Prepectoral vs Partial Subpectoral Two-Stage Implant-Based Breast Reconstruction
Trial Snapshot
- Phase
- Not Applicable
- Status
- Withdrawn
- Locations
- 1
- Primary Endpoint
- Patient satisfaction as measured by BREAST-Q-scores
Study Overview
Brief Summary
The purpose of this study is to investigate the to analyze the patient satisfaction and complication rates under controlled conditions of the increasingly popular prepectoral technique for implant-based breast reconstruction.
Detailed Description
This is a single center, single-blinded, randomized clinical trial involving adult women undergoing two-stage implant-based breast reconstruction for either breast cancer or breast cancer risk reduction. The aim is to generate high quality evidence before establishing the prepectoral technique as routine care. A favorable safety and patient satisfaction profile will bring high quality evidence supporting the adoption of a technique that has shown similar complication rates while eliminating animation deformity and its associated pain and discomfort in retrospective and non-randomized studies.
The mastectomy flap perfusion will be assessed clinically and using SPY fluorescence imaging. Immediately following mastectomy, participants will be randomized to one of two treatment arms.
Group A will be composed of participants who will undergo prepectoral reconstruction with Acellular Dermal Matrix (ADM) by means of the anterior tenting technique. In this technique, two sheets of contour, fenestrated ADM sutured together are trimmed in accordance with the measurement of the expander/implant and fixed to the pectoralis major muscle covering the entire anterior surface of the device
Group B (current standard of care (SOC)) will be composed of participants who will undergo partial subpectoral reconstruction with ADM by means of the sling technique. In this technique the leading edge of the pectoral muscle is elevated and a subpectoral pocket is fashioned. The lower medial origin muscle fibers are released for anatomical expander seating. An ADM sling is sutured from the leading edge of the pectoralis muscle to the inframammary fold (over the expander) and laterally to close the expander pocket.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 19 Years to — (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •- Undergoing two-stage implant-based breast reconstruction for either breast cancer or breast cancer risk reduction
Exclusion Criteria
- •Active use of any tobacco products
- •Uncontrolled diabetes defined by HbA1c greater than 7.5%
- •Class II obesity or higher defined by a body mass index equal or greater than 35 kg/m2
- •History of radiation to the affect breast or chest
- •Immunocompromised patients
- •Clinical evidence of significant mastectomy flap ischemia prior to the initiation of the reconstructive procedure
Arms & Interventions
Prepectoral approach
Immediately following mastectomy, participants will undergo prepectoral reconstruction approach. Intraoperative filling volume will be decided by the attending surgeon based on the pocket dimension and volume capabilities. Participants will be evaluated at 6 time points during the study.
Intervention: Prepectoral approach (Procedure)
Partial subpectoral approach
Immediately following mastectomy, participants will undergo partial subpectoral reconstruction approach. Intraoperative filling volume will be decided by the attending surgeon based on the pocket dimension and volume capabilities. Participants will be evaluated at 6 time points during the study.
Intervention: Partial Subpectoral approach (Procedure)
Outcomes
Primary Outcomes
Patient satisfaction as measured by BREAST-Q-scores
Time Frame: postoperative day 90 +/-30 days
Patient satisfaction will be assessed using BREAST-Q-scores. BREAST-Q is a patient-reported outcome instrument used to assess the outcomes of different breast surgeries among women. Modules selected will be "Psychosocial Well-Being, Physical Well-Being: Chest and Satisfaction with Breasts" within the Reconstruction (Preoperative) module and "Psychosocial Well-Being, Physical Well-Being: Chest, Satisfaction with Breasts and Satisfaction with Implants" within the Reconstruction (Postoperative) module For each BRESAT-Q scale, items are summed and transformed to a score with range from 0 to 100, and with greater values representing more satisfaction and higher levels of breast related quality of life. A two-sample T-test will be used to assess the changes in mean scores of satisfaction between two arms
Patient satisfaction as measured by BREAST-Q-scores
Time Frame: Preoperatively
Patient satisfaction will be assessed using BREAST-Q-scores. BREAST-Q is a patient-reported outcome instrument used to assess the outcomes of different breast surgeries among women. Modules selected will be "Psychosocial Well-Being, Physical Well-Being: Chest and Satisfaction with Breasts" within the Reconstruction (Preoperative) module and "Psychosocial Well-Being, Physical Well-Being: Chest, Satisfaction with Breasts and Satisfaction with Implants" within the Reconstruction (Postoperative) module For each BRESAT-Q scale, items are summed and transformed to a score with range from 0 to 100, and with greater values representing more satisfaction and higher levels of breast related quality of life. A two-sample T-test will be used to assess the changes in mean scores of satisfaction between two arms
Secondary Outcomes
- Overall complication rates(postoperative day 90 +/-30 days)
- Specific complication rates(postoperative day 21 +/-7 days)
- Postoperative pain intensity(postoperative day 21 +/-7 days)
- Overall complication rates(Preoperatively)
- Overall complication rates(Postoperative day 1)
- Overall complication rates(Postoperative day 7 +/-7 days)
- Overall complication rates(Postoperative day 14 +/-7 days)
- Overall complication rates(postoperative day 21 +/-7 days)
- Specific complication rates(Preoperatively)
- Specific complication rates(Postoperative day 1)
- Specific complication rates(Postoperative day 7 +/-7 days)
- Specific complication rates(Postoperative day 14 +/-7 days)
- Postoperative pain intensity(Postoperative day 1)
- Postoperative pain intensity(Postoperative day 7 +/-7 days)
- Postoperative pain intensity(Postoperative day 14 +/-7 days)