Biomarkers of disseminated intravascular coagulation in pediatric intensive care unit in Thailand
© 2018 John Wiley & Sons Ltd Introduction: Disseminated intravascular coagulation (DIC) is a systemic activation of hemostatic system caused by several causes. Biomarkers including antithrombin (AT), protein C (PC), and thrombomodulin (TM) were reported as the additional markers for DIC in adu...
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th-cmuir.6653943832-625902018-11-29T07:53:53Z Biomarkers of disseminated intravascular coagulation in pediatric intensive care unit in Thailand Wiralpat Padungmaneesub Sanit Reungrongrat Suphara Manowong Kanda Fanhchaksai Noppamas Panyasit Rungrote Natesirinilkul Biochemistry, Genetics and Molecular Biology Medicine © 2018 John Wiley & Sons Ltd Introduction: Disseminated intravascular coagulation (DIC) is a systemic activation of hemostatic system caused by several causes. Biomarkers including antithrombin (AT), protein C (PC), and thrombomodulin (TM) were reported as the additional markers for DIC in adults. This study aimed to determine the association between biomarkers among patients with overt DIC (ODIC) and nonovert DIC (NDIC) in children in PICU. Methods: We enrolled 103 subjects, aged 1 month-18 years, who were admitted to PICU at Chiang Mai University (CMU) Hospital >24 hours with underlying conditions predisposing to DIC were enrolled. Biomarkers were tested after 24 hours of admission. Subject who had NDIC on the 1stinvestigations would have other tests on days 3-5 of admission. Results: The incidence of ODIC by the International Society on Thrombosis and Hemostasis (ISTH) DIC score was found 24%. The bleeding, thrombosis, and death were significantly higher in ODIC group (P < 0.05). Mean levels of AT and PC in ODIC group were significantly different from NDIC one (66.9% vs 79.9%, P < 0.001 and 46.1% vs 59.2%, P = 0.004, respectively) while mean level of TM was not different between two groups. Adding AT to DIC score was better than the original score for predict mortality [area under curve (AUC) = 0.662 vs AUC = 0.65] and bleeding (AUC = 0.751 vs AUC = 0.732). Conclusions: ODIC is prevalent among critically ill children. Adverse outcomes were more commonly found in children with ODIC. AT and PC levels after 24 hours of PICU admission seem to be the useful biomarkers for ODIC in PICU. 2018-11-29T07:34:18Z 2018-11-29T07:34:18Z 2018-01-01 Journal 1751553X 17515521 2-s2.0-85053371634 10.1111/ijlh.12917 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053371634&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62590 |
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Biochemistry, Genetics and Molecular Biology Medicine Wiralpat Padungmaneesub Sanit Reungrongrat Suphara Manowong Kanda Fanhchaksai Noppamas Panyasit Rungrote Natesirinilkul Biomarkers of disseminated intravascular coagulation in pediatric intensive care unit in Thailand |
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© 2018 John Wiley & Sons Ltd Introduction: Disseminated intravascular coagulation (DIC) is a systemic activation of hemostatic system caused by several causes. Biomarkers including antithrombin (AT), protein C (PC), and thrombomodulin (TM) were reported as the additional markers for DIC in adults. This study aimed to determine the association between biomarkers among patients with overt DIC (ODIC) and nonovert DIC (NDIC) in children in PICU. Methods: We enrolled 103 subjects, aged 1 month-18 years, who were admitted to PICU at Chiang Mai University (CMU) Hospital >24 hours with underlying conditions predisposing to DIC were enrolled. Biomarkers were tested after 24 hours of admission. Subject who had NDIC on the 1stinvestigations would have other tests on days 3-5 of admission. Results: The incidence of ODIC by the International Society on Thrombosis and Hemostasis (ISTH) DIC score was found 24%. The bleeding, thrombosis, and death were significantly higher in ODIC group (P < 0.05). Mean levels of AT and PC in ODIC group were significantly different from NDIC one (66.9% vs 79.9%, P < 0.001 and 46.1% vs 59.2%, P = 0.004, respectively) while mean level of TM was not different between two groups. Adding AT to DIC score was better than the original score for predict mortality [area under curve (AUC) = 0.662 vs AUC = 0.65] and bleeding (AUC = 0.751 vs AUC = 0.732). Conclusions: ODIC is prevalent among critically ill children. Adverse outcomes were more commonly found in children with ODIC. AT and PC levels after 24 hours of PICU admission seem to be the useful biomarkers for ODIC in PICU. |
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Journal |
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Wiralpat Padungmaneesub Sanit Reungrongrat Suphara Manowong Kanda Fanhchaksai Noppamas Panyasit Rungrote Natesirinilkul |
author_facet |
Wiralpat Padungmaneesub Sanit Reungrongrat Suphara Manowong Kanda Fanhchaksai Noppamas Panyasit Rungrote Natesirinilkul |
author_sort |
Wiralpat Padungmaneesub |
title |
Biomarkers of disseminated intravascular coagulation in pediatric intensive care unit in Thailand |
title_short |
Biomarkers of disseminated intravascular coagulation in pediatric intensive care unit in Thailand |
title_full |
Biomarkers of disseminated intravascular coagulation in pediatric intensive care unit in Thailand |
title_fullStr |
Biomarkers of disseminated intravascular coagulation in pediatric intensive care unit in Thailand |
title_full_unstemmed |
Biomarkers of disseminated intravascular coagulation in pediatric intensive care unit in Thailand |
title_sort |
biomarkers of disseminated intravascular coagulation in pediatric intensive care unit in thailand |
publishDate |
2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053371634&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62590 |
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