Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial

Detalhes bibliográficos
Autor(a) principal: Veiga, Daniela Francescato [UNIFESP]
Data de Publicação: 2013
Outros Autores: Veiga-Filho, Joel, Damasceno, Carlos Americo Veiga, Sales, Edilaine Maria Leci, Morais, Thiago Bezerra, Almeida, Wania Eliza, Novo, Neil Ferreira, Ferreira, Lydia Masako [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/35982
http://dx.doi.org/10.1186/1745-6215-14-58
Resumo: Background: One of the major risk variables for surgical site infection is wound management. Understanding infection risk factors for breast operations is essential in order to develop infection-prevention strategies and improve surgical outcomes. the aim of this trial is to assess the influence of dressing wear time on surgical site infection rates and skin colonization. Patients' perception at self-assessment will also be analyzed.Methods/Design: This is a two-arm randomized controlled trial. Two hundred breast cancer patients undergoing immediate or delayed breast reconstruction will be prospectively enrolled. Patients will be randomly allocated to group I (dressing removed on postoperative day one) or group II (dressing removed on postoperative day six). Surgical site infections will be defined by standard criteria from the Centers for Disease Control and Prevention (CDC). Skin colonization will be assessed by culture of samples collected at predefined time points. Patients will score dressing wear time with regard to safety, comfort and convenience.Discussion: the evidence to support dressing standards for breast surgery wounds is empiric and scarce. CDC recommends protecting, with a sterile dressing for 24 to 48 hours postoperatively, a primarily closed incision, but there is no recommendation to cover this kind of incision beyond 48 hours, or on the appropriate time to shower or bathe with an uncovered incision. the results of the ongoing trial may support standard recommendations regarding dressing wear time after breast reconstruction.
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spelling Veiga, Daniela Francescato [UNIFESP]Veiga-Filho, JoelDamasceno, Carlos Americo VeigaSales, Edilaine Maria LeciMorais, Thiago BezerraAlmeida, Wania ElizaNovo, Neil FerreiraFerreira, Lydia Masako [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Univ Vale do Sapucai2016-01-24T14:31:16Z2016-01-24T14:31:16Z2013-02-22Trials. London: Biomed Central Ltd, v. 14, 6 p., 2013.1745-6215http://repositorio.unifesp.br/handle/11600/35982http://dx.doi.org/10.1186/1745-6215-14-58WOS000315877300002.pdf10.1186/1745-6215-14-58WOS:000315877300002Background: One of the major risk variables for surgical site infection is wound management. Understanding infection risk factors for breast operations is essential in order to develop infection-prevention strategies and improve surgical outcomes. the aim of this trial is to assess the influence of dressing wear time on surgical site infection rates and skin colonization. Patients' perception at self-assessment will also be analyzed.Methods/Design: This is a two-arm randomized controlled trial. Two hundred breast cancer patients undergoing immediate or delayed breast reconstruction will be prospectively enrolled. Patients will be randomly allocated to group I (dressing removed on postoperative day one) or group II (dressing removed on postoperative day six). Surgical site infections will be defined by standard criteria from the Centers for Disease Control and Prevention (CDC). Skin colonization will be assessed by culture of samples collected at predefined time points. Patients will score dressing wear time with regard to safety, comfort and convenience.Discussion: the evidence to support dressing standards for breast surgery wounds is empiric and scarce. CDC recommends protecting, with a sterile dressing for 24 to 48 hours postoperatively, a primarily closed incision, but there is no recommendation to cover this kind of incision beyond 48 hours, or on the appropriate time to shower or bathe with an uncovered incision. the results of the ongoing trial may support standard recommendations regarding dressing wear time after breast reconstruction.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)Universidade Federal de São Paulo, Dept Surg, Div Plast Surg, São Paulo, BrazilUniv Vale do Sapucai, Dept Surg, Div Plast Surg, Pouso Alegre, BrazilUniv Vale do Sapucai, Dept Microbiol, Pouso Alegre, BrazilUniv Vale do Sapucai, Sch Med, Pouso Alegre, BrazilUniv Vale do Sapucai, Dept Bioestat, Pouso Alegre, BrazilUniversidade Federal de São Paulo, Div Plast Surg, BR-04024002 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Surg, Div Plast Surg, São Paulo, BrazilUniversidade Federal de São Paulo, Div Plast Surg, BR-04024002 São Paulo, BrazilCNPq: 480644/2011-0Web of Science6engBiomed Central LtdTrialsBreast cancerBreast reconstructionPostoperative careDressingsSurgical wound infectionBacterial growthPatient satisfactionDressing wear time after breast reconstruction: study protocol for a randomized controlled trialinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALWOS000315877300002.pdfapplication/pdf240433${dspace.ui.url}/bitstream/11600/35982/1/WOS000315877300002.pdf77203bfdaa29694c89776867f04559b1MD51open accessTEXTWOS000315877300002.pdf.txtWOS000315877300002.pdf.txtExtracted texttext/plain30285${dspace.ui.url}/bitstream/11600/35982/2/WOS000315877300002.pdf.txtc012fe00f88e795adc10fe4173ea3fa1MD52open access11600/359822022-09-27 09:48:33.217open accessoai:repositorio.unifesp.br:11600/35982Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:23:28.388013Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial
title Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial
spellingShingle Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial
Veiga, Daniela Francescato [UNIFESP]
Breast cancer
Breast reconstruction
Postoperative care
Dressings
Surgical wound infection
Bacterial growth
Patient satisfaction
title_short Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial
title_full Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial
title_fullStr Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial
title_full_unstemmed Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial
title_sort Dressing wear time after breast reconstruction: study protocol for a randomized controlled trial
author Veiga, Daniela Francescato [UNIFESP]
author_facet Veiga, Daniela Francescato [UNIFESP]
Veiga-Filho, Joel
Damasceno, Carlos Americo Veiga
Sales, Edilaine Maria Leci
Morais, Thiago Bezerra
Almeida, Wania Eliza
Novo, Neil Ferreira
Ferreira, Lydia Masako [UNIFESP]
author_role author
author2 Veiga-Filho, Joel
Damasceno, Carlos Americo Veiga
Sales, Edilaine Maria Leci
Morais, Thiago Bezerra
Almeida, Wania Eliza
Novo, Neil Ferreira
Ferreira, Lydia Masako [UNIFESP]
author2_role author
author
author
author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Univ Vale do Sapucai
dc.contributor.author.fl_str_mv Veiga, Daniela Francescato [UNIFESP]
Veiga-Filho, Joel
Damasceno, Carlos Americo Veiga
Sales, Edilaine Maria Leci
Morais, Thiago Bezerra
Almeida, Wania Eliza
Novo, Neil Ferreira
Ferreira, Lydia Masako [UNIFESP]
dc.subject.eng.fl_str_mv Breast cancer
Breast reconstruction
Postoperative care
Dressings
Surgical wound infection
Bacterial growth
Patient satisfaction
topic Breast cancer
Breast reconstruction
Postoperative care
Dressings
Surgical wound infection
Bacterial growth
Patient satisfaction
description Background: One of the major risk variables for surgical site infection is wound management. Understanding infection risk factors for breast operations is essential in order to develop infection-prevention strategies and improve surgical outcomes. the aim of this trial is to assess the influence of dressing wear time on surgical site infection rates and skin colonization. Patients' perception at self-assessment will also be analyzed.Methods/Design: This is a two-arm randomized controlled trial. Two hundred breast cancer patients undergoing immediate or delayed breast reconstruction will be prospectively enrolled. Patients will be randomly allocated to group I (dressing removed on postoperative day one) or group II (dressing removed on postoperative day six). Surgical site infections will be defined by standard criteria from the Centers for Disease Control and Prevention (CDC). Skin colonization will be assessed by culture of samples collected at predefined time points. Patients will score dressing wear time with regard to safety, comfort and convenience.Discussion: the evidence to support dressing standards for breast surgery wounds is empiric and scarce. CDC recommends protecting, with a sterile dressing for 24 to 48 hours postoperatively, a primarily closed incision, but there is no recommendation to cover this kind of incision beyond 48 hours, or on the appropriate time to shower or bathe with an uncovered incision. the results of the ongoing trial may support standard recommendations regarding dressing wear time after breast reconstruction.
publishDate 2013
dc.date.issued.fl_str_mv 2013-02-22
dc.date.accessioned.fl_str_mv 2016-01-24T14:31:16Z
dc.date.available.fl_str_mv 2016-01-24T14:31:16Z
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dc.identifier.citation.fl_str_mv Trials. London: Biomed Central Ltd, v. 14, 6 p., 2013.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/35982
http://dx.doi.org/10.1186/1745-6215-14-58
dc.identifier.issn.none.fl_str_mv 1745-6215
dc.identifier.file.none.fl_str_mv WOS000315877300002.pdf
dc.identifier.doi.none.fl_str_mv 10.1186/1745-6215-14-58
dc.identifier.wos.none.fl_str_mv WOS:000315877300002
identifier_str_mv Trials. London: Biomed Central Ltd, v. 14, 6 p., 2013.
1745-6215
WOS000315877300002.pdf
10.1186/1745-6215-14-58
WOS:000315877300002
url http://repositorio.unifesp.br/handle/11600/35982
http://dx.doi.org/10.1186/1745-6215-14-58
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dc.publisher.none.fl_str_mv Biomed Central Ltd
publisher.none.fl_str_mv Biomed Central Ltd
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instname:Universidade Federal de São Paulo (UNIFESP)
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