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Prediction of Ischemic Events after Percutaneous Coronary Intervention: Thrombelastography Profiles and Factor XIIIa Activity
Background High plasma fibrin clot strength (MA) measured by thrombelastography (TEG) is associated with increased risk of cardiac events after percutaneous coronary interventions (PCIs). Factor XIIIa (FXIIIa) cross-links soluble fibrin, shortens clot formation time (TEG-K), and increases final clo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Georg Thieme Verlag KG
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419750/ https://www.ncbi.nlm.nih.gov/pubmed/30882064 http://dx.doi.org/10.1055/s-0038-1645876 |
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author | Kreutz, Rolf P. Schmeisser, Glen Schaffter, Andrea Kanuri, Sri Owens, Janelle Maatman, Benjamin Sinha, Anjan von der Lohe, Elisabeth Breall, Jeffrey A. |
author_facet | Kreutz, Rolf P. Schmeisser, Glen Schaffter, Andrea Kanuri, Sri Owens, Janelle Maatman, Benjamin Sinha, Anjan von der Lohe, Elisabeth Breall, Jeffrey A. |
author_sort | Kreutz, Rolf P. |
collection | PubMed |
description | Background High plasma fibrin clot strength (MA) measured by thrombelastography (TEG) is associated with increased risk of cardiac events after percutaneous coronary interventions (PCIs). Factor XIIIa (FXIIIa) cross-links soluble fibrin, shortens clot formation time (TEG-K), and increases final clot strength (MA). Methods We analyzed platelet-poor plasma from patients with previous PCI. Kaolin-activated TEG (R, K, MA) in citrate platelet-poor plasma and FXIIIa were measured ( n = 257). Combined primary endpoint was defined as recurrent myocardial infarction (MI) or cardiovascular death (CVD). Relationship of FXIIIa and TEG measurements on cardiac risk was explored. Results FXIIIa correlated with TEG-MA ( p = 0.002) and inversely with TEG-K ( p < 0.001). High MA (≥35.35 mm; p = 0.001), low K (<1.15 min; p = 0.038), and elevated FXIIIa (≥83.51%; p = 0.011) were associated with increased risk of CVD or MI. Inclusion of FXIIIa activity and low TEG-K in risk scores did not improve risk prediction as compared with high TEG-MA alone. Conclusion FXIIIa is associated with higher plasma TEG-MA and low TEG-K. High FXIIIa activity is associated with a modest increase in cardiovascular risk after PCI, but is less sensitive and specific than TEG-MA. Addition of FXIIIa does not provide additional risk stratification beyond risk associated with high fibrin clot strength phenotype measured by TEG. |
format | Online Article Text |
id | pubmed-6419750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-64197502019-03-15 Prediction of Ischemic Events after Percutaneous Coronary Intervention: Thrombelastography Profiles and Factor XIIIa Activity Kreutz, Rolf P. Schmeisser, Glen Schaffter, Andrea Kanuri, Sri Owens, Janelle Maatman, Benjamin Sinha, Anjan von der Lohe, Elisabeth Breall, Jeffrey A. TH Open Background High plasma fibrin clot strength (MA) measured by thrombelastography (TEG) is associated with increased risk of cardiac events after percutaneous coronary interventions (PCIs). Factor XIIIa (FXIIIa) cross-links soluble fibrin, shortens clot formation time (TEG-K), and increases final clot strength (MA). Methods We analyzed platelet-poor plasma from patients with previous PCI. Kaolin-activated TEG (R, K, MA) in citrate platelet-poor plasma and FXIIIa were measured ( n = 257). Combined primary endpoint was defined as recurrent myocardial infarction (MI) or cardiovascular death (CVD). Relationship of FXIIIa and TEG measurements on cardiac risk was explored. Results FXIIIa correlated with TEG-MA ( p = 0.002) and inversely with TEG-K ( p < 0.001). High MA (≥35.35 mm; p = 0.001), low K (<1.15 min; p = 0.038), and elevated FXIIIa (≥83.51%; p = 0.011) were associated with increased risk of CVD or MI. Inclusion of FXIIIa activity and low TEG-K in risk scores did not improve risk prediction as compared with high TEG-MA alone. Conclusion FXIIIa is associated with higher plasma TEG-MA and low TEG-K. High FXIIIa activity is associated with a modest increase in cardiovascular risk after PCI, but is less sensitive and specific than TEG-MA. Addition of FXIIIa does not provide additional risk stratification beyond risk associated with high fibrin clot strength phenotype measured by TEG. Georg Thieme Verlag KG 2018-05-07 /pmc/articles/PMC6419750/ /pubmed/30882064 http://dx.doi.org/10.1055/s-0038-1645876 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Kreutz, Rolf P. Schmeisser, Glen Schaffter, Andrea Kanuri, Sri Owens, Janelle Maatman, Benjamin Sinha, Anjan von der Lohe, Elisabeth Breall, Jeffrey A. Prediction of Ischemic Events after Percutaneous Coronary Intervention: Thrombelastography Profiles and Factor XIIIa Activity |
title | Prediction of Ischemic Events after Percutaneous Coronary Intervention: Thrombelastography Profiles and Factor XIIIa Activity |
title_full | Prediction of Ischemic Events after Percutaneous Coronary Intervention: Thrombelastography Profiles and Factor XIIIa Activity |
title_fullStr | Prediction of Ischemic Events after Percutaneous Coronary Intervention: Thrombelastography Profiles and Factor XIIIa Activity |
title_full_unstemmed | Prediction of Ischemic Events after Percutaneous Coronary Intervention: Thrombelastography Profiles and Factor XIIIa Activity |
title_short | Prediction of Ischemic Events after Percutaneous Coronary Intervention: Thrombelastography Profiles and Factor XIIIa Activity |
title_sort | prediction of ischemic events after percutaneous coronary intervention: thrombelastography profiles and factor xiiia activity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419750/ https://www.ncbi.nlm.nih.gov/pubmed/30882064 http://dx.doi.org/10.1055/s-0038-1645876 |
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