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...

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Veröffentlicht in:Scandinavian journal of clinical and laboratory investigation 1992-06, Vol.52 (4), p.289-296
Hauptverfasser: Hafner, G., Swars, H., Ehrenthal, W., Schinzel, H., Weilemann, L. S., Prellwitz, W.
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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.
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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 &lt; 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 &amp; 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 &amp; 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. 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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 &amp; 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. 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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 &lt; 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>
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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
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