Platelet function in dogs with chronic liver disease
Objectives To assess platelet function, buccal mucosal bleeding time and plasma von Willebrand factor concentration in dogs with chronic inflammatory and/or fibrotic liver disease and to compare results with those obtained in healthy dogs. Materials and Methods Preliminary study including 18 dogs wi...
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Veröffentlicht in: | Journal of small animal practice 2022-02, Vol.63 (2), p.120-127 |
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creator | Wilkinson, A. Panciera, D. DeMonaco, S. Boes, K. Leib, M. Clapp, K. Ruth, J. Cecere, T. McClendon, D. |
description | Objectives
To assess platelet function, buccal mucosal bleeding time and plasma von Willebrand factor concentration in dogs with chronic inflammatory and/or fibrotic liver disease and to compare results with those obtained in healthy dogs.
Materials and Methods
Preliminary study including 18 dogs with chronic inflammatory and/or fibrotic liver disease undergoing liver biopsy and 18 healthy age‐matched control dogs. Platelet function was assessed by measuring closure time with the PFA‐100® analyser using adenosine diphosphate (ADP) as an agonist. Buccal mucosal bleeding time, closure time and plasma von Willebrand factor antigen were measured in dogs in both groups. After undergoing ultrasound‐guided needle biopsy, dogs were monitored for haemorrhage to determine if there was an association of any measurement with post‐biopsy bleeding.
Results
The closure time was not different between the liver disease group (median 76.3; range 53 to 118.5 seconds) and control group (72.8; 57 to 89.5 seconds). The buccal mucosal bleeding time was longer in the liver disease group (median 138; range 95 to 229 seconds) than the control group (103; 63 to 200 seconds). The plasma von Willebrand factor antigen concentration was not different between the liver disease group (median 203; range 109 to 351%) and control group (165.5; 63 to 246%).
Clinical Significance
In this study, dogs with chronic necroinflammatory and/or fibrotic liver disease did not have overt, clinically relevant derangements in platelet function as assessed by buccal mucosal bleeding time, closure time and von Willebrand factor analysis. In addition, none of the dogs undergoing percutaneous ultrasound‐guided biopsy in the study exhibited bleeding complications post‐biopsy procedure. |
doi_str_mv | 10.1111/jsap.13342 |
format | Article |
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To assess platelet function, buccal mucosal bleeding time and plasma von Willebrand factor concentration in dogs with chronic inflammatory and/or fibrotic liver disease and to compare results with those obtained in healthy dogs.
Materials and Methods
Preliminary study including 18 dogs with chronic inflammatory and/or fibrotic liver disease undergoing liver biopsy and 18 healthy age‐matched control dogs. Platelet function was assessed by measuring closure time with the PFA‐100® analyser using adenosine diphosphate (ADP) as an agonist. Buccal mucosal bleeding time, closure time and plasma von Willebrand factor antigen were measured in dogs in both groups. After undergoing ultrasound‐guided needle biopsy, dogs were monitored for haemorrhage to determine if there was an association of any measurement with post‐biopsy bleeding.
Results
The closure time was not different between the liver disease group (median 76.3; range 53 to 118.5 seconds) and control group (72.8; 57 to 89.5 seconds). The buccal mucosal bleeding time was longer in the liver disease group (median 138; range 95 to 229 seconds) than the control group (103; 63 to 200 seconds). The plasma von Willebrand factor antigen concentration was not different between the liver disease group (median 203; range 109 to 351%) and control group (165.5; 63 to 246%).
Clinical Significance
In this study, dogs with chronic necroinflammatory and/or fibrotic liver disease did not have overt, clinically relevant derangements in platelet function as assessed by buccal mucosal bleeding time, closure time and von Willebrand factor analysis. In addition, none of the dogs undergoing percutaneous ultrasound‐guided biopsy in the study exhibited bleeding complications post‐biopsy procedure.</description><identifier>ISSN: 0022-4510</identifier><identifier>EISSN: 1748-5827</identifier><identifier>DOI: 10.1111/jsap.13342</identifier><identifier>PMID: 33900656</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenosine ; Animals ; Antigens ; Biopsy ; Bleeding ; Dog Diseases ; Dogs ; Factor analysis ; Hemorrhage ; Inflammation ; Liver diseases ; Liver Diseases - veterinary ; Mucosa ; Platelet Function Tests - veterinary ; Platelets ; Ultrasonic imaging ; Ultrasound ; Von Willebrand factor ; von Willebrand Factor - analysis</subject><ispartof>Journal of small animal practice, 2022-02, Vol.63 (2), p.120-127</ispartof><rights>2021 British Small Animal Veterinary Association</rights><rights>2021 British Small Animal Veterinary Association.</rights><rights>2022 British Small Animal Veterinary Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3932-6797ccb0d94fde49e5e9f52ffe9d7929a4651b556798375b29834bca3dd3fdf63</citedby><cites>FETCH-LOGICAL-c3932-6797ccb0d94fde49e5e9f52ffe9d7929a4651b556798375b29834bca3dd3fdf63</cites><orcidid>0000-0001-6170-2709</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%2Fjsap.13342$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjsap.13342$$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/33900656$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wilkinson, A.</creatorcontrib><creatorcontrib>Panciera, D.</creatorcontrib><creatorcontrib>DeMonaco, S.</creatorcontrib><creatorcontrib>Boes, K.</creatorcontrib><creatorcontrib>Leib, M.</creatorcontrib><creatorcontrib>Clapp, K.</creatorcontrib><creatorcontrib>Ruth, J.</creatorcontrib><creatorcontrib>Cecere, T.</creatorcontrib><creatorcontrib>McClendon, D.</creatorcontrib><title>Platelet function in dogs with chronic liver disease</title><title>Journal of small animal practice</title><addtitle>J Small Anim Pract</addtitle><description>Objectives
To assess platelet function, buccal mucosal bleeding time and plasma von Willebrand factor concentration in dogs with chronic inflammatory and/or fibrotic liver disease and to compare results with those obtained in healthy dogs.
Materials and Methods
Preliminary study including 18 dogs with chronic inflammatory and/or fibrotic liver disease undergoing liver biopsy and 18 healthy age‐matched control dogs. Platelet function was assessed by measuring closure time with the PFA‐100® analyser using adenosine diphosphate (ADP) as an agonist. Buccal mucosal bleeding time, closure time and plasma von Willebrand factor antigen were measured in dogs in both groups. After undergoing ultrasound‐guided needle biopsy, dogs were monitored for haemorrhage to determine if there was an association of any measurement with post‐biopsy bleeding.
Results
The closure time was not different between the liver disease group (median 76.3; range 53 to 118.5 seconds) and control group (72.8; 57 to 89.5 seconds). The buccal mucosal bleeding time was longer in the liver disease group (median 138; range 95 to 229 seconds) than the control group (103; 63 to 200 seconds). The plasma von Willebrand factor antigen concentration was not different between the liver disease group (median 203; range 109 to 351%) and control group (165.5; 63 to 246%).
Clinical Significance
In this study, dogs with chronic necroinflammatory and/or fibrotic liver disease did not have overt, clinically relevant derangements in platelet function as assessed by buccal mucosal bleeding time, closure time and von Willebrand factor analysis. In addition, none of the dogs undergoing percutaneous ultrasound‐guided biopsy in the study exhibited bleeding complications post‐biopsy procedure.</description><subject>Adenosine</subject><subject>Animals</subject><subject>Antigens</subject><subject>Biopsy</subject><subject>Bleeding</subject><subject>Dog Diseases</subject><subject>Dogs</subject><subject>Factor analysis</subject><subject>Hemorrhage</subject><subject>Inflammation</subject><subject>Liver diseases</subject><subject>Liver Diseases - veterinary</subject><subject>Mucosa</subject><subject>Platelet Function Tests - veterinary</subject><subject>Platelets</subject><subject>Ultrasonic imaging</subject><subject>Ultrasound</subject><subject>Von Willebrand factor</subject><subject>von Willebrand Factor - analysis</subject><issn>0022-4510</issn><issn>1748-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKw0AUQAdRbK1u_AAJuBEhdd6TWZbik4IFdT0k87BT0qRmEkv_3qmpLlx4N5cLh8PlAHCO4BjFuVmGfD1GhFB8AIZI0CxlGRaHYAghxillCA7ASQjLeHIq4DEYECIh5IwPAZ2XeWtL2yauq3Tr6yrxVWLq95BsfLtI9KKpK6-T0n_aJjE-2DzYU3Dk8jLYs_0egbe729fpQzp7vn-cTmapJpLglAsptC6gkdQZS6VlVjqGnbPSCIllTjlDBWORy4hgBY6LFjonxhBnHCcjcNV710390dnQqpUP2pZlXtm6CwozlAkiGWcRvfyDLuuuqeJ3CnMsCIMy2kfguqd0U4fQWKfWjV_lzVYhqHYt1a6l-m4Z4Yu9sitW1vyiP_EigHpg40u7_Uelnl4m8176BUdDfRs</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Wilkinson, A.</creator><creator>Panciera, D.</creator><creator>DeMonaco, S.</creator><creator>Boes, K.</creator><creator>Leib, M.</creator><creator>Clapp, K.</creator><creator>Ruth, J.</creator><creator>Cecere, T.</creator><creator>McClendon, D.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6170-2709</orcidid></search><sort><creationdate>202202</creationdate><title>Platelet function in dogs with chronic liver disease</title><author>Wilkinson, A. ; Panciera, D. ; DeMonaco, S. ; Boes, K. ; Leib, M. ; Clapp, K. ; Ruth, J. ; Cecere, T. ; McClendon, D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3932-6797ccb0d94fde49e5e9f52ffe9d7929a4651b556798375b29834bca3dd3fdf63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adenosine</topic><topic>Animals</topic><topic>Antigens</topic><topic>Biopsy</topic><topic>Bleeding</topic><topic>Dog Diseases</topic><topic>Dogs</topic><topic>Factor analysis</topic><topic>Hemorrhage</topic><topic>Inflammation</topic><topic>Liver diseases</topic><topic>Liver Diseases - veterinary</topic><topic>Mucosa</topic><topic>Platelet Function Tests - veterinary</topic><topic>Platelets</topic><topic>Ultrasonic imaging</topic><topic>Ultrasound</topic><topic>Von Willebrand factor</topic><topic>von Willebrand Factor - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilkinson, A.</creatorcontrib><creatorcontrib>Panciera, D.</creatorcontrib><creatorcontrib>DeMonaco, S.</creatorcontrib><creatorcontrib>Boes, K.</creatorcontrib><creatorcontrib>Leib, M.</creatorcontrib><creatorcontrib>Clapp, K.</creatorcontrib><creatorcontrib>Ruth, J.</creatorcontrib><creatorcontrib>Cecere, T.</creatorcontrib><creatorcontrib>McClendon, D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of small animal practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wilkinson, A.</au><au>Panciera, D.</au><au>DeMonaco, S.</au><au>Boes, K.</au><au>Leib, M.</au><au>Clapp, K.</au><au>Ruth, J.</au><au>Cecere, T.</au><au>McClendon, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Platelet function in dogs with chronic liver disease</atitle><jtitle>Journal of small animal practice</jtitle><addtitle>J Small Anim Pract</addtitle><date>2022-02</date><risdate>2022</risdate><volume>63</volume><issue>2</issue><spage>120</spage><epage>127</epage><pages>120-127</pages><issn>0022-4510</issn><eissn>1748-5827</eissn><abstract>Objectives
To assess platelet function, buccal mucosal bleeding time and plasma von Willebrand factor concentration in dogs with chronic inflammatory and/or fibrotic liver disease and to compare results with those obtained in healthy dogs.
Materials and Methods
Preliminary study including 18 dogs with chronic inflammatory and/or fibrotic liver disease undergoing liver biopsy and 18 healthy age‐matched control dogs. Platelet function was assessed by measuring closure time with the PFA‐100® analyser using adenosine diphosphate (ADP) as an agonist. Buccal mucosal bleeding time, closure time and plasma von Willebrand factor antigen were measured in dogs in both groups. After undergoing ultrasound‐guided needle biopsy, dogs were monitored for haemorrhage to determine if there was an association of any measurement with post‐biopsy bleeding.
Results
The closure time was not different between the liver disease group (median 76.3; range 53 to 118.5 seconds) and control group (72.8; 57 to 89.5 seconds). The buccal mucosal bleeding time was longer in the liver disease group (median 138; range 95 to 229 seconds) than the control group (103; 63 to 200 seconds). The plasma von Willebrand factor antigen concentration was not different between the liver disease group (median 203; range 109 to 351%) and control group (165.5; 63 to 246%).
Clinical Significance
In this study, dogs with chronic necroinflammatory and/or fibrotic liver disease did not have overt, clinically relevant derangements in platelet function as assessed by buccal mucosal bleeding time, closure time and von Willebrand factor analysis. In addition, none of the dogs undergoing percutaneous ultrasound‐guided biopsy in the study exhibited bleeding complications post‐biopsy procedure.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>33900656</pmid><doi>10.1111/jsap.13342</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-6170-2709</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Wiley Journals |
subjects | Adenosine Animals Antigens Biopsy Bleeding Dog Diseases Dogs Factor analysis Hemorrhage Inflammation Liver diseases Liver Diseases - veterinary Mucosa Platelet Function Tests - veterinary Platelets Ultrasonic imaging Ultrasound Von Willebrand factor von Willebrand Factor - analysis |
title | Platelet function in dogs with chronic liver disease |
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