Comparison of the in vitro effects of saline, hypertonic hydroxyethyl starch, hypertonic saline, and two forms of hydroxyethyl starch on whole blood coagulation and platelet function in dogs

OBJECTIVE: To compare the in vitro effects of hypertonic solutions and colloids to saline on coagulation in dogs. DESIGN: In vitro experimental study. SETTING: Veterinary teaching hospital. ANIMALS: Twenty‐one adult dogs. INTERVENTIONS: Blood samples were diluted with saline, 7.2% hypertonic saline...

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Veröffentlicht in:Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000) Tex. : 2000), 2015-07, Vol.25 (4), p.474-487
Hauptverfasser: Wurlod, Virginie A., Howard, Judith, Francey, Thierry, Schweighauser, Ariane, Adamik, Katja N.
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container_issue 4
container_start_page 474
container_title Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000)
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creator Wurlod, Virginie A.
Howard, Judith
Francey, Thierry
Schweighauser, Ariane
Adamik, Katja N.
description OBJECTIVE: To compare the in vitro effects of hypertonic solutions and colloids to saline on coagulation in dogs. DESIGN: In vitro experimental study. SETTING: Veterinary teaching hospital. ANIMALS: Twenty‐one adult dogs. INTERVENTIONS: Blood samples were diluted with saline, 7.2% hypertonic saline solution with 6% hydroxyethylstarch with an average molecular weight of 200 kDa and a molar substitution of 0.4 (HH), 7.2% hypertonic saline (HTS), hydroxyethyl starch (HES) 130/0.4 or hydroxyethyl starch 600/0.75 at ratios of 1:22 and 1:9, and with saline and HES at a ratio of 1:3. MEASUREMENTS AND MAIN RESULTS: Whole blood coagulation was analyzed using rotational thromboelastometry (extrinsic thromboelastometry‐cloting time (ExTEM‐CT), maximal clot firmness (MCF) and clot formation time (CFT) and fibrinogen function TEM‐CT (FibTEM‐CT) and MCF) and platelet function was analyzed using a platelet function analyzer (closure time, CTPFA). All parameters measured were impaired by saline dilution. The CTPFA was prolonged by 7.2% hypertonic saline solution with 6% hydroxyethylstarch with an average molecular weight of 200 kDa and a molar substitution of 0.4 (HH) and HTS but not by HES solutions. At clinical dilutions equivalent to those generally administered for shock (saline 1:3, HES 1:9, and hypertonic solutions 1:22), CTPFA was more prolonged by HH and HTS than other solutions but more by saline than HES. No difference was found between the HES solutions or the hypertonic solutions. ExTEM‐CFT and MCF were impaired by HH and HTS but only mildly by HES solutions. At clinically relevant dilutions, no difference was found in ExTEM‐CFT between HTS and saline or in ExTEM‐MCF between HH and saline. No consistent difference was found between the 2 HES solutions but HH impaired ExTEM‐CFT and MCF more than HTS. At high dilutions, FibTEM‐CT and ‐MCF and ExTEM‐CT were impaired by HES. CONCLUSIONS: Hypertonic solutions affect platelet function and whole blood coagulation to a greater extent than saline and HES. At clinically relevant dilutions, only CTPFA was markedly more affected by hypertonic solutions than by saline. At high dilutions, HES significantly affects coagulation but to no greater extent than saline at clinically relevant dilutions.
doi_str_mv 10.1111/vec.12320
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DESIGN: In vitro experimental study. SETTING: Veterinary teaching hospital. ANIMALS: Twenty‐one adult dogs. INTERVENTIONS: Blood samples were diluted with saline, 7.2% hypertonic saline solution with 6% hydroxyethylstarch with an average molecular weight of 200 kDa and a molar substitution of 0.4 (HH), 7.2% hypertonic saline (HTS), hydroxyethyl starch (HES) 130/0.4 or hydroxyethyl starch 600/0.75 at ratios of 1:22 and 1:9, and with saline and HES at a ratio of 1:3. MEASUREMENTS AND MAIN RESULTS: Whole blood coagulation was analyzed using rotational thromboelastometry (extrinsic thromboelastometry‐cloting time (ExTEM‐CT), maximal clot firmness (MCF) and clot formation time (CFT) and fibrinogen function TEM‐CT (FibTEM‐CT) and MCF) and platelet function was analyzed using a platelet function analyzer (closure time, CTPFA). All parameters measured were impaired by saline dilution. The CTPFA was prolonged by 7.2% hypertonic saline solution with 6% hydroxyethylstarch with an average molecular weight of 200 kDa and a molar substitution of 0.4 (HH) and HTS but not by HES solutions. At clinical dilutions equivalent to those generally administered for shock (saline 1:3, HES 1:9, and hypertonic solutions 1:22), CTPFA was more prolonged by HH and HTS than other solutions but more by saline than HES. No difference was found between the HES solutions or the hypertonic solutions. ExTEM‐CFT and MCF were impaired by HH and HTS but only mildly by HES solutions. At clinically relevant dilutions, no difference was found in ExTEM‐CFT between HTS and saline or in ExTEM‐MCF between HH and saline. No consistent difference was found between the 2 HES solutions but HH impaired ExTEM‐CFT and MCF more than HTS. At high dilutions, FibTEM‐CT and ‐MCF and ExTEM‐CT were impaired by HES. CONCLUSIONS: Hypertonic solutions affect platelet function and whole blood coagulation to a greater extent than saline and HES. At clinically relevant dilutions, only CTPFA was markedly more affected by hypertonic solutions than by saline. At high dilutions, HES significantly affects coagulation but to no greater extent than saline at clinically relevant dilutions.</description><identifier>ISSN: 1479-3261</identifier><identifier>EISSN: 1476-4431</identifier><identifier>DOI: 10.1111/vec.12320</identifier><identifier>PMID: 26037241</identifier><language>eng</language><publisher>United States: Veterinary Emergency &amp; Critical Care Society</publisher><subject>Adolescent ; Animals ; Blood Coagulation - drug effects ; Blood Coagulation Tests ; Blood Platelets - drug effects ; canine ; colloids ; dilutional coagulopathy ; Dogs ; Fibrinogen - drug effects ; Humans ; Hydroxyethyl Starch Derivatives - pharmacology ; Male ; platelet function analyzer ; Platelet Function Tests - veterinary ; ROTEM ; Saline Solution, Hypertonic - pharmacology ; Sodium Chloride - pharmacology ; Thrombelastography - veterinary ; thromboelastometry</subject><ispartof>Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000), 2015-07, Vol.25 (4), p.474-487</ispartof><rights>Veterinary Emergency and Critical Care Society 2015</rights><rights>Veterinary Emergency and Critical Care Society 2015.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4570-47eaeab9aba404471453505487c2f591be85a766fd4d4ea5919ef0b1138062703</citedby><cites>FETCH-LOGICAL-c4570-47eaeab9aba404471453505487c2f591be85a766fd4d4ea5919ef0b1138062703</cites><orcidid>0000-0002-6693-5365</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fvec.12320$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fvec.12320$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26037241$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wurlod, Virginie A.</creatorcontrib><creatorcontrib>Howard, Judith</creatorcontrib><creatorcontrib>Francey, Thierry</creatorcontrib><creatorcontrib>Schweighauser, Ariane</creatorcontrib><creatorcontrib>Adamik, Katja N.</creatorcontrib><title>Comparison of the in vitro effects of saline, hypertonic hydroxyethyl starch, hypertonic saline, and two forms of hydroxyethyl starch on whole blood coagulation and platelet function in dogs</title><title>Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000)</title><addtitle>Journal of Veterinary Emergency and Critical Care</addtitle><description>OBJECTIVE: To compare the in vitro effects of hypertonic solutions and colloids to saline on coagulation in dogs. DESIGN: In vitro experimental study. SETTING: Veterinary teaching hospital. ANIMALS: Twenty‐one adult dogs. INTERVENTIONS: Blood samples were diluted with saline, 7.2% hypertonic saline solution with 6% hydroxyethylstarch with an average molecular weight of 200 kDa and a molar substitution of 0.4 (HH), 7.2% hypertonic saline (HTS), hydroxyethyl starch (HES) 130/0.4 or hydroxyethyl starch 600/0.75 at ratios of 1:22 and 1:9, and with saline and HES at a ratio of 1:3. MEASUREMENTS AND MAIN RESULTS: Whole blood coagulation was analyzed using rotational thromboelastometry (extrinsic thromboelastometry‐cloting time (ExTEM‐CT), maximal clot firmness (MCF) and clot formation time (CFT) and fibrinogen function TEM‐CT (FibTEM‐CT) and MCF) and platelet function was analyzed using a platelet function analyzer (closure time, CTPFA). All parameters measured were impaired by saline dilution. The CTPFA was prolonged by 7.2% hypertonic saline solution with 6% hydroxyethylstarch with an average molecular weight of 200 kDa and a molar substitution of 0.4 (HH) and HTS but not by HES solutions. At clinical dilutions equivalent to those generally administered for shock (saline 1:3, HES 1:9, and hypertonic solutions 1:22), CTPFA was more prolonged by HH and HTS than other solutions but more by saline than HES. No difference was found between the HES solutions or the hypertonic solutions. ExTEM‐CFT and MCF were impaired by HH and HTS but only mildly by HES solutions. At clinically relevant dilutions, no difference was found in ExTEM‐CFT between HTS and saline or in ExTEM‐MCF between HH and saline. No consistent difference was found between the 2 HES solutions but HH impaired ExTEM‐CFT and MCF more than HTS. At high dilutions, FibTEM‐CT and ‐MCF and ExTEM‐CT were impaired by HES. CONCLUSIONS: Hypertonic solutions affect platelet function and whole blood coagulation to a greater extent than saline and HES. At clinically relevant dilutions, only CTPFA was markedly more affected by hypertonic solutions than by saline. At high dilutions, HES significantly affects coagulation but to no greater extent than saline at clinically relevant dilutions.</description><subject>Adolescent</subject><subject>Animals</subject><subject>Blood Coagulation - drug effects</subject><subject>Blood Coagulation Tests</subject><subject>Blood Platelets - drug effects</subject><subject>canine</subject><subject>colloids</subject><subject>dilutional coagulopathy</subject><subject>Dogs</subject><subject>Fibrinogen - drug effects</subject><subject>Humans</subject><subject>Hydroxyethyl Starch Derivatives - pharmacology</subject><subject>Male</subject><subject>platelet function analyzer</subject><subject>Platelet Function Tests - veterinary</subject><subject>ROTEM</subject><subject>Saline Solution, Hypertonic - pharmacology</subject><subject>Sodium Chloride - pharmacology</subject><subject>Thrombelastography - veterinary</subject><subject>thromboelastometry</subject><issn>1479-3261</issn><issn>1476-4431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1ks1u1DAUhSMEoj-w4AXAS5BIazuOPVmioS1IFSyYwtJynOuJIROnttNpXo5nwzPpVEICb3x1_J3jK92bZa8IPiPpnN-BPiO0oPhJdkyY4DljBXm6r6u8oJwcZSch_MSYVFVJn2dHlONCUEaOs99LtxmUt8H1yBkUW0C2R3c2eofAGNAx7PSgOtvDe9ROA_joeqtT2Xh3P0Fspw6FqLxu_3o_WFTfoLh1yDi_2Wf9w4jS79vWdYDqzrkGaafWY6eiTfrOP6QaOojIjL3eq6nJxq3Di-yZUV2Alw_3aXZzebFafsqvv159Xn64zjUrBc6ZAAWqrlStGGZMEFYWJS7ZQmhqyorUsCiV4Nw0rGGgklKBwTUhxQJzKnBxmr2dcwfvbkcIUW5s0NB1qgc3BkkEprzEmIuEvptR7V0IHowcvN0oP0mC5W5cMo1L7seV2NcPsWO9geaRPMwnAeczsLUdTP9Pkt8vlofIfHbYEOH-0aH8L5maE6X88eVK8lVFPlZ4JYvEv5l5o5xU67QJ8uYbxYSnbSkxIaL4A42WusM</recordid><startdate>201507</startdate><enddate>201507</enddate><creator>Wurlod, Virginie A.</creator><creator>Howard, Judith</creator><creator>Francey, Thierry</creator><creator>Schweighauser, Ariane</creator><creator>Adamik, Katja N.</creator><general>Veterinary Emergency &amp; 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DESIGN: In vitro experimental study. SETTING: Veterinary teaching hospital. ANIMALS: Twenty‐one adult dogs. INTERVENTIONS: Blood samples were diluted with saline, 7.2% hypertonic saline solution with 6% hydroxyethylstarch with an average molecular weight of 200 kDa and a molar substitution of 0.4 (HH), 7.2% hypertonic saline (HTS), hydroxyethyl starch (HES) 130/0.4 or hydroxyethyl starch 600/0.75 at ratios of 1:22 and 1:9, and with saline and HES at a ratio of 1:3. MEASUREMENTS AND MAIN RESULTS: Whole blood coagulation was analyzed using rotational thromboelastometry (extrinsic thromboelastometry‐cloting time (ExTEM‐CT), maximal clot firmness (MCF) and clot formation time (CFT) and fibrinogen function TEM‐CT (FibTEM‐CT) and MCF) and platelet function was analyzed using a platelet function analyzer (closure time, CTPFA). All parameters measured were impaired by saline dilution. The CTPFA was prolonged by 7.2% hypertonic saline solution with 6% hydroxyethylstarch with an average molecular weight of 200 kDa and a molar substitution of 0.4 (HH) and HTS but not by HES solutions. At clinical dilutions equivalent to those generally administered for shock (saline 1:3, HES 1:9, and hypertonic solutions 1:22), CTPFA was more prolonged by HH and HTS than other solutions but more by saline than HES. No difference was found between the HES solutions or the hypertonic solutions. ExTEM‐CFT and MCF were impaired by HH and HTS but only mildly by HES solutions. At clinically relevant dilutions, no difference was found in ExTEM‐CFT between HTS and saline or in ExTEM‐MCF between HH and saline. No consistent difference was found between the 2 HES solutions but HH impaired ExTEM‐CFT and MCF more than HTS. At high dilutions, FibTEM‐CT and ‐MCF and ExTEM‐CT were impaired by HES. CONCLUSIONS: Hypertonic solutions affect platelet function and whole blood coagulation to a greater extent than saline and HES. At clinically relevant dilutions, only CTPFA was markedly more affected by hypertonic solutions than by saline. At high dilutions, HES significantly affects coagulation but to no greater extent than saline at clinically relevant dilutions.</abstract><cop>United States</cop><pub>Veterinary Emergency &amp; Critical Care Society</pub><pmid>26037241</pmid><doi>10.1111/vec.12320</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-6693-5365</orcidid></addata></record>
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ispartof Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000), 2015-07, Vol.25 (4), p.474-487
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subjects Adolescent
Animals
Blood Coagulation - drug effects
Blood Coagulation Tests
Blood Platelets - drug effects
canine
colloids
dilutional coagulopathy
Dogs
Fibrinogen - drug effects
Humans
Hydroxyethyl Starch Derivatives - pharmacology
Male
platelet function analyzer
Platelet Function Tests - veterinary
ROTEM
Saline Solution, Hypertonic - pharmacology
Sodium Chloride - pharmacology
Thrombelastography - veterinary
thromboelastometry
title Comparison of the in vitro effects of saline, hypertonic hydroxyethyl starch, hypertonic saline, and two forms of hydroxyethyl starch on whole blood coagulation and platelet function in dogs
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