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Bioengineered skin equivalent
Negative pressure wound therapy
Acellular dermal matrix
Diabetic neuropathy
Silver dressings
Enzymatic debridement

Autolytic debridement
Wound necrosis
Surgical debridement
Mechanical debridement
Wound fibroblasts
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583
Wounds - ISSN: 1044-7946 - Volume 18 - Issue 5 - May 2006
Editor's Message:
Editorial Message
David T. Rovee, PhD
Evidence Corner:
Evidence Corner
Laura L. Bolton, PhD, FAPWCA
Brian F. McCrary, DO, MPH
Abstract: A proposal for a post-treatment wound outcome tool is presented to help in documenting and tracking the final outcome of a wound treated at a health facility or clinic or by a provider. It is expected that a measure of the final treatment outcome will become more important in the future and affect reimbursement for care.

Composition of Wound Fluid from Pressure Ulcers Treated with Negative Pressure Wound Therapy Using V.A.C.® Therapy in Home Health or Extended Care Patients: A Pilot Study
Deepak V. Kilpadi, PhD, MBA;1 Joyce K. Stechmiller, ARNP, PhD, CS;2 Beverly Childress, ARNP, PhD;3 Linda Cowan, ARNP;2 Melissa Comerio, RN, BSN;1 Kristine Kieswetter, PhD, MBA;1 Gregory Schultz, PhD4
Abstract: The purpose of this pilot study was to characterize changes in concentrations of tumor necrosis factor (TNF)-a, interleukin (IL)-1b, matrix metalloproteinase (MMP)-3, MMP-9, and tissue inhibitor of metalloproteinase (TIMP)-1 in wound fluid collected from pressure ulcers in adults treated with negative pressure wound therapy (NPWT; V.A.C.® Therapy, KCI, San Antonio, Tex). Wound fluids were collected from 8 patients with Stage III or IV pressure ulcers in home care and extended care settings. Concentrations of analytes were measured immediately prior to initiation of NPWT (Day 0) and at Days 1, 3, and 7 continuous NPWT. There were statistically significant (P < 0.05) decreases from baseline in the levels of MMP-3 (Day 0 > [Day 1 ~ Day 3 ~ Day 7]), MMP-9 (Day 0 > [Day 1 ~ Day 3]), and MMP-3:TIMP-1 ratios (Day 0 > [Day 1 ~ Day 3 ~ Day 7]). No other significant differences were detected. Previous studies have shown a consistent decrease in protease levels to have prognostic value

Newer Antistaphylococcal Agents: In-Vitro Studies and Emerging Trends in Staphylococcus aureus Resistance
Adebayo Shittu, BSc, MSc, PhD,1,2 and Johnson Lin, BSc, MSc, PhD2
Abstract: Although remarkable advances in the development of antibacterial agents for infections caused by Staphylococcus aureus began in the 1940s, treatment of this pathogen is still a challenge for clinicians. The emergence of S aureus strains with resistance to penicillin and methicillin in 1948 and 1961 and the recent reports of vancomycin-resistant strains indicate that the battle against this versatile pathogen is not yet over. This review discusses the newly developed antimicrobial agents, mechanisms of action, in-vitro studies, and emerging trends in S aureus resistance to these antibacterial agents. The availability of linezolid in intravenous and oral form is an advantage for the treatment of pneumonia and skin and soft tissue infection. Daptomycin is recommended for the treatment of deep-seated infections, such as endocarditis or osteomyelitis caused by methicillin-resistant S aureus. Tigecycline is a promising antibacterial agent in cases of complicated intra-abdominal inf
Industry News:
May 2006
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May 2006



Supplements:

Special Publication:
The following is a collection of publications from Healthpoint intended to facilitate expeditious, cost-effective wound care management. There will be nine publications total.

Related Links:
Symposium on Advanced Wound Care (SAWC)
The Buck Stops Here
Association of Advanced Wound Care
Ostomy/Wound Management
Podiatry Today
Vascular Disease Management
Wound Healing Society

Article Submission:
All submissions for consideration should be submitted online using the Rapid Review Web-Based Review System at www.rapidreview.com. Authors should scroll down to HMP Communications and click on Author.


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