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
Hauptverfasser: Wilkinson, A., Panciera, D., DeMonaco, S., Boes, K., Leib, M., Clapp, K., Ruth, J., Cecere, T., McClendon, D.
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container_end_page 127
container_issue 2
container_start_page 120
container_title Journal of small animal practice
container_volume 63
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
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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. 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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 &amp; 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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). 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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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