<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-29T01:19:21Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/116269" metadataPrefix="marc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/116269</identifier><datestamp>2025-01-28T01:09:47Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Simon-Talero M</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">García Martínez, Rita</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Cordoba J</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2013-12</subfield>
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      <subfield code="a">Background &amp; Aims Episodic hepatic encephalopathy is frequently precipitated by factors that induce circulatory dysfunction, cause oxidative stress-mediated damage or enhance astrocyte swelling. The administration of albumin could modify these factors and improve the outcome of hepatic encephalopathy. The aim of this study is to assess the efficacy of albumin in a multicenter, prospective, double-blind, controlled trial (ClinicalTrials.gov number, NCT00886925). Methods Cirrhotic patients with an acute episode of hepatic encephalopathy (grade II-IV) were randomized to receive albumin (1.5 g/kg on day 1 and 1.0 g/kg on day 3) or isotonic saline, in addition to the usual treatment (laxatives, rifaximin 1200 mg per day). The primary end point was the proportion of patients in which encephalopathy was resolved on day 4. The secondary end points included survival, length of hospital stay, and biochemical parameters. Results Fifty-six patients were randomly assigned to albumin (n = 26) or saline (n = 30) stratified by the severity of HE. Both groups were comparable regarding to demographic data, liver function, and precipitating factors. The percentage of patients without hepatic encephalopathy at day 4 did not differ between both groups (albumin: 57.7% vs. saline: 53.3%; p >0.05). However, significant differences in survival were found at day 90 (albumin: 69.2% vs. saline: 40.0%; p = 0.02). Conclusions Albumin does not improve the resolution of hepatic encephalopathy during hospitalization. However, differences in survival after hospitalization suggest that the development of encephalopathy may identify a subgroup of patients with advanced cirrhosis that may benefit from the administration of albumin.</subfield>
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      <subfield code="a">Effects of intravenous albumin in patients with cirrhosis and episodic hepatic encephalopathy: A randomized double-blind study Simón-Talero, Macarena et al. Journal of Hepatology, Volume 59, Issue 6, 1184 - 1192</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">10.1016/j.jhep.2013.07.020</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.14352/116269</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">http://dx.doi.org/10.1016/j.jhep.2013.07.020</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">https://pubmed.ncbi.nlm.nih.gov/23872605/</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">https://www.sciencedirect.com/science/article/pii/S016882781300531X?via%3Dihub</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Effects of intravenous albumin in patients with cirrhosis and episodic hepatic encephalopathy: a randomized double-blind study</subfield>
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