CHAPTER 58 Microdermabrasion and Dermalinfusion
Mechanism of Action
Epidermal Effects of Microdermabrasion
The micrographs in Figure 58-1 exhibit the immediate sequential thinning and smoothing of epidermal structures as a result of the abrasive effect of the aluminum oxide crystals moving rapidly across the skin surface. The gentle planing of the upper layers of the skin removes pigmentary impurities and debris held within the stratum corneum and yields a smoother, softer skin surface. Each pass of the MDA handpiece is estimated to ablate approximately 15 µm of skin, roughly equal to one pass of the erbium laser. In addition to the immediate smoothing of the skin, the abrasive process seems to stimulate keratinocyte turnover over the long-term. Larson and Shehadi and colleagues have shown increases in epidermal thickness in porcine skin by 9% with MDA.
Indications
Clinical indications for MDA include the following skin conditions:
Patients with stage I, II, or III acne have done well when MDA is combined with topical retinoid therapy (Fig. 58-2). In this instance, MDA’s action on the stratum corneum allows for better absorption of topical medications. Although MDA does not entirely eliminate stretch marks, it can be an effective treatment option when combined with topical therapies. In a study by Abdel-Latif and Elbendary (2008), better results were seen when treating striae rubra than for striae alba, suggesting that treatment may be limited to more recent-onset stretch marks. Moreover, molecular studies showed that type I collagen expression was upregulated in the skin of patients with striae post-MDA treatment. This provides a biologic mechanism for the clinical benefits of MDA treatment in patients with striae rubra. More recently, cosmeceutical agents such as vitamin C have been proposed as therapies for striae. In addition, work by Lee and colleagues (2003) demonstrated that treatment of ex vivo skin with MDA can significantly increase the uptake of vitamin C. It will be interesting to see whether the combination of MDA and topical vitamin C results in improved clinical outcomes for striae treatment.
Dermalinfusion
Background
In an unpublished histologic study conducted by Moy (www.plasticsurgerypractice.com/issues/articles/2007-01_06.asp), patients were pretreated with dermalinfusion in the preauricular area 1 to 3 days before undergoing an elective facelift. During the procedure, the marked dermalinfusion-treated area was removed, fixed with formalin, processed, and then analyzed. The author found that the dermalinfusion treatment created a smooth and uniform abraded surface confined to the granular layer approximately 30 to 35 µm deep. The epidermal layer, and the keratinosomes in it that help create the hydrophobic barrier, remained intact after treatment. Moreover, addition of a hydrating serum to the abrasive surface showed vacuolization of keratinocytes, displacement of the nucleus, and edema around collagen fibers near the upper papillary dermis. Furthermore, epidermal thickness was increased by 70% after dermalinfusion, consistent with effective absorption and penetration into the papillary dermis. These findings are consistent with rapid hydration of the underlying dermis and help explain the mechanism for the observed clinical improvement in fine wrinkles after MDA plus dermalinfusion treatment.
Rosacea Treatment
Current treatments of rosacea include avoiding triggers such as sunlight exposure, administration of topical and oral antibiotics, and use of laser and light therapies. Treatment usually lasts 3 to 6 months and is associated with side effects such as skin irritation and dryness, erythema, bruising, and photosensitivity. Moreover, MDA is not recommended for patients with rosacea because it can further aggravate the skin, causing angiogenesis, inflammation, and reactive oxygen species. Dermalinfusion, however, will not exacerbate the deeper epidermal layers and can be considered an alternative monotherapy for patients with rosacea. In a recent study by Desai and colleagues (2006), 30 patients with erythematotelangiectatic or papulopustular rosacea underwent MDA plus dermalinfusion treatment twice a month for a total of 12 weeks. The authors chose to use 2% erythromycin and 2% salicylic acid as their infusion solution to decrease inflammation and induce exfoliation, respectively. Twenty patients completed the entire study: 6 patients with erythematotelangiectatic rosacea and 14 patients with papulopustular rosacea. There was a statistically significant reduction in erythema, papules, and pustules in all patients by the 12th week, with a reduction noted as early as week 4. The authors reported a 42% improvement in erythema in the erythematotelangiectatic group and a 69% decrease in papules and 55% decrease in pustules in the papulopustular group. In addition, photographs taken throughout the study documented an overall improvement in the patients’ condition, and there was positive patient feedback regarding tolerability, satisfaction, and overall quality of life. The adverse event most commonly reported by the study participants was transient erythema, which resolved in 3 to 6 hours.
Tattoo Treatment
An interesting case report by Wray and colleagues (2005) documents the first successful treatment of traumatic tattoo with SilkPeel (Envy Medical, Inc., Westlake Village, Calif) MDA treatment during isotretinoin (Accutane) therapy. The adolescent male patient had suffered a traumatic tattoo around the upper and lower eyelids after an explosive accident. The first treatment was performed 48 hours after the accident, with two other treatments on days 3 and 12 postaccident. In addition, comedonal extractors and Vigilon were used as adjunctive therapy for greater efficacy. After the first treatment, more than half of the tattoo marks disappeared, with further improvement reported with each ensuing treatment. The patient was extremely satisfied with the cosmetic outcome, and no complications were reported.
Hyperpigmentation Treatment
More recently, Envy Medical (formerly Emed, Inc.), the manufacturer of the SilkPeel MDA system, has introduced a novel approach for the treatment of hyperpigmentation that involves four MDA treatments spaced 1 week apart, in combination with infusion of a novel skin-lightening solution (Lumixyl) developed by the same company. Although results are preliminary, this new approach represents a potential breakthrough in the treatment of hyperpigmentation because the skin-lightening formulation does not include the more toxic hydroquinone and can thus be used safely in women of child-bearing age, even if pregnant or breast-feeding. In addition, results from the pilot study indicate that no skin irritation or skin thinning would be expected from this treatment because the formulation does not include retinoids or corticosteroids, respectively. Figure 58-3 shows the results for an Asian patient with Fitzpatrick type IV skin before and after four weekly treatments using this approach.
Other Dermalinfusion Systems
In a study by Freedman (2008), two study groups were randomized to either a series of hydradermabrasion treatments with antioxidant dermalinfusion or treatments with the same antioxidant applied manually. Histologic and clinical assessments showed improvement in skin quality in the hydradermabrasion group. The treated skin showed in a statistically significant increase in antioxidant levels and an increase in epidermal and papillary dermal thickness, collagen hyalinization, and fibroblast density. There was also a decrease in wrinkles, pore size, and hyperpigmentation after hydradermabrasion treatment. The skin with manually applied antioxidant, however, showed no detectable change in structure or antioxidant levels. MDA with antioxidants as an infusion agent may be a reasonable treatment option for those patients who wish to prevent or stop the signs of aging.
In another study by Freedman (2009), 10 patients were treated in split-face fashion with either MDA with infusion of an antioxidant serum or MDA alone. Patients underwent a total of six treatments, each 1 week apart. Histologic assessment of post-treatment biopsy samples revealed that patients treated with MDA plus antioxidants had a marked increase in epidermal and papillary dermal thickness, as well as an increase in fibroblast density and deposition of collagen. Digital photography indicated that skin quality improved more with the combined treatment than MDA alone. Raman spectroscopy was used to measure skin polyphenolic levels. The dermalinfusion-treated skin was found to have a 32% increase in antioxidant levels. Unfortunately, the author did not report the effect of MDA alone on polyphenolic levels, so it remains unclear whether the increase in antioxidant levels is attributable to topical infusion therapy, MDA, or a combination of the two. Further studies are required to clarify this issue.