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Terlipressin versus albumin in paracentesis-induced circulatory dysfunction in cirrhosis: A randomized study

Background:  Therapeutic paracentesis in patients with cirrhosis induces arterial vasodilatation, causes a decrease in effective arterial blood volume and leads to circulatory dysfunction, which can be prevented by intravenous albumin. However, the use of albumin, being a blood product, is controver...

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Published in:Journal of gastroenterology and hepatology 2006-01, Vol.21 (1), p.303-307
Main Authors: Singh, Virendra, Kumar, Ramesh, Nain, Chander Kanwal, Singh, Baljinder, Sharma, Arun K
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Kumar, Ramesh
Nain, Chander Kanwal
Singh, Baljinder
Sharma, Arun K
description Background:  Therapeutic paracentesis in patients with cirrhosis induces arterial vasodilatation, causes a decrease in effective arterial blood volume and leads to circulatory dysfunction, which can be prevented by intravenous albumin. However, the use of albumin, being a blood product, is controversial. Recently, terlipressin, a vasoconstrictor, has been successfully used to combat this adverse effect of therapeutic paracentesis. Therefore, the aim of the present study was to investigate the preventive effect of terlipressin on paracentesis‐induced circulatory dysfunction in patients with cirrhosis after therapeutic paracentesis and compared with that of intravenous albumin. Methods:  Forty patients with cirrhosis and tense ascites underwent therapeutic paracentesis with albumin or terlipressin in a randomized pilot study at a tertiary center. Effective arterial blood volume was assessed by measuring plasma renin activity at baseline and at 4–6 days after treatment. Results:  Effective arterial blood volumes as indicated by plasma renin activity before and 4–6 days after paracentesis did not differ in the two groups (19.15 ± 12.1 to 20.33 ± 12.8 ng/mL per h, P = 0.46 in the albumin group; and 20.11 ± 10.6 to 21.08 ± 10.52 ng/mL per h, P = 0.44 in the terlipressin group). Plasma aldosterone concentrations before and 4–6 days after paracentesis were also similar in both groups (1334.75 ± 1058 to 1440.0 ± 1161 pg/mL, P = 0.06 in the albumin group; and 1473.0 ± 1168 to 1572.29 ± 1182 pg/mL, P = 0.24 in the terlipressin group). Both terlipressin and albumin prevented paracentesis‐induced renal impairment in these patients. Conclusions:  Terlipressin may be as effective as intravenous albumin in preventing paracentesis‐induced circulatory dysfunction in patients with cirrhosis after therapeutic paracentesis.
doi_str_mv 10.1111/j.1440-1746.2006.04182.x
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However, the use of albumin, being a blood product, is controversial. Recently, terlipressin, a vasoconstrictor, has been successfully used to combat this adverse effect of therapeutic paracentesis. Therefore, the aim of the present study was to investigate the preventive effect of terlipressin on paracentesis‐induced circulatory dysfunction in patients with cirrhosis after therapeutic paracentesis and compared with that of intravenous albumin. Methods:  Forty patients with cirrhosis and tense ascites underwent therapeutic paracentesis with albumin or terlipressin in a randomized pilot study at a tertiary center. Effective arterial blood volume was assessed by measuring plasma renin activity at baseline and at 4–6 days after treatment. Results:  Effective arterial blood volumes as indicated by plasma renin activity before and 4–6 days after paracentesis did not differ in the two groups (19.15 ± 12.1 to 20.33 ± 12.8 ng/mL per h, P = 0.46 in the albumin group; and 20.11 ± 10.6 to 21.08 ± 10.52 ng/mL per h, P = 0.44 in the terlipressin group). Plasma aldosterone concentrations before and 4–6 days after paracentesis were also similar in both groups (1334.75 ± 1058 to 1440.0 ± 1161 pg/mL, P = 0.06 in the albumin group; and 1473.0 ± 1168 to 1572.29 ± 1182 pg/mL, P = 0.24 in the terlipressin group). Both terlipressin and albumin prevented paracentesis‐induced renal impairment in these patients. 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However, the use of albumin, being a blood product, is controversial. Recently, terlipressin, a vasoconstrictor, has been successfully used to combat this adverse effect of therapeutic paracentesis. Therefore, the aim of the present study was to investigate the preventive effect of terlipressin on paracentesis‐induced circulatory dysfunction in patients with cirrhosis after therapeutic paracentesis and compared with that of intravenous albumin. Methods:  Forty patients with cirrhosis and tense ascites underwent therapeutic paracentesis with albumin or terlipressin in a randomized pilot study at a tertiary center. Effective arterial blood volume was assessed by measuring plasma renin activity at baseline and at 4–6 days after treatment. Results:  Effective arterial blood volumes as indicated by plasma renin activity before and 4–6 days after paracentesis did not differ in the two groups (19.15 ± 12.1 to 20.33 ± 12.8 ng/mL per h, P = 0.46 in the albumin group; and 20.11 ± 10.6 to 21.08 ± 10.52 ng/mL per h, P = 0.44 in the terlipressin group). Plasma aldosterone concentrations before and 4–6 days after paracentesis were also similar in both groups (1334.75 ± 1058 to 1440.0 ± 1161 pg/mL, P = 0.06 in the albumin group; and 1473.0 ± 1168 to 1572.29 ± 1182 pg/mL, P = 0.24 in the terlipressin group). Both terlipressin and albumin prevented paracentesis‐induced renal impairment in these patients. Conclusions:  Terlipressin may be as effective as intravenous albumin in preventing paracentesis‐induced circulatory dysfunction in patients with cirrhosis after therapeutic paracentesis.</description><subject>albumin</subject><subject>Albumins - therapeutic use</subject><subject>Aldosterone - blood</subject><subject>Ascites - etiology</subject><subject>Ascites - therapy</subject><subject>ascitis</subject><subject>Biological and medical sciences</subject><subject>Blood Volume</subject><subject>cirrhosis</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>Liver Cirrhosis - complications</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Lypressin - analogs &amp; derivatives</subject><subject>Lypressin - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Other diseases. Semiology</subject><subject>paracentesis</subject><subject>Paracentesis - adverse effects</subject><subject>Plasma Substitutes - therapeutic use</subject><subject>Renin - blood</subject><subject>terlipressin</subject><subject>Vasoconstrictor Agents - therapeutic use</subject><issn>0815-9319</issn><issn>1440-1746</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqNkE-P1CAYh4nRuOPqVzC96K2Vfy2tiYfNxJ1ZXTUmazwSCjQy0naWt-h0P710Z7J7lUCA8Pzg5UEoI7ggqb3bFYRznBPBq4JiXBWYk5oWhydo9XDwFK1wTcq8YaQ5Qy8AdhhjjkX5HJ2RileYN2SF_I0N3u2DBXBD9scGiJAp38Y-bVPfq6C0HSYLDnI3mKitybQLOno1jWHOzAxdHPTkxns-HYVfY4LfZxdZUIMZe3eXIjBFM79Ezzrlwb46zefox-XHm_U2v_62uVpfXOeas5LmQhnMurYzpBW6Kxk3bWlb1mFmmKGmVRVtGSWC1LYlxgqcUEpK3JRcM53GOXp7vHcfxttoYZK9A229V4MdI8hKVKzBlCawPoI6jADBdnIfXK_CLAmWi2m5k4tQuQiVi2l5b1oeUvT16Y3Y9tY8Bk9qE_DmBCjQyndJhnbwyIlqKblO3Icj99d5O_93AfLTZrusUj4_5h1M9vCQV-F3-icTpfz5dSPXXz5vvm8va9mwf-rhq8k</recordid><startdate>200601</startdate><enddate>200601</enddate><creator>Singh, Virendra</creator><creator>Kumar, Ramesh</creator><creator>Nain, Chander Kanwal</creator><creator>Singh, Baljinder</creator><creator>Sharma, Arun K</creator><general>Blackwell Publishing Asia</general><general>Blackwell Science</general><scope>BSCLL</scope><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>200601</creationdate><title>Terlipressin versus albumin in paracentesis-induced circulatory dysfunction in cirrhosis: A randomized study</title><author>Singh, Virendra ; Kumar, Ramesh ; Nain, Chander Kanwal ; Singh, Baljinder ; Sharma, Arun K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4352-7ad03fbfd1b7cf534db5eb3f03d3d2dba62b321718eb1de70bfd2150954c3c4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>albumin</topic><topic>Albumins - therapeutic use</topic><topic>Aldosterone - blood</topic><topic>Ascites - etiology</topic><topic>Ascites - therapy</topic><topic>ascitis</topic><topic>Biological and medical sciences</topic><topic>Blood Volume</topic><topic>cirrhosis</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>Liver Cirrhosis - complications</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Lypressin - analogs &amp; derivatives</topic><topic>Lypressin - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Other diseases. Semiology</topic><topic>paracentesis</topic><topic>Paracentesis - adverse effects</topic><topic>Plasma Substitutes - therapeutic use</topic><topic>Renin - blood</topic><topic>terlipressin</topic><topic>Vasoconstrictor Agents - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Singh, Virendra</creatorcontrib><creatorcontrib>Kumar, Ramesh</creatorcontrib><creatorcontrib>Nain, Chander Kanwal</creatorcontrib><creatorcontrib>Singh, Baljinder</creatorcontrib><creatorcontrib>Sharma, Arun K</creatorcontrib><collection>Istex</collection><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>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Singh, Virendra</au><au>Kumar, Ramesh</au><au>Nain, Chander Kanwal</au><au>Singh, Baljinder</au><au>Sharma, Arun K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Terlipressin versus albumin in paracentesis-induced circulatory dysfunction in cirrhosis: A randomized study</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>2006-01</date><risdate>2006</risdate><volume>21</volume><issue>1</issue><spage>303</spage><epage>307</epage><pages>303-307</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>Background:  Therapeutic paracentesis in patients with cirrhosis induces arterial vasodilatation, causes a decrease in effective arterial blood volume and leads to circulatory dysfunction, which can be prevented by intravenous albumin. However, the use of albumin, being a blood product, is controversial. Recently, terlipressin, a vasoconstrictor, has been successfully used to combat this adverse effect of therapeutic paracentesis. Therefore, the aim of the present study was to investigate the preventive effect of terlipressin on paracentesis‐induced circulatory dysfunction in patients with cirrhosis after therapeutic paracentesis and compared with that of intravenous albumin. Methods:  Forty patients with cirrhosis and tense ascites underwent therapeutic paracentesis with albumin or terlipressin in a randomized pilot study at a tertiary center. Effective arterial blood volume was assessed by measuring plasma renin activity at baseline and at 4–6 days after treatment. Results:  Effective arterial blood volumes as indicated by plasma renin activity before and 4–6 days after paracentesis did not differ in the two groups (19.15 ± 12.1 to 20.33 ± 12.8 ng/mL per h, P = 0.46 in the albumin group; and 20.11 ± 10.6 to 21.08 ± 10.52 ng/mL per h, P = 0.44 in the terlipressin group). Plasma aldosterone concentrations before and 4–6 days after paracentesis were also similar in both groups (1334.75 ± 1058 to 1440.0 ± 1161 pg/mL, P = 0.06 in the albumin group; and 1473.0 ± 1168 to 1572.29 ± 1182 pg/mL, P = 0.24 in the terlipressin group). Both terlipressin and albumin prevented paracentesis‐induced renal impairment in these patients. 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1440-1746
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source Wiley-Blackwell Read & Publish Collection
subjects albumin
Albumins - therapeutic use
Aldosterone - blood
Ascites - etiology
Ascites - therapy
ascitis
Biological and medical sciences
Blood Volume
cirrhosis
Female
Gastroenterology. Liver. Pancreas. Abdomen
Hemodynamics
Humans
Liver Cirrhosis - complications
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Lypressin - analogs & derivatives
Lypressin - therapeutic use
Male
Medical sciences
Middle Aged
Other diseases. Semiology
paracentesis
Paracentesis - adverse effects
Plasma Substitutes - therapeutic use
Renin - blood
terlipressin
Vasoconstrictor Agents - therapeutic use
title Terlipressin versus albumin in paracentesis-induced circulatory dysfunction in cirrhosis: A randomized study
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