{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,23]],"date-time":"2026-10-23T21:20:08Z","timestamp":1792790408130,"version":"4.5.0"},"reference-count":37,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2017,8,24]],"date-time":"2017-08-24T00:00:00Z","timestamp":1503532800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100004332","name":"Seoul National University Hospital","doi-asserted-by":"publisher","award":["3020160190 [2016\u20101388]"],"award-info":[{"award-number":["3020160190 [2016\u20101388]"]}],"id":[{"id":"10.13039\/501100004332","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Aliment Pharmacol Ther"],"published-print":{"date-parts":[[2017,11]]},"abstract":"<jats:title>Summary<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Rifaximin might decrease the risk of portal hypertension\u2010related complications by controlling small intestinal bacterial overgrowth.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Aim<\/jats:title>\n                    <jats:p>To evaluate whether rifaximin was associated with the risk of death and cirrhotic complications.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      We conducted a retrospective study that included 1042 patients experiencing hepatic encephalopathy (\n                      <jats:styled-content style=\"fixed-case\">HE<\/jats:styled-content>\n                      ): 421 patients without hepatocellular carcinoma (\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      ; the non\u2010\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      cohort) and 621 patients with\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      (the\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      cohort). The primary endpoint was overall survival and secondary endpoints were recurrence of\n                      <jats:styled-content style=\"fixed-case\">HE<\/jats:styled-content>\n                      and the development of spontaneous bacterial peritonitis (\n                      <jats:styled-content style=\"fixed-case\">SBP<\/jats:styled-content>\n                      ), hepatorenal syndrome (\n                      <jats:styled-content style=\"fixed-case\">HRS<\/jats:styled-content>\n                      ) and variceal bleeding.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      In the non\u2010\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      cohort, 145 patients received rifaximin plus lactulose (the rifaximin group) and 276 patients received lactulose alone (the control group). The multivariate analysis revealed that rifaximin was significantly associated with lower risk of death (adjusted hazard ratio [\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      ], 0.697;\n                      <jats:italic>P<\/jats:italic>\n                      = .024) and reduced the risk of recurrent\n                      <jats:styled-content style=\"fixed-case\">HE<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      , 0.452;\n                      <jats:italic>P<\/jats:italic>\n                      &lt; .001),\n                      <jats:styled-content style=\"fixed-case\">SBP<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      , 0.210;\n                      <jats:italic>P<\/jats:italic>\n                      &lt; .001) and variceal bleeding (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      , 0.425;\n                      <jats:italic>P<\/jats:italic>\n                      = .011) but not\n                      <jats:styled-content style=\"fixed-case\">HRS<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      , 0.598;\n                      <jats:italic>P<\/jats:italic>\n                      = .08). In the\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      cohort, 173 patients received rifaximin plus lactulose and 448 patients received lactulose. Rifaximin was not associated with the risk of death (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      , 1.177;\n                      <jats:italic>P<\/jats:italic>\n                      = .121). Rifaximin was associated with lower risk of\n                      <jats:styled-content style=\"fixed-case\">SBP<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      , 0.323;\n                      <jats:italic>P<\/jats:italic>\n                      &lt; .001) but not with variceal bleeding (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      , 0.660;\n                      <jats:italic>P<\/jats:italic>\n                      = .104) or recurrent\n                      <jats:styled-content style=\"fixed-case\">HE<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      , 0.689;\n                      <jats:italic>P<\/jats:italic>\n                      = .057). The risk of\n                      <jats:italic>Clostridium difficile<\/jats:italic>\n                      \u2010associated diarrhoea was not different between the groups (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      , 0.028;\n                      <jats:italic>P<\/jats:italic>\n                      = .338).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      In patients without\n                      <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>\n                      , rifaximin treatment was significantly associated with prolonged overall survival and reduced risks of spontaneous bacterial peritonitis, variceal bleeding and recurrent hepatic encephalopathy.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/apt.14275","type":"journal-article","created":{"date-parts":[[2017,8,24]],"date-time":"2017-08-24T08:49:23Z","timestamp":1503564563000},"page":"845-855","source":"Crossref","is-referenced-by-count":92,"title":["Rifaximin treatment is associated with reduced risk of cirrhotic complications and prolonged overall survival in patients experiencing hepatic encephalopathy"],"prefix":"10.1111","volume":"46","author":[{"given":"S. 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