Acticoat™ stimulates inflammation, but does not delay healing, in acute full-thickness excisional wounds
Acticoat™ has antimicrobial and anti‐inflammatory effects which aid wound healing. However, in vitro studies indicate that Acticoat™ is cytotoxic and clinical and in vivo studies suggest that it may delay healing in acute wounds. Therefore, this study investigated the effects of Acticoat™ on healing...
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Veröffentlicht in: | International wound journal 2016-12, Vol.13 (6), p.1344-1348 |
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description | Acticoat™ has antimicrobial and anti‐inflammatory effects which aid wound healing. However, in vitro studies indicate that Acticoat™ is cytotoxic and clinical and in vivo studies suggest that it may delay healing in acute wounds. Therefore, this study investigated the effects of Acticoat™ on healing in acute full‐thickness excisional wounds. Using a porcine model, healing was assessed on days 3, 6, 9 and 15 post‐wounding. Five wounds dressed with Acticoat™ and five wounds dressed with polyurethane film (control) were assessed per day (n = 40 wounds). The rate of healing, inflammatory response, restoration of the epithelium and blood vessel and collagen formation were evaluated. No difference was found in the rate of healing between wounds treated with Acticoat™ and the control wounds. Inflammation was increased in Acticoat™‐treated wounds on day 3 post‐wounding compared to the control wounds. However, by day 15 post‐wounding, the epithelium of the Acticoat™‐treated wounds closely resembled normal epithelium. Acticoat™‐treated wounds also contained a higher proportion of mature blood vessels, and differences in collagen deposition were apparent. Despite inducing an inflammatory response, Acticoat™ did not delay healing in acute wounds. Conversely, the improved quality of the epithelium and blood vessels within Acticoat™‐treated wounds indicates that Acticoat™ has a beneficial effect on healing. |
doi_str_mv | 10.1111/iwj.12525 |
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However, in vitro studies indicate that Acticoat™ is cytotoxic and clinical and in vivo studies suggest that it may delay healing in acute wounds. Therefore, this study investigated the effects of Acticoat™ on healing in acute full‐thickness excisional wounds. Using a porcine model, healing was assessed on days 3, 6, 9 and 15 post‐wounding. Five wounds dressed with Acticoat™ and five wounds dressed with polyurethane film (control) were assessed per day (n = 40 wounds). The rate of healing, inflammatory response, restoration of the epithelium and blood vessel and collagen formation were evaluated. No difference was found in the rate of healing between wounds treated with Acticoat™ and the control wounds. Inflammation was increased in Acticoat™‐treated wounds on day 3 post‐wounding compared to the control wounds. However, by day 15 post‐wounding, the epithelium of the Acticoat™‐treated wounds closely resembled normal epithelium. Acticoat™‐treated wounds also contained a higher proportion of mature blood vessels, and differences in collagen deposition were apparent. Despite inducing an inflammatory response, Acticoat™ did not delay healing in acute wounds. Conversely, the improved quality of the epithelium and blood vessels within Acticoat™‐treated wounds indicates that Acticoat™ has a beneficial effect on healing.</description><identifier>ISSN: 1742-4801</identifier><identifier>EISSN: 1742-481X</identifier><identifier>DOI: 10.1111/iwj.12525</identifier><identifier>PMID: 26561384</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Acticoat ; Animals ; Bandages ; Biopsy, Needle ; Disease Models, Animal ; Female ; Immunohistochemistry ; Inflammation ; Inflammation - physiopathology ; Nanocrystalline silver ; Nanoparticles ; Original ; Random Allocation ; Silver - pharmacology ; Statistics, Nonparametric ; Sus scrofa ; Swine ; Time Factors ; Wound healing ; Wound Healing - physiology ; Wounds and Injuries - pathology ; Wounds and Injuries - therapy</subject><ispartof>International wound journal, 2016-12, Vol.13 (6), p.1344-1348</ispartof><rights>2015 Medicalhelplines.com Inc and John Wiley & Sons Ltd</rights><rights>2015 Medicalhelplines.com Inc and John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4535-237530430425f5788089236134cf1f8926496351cb4e73c0759ab8106e5c06b73</citedby><cites>FETCH-LOGICAL-c4535-237530430425f5788089236134cf1f8926496351cb4e73c0759ab8106e5c06b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7949776/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7949776/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,1411,11541,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fiwj.12525$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26561384$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hartmann, Carol A</creatorcontrib><creatorcontrib>Rode, Heinz</creatorcontrib><creatorcontrib>Kramer, Beverley</creatorcontrib><title>Acticoat™ stimulates inflammation, but does not delay healing, in acute full-thickness excisional wounds</title><title>International wound journal</title><addtitle>Int Wound J</addtitle><description>Acticoat™ has antimicrobial and anti‐inflammatory effects which aid wound healing. However, in vitro studies indicate that Acticoat™ is cytotoxic and clinical and in vivo studies suggest that it may delay healing in acute wounds. Therefore, this study investigated the effects of Acticoat™ on healing in acute full‐thickness excisional wounds. Using a porcine model, healing was assessed on days 3, 6, 9 and 15 post‐wounding. Five wounds dressed with Acticoat™ and five wounds dressed with polyurethane film (control) were assessed per day (n = 40 wounds). The rate of healing, inflammatory response, restoration of the epithelium and blood vessel and collagen formation were evaluated. No difference was found in the rate of healing between wounds treated with Acticoat™ and the control wounds. Inflammation was increased in Acticoat™‐treated wounds on day 3 post‐wounding compared to the control wounds. However, by day 15 post‐wounding, the epithelium of the Acticoat™‐treated wounds closely resembled normal epithelium. Acticoat™‐treated wounds also contained a higher proportion of mature blood vessels, and differences in collagen deposition were apparent. Despite inducing an inflammatory response, Acticoat™ did not delay healing in acute wounds. Conversely, the improved quality of the epithelium and blood vessels within Acticoat™‐treated wounds indicates that Acticoat™ has a beneficial effect on healing.</description><subject>Acticoat</subject><subject>Animals</subject><subject>Bandages</subject><subject>Biopsy, Needle</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>Inflammation - physiopathology</subject><subject>Nanocrystalline silver</subject><subject>Nanoparticles</subject><subject>Original</subject><subject>Random Allocation</subject><subject>Silver - pharmacology</subject><subject>Statistics, Nonparametric</subject><subject>Sus scrofa</subject><subject>Swine</subject><subject>Time Factors</subject><subject>Wound healing</subject><subject>Wound Healing - physiology</subject><subject>Wounds and Injuries - pathology</subject><subject>Wounds and Injuries - therapy</subject><issn>1742-4801</issn><issn>1742-481X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kd1OFDEYhhuiEUQPuAHSQ00Y6H9nTkzIRvkJYmIgcNZ0uh22S6ddpx2XPfdKvDSvxOrCBg9smvRL-7zv96UvAHsYHeKyjtxyfogJJ3wL7GDJSMVqfPtiUyO8DV6nNEeINJzLV2CbCC4wrdkOmB-b7EzU-dePnzBl149eZ5ugC53Xfa-zi-EAtmOG01iuQyyF9XoFZ1Z7F-4OCgm1GbOF3eh9lWfO3AebErQPxqWi1h4u4xim6Q142Wmf7NvHcxdcf_p4NTmtLr6cnE2OLyrDOOUVoZJTxMomvOOyrlHdEFrGZabDXakFawTl2LTMSmqQ5I1ua4yE5QaJVtJd8GHtuxjb3k6NDXnQXi0G1-thpaJ26t-X4GbqLn5XsmGNlKIYvHs0GOK30aasepeM9V4HG8ekcE2EoEIQXND3a9QMMaXBdps2GKk_2aiSjfqbTWH3n8-1IZ_CKMDRGlg6b1f_d1JnN-dPltVa4VK2DxuFHu6VkOUf1c3lifp8Tr5eNrenakJ_Aw-Xqaw</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Hartmann, Carol A</creator><creator>Rode, Heinz</creator><creator>Kramer, Beverley</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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><scope>5PM</scope></search><sort><creationdate>201612</creationdate><title>Acticoat™ stimulates inflammation, but does not delay healing, in acute full-thickness excisional wounds</title><author>Hartmann, Carol A ; Rode, Heinz ; Kramer, Beverley</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4535-237530430425f5788089236134cf1f8926496351cb4e73c0759ab8106e5c06b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acticoat</topic><topic>Animals</topic><topic>Bandages</topic><topic>Biopsy, Needle</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Immunohistochemistry</topic><topic>Inflammation</topic><topic>Inflammation - physiopathology</topic><topic>Nanocrystalline silver</topic><topic>Nanoparticles</topic><topic>Original</topic><topic>Random Allocation</topic><topic>Silver - pharmacology</topic><topic>Statistics, Nonparametric</topic><topic>Sus scrofa</topic><topic>Swine</topic><topic>Time Factors</topic><topic>Wound healing</topic><topic>Wound Healing - physiology</topic><topic>Wounds and Injuries - pathology</topic><topic>Wounds and Injuries - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hartmann, Carol A</creatorcontrib><creatorcontrib>Rode, Heinz</creatorcontrib><creatorcontrib>Kramer, Beverley</creatorcontrib><collection>Istex</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>International wound journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Hartmann, Carol A</au><au>Rode, Heinz</au><au>Kramer, Beverley</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acticoat™ stimulates inflammation, but does not delay healing, in acute full-thickness excisional wounds</atitle><jtitle>International wound journal</jtitle><addtitle>Int Wound J</addtitle><date>2016-12</date><risdate>2016</risdate><volume>13</volume><issue>6</issue><spage>1344</spage><epage>1348</epage><pages>1344-1348</pages><issn>1742-4801</issn><eissn>1742-481X</eissn><abstract>Acticoat™ has antimicrobial and anti‐inflammatory effects which aid wound healing. However, in vitro studies indicate that Acticoat™ is cytotoxic and clinical and in vivo studies suggest that it may delay healing in acute wounds. Therefore, this study investigated the effects of Acticoat™ on healing in acute full‐thickness excisional wounds. Using a porcine model, healing was assessed on days 3, 6, 9 and 15 post‐wounding. Five wounds dressed with Acticoat™ and five wounds dressed with polyurethane film (control) were assessed per day (n = 40 wounds). The rate of healing, inflammatory response, restoration of the epithelium and blood vessel and collagen formation were evaluated. No difference was found in the rate of healing between wounds treated with Acticoat™ and the control wounds. Inflammation was increased in Acticoat™‐treated wounds on day 3 post‐wounding compared to the control wounds. However, by day 15 post‐wounding, the epithelium of the Acticoat™‐treated wounds closely resembled normal epithelium. Acticoat™‐treated wounds also contained a higher proportion of mature blood vessels, and differences in collagen deposition were apparent. Despite inducing an inflammatory response, Acticoat™ did not delay healing in acute wounds. Conversely, the improved quality of the epithelium and blood vessels within Acticoat™‐treated wounds indicates that Acticoat™ has a beneficial effect on healing.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>26561384</pmid><doi>10.1111/iwj.12525</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acticoat Animals Bandages Biopsy, Needle Disease Models, Animal Female Immunohistochemistry Inflammation Inflammation - physiopathology Nanocrystalline silver Nanoparticles Original Random Allocation Silver - pharmacology Statistics, Nonparametric Sus scrofa Swine Time Factors Wound healing Wound Healing - physiology Wounds and Injuries - pathology Wounds and Injuries - therapy |
title | Acticoat™ stimulates inflammation, but does not delay healing, in acute full-thickness excisional wounds |
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