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https://hdl.handle.net/11499/10742
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DC Field | Value | Language |
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dc.contributor.author | Facciorusso, A. | - |
dc.contributor.author | Roy, S. | - |
dc.contributor.author | Livadas, S. | - |
dc.contributor.author | Fevrier-Paul, A. | - |
dc.contributor.author | Wekesa, C. | - |
dc.contributor.author | Kılıç, İsmail Doğu | - |
dc.contributor.author | Chaurasia, A.K. | - |
dc.date.accessioned | 2019-08-16T13:32:41Z | |
dc.date.available | 2019-08-16T13:32:41Z | |
dc.date.issued | 2018 | - |
dc.identifier.issn | 0163-2116 | - |
dc.identifier.uri | https://hdl.handle.net/11499/10742 | - |
dc.identifier.uri | https://doi.org/10.1007/s10620-018-5092-6 | - |
dc.description.abstract | Background: The role of nonselective beta-blockers in cirrhotic patients with ascites has been recently questioned; however, definitive evidence in this regard is still lacking. Aims: To analyze published data on the influence of nonselective beta-blockers as compared to control group on survival of cirrhotic patients with ascites. Methods: Computerized bibliographic search on the main databases was performed. Hazard ratios from Kaplan–Meier curves were extracted in order to perform an unbiased comparison of survival estimates. Secondary outcomes were mortality in patients with refractory ascites, pooled rate of nonselective beta-blockers interruption, spontaneous bacterial peritonitis and hepato-renal syndrome incidence. Results: Three randomized controlled trials and 13 observational studies with 8279 patients were included. Overall survival was comparable between the two groups (hazard ratio = 0.86, 0.71–1.03, p = 0.11). Study design resulted as the main source of heterogeneity in sensitivity analysis and meta-regression. Mortality in refractory ascites patients was similar in the two groups (odds ratio = 0.90, 0.45–1.79; p = 0.76). No difference in spontaneous bacterial peritonitis (odds ratio = 0.78, 0.47–1.29, p = 0.33) and hepato-renal syndrome incidence (odds ratio = 1.22, 0.48–3.09; p = 0.67) was observed. Pooled rate of nonselective beta-blockers interruption was 18.6% (5.2–32.1%). Conclusions: Based on our findings, nonselective beta-blockers should not be routinely withheld in patients with cirrhosis and ascites, even if refractory. © 2018, Springer Science+Business Media, LLC, part of Springer Nature. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Springer New York LLC | en_US |
dc.relation.ispartof | Digestive Diseases and Sciences | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Cirrhosis | en_US |
dc.subject | Hazard ratio | en_US |
dc.subject | Mortality | en_US |
dc.subject | NSBB | en_US |
dc.subject | beta adrenergic receptor blocking agent | en_US |
dc.subject | ascites | en_US |
dc.subject | bacterial peritonitis | en_US |
dc.subject | controlled study | en_US |
dc.subject | hepatorenal syndrome | en_US |
dc.subject | human | en_US |
dc.subject | incidence | en_US |
dc.subject | liver cirrhosis | en_US |
dc.subject | mortality | en_US |
dc.subject | overall survival | en_US |
dc.subject | priority journal | en_US |
dc.subject | Review | en_US |
dc.subject | sensitivity analysis | en_US |
dc.subject | chi square distribution | en_US |
dc.subject | complication | en_US |
dc.subject | Kaplan Meier method | en_US |
dc.subject | meta analysis | en_US |
dc.subject | microbiology | en_US |
dc.subject | odds ratio | en_US |
dc.subject | peritonitis | en_US |
dc.subject | risk factor | en_US |
dc.subject | time factor | en_US |
dc.subject | treatment outcome | en_US |
dc.subject | Adrenergic beta-Antagonists | en_US |
dc.subject | Ascites | en_US |
dc.subject | Chi-Square Distribution | en_US |
dc.subject | Hepatorenal Syndrome | en_US |
dc.subject | Humans | en_US |
dc.subject | Incidence | en_US |
dc.subject | Kaplan-Meier Estimate | en_US |
dc.subject | Liver Cirrhosis | en_US |
dc.subject | Odds Ratio | en_US |
dc.subject | Peritonitis | en_US |
dc.subject | Risk Factors | en_US |
dc.subject | Time Factors | en_US |
dc.subject | Treatment Outcome | en_US |
dc.title | Nonselective beta-blockers do not affect survival in cirrhotic patients with ascites | en_US |
dc.type | Review | en_US |
dc.identifier.volume | 63 | en_US |
dc.identifier.issue | 7 | en_US |
dc.identifier.startpage | 1737 | |
dc.identifier.startpage | 1737 | en_US |
dc.identifier.endpage | 1746 | en_US |
dc.identifier.doi | 10.1007/s10620-018-5092-6 | - |
dc.relation.publicationcategory | Diğer | en_US |
dc.identifier.pmid | 29725793 | en_US |
dc.identifier.scopus | 2-s2.0-85046420580 | en_US |
dc.identifier.wos | WOS:000435949100010 | en_US |
dc.identifier.scopusquality | Q1 | - |
dc.owner | Pamukkale University | - |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
item.openairetype | Review | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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