The control of anti-coagulation in acute dialyses with sensitive laboratory parameters
In seven patients who had to be dialysed between four and 13 times due to acute renal failure, low molecular weight heparin (LMWH) Fragmin was used for anticoagulation. According to dose-finding studies, 80-90 U kg-1 body weight of LMWH as a single bolus were administered initially, producing dose-r...
Gespeichert in:
Veröffentlicht in: | Scandinavian journal of clinical and laboratory investigation 1992-06, Vol.52 (4), p.289-296 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 296 |
---|---|
container_issue | 4 |
container_start_page | 289 |
container_title | Scandinavian journal of clinical and laboratory investigation |
container_volume | 52 |
creator | Hafner, G. Swars, H. Ehrenthal, W. Schinzel, H. Weilemann, L. S. Prellwitz, W. |
description | In seven patients who had to be dialysed between four and 13 times due to acute renal failure, low molecular weight heparin (LMWH) Fragmin was used for anticoagulation. According to dose-finding studies, 80-90 U kg-1 body weight of LMWH as a single bolus were administered initially, producing dose-related levels of 0.3-1.5 anti-factor Xa U ml-1 in plasma. Apart from the anti-Xa activity in the plasma, the thrombin anti-thrombin III complex (TAT complex) and a fibrin degradation product (D-dimer) were measured as parameters of a coagulation activation. A sufficient anti-coagulation during dialysis was supposed to exist at a normal range (5.0 μg l-1 or below) of TAT complex. Pathological TAT concentrations at the end of dialysis indicated the requirement of an increased dose for the next dialysis. These concentrations reflected a need for more heparin if, for example, inflammation, indicated by increasing C-reactive protein levels (CRP), occurred. The increase of TAT complex and D-dimer during dialysis showed a good agreement (p < 0.001). Due to a single bolus application before dialysis, one measurement of TAT at the end of the dialysis was sufficient. The determination of the TAT complex concentration enabled a heparinization better adapted to the clinical situation of intensive-care patients undergoing acute dialyses, so that the coagulation system was not additionally activated by the extracorporeal circulation. |
doi_str_mv | 10.1080/00365519209088361 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmed_primary_1332180</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73360533</sourcerecordid><originalsourceid>FETCH-LOGICAL-c345t-377316e24572fe69fcd10065733c477158cbbf458bef2407727a18e6d419c4343</originalsourceid><addsrcrecordid>eNp9kM1rFTEUxYMo9Vn9A1wIWYi7sclk8jHoRopfUHDTdjvcydz4UjLJM8lY3n_v1PdUpNDV5XJ-53DvIeQlZ285M-yMMaGk5H3LemaMUPwR2XDJ2kYrox6TzZ3erIB4Sp6VcsPWXZjuhJxwIVpu2IZcX26R2hRrToEmRyFW39gE35cA1adIfaRgl4p08hD2BQu99XVLC8biq_-JNMCYMtSU93QHGWasmMtz8sRBKPjiOE_J1aePl-dfmotvn7-ef7horOhkbYTWgitsO6lbh6p3duKMKamFsJ3WXBo7jq6TZkTXdkzrVgM3qKaO97YTnTglbw65u5x-LFjqMPtiMQSImJYyrEGKSSFWkB9Am1MpGd2wy36GvB84G-66HO51uXpeHcOXccbpn-NQ3qq_PupQLASXIVpf_mLrfb35HfP-gPnoUp7hNuUwDRX2IeU_HvHQFe_-s28RQt1ayDjcpCXHtd4HfvgFsXGgXQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73360533</pqid></control><display><type>article</type><title>The control of anti-coagulation in acute dialyses with sensitive laboratory parameters</title><source>MEDLINE</source><source>Taylor & Francis Medical Library - CRKN</source><source>Access via Taylor & Francis</source><creator>Hafner, G. ; Swars, H. ; Ehrenthal, W. ; Schinzel, H. ; Weilemann, L. S. ; Prellwitz, W.</creator><creatorcontrib>Hafner, G. ; Swars, H. ; Ehrenthal, W. ; Schinzel, H. ; Weilemann, L. S. ; Prellwitz, W.</creatorcontrib><description>In seven patients who had to be dialysed between four and 13 times due to acute renal failure, low molecular weight heparin (LMWH) Fragmin was used for anticoagulation. According to dose-finding studies, 80-90 U kg-1 body weight of LMWH as a single bolus were administered initially, producing dose-related levels of 0.3-1.5 anti-factor Xa U ml-1 in plasma. Apart from the anti-Xa activity in the plasma, the thrombin anti-thrombin III complex (TAT complex) and a fibrin degradation product (D-dimer) were measured as parameters of a coagulation activation. A sufficient anti-coagulation during dialysis was supposed to exist at a normal range (5.0 μg l-1 or below) of TAT complex. Pathological TAT concentrations at the end of dialysis indicated the requirement of an increased dose for the next dialysis. These concentrations reflected a need for more heparin if, for example, inflammation, indicated by increasing C-reactive protein levels (CRP), occurred. The increase of TAT complex and D-dimer during dialysis showed a good agreement (p < 0.001). Due to a single bolus application before dialysis, one measurement of TAT at the end of the dialysis was sufficient. The determination of the TAT complex concentration enabled a heparinization better adapted to the clinical situation of intensive-care patients undergoing acute dialyses, so that the coagulation system was not additionally activated by the extracorporeal circulation.</description><identifier>ISSN: 0036-5513</identifier><identifier>EISSN: 1502-7686</identifier><identifier>DOI: 10.1080/00365519209088361</identifier><identifier>PMID: 1332180</identifier><identifier>CODEN: SJCLAY</identifier><language>eng</language><publisher>Oslo: Informa Healthcare</publisher><subject>Acute Kidney Injury - blood ; Acute Kidney Injury - therapy ; Aged ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Anticoagulants - administration & dosage ; Antithrombin III - metabolism ; Biological and medical sciences ; Blood Coagulation - drug effects ; D-dimer ; Emergency and intensive care: renal failure. Dialysis management ; extracorporeal circulation ; Factor Xa Inhibitors ; Fibrin Fibrinogen Degradation Products - metabolism ; Heparin, Low-Molecular-Weight - administration & dosage ; Humans ; individual anti-coagulation ; Intensive care medicine ; Male ; Medical sciences ; Middle Aged ; Peptide Hydrolases - metabolism ; Renal Dialysis - adverse effects ; Renal Dialysis - methods ; septicaemia ; TAT complex</subject><ispartof>Scandinavian journal of clinical and laboratory investigation, 1992-06, Vol.52 (4), p.289-296</ispartof><rights>1992 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1992</rights><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-377316e24572fe69fcd10065733c477158cbbf458bef2407727a18e6d419c4343</citedby><cites>FETCH-LOGICAL-c345t-377316e24572fe69fcd10065733c477158cbbf458bef2407727a18e6d419c4343</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/00365519209088361$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/00365519209088361$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>315,781,785,27929,27930,59652,59758,60441,60547,61226,61261,61407,61442</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4349861$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1332180$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hafner, G.</creatorcontrib><creatorcontrib>Swars, H.</creatorcontrib><creatorcontrib>Ehrenthal, W.</creatorcontrib><creatorcontrib>Schinzel, H.</creatorcontrib><creatorcontrib>Weilemann, L. S.</creatorcontrib><creatorcontrib>Prellwitz, W.</creatorcontrib><title>The control of anti-coagulation in acute dialyses with sensitive laboratory parameters</title><title>Scandinavian journal of clinical and laboratory investigation</title><addtitle>Scand J Clin Lab Invest</addtitle><description>In seven patients who had to be dialysed between four and 13 times due to acute renal failure, low molecular weight heparin (LMWH) Fragmin was used for anticoagulation. According to dose-finding studies, 80-90 U kg-1 body weight of LMWH as a single bolus were administered initially, producing dose-related levels of 0.3-1.5 anti-factor Xa U ml-1 in plasma. Apart from the anti-Xa activity in the plasma, the thrombin anti-thrombin III complex (TAT complex) and a fibrin degradation product (D-dimer) were measured as parameters of a coagulation activation. A sufficient anti-coagulation during dialysis was supposed to exist at a normal range (5.0 μg l-1 or below) of TAT complex. Pathological TAT concentrations at the end of dialysis indicated the requirement of an increased dose for the next dialysis. These concentrations reflected a need for more heparin if, for example, inflammation, indicated by increasing C-reactive protein levels (CRP), occurred. The increase of TAT complex and D-dimer during dialysis showed a good agreement (p < 0.001). Due to a single bolus application before dialysis, one measurement of TAT at the end of the dialysis was sufficient. The determination of the TAT complex concentration enabled a heparinization better adapted to the clinical situation of intensive-care patients undergoing acute dialyses, so that the coagulation system was not additionally activated by the extracorporeal circulation.</description><subject>Acute Kidney Injury - blood</subject><subject>Acute Kidney Injury - therapy</subject><subject>Aged</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Anticoagulants - administration & dosage</subject><subject>Antithrombin III - metabolism</subject><subject>Biological and medical sciences</subject><subject>Blood Coagulation - drug effects</subject><subject>D-dimer</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>extracorporeal circulation</subject><subject>Factor Xa Inhibitors</subject><subject>Fibrin Fibrinogen Degradation Products - metabolism</subject><subject>Heparin, Low-Molecular-Weight - administration & dosage</subject><subject>Humans</subject><subject>individual anti-coagulation</subject><subject>Intensive care medicine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Peptide Hydrolases - metabolism</subject><subject>Renal Dialysis - adverse effects</subject><subject>Renal Dialysis - methods</subject><subject>septicaemia</subject><subject>TAT complex</subject><issn>0036-5513</issn><issn>1502-7686</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1rFTEUxYMo9Vn9A1wIWYi7sclk8jHoRopfUHDTdjvcydz4UjLJM8lY3n_v1PdUpNDV5XJ-53DvIeQlZ285M-yMMaGk5H3LemaMUPwR2XDJ2kYrox6TzZ3erIB4Sp6VcsPWXZjuhJxwIVpu2IZcX26R2hRrToEmRyFW39gE35cA1adIfaRgl4p08hD2BQu99XVLC8biq_-JNMCYMtSU93QHGWasmMtz8sRBKPjiOE_J1aePl-dfmotvn7-ef7horOhkbYTWgitsO6lbh6p3duKMKamFsJ3WXBo7jq6TZkTXdkzrVgM3qKaO97YTnTglbw65u5x-LFjqMPtiMQSImJYyrEGKSSFWkB9Am1MpGd2wy36GvB84G-66HO51uXpeHcOXccbpn-NQ3qq_PupQLASXIVpf_mLrfb35HfP-gPnoUp7hNuUwDRX2IeU_HvHQFe_-s28RQt1ayDjcpCXHtd4HfvgFsXGgXQ</recordid><startdate>199206</startdate><enddate>199206</enddate><creator>Hafner, G.</creator><creator>Swars, H.</creator><creator>Ehrenthal, W.</creator><creator>Schinzel, H.</creator><creator>Weilemann, L. S.</creator><creator>Prellwitz, W.</creator><general>Informa Healthcare</general><general>Taylor & Francis</general><general>Scandinavian University Press</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>199206</creationdate><title>The control of anti-coagulation in acute dialyses with sensitive laboratory parameters</title><author>Hafner, G. ; Swars, H. ; Ehrenthal, W. ; Schinzel, H. ; Weilemann, L. S. ; Prellwitz, W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-377316e24572fe69fcd10065733c477158cbbf458bef2407727a18e6d419c4343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Acute Kidney Injury - blood</topic><topic>Acute Kidney Injury - therapy</topic><topic>Aged</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Anticoagulants - administration & dosage</topic><topic>Antithrombin III - metabolism</topic><topic>Biological and medical sciences</topic><topic>Blood Coagulation - drug effects</topic><topic>D-dimer</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>extracorporeal circulation</topic><topic>Factor Xa Inhibitors</topic><topic>Fibrin Fibrinogen Degradation Products - metabolism</topic><topic>Heparin, Low-Molecular-Weight - administration & dosage</topic><topic>Humans</topic><topic>individual anti-coagulation</topic><topic>Intensive care medicine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Peptide Hydrolases - metabolism</topic><topic>Renal Dialysis - adverse effects</topic><topic>Renal Dialysis - methods</topic><topic>septicaemia</topic><topic>TAT complex</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hafner, G.</creatorcontrib><creatorcontrib>Swars, H.</creatorcontrib><creatorcontrib>Ehrenthal, W.</creatorcontrib><creatorcontrib>Schinzel, H.</creatorcontrib><creatorcontrib>Weilemann, L. S.</creatorcontrib><creatorcontrib>Prellwitz, W.</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>Scandinavian journal of clinical and laboratory investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hafner, G.</au><au>Swars, H.</au><au>Ehrenthal, W.</au><au>Schinzel, H.</au><au>Weilemann, L. S.</au><au>Prellwitz, W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The control of anti-coagulation in acute dialyses with sensitive laboratory parameters</atitle><jtitle>Scandinavian journal of clinical and laboratory investigation</jtitle><addtitle>Scand J Clin Lab Invest</addtitle><date>1992-06</date><risdate>1992</risdate><volume>52</volume><issue>4</issue><spage>289</spage><epage>296</epage><pages>289-296</pages><issn>0036-5513</issn><eissn>1502-7686</eissn><coden>SJCLAY</coden><abstract>In seven patients who had to be dialysed between four and 13 times due to acute renal failure, low molecular weight heparin (LMWH) Fragmin was used for anticoagulation. According to dose-finding studies, 80-90 U kg-1 body weight of LMWH as a single bolus were administered initially, producing dose-related levels of 0.3-1.5 anti-factor Xa U ml-1 in plasma. Apart from the anti-Xa activity in the plasma, the thrombin anti-thrombin III complex (TAT complex) and a fibrin degradation product (D-dimer) were measured as parameters of a coagulation activation. A sufficient anti-coagulation during dialysis was supposed to exist at a normal range (5.0 μg l-1 or below) of TAT complex. Pathological TAT concentrations at the end of dialysis indicated the requirement of an increased dose for the next dialysis. These concentrations reflected a need for more heparin if, for example, inflammation, indicated by increasing C-reactive protein levels (CRP), occurred. The increase of TAT complex and D-dimer during dialysis showed a good agreement (p < 0.001). Due to a single bolus application before dialysis, one measurement of TAT at the end of the dialysis was sufficient. The determination of the TAT complex concentration enabled a heparinization better adapted to the clinical situation of intensive-care patients undergoing acute dialyses, so that the coagulation system was not additionally activated by the extracorporeal circulation.</abstract><cop>Oslo</cop><pub>Informa Healthcare</pub><pmid>1332180</pmid><doi>10.1080/00365519209088361</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0036-5513 |
ispartof | Scandinavian journal of clinical and laboratory investigation, 1992-06, Vol.52 (4), p.289-296 |
issn | 0036-5513 1502-7686 |
language | eng |
recordid | cdi_pubmed_primary_1332180 |
source | MEDLINE; Taylor & Francis Medical Library - CRKN; Access via Taylor & Francis |
subjects | Acute Kidney Injury - blood Acute Kidney Injury - therapy Aged Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Anticoagulants - administration & dosage Antithrombin III - metabolism Biological and medical sciences Blood Coagulation - drug effects D-dimer Emergency and intensive care: renal failure. Dialysis management extracorporeal circulation Factor Xa Inhibitors Fibrin Fibrinogen Degradation Products - metabolism Heparin, Low-Molecular-Weight - administration & dosage Humans individual anti-coagulation Intensive care medicine Male Medical sciences Middle Aged Peptide Hydrolases - metabolism Renal Dialysis - adverse effects Renal Dialysis - methods septicaemia TAT complex |
title | The control of anti-coagulation in acute dialyses with sensitive laboratory parameters |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T19%3A36%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20control%20of%20anti-coagulation%20in%20acute%20dialyses%20with%20sensitive%20laboratory%20parameters&rft.jtitle=Scandinavian%20journal%20of%20clinical%20and%20laboratory%20investigation&rft.au=Hafner,%20G.&rft.date=1992-06&rft.volume=52&rft.issue=4&rft.spage=289&rft.epage=296&rft.pages=289-296&rft.issn=0036-5513&rft.eissn=1502-7686&rft.coden=SJCLAY&rft_id=info:doi/10.1080/00365519209088361&rft_dat=%3Cproquest_pubme%3E73360533%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=73360533&rft_id=info:pmid/1332180&rfr_iscdi=true |