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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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 & 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 & Critical Care Society</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6693-5365</orcidid></search><sort><creationdate>201507</creationdate><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><author>Wurlod, Virginie A. ; Howard, Judith ; Francey, Thierry ; Schweighauser, Ariane ; Adamik, Katja N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4570-47eaeab9aba404471453505487c2f591be85a766fd4d4ea5919ef0b1138062703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Animals</topic><topic>Blood Coagulation - drug effects</topic><topic>Blood Coagulation Tests</topic><topic>Blood Platelets - drug effects</topic><topic>canine</topic><topic>colloids</topic><topic>dilutional coagulopathy</topic><topic>Dogs</topic><topic>Fibrinogen - drug effects</topic><topic>Humans</topic><topic>Hydroxyethyl Starch Derivatives - pharmacology</topic><topic>Male</topic><topic>platelet function analyzer</topic><topic>Platelet Function Tests - veterinary</topic><topic>ROTEM</topic><topic>Saline Solution, Hypertonic - pharmacology</topic><topic>Sodium Chloride - pharmacology</topic><topic>Thrombelastography - veterinary</topic><topic>thromboelastometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wurlod, Virginie A.</creatorcontrib><creatorcontrib>Howard, Judith</creatorcontrib><creatorcontrib>Francey, Thierry</creatorcontrib><creatorcontrib>Schweighauser, Ariane</creatorcontrib><creatorcontrib>Adamik, Katja N.</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wurlod, Virginie A.</au><au>Howard, Judith</au><au>Francey, Thierry</au><au>Schweighauser, Ariane</au><au>Adamik, Katja N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000)</jtitle><addtitle>Journal of Veterinary Emergency and Critical Care</addtitle><date>2015-07</date><risdate>2015</risdate><volume>25</volume><issue>4</issue><spage>474</spage><epage>487</epage><pages>474-487</pages><issn>1479-3261</issn><eissn>1476-4431</eissn><abstract>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.</abstract><cop>United States</cop><pub>Veterinary Emergency & 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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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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