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Patient-reported outcomes of immediate implant-based breast reconstruction with and without biological or synthetic mesh.
Sewart, E; Turner, N L; Conroy, E J; Cutress, R I; Skillman, J; Whisker, L; Thrush, S; Barnes, N; Holcombe, C; Potter, S.
Afiliación
  • Sewart E; Population Health Sciences, Bristol Centre for Surgical Research, Bristol Medical School, Bristol, UK.
  • Turner NL; Population Health Sciences, Bristol Centre for Surgical Research, Bristol Medical School, Bristol, UK.
  • Conroy EJ; Liverpool Clinical Trials Centre, University of Liverpool, Liverpool, UK.
  • Cutress RI; Cancer Sciences Unit, Faculty of Medicine, University of Southampton, University Hospital Southampton, Southampton, UK.
  • Skillman J; Department of Plastic Surgery, University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
  • Whisker L; Nottingham Breast Institute, Nottingham University Hospitals NHS Trust, Nottingham, UK.
  • Thrush S; Breast Unit, Worcester Royal Hospital, Worcester, UK.
  • Barnes N; Nightingale Breast Unit, Manchester University NHS Foundation Trust, Manchester, UK.
  • Holcombe C; Linda McCartney Centre, Royal Liverpool and Broadgreen University Hospital, Liverpool, UK.
  • Potter S; Population Health Sciences, Bristol Centre for Surgical Research, Bristol Medical School, Bristol, UK.
BJS Open ; 5(1)2021 01 08.
Article en En | MEDLINE | ID: mdl-33609398
ABSTRACT

BACKGROUND:

Biological and synthetic meshes may improve the outcomes of immediate implant-based breast reconstruction (IBBR) by facilitating single-stage procedures and improving cosmesis. Supporting evidence is, however, limited. The aim of this study was to explore the impact of biological and synthetic mesh on patient-reported outcomes (PROs) of IBBR 18 months after surgery.

METHODS:

Consecutive women undergoing immediate IBBR between February 2014 and June 2016 were recruited to the study. Demographic, operative, oncological and 3-month complication data were collected, and patients received validated BREAST-Q questionnaires at 18 months. The impact of different IBBR techniques on PROs were explored using mixed-effects regression models adjusted for clinically relevant confounders, and including a random effect to account for clustering by centre.

RESULTS:

A total of 1470 participants consented to receive the questionnaire and 891 completed it. Of these, 67 women underwent two-stage submuscular reconstructions. Some 764 patients had a submuscular reconstruction with biological mesh (495 women), synthetic mesh (95) or dermal sling (174). Fourteen patients had a prepectoral reconstruction. Compared with two-stage submuscular reconstructions, no significant differences in PROs were seen in biological or synthetic mesh-assisted or dermal sling procedures. However, patients undergoing prepectoral IBBR reported better satisfaction with breasts (adjusted mean difference +6.63, 95 per cent c.i. 1.65 to11.61; P = 0.009). PROs were similar to those in the National Mastectomy and Breast Reconstruction Audit 2008-2009 cohort, which included two-stage submuscular procedures only.

CONCLUSION:

This study found no difference in PROs of subpectoral IBBR with or without biological or synthetic mesh, but provides early data to suggest improved satisfaction with breasts following prepectoral reconstruction. Robust evaluation is required before this approach can be adopted as standard practice.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Mallas Quirúrgicas / Neoplasias de la Mama / Implantación de Mama / Medición de Resultados Informados por el Paciente / Mastectomía Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: BJS Open Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Mallas Quirúrgicas / Neoplasias de la Mama / Implantación de Mama / Medición de Resultados Informados por el Paciente / Mastectomía Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: BJS Open Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido