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DOI: 10.1055/s-0043-1775592
Smooth versus Textured Tissue Expanders: Comparison of Outcomes and Complications in 536 Implants
Funding This study was completed in part with financial support from a research grant from the Mentor Corporation (grant no: 20-002996).

Abstract
Background Increasing concerns regarding the safety of textured surface implants have resulted in surgeons transitioning from textured tissue expanders (TEs) to smooth TEs. Given this change has only recently occurred, this study evaluated outcomes between smooth and textured TEs.
Methods Women who underwent two-stage breast reconstruction using TEs from 2013 to 2022 were included. TE-specific variables, perioperative information, pain scores, and complications were collected. Chi-squared, t-test, and linear regression analyses were performed.
Results A total of 320 patients received a total of 384 textured and 152 smooth TEs. Note that 216 patients received bilateral reconstruction. TEs were removed in 9 cases. No significant differences existed between groups regarding comorbidities. Smooth TEs had a higher proportion of prepectoral placement (p < 0.001). Smooth TEs had less fills (3 ± 1 vs. 4 ± 2, p < 0.001), shorter expansion periods (60 ± 44 vs. 90 ± 77 days, p < 0.001), smaller expander fill volumes (390 ± 168 vs. 478 ± 177 mL, p < 0.001), and shorter time to exchange (80 ± 43 vs. 104 ± 39 days, p < 0.001). Complication rates between textured and smooth TEs were comparable. Smooth TE had a greater proportion of TE replacements (p = 0.030). On regression analysis, pain scores were more closely associated with age (p = 0.018) and TE texture (p = 0.046). Additional procedures at time of TE exchange (p < 0.001) and textured TE (p = 0.017) led to longer operative times.
Conclusion As many surgeons have transitioned away from textured implants, our study shows that smooth TEs have similar outcomes to the textured alternatives.
Ethical Approval
This study was done in accordance with the Helsinki Declaration and with Institutional Review Board approval.
Patient Consent
Signed consent was waived by the Institutional Review Board at Yale University.
Authors' Contributions
O.A.: Conceptualization, methodology, data curation, and writing-original draft.
J.D.: Conceptualization, methodology, data curation, writing-original draft, and formal analysis.
M.N.A.: Data curation, writing- review and editing, and formal analysis.
A.J.: Data curation, writing-original draft, and methodology.
M.A.M.: Data curation and writing-original draft.
R.S.: Data curation and writing-original draft.
L.C.: Data curation and writing-review and editing.
O.O.: Data curation and writing-original draft.
S.M.: Data curation and writing-review and editing.
K.E.P.: Data curation and writing-review and editing.
T.A.: Supervision and writing-review and editing.
M.A.: Supervision and writing-review and editing.
* Co-First Author.
Publication History
Received: 03 February 2023
Accepted: 27 July 2023
Article published online:
07 February 2024
© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
Thieme Medical Publishers, Inc.
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