Posts Tagged ‘Diabetic foot ulcers’

Diabetic Foot Ulcer Case Studies: Not All DFU’s are the Same

Friday, July 8th, 2011

Diabetic Foot Wounds

Diabetic Foot Ulcer Case Studie: Not All DFU’s are the same will be presented by Jeffrey Jensen DPM, FACFAS, Dean of Barry University School of Podiatric Medicine at this year’s Wild On Wounds National Conference in Las Vegas, September 7-10, 2011

Diagnosis and treatment of diabetic foot ulcerations goes far beyond which dressing to use at a particular time. In this session we will discuss time tested diagnostic approaches, treatment guidelines, and the latest in technologies to assist in healing this difficult patient population.

This dove tails nicely to those who have already obtained their DWC (Diabetic Wound Certification) and for those considering taking the course through the Wound Care Education Institute. If you are coming to this year’s Wild on Wounds National Conference, make sure you catch this session.

Dermagraft and Diabetic Foot Ulcers

Thursday, January 13th, 2011


As Wound Care Certified Professionals, it is with certainty that we have come across and treat patients with diabetic foot ulcers. Its a growing epidemic among the population of people who suffer from diabetes. So what modalities and treatment regimens are you utilizing to deliver the care to the patients who suffer from these ulcerations? One such product that is being used in the Operating rooms, Surgi-centers and Outpatient Wound Care Centers is a product called Dermagraft.

Below is a brief video about Dermagraft, followed by some information that I found on Dermagraft’s Website.

Dermagraft® is a cryopreserved human fibroblast-derived dermal substitute; it is composed of fibroblasts, extracellular matrix, and a bioabsorbable scaffold.

Dermagraft is manufactured from human fibroblast cells derived from newborn foreskin tissue. During the manufacturing process, the human fibroblasts are seeded onto a bioabsorbable polyglactin mesh scaffold. The fibroblasts proliferate to fill the interstices of this scaffold and secrete human dermal collagen, matrix proteins, growth factors, and cytokines to create a three-dimensional human dermal substitute containing metabolically active, living cells. Dermagraft does not contain macrophages, lymphocytes, blood vessels, or hair follicles.

Dermagraft is supplied frozen in a clear bag containing one piece of approximately 2” x 3” for a single-use application.

Dermagraft Overview

  • Description – Human fibroblast-derived dermal substitute
  • Composition – Composed of human fibroblasts, extracellular matrix, and bioabsorbable scaffold; does not contain macrophages, lymphocytes, blood vessels, or hair follicles
  • Cultured In Vitro
  • Mode of Action – Re-epithelialization — assists in the restoration of the dermal bed, allowing wounds to heal (when implanted into adequately prepared diabetic foot ulcers)
  • Primary Indication – For use in the treatment of full-thickness diabetic foot ulcers
  • Product Number – 11045

Dermagraft Indication

Dermagraft is indicated for use in the treatment of full-thickness diabetic foot ulcers greater than 6 weeks duration, which extend through the dermis, but without tendon, muscle, joint capsule, or bone exposure. Dermagraft should be used in conjunction with standard wound care regimens and in patients who have adequate blood supply to the involved foot.


  • Dermagraft is contraindicated for use in ulcers that have signs of clinical infection or in ulcers with sinus tracts
  • Dermagraft is contraindicated in patients with known hypersensitivity to bovine products, as it may contain trace amounts of bovine proteins from the manufacturing medium and storage solution

Adverse events included local wound infection, osteomyelitis, and/or cellulitis.1

Dermagraft Safely Gets Patients Back in Action

Proprietary Cryopreservation Process Ensures Confidence

Dermagraft is cryopreserved to allow long-term maintenance of tissue integrity and cellular viability. Cryopreservation of Dermagraft offers a number of additional product benefits:

  • Allows for safety testing prior to shipping and application
  • Provides longer shelf life-long-term storage (up to 6 months) when stored at -75°C ± 10°C

There have been no reported immunological responses or rejections from patients that received Dermagraft.

Manufacturing Safety

Each lot of Dermagraft is tested and results are known before it is released.

Final product microbiological testing:

  • Final product sterility
  • Endotoxin (cryopreservation solution)
  • Endotoxin (tissue)
  • Mycoplasma by DNA fluorochrome stain
  • Direct cultivation of mycoplasma
(28 day test by approved 3rd party laboratory)

Adverse Events

Dermagraft was safe and well-tolerated. The most common adverse effects occurring in the Dermagraft (n=163) and control (n=151) groups included all randomized patients, respectively, were infection at study wound (10.4% vs 19.9%), infection not at study wound all randomized patients (10.4% vs 9.3%), accidental injury (10.4% vs 11.9%), and skin dysfunction/blister (9.8% vs 13.2%). The overall incidence of adverse events was approximately the same for both the Dermagraft and control groups. No adverse laboratory findings were associated with the use of Dermagraft and no adverse device effects were reported in the study. The number of patients who developed study ulcer-related adverse events (ie, local wound infection, osteomyelitis, cellulitis) was significantly lower in the Dermagraft-treated group (19%) as compared with the control group (32.5%, P=0.007; Table 3).

Event Dermagraft (n=163) Control (n=151)
Infection 17 (10.4%)* 27 (17.9%)
Osteomyelitis 14 (8.6%) 13 (8.6%)
Cellulitis 12 (7.4%) 14 (9.3%)
Overall 31 (19.0%)† 49 (32.5%)

*P=0.073 vs control; †P=0.007 vs control.

For full safety information, please reference the Dermagraft Directions for Use.

Advanced BioHealing, Inc, (ABH) is a leader in regenerative medicine focused on the development and marketing of cell-based and tissue-engineered products. For more information about ABH and Dermagraft, visit, or click here for other inquiries.

  1. Marston WA, Hanft J, Norwood P, Pollak R; Dermagraft Diabetic Foot Ulcer Study Group. The efficacy and safety of Dermagraft in improving the healing of chronic diabetic foot ulcers: results of a prospective randomized trial. Diabetes Care. 2003;26(6):1701-1705.

I was able to find another video from Advanced BioHealing on the Manufacturing Process. It may be useful to understand the overview:

For more information about Dermagraft please visit their website at

For more information about becoming Wound Care Certified, please visit

Arobella Medical Presented at the Wild on Wounds Conference 2009 in Las Vegas NV

Sunday, September 20th, 2009

WCEI caught up with Charlie of Arobella Medical at the recent Wild on Wounds Conference in Las Vegas NV, held at The Paris Hotel. Charlie was able to give us a brief demonstration of the Qoustic System by Arobella Medical. Below is a short clip and demonstration of the Qoustic System by Arobella Medical.

For more information about the Qoustic System, please visit

Qoustic Wound Therapy System™

For wounds, burns and hard & soft tissues

Arobella Medical, LLC is an innovative company committed to providing wound care professionals with sophisticated technology to manage today’s most difficult cases.

The Qoustic Wound Therapy System™, patented and patent pending, uses ultrasonic energy for the selective dissection and fragmentation of tissues, wound debridement (acute and chronic wounds, burns, diseased or necrotic tissue) and cleansing saline irrigation of the site for the removal of debris, exudates, fragments, and other matter. Not only does the Qoustic Wound Therapy System™ provide a superior debriding process, but it also allows for more control over the procedure. The unique domed shape of the Qoustic Qurette™ significantly advances state-of-the-art technology by permitting controlled volumetric removal of unwanted tissue while focusing ultrasonic energy directly on the area of the wound being treated.

The Qoustic Wound Therapy System™ allows:

* Selective, precise, and gentle fragmentation of soft and hard tissues
* Preservation of healthy tissue through ultrasonic separation of damaged tissue
* Cleansing of the wound area with less pressure and pain
* Reduction of splash created by residuals of sharp debridement and saline wash
* Improvement in granulation of treated tissue
* Stable delivery of ultrasound energy during procedure

Recommended treatment:

This process is directed for single (1) treatment, and total recommended treatment shall be no more than three (3) times per week; typically treatment regimen is approximately two (2) weeks or more, depending on the size and nature/condition of the treated area as well as other subject dependent factors, but may be prescribed longer on the order of a physician.
Basic Information:

* This product has been cleared by the FDA for sale in the United States. Cleared indications for use (K062544)
o Selective dissection and fragmentation of tissue, wound debridement (acute and chronic wounds, burns, diseased or necrotic tissue), and cleansing irrigation of the site for the removal of debris, exudates, fragments, and other matter.
* Patent Pending
* Ideal for
o Wound Management
o Treating specific types of wounds including:
+ Diabetic foot ulcers
+ Pressure ulcers
+ Venous Insufficiency Ulcers
+ Arterial Wounds
+ Compromised Surgical Wounds
+ Burns
+ Osteomyelitis
+ Fistulas
+ Infected, Eczematous, Ulcerated or Devitalized Skin