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Prevena Central for plastic surgery
Convenient. Curated. Connected. Training for the use of 3M™ Prevena™ Therapy in plastic surgery.
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In a prospective, single-center, randomised controlled trial with patients undergoing breast reconstruction, Prevena Therapy aided in:
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Reduction in SSCs1,*
90-day post-operatively
8.5% (28/331) Prevena Therapy vs.
15.9% (53/334) SOC (p=0.0092)* -
Reduction in SSIs1,*
90-day post-operatively
2.1% (7/331) Prevena Therapy vs.
4.5% (15/334) SOC (p=0.00225)* -
Reduction in seroma1,*
90-day post-operatively
1.8% (6/331) Prevena Therapy vs. 5.7% (19/334) SOC
(p=0.0106)*
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Calculations are derived based on relative patient group incidence rate reported in this study.
*Statistically significant (p<0.05).
1 Gabriel A, et al. (Loma Linda University). The Impact of Closed Incision Negative Pressure Therapy on Postoperative Breast Reconstruction Outcomes. Plast Reconstr Surg Glob Open. 2018;6:e1880.
Webinar Videos
Here are some webinar videos by experts highlighting the role of ciNPWT in optimising outcomes and navigating the challenges of complex reconstructive surgeries.
Resource Library
Find clinical compendiums, case studies, eGuides and more to enrich patient experiences in our resource library.
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Regina M. Fearmonti, MD; San Antonio, TX
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Allen Gabriel, MD, FACS; Camas, WA
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Abhishek Chatterjee, MD, MBA; Boston, MA
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3M™ Prevena Restor™ Bella·Form™ Incision Management System application video (8:46)
Connect with a 3M representative
Learn more about the use of Prevena Therapy in plastic surgery or request a product demonstration.
The Prevena Incision Management System is intended to manage the environment of closed surgical incisions and surrounding intact skin in patients at risk for developing post-operative complications, such as infection, by maintaining a closed environment via the application of a negative pressure wound therapy system to the incision. The Prevena Incision Dressing skin interface layer with silver reduces microbial colonization in the fabric.
The effectiveness of Prevena Therapy in reducing the incidence of SSIs and seroma in all surgical procedures and populations has not been demonstrated.
NOTE: Specific indications, limitations, contraindications, warnings, precautions and safety information exist for these products and therapies. Please consult a clinician and product instructions for use prior to application. This material is intended for healthcare professionals.
