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Pumactant in the prevention of postoperative adhesions: A randomized trial

Abstract Background Postoperative intraperitoneal adhesions are a considerable source of morbidity. Supplementing compromised endogenous intraperitoneal phospholipids can reduce postoperative adhesions. A randomised, controlled, parallel group study was performed to evaluate the efficacy, safety and...

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Published in:The Journal of surgical research 2012-12, Vol.178 (2), p.677-684
Main Authors: Shimi, Sami M., MD, FRCS, Loudon, Malcolm A., MD, FRCS
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Language:English
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cited_by cdi_FETCH-LOGICAL-c441t-661afad597b7687279c6da1ec4a16d34b9026287e42b6664030e719c6770563c3
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Loudon, Malcolm A., MD, FRCS
description Abstract Background Postoperative intraperitoneal adhesions are a considerable source of morbidity. Supplementing compromised endogenous intraperitoneal phospholipids can reduce postoperative adhesions. A randomised, controlled, parallel group study was performed to evaluate the efficacy, safety and tolerability of pumactant in the prevention of peritoneal adhesions after abdominal colorectal surgery. Materials and methods A total of 134 patients undergoing partial colectomy and colostomy or ileostomy were randomized to receive either 240 mg of pumactant or placebo (carbon dioxide) sprayed into the peritoneal cavity. The outcome measures were efficacy (adhesion incidence and extent and severity at the second surgery) and the safety of pumactant in the peritoneal cavity after abdominal surgery. Results The mean adhesion score increased from surgery 1 to surgery 2 in the pumactant group and decreased in the placebo group, and the incidence and extent of adhesions increased in both groups. A total of 2149 adverse events were reported, of which 158 were serious. The overall adverse event profile for the two groups (pumactant and placebo) was very similar. Conclusions Although pumactant is relatively safe by the intraperitoneal route, 240 mg powdered pumactant is not effective in reducing postoperative peritoneal adhesions.
doi_str_mv 10.1016/j.jss.2012.06.060
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Supplementing compromised endogenous intraperitoneal phospholipids can reduce postoperative adhesions. A randomised, controlled, parallel group study was performed to evaluate the efficacy, safety and tolerability of pumactant in the prevention of peritoneal adhesions after abdominal colorectal surgery. Materials and methods A total of 134 patients undergoing partial colectomy and colostomy or ileostomy were randomized to receive either 240 mg of pumactant or placebo (carbon dioxide) sprayed into the peritoneal cavity. The outcome measures were efficacy (adhesion incidence and extent and severity at the second surgery) and the safety of pumactant in the peritoneal cavity after abdominal surgery. Results The mean adhesion score increased from surgery 1 to surgery 2 in the pumactant group and decreased in the placebo group, and the incidence and extent of adhesions increased in both groups. A total of 2149 adverse events were reported, of which 158 were serious. The overall adverse event profile for the two groups (pumactant and placebo) was very similar. Conclusions Although pumactant is relatively safe by the intraperitoneal route, 240 mg powdered pumactant is not effective in reducing postoperative peritoneal adhesions.</description><identifier>ISSN: 0022-4804</identifier><identifier>EISSN: 1095-8673</identifier><identifier>DOI: 10.1016/j.jss.2012.06.060</identifier><identifier>PMID: 22789134</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Abdominal surgery ; Adult ; Aged ; Colectomy ; Colostomy ; Double-Blind Method ; Female ; Humans ; Ileostomy ; Male ; Middle Aged ; Postoperative adhesions ; Postoperative Complications - prevention &amp; control ; Pulmonary Surfactants - therapeutic use ; Pumactant ; Surgery ; Tissue Adhesions - prevention &amp; control</subject><ispartof>The Journal of surgical research, 2012-12, Vol.178 (2), p.677-684</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-661afad597b7687279c6da1ec4a16d34b9026287e42b6664030e719c6770563c3</citedby><cites>FETCH-LOGICAL-c441t-661afad597b7687279c6da1ec4a16d34b9026287e42b6664030e719c6770563c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22789134$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shimi, Sami M., MD, FRCS</creatorcontrib><creatorcontrib>Loudon, Malcolm A., MD, FRCS</creatorcontrib><title>Pumactant in the prevention of postoperative adhesions: A randomized trial</title><title>The Journal of surgical research</title><addtitle>J Surg Res</addtitle><description>Abstract Background Postoperative intraperitoneal adhesions are a considerable source of morbidity. Supplementing compromised endogenous intraperitoneal phospholipids can reduce postoperative adhesions. A randomised, controlled, parallel group study was performed to evaluate the efficacy, safety and tolerability of pumactant in the prevention of peritoneal adhesions after abdominal colorectal surgery. Materials and methods A total of 134 patients undergoing partial colectomy and colostomy or ileostomy were randomized to receive either 240 mg of pumactant or placebo (carbon dioxide) sprayed into the peritoneal cavity. The outcome measures were efficacy (adhesion incidence and extent and severity at the second surgery) and the safety of pumactant in the peritoneal cavity after abdominal surgery. Results The mean adhesion score increased from surgery 1 to surgery 2 in the pumactant group and decreased in the placebo group, and the incidence and extent of adhesions increased in both groups. A total of 2149 adverse events were reported, of which 158 were serious. The overall adverse event profile for the two groups (pumactant and placebo) was very similar. 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Supplementing compromised endogenous intraperitoneal phospholipids can reduce postoperative adhesions. A randomised, controlled, parallel group study was performed to evaluate the efficacy, safety and tolerability of pumactant in the prevention of peritoneal adhesions after abdominal colorectal surgery. Materials and methods A total of 134 patients undergoing partial colectomy and colostomy or ileostomy were randomized to receive either 240 mg of pumactant or placebo (carbon dioxide) sprayed into the peritoneal cavity. The outcome measures were efficacy (adhesion incidence and extent and severity at the second surgery) and the safety of pumactant in the peritoneal cavity after abdominal surgery. Results The mean adhesion score increased from surgery 1 to surgery 2 in the pumactant group and decreased in the placebo group, and the incidence and extent of adhesions increased in both groups. A total of 2149 adverse events were reported, of which 158 were serious. The overall adverse event profile for the two groups (pumactant and placebo) was very similar. Conclusions Although pumactant is relatively safe by the intraperitoneal route, 240 mg powdered pumactant is not effective in reducing postoperative peritoneal adhesions.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22789134</pmid><doi>10.1016/j.jss.2012.06.060</doi><tpages>8</tpages></addata></record>
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subjects Abdominal surgery
Adult
Aged
Colectomy
Colostomy
Double-Blind Method
Female
Humans
Ileostomy
Male
Middle Aged
Postoperative adhesions
Postoperative Complications - prevention & control
Pulmonary Surfactants - therapeutic use
Pumactant
Surgery
Tissue Adhesions - prevention & control
title Pumactant in the prevention of postoperative adhesions: A randomized trial
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