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SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0

SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0

SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0

Product catalog summary
Introduction
This document is a case study on the use of Integra® SurgiMend® Collagen Matrix for soft tissue reconstruction, specifically in the management of a giant ventral hernia over a two-year period.

Patient Presentation
A 36-year-old male with multiple trans-abdominal gunshot wounds developed severe systemic inflammatory response syndrome (SIRS) and required multiple surgeries, including negative pressure wound therapy (NPWT) and a right hemi-colectomy.

Surgical Intervention
In November 2009, a 20 cm by 30 cm SurgiMend 3.0 mesh was used to bridge a 13 cm by 35 cm defect in the abdominal wall. The mesh was placed using a modified Rives-Stoppa technique. Despite complications, including an anastomotic leak, the patient was eventually discharged.

Interim Clinical Outcomes
The patient was discharged after a prolonged hospital stay, with instructions to exercise and lose weight. He successfully lost 60 lbs over the following year and was scheduled for further surgery to address a fistula.

Long-Term Follow-up
In November 2011, the patient underwent surgery for fistula excision and abdominal reconstruction using Trans-Abdominal Wall Reconstruction (TAWT). The procedure aimed to achieve definitive myofascial closure. The patient recovered well and returned to work.

Product Description and Indications
SurgiMend is an acellular dermal tissue derived from bovine dermis, used to reinforce soft tissue where weakness exists. It is indicated for plastic and reconstructive surgery, muscle flap reinforcement, and hernia repair.

Contraindications and Precautions
SurgiMend should not be used in patients with hypersensitivity to collagen or bovine products. It should be used with caution in areas with limited blood supply or infection. The product is for single patient use and should not be resterilized.

Potential Complications
Risks include infection, allergic reactions, pain, swelling, foreign body reactions, and repair laxity. Physicians must inform patients of these risks.

Contact Information
For more information or to place an order, contact Integra LifeSciences Corporation.
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Catalog excerpts

SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0-1

Integra SurgiMend® Collagen Matrix for Soft Tissue Reconstruction CASE STUDY Successful Management of Giant Ventral Hernia using SurgiMend 3.0 LIMIT UNCERTAINTY

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SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0-2

Integra® SurgiMend® Collagen Matrix for Soft Tissue Reconstruction Surgeon Profile Andrew Dennis, DO, FACOS Cook County Hospital, Chicago, IL Dr. Dennis is the Chair of the Division of Pre-Hospital and Emergency Services in the Department of Trauma and Burn at the Cook County Hospital in Chicago, IL. He is an Associate Professor of Surgery at Rush Medical College and Chairman of the Department of Surgery at Midwestern University College of Osteopathic Medicine. Successful Management of Giant Ventral Hernia using SurgiMend 3.0: A Two-Year Journey From Bridge to Re-Enforced Closure Patient Presentation...

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SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0-3

dressing changes and abdominal washouts. A subsequent operation included a right hemi-colectomy with primary ileocolic anastomosis for breakdown of his prior repair. During the course of the multiple returns to the operating room, it was discovered that he had developed an anastomotic leak at the ileocolic anastomosis. This was repaired primarily on two occasions, but the leak recurred. At this time, primary fascial closure of the abdominal muscles was not considered possible due to the extensive loss of domain (Figure 1A). Surgical Intervention for Abdominal Wall Closure In November 2009, abdominal...

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SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0-4

Integra® SurgiMend® Collagen Matrix for Soft Tissue Reconstruction The patient was seen multiple times in follow-up. His instructions upon discharge were to exercise daily and continue weight loss, as his initial weight prior to hospitalization was well over 300 lbs and his discharge weight was 240 lbs. The patient was instructed to refrain from smoking and to continue to lose weight. He was followed by the trauma nutrition service monthly, and he successfully lost 60 lbs over the next year. During his follow-up, he demonstrated only mild eventration of his bridge mesh graft. He was able to do...

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SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0-5

was placed along with an internal plastic adhesion barrier, and the patient was taken back to the trauma intensive care unit to be resuscitated. He was placed into the Trauma Open Abdomen Protocol (OAP) which delays TAWT placement until edema is reduced and a physiologic steady state is achieved. The patient returned to the operating room three days later for washout and replacement of NPWT dressings. TAWT was again delayed as the patient’s edema was not under control. After another three days, he was again returned to the OR for washout and evaluation for TAWT. At this time the edema was reduced...

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SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0-6

Integra® SurgiMend® Collagen Matrix for Soft Tissue Reconstruction Figure 6A. Following removal of the TAWT device, definitive closure was achieved. Figure 6B. Reinforced with a 10 cm by 15 cm piece of SurgiMend 3.0 placed under moderate tension as an underlay. Figure 7. The patient recovered from the last procedure without significant complications (seen here at two months). Now more than a year removed from the definitive closure, the patient has no signs of recurrence and is back to work as a laborer.

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SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0-7

SurgiMend Collagen Matrix for Soft Tissue Reconstruction is part of a family of soft tissue repair products Description SurgiMend is an acellular dermal tissue derived from bovine dermis. The device is supplied sterile in a variety of sizes, shapes, and thicknesses to be trimmed by the physician to meet the individual patient's needs. Indications SurgiMend is intended for implantation to reinforce soft tissue where weakness exists and for surgical repair of damaged or ruptured soft tissue membranes. SurgiMend is specifically indicated for: • Plastic and reconstructive surgery • Muscle flap reinforcement •...

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SurgiMend® Case Study: Successful Management of Giant Ventral Hernia Using SurgiMend® 3.0-8

Integra® SurgiMend® Collagen Matrix for Soft Tissue Reconstruction Availability of these products might vary from a given country or region to another, as a result of specific local regulatory approval or clearance requirements for sale in such country or region. Always refer to the appropriate instructions for use for complete clinical instructions. Non contractual document. The manufacturer reserves the right, without prior notice, to modify the products in order to improve their quality. Warning: Applicable laws restrict these products to sale by or on the order of a physician. n n n For more...

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*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.