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Establishing a protocol for thromboelastography in sea turtles

Thromboelastography (TEG) provides a global evaluation of haemostasis. This diagnostic test is widely used in mammals but has not previously been performed in reptiles, mainly due to the limited availability of taxon-specific reagents. The objective of this pilot study was to establish a protocol to...

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Autores principales: Barratclough, Ashley, Hanel, Rita, Stacy, Nicole I, Ruterbories, Laura K, Christiansen, Emily, Harms, Craig A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109949/
https://www.ncbi.nlm.nih.gov/pubmed/30167312
http://dx.doi.org/10.1136/vetreco-2017-000240
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author Barratclough, Ashley
Hanel, Rita
Stacy, Nicole I
Ruterbories, Laura K
Christiansen, Emily
Harms, Craig A
author_facet Barratclough, Ashley
Hanel, Rita
Stacy, Nicole I
Ruterbories, Laura K
Christiansen, Emily
Harms, Craig A
author_sort Barratclough, Ashley
collection PubMed
description Thromboelastography (TEG) provides a global evaluation of haemostasis. This diagnostic test is widely used in mammals but has not previously been performed in reptiles, mainly due to the limited availability of taxon-specific reagents. The objective of this pilot study was to establish a protocol to perform TEG in sea turtles. Pooled citrated plasma, stored at −80°C, from four green turtles (Chelonia mydas) was assayed on a TEG 5000. Several initiators were evaluated: kaolin (n=2), RapidTEG (n=2), fresh (n=2) and frozen (n=6) thromboplastin extracted from pooled brain tissue from several chelonian species, human recombinant tissue factor at 1:100 (n=1), Reptilase (n=2), and rabbit thromboplastin (n=1). Both fresh and frozen chelonian thromboplastin were superior in producing quantifiable TEG reaction time compared with all other reagents. These findings are consistent with the lack of an intrinsic pathway in turtles and confirmed a lack of coagulation in the turtle samples in response to mammalian thromboplastin. A TEG protocol was subsequently established for harvested species-specific frozen thromboplastin. The frozen thromboplastin reagent remained stable after one year of storage at −80°C. The developed protocol will be useful as a basis for future studies that aim to understand the pathophysiology of haemostatic disorders in various stranding conditions of sea turtles.
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spelling pubmed-61099492018-08-30 Establishing a protocol for thromboelastography in sea turtles Barratclough, Ashley Hanel, Rita Stacy, Nicole I Ruterbories, Laura K Christiansen, Emily Harms, Craig A Vet Rec Open Wildlife Thromboelastography (TEG) provides a global evaluation of haemostasis. This diagnostic test is widely used in mammals but has not previously been performed in reptiles, mainly due to the limited availability of taxon-specific reagents. The objective of this pilot study was to establish a protocol to perform TEG in sea turtles. Pooled citrated plasma, stored at −80°C, from four green turtles (Chelonia mydas) was assayed on a TEG 5000. Several initiators were evaluated: kaolin (n=2), RapidTEG (n=2), fresh (n=2) and frozen (n=6) thromboplastin extracted from pooled brain tissue from several chelonian species, human recombinant tissue factor at 1:100 (n=1), Reptilase (n=2), and rabbit thromboplastin (n=1). Both fresh and frozen chelonian thromboplastin were superior in producing quantifiable TEG reaction time compared with all other reagents. These findings are consistent with the lack of an intrinsic pathway in turtles and confirmed a lack of coagulation in the turtle samples in response to mammalian thromboplastin. A TEG protocol was subsequently established for harvested species-specific frozen thromboplastin. The frozen thromboplastin reagent remained stable after one year of storage at −80°C. The developed protocol will be useful as a basis for future studies that aim to understand the pathophysiology of haemostatic disorders in various stranding conditions of sea turtles. BMJ Publishing Group 2018-08-13 /pmc/articles/PMC6109949/ /pubmed/30167312 http://dx.doi.org/10.1136/vetreco-2017-000240 Text en © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Wildlife
Barratclough, Ashley
Hanel, Rita
Stacy, Nicole I
Ruterbories, Laura K
Christiansen, Emily
Harms, Craig A
Establishing a protocol for thromboelastography in sea turtles
title Establishing a protocol for thromboelastography in sea turtles
title_full Establishing a protocol for thromboelastography in sea turtles
title_fullStr Establishing a protocol for thromboelastography in sea turtles
title_full_unstemmed Establishing a protocol for thromboelastography in sea turtles
title_short Establishing a protocol for thromboelastography in sea turtles
title_sort establishing a protocol for thromboelastography in sea turtles
topic Wildlife
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109949/
https://www.ncbi.nlm.nih.gov/pubmed/30167312
http://dx.doi.org/10.1136/vetreco-2017-000240
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