Short-term safety outcomes of mastectomy and immediate prepectoral implant-based breast reconstruction: Pre-BRA prospective multicentre cohort study

Author:

Harvey Kate L1,Sinai Parisa1,Mills Nicola1,White Paul2,Holcombe Christopher3,Potter Shelley14ORCID,Barry Peter,O'Connell Rachel,Cawthorn Simon,Gardiner Matthew,Irwin Gareth,Kirwan Cliona,McKenzie Mairead,McKenzie Shireen,Oni Georgette,Whisker Lisa,Rattay Tim,Roy Pankaj,Skillman Joanna,Soumian Soni,Vidya Raghavan,Williams Samantha,

Affiliation:

1. National Institute for Health Research Bristol Biomedical Research Centre, University Hospitals Bristol NHS Foundation Trust and University of Bristol, Bristol, UK

2. Applied Statistics Group, University of the West of England, Bristol, UK

3. Breast Unit, Royal Liverpool University Hospital, Liverpool, UK

4. Bristol Breast Care Centre, North Bristol NHS Trust, Bristol, UK

Abstract

Abstract Background Prepectoral breast reconstruction (PPBR) has recently been introduced to reduce postoperative pain and improve cosmetic outcomes in women having implant-based procedures. High-quality evidence to support the practice of PPBR, however, is lacking. Pre-BRA is an IDEAL stage 2a/2b study that aimed to establish the safety, effectiveness, and stability of PPBR before definitive evaluation in an RCT. The short-term safety endpoints at 3 months after surgery are reported here. Methods Consecutive patients electing to undergo immediate PPBR at participating UK centres between July 2019 and December 2020 were invited to participate. Demographic, operative, oncology, and complication data were collected. The primary outcome was implant loss at 3 months. Other outcomes of interest included readmission, reoperation, and infection. Results Some 347 women underwent 424 immediate implant-based reconstructions at 40 centres. Most were single-stage direct-to-implant (357, 84.2 per cent) biological mesh-assisted (341, 80.4 per cent) procedures. Conversion to subpectoral reconstruction was necessary in four patients (0.9 per cent) owing to poor skin-flap quality. Of the 343 women who underwent PPBR, 144 (42.0 per cent) experienced at least one postoperative complication. Implant loss occurred in 28 women (8.2 per cent), 67 (19.5 per cent) experienced an infection, 60 (17.5 per cent) were readmitted for a complication, and 55 (16.0 per cent) required reoperation within 3 months of reconstruction. Conclusion Complication rates following PPBR are high and implant loss is comparable to that associated with subpectoral mesh-assisted implant-based techniques. These findings support the need for a well-designed RCT comparing prepectoral and subpectoral reconstruction to establish best practice for implant-based breast reconstruction.

Funder

One Year Royal College of Surgeons Blond McIndoe Foundation

NIHR Biomedical Research Centre

University Hospitals Bristol NHS Foundation Trust

University of Bristol

Publisher

Oxford University Press (OUP)

Subject

Surgery

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