Evidence map›Paper›PMID 40614234›Full record

ArticleAesthetic surgery journal2025

Histomorphologic Outcomes of GalaFLEX Scaffold Used in Breast Surgery: Clinical Follow-up From 6 Weeks to 63 Months.

Bruce W Van Natta, Catalina Pineda Molina, Vincent Antonelli, George S Hussey, Stephen F Badylak

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Article in Aesthetic surgery journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Bruce W Van NattaORCID 0000-0003-1792-1247
Catalina Pineda MolinaORCID 0000-0001-7710-6119
Vincent Antonelli
George S Hussey
Stephen F Badylak

Funding

Postdoctoral Research Training in Biotherapy of CancerT32CA113263 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Udai S Kammula · 2006 to 2026
$3.6M
National Cancer Institute of the National Institutes of Health (Bethesda, MD, USA) T32CA113263NCI NIH HHS T32 CA113263
6 · The paper itself

Abstract

backgroundThe use of scaffolds in reconstructive and aesthetic breast surgeries for soft tissue reinforcement has increased over time. However, histomorphologic outcomes with the use of such materials are not typically reported. The present study describes the histologic findings associated with the use of the GalaFLEX Scaffold by BD (Franklin Lakes, NJ), an absorbable biosynthetic material, when used as soft tissue support in breast surgery.

objectivesThe present study evaluates the histomorphologic patterns of a 10-patient cohort that received GalaFLEX Scaffolds as soft tissue support in breast surgery, with and without breast implants.

methodsTissue biopsy specimens that included the implanted GalaFLEX Scaffold were collected during revision from 6 weeks to 63 months postimplantation. General staining and specific immunolabeling were used to determine cellular infiltration, tissue composition and organization, and vascularization.

resultsBiopsy specimens showed slow degradation of the GalaFLEX Scaffold, robust vascularization, mononuclear cell infiltration that decreased with time, and deposition of an organized collagenous connective tissue matrix in the interfiber space of the GalaFLEX Scaffold. There was no evidence for chronic inflammation or a foreign body response. The pattern of tissue remodeling around and within the fibers suggests a constructive tissue remodeling process rather than the formation of dense capsular tissue with contraction.

conclusionsImplantation of the GalaFLEX Scaffold for reconstructive and cosmetic breast surgery appears to be safe and is associated with slow scaffold degradation, neovascularization, and mononuclear cell infiltration that diminishes with time, and a constructive remodeling response devoid of chronic inflammation or foreign body response. These conclusions are limited by the size of the 10-patient cohort. LEVEL OF EVIDENCE: 4 (THERAPEUTIC):

Indexed as

Absorbable ImplantsBreastBreast ImplantationBreast ImplantsMammaplastyTissue ScaffoldsAdultBiopsyFemaleFollow-Up StudiesHumansMiddle AgedTime FactorsTreatment Outcome

Identifiers

PMID40614234
PMCPMC12461751

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