Cyanoacrylate mesh fixation for laparoscopic inguinal hernia repair: a prospective, multicenter, single-arm study

Background Inguinal hernia repair is among the most frequently performed surgical procedures. Alternatives to penetrating mesh fixation, such as surgical glue, are being investigated for their potential benefit in reducing chronic pain. The aim of this study was to assess the efficacy of the n -hexy...

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Veröffentlicht in:Surgical endoscopy 2023-12, Vol.37 (12), p.9105-9115
Hauptverfasser: Dams, Anne, Vankeirsbilck, Joost, Poelmans, Stephan, Kerschaever, Ivan, Borreman, Philippe, Berwouts, Luc, De Mulder, Wim, Colle, Julien, Beunis, Anthony, Dhooghe, Vicky, Van De Winkel, Nele, Allaeys, Mathias, Ruyssers, Michael, Haesen, Dorien, Van der Speeten, Kurt
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container_end_page 9115
container_issue 12
container_start_page 9105
container_title Surgical endoscopy
container_volume 37
creator Dams, Anne
Vankeirsbilck, Joost
Poelmans, Stephan
Kerschaever, Ivan
Borreman, Philippe
Berwouts, Luc
De Mulder, Wim
Colle, Julien
Beunis, Anthony
Dhooghe, Vicky
Van De Winkel, Nele
Allaeys, Mathias
Ruyssers, Michael
Haesen, Dorien
Van der Speeten, Kurt
description Background Inguinal hernia repair is among the most frequently performed surgical procedures. Alternatives to penetrating mesh fixation, such as surgical glue, are being investigated for their potential benefit in reducing chronic pain. The aim of this study was to assess the efficacy of the n -hexyl cyanoacrylate glue Ifabond™ for mesh fixation in laparoscopic inguinal hernia repair. Methods This prospective, multicenter, single-arm study collected data from laparoscopic inguinal hernia repairs using Ifabond™ (Peters Surgical, Boulogne-Billancourt Cedex, France) and a standard [Promesh® SURG ST (Peters Surgical)/Biomesh® P1 (Cousin Biotech, Wervicq-Sud, France)] or lightweight [Promesh® SURG LI (Peters Surgical)/Premium® Implant (Cousin Biotech)] polypropylene mesh. The primary endpoint was postoperative pain [100-scale Visual Analog Scale (VAS)]. Secondary endpoints were complications, hernia recurrences, and quality of life (QoL) (EQ-5D-3L health index and EQ-VAS). Patients were followed up at 5 weeks and 12 months after surgery. Results Six-hundred and thirteen patients underwent laparoscopic inguinal hernia repair. Postoperative pain decreased at 5-week (3.97 ± 10.04; p  
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Alternatives to penetrating mesh fixation, such as surgical glue, are being investigated for their potential benefit in reducing chronic pain. The aim of this study was to assess the efficacy of the n -hexyl cyanoacrylate glue Ifabond™ for mesh fixation in laparoscopic inguinal hernia repair. Methods This prospective, multicenter, single-arm study collected data from laparoscopic inguinal hernia repairs using Ifabond™ (Peters Surgical, Boulogne-Billancourt Cedex, France) and a standard [Promesh® SURG ST (Peters Surgical)/Biomesh® P1 (Cousin Biotech, Wervicq-Sud, France)] or lightweight [Promesh® SURG LI (Peters Surgical)/Premium® Implant (Cousin Biotech)] polypropylene mesh. The primary endpoint was postoperative pain [100-scale Visual Analog Scale (VAS)]. Secondary endpoints were complications, hernia recurrences, and quality of life (QoL) (EQ-5D-3L health index and EQ-VAS). Patients were followed up at 5 weeks and 12 months after surgery. Results Six-hundred and thirteen patients underwent laparoscopic inguinal hernia repair. Postoperative pain decreased at 5-week (3.97 ± 10.04; p  < 0.0001) and 12-month (3.83 ± 11.26; p  < 0.0001) follow-up compared with before surgery (26.96 ± 19.42). One hundred and fifteen patients (13.74%) experienced chronic pain in the groin at 12-month follow-up, of whom 14 (2.67%) required analgesics. There were 6 patients with major morbidities and one patient died of an unrelated cause. Two hernia recurrences occurred within 12-month follow-up. Patients’ QoL increased from an EQ-5D-3L index score of 0.82 ± 0.19 preoperatively to 0.90 ± 0.15 at 5 weeks ( p  < 0.0001) and 0.92 ± 0.15 at 12 months after surgery ( p  < 0.0001). The EQ-VAS general health scoring increased from 79.03 ± 12.69 preoperatively to 84.31 ± 9.97 at 5-week ( p  < 0.0001) and 84.16 ± 14.48 at 12-month follow-up ( p  < 0.0001). Conclusions Ifabond™ (Peters Surgical) is a safe, reliable, and feasible fixation method for laparoscopic inguinal hernia repair with a very high surgeon satisfaction score, improved patients’ QoL, and comparable risk of developing chronic pain and postoperative complications as described in the literature.]]></description><identifier>ISSN: 0930-2794</identifier><identifier>EISSN: 1432-2218</identifier><identifier>DOI: 10.1007/s00464-023-10439-6</identifier><identifier>PMID: 37798529</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Abdominal Surgery ; Chronic pain ; Gastroenterology ; Gynecology ; Hepatology ; Hernias ; Laparoscopy ; Medicine ; Medicine &amp; Public Health ; Proctology ; Surgery ; Surgical mesh ; Surgical outcomes</subject><ispartof>Surgical endoscopy, 2023-12, Vol.37 (12), p.9105-9115</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c326t-6c2c7bac9a02bce95709eed5c6ac97a570db0cc717c2b62f5f93ebd4114264fd3</cites><orcidid>0000-0001-8899-7834</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00464-023-10439-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00464-023-10439-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37798529$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dams, Anne</creatorcontrib><creatorcontrib>Vankeirsbilck, Joost</creatorcontrib><creatorcontrib>Poelmans, Stephan</creatorcontrib><creatorcontrib>Kerschaever, Ivan</creatorcontrib><creatorcontrib>Borreman, Philippe</creatorcontrib><creatorcontrib>Berwouts, Luc</creatorcontrib><creatorcontrib>De Mulder, Wim</creatorcontrib><creatorcontrib>Colle, Julien</creatorcontrib><creatorcontrib>Beunis, Anthony</creatorcontrib><creatorcontrib>Dhooghe, Vicky</creatorcontrib><creatorcontrib>Van De Winkel, Nele</creatorcontrib><creatorcontrib>Allaeys, Mathias</creatorcontrib><creatorcontrib>Ruyssers, Michael</creatorcontrib><creatorcontrib>Haesen, Dorien</creatorcontrib><creatorcontrib>Van der Speeten, Kurt</creatorcontrib><title>Cyanoacrylate mesh fixation for laparoscopic inguinal hernia repair: a prospective, multicenter, single-arm study</title><title>Surgical endoscopy</title><addtitle>Surg Endosc</addtitle><addtitle>Surg Endosc</addtitle><description><![CDATA[Background Inguinal hernia repair is among the most frequently performed surgical procedures. Alternatives to penetrating mesh fixation, such as surgical glue, are being investigated for their potential benefit in reducing chronic pain. The aim of this study was to assess the efficacy of the n -hexyl cyanoacrylate glue Ifabond™ for mesh fixation in laparoscopic inguinal hernia repair. Methods This prospective, multicenter, single-arm study collected data from laparoscopic inguinal hernia repairs using Ifabond™ (Peters Surgical, Boulogne-Billancourt Cedex, France) and a standard [Promesh® SURG ST (Peters Surgical)/Biomesh® P1 (Cousin Biotech, Wervicq-Sud, France)] or lightweight [Promesh® SURG LI (Peters Surgical)/Premium® Implant (Cousin Biotech)] polypropylene mesh. The primary endpoint was postoperative pain [100-scale Visual Analog Scale (VAS)]. Secondary endpoints were complications, hernia recurrences, and quality of life (QoL) (EQ-5D-3L health index and EQ-VAS). Patients were followed up at 5 weeks and 12 months after surgery. Results Six-hundred and thirteen patients underwent laparoscopic inguinal hernia repair. Postoperative pain decreased at 5-week (3.97 ± 10.04; p  < 0.0001) and 12-month (3.83 ± 11.26; p  < 0.0001) follow-up compared with before surgery (26.96 ± 19.42). One hundred and fifteen patients (13.74%) experienced chronic pain in the groin at 12-month follow-up, of whom 14 (2.67%) required analgesics. There were 6 patients with major morbidities and one patient died of an unrelated cause. Two hernia recurrences occurred within 12-month follow-up. Patients’ QoL increased from an EQ-5D-3L index score of 0.82 ± 0.19 preoperatively to 0.90 ± 0.15 at 5 weeks ( p  < 0.0001) and 0.92 ± 0.15 at 12 months after surgery ( p  < 0.0001). The EQ-VAS general health scoring increased from 79.03 ± 12.69 preoperatively to 84.31 ± 9.97 at 5-week ( p  < 0.0001) and 84.16 ± 14.48 at 12-month follow-up ( p  < 0.0001). Conclusions Ifabond™ (Peters Surgical) is a safe, reliable, and feasible fixation method for laparoscopic inguinal hernia repair with a very high surgeon satisfaction score, improved patients’ QoL, and comparable risk of developing chronic pain and postoperative complications as described in the literature.]]></description><subject>Abdominal Surgery</subject><subject>Chronic pain</subject><subject>Gastroenterology</subject><subject>Gynecology</subject><subject>Hepatology</subject><subject>Hernias</subject><subject>Laparoscopy</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Proctology</subject><subject>Surgery</subject><subject>Surgical mesh</subject><subject>Surgical outcomes</subject><issn>0930-2794</issn><issn>1432-2218</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kU1PFTEUhhuikQv6B1yYJm5YUGlPZ6ZTd-ZG0ISEDaybM50zUDJftDOG--8pXsTEhaum7fO-7cnD2EclvygpzVmSsqgKIUELJQttRXXANqrQIABU_YZtpNVSgLHFITtK6V5m3qryHTvUxti6BLthD9sdjhP6uOtxIT5QuuNdeMQlTCPvpsh7nDFOyU9z8DyMt2sYsed3FMeAPNKMIX7lyOfMzOSX8ItO-bD2S_A0LhRPecqhngTGgadlbXfv2dsO-0QfXtZjdnP-_Xr7Q1xeXfzcfrsUXkO1iMqDNw16ixIaT7Y00hK1pa_ymcG8bRvpvVHGQ1NBV3ZWU9MWShVQFV2rj9nJvjd_7WGltLghJE99jyNNa3JQm0xKCXVGP_-D3k9rzHM-U9aWCmqwmYI95fOsKVLn5hgGjDunpHsW4vZCXBbifgtxVQ59eqlem4Ha18gfAxnQeyDlq_GW4t-3_1P7BF5gmEQ</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Dams, Anne</creator><creator>Vankeirsbilck, Joost</creator><creator>Poelmans, Stephan</creator><creator>Kerschaever, Ivan</creator><creator>Borreman, Philippe</creator><creator>Berwouts, Luc</creator><creator>De Mulder, Wim</creator><creator>Colle, Julien</creator><creator>Beunis, Anthony</creator><creator>Dhooghe, Vicky</creator><creator>Van De Winkel, Nele</creator><creator>Allaeys, Mathias</creator><creator>Ruyssers, Michael</creator><creator>Haesen, Dorien</creator><creator>Van der Speeten, Kurt</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</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>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8899-7834</orcidid></search><sort><creationdate>20231201</creationdate><title>Cyanoacrylate mesh fixation for laparoscopic inguinal hernia repair: a prospective, multicenter, single-arm study</title><author>Dams, Anne ; Vankeirsbilck, Joost ; Poelmans, Stephan ; Kerschaever, Ivan ; Borreman, Philippe ; Berwouts, Luc ; De Mulder, Wim ; Colle, Julien ; Beunis, Anthony ; Dhooghe, Vicky ; Van De Winkel, Nele ; Allaeys, Mathias ; Ruyssers, Michael ; Haesen, Dorien ; Van der Speeten, Kurt</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-6c2c7bac9a02bce95709eed5c6ac97a570db0cc717c2b62f5f93ebd4114264fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abdominal Surgery</topic><topic>Chronic pain</topic><topic>Gastroenterology</topic><topic>Gynecology</topic><topic>Hepatology</topic><topic>Hernias</topic><topic>Laparoscopy</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Proctology</topic><topic>Surgery</topic><topic>Surgical mesh</topic><topic>Surgical outcomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dams, Anne</creatorcontrib><creatorcontrib>Vankeirsbilck, Joost</creatorcontrib><creatorcontrib>Poelmans, Stephan</creatorcontrib><creatorcontrib>Kerschaever, Ivan</creatorcontrib><creatorcontrib>Borreman, Philippe</creatorcontrib><creatorcontrib>Berwouts, Luc</creatorcontrib><creatorcontrib>De Mulder, Wim</creatorcontrib><creatorcontrib>Colle, Julien</creatorcontrib><creatorcontrib>Beunis, Anthony</creatorcontrib><creatorcontrib>Dhooghe, Vicky</creatorcontrib><creatorcontrib>Van De Winkel, Nele</creatorcontrib><creatorcontrib>Allaeys, Mathias</creatorcontrib><creatorcontrib>Ruyssers, Michael</creatorcontrib><creatorcontrib>Haesen, Dorien</creatorcontrib><creatorcontrib>Van der Speeten, Kurt</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Surgical endoscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dams, Anne</au><au>Vankeirsbilck, Joost</au><au>Poelmans, Stephan</au><au>Kerschaever, Ivan</au><au>Borreman, Philippe</au><au>Berwouts, Luc</au><au>De Mulder, Wim</au><au>Colle, Julien</au><au>Beunis, Anthony</au><au>Dhooghe, Vicky</au><au>Van De Winkel, Nele</au><au>Allaeys, Mathias</au><au>Ruyssers, Michael</au><au>Haesen, Dorien</au><au>Van der Speeten, Kurt</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cyanoacrylate mesh fixation for laparoscopic inguinal hernia repair: a prospective, multicenter, single-arm study</atitle><jtitle>Surgical endoscopy</jtitle><stitle>Surg Endosc</stitle><addtitle>Surg Endosc</addtitle><date>2023-12-01</date><risdate>2023</risdate><volume>37</volume><issue>12</issue><spage>9105</spage><epage>9115</epage><pages>9105-9115</pages><issn>0930-2794</issn><eissn>1432-2218</eissn><abstract><![CDATA[Background Inguinal hernia repair is among the most frequently performed surgical procedures. Alternatives to penetrating mesh fixation, such as surgical glue, are being investigated for their potential benefit in reducing chronic pain. The aim of this study was to assess the efficacy of the n -hexyl cyanoacrylate glue Ifabond™ for mesh fixation in laparoscopic inguinal hernia repair. Methods This prospective, multicenter, single-arm study collected data from laparoscopic inguinal hernia repairs using Ifabond™ (Peters Surgical, Boulogne-Billancourt Cedex, France) and a standard [Promesh® SURG ST (Peters Surgical)/Biomesh® P1 (Cousin Biotech, Wervicq-Sud, France)] or lightweight [Promesh® SURG LI (Peters Surgical)/Premium® Implant (Cousin Biotech)] polypropylene mesh. The primary endpoint was postoperative pain [100-scale Visual Analog Scale (VAS)]. Secondary endpoints were complications, hernia recurrences, and quality of life (QoL) (EQ-5D-3L health index and EQ-VAS). Patients were followed up at 5 weeks and 12 months after surgery. Results Six-hundred and thirteen patients underwent laparoscopic inguinal hernia repair. Postoperative pain decreased at 5-week (3.97 ± 10.04; p  < 0.0001) and 12-month (3.83 ± 11.26; p  < 0.0001) follow-up compared with before surgery (26.96 ± 19.42). One hundred and fifteen patients (13.74%) experienced chronic pain in the groin at 12-month follow-up, of whom 14 (2.67%) required analgesics. There were 6 patients with major morbidities and one patient died of an unrelated cause. Two hernia recurrences occurred within 12-month follow-up. Patients’ QoL increased from an EQ-5D-3L index score of 0.82 ± 0.19 preoperatively to 0.90 ± 0.15 at 5 weeks ( p  < 0.0001) and 0.92 ± 0.15 at 12 months after surgery ( p  < 0.0001). The EQ-VAS general health scoring increased from 79.03 ± 12.69 preoperatively to 84.31 ± 9.97 at 5-week ( p  < 0.0001) and 84.16 ± 14.48 at 12-month follow-up ( p  < 0.0001). Conclusions Ifabond™ (Peters Surgical) is a safe, reliable, and feasible fixation method for laparoscopic inguinal hernia repair with a very high surgeon satisfaction score, improved patients’ QoL, and comparable risk of developing chronic pain and postoperative complications as described in the literature.]]></abstract><cop>New York</cop><pub>Springer US</pub><pmid>37798529</pmid><doi>10.1007/s00464-023-10439-6</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-8899-7834</orcidid></addata></record>
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subjects Abdominal Surgery
Chronic pain
Gastroenterology
Gynecology
Hepatology
Hernias
Laparoscopy
Medicine
Medicine & Public Health
Proctology
Surgery
Surgical mesh
Surgical outcomes
title Cyanoacrylate mesh fixation for laparoscopic inguinal hernia repair: a prospective, multicenter, single-arm study
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