DERMABOND ADVANCED™ Topical Skin Adhesive
DERMABOND ADVANCED™ Topical Skin Adhesive holds wound edges together following surgical incisions and lacerations.1 It delivers a microbial barrier with 99% effectiveness for 72 hours in vitro, guarding against organisms commonly responsible for surgical site infections (SSIs).2A Patients also benefit from significantly improved comfort and satisfaction when compared to sutured closures.3,4B
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About this device
DERMABOND ADVANCED™ has a unique formulation that provides a strong, flexible skin closure plus microbial barrier protection.5,6 It allows for improved control during application due to its ergonomic design and high viscosity. Designed for both wide and fine applications, it polymerizes within minutes and stays securely in place, creating a protective barrier that naturally sloughs off within 5-10 days.1
Specialties
GYN, Thoracic
Procedures
C-Section, Lobectomy
Economic benefits
In retrospective analyses, DERMABOND ADVANCED™ was associated with:
- 25% reduction in length of stay for sternal closure patients in cardiac surgery7
- $500 reduction in total Ceasarean hospital costs when compared to staples and sutures8C
Clinical outcomes
In a randomized trial comparing topical skin adhesives and sutures in the management of lacerations, DERMABOND™ Adhesive was associated with9:
- Shorter procedure time (3.6 minutes vs. 12.4 minutes; P <0.001)
- Less patient pain (visual analog pain scores, 7.2 mm vs. 18.0 mm; P<0.001)
Features & benefits
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Protection
Provides 99% protection in vitro for 72 hours against organisms commonly responsible for SSIs, including Staphylococcus epidermidis, Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa and Enterococcus faecium.2A
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Strength
Provides strength to maintain barrier and wound closure integrity during the critical wound healing period (48 hours).5,9 When used in addition to sutures, DERMABOND ADVANCED™ Topical Skin Adhesive was shown ex vivo to add 75% more strength to the wound closure than sutures alone.10
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Patient satisfaction
Leads to excellent cosmetic appearance and improved patient satisfaction.11 The patient does not need to return visit for staple or suture removal— sloughs off naturally within 5-10 days.1
Learn how to use this device
DERMABOND ADVANCED™ and Mini Topical Skin Adhesives
Supporting documentation
Related products
DERMABOND™ PRINEO™ Skin Closure System
The DERMABOND™ PRINEO™ Skin Closure System offers a powerful, non-invasive alternative to traditional skin sutures and staples. It combines the strength, flexibility, and microbial protection of DERMABOND ADVANCED™ Topical Skin Adhesive with a secure, latex-free, self-adhering mesh to facilitate optimal skin closure and healing.1-7A In a clinical study, the DERMABOND™ PRINEO™ System was associated with a better cosmetic outcome than conventional suturing in skin closure. 8B
References
A. Clinical significance unknown.
B. Patients experienced significantly greater comfort with DERMABOND ADVANCED Adhesive at 6 weeks (P < 0.05) and 6 months (P < 0.01). In a similar retrospective study of 670 patients, patient comfort and satisfaction were also superior with DERMABOND ADVANCED Adhesive.
C. Premier Perspective™ Comparative Database.
- DERMABOND ADVANCED™ Topical Skin Adhesive Instructions for Use. Ethicon, Inc.
- Su W. Study Report for in vitro evaluation of microbial barrier properties of Dermabond® Protape. 06TR071. December 4, 2006. Ethicon, Inc.
- Nipshagen MD, Hage JJ, Beekman WH. Use of 2‐octyl‐ cyanoacrylate skin adhesive (DERMABOND™) for wound closure following reduction mammaplasty: a prospective, randomized intervention study. Plast Reconstr Surg. 2008;122(1):10‐18.
- Scott GR, Carson CL, Borah GL. Dermabond skin closures for bilateral reduction mammaplasties: a review of 255 consecutive cases. Plast Reconstr Surg. 2007;120(6):1460‐ 1465.
- Singer AJ, Perry LC, Allen RL. In v iv o study of wound-bursting strength and compliance of topical skin adhesives. Acad Emerg Med. 2008;15(12):1290-1294.
- Keplinger, S. Comparison of setting times of topical skin adhesive products. Report 11TR053. August 16, 2011. Ethicon, Inc. Annotation> Dermabond uses a chemical initiation system
- Souza EC, FitaroniRB, JanuzelliDM, et al. Use of 2-octylcyanoacrylate for skin closure of sternal incisions in cardiac surgery : observations of microbial barrier effects. CurrMed Res Opin. 2008;24(1):151-155.
- Murrmann SG, Markowitz JS, Gutterman EM, Magee G. Health and economic outcomes after OBGY N surgery : a comparison of skin closure techniques. Poster presentation at 2008 Annual Clinical Meeting of The American College of Obstetricians and Gynecologists; May 37, 2008; New Orleans, LA
- Quinn J, Wells G, Sutcliffe T, et al. A randomized trial comparing octylcyanoacrylate tissue adhesive and sutures in the management of lacerations. JAMA. 1997;277(19):1527‐ 1530.
- Protocol To Determine The Strength Benifits When Adding Dermabond Advanced Topical Skin Adhesive To A Wound Or Incision Using Suture As The Primary Closure Report. 2013: p.3. Data Normality Evaluation.
- Krishnamoorthy B, Najam O, Khan UA, et al. Randomized prospective study comparing conventional subcuticular skin closure with DERMABOND™ skin glue after saphenous vein harvesting. Ann Thorac Surg. 2009;88(5):1445-1449
For complete indications, contraindications, warnings, precautions, and adverse reactions, please reference full package insert.
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