Microdermabrasion and Dermalinfusion

CHAPTER 58 Microdermabrasion and Dermalinfusion




Microdermabrasion: Background


The concept of smoothing the skin by removing or abrading the upper layers can be dated as far back as 1500 BC, when Egyptian physicians used a type of “sandpaper” to treat scars. Modern dermabrasion was developed in Germany in the early 1900s by Kromayer, who used human-powered rotating wheels and rasps as a means of removing the epidermis and superficial portions of the dermis. This new technology was mainly used to treat scars, hyperpigmentation, and keratoses; however, acceptance was not forthcoming. It was not until Kurtin, Burks, and others began using motorized wire brushes in the early to mid-1950s that the power of the technology began to be realized. In spite of the great benefits possible with dermabrasion, there are many potential negatives: need for anesthesia, scarring, prolonged downtime, wound care, infection, and contaminated operative field with aerosolized particles that endanger the practitioner and staff. Many of these problems are also encountered with other techniques, such as laser resurfacing and deep chemical peels. These factors, as well as economic considerations, have pushed for development of a new technology that is less debilitating, safer, and more affordable: microdermabrasion (MDA).


MDA was developed in Italy in 1985 and introduced to the American market during the mid-1990s. MDA has spread at an explosive rate. According to data from the American Society for Aesthetic Plastic Surgery, an estimated 557,131 MDA procedures were performed in the United States in 2008. The aim of this chapter is to help the reader better understand MDA’s mechanism of action, clinical indications, contraindications, patient selection and initial evaluation criteria, procedure methods, and complications encountered following treatment.



Mechanism of Action


The most superficial layer of the skin is the stratum corneum, which is a lifeless accumulation of protein and lipid material derived from flattened, dead keratinocytes that forms a barrier to protect the skin from a myriad of invasive insults. From the time a keratinocyte is formed in younger skin, it takes approximately 28 days to mature, die, and flake off the skin surface as dander. As humans age, keratinocyte transit times dramatically increase, trapping pigment and debris in the superficial epidermal layers to give the characteristic stained appearance of aging or solar (actinic) damage. Another skin cell of major importance is the dermal fibroblast, which lies within the dermis and synthesizes extracellular matrix (ECM) components, including proteoglycans (e.g., dermatan sulfate), glycosaminoglycans (e.g., hyaluronic acid), collagen, and elastin. This function decreases with aging and actinic damage. The process of MDA addresses both the stained, debris-laden epidermis and the sluggish fibroblast production of ECM, especially collagen.



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.




Dermal Effects of Microdermabrasion


Most MDA machines are quite simple in principle, having a crystal reservoir that supplies abrasive crystals through a flexible tube to a handpiece that is moved across the skin by the operator. The skin is “tented up” by the negative pressure generated in the machine, and abrasive crystals, usually aluminum oxide (corundum), are simultaneously blown and “sucked” across the skin to remove the upper layers of the epidermis. This can be compared with a fine “sandblasting” technique. Other types of particulate materials are occasionally used for the abrasion process, such as sodium chloride crystals, sodium bicarbonate (baking soda), and magnesium oxide crystals. However, aluminum oxide seems ideal because it is widely available, inert, very hard, has multiple sharp edges, does not readily absorb liquid, and is nontoxic even if inadvertently inhaled. Used crystals and cutaneous debris are removed through suction and collected in a separate waste container, thus creating a closed-loop system that avoids the airborne contaminants of open dermabrasion. The handpieces usually can be fitted with reusable metal tips or disposable plastic tips. The metal tips must be sterilized before use with different patients.


Treatments are superficial enough that they do not cause bleeding or “serum ooze.” Some patients with very sensitive skin may experience slight discomfort, but treatments are certainly not painful and are generally well tolerated. No topical anesthetics are needed. After each pass, the bulk of crystals should be removed before continuing. The second pass should be at right angles, or perpendicular, to the direction of the first pass. An optional third pass is performed with a swirling or circular motion, making sure that the skin is taut and the handpiece tip is moving and not stationary over a single skin point. Skilled operators also pay close attention to the direction of lymphatic flow, especially in areas such as the face, in order not to obstruct drainage and prevent unnecessary edema.


Skin changes are cumulative and treatment sessions are recommended at 7- to 14-day intervals. Depending on the type and severity of the skin problem(s), usually between 4 and 15 treatments are offered on an as-needed basis between 1 and 4 months. The patient is usually able to return to most normal activities immediately, unless the skin is extremely sensitive. Mild erythema may be observed, and usually resolves within 12 to 24 hours after treatment.


The operator has great flexibility in treating patients and improving outcomes by varying the depth of penetration to match each patient’s unique circumstances and requirements. This is accomplished by controlling the following four factors:






In rare instances (e.g., acne scarring), high vacuum settings (≥20 mm Hg) may be required. The operator should expect variability in vacuum settings and crystal flow with different machines.



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


Dermalinfusion is an innovative procedure that uses MDA technology to increase delivery of active ingredients to treat specific skin conditions such as hyperpigmentation, telangiectasia, papulopustular acne, eczema, photodamage, dehydration, rosacea, and fine lines. It is unique in that it uses a closed-loop vacuum system with a recessed diamond tip rather than microcrystals to exfoliate the skin while simultaneously infusing the topical dermaceutical into the deeper dermal layers. The size, coarseness of the diamond tip, vacuum, and flow rates can all be adjusted depending on the patient’s treatment. A major advantage of dermalinfusion is minimal post-treatment erythema and decreased risk of PIH compared with the harsh and abrasive standard MDA treatments. Furthermore, dermalinfusion is ideal for treatment of the lips, papulopustular acne, as well as rosacea, which are all relatively contraindicated with crystal-based MDA. The optimal treatment regimen involves four to six treatments every 1 to 2 weeks and monthly treatments thereafter.


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.




Other Dermalinfusion Systems


HydraFacial, manufactured by Edge Systems (Signal Hill, Calif), is another dermalinfusion unit currently used by dermatologists and aestheticians. Similar to SilkPeel, the HydraFacial device simultaneously resurfaces the stratum corneum and delivers active serum into the treated tissue. The exfoliation is achieved with a patented crystal-free tip, patented disposable HydroPeel tip, or a Spa Aggression tip. Various skin-specific solutions such as glucosamine, lactic acid, salicylic acid, and antioxidants (vitamins A and E and white tea extract) are used for infusion. The Tissue Nutrient Solution (TNS) serum developed by SkinMedica (Carlsbad, Calif) is exclusively designed for the HydraFacial system. The serum consists of NouriCel-MD, a patented formulation of human growth factors, cytokines, soluble collagen, antioxidants, and matrix proteins that enables greater skin rejuvenation.


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.


Although a number of other MDA infusion systems have been commercially developed, only the HydraFacial and SilkPeel systems have appropriate patent protection. Therefore, no other systems are reviewed in this chapter.

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May 14, 2017 | Posted by in GENERAL & FAMILY MEDICINE | Comments Off on Microdermabrasion and Dermalinfusion

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