Enoxaparin Prevents Portal Vein Thrombosis and Liver Decompensation in Patients With Advanced Cirrhosis

Background & Aims We performed a randomized controlled trial to evaluate the safety and efficacy of enoxaparin, a low-molecular-weight heparin, in preventing portal vein thrombosis (PVT) in patients with advanced cirrhosis. Methods In a nonblinded, single-center study, 70 outpatients with cirrho...

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Veröffentlicht in:Gastroenterology (New York, N.Y. 1943) N.Y. 1943), 2012-11, Vol.143 (5), p.1253-1260.e4
Hauptverfasser: Villa, Erica, Cammà, Calogero, Marietta, Marco, Luongo, Monica, Critelli, Rosina, Colopi, Stefano, Tata, Cristina, Zecchini, Ramona, Gitto, Stefano, Petta, Salvatore, Lei, Barbara, Bernabucci, Veronica, Vukotic, Ranka, De Maria, Nicola, Schepis, Filippo, Karampatou, Aimilia, Caporali, Cristian, Simoni, Luisa, Del Buono, Mariagrazia, Zambotto, Beatrice, Turola, Elena, Fornaciari, Giovanni, Schianchi, Susanna, Ferrari, Anna, Valla, Dominique
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container_issue 5
container_start_page 1253
container_title Gastroenterology (New York, N.Y. 1943)
container_volume 143
creator Villa, Erica
Cammà, Calogero
Marietta, Marco
Luongo, Monica
Critelli, Rosina
Colopi, Stefano
Tata, Cristina
Zecchini, Ramona
Gitto, Stefano
Petta, Salvatore
Lei, Barbara
Bernabucci, Veronica
Vukotic, Ranka
De Maria, Nicola
Schepis, Filippo
Karampatou, Aimilia
Caporali, Cristian
Simoni, Luisa
Del Buono, Mariagrazia
Zambotto, Beatrice
Turola, Elena
Fornaciari, Giovanni
Schianchi, Susanna
Ferrari, Anna
Valla, Dominique
description Background & Aims We performed a randomized controlled trial to evaluate the safety and efficacy of enoxaparin, a low-molecular-weight heparin, in preventing portal vein thrombosis (PVT) in patients with advanced cirrhosis. Methods In a nonblinded, single-center study, 70 outpatients with cirrhosis (Child–Pugh classes B7–C10) with demonstrated patent portal veins and without hepatocellular carcinoma were assigned randomly to groups that were given enoxaparin (4000 IU/day, subcutaneously for 48 weeks; n = 34) or no treatment (controls, n = 36). Ultrasonography (every 3 months) and computed tomography (every 6 months) were performed to check the portal vein axis. The primary outcome was prevention of PVT. Radiologists and hepatologists that assessed outcomes were blinded to group assignments. Analysis was by intention to treat. Results At 48 weeks, none of the patients in the enoxaparin group had developed PVT, compared with 6 of 36 (16.6%) controls ( P = .025). At 96 weeks, no patient developed PVT in the enoxaparin group, compared with 10 of 36 (27.7%) controls ( P = .001). At the end of the follow-up period, 8.8% of patients in the enoxaparin group and 27.7% of controls developed PVT ( P = .048). The actuarial probability of PVT was lower in the enoxaparin group ( P = .006). Liver decompensation was less frequent among patients given enoxaparin (11.7%) than controls (59.4%) ( P < .0001); overall values were 38.2% vs 83.0%, respectively ( P < .0001). The actuarial probability of liver decompensation was lower in the enoxaparin group ( P < .0001). Eight patients in the enoxaparin group and 13 controls died. The actuarial probability of survival was higher in the enoxaparin group ( P = .020). No relevant side effects or hemorrhagic events were reported. Conclusions In a small randomized controlled trial, a 12-month course of enoxaparin was safe and effective in preventing PVT in patients with cirrhosis and a Child–Pugh score of 7–10. Enoxaparin appeared to delay the occurrence of hepatic decompensation and to improve survival. www.isrctn.>org : ISRCTN32383354; www.clinicaltrialsregister.eu : EudraCT2007-007890-22.
doi_str_mv 10.1053/j.gastro.2012.07.018
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Methods In a nonblinded, single-center study, 70 outpatients with cirrhosis (Child–Pugh classes B7–C10) with demonstrated patent portal veins and without hepatocellular carcinoma were assigned randomly to groups that were given enoxaparin (4000 IU/day, subcutaneously for 48 weeks; n = 34) or no treatment (controls, n = 36). Ultrasonography (every 3 months) and computed tomography (every 6 months) were performed to check the portal vein axis. The primary outcome was prevention of PVT. Radiologists and hepatologists that assessed outcomes were blinded to group assignments. Analysis was by intention to treat. Results At 48 weeks, none of the patients in the enoxaparin group had developed PVT, compared with 6 of 36 (16.6%) controls ( P = .025). At 96 weeks, no patient developed PVT in the enoxaparin group, compared with 10 of 36 (27.7%) controls ( P = .001). At the end of the follow-up period, 8.8% of patients in the enoxaparin group and 27.7% of controls developed PVT ( P = .048). The actuarial probability of PVT was lower in the enoxaparin group ( P = .006). Liver decompensation was less frequent among patients given enoxaparin (11.7%) than controls (59.4%) ( P &lt; .0001); overall values were 38.2% vs 83.0%, respectively ( P &lt; .0001). The actuarial probability of liver decompensation was lower in the enoxaparin group ( P &lt; .0001). Eight patients in the enoxaparin group and 13 controls died. The actuarial probability of survival was higher in the enoxaparin group ( P = .020). No relevant side effects or hemorrhagic events were reported. Conclusions In a small randomized controlled trial, a 12-month course of enoxaparin was safe and effective in preventing PVT in patients with cirrhosis and a Child–Pugh score of 7–10. Enoxaparin appeared to delay the occurrence of hepatic decompensation and to improve survival. www.isrctn.&gt;org : ISRCTN32383354; www.clinicaltrialsregister.eu : EudraCT2007-007890-22.</description><identifier>ISSN: 0016-5085</identifier><identifier>EISSN: 1528-0012</identifier><identifier>DOI: 10.1053/j.gastro.2012.07.018</identifier><identifier>PMID: 22819864</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Anticoagulant Therapy ; Anticoagulants - adverse effects ; Anticoagulants - therapeutic use ; Bacterial Infections - blood ; Bacterial Translocation ; Biomarkers - blood ; DNA, Bacterial - blood ; Enoxaparin - adverse effects ; Enoxaparin - therapeutic use ; Fatty Acid-Binding Proteins - blood ; Female ; Gastroenterology and Hepatology ; Humans ; Interleukin-6 - blood ; Kaplan-Meier Estimate ; Lipopolysaccharide Receptors - blood ; Liver Cirrhosis - complications ; Liver Failure - etiology ; Liver Failure - prevention &amp; control ; Male ; Middle Aged ; Portal Hypertension ; Prophylaxis ; Proportional Hazards Models ; Renal Veins ; Statistics, Nonparametric ; Thrombosis - complications ; Thrombosis - prevention &amp; control</subject><ispartof>Gastroenterology (New York, N.Y. 1943), 2012-11, Vol.143 (5), p.1253-1260.e4</ispartof><rights>AGA Institute</rights><rights>2012 AGA Institute</rights><rights>Copyright © 2012 AGA Institute. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-524a192665721e94ad7755f3d791f8ecffab99eebada8b7c2a064a76cfc92c9e3</citedby><cites>FETCH-LOGICAL-c463t-524a192665721e94ad7755f3d791f8ecffab99eebada8b7c2a064a76cfc92c9e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0016508512010116$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22819864$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Villa, Erica</creatorcontrib><creatorcontrib>Cammà, Calogero</creatorcontrib><creatorcontrib>Marietta, Marco</creatorcontrib><creatorcontrib>Luongo, Monica</creatorcontrib><creatorcontrib>Critelli, Rosina</creatorcontrib><creatorcontrib>Colopi, Stefano</creatorcontrib><creatorcontrib>Tata, Cristina</creatorcontrib><creatorcontrib>Zecchini, Ramona</creatorcontrib><creatorcontrib>Gitto, Stefano</creatorcontrib><creatorcontrib>Petta, Salvatore</creatorcontrib><creatorcontrib>Lei, Barbara</creatorcontrib><creatorcontrib>Bernabucci, Veronica</creatorcontrib><creatorcontrib>Vukotic, Ranka</creatorcontrib><creatorcontrib>De Maria, Nicola</creatorcontrib><creatorcontrib>Schepis, Filippo</creatorcontrib><creatorcontrib>Karampatou, Aimilia</creatorcontrib><creatorcontrib>Caporali, Cristian</creatorcontrib><creatorcontrib>Simoni, Luisa</creatorcontrib><creatorcontrib>Del Buono, Mariagrazia</creatorcontrib><creatorcontrib>Zambotto, Beatrice</creatorcontrib><creatorcontrib>Turola, Elena</creatorcontrib><creatorcontrib>Fornaciari, Giovanni</creatorcontrib><creatorcontrib>Schianchi, Susanna</creatorcontrib><creatorcontrib>Ferrari, Anna</creatorcontrib><creatorcontrib>Valla, Dominique</creatorcontrib><title>Enoxaparin Prevents Portal Vein Thrombosis and Liver Decompensation in Patients With Advanced Cirrhosis</title><title>Gastroenterology (New York, N.Y. 1943)</title><addtitle>Gastroenterology</addtitle><description>Background &amp; Aims We performed a randomized controlled trial to evaluate the safety and efficacy of enoxaparin, a low-molecular-weight heparin, in preventing portal vein thrombosis (PVT) in patients with advanced cirrhosis. Methods In a nonblinded, single-center study, 70 outpatients with cirrhosis (Child–Pugh classes B7–C10) with demonstrated patent portal veins and without hepatocellular carcinoma were assigned randomly to groups that were given enoxaparin (4000 IU/day, subcutaneously for 48 weeks; n = 34) or no treatment (controls, n = 36). Ultrasonography (every 3 months) and computed tomography (every 6 months) were performed to check the portal vein axis. The primary outcome was prevention of PVT. Radiologists and hepatologists that assessed outcomes were blinded to group assignments. Analysis was by intention to treat. Results At 48 weeks, none of the patients in the enoxaparin group had developed PVT, compared with 6 of 36 (16.6%) controls ( P = .025). At 96 weeks, no patient developed PVT in the enoxaparin group, compared with 10 of 36 (27.7%) controls ( P = .001). At the end of the follow-up period, 8.8% of patients in the enoxaparin group and 27.7% of controls developed PVT ( P = .048). The actuarial probability of PVT was lower in the enoxaparin group ( P = .006). Liver decompensation was less frequent among patients given enoxaparin (11.7%) than controls (59.4%) ( P &lt; .0001); overall values were 38.2% vs 83.0%, respectively ( P &lt; .0001). The actuarial probability of liver decompensation was lower in the enoxaparin group ( P &lt; .0001). Eight patients in the enoxaparin group and 13 controls died. The actuarial probability of survival was higher in the enoxaparin group ( P = .020). No relevant side effects or hemorrhagic events were reported. Conclusions In a small randomized controlled trial, a 12-month course of enoxaparin was safe and effective in preventing PVT in patients with cirrhosis and a Child–Pugh score of 7–10. Enoxaparin appeared to delay the occurrence of hepatic decompensation and to improve survival. www.isrctn.&gt;org : ISRCTN32383354; www.clinicaltrialsregister.eu : EudraCT2007-007890-22.</description><subject>Anticoagulant Therapy</subject><subject>Anticoagulants - adverse effects</subject><subject>Anticoagulants - therapeutic use</subject><subject>Bacterial Infections - blood</subject><subject>Bacterial Translocation</subject><subject>Biomarkers - blood</subject><subject>DNA, Bacterial - blood</subject><subject>Enoxaparin - adverse effects</subject><subject>Enoxaparin - therapeutic use</subject><subject>Fatty Acid-Binding Proteins - blood</subject><subject>Female</subject><subject>Gastroenterology and Hepatology</subject><subject>Humans</subject><subject>Interleukin-6 - blood</subject><subject>Kaplan-Meier Estimate</subject><subject>Lipopolysaccharide Receptors - blood</subject><subject>Liver Cirrhosis - complications</subject><subject>Liver Failure - etiology</subject><subject>Liver Failure - prevention &amp; control</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Portal Hypertension</subject><subject>Prophylaxis</subject><subject>Proportional Hazards Models</subject><subject>Renal Veins</subject><subject>Statistics, Nonparametric</subject><subject>Thrombosis - complications</subject><subject>Thrombosis - prevention &amp; control</subject><issn>0016-5085</issn><issn>1528-0012</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhi0EotvCGyDkI5cEjxM78QWp2paCtBKVKHC0HGfS9ZLYi51d0bfHYQsHLpzGGv3fjPwNIa-AlcBE9XZX3ps0x1ByBrxkTcmgfUJWIHhbsNx6Sla5yEKwVpyR85R2jDFVtfCcnHHegmplvSL31z78NHsTnae3EY_o50RvQ5zNSL9ibt5tY5i6kFyixvd0444Y6RXaMO3RJzO74OnC5tdv9pubt_SyPxpvsadrF-N2gV-QZ4MZE758rBfky_vru_WHYvPp5uP6clPYWlZzIXhtQHEpRcMBVW36phFiqPpGwdCiHQbTKYXYmd60XWO5YbI2jbSDVdwqrC7Im9PcfQw_DphmPblkcRyNx3BIGgAEk1wC5Gh9itoYUoo46H10k4kPGpheFOudPinWi2LNGp0VZ-z144ZDN2H_F_rjNAfenQKY_3l0GHWy2U3W4SLaWffB_W_DvwPs6LyzZvyOD5h24RB9dqhBp8zoz8uZlytDHsIAZPULQxCldw</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Villa, Erica</creator><creator>Cammà, Calogero</creator><creator>Marietta, Marco</creator><creator>Luongo, Monica</creator><creator>Critelli, Rosina</creator><creator>Colopi, Stefano</creator><creator>Tata, Cristina</creator><creator>Zecchini, Ramona</creator><creator>Gitto, Stefano</creator><creator>Petta, Salvatore</creator><creator>Lei, Barbara</creator><creator>Bernabucci, Veronica</creator><creator>Vukotic, Ranka</creator><creator>De Maria, Nicola</creator><creator>Schepis, Filippo</creator><creator>Karampatou, Aimilia</creator><creator>Caporali, Cristian</creator><creator>Simoni, Luisa</creator><creator>Del Buono, Mariagrazia</creator><creator>Zambotto, Beatrice</creator><creator>Turola, Elena</creator><creator>Fornaciari, Giovanni</creator><creator>Schianchi, Susanna</creator><creator>Ferrari, Anna</creator><creator>Valla, Dominique</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>20121101</creationdate><title>Enoxaparin Prevents Portal Vein Thrombosis and Liver Decompensation in Patients With Advanced Cirrhosis</title><author>Villa, Erica ; Cammà, Calogero ; Marietta, Marco ; Luongo, Monica ; Critelli, Rosina ; Colopi, Stefano ; Tata, Cristina ; Zecchini, Ramona ; Gitto, Stefano ; Petta, Salvatore ; Lei, Barbara ; Bernabucci, Veronica ; Vukotic, Ranka ; De Maria, Nicola ; Schepis, Filippo ; Karampatou, Aimilia ; Caporali, Cristian ; Simoni, Luisa ; Del Buono, Mariagrazia ; Zambotto, Beatrice ; Turola, Elena ; Fornaciari, Giovanni ; Schianchi, Susanna ; Ferrari, Anna ; Valla, Dominique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-524a192665721e94ad7755f3d791f8ecffab99eebada8b7c2a064a76cfc92c9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Anticoagulant Therapy</topic><topic>Anticoagulants - adverse effects</topic><topic>Anticoagulants - therapeutic use</topic><topic>Bacterial Infections - blood</topic><topic>Bacterial Translocation</topic><topic>Biomarkers - blood</topic><topic>DNA, Bacterial - blood</topic><topic>Enoxaparin - adverse effects</topic><topic>Enoxaparin - therapeutic use</topic><topic>Fatty Acid-Binding Proteins - blood</topic><topic>Female</topic><topic>Gastroenterology and Hepatology</topic><topic>Humans</topic><topic>Interleukin-6 - blood</topic><topic>Kaplan-Meier Estimate</topic><topic>Lipopolysaccharide Receptors - blood</topic><topic>Liver Cirrhosis - complications</topic><topic>Liver Failure - etiology</topic><topic>Liver Failure - prevention &amp; 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Aims We performed a randomized controlled trial to evaluate the safety and efficacy of enoxaparin, a low-molecular-weight heparin, in preventing portal vein thrombosis (PVT) in patients with advanced cirrhosis. Methods In a nonblinded, single-center study, 70 outpatients with cirrhosis (Child–Pugh classes B7–C10) with demonstrated patent portal veins and without hepatocellular carcinoma were assigned randomly to groups that were given enoxaparin (4000 IU/day, subcutaneously for 48 weeks; n = 34) or no treatment (controls, n = 36). Ultrasonography (every 3 months) and computed tomography (every 6 months) were performed to check the portal vein axis. The primary outcome was prevention of PVT. Radiologists and hepatologists that assessed outcomes were blinded to group assignments. Analysis was by intention to treat. Results At 48 weeks, none of the patients in the enoxaparin group had developed PVT, compared with 6 of 36 (16.6%) controls ( P = .025). At 96 weeks, no patient developed PVT in the enoxaparin group, compared with 10 of 36 (27.7%) controls ( P = .001). At the end of the follow-up period, 8.8% of patients in the enoxaparin group and 27.7% of controls developed PVT ( P = .048). The actuarial probability of PVT was lower in the enoxaparin group ( P = .006). Liver decompensation was less frequent among patients given enoxaparin (11.7%) than controls (59.4%) ( P &lt; .0001); overall values were 38.2% vs 83.0%, respectively ( P &lt; .0001). The actuarial probability of liver decompensation was lower in the enoxaparin group ( P &lt; .0001). Eight patients in the enoxaparin group and 13 controls died. The actuarial probability of survival was higher in the enoxaparin group ( P = .020). No relevant side effects or hemorrhagic events were reported. Conclusions In a small randomized controlled trial, a 12-month course of enoxaparin was safe and effective in preventing PVT in patients with cirrhosis and a Child–Pugh score of 7–10. Enoxaparin appeared to delay the occurrence of hepatic decompensation and to improve survival. www.isrctn.&gt;org : ISRCTN32383354; www.clinicaltrialsregister.eu : EudraCT2007-007890-22.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22819864</pmid><doi>10.1053/j.gastro.2012.07.018</doi><oa>free_for_read</oa></addata></record>
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language eng
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source MEDLINE; Elsevier ScienceDirect Journals; Alma/SFX Local Collection
subjects Anticoagulant Therapy
Anticoagulants - adverse effects
Anticoagulants - therapeutic use
Bacterial Infections - blood
Bacterial Translocation
Biomarkers - blood
DNA, Bacterial - blood
Enoxaparin - adverse effects
Enoxaparin - therapeutic use
Fatty Acid-Binding Proteins - blood
Female
Gastroenterology and Hepatology
Humans
Interleukin-6 - blood
Kaplan-Meier Estimate
Lipopolysaccharide Receptors - blood
Liver Cirrhosis - complications
Liver Failure - etiology
Liver Failure - prevention & control
Male
Middle Aged
Portal Hypertension
Prophylaxis
Proportional Hazards Models
Renal Veins
Statistics, Nonparametric
Thrombosis - complications
Thrombosis - prevention & control
title Enoxaparin Prevents Portal Vein Thrombosis and Liver Decompensation in Patients With Advanced Cirrhosis
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