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Presidential Greeting - American Society for Laser Medicine and ...

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26 <strong>American</strong> <strong>Society</strong> <strong>for</strong> <strong>Laser</strong> <strong>Medicine</strong> <strong>and</strong> Surgery Abstracts<br />

Study: A porcine model was chosen due to the morphological<br />

similarities between swine skin <strong>and</strong> human skin. Allogeneic cells<br />

were obtained by bone marrow aspiration from a donor pig.<br />

Mesenchymal stem cells were isolated from the donor bone<br />

marrow aspirate <strong>and</strong> transduced with a lentiviral vector<br />

containing a fluorescent marker gene. One recipient pig was<br />

placed under general anesthesia <strong>and</strong> 60 full thickness skin<br />

wounds were made using a 10 mm punch biopsy. The wounds were<br />

r<strong>and</strong>omly assigned to two laser treatment regimens: laser CO 2/<br />

MSC <strong>and</strong> laser Er:YAG/MSC. After AFL the stem cells were<br />

pipetted into the vertical channels. Wounds were covered with an<br />

occlusive polyurethane film dressing. Three punch <strong>and</strong> wedge<br />

biopsies were taken from each group on days 5, 7, <strong>and</strong> 21.<br />

Results: Labeled allogeneic bone marrow cells were observed in<br />

papillary <strong>and</strong> reticular dermis on days 5 <strong>and</strong> 7 in both the Er:YAG<br />

<strong>and</strong> CO 2 laser treated wounds. Some labeled cells were noted in<br />

close proximity to the ablated vertical channels created by laser<br />

treatment. Allogeneic cell showed persistence in the treated<br />

wounds despite intense inflammation associated with the full<br />

thickness wounds created.<br />

Conclusion: Preliminary study suggests that ablative fractional<br />

lasers may be useful technology to deliver mesenchymal stem<br />

cells <strong>and</strong> this has broad implications <strong>for</strong> many branches of<br />

medicine.<br />

#81<br />

A SPLIT-FACE STUDY INVESTIGATING<br />

ALLUMERA COMBINED WITH MULTIPLE LASER<br />

AND LIGHT SOURCES FOR<br />

PHOTOREJUVENATION<br />

Sabrina Fabi, Jennifer Peterson, Mitchel Goldman<br />

Goldman Butterwick & Associates, Cosmetic <strong>Laser</strong> Surgery,<br />

San Diego, CA<br />

Background: Chronic exposure to sun can result in<br />

photodamage manifested as fine lines/wrinkling, erythema,<br />

tactile roughness, hyperpigmented macules <strong>and</strong> patches,<br />

sallowness, skin laxity, <strong>and</strong> telangiectasias. Photodynamic<br />

therapy (PDT) uses a photosensitizer such as aminolevulinic acid<br />

or methyl aminolevulinic which is converted to protoporphyrin IX<br />

in vivo. These photosensitizers concentrate in rapidly<br />

proliferating cells, sebaceous gl<strong>and</strong>s, superficial melanin, <strong>and</strong><br />

vasculature. When visible light radiation is applied, reactive<br />

oxygen species are generated. While originally indicated <strong>for</strong> the<br />

treatment of nonhyperkeratotic actinic keratosis, improvement in<br />

the signs of photoaging was noticed as an advantageous side<br />

effect. Most commonly, blue fluorescent light or a red light<br />

emitting diode is used to activate the photosensitizer; however,<br />

any laser or light source that emits visible light radiation can be<br />

used including the pulsed dye laser (PDL) <strong>and</strong> intense pulsed light<br />

(IPL). When administering PDT in our practice, a sequence of four<br />

laser <strong>and</strong> light sources are used: PDL, IPL, blue light, <strong>and</strong> red<br />

light to work synergistically to activate the photosensitizer.<br />

Photocure has developed Allumera cream (Photocure ASA, Oslo,<br />

Norway), a precursor to photoactive protoporphyrins (PAP), that<br />

enhances the skin appearance. This product is applied without<br />

occlusion <strong>and</strong> allowed to incubate be<strong>for</strong>e activation by visible light<br />

radiation. The purpose of this study is to investigate if the<br />

addition of Allumera to a series of laser <strong>and</strong> light sources results in<br />

further improvement of photoaging as compared to a placebo.<br />

Study: The primary objective of this study was to evaluate the<br />

efficacy of Allumera versus placebo combined with a series of laser<br />

<strong>and</strong> light sources in the improvement of photoaging as measured<br />

by the Global Score <strong>for</strong> Photoaging. Secondary objectives included:<br />

improvement of fine/lines, hyperpigmentation, telangiectasias,<br />

tactile roughness, erythema, sallowness, global evaluation of<br />

response to treatment, patient evaluation of photoaging, patient<br />

preference <strong>and</strong> patient satisfaction. A total of 20 patients were<br />

r<strong>and</strong>omized to receive split face treatment with Allumera cream<br />

or placebo cream. On day 1 (Visit 1), day 30 (Visit 2), <strong>and</strong> day 60<br />

(Visit 3), the face of study subjects was pretreated with<br />

microdermabrasion <strong>and</strong> acetone wash, followed by r<strong>and</strong>omized<br />

treatment to half of the face with Allumera cream (Photocure<br />

ASA, Oslo, Norway), <strong>and</strong> the other half with placebo cream, with<br />

unoccluded application <strong>for</strong> 1 hour. Photoactivation followed with<br />

first pulsed dye laser (PDL) to individual lesions, then intense<br />

pulsed light (IPL) to the entire treatment area, <strong>and</strong> finally<br />

treatment to entire face with both red <strong>and</strong> blue light sources.<br />

Investigator assessment of global photoaging, fine lines/wrinkles,<br />

hyperpigmentation, tactile roughness, sallowness,<br />

telangiectasias, erythema, <strong>and</strong> adverse events (using a 5-point<br />

scale) occurred prior to treatment at day 1 (Visit 1), day 30 (Visit<br />

2), day 60 (Visit 3), <strong>and</strong> on day 90 (Visit 4). Patient questionnaires<br />

were completed after day 1 (Visit 1), day 30 (Visit 2), <strong>and</strong> day 60<br />

(Visit 3), <strong>for</strong> a total of 1 week after treatment. St<strong>and</strong>ardized<br />

photography was completed at day 1 (Visit 1) <strong>and</strong> day 90 (Visit 4).<br />

Results: Eighteen of 20 patients (18 females), aged 32–64 years<br />

old (mean 52.11), had completed visit 2 (day 30) of the study at the<br />

time of data analysis; <strong>and</strong> 8 patients of those patients (8 females),<br />

had completed visit 3 (day 60) by the time of data analysis. All<br />

patients were Fitzpatrick skin types II–IV with moderate to<br />

severe photodamage. Investigator assessment (using a 5 point<br />

scale) comparing baseline to day 30 found a trend towards<br />

improvement in global photoaging, fine lines/wrinkles,<br />

hyperpigmentation, tactile roughness, sallowness,<br />

telangiectasias, <strong>and</strong> erythema. Comparing baseline to day 60, a<br />

statistical significance in improvement was noted in global<br />

photoaging, fine lines/wrinkles, hyperpigmentation, tactile<br />

roughness, <strong>and</strong> sallowness. There was no significant difference<br />

noted in post-treatment pain, erythema <strong>and</strong> edema, between the<br />

Allumera versus placebo-treated side by patients. Patient<br />

assessment of pain, redness, swelling, <strong>and</strong> itching <strong>for</strong> seven days<br />

following Visit 1 did not show a statistically significant difference<br />

between the Allumera versus placebo-treated sides.<br />

Conclusion: Treatment with Allumera shows a trend towards<br />

improvement in global photoaging, fine lines/wrinkles,<br />

hyperpigmentation, tactile roughness, sallowness,<br />

telangiectasias, <strong>and</strong> erythema. Allumera is well tolerated by<br />

patients <strong>and</strong> does not result in significant post-treatment pain,<br />

erythema <strong>and</strong> edema compared to placebo. Preliminary data are<br />

presented. This is a single-site study of a small cohort of patients<br />

followed <strong>for</strong> an average of 45 days at the time of data analysis.<br />

This study will be completed by February 28, 2011, by which time<br />

we will have followed all 20 patients <strong>for</strong> a total of 120 days, <strong>and</strong> all<br />

patients will have received an additional photodynamic therapy<br />

session with Allumera.<br />

#82<br />

COMPARISON STUDY OF NON-ABLATIVE<br />

FRACTIONAL TREATMENT WITH AND WITHOUT<br />

ADVANCED SKIN COMPRESSION TECHNIQUE<br />

Taro Kono, Motoko Nakata, Hiroyuki Sakurai,<br />

Henry Chan<br />

Tokyo Women’s Medical University, Tokyo, Japan; University of<br />

Hong Kong, Hong Kong, China

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