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The healing of colon anastomosis covered with fibrin glue after early postoperative intraperitoneal chemotherapy
After colon resection for colonic cancer, the administration of antineoplastic agents may prolong survival by killing residual cancer calls and preventing metastasis, but may also slow anastomotic healing. This study was designed to determine the effects of 5-fluorouracil (5-FU) and leucovorin (LEV)...
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Published in: | Techniques in coloproctology 2006-06, Vol.10 (2), p.115-120 |
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description | After colon resection for colonic cancer, the administration of antineoplastic agents may prolong survival by killing residual cancer calls and preventing metastasis, but may also slow anastomotic healing. This study was designed to determine the effects of 5-fluorouracil (5-FU) and leucovorin (LEV), injected intraperitoneally, on the healing of colonic anastomoses with or without fibrin glue (FG) covering.
Sixty rats were randomized to one of four groups. After resection of a transverse colon segment, an end-to-end sutured anastomosis was performed. Rats in the 5-FU+LEV and the 5- FU+LEV+FG groups received 5-FU+LEV intraperitoneally. The colonic anastomoses of the rats in the FG group and in the 5-FU+LEV+FG group were covered with fibrin glue. All rats were killed on postoperative day 8. Bursting pressure measurements were recorded and the anastomoses were examined macroscopically and histologically.
The leakage rate of the anastomoses was significantly different among groups. Specifically, the leakage rate was significantly higher in the 5-FU+LEV group (40%) than in the FG and in the 5-FU+LEV+FG groups where there were no leakages (p=0.017). The mean adhesion formation score was significantly higher in rats of the 5-FU+LEV group, compared to the control (p=0.023), the FG (p=0.006) and the 5-FU+LEV+FG (p=0.006) groups. Bursting pressures were significantly lower in the 5-FU+LEV group than in the other groups (p |
doi_str_mv | 10.1007/s10151-006-0263-4 |
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Sixty rats were randomized to one of four groups. After resection of a transverse colon segment, an end-to-end sutured anastomosis was performed. Rats in the 5-FU+LEV and the 5- FU+LEV+FG groups received 5-FU+LEV intraperitoneally. The colonic anastomoses of the rats in the FG group and in the 5-FU+LEV+FG group were covered with fibrin glue. All rats were killed on postoperative day 8. Bursting pressure measurements were recorded and the anastomoses were examined macroscopically and histologically.
The leakage rate of the anastomoses was significantly different among groups. Specifically, the leakage rate was significantly higher in the 5-FU+LEV group (40%) than in the FG and in the 5-FU+LEV+FG groups where there were no leakages (p=0.017). The mean adhesion formation score was significantly higher in rats of the 5-FU+LEV group, compared to the control (p=0.023), the FG (p=0.006) and the 5-FU+LEV+FG (p=0.006) groups. Bursting pressures were significantly lower in the 5-FU+LEV group than in the other groups (p<0.001). Also, bursting pressures were significantly lower in the control group compared to the FG and 5-FU+LEV+FG groups (p<0.001). Rats in the 5-FU+LEV+FG group had significantly greater neoangiogenesis and fibroblast activity than those in the 5-FU+LEV group (p=0.025).
The early intraperitoneal postoperative administration of 5-fluorouracil plus leucovorin impaired colonic wound healing. However, the application of fibrin glue prevented the deleterious effect of chemotherapy.</description><identifier>ISSN: 1123-6337</identifier><identifier>EISSN: 1128-045X</identifier><identifier>DOI: 10.1007/s10151-006-0263-4</identifier><identifier>PMID: 16773289</identifier><identifier>CODEN: TECOFO</identifier><language>eng</language><publisher>Italy: Springer Nature B.V</publisher><subject>Anastomosis, Surgical ; Animals ; Antimetabolites, Antineoplastic - administration & dosage ; Antimetabolites, Antineoplastic - pharmacology ; Colon - surgery ; Fibrin Tissue Adhesive ; Fluorouracil - administration & dosage ; Fluorouracil - pharmacology ; Injections, Intraperitoneal ; Leucovorin - administration & dosage ; Leucovorin - pharmacology ; Male ; Rats ; Rats, Wistar ; Vitamin B Complex - administration & dosage ; Vitamin B Complex - pharmacology ; Wound Healing - drug effects</subject><ispartof>Techniques in coloproctology, 2006-06, Vol.10 (2), p.115-120</ispartof><rights>Springer-Verlag Italia 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c241t-5563b3650069f1fe54192ecc7716ebf502d5b7e48446bae96b69163ef2682c833</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16773289$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kanellos, I</creatorcontrib><creatorcontrib>Christoforidis, E</creatorcontrib><creatorcontrib>Kanellos, D</creatorcontrib><creatorcontrib>Pramateftakis, M G</creatorcontrib><creatorcontrib>Sakkas, L</creatorcontrib><creatorcontrib>Betsis, D</creatorcontrib><title>The healing of colon anastomosis covered with fibrin glue after early postoperative intraperitoneal chemotherapy</title><title>Techniques in coloproctology</title><addtitle>Tech Coloproctol</addtitle><description>After colon resection for colonic cancer, the administration of antineoplastic agents may prolong survival by killing residual cancer calls and preventing metastasis, but may also slow anastomotic healing. This study was designed to determine the effects of 5-fluorouracil (5-FU) and leucovorin (LEV), injected intraperitoneally, on the healing of colonic anastomoses with or without fibrin glue (FG) covering.
Sixty rats were randomized to one of four groups. After resection of a transverse colon segment, an end-to-end sutured anastomosis was performed. Rats in the 5-FU+LEV and the 5- FU+LEV+FG groups received 5-FU+LEV intraperitoneally. The colonic anastomoses of the rats in the FG group and in the 5-FU+LEV+FG group were covered with fibrin glue. All rats were killed on postoperative day 8. Bursting pressure measurements were recorded and the anastomoses were examined macroscopically and histologically.
The leakage rate of the anastomoses was significantly different among groups. Specifically, the leakage rate was significantly higher in the 5-FU+LEV group (40%) than in the FG and in the 5-FU+LEV+FG groups where there were no leakages (p=0.017). The mean adhesion formation score was significantly higher in rats of the 5-FU+LEV group, compared to the control (p=0.023), the FG (p=0.006) and the 5-FU+LEV+FG (p=0.006) groups. Bursting pressures were significantly lower in the 5-FU+LEV group than in the other groups (p<0.001). Also, bursting pressures were significantly lower in the control group compared to the FG and 5-FU+LEV+FG groups (p<0.001). Rats in the 5-FU+LEV+FG group had significantly greater neoangiogenesis and fibroblast activity than those in the 5-FU+LEV group (p=0.025).
The early intraperitoneal postoperative administration of 5-fluorouracil plus leucovorin impaired colonic wound healing. However, the application of fibrin glue prevented the deleterious effect of chemotherapy.</description><subject>Anastomosis, Surgical</subject><subject>Animals</subject><subject>Antimetabolites, Antineoplastic - administration & dosage</subject><subject>Antimetabolites, Antineoplastic - pharmacology</subject><subject>Colon - surgery</subject><subject>Fibrin Tissue Adhesive</subject><subject>Fluorouracil - administration & dosage</subject><subject>Fluorouracil - pharmacology</subject><subject>Injections, Intraperitoneal</subject><subject>Leucovorin - administration & dosage</subject><subject>Leucovorin - pharmacology</subject><subject>Male</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Vitamin B Complex - administration & dosage</subject><subject>Vitamin B Complex - pharmacology</subject><subject>Wound Healing - drug effects</subject><issn>1123-6337</issn><issn>1128-045X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNpFUE1LxDAQDaL4_QO8SPBezSRN0h5F_ALBi4K3kHYnNtJtapJV9t8b3QVP8_Xem5lHyBmwS2BMXyVgIKFiTFWMK1HVO-QQgDcVq-Xb7l8uKiWEPiBHKX0wBlpL2CcHoLQWvGkPyfwyIB3Qjn56p8HRPoxhonayKYdlSD6VzhdGXNBvnwfqfBf9RN_HFVLrMkaKNo5rOoeCnzHa7L-Q-ilHWyqfw1SkaT_gMuShjOf1Cdlzdkx4uo3H5PXu9uXmoXp6vn-8uX6qel5DrqRUohNKlt9aBw5lDS3HvtcaFHZOMr6Qnca6qWvVWWxVp1pQAh1XDe8bIY7JxUZ3juFzhSmbj7CKU1lpuJAamABZQLAB9TGkFNGZOfqljWsDzPxabDYWm3KG-bXY1IVzvhVedUtc_DO2noofJcJ4jw</recordid><startdate>200606</startdate><enddate>200606</enddate><creator>Kanellos, I</creator><creator>Christoforidis, E</creator><creator>Kanellos, D</creator><creator>Pramateftakis, M G</creator><creator>Sakkas, L</creator><creator>Betsis, D</creator><general>Springer Nature B.V</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>200606</creationdate><title>The healing of colon anastomosis covered with fibrin glue after early postoperative intraperitoneal chemotherapy</title><author>Kanellos, I ; Christoforidis, E ; Kanellos, D ; Pramateftakis, M G ; Sakkas, L ; Betsis, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c241t-5563b3650069f1fe54192ecc7716ebf502d5b7e48446bae96b69163ef2682c833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Anastomosis, Surgical</topic><topic>Animals</topic><topic>Antimetabolites, Antineoplastic - administration & dosage</topic><topic>Antimetabolites, Antineoplastic - pharmacology</topic><topic>Colon - surgery</topic><topic>Fibrin Tissue Adhesive</topic><topic>Fluorouracil - administration & dosage</topic><topic>Fluorouracil - pharmacology</topic><topic>Injections, Intraperitoneal</topic><topic>Leucovorin - administration & dosage</topic><topic>Leucovorin - pharmacology</topic><topic>Male</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Vitamin B Complex - administration & dosage</topic><topic>Vitamin B Complex - pharmacology</topic><topic>Wound Healing - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kanellos, I</creatorcontrib><creatorcontrib>Christoforidis, E</creatorcontrib><creatorcontrib>Kanellos, D</creatorcontrib><creatorcontrib>Pramateftakis, M G</creatorcontrib><creatorcontrib>Sakkas, L</creatorcontrib><creatorcontrib>Betsis, D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Techniques in coloproctology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kanellos, I</au><au>Christoforidis, E</au><au>Kanellos, D</au><au>Pramateftakis, M G</au><au>Sakkas, L</au><au>Betsis, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The healing of colon anastomosis covered with fibrin glue after early postoperative intraperitoneal chemotherapy</atitle><jtitle>Techniques in coloproctology</jtitle><addtitle>Tech Coloproctol</addtitle><date>2006-06</date><risdate>2006</risdate><volume>10</volume><issue>2</issue><spage>115</spage><epage>120</epage><pages>115-120</pages><issn>1123-6337</issn><eissn>1128-045X</eissn><coden>TECOFO</coden><abstract>After colon resection for colonic cancer, the administration of antineoplastic agents may prolong survival by killing residual cancer calls and preventing metastasis, but may also slow anastomotic healing. This study was designed to determine the effects of 5-fluorouracil (5-FU) and leucovorin (LEV), injected intraperitoneally, on the healing of colonic anastomoses with or without fibrin glue (FG) covering.
Sixty rats were randomized to one of four groups. After resection of a transverse colon segment, an end-to-end sutured anastomosis was performed. Rats in the 5-FU+LEV and the 5- FU+LEV+FG groups received 5-FU+LEV intraperitoneally. The colonic anastomoses of the rats in the FG group and in the 5-FU+LEV+FG group were covered with fibrin glue. All rats were killed on postoperative day 8. Bursting pressure measurements were recorded and the anastomoses were examined macroscopically and histologically.
The leakage rate of the anastomoses was significantly different among groups. Specifically, the leakage rate was significantly higher in the 5-FU+LEV group (40%) than in the FG and in the 5-FU+LEV+FG groups where there were no leakages (p=0.017). The mean adhesion formation score was significantly higher in rats of the 5-FU+LEV group, compared to the control (p=0.023), the FG (p=0.006) and the 5-FU+LEV+FG (p=0.006) groups. Bursting pressures were significantly lower in the 5-FU+LEV group than in the other groups (p<0.001). Also, bursting pressures were significantly lower in the control group compared to the FG and 5-FU+LEV+FG groups (p<0.001). Rats in the 5-FU+LEV+FG group had significantly greater neoangiogenesis and fibroblast activity than those in the 5-FU+LEV group (p=0.025).
The early intraperitoneal postoperative administration of 5-fluorouracil plus leucovorin impaired colonic wound healing. However, the application of fibrin glue prevented the deleterious effect of chemotherapy.</abstract><cop>Italy</cop><pub>Springer Nature B.V</pub><pmid>16773289</pmid><doi>10.1007/s10151-006-0263-4</doi><tpages>6</tpages></addata></record> |
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subjects | Anastomosis, Surgical Animals Antimetabolites, Antineoplastic - administration & dosage Antimetabolites, Antineoplastic - pharmacology Colon - surgery Fibrin Tissue Adhesive Fluorouracil - administration & dosage Fluorouracil - pharmacology Injections, Intraperitoneal Leucovorin - administration & dosage Leucovorin - pharmacology Male Rats Rats, Wistar Vitamin B Complex - administration & dosage Vitamin B Complex - pharmacology Wound Healing - drug effects |
title | The healing of colon anastomosis covered with fibrin glue after early postoperative intraperitoneal chemotherapy |
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