TY - JOUR
T1 - Successful treatment of atrophic postoperative and traumatic scarring with carbon dioxide ablative fractional resurfacing
T2 - Quantitative volumetric scar improvement
AU - Weiss, Elliot T.
AU - Chapas, Anne
AU - Brightman, Lori
AU - Hunzeker, Christopher
AU - Hale, Elizabeth K.
AU - Karen, Julie K.
AU - Bernstein, Leonard
AU - Geronemus, Roy G.
PY - 2010/2
Y1 - 2010/2
N2 - Objective: To assess the safety and efficacy of ablative fractional resurfacing (AFR) for nonacne atrophic scarring. Design: In this before-and-after trial, each scar received 3 AFR treatments and 6 months of follow-up. Setting: Private academic practice. Patients: Fifteen women with Fitzpatrick skin types I to IV, aged 21 to 66 years, presented with 22 nonacne atrophic scars between June 1 and November 30, 2007. Three patients (3 scars) were excluded from the study after receiving 1 AFR treatment and not returning for follow-up visits. The remaining 12 patients (19 scars) completed all 3 treatments and 6 months of follow-up. Interventions: Each scar received 3 AFR treatments at 1- to 4-month intervals. Main Outcome Measures: Erythema, edema, petechiae, scarring, crusting, and dyschromia were graded after treatment and through 6 months of follow-up. Skin texture, pigmentation, atrophy, and overall appearance were evaluated after treatment and through 6 months of follow-up by the patient and a nonblinded investigator. A 3-dimensional optical profiling system generated highresolution topographic representations of atrophic scars for objective measurement of changes in scar volume and depth. Results: Adverse effects of treatment were mild to moderate, and no scarring or delayed-onset hypopigmentation was observed. At the 6-month follow-up visit, patient and investigator scores demonstrated improvements in skin texture for all scars (patient range, 1-4 [mean, 2.79]; investigator range, 2-4 [mean, 2.95]), pigmentation for all scars (patient range, 1-4 [mean, 2.32]; investigator range, 1-4 [mean, 2.21]), atrophy for all scars (patient range, 1-4 [mean, 2.26]; investigator range, 2-4 [mean, 2.95]), and overall scar appearance for all scars (patient range, 2-4 [mean, 2.89]; investigator range, 2-4 [mean, 3.05]). Image analysis revealed a 38.0% mean reduction of volume and 35.6% mean reduction of maximum scar depth. Conclusion: The AFR treatments represent a safe, effective treatment modality for improving atrophic scarring due to surgery or trauma.
AB - Objective: To assess the safety and efficacy of ablative fractional resurfacing (AFR) for nonacne atrophic scarring. Design: In this before-and-after trial, each scar received 3 AFR treatments and 6 months of follow-up. Setting: Private academic practice. Patients: Fifteen women with Fitzpatrick skin types I to IV, aged 21 to 66 years, presented with 22 nonacne atrophic scars between June 1 and November 30, 2007. Three patients (3 scars) were excluded from the study after receiving 1 AFR treatment and not returning for follow-up visits. The remaining 12 patients (19 scars) completed all 3 treatments and 6 months of follow-up. Interventions: Each scar received 3 AFR treatments at 1- to 4-month intervals. Main Outcome Measures: Erythema, edema, petechiae, scarring, crusting, and dyschromia were graded after treatment and through 6 months of follow-up. Skin texture, pigmentation, atrophy, and overall appearance were evaluated after treatment and through 6 months of follow-up by the patient and a nonblinded investigator. A 3-dimensional optical profiling system generated highresolution topographic representations of atrophic scars for objective measurement of changes in scar volume and depth. Results: Adverse effects of treatment were mild to moderate, and no scarring or delayed-onset hypopigmentation was observed. At the 6-month follow-up visit, patient and investigator scores demonstrated improvements in skin texture for all scars (patient range, 1-4 [mean, 2.79]; investigator range, 2-4 [mean, 2.95]), pigmentation for all scars (patient range, 1-4 [mean, 2.32]; investigator range, 1-4 [mean, 2.21]), atrophy for all scars (patient range, 1-4 [mean, 2.26]; investigator range, 2-4 [mean, 2.95]), and overall scar appearance for all scars (patient range, 2-4 [mean, 2.89]; investigator range, 2-4 [mean, 3.05]). Image analysis revealed a 38.0% mean reduction of volume and 35.6% mean reduction of maximum scar depth. Conclusion: The AFR treatments represent a safe, effective treatment modality for improving atrophic scarring due to surgery or trauma.
UR - http://www.scopus.com/inward/record.url?scp=76749140451&partnerID=8YFLogxK
U2 - 10.1001/archdermatol.2009.358
DO - 10.1001/archdermatol.2009.358
M3 - Article
C2 - 20157023
AN - SCOPUS:76749140451
SN - 2168-6068
VL - 146
SP - 133
EP - 140
JO - JAMA Dermatology
JF - JAMA Dermatology
IS - 2
ER -