Abstract
Perioperative identification of ischemic-hypoxic tissue is essential for reducing the risk of mastectomy skin flap necrosis (MSFN), a major complication following mastectomy. Implant-based breast reconstruction is jeopardized in the presence of MSFN. However, existing technologies are limited by depth insensitivity, dye-related risks, the need for contact sensors, and an inability to simultaneously assess both blood flow and oxygenation. A multi-wavelength speckle contrast diffuse correlation tomography (MW-scDCT) system was developed for noncontact, dye-free, and depth-sensitive imaging of tissue hemodynamics in a rat model incorporating four distinct flap scenarios: sham (SH), implant (IM), half necrosis (HN), and full necrosis (FN), representing varying degrees of tissue viability. MW-scDCT measured longitudinal changes in relative blood flow index (rBFI) and oxy- and deoxy-hemoglobin concentrations (∆[HbO2] and ∆[Hb]) over seven days. Repeated measures analysis of variance and quadratic discriminant analysis were employed for statistical analysis. MW-scDCT enabled longitudinal imaging of tissue blood flow and oxygenation distributions, revealing significant differences across flap types and over time. In terms of discriminative power, integrating rBFI, ∆[HbO2], and ∆[Hb] into a multivariable classification model substantially improved accuracy, achieving 80-95% compared to 40-70% using individual parameters. Binary classification of necrotic (FN + HN) versus non-necrotic (SH + IM) flaps showed up to 50% improvement in accuracy gains. MW-scDCT effectively distinguished necrotic from viable flaps and provided critical early postoperative insights into MSFN. These findings support its potential clinical utility as a perioperative monitoring tool to guide decision-making, reduce flap failure risk, and improve reconstructive outcomes.
| Original language | English |
|---|---|
| Pages (from-to) | 3740-3758 |
| Number of pages | 19 |
| Journal | Biomedical Optics Express |
| Volume | 16 |
| Issue number | 9 |
| DOIs | |
| State | Published - Sep 1 2025 |
Bibliographical note
Publisher Copyright:© 2025 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement.
Funding
Acknowledgements. We acknowledge financial support from the National Institutes of Health (NIH) under grants R01 EB028792, R01-HD101508, R41-NS122722, and R42-MH135825 (G.Y.). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
| Funders | Funder number |
|---|---|
| National Institutes of Health (NIH) | R01 EB028792, R01-HD101508, R42-MH135825, R41-NS122722 |
ASJC Scopus subject areas
- Biotechnology
- Atomic and Molecular Physics, and Optics