Preservation of platelet function in patients with cirrhosis and thrombocytopenia undergoing esophageal variceal ligation
Thrombocytopenia is a possible risk factor for bleeding after band ligation of esophageal varices. However, elevated von Willebrand factor (VWF) in cirrhosis improves platelet function and could decrease this risk. Our objective was to assess platelet function in patients with cirrhosis undergoing e...
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creator | de Oliveira Souza, Evandro D'Amico, Élbio Antônio Flores da Rocha, Tânia Rúbia Marcondes Ferreira, Caroline Medeiros Batista, Juliana Carneiro D'Albuquerque, Luiz Augusto Carrilho, Flair José Queiroz Farias, Alberto |
description | Thrombocytopenia is a possible risk factor for bleeding after band ligation of esophageal varices. However, elevated von Willebrand factor (VWF) in cirrhosis improves platelet function and could decrease this risk. Our objective was to assess platelet function in patients with cirrhosis undergoing esophageal variceal ligation (EVL).
The assessment consisted of platelet count, antigen and activity of VWF and VWF-cleaving protease ADAMTS-13 activity, and a platelet adhesion and aggregation test simulating vascular flow in vivo (Impact-RⓇ) prior to EVL.
Totally 111 patients were divided into three groups according to platelet count: (1) < 50 × 109/L (n = 38, 34.2%); (2) 50 × 109/L to 100 × 109/L (n = 47, 42.3%); and (3) > 100 × 109/L (n = 26, 23.4%). No statistically significant difference was found in the aggregate size of platelets [group 1: 41.0 (31.8–67.3) µm2; group 2: 47.0 (33.8–71.3) µm2; and group 3: 47.0 (34.0–66.0) µm2; P = 0.60] and no significant correlation was found between aggregate size and platelet count (Spearman r = 0.07; P = 0.47). Surface coverage was 4.1% (2.8%–6.7%), 8.5% (4.0%–10.0%), and 9.0% (7.1%–12.0%) (P < 0.001) in groups 1, 2 and 3, respectively and correlated with platelet count (Spearman r = 0.39; P < 0.0001). There was no significant difference between groups in VWF or ADAMTS-13. Post-EVL bleeding occurred in six (5.4%) patients (n = 2 in group 1, n = 1 in group 2, and n = 3 in group 3; P = 0.32). Patients with bleeding had higher MELD scores [15.0 (11.3–20.3) versus 12.0 (10.0–15.0); P = 0.025], but no difference was demonstrated for platelet function parameters.
Platelet function is preserved even in the presence of thrombocytopenia, including in the patients with post-EVL bleeding. |
doi_str_mv | 10.1016/j.hbpd.2019.12.009 |
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The assessment consisted of platelet count, antigen and activity of VWF and VWF-cleaving protease ADAMTS-13 activity, and a platelet adhesion and aggregation test simulating vascular flow in vivo (Impact-RⓇ) prior to EVL.
Totally 111 patients were divided into three groups according to platelet count: (1) < 50 × 109/L (n = 38, 34.2%); (2) 50 × 109/L to 100 × 109/L (n = 47, 42.3%); and (3) > 100 × 109/L (n = 26, 23.4%). No statistically significant difference was found in the aggregate size of platelets [group 1: 41.0 (31.8–67.3) µm2; group 2: 47.0 (33.8–71.3) µm2; and group 3: 47.0 (34.0–66.0) µm2; P = 0.60] and no significant correlation was found between aggregate size and platelet count (Spearman r = 0.07; P = 0.47). Surface coverage was 4.1% (2.8%–6.7%), 8.5% (4.0%–10.0%), and 9.0% (7.1%–12.0%) (P < 0.001) in groups 1, 2 and 3, respectively and correlated with platelet count (Spearman r = 0.39; P < 0.0001). There was no significant difference between groups in VWF or ADAMTS-13. Post-EVL bleeding occurred in six (5.4%) patients (n = 2 in group 1, n = 1 in group 2, and n = 3 in group 3; P = 0.32). Patients with bleeding had higher MELD scores [15.0 (11.3–20.3) versus 12.0 (10.0–15.0); P = 0.025], but no difference was demonstrated for platelet function parameters.
Platelet function is preserved even in the presence of thrombocytopenia, including in the patients with post-EVL bleeding.</description><identifier>ISSN: 1499-3872</identifier><identifier>EISSN: 2352-9377</identifier><identifier>DOI: 10.1016/j.hbpd.2019.12.009</identifier><identifier>PMID: 31982344</identifier><language>eng</language><publisher>AMSTERDAM: Elsevier B.V</publisher><subject>Cirrhosis ; Endoscopy ; Gastroenterology & Hepatology ; Hemorrage ; Hemostasis ; Life Sciences & Biomedicine ; Platelet aggregation ; Science & Technology ; Thrombocytopenia</subject><ispartof>Hepatobiliary & pancreatic diseases international, 2020-12, Vol.19 (6), p.555-560</ispartof><rights>2020 First Affiliated Hospital, Zhejiang University School of Medicine in China</rights><rights>Copyright © 2020 First Affiliated Hospital, Zhejiang University School of Medicine in China. Published by Elsevier B.V. All rights reserved.</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>2</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000600647100007</woscitedreferencesoriginalsourcerecordid><cites>FETCH-LOGICAL-c343t-8877ee7d85eddb945f4a5c715ce86814b706f910cd514b62009c9bd1c1ffc2613</cites><orcidid>0000-0002-5572-663X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/gjgdybzz-z/gjgdybzz-z.jpg</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.hbpd.2019.12.009$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31982344$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Oliveira Souza, Evandro</creatorcontrib><creatorcontrib>D'Amico, Élbio Antônio</creatorcontrib><creatorcontrib>Flores da Rocha, Tânia Rúbia</creatorcontrib><creatorcontrib>Marcondes Ferreira, Caroline</creatorcontrib><creatorcontrib>Medeiros Batista, Juliana</creatorcontrib><creatorcontrib>Carneiro D'Albuquerque, Luiz Augusto</creatorcontrib><creatorcontrib>Carrilho, Flair José</creatorcontrib><creatorcontrib>Queiroz Farias, Alberto</creatorcontrib><title>Preservation of platelet function in patients with cirrhosis and thrombocytopenia undergoing esophageal variceal ligation</title><title>Hepatobiliary & pancreatic diseases international</title><addtitle>HEPATOB PANCREAT DIS</addtitle><addtitle>Hepatobiliary Pancreat Dis Int</addtitle><description>Thrombocytopenia is a possible risk factor for bleeding after band ligation of esophageal varices. However, elevated von Willebrand factor (VWF) in cirrhosis improves platelet function and could decrease this risk. Our objective was to assess platelet function in patients with cirrhosis undergoing esophageal variceal ligation (EVL).
The assessment consisted of platelet count, antigen and activity of VWF and VWF-cleaving protease ADAMTS-13 activity, and a platelet adhesion and aggregation test simulating vascular flow in vivo (Impact-RⓇ) prior to EVL.
Totally 111 patients were divided into three groups according to platelet count: (1) < 50 × 109/L (n = 38, 34.2%); (2) 50 × 109/L to 100 × 109/L (n = 47, 42.3%); and (3) > 100 × 109/L (n = 26, 23.4%). No statistically significant difference was found in the aggregate size of platelets [group 1: 41.0 (31.8–67.3) µm2; group 2: 47.0 (33.8–71.3) µm2; and group 3: 47.0 (34.0–66.0) µm2; P = 0.60] and no significant correlation was found between aggregate size and platelet count (Spearman r = 0.07; P = 0.47). Surface coverage was 4.1% (2.8%–6.7%), 8.5% (4.0%–10.0%), and 9.0% (7.1%–12.0%) (P < 0.001) in groups 1, 2 and 3, respectively and correlated with platelet count (Spearman r = 0.39; P < 0.0001). There was no significant difference between groups in VWF or ADAMTS-13. Post-EVL bleeding occurred in six (5.4%) patients (n = 2 in group 1, n = 1 in group 2, and n = 3 in group 3; P = 0.32). Patients with bleeding had higher MELD scores [15.0 (11.3–20.3) versus 12.0 (10.0–15.0); P = 0.025], but no difference was demonstrated for platelet function parameters.
Platelet function is preserved even in the presence of thrombocytopenia, including in the patients with post-EVL bleeding.</description><subject>Cirrhosis</subject><subject>Endoscopy</subject><subject>Gastroenterology & Hepatology</subject><subject>Hemorrage</subject><subject>Hemostasis</subject><subject>Life Sciences & Biomedicine</subject><subject>Platelet aggregation</subject><subject>Science & Technology</subject><subject>Thrombocytopenia</subject><issn>1499-3872</issn><issn>2352-9377</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><recordid>eNqNkUuP0zAUhSMEYsrAH2CBvERCCbbzcCyxQdXwkEaCBawtx75JXKV2sJ2O2l-P05YRK8TKr-_ce31Olr0muCCYNO93xdjNuqCY8ILQAmP-JNvQsqY5Lxl7mm1IxXletozeZC9C2GFM27Zunmc3JeEtLatqkx2_ewjgDzIaZ5Hr0TzJCBNE1C9WnS-NRXN6BhsDejBxRMp4P7pgApJWozh6t--cOkY3gzUSLVaDH5yxA4Lg5lEOICd0kN6odTOZ4dzsZfasl1OAV9f1Nvv56e7H9kt-_-3z1-3H-1yVVRnztmUMgOm2Bq07XtV9JWvFSK2gbVpSdQw3PSdY6TodGppcULzTRJG-V7Qh5W327lL3Qdpe2kHs3OJt6iiG3aCP3ekkThQnXYMJTvTbCz1792uBEMXeBAXTJC24JYjkWkN5U9IVpRdUeReCh17M3uylPwqCxRqQ2Ik1ILEGJAgVabQkenOtv3R70I-SP4n8NS50rg8q-a7gEcPrmLipGEk7zBLd_j-9NfHs_NYtNibph4sUkvkHA15c5dp4UFFoZ_71kd8MmcVy</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>de Oliveira Souza, Evandro</creator><creator>D'Amico, Élbio Antônio</creator><creator>Flores da Rocha, Tânia Rúbia</creator><creator>Marcondes Ferreira, Caroline</creator><creator>Medeiros Batista, Juliana</creator><creator>Carneiro D'Albuquerque, Luiz Augusto</creator><creator>Carrilho, Flair José</creator><creator>Queiroz Farias, Alberto</creator><general>Elsevier B.V</general><general>Elsevier</general><general>Division of Gastroenterology and Hepatology,University of Sao Paulo School of Medicine,Av. Dr. Eneas Carvalho de Aguiar,255,9th floor,office 9159,Sao Paulo,SP 05403-000,Brazil%Hemostasis Laboratory,Hematology Service,University of Sao Paulo School of Medicine,Av. 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However, elevated von Willebrand factor (VWF) in cirrhosis improves platelet function and could decrease this risk. Our objective was to assess platelet function in patients with cirrhosis undergoing esophageal variceal ligation (EVL).
The assessment consisted of platelet count, antigen and activity of VWF and VWF-cleaving protease ADAMTS-13 activity, and a platelet adhesion and aggregation test simulating vascular flow in vivo (Impact-RⓇ) prior to EVL.
Totally 111 patients were divided into three groups according to platelet count: (1) < 50 × 109/L (n = 38, 34.2%); (2) 50 × 109/L to 100 × 109/L (n = 47, 42.3%); and (3) > 100 × 109/L (n = 26, 23.4%). No statistically significant difference was found in the aggregate size of platelets [group 1: 41.0 (31.8–67.3) µm2; group 2: 47.0 (33.8–71.3) µm2; and group 3: 47.0 (34.0–66.0) µm2; P = 0.60] and no significant correlation was found between aggregate size and platelet count (Spearman r = 0.07; P = 0.47). Surface coverage was 4.1% (2.8%–6.7%), 8.5% (4.0%–10.0%), and 9.0% (7.1%–12.0%) (P < 0.001) in groups 1, 2 and 3, respectively and correlated with platelet count (Spearman r = 0.39; P < 0.0001). There was no significant difference between groups in VWF or ADAMTS-13. Post-EVL bleeding occurred in six (5.4%) patients (n = 2 in group 1, n = 1 in group 2, and n = 3 in group 3; P = 0.32). Patients with bleeding had higher MELD scores [15.0 (11.3–20.3) versus 12.0 (10.0–15.0); P = 0.025], but no difference was demonstrated for platelet function parameters.
Platelet function is preserved even in the presence of thrombocytopenia, including in the patients with post-EVL bleeding.</abstract><cop>AMSTERDAM</cop><pub>Elsevier B.V</pub><pmid>31982344</pmid><doi>10.1016/j.hbpd.2019.12.009</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-5572-663X</orcidid></addata></record> |
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subjects | Cirrhosis Endoscopy Gastroenterology & Hepatology Hemorrage Hemostasis Life Sciences & Biomedicine Platelet aggregation Science & Technology Thrombocytopenia |
title | Preservation of platelet function in patients with cirrhosis and thrombocytopenia undergoing esophageal variceal ligation |
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