Floor plan - 2013 Annual Meeting - American Association for Hand ...
Floor plan - 2013 Annual Meeting - American Association for Hand ...
Floor plan - 2013 Annual Meeting - American Association for Hand ...
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Understanding the Physiologic Process Behind VAC®: Comparison of Wound Healing<br />
Markers with Non-VAC® Treated Wounds<br />
Institution where the work was prepared: Penn State College of Medicine, Hershey, PA, USA<br />
Rachel H. Noone, BA; Robert Grunfeld, MA; Sprague W. Hazard, MD; Noel B. Natoli, MD; Justin Zelones, BS; Brad Morrow,<br />
BS; Jason Hancey, MD; Paul Ehrlich, PhD; Donald R. Mackay, MD; Reza Miraliakbari, MD; Penn State College of Medicine<br />
INTRODUCTION:<br />
The success of Vacuum Assisted Closure (VAC®) in treatment of wounds is evidenced by its popularity and wide spectrum of clinical<br />
application. Recent studies have examined the effect of VAC® on the biochemical composition of wound fluids by cytokine assay. No<br />
direct data exist as how these findings are different from the non-VAC treated fluid. We propose to study the effect of VAC by comparing<br />
physiologic assays (fibroblast migration and proliferation) as well as the cytokine profiles of wound fluid from patients treated with<br />
VAC®, to closed wounds treated with closed suction JP (Jackson-Pratt) systems.<br />
METHODS:<br />
Wound fluid was collected from 34 VAC® treated patients, and 11 patients with JP drains. Diabetic patients were purposely excluded.<br />
Wound fluid was collected from VAC® canisters and JP bulbs roughly every two days <strong>for</strong> a period of 7 days (at least three collections).<br />
VEGF, IL-1, MMP-13, collagen type I and EDA-Fibronectin levels were analyzed. Also, effects of wound fluid on cultured fibroblast migration<br />
and proliferation were tested on all samples.<br />
RESULTS:<br />
VAC® treated wound fluid showed a significant increase in IL-1 (p = 0.0027). and VEGF (p = 0.016) levels at all time points compared<br />
to JP drained wounds There were no significances detected when comparing the two wound fluids with respect to collagen, fibronectin,<br />
MMP13, or cultures fibroblast migration or proliferation.<br />
CONCLUSIONS:<br />
The mechanism <strong>for</strong> VAC® treatment's success is undefined. This study reports significant elevation of IL-1 and VEGF in VAC treated<br />
wounds compared to non treated wounds. These findings, viewed in isolation, may speak to VAC®'s success. However, once the larger<br />
picture (wound fluid effects on cultured cells) is taken into account, more questions will be raised, regarding the mechanism <strong>for</strong><br />
VAC®'s success. Non- VAC® treated wounds did not differ from VAC® treated wounds in regard to: cell migration, proliferation, collagen<br />
and fibronectin production, as well as MMP13 levels. Further wound fluid analysis is underway to clarify the physiological processes<br />
underlying VAC®'s effectiveness in promoting wound closure.<br />
Cold Ischemia Facilitates Free TRAM and DIEP Flap Breast Reconstruction<br />
Institution where the work was prepared: Stan<strong>for</strong>d University, Palo Alto, CA, USA<br />
Ali Salim, MD; Gordon K. Lee; Stan<strong>for</strong>d University<br />
INTRODUCTION:<br />
The free TRAM flap is a well-established method of autologous tissue breast reconstruction. A drawback to this and other microvascular-based<br />
approaches is the length of operation, which may be 6 hours <strong>for</strong> unilateral and 8 hours <strong>for</strong> bilateral breast reconstruction.<br />
Longer operative times have been reported <strong>for</strong> per<strong>for</strong>ator-based reconstructions, including the DIEP flap. As this may take a significant<br />
physical toll on the surgical team, we have adopted a two-surgeon protocol in which flaps are placed under cold ischemia immediately<br />
after harvest. We believe this (a) reduces surgeon fatigue by facilitating per<strong>for</strong>mance of the operation and (b) is a safe modification<br />
which does not increase operative time or compromise flap viability.<br />
METHODS:<br />
We per<strong>for</strong>med 84 consecutive breast reconstructions (free TRAM, muscle-sparing TRAM, and DIEP flaps) over 36 months. All flaps were<br />
exposed to post-harvest cold ischemia as follows: immediately after harvest, each flap was wrapped in a moist sponge, sealed in a<br />
bowel bag, and placed in an ice slush bath. With the flap(s) on ice, one member of the team proceeds with closure of the abdominal<br />
fascia while the other member takes a break. The surgeons then alternate roles, such that by the time the microvascular anastomosis is<br />
per<strong>for</strong>med, both surgeons are refreshed mentally and physically <strong>for</strong> this delicate part of the operation. A second assistant can close the<br />
skin layer of the abdomen and per<strong>for</strong>m the umbilicoplasty at the same as the microsurgery. We then retrospectively reviewed flap<br />
ischemia times, operative times, and the rate of complications including flap loss, microvascular thrombosis, and fat necrosis evident<br />
upon physical exam.<br />
RESULTS:<br />
Average cold ischemia time <strong>for</strong> unilateral reconstruction was 1 hour 45 minutes, and <strong>for</strong> bilateral reconstruction was 2 hours 5 minutes<br />
<strong>for</strong> the first flap and 3 hours 35 minutes <strong>for</strong> the second flap. There was 1 flap loss (1.2%) which was due to vascular thrombosis; this complication<br />
was not associated with a statistically significant increase in ischemia time. Fat necrosis rate was 3% and average patient follow-up<br />
was 22 months.<br />
CONCLUSION:<br />
As our operative times and complication rates compare to other large published series, we believe that cold ischemia is well-tolerated<br />
by the free TRAM flap, and in fact facilitates the operation significantly by contributing to decreased surgeon fatigue.<br />
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