Neocytopheresis: a new approach for the transfusion of patients with thalassaemia major
At present the treatment of thalassaemia major consists of regular blood transfusions coupled with chelation therapy using deferoxamine. A complementary approach to the problem is the use of blood units enriched with young red cells (neocytes), which reduce the transfusional frequency and thereby di...
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Veröffentlicht in: | European journal of pediatrics 1986-04, Vol.145 (1-2), p.10-13 |
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container_title | European journal of pediatrics |
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creator | TRIADOU, P GIROT, R LEMAU, D MATTLINGER, B BOLO, P MAIER-REDELSPERGER, M BARRITAULT, L |
description | At present the treatment of thalassaemia major consists of regular blood transfusions coupled with chelation therapy using deferoxamine. A complementary approach to the problem is the use of blood units enriched with young red cells (neocytes), which reduce the transfusional frequency and thereby diminish the risk of iron overload. Young red cell units were collected from blood from 60 volunteer donors using a cell separator (IBM 2997). Donors' blood was anticoagulated and the young red cell harvesting carried out over 4 h at a constant rotor speed of 500 rpm. Three biological criteria were used to evaluate young red cell quality: the number of reticulocytes, the pyruvate kinase activity and the mean corpuscular volume, all of which show an enrichment of young red cells as compared to standard donor units. The 51Cr young red cell survival in four normal donors and in two splenectomized patients showed an increased red cell half-life compared to the same study performed with standard blood units. Blood consumption was diminished significantly when the two patients were transfused with young red cell units. It must be emphasized that, despite the high cost of this blood product, the efficiency of this transfusion technique, by reducing blood consumption, represents important progress and a hopeful treatment for chronic anaemia. |
doi_str_mv | 10.1007/BF00441844 |
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A complementary approach to the problem is the use of blood units enriched with young red cells (neocytes), which reduce the transfusional frequency and thereby diminish the risk of iron overload. Young red cell units were collected from blood from 60 volunteer donors using a cell separator (IBM 2997). Donors' blood was anticoagulated and the young red cell harvesting carried out over 4 h at a constant rotor speed of 500 rpm. Three biological criteria were used to evaluate young red cell quality: the number of reticulocytes, the pyruvate kinase activity and the mean corpuscular volume, all of which show an enrichment of young red cells as compared to standard donor units. The 51Cr young red cell survival in four normal donors and in two splenectomized patients showed an increased red cell half-life compared to the same study performed with standard blood units. Blood consumption was diminished significantly when the two patients were transfused with young red cell units. It must be emphasized that, despite the high cost of this blood product, the efficiency of this transfusion technique, by reducing blood consumption, represents important progress and a hopeful treatment for chronic anaemia.</description><identifier>ISSN: 0340-6199</identifier><identifier>EISSN: 1432-1076</identifier><identifier>DOI: 10.1007/BF00441844</identifier><identifier>PMID: 3732311</identifier><identifier>CODEN: EJPEDT</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Anemias. Hemoglobinopathies ; Biological and medical sciences ; Blood Donors ; Blood Preservation ; Blood Transfusion ; Cell Separation ; Diseases of red blood cells ; Erythrocyte Aging ; Erythrocyte Count ; Erythrocyte Indices ; Erythrocyte Transfusion ; Erythrocytes - enzymology ; Hematologic and hematopoietic diseases ; Humans ; Medical sciences ; Pyruvate Kinase - blood ; Reticulocytes ; Thalassemia - blood ; Thalassemia - therapy ; Time Factors</subject><ispartof>European journal of pediatrics, 1986-04, Vol.145 (1-2), p.10-13</ispartof><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c226t-cb54a60b90fcee65cfa689fcd68b1d244585d05f2732a45d889f2728bbc572773</citedby><cites>FETCH-LOGICAL-c226t-cb54a60b90fcee65cfa689fcd68b1d244585d05f2732a45d889f2728bbc572773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8761636$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3732311$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TRIADOU, P</creatorcontrib><creatorcontrib>GIROT, R</creatorcontrib><creatorcontrib>LEMAU, D</creatorcontrib><creatorcontrib>MATTLINGER, B</creatorcontrib><creatorcontrib>BOLO, P</creatorcontrib><creatorcontrib>MAIER-REDELSPERGER, M</creatorcontrib><creatorcontrib>BARRITAULT, L</creatorcontrib><title>Neocytopheresis: a new approach for the transfusion of patients with thalassaemia major</title><title>European journal of pediatrics</title><addtitle>Eur J Pediatr</addtitle><description>At present the treatment of thalassaemia major consists of regular blood transfusions coupled with chelation therapy using deferoxamine. A complementary approach to the problem is the use of blood units enriched with young red cells (neocytes), which reduce the transfusional frequency and thereby diminish the risk of iron overload. Young red cell units were collected from blood from 60 volunteer donors using a cell separator (IBM 2997). Donors' blood was anticoagulated and the young red cell harvesting carried out over 4 h at a constant rotor speed of 500 rpm. Three biological criteria were used to evaluate young red cell quality: the number of reticulocytes, the pyruvate kinase activity and the mean corpuscular volume, all of which show an enrichment of young red cells as compared to standard donor units. The 51Cr young red cell survival in four normal donors and in two splenectomized patients showed an increased red cell half-life compared to the same study performed with standard blood units. Blood consumption was diminished significantly when the two patients were transfused with young red cell units. It must be emphasized that, despite the high cost of this blood product, the efficiency of this transfusion technique, by reducing blood consumption, represents important progress and a hopeful treatment for chronic anaemia.</description><subject>Anemias. Hemoglobinopathies</subject><subject>Biological and medical sciences</subject><subject>Blood Donors</subject><subject>Blood Preservation</subject><subject>Blood Transfusion</subject><subject>Cell Separation</subject><subject>Diseases of red blood cells</subject><subject>Erythrocyte Aging</subject><subject>Erythrocyte Count</subject><subject>Erythrocyte Indices</subject><subject>Erythrocyte Transfusion</subject><subject>Erythrocytes - enzymology</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Pyruvate Kinase - blood</subject><subject>Reticulocytes</subject><subject>Thalassemia - blood</subject><subject>Thalassemia - therapy</subject><subject>Time Factors</subject><issn>0340-6199</issn><issn>1432-1076</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLxDAUhYMoOj427oUsxIVQTdI0Sd2p-ALRjeKy3KYJ06Ftam4HmX9vZIZxdRbn43D4CDnl7Iozpq_vHhmTkhspd8iMy1xknGm1S2YslyxTvCwPyCHigiW45Gaf7Oc6FznnM_L15oJdTWGcu-iwxRsKdHA_FMYxBrBz6kOk09zRKcKAfoltGGjwdISpdcOE9Ked5gmADhDB9S3QHhYhHpM9Dx26k00ekc_Hh4_75-z1_enl_vY1s0KoKbN1IUGxumTeOqcK60GZ0ttGmZo3QsrCFA0rvEh_QRaNSaXQwtS1LbTQOj8iF-vddPd76XCq-hat6zoYXFhipVVZCMVNAi_XoI0BMTpfjbHtIa4qzqo_i9W_xQSfbVaXde-aLbrRlvrzTQ9oofPJjW1xixmtuMpV_gssK3mM</recordid><startdate>198604</startdate><enddate>198604</enddate><creator>TRIADOU, P</creator><creator>GIROT, R</creator><creator>LEMAU, D</creator><creator>MATTLINGER, B</creator><creator>BOLO, P</creator><creator>MAIER-REDELSPERGER, M</creator><creator>BARRITAULT, L</creator><general>Springer</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>198604</creationdate><title>Neocytopheresis: a new approach for the transfusion of patients with thalassaemia major</title><author>TRIADOU, P ; GIROT, R ; LEMAU, D ; MATTLINGER, B ; BOLO, P ; MAIER-REDELSPERGER, M ; BARRITAULT, L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c226t-cb54a60b90fcee65cfa689fcd68b1d244585d05f2732a45d889f2728bbc572773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Anemias. Hemoglobinopathies</topic><topic>Biological and medical sciences</topic><topic>Blood Donors</topic><topic>Blood Preservation</topic><topic>Blood Transfusion</topic><topic>Cell Separation</topic><topic>Diseases of red blood cells</topic><topic>Erythrocyte Aging</topic><topic>Erythrocyte Count</topic><topic>Erythrocyte Indices</topic><topic>Erythrocyte Transfusion</topic><topic>Erythrocytes - enzymology</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Pyruvate Kinase - blood</topic><topic>Reticulocytes</topic><topic>Thalassemia - blood</topic><topic>Thalassemia - therapy</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TRIADOU, P</creatorcontrib><creatorcontrib>GIROT, R</creatorcontrib><creatorcontrib>LEMAU, D</creatorcontrib><creatorcontrib>MATTLINGER, B</creatorcontrib><creatorcontrib>BOLO, P</creatorcontrib><creatorcontrib>MAIER-REDELSPERGER, M</creatorcontrib><creatorcontrib>BARRITAULT, L</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>European journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TRIADOU, P</au><au>GIROT, R</au><au>LEMAU, D</au><au>MATTLINGER, B</au><au>BOLO, P</au><au>MAIER-REDELSPERGER, M</au><au>BARRITAULT, L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neocytopheresis: a new approach for the transfusion of patients with thalassaemia major</atitle><jtitle>European journal of pediatrics</jtitle><addtitle>Eur J Pediatr</addtitle><date>1986-04</date><risdate>1986</risdate><volume>145</volume><issue>1-2</issue><spage>10</spage><epage>13</epage><pages>10-13</pages><issn>0340-6199</issn><eissn>1432-1076</eissn><coden>EJPEDT</coden><abstract>At present the treatment of thalassaemia major consists of regular blood transfusions coupled with chelation therapy using deferoxamine. A complementary approach to the problem is the use of blood units enriched with young red cells (neocytes), which reduce the transfusional frequency and thereby diminish the risk of iron overload. Young red cell units were collected from blood from 60 volunteer donors using a cell separator (IBM 2997). Donors' blood was anticoagulated and the young red cell harvesting carried out over 4 h at a constant rotor speed of 500 rpm. Three biological criteria were used to evaluate young red cell quality: the number of reticulocytes, the pyruvate kinase activity and the mean corpuscular volume, all of which show an enrichment of young red cells as compared to standard donor units. The 51Cr young red cell survival in four normal donors and in two splenectomized patients showed an increased red cell half-life compared to the same study performed with standard blood units. Blood consumption was diminished significantly when the two patients were transfused with young red cell units. It must be emphasized that, despite the high cost of this blood product, the efficiency of this transfusion technique, by reducing blood consumption, represents important progress and a hopeful treatment for chronic anaemia.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><pub>Springer</pub><pmid>3732311</pmid><doi>10.1007/BF00441844</doi><tpages>4</tpages></addata></record> |
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subjects | Anemias. Hemoglobinopathies Biological and medical sciences Blood Donors Blood Preservation Blood Transfusion Cell Separation Diseases of red blood cells Erythrocyte Aging Erythrocyte Count Erythrocyte Indices Erythrocyte Transfusion Erythrocytes - enzymology Hematologic and hematopoietic diseases Humans Medical sciences Pyruvate Kinase - blood Reticulocytes Thalassemia - blood Thalassemia - therapy Time Factors |
title | Neocytopheresis: a new approach for the transfusion of patients with thalassaemia major |
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