiopulmonary Bypass</topic><topic>Cell Count</topic><topic>Cell Size</topic><topic>Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care</topic><topic>Female</topic><topic>Hemofiltration</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Megakaryocytes - physiology</topic><topic>Megakaryocytes - ultrastructure</topic><topic>Middle Aged</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woods, M.J.</creatorcontrib><creatorcontrib>Greaves, M.</creatorcontrib><creatorcontrib>Smith, G.H.</creatorcontrib><creatorcontrib>Trowbridge, E.A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Woods, M.J.</au><au>Greaves, M.</au><au>Smith, G.H.</au><au>Trowbridge, E.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The fate of circulating megakaryocytes during cardiopulmonary bypass</atitle><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle><addtitle>J Thorac Cardiovasc Surg</addtitle><date>1993-10-01</date><risdate>1993</risdate><volume>106</volume><issue>4</issue><spage>658</spage><epage>663</epage><pages>658-663</pages><issn>0022-5223</issn><eissn>1097-685X</eissn><coden>JTCSAQ</coden><abstract>Megakaryocytes with intact cytoplasm normally leave the bone marrow, enter central venous blood, and are filtered in the lungs. During cardiopulmonary bypass, large megakaryocytes are not filtered by the lungs and may not be removed in the extracorporeal circuit by arterial line filters. In such circumstances, they could enter the systemic circulation and block smaller cerebral vessels, resulting in neurologic impairment. To investigate the fate of circulating megakaryocytes during cardiopulmonary bypass, central venous blood and oxygenated blood samples before and after arterial line filtration (40 µm polyester screen filter) were obtained from 10 patients undergoing cardiopulmonary bypass. Megakaryocytes were isolated by whole blood filtration and identified by their characteristic structure after May-Grunwald-Giemsa staining. In preliminary studies, megakaryocyte identification was verified by immunolabeling. All samples contained megakaryocytes with copious cytoplasm. Their frequencies in central venous blood and oxygenated blood before and after the arterial line filtration (corrected for hemodilution) were 23.4 ± 9.3 per milliliter (mean ± standard error of the mean, range 3.1 to 89.7 per milliliter), 21.0 ± 8.2 per milliliter (2.0 to 84.2 per milliliter) and 17.1 ± 7.4 per milliliter (3.1 to 80.4 per milliliter), respectively. Megakaryocytes with scant or no visible cytoplasm were also observed. The results confirm that circulating megakaryocytes are a normal physiologic component. During cardiopulmonary bypass, megakaryocytes with copious cytoplasm (mean diameter 42.7 µm, range 22 to 78 µm) can pass through the extracorporeal circuit. In the absence of filtration by the lungs, these large cells have access to the systemic circulation. This study supports a possible role for circulating megakaryocytes in the development of cerebral dysfunction after cardiopulmonary bypass. 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subjects Adult
Aged
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Cardiopulmonary Bypass
Cell Count
Cell Size
Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care
Female
Hemofiltration
Humans
Intensive care medicine
Male
Medical sciences
Megakaryocytes - physiology
Megakaryocytes - ultrastructure
Middle Aged
title The fate of circulating megakaryocytes during cardiopulmonary bypass
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