Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1186/s13063-016-1700-y https://repositorio.unifesp.br/handle/11600/56699 |
Resumo: | Background: The role of antibiotics in surgical procedures where the risk of surgical site infection (SSI) is low remains uncertain. There is, to date, no evidence to justify the routine use of antibiotics in postoperative reduction mammaplasty. The aim of this study is to evaluate the effect of postoperative antibiotic treatment on the occurrence of SSI after breast reduction surgery. Methods: This is a double-blind randomized clinical trial with 124 breast hypertrophy patients allocated to two treatment groups: antibiotic (n = 62) and placebo (n = 62). All patients will undergo reduction mammoplasty, performed by the same surgical team. The surgeons will raise the nipple-areola complex by the superomedial pedicle technique. The patients will receive antibiotics intravenously during anesthetic induction and every 6 hours thereafter during their 24-hour hospital stay. During discharge from the hospital, each patient will receive a numbered package containing either cephalexin or placebo capsules and will be directed to take one capsule every 6 hours for 7 days. Neither the surgery team nor the patients will know the contents of the capsules. Patients will be monitored for the occurrence of SSI once weekly during the first 30 days following hospital discharge by a single surgeon who is blinded to their treatment group. SSI will be evaluated based on the definition adopted by the Centers for Disease Control and Prevention. Discussion: Due to the variety of risk factors for SSI and limited case studies, conclusions regarding the effect of antibiotics on the occurrence of SSIs following reduction mammaplasty are potentially biased. In recent studies, perioperative antibiotic prophylaxis was effective in preventing infection and is therefore recommended in clinical practice. However, antibiotic use in the postoperative period still remains controversial. |
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Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trialPlastic surgeryMammaplastyWound infectionProphylaxisBackground: The role of antibiotics in surgical procedures where the risk of surgical site infection (SSI) is low remains uncertain. There is, to date, no evidence to justify the routine use of antibiotics in postoperative reduction mammaplasty. The aim of this study is to evaluate the effect of postoperative antibiotic treatment on the occurrence of SSI after breast reduction surgery. Methods: This is a double-blind randomized clinical trial with 124 breast hypertrophy patients allocated to two treatment groups: antibiotic (n = 62) and placebo (n = 62). All patients will undergo reduction mammoplasty, performed by the same surgical team. The surgeons will raise the nipple-areola complex by the superomedial pedicle technique. The patients will receive antibiotics intravenously during anesthetic induction and every 6 hours thereafter during their 24-hour hospital stay. During discharge from the hospital, each patient will receive a numbered package containing either cephalexin or placebo capsules and will be directed to take one capsule every 6 hours for 7 days. Neither the surgery team nor the patients will know the contents of the capsules. Patients will be monitored for the occurrence of SSI once weekly during the first 30 days following hospital discharge by a single surgeon who is blinded to their treatment group. SSI will be evaluated based on the definition adopted by the Centers for Disease Control and Prevention. Discussion: Due to the variety of risk factors for SSI and limited case studies, conclusions regarding the effect of antibiotics on the occurrence of SSIs following reduction mammaplasty are potentially biased. In recent studies, perioperative antibiotic prophylaxis was effective in preventing infection and is therefore recommended in clinical practice. However, antibiotic use in the postoperative period still remains controversial.Univ Fed Sao Paulo, Translat Surg Grad Program, Rua Napoleao Barros 725,4th Floor, BR-04024002 Sao Paulo, SP, BrazilUniv Vale Sapucai, Div Plast Surg, Ctr, Rua Comendador Jose Garcia 777, BR-37550000 Pouso Alegre, MG, BrazilTranslational Surgery Graduate Program, Universidade Federal de São Paulo (UNIFESP), Rua Napoleão de Barros, 725, 4th Floor, Vila Clementino, CEP: 04024-002 São Paulo, SP, BrazilWeb of ScienceConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)CNPq: 444087/2014FAPEMIG: APQ-00995-15Biomed Central Ltd2020-07-31T12:47:15Z2020-07-31T12:47:15Z2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion-application/pdfhttp://dx.doi.org/10.1186/s13063-016-1700-yTrials. London, v. 17, p. -, 2016.10.1186/s13063-016-1700-yWOS000388901200001.pdf1745-6215https://repositorio.unifesp.br/handle/11600/56699WOS:000388901200001engTrialsLondoninfo:eu-repo/semantics/openAccessGarcia, Edgard Silva [UNIFESP]Veiga, Daniela Francescato [UNIFESP]Veiga-Filho, JoelCabral, Isaias VieiraLarcher Pinto, Natylia LanaNovo, Neil Ferreira [UNIFESP]Sabino Neto, Miguel [UNIFESP]Ferreira, Lydia Masako [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-11T13:32:17Zoai:repositorio.unifesp.br/:11600/56699Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-11T13:32:17Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial |
title |
Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial |
spellingShingle |
Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial Garcia, Edgard Silva [UNIFESP] Plastic surgery Mammaplasty Wound infection Prophylaxis |
title_short |
Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial |
title_full |
Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial |
title_fullStr |
Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial |
title_full_unstemmed |
Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial |
title_sort |
Antibiotic prophylaxis in reduction mammaplasty: study protocol for a randomized controlled trial |
author |
Garcia, Edgard Silva [UNIFESP] |
author_facet |
Garcia, Edgard Silva [UNIFESP] Veiga, Daniela Francescato [UNIFESP] Veiga-Filho, Joel Cabral, Isaias Vieira Larcher Pinto, Natylia Lana Novo, Neil Ferreira [UNIFESP] Sabino Neto, Miguel [UNIFESP] Ferreira, Lydia Masako [UNIFESP] |
author_role |
author |
author2 |
Veiga, Daniela Francescato [UNIFESP] Veiga-Filho, Joel Cabral, Isaias Vieira Larcher Pinto, Natylia Lana Novo, Neil Ferreira [UNIFESP] Sabino Neto, Miguel [UNIFESP] Ferreira, Lydia Masako [UNIFESP] |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Garcia, Edgard Silva [UNIFESP] Veiga, Daniela Francescato [UNIFESP] Veiga-Filho, Joel Cabral, Isaias Vieira Larcher Pinto, Natylia Lana Novo, Neil Ferreira [UNIFESP] Sabino Neto, Miguel [UNIFESP] Ferreira, Lydia Masako [UNIFESP] |
dc.subject.por.fl_str_mv |
Plastic surgery Mammaplasty Wound infection Prophylaxis |
topic |
Plastic surgery Mammaplasty Wound infection Prophylaxis |
description |
Background: The role of antibiotics in surgical procedures where the risk of surgical site infection (SSI) is low remains uncertain. There is, to date, no evidence to justify the routine use of antibiotics in postoperative reduction mammaplasty. The aim of this study is to evaluate the effect of postoperative antibiotic treatment on the occurrence of SSI after breast reduction surgery. Methods: This is a double-blind randomized clinical trial with 124 breast hypertrophy patients allocated to two treatment groups: antibiotic (n = 62) and placebo (n = 62). All patients will undergo reduction mammoplasty, performed by the same surgical team. The surgeons will raise the nipple-areola complex by the superomedial pedicle technique. The patients will receive antibiotics intravenously during anesthetic induction and every 6 hours thereafter during their 24-hour hospital stay. During discharge from the hospital, each patient will receive a numbered package containing either cephalexin or placebo capsules and will be directed to take one capsule every 6 hours for 7 days. Neither the surgery team nor the patients will know the contents of the capsules. Patients will be monitored for the occurrence of SSI once weekly during the first 30 days following hospital discharge by a single surgeon who is blinded to their treatment group. SSI will be evaluated based on the definition adopted by the Centers for Disease Control and Prevention. Discussion: Due to the variety of risk factors for SSI and limited case studies, conclusions regarding the effect of antibiotics on the occurrence of SSIs following reduction mammaplasty are potentially biased. In recent studies, perioperative antibiotic prophylaxis was effective in preventing infection and is therefore recommended in clinical practice. However, antibiotic use in the postoperative period still remains controversial. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2020-07-31T12:47:15Z 2020-07-31T12:47:15Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1186/s13063-016-1700-y Trials. London, v. 17, p. -, 2016. 10.1186/s13063-016-1700-y WOS000388901200001.pdf 1745-6215 https://repositorio.unifesp.br/handle/11600/56699 WOS:000388901200001 |
url |
http://dx.doi.org/10.1186/s13063-016-1700-y https://repositorio.unifesp.br/handle/11600/56699 |
identifier_str_mv |
Trials. London, v. 17, p. -, 2016. 10.1186/s13063-016-1700-y WOS000388901200001.pdf 1745-6215 WOS:000388901200001 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Trials |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
- application/pdf |
dc.coverage.none.fl_str_mv |
London |
dc.publisher.none.fl_str_mv |
Biomed Central Ltd |
publisher.none.fl_str_mv |
Biomed Central Ltd |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268350200545280 |