The effects of pneumatic tube system transport on ROTEM analysis and contact activation assessed by thrombin generation test

Abstract Thromboelastometry (ROTEM) is a popular point-of-care test. It generates results quickly and may benefit individualised guided haemostatic therapy. However, processing of specimens by non-technicians might decrease the quality and reproducibility of results. Centralised laboratory equipment...

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Veröffentlicht in:Thrombosis research 2012-09, Vol.130 (3), p.e147-e150
Hauptverfasser: Lancé, Marcus D, Kuiper, Gerhardus J.A.J.M, Sloep, Matthijs, Spronk, Henri M.H, van Oerle, René, ten Cate, Hugo, Marcus, Marco A.E, Henskens, Yvonne M.C
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container_end_page e150
container_issue 3
container_start_page e147
container_title Thrombosis research
container_volume 130
creator Lancé, Marcus D
Kuiper, Gerhardus J.A.J.M
Sloep, Matthijs
Spronk, Henri M.H
van Oerle, René
ten Cate, Hugo
Marcus, Marco A.E
Henskens, Yvonne M.C
description Abstract Thromboelastometry (ROTEM) is a popular point-of-care test. It generates results quickly and may benefit individualised guided haemostatic therapy. However, processing of specimens by non-technicians might decrease the quality and reproducibility of results. Centralised laboratory equipment receiving specimens through a pneumatic tube system (PTS) could avoid this. This study aimed to evaluate the influence of PTS transport on ROTEM results and its contribution to contact activation assessed by thrombin generation (TG). Methods Specimens from 44 patients were drawn immediately after arterial puncture. Two were anticoagulated by citrate and two by citrate/corn trypsin inhibitor, a Factor XIIa pathway inhibitor. Both types of samples were transported by walking and PTS. Subsequently, analysis was performed: ROTEM on citrated blood, and TG on citrated and corn trypsin inhibitor (CTI) blood using either 0 or 1 pM tissue factor (TF). Results In ROTEM analysis the NATEM assay showed significant differences. The EXTEM assay revealed small significant differences for clot formation time: 65 seconds (SD ± 20) versus 67 seconds (SD ± 17), and alpha angle 79° (SD ± 3) versus 77° (SD ± 3). The results remained within reference range. TG was not significantly affected by the type of tube transport, independent of the amount of TF. Conclusion PTS for ROTEM analysis is feasible except for NATEM assays. The amount of contact activation via Factor XIIa in terms of TG is independent of transport type. However, due to the different characteristics of pneumatic systems, hospitals should check its impact on the results before introducing this route of transport.
doi_str_mv 10.1016/j.thromres.2012.05.002
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It generates results quickly and may benefit individualised guided haemostatic therapy. However, processing of specimens by non-technicians might decrease the quality and reproducibility of results. Centralised laboratory equipment receiving specimens through a pneumatic tube system (PTS) could avoid this. This study aimed to evaluate the influence of PTS transport on ROTEM results and its contribution to contact activation assessed by thrombin generation (TG). Methods Specimens from 44 patients were drawn immediately after arterial puncture. Two were anticoagulated by citrate and two by citrate/corn trypsin inhibitor, a Factor XIIa pathway inhibitor. Both types of samples were transported by walking and PTS. Subsequently, analysis was performed: ROTEM on citrated blood, and TG on citrated and corn trypsin inhibitor (CTI) blood using either 0 or 1 pM tissue factor (TF). Results In ROTEM analysis the NATEM assay showed significant differences. The EXTEM assay revealed small significant differences for clot formation time: 65 seconds (SD ± 20) versus 67 seconds (SD ± 17), and alpha angle 79° (SD ± 3) versus 77° (SD ± 3). The results remained within reference range. TG was not significantly affected by the type of tube transport, independent of the amount of TF. Conclusion PTS for ROTEM analysis is feasible except for NATEM assays. The amount of contact activation via Factor XIIa in terms of TG is independent of transport type. However, due to the different characteristics of pneumatic systems, hospitals should check its impact on the results before introducing this route of transport.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/j.thromres.2012.05.002</identifier><identifier>PMID: 22633532</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Aged ; Contact activation ; Equipment Design ; Equipment Failure Analysis ; Female ; Hematology, Oncology and Palliative Medicine ; Humans ; Male ; Pneumatic tube system ; Point-of-care monitoring ; Pressure ; Reproducibility of Results ; Rheology - instrumentation ; ROTEM ; Sensitivity and Specificity ; Thrombelastography - instrumentation ; Thrombin Time ; Thromboelastometry</subject><ispartof>Thrombosis research, 2012-09, Vol.130 (3), p.e147-e150</ispartof><rights>2012</rights><rights>Crown Copyright © 2012. Published by Elsevier Ltd. 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It generates results quickly and may benefit individualised guided haemostatic therapy. However, processing of specimens by non-technicians might decrease the quality and reproducibility of results. Centralised laboratory equipment receiving specimens through a pneumatic tube system (PTS) could avoid this. This study aimed to evaluate the influence of PTS transport on ROTEM results and its contribution to contact activation assessed by thrombin generation (TG). Methods Specimens from 44 patients were drawn immediately after arterial puncture. Two were anticoagulated by citrate and two by citrate/corn trypsin inhibitor, a Factor XIIa pathway inhibitor. Both types of samples were transported by walking and PTS. Subsequently, analysis was performed: ROTEM on citrated blood, and TG on citrated and corn trypsin inhibitor (CTI) blood using either 0 or 1 pM tissue factor (TF). Results In ROTEM analysis the NATEM assay showed significant differences. The EXTEM assay revealed small significant differences for clot formation time: 65 seconds (SD ± 20) versus 67 seconds (SD ± 17), and alpha angle 79° (SD ± 3) versus 77° (SD ± 3). The results remained within reference range. TG was not significantly affected by the type of tube transport, independent of the amount of TF. Conclusion PTS for ROTEM analysis is feasible except for NATEM assays. The amount of contact activation via Factor XIIa in terms of TG is independent of transport type. However, due to the different characteristics of pneumatic systems, hospitals should check its impact on the results before introducing this route of transport.</description><subject>Aged</subject><subject>Contact activation</subject><subject>Equipment Design</subject><subject>Equipment Failure Analysis</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Male</subject><subject>Pneumatic tube system</subject><subject>Point-of-care monitoring</subject><subject>Pressure</subject><subject>Reproducibility of Results</subject><subject>Rheology - instrumentation</subject><subject>ROTEM</subject><subject>Sensitivity and Specificity</subject><subject>Thrombelastography - instrumentation</subject><subject>Thrombin Time</subject><subject>Thromboelastometry</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS0EokvhL1Q-ckmwncTZXBCoagGpqBIsZ8uxx9RLYi8ep1IkfjxetuXABcmWLfm9Gb9vCLngrOaMyzf7Ot-lOCfAWjAuatbVjIknZMO3_VCJthdPyYaxdqiabbs9Iy8Q94zxng_dc3ImhGyarhEb8mt3BxScA5ORRkcPAZZZZ29oXkaguGKGmeakAx5iyjQG-uV2d_WZ6qCnFT2Wi6UmhqxNpmX7--IuKo0IZVk6rvTPV0cf6HcIkE7vGTC_JM-cnhBePZzn5Nv11e7yY3Vz--HT5fubyrQ9z1U_GhDt0PWDM1aWOMbIxg6s4VvdWauZ40y0XDBrhNVWCmcHPRot5MgdN6I5J69PdQ8p_lxKYzV7NDBNOkBcUHHWtLIbpOiLVJ6kJkXEBE4dkp91WotIHcmrvXokr47kFetUIV-MFw89lnEG-9f2iLoI3p0EUJLee0gKjYdgwPpU6Csb_f97vP2nhJl88EZPP2AF3McllamUPAqLR309zv84_oKGCTZ0zW-KOLAl</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Lancé, Marcus D</creator><creator>Kuiper, Gerhardus J.A.J.M</creator><creator>Sloep, Matthijs</creator><creator>Spronk, Henri M.H</creator><creator>van Oerle, René</creator><creator>ten Cate, Hugo</creator><creator>Marcus, Marco A.E</creator><creator>Henskens, Yvonne M.C</creator><general>Elsevier Ltd</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>20120901</creationdate><title>The effects of pneumatic tube system transport on ROTEM analysis and contact activation assessed by thrombin generation test</title><author>Lancé, Marcus D ; Kuiper, Gerhardus J.A.J.M ; Sloep, Matthijs ; Spronk, Henri M.H ; van Oerle, René ; ten Cate, Hugo ; Marcus, Marco A.E ; Henskens, Yvonne M.C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-7bce249579fcd6848cc63d90318a5dda0f1024120dc2dad62fd9abca26b1f1c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Contact activation</topic><topic>Equipment Design</topic><topic>Equipment Failure Analysis</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Male</topic><topic>Pneumatic tube system</topic><topic>Point-of-care monitoring</topic><topic>Pressure</topic><topic>Reproducibility of Results</topic><topic>Rheology - instrumentation</topic><topic>ROTEM</topic><topic>Sensitivity and Specificity</topic><topic>Thrombelastography - instrumentation</topic><topic>Thrombin Time</topic><topic>Thromboelastometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lancé, Marcus D</creatorcontrib><creatorcontrib>Kuiper, Gerhardus J.A.J.M</creatorcontrib><creatorcontrib>Sloep, Matthijs</creatorcontrib><creatorcontrib>Spronk, Henri M.H</creatorcontrib><creatorcontrib>van Oerle, René</creatorcontrib><creatorcontrib>ten Cate, Hugo</creatorcontrib><creatorcontrib>Marcus, Marco A.E</creatorcontrib><creatorcontrib>Henskens, Yvonne M.C</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>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lancé, Marcus D</au><au>Kuiper, Gerhardus J.A.J.M</au><au>Sloep, Matthijs</au><au>Spronk, Henri M.H</au><au>van Oerle, René</au><au>ten Cate, Hugo</au><au>Marcus, Marco A.E</au><au>Henskens, Yvonne M.C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effects of pneumatic tube system transport on ROTEM analysis and contact activation assessed by thrombin generation test</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>130</volume><issue>3</issue><spage>e147</spage><epage>e150</epage><pages>e147-e150</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><abstract>Abstract Thromboelastometry (ROTEM) is a popular point-of-care test. It generates results quickly and may benefit individualised guided haemostatic therapy. However, processing of specimens by non-technicians might decrease the quality and reproducibility of results. Centralised laboratory equipment receiving specimens through a pneumatic tube system (PTS) could avoid this. This study aimed to evaluate the influence of PTS transport on ROTEM results and its contribution to contact activation assessed by thrombin generation (TG). Methods Specimens from 44 patients were drawn immediately after arterial puncture. Two were anticoagulated by citrate and two by citrate/corn trypsin inhibitor, a Factor XIIa pathway inhibitor. Both types of samples were transported by walking and PTS. Subsequently, analysis was performed: ROTEM on citrated blood, and TG on citrated and corn trypsin inhibitor (CTI) blood using either 0 or 1 pM tissue factor (TF). Results In ROTEM analysis the NATEM assay showed significant differences. The EXTEM assay revealed small significant differences for clot formation time: 65 seconds (SD ± 20) versus 67 seconds (SD ± 17), and alpha angle 79° (SD ± 3) versus 77° (SD ± 3). The results remained within reference range. TG was not significantly affected by the type of tube transport, independent of the amount of TF. Conclusion PTS for ROTEM analysis is feasible except for NATEM assays. The amount of contact activation via Factor XIIa in terms of TG is independent of transport type. However, due to the different characteristics of pneumatic systems, hospitals should check its impact on the results before introducing this route of transport.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>22633532</pmid><doi>10.1016/j.thromres.2012.05.002</doi><oa>free_for_read</oa></addata></record>
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subjects Aged
Contact activation
Equipment Design
Equipment Failure Analysis
Female
Hematology, Oncology and Palliative Medicine
Humans
Male
Pneumatic tube system
Point-of-care monitoring
Pressure
Reproducibility of Results
Rheology - instrumentation
ROTEM
Sensitivity and Specificity
Thrombelastography - instrumentation
Thrombin Time
Thromboelastometry
title The effects of pneumatic tube system transport on ROTEM analysis and contact activation assessed by thrombin generation test
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