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Effect of Hemodilution In Vitro with Hydroxyethyl Starch on Hemostasis
BACKGROUND: Hydroxyethyl starch (HES) solutions are used for volume expansion during surgery. We aimed to investigate how 6%HES 130/0.4 affects hemostasis. MATERIAL/METHODS: Blood samples were collected from 12 healthy adult volunteers, diluting with 6%HES 130/0.4 (HES group) or Ringer lactate solut...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436429/ https://www.ncbi.nlm.nih.gov/pubmed/28481865 http://dx.doi.org/10.12659/MSM.901588 |
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author | Jin, Shanliang Yu, Guifang Hou, Ruijiao Shen, Boxiong Jiang, Hong |
author_facet | Jin, Shanliang Yu, Guifang Hou, Ruijiao Shen, Boxiong Jiang, Hong |
author_sort | Jin, Shanliang |
collection | PubMed |
description | BACKGROUND: Hydroxyethyl starch (HES) solutions are used for volume expansion during surgery. We aimed to investigate how 6%HES 130/0.4 affects hemostasis. MATERIAL/METHODS: Blood samples were collected from 12 healthy adult volunteers, diluting with 6%HES 130/0.4 (HES group) or Ringer lactate solution (RL control group). The hemodilution ratio (HR) of citrated blood volume to plasma substitute volume was 10: 0 (undiluted), 10: 2, 10: 4, and 10: 6. Clotting factors activity was measured. Thrombin generation was monitored. Platelet function was analyzed. RESULTS: 1) Activity of coagulation factor was decreased with increasing HR compared to undiluted baseline, and the activity of FVIII was significantly decreased in HES vs. RL. 2) Calibrated automated thrombography (CAT) results showed HES extended lag time, time to peak (ttpeak), start tail, and decreased peak of thrombin generation. Although lag time and ttpeak were significantly prolonged in HES vs. RL, endogenous thrombin potential (ETP) did not change. 3) Flow cytometric (FCM) analysis showed that HES reduced platelet phospholipids serine (PS) vs. baseline and RL. 4) HES significantly decreased antithrombin activity (AT: A) of the anticoagulant system with increasing HR vs. baseline and RL. 5) For fibrinolytic system, HES did not affect fibrinogen degradation products (FDP) and D-dimers (D-D) vs. baseline, or α(2)-antiplasmin (α2-AP) vs. RL. CONCLUSIONS: By reducing FVIII activity and platelet PS expression, HES interfered with PS combining to FXIa, FVIIIa, and FVa, which affected the acceleration and explosion stage of thrombin. The decreased velocity and peak of thrombin generation delays and reduces clot formation. Combined 6%HES 130/0.4 decreased anticoagulant activity and may have clinical utility. |
format | Online Article Text |
id | pubmed-5436429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54364292017-05-24 Effect of Hemodilution In Vitro with Hydroxyethyl Starch on Hemostasis Jin, Shanliang Yu, Guifang Hou, Ruijiao Shen, Boxiong Jiang, Hong Med Sci Monit Lab/In Vitro Research BACKGROUND: Hydroxyethyl starch (HES) solutions are used for volume expansion during surgery. We aimed to investigate how 6%HES 130/0.4 affects hemostasis. MATERIAL/METHODS: Blood samples were collected from 12 healthy adult volunteers, diluting with 6%HES 130/0.4 (HES group) or Ringer lactate solution (RL control group). The hemodilution ratio (HR) of citrated blood volume to plasma substitute volume was 10: 0 (undiluted), 10: 2, 10: 4, and 10: 6. Clotting factors activity was measured. Thrombin generation was monitored. Platelet function was analyzed. RESULTS: 1) Activity of coagulation factor was decreased with increasing HR compared to undiluted baseline, and the activity of FVIII was significantly decreased in HES vs. RL. 2) Calibrated automated thrombography (CAT) results showed HES extended lag time, time to peak (ttpeak), start tail, and decreased peak of thrombin generation. Although lag time and ttpeak were significantly prolonged in HES vs. RL, endogenous thrombin potential (ETP) did not change. 3) Flow cytometric (FCM) analysis showed that HES reduced platelet phospholipids serine (PS) vs. baseline and RL. 4) HES significantly decreased antithrombin activity (AT: A) of the anticoagulant system with increasing HR vs. baseline and RL. 5) For fibrinolytic system, HES did not affect fibrinogen degradation products (FDP) and D-dimers (D-D) vs. baseline, or α(2)-antiplasmin (α2-AP) vs. RL. CONCLUSIONS: By reducing FVIII activity and platelet PS expression, HES interfered with PS combining to FXIa, FVIIIa, and FVa, which affected the acceleration and explosion stage of thrombin. The decreased velocity and peak of thrombin generation delays and reduces clot formation. Combined 6%HES 130/0.4 decreased anticoagulant activity and may have clinical utility. International Scientific Literature, Inc. 2017-05-08 /pmc/articles/PMC5436429/ /pubmed/28481865 http://dx.doi.org/10.12659/MSM.901588 Text en © Med Sci Monit, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Lab/In Vitro Research Jin, Shanliang Yu, Guifang Hou, Ruijiao Shen, Boxiong Jiang, Hong Effect of Hemodilution In Vitro with Hydroxyethyl Starch on Hemostasis |
title | Effect of Hemodilution In Vitro with Hydroxyethyl Starch on Hemostasis |
title_full | Effect of Hemodilution In Vitro with Hydroxyethyl Starch on Hemostasis |
title_fullStr | Effect of Hemodilution In Vitro with Hydroxyethyl Starch on Hemostasis |
title_full_unstemmed | Effect of Hemodilution In Vitro with Hydroxyethyl Starch on Hemostasis |
title_short | Effect of Hemodilution In Vitro with Hydroxyethyl Starch on Hemostasis |
title_sort | effect of hemodilution in vitro with hydroxyethyl starch on hemostasis |
topic | Lab/In Vitro Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436429/ https://www.ncbi.nlm.nih.gov/pubmed/28481865 http://dx.doi.org/10.12659/MSM.901588 |
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