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. 2022 Mar 18;10(3):e4179.
doi: 10.1097/GOX.0000000000004179. eCollection 2022 Mar.

Implant-based Breast Reconstruction after Mastectomy for Breast Cancer: A Systematic Review and Meta-analysis

Affiliations

Implant-based Breast Reconstruction after Mastectomy for Breast Cancer: A Systematic Review and Meta-analysis

Ian J Saldanha et al. Plast Reconstr Surg Glob Open. .

Abstract

Women undergoing implant-based reconstruction (IBR) after mastectomy for breast cancer have numerous options, including timing of IBR relative to radiation and chemotherapy, implant materials, anatomic planes, and use of human acellular dermal matrices. We conducted a systematic review to evaluate these options.

Methods: We searched Medline, Embase, Cochrane CENTRAL, CINAHL, and ClinicalTrials.gov for studies, from inception to March 23, 2021, without language restriction. We assessed risk of bias and strength of evidence (SoE) using standard methods.

Results: We screened 15,936 citations. Thirty-six mostly high or moderate risk of bias studies (48,419 patients) met criteria. Timing of IBR before or after radiation may result in comparable physical, psychosocial, and sexual well-being, and satisfaction with breasts (all low SoE), and probably comparable risks of implant failure/loss or explantation (moderate SoE). No studies addressed timing relative to chemotherapy. Silicone and saline implants may result in clinically comparable satisfaction with breasts (low SoE). Whether the implant is in the prepectoral or total submuscular plane may not impact risk of infections (low SoE). Acellular dermal matrix use probably increases the risk of implant failure/loss or need for explant surgery (moderate SoE) and may increase the risk of infections (low SoE). Risks of seroma and unplanned repeat surgeries for revision are probably comparable (moderate SoE), and risk of necrosis may be comparable with or without human acellular dermal matrices (low SoE).

Conclusions: Evidence regarding IBR options is mostly of low SoE. New high-quality research is needed, especially for timing, implant materials, and anatomic planes of implant placement.

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Figures

Fig. 1.
Fig. 1.
PRISMA diagram depicting identification of studies in this SR.
Fig. 2.
Fig. 2.
Meta-analysis for timing of IBR relative to radiation (Outcome: Implant failure/loss or need for explant surgery). Abbreviations: adj = adjusted, CI = confidence interval, HR = hazard ratio = IBR = implant-based reconstruction, I2 = measure of statistical heterogeneity (% of total variability that is due to between-study variability), NR = not reported, OR = odds ratio, RTX = radiation therapy, y = years.
Fig. 3.
Fig. 3.
Meta-analyses for ADM use during IBR: A, Outcome: implant failure/loss or need for explant surgery. B, Outcome: infections. Abbreviations: ADM = acellular dermal matrix, CI = confidence interval, IBR = implant-based reconstruction, I2 = measure of statistical heterogeneity (% of total variability that is due to between-study variability), mo = months, NR = not reported, NRCS = nonrandomized comparative study, OR = odds ratio, RCT = randomized controlled trial, y = years.
Fig. 4.
Fig. 4.
Meta-analyses for ADM use during IBR: A, Outcome: necrosis. B, Outcome: Seroma. Abbreviations: ADM = acellular dermal matrix, CI = confidence interval, IBR = implant-based reconstruction, I2 = measure of statistical heterogeneity (% of total variability that is due to between-study variability), NR = not reported, OR = odds ratio.

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