Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/148219
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dc.contributor.authorTurco, Laura-
dc.contributor.authorVillanueva, Candid-
dc.contributor.authorMura, Vincenzo La-
dc.contributor.authorGarcía Pagán, Juan Carlos-
dc.contributor.authorReiberger, Thomas-
dc.contributor.authorGenescà, Joan-
dc.contributor.authorGroszmann, Roberto J.-
dc.contributor.authorSharma, Barjesh C.-
dc.contributor.authorMerkel, Carlo-
dc.contributor.authorBureau, Christophe-
dc.contributor.authorAlvarado Tapias, Edilmar-
dc.contributor.authorGonzález-Abraldes Iglesias, Juan-
dc.contributor.authorAlbillos, Agustín-
dc.contributor.authorBañares, Rafael-
dc.contributor.authorPeck-Radosavljevic, Markus-
dc.contributor.authorAugustin, Salvador-
dc.contributor.authorSarin, Shiv K.-
dc.contributor.authorBosch, Jaime-
dc.contributor.authorGarcía-Tsao, Guadalupe-
dc.date.accessioned2020-01-20T12:51:26Z-
dc.date.available2020-01-20T12:51:26Z-
dc.date.issued2020-01-01-
dc.identifier.urihttp://hdl.handle.net/2445/148219-
dc.description.abstractBackground & Aims: In unselected patients with cirrhosis, those with reductions in hepatic venous pressure gradient (HVPG) to below a defined threshold (responders) have a reduced risk of variceal hemorrhage (VH) and death. We performed a meta-analysis to compare this effect in patients with vs without ascites. Methods: We collected data from 15 studies of primary or secondary prophylaxis of VH that reported data on VH and death in responders vs nonresponders. We included studies in which data on ascites at baseline and on other relevant outcomes during follow-up evaluation were available. We performed separate meta-analyses for patients with vs without ascites. Results: Of the 1113 patients included in the studies, 968 patients (87%) had been treated with nonselective β-blockers. In 993 patients (89%), HVPG response was defined as a decrease of more than 20% from baseline (>10% in 11% of patients) or to less than 12 mm Hg. In the 661 patients without ascites, responders (n = 329; 50%) had significantly lower odds of events (ascites, VH, or encephalopathy) than nonresponders (odds ratio [OR], 0.35; 95% CI, 0.22–0.56). Odds of death or liver transplantation were also significantly lower among responders than nonresponders (OR, 0.50, 95% CI, 0.32–0.78). In the 452 patients with ascites, responders (n = 188; 42%) had significantly lower odds of events (VH, refractory ascites, spontaneous bacterial peritonitis, or hepatorenal syndrome) than nonresponders (OR, 0.27; 95% CI, 0.16–0.43). Overall, odds of death or liver transplantation were lower among responders (OR, 0.47; 95% CI, 0.29–0.75). No heterogeneity was observed among studies. Conclusions: In a meta-analysis of clinical trials, we found that patients with cirrhosis with and without ascites who respond to treatment with nonselective β-blockers (based on reductions in HVPG) have a reduced risk of events, death, or liver transplantation.-
dc.format.extent15 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.cgh.2019.05.050-
dc.relation.ispartofClinical Gastroenterology and Hepatology, 2020, vol. 18, num. 2, p. 313-327.e6-
dc.relation.urihttps://doi.org/10.1016/j.cgh.2019.05.050-
dc.rights(c) AGA Institute, 2020-
dc.sourceArticles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)-
dc.subject.classificationCirrosi hepàtica-
dc.subject.classificationHipertensió portal-
dc.subject.otherHepatic cirrhosis-
dc.subject.otherPortal hypertension-
dc.titleLowering Portal Pressure Improves Outcomes of Patients With Cirrhosis, With or Without Ascites: A Meta-Analysis-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.date.updated2020-01-08T12:16:45Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.idimarina5563933-
dc.identifier.pmid31176013-
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)



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