Randomized trial comparing albumin and saline in the prevention of paracentesis-induced circulatory dysfunction in cirrhotic patients with ascites
Paracentesis-induced circulatory dysfunction (PICD) is a recently described complication that can be prevented with the administration of plasma expanders. The aim of this study was to compare the efficacy of saline versus albumin in the prevention of PICD. Patients were randomized to receive albumi...
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creator | Sola-Vera, Javier Miñana, Josep Ricart, Elena Planella, Montserrat González, Begoña Torras, Xavier Rodrı́ guez, Jose Such, José Pascual, Sonia Soriano, Germán Pérez-Mateo, Miguel Guarner, Carlos |
description | Paracentesis-induced circulatory dysfunction (PICD) is a recently described complication that can be prevented with the administration of plasma expanders. The aim of this study was to compare the efficacy of saline versus albumin in the prevention of PICD. Patients were randomized to receive albumin or saline after total paracentesis. Patients readmitted as a consequence of a second episode of tense ascites were treated with total paracentesis and the alternative plasma expander. After randomization, 35 patients received saline and 37 received albumin. Twenty-one patients were readmitted for tense ascites and treated with the alternative expander. Significant increases in plasma renin activity (PRA) were found 24 hours and 6 days after paracentesis when saline was used (baseline, 5.6 ± 5.7; 24 hours, 7.6 ± 6.9; 6 days, 8.5 ± 8.0 ng · mL
−1 · hr
−1;
P < .05 and
P < .01 vs. baseline, respectively), whereas no significant changes were observed with albumin. The incidence of PICD was significantly higher in the saline group versus the albumin group (33.3% vs. 11.4%, respectively;
P = .03). However, no significant differences were found when less than 6 L of ascitic fluid was evacuated (6.7% vs. 5.6% in the saline and albumin groups, respectively;
P = .9). Similar results were observed when analyzing patients who received 2 consecutive paracentesis (
i.e., a significant increase in PRA after saline [
P < .01] without significant variations after albumin). In conclusion, albumin is more effective than saline in the prevention of PICD. Saline is a valid alternative to albumin when less than 6 L of ascitic fluid is evacuated. (H
epatology 2003;37:1147-1153.) |
doi_str_mv | 10.1053/jhep.2003.50169 |
format | Article |
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−1 · hr
−1;
P < .05 and
P < .01 vs. baseline, respectively), whereas no significant changes were observed with albumin. The incidence of PICD was significantly higher in the saline group versus the albumin group (33.3% vs. 11.4%, respectively;
P = .03). However, no significant differences were found when less than 6 L of ascitic fluid was evacuated (6.7% vs. 5.6% in the saline and albumin groups, respectively;
P = .9). Similar results were observed when analyzing patients who received 2 consecutive paracentesis (
i.e., a significant increase in PRA after saline [
P < .01] without significant variations after albumin). In conclusion, albumin is more effective than saline in the prevention of PICD. Saline is a valid alternative to albumin when less than 6 L of ascitic fluid is evacuated. (H
epatology 2003;37:1147-1153.)</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1053/jhep.2003.50169</identifier><identifier>PMID: 12717396</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>Aged ; Albumins - administration & dosage ; Ascites - diagnosis ; Ascites - therapy ; Biological and medical sciences ; Cardiovascular Diseases - epidemiology ; Cardiovascular Diseases - etiology ; Cardiovascular Diseases - prevention & control ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Hemodynamics - drug effects ; Humans ; Incidence ; Kidney Diseases - epidemiology ; Kidney Diseases - etiology ; Kidney Diseases - prevention & control ; Liver Cirrhosis - diagnosis ; Liver Cirrhosis - therapy ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Other diseases. Semiology ; Paracentesis - adverse effects ; Plasma Substitutes - administration & dosage ; Predictive Value of Tests ; Recurrence ; Sodium Chloride - administration & dosage ; Treatment Outcome</subject><ispartof>Hepatology (Baltimore, Md.), 2003-05, Vol.37 (5), p.1147-1153</ispartof><rights>2003 The American Association for the Study of Liver Diseases</rights><rights>Copyright © 2003 by the American Association for the Study of Liver Diseases</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4644-345ac0fdbaed2d138ad5487e9ba8b6b004fb20864ae2bbe0b220d2b4a587f09d3</citedby><cites>FETCH-LOGICAL-c4644-345ac0fdbaed2d138ad5487e9ba8b6b004fb20864ae2bbe0b220d2b4a587f09d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1053%2Fjhep.2003.50169$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1053%2Fjhep.2003.50169$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14805595$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12717396$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sola-Vera, Javier</creatorcontrib><creatorcontrib>Miñana, Josep</creatorcontrib><creatorcontrib>Ricart, Elena</creatorcontrib><creatorcontrib>Planella, Montserrat</creatorcontrib><creatorcontrib>González, Begoña</creatorcontrib><creatorcontrib>Torras, Xavier</creatorcontrib><creatorcontrib>Rodrı&#x0301;guez, Jose</creatorcontrib><creatorcontrib>Such, José</creatorcontrib><creatorcontrib>Pascual, Sonia</creatorcontrib><creatorcontrib>Soriano, Germán</creatorcontrib><creatorcontrib>Pérez-Mateo, Miguel</creatorcontrib><creatorcontrib>Guarner, Carlos</creatorcontrib><title>Randomized trial comparing albumin and saline in the prevention of paracentesis-induced circulatory dysfunction in cirrhotic patients with ascites</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>Paracentesis-induced circulatory dysfunction (PICD) is a recently described complication that can be prevented with the administration of plasma expanders. The aim of this study was to compare the efficacy of saline versus albumin in the prevention of PICD. Patients were randomized to receive albumin or saline after total paracentesis. Patients readmitted as a consequence of a second episode of tense ascites were treated with total paracentesis and the alternative plasma expander. After randomization, 35 patients received saline and 37 received albumin. Twenty-one patients were readmitted for tense ascites and treated with the alternative expander. Significant increases in plasma renin activity (PRA) were found 24 hours and 6 days after paracentesis when saline was used (baseline, 5.6 ± 5.7; 24 hours, 7.6 ± 6.9; 6 days, 8.5 ± 8.0 ng · mL
−1 · hr
−1;
P < .05 and
P < .01 vs. baseline, respectively), whereas no significant changes were observed with albumin. The incidence of PICD was significantly higher in the saline group versus the albumin group (33.3% vs. 11.4%, respectively;
P = .03). However, no significant differences were found when less than 6 L of ascitic fluid was evacuated (6.7% vs. 5.6% in the saline and albumin groups, respectively;
P = .9). Similar results were observed when analyzing patients who received 2 consecutive paracentesis (
i.e., a significant increase in PRA after saline [
P < .01] without significant variations after albumin). In conclusion, albumin is more effective than saline in the prevention of PICD. Saline is a valid alternative to albumin when less than 6 L of ascitic fluid is evacuated. (H
epatology 2003;37:1147-1153.)</description><subject>Aged</subject><subject>Albumins - administration & dosage</subject><subject>Ascites - diagnosis</subject><subject>Ascites - therapy</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>Cardiovascular Diseases - etiology</subject><subject>Cardiovascular Diseases - prevention & control</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hemodynamics - drug effects</subject><subject>Humans</subject><subject>Incidence</subject><subject>Kidney Diseases - epidemiology</subject><subject>Kidney Diseases - etiology</subject><subject>Kidney Diseases - prevention & control</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver Cirrhosis - therapy</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Other diseases. Semiology</subject><subject>Paracentesis - adverse effects</subject><subject>Plasma Substitutes - administration & dosage</subject><subject>Predictive Value of Tests</subject><subject>Recurrence</subject><subject>Sodium Chloride - administration & dosage</subject><subject>Treatment Outcome</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS0EosPAmh3yBnaZ3viRxEtUtRSpEgjB2vLjhnGVOIOdtBp-Br8YT2ekWSFW1pW_c67uOYS8rWFTg-SX91vcbRgA30ioG_WMrGrJ2opzCc_JClgLlaq5uiCvcr4HACVY95Jc1KytW66aFfnzzUQ_jeE3ejqnYAbqpnFnUog_qRnsMoZIC0GzGUJEWqZ5i3SX8AHjHKZIp54W3LgyYg65CtEvrpi5kNwymHlKe-r3uV-ie-KLQ_lK22kOrijnUISZPoZ5S012oZi8Ji96M2R8c3rX5MfN9fer2-ruy6fPVx_vKicaISoupHHQe2vQM1_zzngpuhaVNZ1tLIDoLYOuEQaZtQiWMfDMCiO7tgfl-Zp8OPru0vRrwTzrMWSHw2AiTkvWLWdCsRLfmlweQZemnBP2epfCaNJe16APNehDDfpQg36qoSjenawXO6I_86fcC_D-BJSjzdAnE13IZ050IKWShVNH7jEMuP_fXn17_VXWwFuQTJy1WEJ8CJh0yRdjKSckdLP2U_jnAX8BqO252Q</recordid><startdate>200305</startdate><enddate>200305</enddate><creator>Sola-Vera, Javier</creator><creator>Miñana, Josep</creator><creator>Ricart, Elena</creator><creator>Planella, Montserrat</creator><creator>González, Begoña</creator><creator>Torras, Xavier</creator><creator>Rodrı&#x0301;guez, Jose</creator><creator>Such, José</creator><creator>Pascual, Sonia</creator><creator>Soriano, Germán</creator><creator>Pérez-Mateo, Miguel</creator><creator>Guarner, Carlos</creator><general>Elsevier Inc</general><general>W.B. Saunders</general><general>Wiley</general><scope>IQODW</scope><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>200305</creationdate><title>Randomized trial comparing albumin and saline in the prevention of paracentesis-induced circulatory dysfunction in cirrhotic patients with ascites</title><author>Sola-Vera, Javier ; Miñana, Josep ; Ricart, Elena ; Planella, Montserrat ; González, Begoña ; Torras, Xavier ; Rodrı&#x0301;guez, Jose ; Such, José ; Pascual, Sonia ; Soriano, Germán ; Pérez-Mateo, Miguel ; Guarner, Carlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4644-345ac0fdbaed2d138ad5487e9ba8b6b004fb20864ae2bbe0b220d2b4a587f09d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Aged</topic><topic>Albumins - administration & dosage</topic><topic>Ascites - diagnosis</topic><topic>Ascites - therapy</topic><topic>Biological and medical sciences</topic><topic>Cardiovascular Diseases - epidemiology</topic><topic>Cardiovascular Diseases - etiology</topic><topic>Cardiovascular Diseases - prevention & control</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Hemodynamics - drug effects</topic><topic>Humans</topic><topic>Incidence</topic><topic>Kidney Diseases - epidemiology</topic><topic>Kidney Diseases - etiology</topic><topic>Kidney Diseases - prevention & control</topic><topic>Liver Cirrhosis - diagnosis</topic><topic>Liver Cirrhosis - therapy</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Other diseases. Semiology</topic><topic>Paracentesis - adverse effects</topic><topic>Plasma Substitutes - administration & dosage</topic><topic>Predictive Value of Tests</topic><topic>Recurrence</topic><topic>Sodium Chloride - administration & dosage</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sola-Vera, Javier</creatorcontrib><creatorcontrib>Miñana, Josep</creatorcontrib><creatorcontrib>Ricart, Elena</creatorcontrib><creatorcontrib>Planella, Montserrat</creatorcontrib><creatorcontrib>González, Begoña</creatorcontrib><creatorcontrib>Torras, Xavier</creatorcontrib><creatorcontrib>Rodrı&#x0301;guez, Jose</creatorcontrib><creatorcontrib>Such, José</creatorcontrib><creatorcontrib>Pascual, Sonia</creatorcontrib><creatorcontrib>Soriano, Germán</creatorcontrib><creatorcontrib>Pérez-Mateo, Miguel</creatorcontrib><creatorcontrib>Guarner, Carlos</creatorcontrib><collection>Pascal-Francis</collection><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>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sola-Vera, Javier</au><au>Miñana, Josep</au><au>Ricart, Elena</au><au>Planella, Montserrat</au><au>González, Begoña</au><au>Torras, Xavier</au><au>Rodrı&#x0301;guez, Jose</au><au>Such, José</au><au>Pascual, Sonia</au><au>Soriano, Germán</au><au>Pérez-Mateo, Miguel</au><au>Guarner, Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Randomized trial comparing albumin and saline in the prevention of paracentesis-induced circulatory dysfunction in cirrhotic patients with ascites</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>2003-05</date><risdate>2003</risdate><volume>37</volume><issue>5</issue><spage>1147</spage><epage>1153</epage><pages>1147-1153</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>Paracentesis-induced circulatory dysfunction (PICD) is a recently described complication that can be prevented with the administration of plasma expanders. The aim of this study was to compare the efficacy of saline versus albumin in the prevention of PICD. Patients were randomized to receive albumin or saline after total paracentesis. Patients readmitted as a consequence of a second episode of tense ascites were treated with total paracentesis and the alternative plasma expander. After randomization, 35 patients received saline and 37 received albumin. Twenty-one patients were readmitted for tense ascites and treated with the alternative expander. Significant increases in plasma renin activity (PRA) were found 24 hours and 6 days after paracentesis when saline was used (baseline, 5.6 ± 5.7; 24 hours, 7.6 ± 6.9; 6 days, 8.5 ± 8.0 ng · mL
−1 · hr
−1;
P < .05 and
P < .01 vs. baseline, respectively), whereas no significant changes were observed with albumin. The incidence of PICD was significantly higher in the saline group versus the albumin group (33.3% vs. 11.4%, respectively;
P = .03). However, no significant differences were found when less than 6 L of ascitic fluid was evacuated (6.7% vs. 5.6% in the saline and albumin groups, respectively;
P = .9). Similar results were observed when analyzing patients who received 2 consecutive paracentesis (
i.e., a significant increase in PRA after saline [
P < .01] without significant variations after albumin). In conclusion, albumin is more effective than saline in the prevention of PICD. Saline is a valid alternative to albumin when less than 6 L of ascitic fluid is evacuated. (H
epatology 2003;37:1147-1153.)</abstract><cop>Philadelphia, PA</cop><pub>Elsevier Inc</pub><pmid>12717396</pmid><doi>10.1053/jhep.2003.50169</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Albumins - administration & dosage Ascites - diagnosis Ascites - therapy Biological and medical sciences Cardiovascular Diseases - epidemiology Cardiovascular Diseases - etiology Cardiovascular Diseases - prevention & control Female Gastroenterology. Liver. Pancreas. Abdomen Hemodynamics - drug effects Humans Incidence Kidney Diseases - epidemiology Kidney Diseases - etiology Kidney Diseases - prevention & control Liver Cirrhosis - diagnosis Liver Cirrhosis - therapy Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Middle Aged Other diseases. Semiology Paracentesis - adverse effects Plasma Substitutes - administration & dosage Predictive Value of Tests Recurrence Sodium Chloride - administration & dosage Treatment Outcome |
title | Randomized trial comparing albumin and saline in the prevention of paracentesis-induced circulatory dysfunction in cirrhotic patients with ascites |
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