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The Role of Whole Blood Impedance Aggregometry and Its Utilisation in the Diagnosis and Prognosis of Patients with Systemic Inflammatory Response Syndrome and Sepsis in Acute Critical Illness
PLoS ONE, Volume: 9, Issue: 9, Start page: e108589
Swansea University Authors: Gareth Davies , Matthew Lawrence, Ceri Battle, Karl Hawkins , Rhodri Williams , Adrian Evans
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DOI (Published version): 10.1371/journal.pone.0108589
Abstract
ObjectiveTo assess the prognostic and diagnostic value of whole blood impedance aggregometry in patients with sepsis and SIRS and to compare with whole blood parameters (platelet count, haemoglobin, haematocrit and white cell count).MethodsWe performed an observational, prospective study in the acut...
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ISSN: | 1932-6203 |
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2014
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Platelet function was determined using whole blood impedance aggregometry (multiplate) on admission to the Emergency Department or Intensive Care Unit and at 6 and 24 hours post admission. Platelet count, haemoglobin, haematocrit and white cell count were also determined.Results106 adult patients that met SIRS and sepsis criteria were included. Platelet aggregation was significantly reduced in patients with severe sepsis/septic shock when compared to SIRS/uncomplicated sepsis (ADP: 90.7±37.6 vs 61.4±40.6; p<0.001, Arachadonic Acid 99.9±48.3 vs 66.3±50.2; p = 0.001, Collagen 102.6±33.0 vs 79.1±38.8; p = 0.001; SD ± mean)). Furthermore platelet aggregation was significantly reduced in the 28 day mortality group when compared with the survival group (Arachadonic Acid 58.8±47.7 vs 91.1±50.9; p<0.05, Collagen 36.6±36.6 vs 98.0±35.1; p = 0.001; SD ± mean)). However haemoglobin, haematocrit and platelet count were more effective at distinguishing between subgroups and were equally effective indicators of prognosis. Significant positive correlations were observed between whole blood impedance aggregometry and platelet count (ADP 0.588 p<0.0001, Arachadonic Acid 0.611 p<0.0001, Collagen 0.599 p<0.0001 (Pearson correlation)).ConclusionsReduced platelet aggregometry responses were not only significantly associated with morbidity and mortality in sepsis and SIRS patients, but also correlated with the different pathological groups. Whole blood aggregometry significantly correlated with platelet count, however, when we adjust for the different groups we investigated, the effect of platelet count appears to be non-significant.</abstract><type>Journal Article</type><journal>PLoS ONE</journal><volume>9</volume><journalNumber>9</journalNumber><paginationStart>e108589</paginationStart><paginationEnd/><publisher>Public Library of Science (PLoS)</publisher><placeOfPublication/><isbnPrint/><isbnElectronic/><issnPrint/><issnElectronic>1932-6203</issnElectronic><keywords/><publishedDay>30</publishedDay><publishedMonth>9</publishedMonth><publishedYear>2014</publishedYear><publishedDate>2014-09-30</publishedDate><doi>10.1371/journal.pone.0108589</doi><url/><notes>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permitsunrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</notes><college>COLLEGE NANME</college><department>Biomedical Sciences</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>BMS</DepartmentCode><institution>Swansea University</institution><apcterm/><funders/><projectreference/><lastEdited>2022-11-02T16:38:34.5673669</lastEdited><Created>2015-05-06T15:20:14.6116632</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">Swansea University Medical School - Medicine</level></path><authors><author><firstname>Gareth</firstname><surname>Davies</surname><orcid>0000-0002-0863-9234</orcid><order>1</order></author><author><firstname>Gavin M.</firstname><surname>Mills</surname><order>2</order></author><author><firstname>Matthew</firstname><surname>Lawrence</surname><order>3</order></author><author><firstname>Ceri</firstname><surname>Battle</surname><order>4</order></author><author><firstname>Keith</firstname><surname>Morris</surname><order>5</order></author><author><firstname>Karl</firstname><surname>Hawkins</surname><orcid>0000-0003-0174-4151</orcid><order>6</order></author><author><firstname>Rhodri</firstname><surname>Williams</surname><orcid>0000-0002-6912-5288</orcid><order>7</order></author><author><firstname>Simon</firstname><surname>Davidson</surname><order>8</order></author><author><firstname>Dafydd</firstname><surname>Thomas</surname><order>9</order></author><author><firstname>Adrian</firstname><surname>Evans</surname><orcid>0000-0002-0814-5162</orcid><order>10</order></author></authors><documents><document><filename>0021117-22072016095820.pdf</filename><originalFilename>davies2015v2.pdf</originalFilename><uploaded>2016-07-22T09:58:20.7670000</uploaded><type>Output</type><contentLength>830677</contentLength><contentType>application/pdf</contentType><version>Version of Record</version><cronfaStatus>true</cronfaStatus><embargoDate>2016-07-22T00:00:00.0000000</embargoDate><documentNotes>Distributed under the terms of a Creative Commons Attribution (CC-BY-4.0)</documentNotes><copyrightCorrect>true</copyrightCorrect></document></documents><OutputDurs/></rfc1807> |
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2022-11-02T16:38:34.5673669 v2 21117 2015-05-06 The Role of Whole Blood Impedance Aggregometry and Its Utilisation in the Diagnosis and Prognosis of Patients with Systemic Inflammatory Response Syndrome and Sepsis in Acute Critical Illness 3959a373060151515e05594d4cbcd6b1 0000-0002-0863-9234 Gareth Davies Gareth Davies true false 262d0cae7663ded863d6e2de15757f3c Matthew Lawrence Matthew Lawrence true false 9ae21f1afb903db3c39684cd47b94760 Ceri Battle Ceri Battle true false 77c39404a9a98c6e2283d84815cba053 0000-0003-0174-4151 Karl Hawkins Karl Hawkins true false 642bf793695f412ed932f1ea4d9bc3f1 0000-0002-6912-5288 Rhodri Williams Rhodri Williams true false 21761f6eb805546a561c9f036e85405b 0000-0002-0814-5162 Adrian Evans Adrian Evans true false 2015-05-06 BMS ObjectiveTo assess the prognostic and diagnostic value of whole blood impedance aggregometry in patients with sepsis and SIRS and to compare with whole blood parameters (platelet count, haemoglobin, haematocrit and white cell count).MethodsWe performed an observational, prospective study in the acute setting. Platelet function was determined using whole blood impedance aggregometry (multiplate) on admission to the Emergency Department or Intensive Care Unit and at 6 and 24 hours post admission. Platelet count, haemoglobin, haematocrit and white cell count were also determined.Results106 adult patients that met SIRS and sepsis criteria were included. Platelet aggregation was significantly reduced in patients with severe sepsis/septic shock when compared to SIRS/uncomplicated sepsis (ADP: 90.7±37.6 vs 61.4±40.6; p<0.001, Arachadonic Acid 99.9±48.3 vs 66.3±50.2; p = 0.001, Collagen 102.6±33.0 vs 79.1±38.8; p = 0.001; SD ± mean)). Furthermore platelet aggregation was significantly reduced in the 28 day mortality group when compared with the survival group (Arachadonic Acid 58.8±47.7 vs 91.1±50.9; p<0.05, Collagen 36.6±36.6 vs 98.0±35.1; p = 0.001; SD ± mean)). However haemoglobin, haematocrit and platelet count were more effective at distinguishing between subgroups and were equally effective indicators of prognosis. Significant positive correlations were observed between whole blood impedance aggregometry and platelet count (ADP 0.588 p<0.0001, Arachadonic Acid 0.611 p<0.0001, Collagen 0.599 p<0.0001 (Pearson correlation)).ConclusionsReduced platelet aggregometry responses were not only significantly associated with morbidity and mortality in sepsis and SIRS patients, but also correlated with the different pathological groups. Whole blood aggregometry significantly correlated with platelet count, however, when we adjust for the different groups we investigated, the effect of platelet count appears to be non-significant. Journal Article PLoS ONE 9 9 e108589 Public Library of Science (PLoS) 1932-6203 30 9 2014 2014-09-30 10.1371/journal.pone.0108589 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permitsunrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. COLLEGE NANME Biomedical Sciences COLLEGE CODE BMS Swansea University 2022-11-02T16:38:34.5673669 2015-05-06T15:20:14.6116632 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Gareth Davies 0000-0002-0863-9234 1 Gavin M. Mills 2 Matthew Lawrence 3 Ceri Battle 4 Keith Morris 5 Karl Hawkins 0000-0003-0174-4151 6 Rhodri Williams 0000-0002-6912-5288 7 Simon Davidson 8 Dafydd Thomas 9 Adrian Evans 0000-0002-0814-5162 10 0021117-22072016095820.pdf davies2015v2.pdf 2016-07-22T09:58:20.7670000 Output 830677 application/pdf Version of Record true 2016-07-22T00:00:00.0000000 Distributed under the terms of a Creative Commons Attribution (CC-BY-4.0) true |
title |
The Role of Whole Blood Impedance Aggregometry and Its Utilisation in the Diagnosis and Prognosis of Patients with Systemic Inflammatory Response Syndrome and Sepsis in Acute Critical Illness |
spellingShingle |
The Role of Whole Blood Impedance Aggregometry and Its Utilisation in the Diagnosis and Prognosis of Patients with Systemic Inflammatory Response Syndrome and Sepsis in Acute Critical Illness Gareth Davies Matthew Lawrence Ceri Battle Karl Hawkins Rhodri Williams Adrian Evans |
title_short |
The Role of Whole Blood Impedance Aggregometry and Its Utilisation in the Diagnosis and Prognosis of Patients with Systemic Inflammatory Response Syndrome and Sepsis in Acute Critical Illness |
title_full |
The Role of Whole Blood Impedance Aggregometry and Its Utilisation in the Diagnosis and Prognosis of Patients with Systemic Inflammatory Response Syndrome and Sepsis in Acute Critical Illness |
title_fullStr |
The Role of Whole Blood Impedance Aggregometry and Its Utilisation in the Diagnosis and Prognosis of Patients with Systemic Inflammatory Response Syndrome and Sepsis in Acute Critical Illness |
title_full_unstemmed |
The Role of Whole Blood Impedance Aggregometry and Its Utilisation in the Diagnosis and Prognosis of Patients with Systemic Inflammatory Response Syndrome and Sepsis in Acute Critical Illness |
title_sort |
The Role of Whole Blood Impedance Aggregometry and Its Utilisation in the Diagnosis and Prognosis of Patients with Systemic Inflammatory Response Syndrome and Sepsis in Acute Critical Illness |
author_id_str_mv |
3959a373060151515e05594d4cbcd6b1 262d0cae7663ded863d6e2de15757f3c 9ae21f1afb903db3c39684cd47b94760 77c39404a9a98c6e2283d84815cba053 642bf793695f412ed932f1ea4d9bc3f1 21761f6eb805546a561c9f036e85405b |
author_id_fullname_str_mv |
3959a373060151515e05594d4cbcd6b1_***_Gareth Davies 262d0cae7663ded863d6e2de15757f3c_***_Matthew Lawrence 9ae21f1afb903db3c39684cd47b94760_***_Ceri Battle 77c39404a9a98c6e2283d84815cba053_***_Karl Hawkins 642bf793695f412ed932f1ea4d9bc3f1_***_Rhodri Williams 21761f6eb805546a561c9f036e85405b_***_Adrian Evans |
author |
Gareth Davies Matthew Lawrence Ceri Battle Karl Hawkins Rhodri Williams Adrian Evans |
author2 |
Gareth Davies Gavin M. Mills Matthew Lawrence Ceri Battle Keith Morris Karl Hawkins Rhodri Williams Simon Davidson Dafydd Thomas Adrian Evans |
format |
Journal article |
container_title |
PLoS ONE |
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9 |
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9 |
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e108589 |
publishDate |
2014 |
institution |
Swansea University |
issn |
1932-6203 |
doi_str_mv |
10.1371/journal.pone.0108589 |
publisher |
Public Library of Science (PLoS) |
college_str |
Faculty of Medicine, Health and Life Sciences |
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|
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facultyofmedicinehealthandlifesciences |
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Faculty of Medicine, Health and Life Sciences |
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facultyofmedicinehealthandlifesciences |
hierarchy_parent_title |
Faculty of Medicine, Health and Life Sciences |
department_str |
Swansea University Medical School - Medicine{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}Swansea University Medical School - Medicine |
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description |
ObjectiveTo assess the prognostic and diagnostic value of whole blood impedance aggregometry in patients with sepsis and SIRS and to compare with whole blood parameters (platelet count, haemoglobin, haematocrit and white cell count).MethodsWe performed an observational, prospective study in the acute setting. Platelet function was determined using whole blood impedance aggregometry (multiplate) on admission to the Emergency Department or Intensive Care Unit and at 6 and 24 hours post admission. Platelet count, haemoglobin, haematocrit and white cell count were also determined.Results106 adult patients that met SIRS and sepsis criteria were included. Platelet aggregation was significantly reduced in patients with severe sepsis/septic shock when compared to SIRS/uncomplicated sepsis (ADP: 90.7±37.6 vs 61.4±40.6; p<0.001, Arachadonic Acid 99.9±48.3 vs 66.3±50.2; p = 0.001, Collagen 102.6±33.0 vs 79.1±38.8; p = 0.001; SD ± mean)). Furthermore platelet aggregation was significantly reduced in the 28 day mortality group when compared with the survival group (Arachadonic Acid 58.8±47.7 vs 91.1±50.9; p<0.05, Collagen 36.6±36.6 vs 98.0±35.1; p = 0.001; SD ± mean)). However haemoglobin, haematocrit and platelet count were more effective at distinguishing between subgroups and were equally effective indicators of prognosis. Significant positive correlations were observed between whole blood impedance aggregometry and platelet count (ADP 0.588 p<0.0001, Arachadonic Acid 0.611 p<0.0001, Collagen 0.599 p<0.0001 (Pearson correlation)).ConclusionsReduced platelet aggregometry responses were not only significantly associated with morbidity and mortality in sepsis and SIRS patients, but also correlated with the different pathological groups. Whole blood aggregometry significantly correlated with platelet count, however, when we adjust for the different groups we investigated, the effect of platelet count appears to be non-significant. |
published_date |
2014-09-30T03:25:01Z |
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1763750865576919040 |
score |
11.037056 |