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dc.contributor.authorAcea Nebril, Benigno 
dc.contributor.authorGarcía-Novoa, A.
dc.contributor.authorJiménez, L.G.
dc.date.accessioned2025-08-26T11:07:47Z
dc.date.available2025-08-26T11:07:47Z
dc.date.issued2022
dc.identifier.citationAcea-Nebril B, García-Novoa A, Jiménez LG. The PreQ-20 TRIAL: A prospective cohort study of the oncologic safety, quality of life and cosmetic outcomes of patients undergoing prepectoral breast reconstruction. PLoS ONE. 2022;17(7 July).
dc.identifier.issn1932-6203
dc.identifier.otherhttps://portalcientifico.sergas.gal/documentos/6505d4a57ef4a16255edb6e9*
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20855
dc.description.abstractBackground Mastectomy currently constitutes a necessary surgical procedure in the oncologic setting and in the context of high risk. Prepectoral breast reconstruction (PBR) has been proposed as a surgical alternative to retropectoral techniques by providing less postoperative morbidity and a better cosmetic result. However, there is a lack of prospective studies that have evaluated its safety and patient-reported satisfaction. Methods We conducted a prospective cohort study to assess the safety, quality of life and cosmetic sequelae of PBR in women with breast cancer and high risk. The study's main objective is to assess the safety of PBR in terms of postsurgical complications and the feasibility of reconstruction (loss of implants). The secondary objectives are to evaluate oncologic safety (local relapses, residual glandular tissue) and to identify factors related to quality of life and cosmetic sequelae. The evaluation of residual tissue will be conducted by MRI 12 to 18 months after the surgery, and the quality-of-life assessment will be performed using the Breast-Q questionnaire. An initial patient evaluation will be conducted 12-18 months after the surgery, and a second evaluation will be performed at 5 years. The estimated sample size is 81 patients. Discussion The PreQ-20 study will analyze the impact of PBR on 3 separate measures: safety, quality of life and cosmetic sequelae. Unlike other studies that analyzed these three measures jointly for women with breast cancer and high risk, this study will individualize the results for these 2 patient groups. This differentiation is necessary from the methodological point of view, given that the 2 patient groups have separate clinical and emotional implications. The assessment of these groups will focus on the following aspects: postoperative complications, local relapses, evaluation of residual glandular tissue and incidence rate of primary tumors in the same, the cosmetic sequelae and the satisfaction and the quality-of-life assessment by the patients.en
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleThe PreQ-20 TRIAL: A prospective cohort study of the oncologic safety, quality of life and cosmetic outcomes of patients undergoing prepectoral breast reconstruction*
dc.typeArticleen
dc.authorsophosAcea-Nebril, L. G. B.
dc.authorsophosGarcía-Novoa, A.
dc.authorsophosJiménez
dc.identifier.doi10.1371/journal.pone.0269426
dc.identifier.sophos6505d4a57ef4a16255edb6e9
dc.issue.number7 July
dc.journal.titlePLoS ONE*
dc.relation.publisherversionhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0269426&type=printablees
dc.rights.accessRightsopenAccess
dc.subject.keywordINIBICes
dc.subject.keywordAS Coruñaes
dc.subject.keywordCHUACes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number17


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