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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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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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1115062611</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0016508512010116</els_id><sourcerecordid>1115062611</sourcerecordid><originalsourceid>FETCH-LOGICAL-c463t-524a192665721e94ad7755f3d791f8ecffab99eebada8b7c2a064a76cfc92c9e3</originalsourceid><addsrcrecordid>eNqFkcFu1DAQhi0EotvCGyDkI5cEjxM78QWp2paCtBKVKHC0HGfS9ZLYi51d0bfHYQsHLpzGGv3fjPwNIa-AlcBE9XZX3ps0x1ByBrxkTcmgfUJWIHhbsNx6Sla5yEKwVpyR85R2jDFVtfCcnHHegmplvSL31z78NHsTnae3EY_o50RvQ5zNSL9ibt5tY5i6kFyixvd0444Y6RXaMO3RJzO74OnC5tdv9pubt_SyPxpvsadrF-N2gV-QZ4MZE758rBfky_vru_WHYvPp5uP6clPYWlZzIXhtQHEpRcMBVW36phFiqPpGwdCiHQbTKYXYmd60XWO5YbI2jbSDVdwqrC7Im9PcfQw_DphmPblkcRyNx3BIGgAEk1wC5Gh9itoYUoo46H10k4kPGpheFOudPinWi2LNGp0VZ-z144ZDN2H_F_rjNAfenQKY_3l0GHWy2U3W4SLaWffB_W_DvwPs6LyzZvyOD5h24RB9dqhBp8zoz8uZlytDHsIAZPULQxCldw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1115062611</pqid></control><display><type>article</type><title>Enoxaparin Prevents Portal Vein Thrombosis and Liver Decompensation in Patients With Advanced Cirrhosis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>Alma/SFX Local Collection</source><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</creator><creatorcontrib>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</creatorcontrib><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.</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 & control ; Male ; Middle Aged ; Portal Hypertension ; Prophylaxis ; Proportional Hazards Models ; Renal Veins ; Statistics, Nonparametric ; Thrombosis - complications ; Thrombosis - prevention & 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 & 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.</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 & 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 & 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 & control</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Portal Hypertension</topic><topic>Prophylaxis</topic><topic>Proportional Hazards Models</topic><topic>Renal Veins</topic><topic>Statistics, Nonparametric</topic><topic>Thrombosis - complications</topic><topic>Thrombosis - prevention & control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><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>Gastroenterology (New York, N.Y. 1943)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Villa, Erica</au><au>Cammà, Calogero</au><au>Marietta, Marco</au><au>Luongo, Monica</au><au>Critelli, Rosina</au><au>Colopi, Stefano</au><au>Tata, Cristina</au><au>Zecchini, Ramona</au><au>Gitto, Stefano</au><au>Petta, Salvatore</au><au>Lei, Barbara</au><au>Bernabucci, Veronica</au><au>Vukotic, Ranka</au><au>De Maria, Nicola</au><au>Schepis, Filippo</au><au>Karampatou, Aimilia</au><au>Caporali, Cristian</au><au>Simoni, Luisa</au><au>Del Buono, Mariagrazia</au><au>Zambotto, Beatrice</au><au>Turola, Elena</au><au>Fornaciari, Giovanni</au><au>Schianchi, Susanna</au><au>Ferrari, Anna</au><au>Valla, Dominique</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enoxaparin Prevents Portal Vein Thrombosis and Liver Decompensation in Patients With Advanced Cirrhosis</atitle><jtitle>Gastroenterology (New York, N.Y. 1943)</jtitle><addtitle>Gastroenterology</addtitle><date>2012-11-01</date><risdate>2012</risdate><volume>143</volume><issue>5</issue><spage>1253</spage><epage>1260.e4</epage><pages>1253-1260.e4</pages><issn>0016-5085</issn><eissn>1528-0012</eissn><abstract>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.</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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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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