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Chapter 6 6 Pearl E. Grimes

The author has no financial interest in any of the products or equipment mentioned in this chapter.

Contents 6.2 Chemical Background/Properties 6.1 History ...... 49 Salicylic acid (ortho-hydroxybenzoic acid) is a 6.2 Chemical Background/Properties . . . 49 beta hydroxy acid agent (Fig. 6.1). It is a lipo- 6.3 Formulations ...... 50 philic compound which removes intercellular 6.4 Indications ...... 50 lipids that are covalently linked to the cornified envelope surrounding cornified epithelioid 6.5 Contraindications ...... 50 cells [1]. Due to its antihyperplastic effects on 6.6 Patient Preparation ...... 51 the epidermis, multiple investigators have used 6.7 Peeling Technique ...... 51 salicylic acid as a peeling agent [2, 3, 4]. Recent- ly, histologic assessments using salicylic acid 6.8 Post-peeling Care and Complications . 55 peels in hairless mice reported loss of cornified 6.9 Advantages ...... 55 cells followed by activation of epidermal basal 6.10 Disadvantages ...... 56 cells and underlying fibroblasts. These findings suggest that salicylic acid peeling can alter the 6.11 Side Effects ...... 56 underlying dermal tissue without directly 6.12 Patient’s Informed Consent ...... 56 wounding the tissue or causing inflammation References ...... 57 [5]. Salicylic acid has also been shown to have anti-inflammatory and antimicrobial proper- ties. When used in combination with in Whitfield’s ointment, it has fungicidal properties. 6.1 History

P.G. Unna, a German dermatologist, was the first to describe the properties and use of sali- cylic acid. It has since been used for many decades as a agent in concentrations of 3 to 6%. Salicylic acid is frequently utilized in topical preparations because of its comed- olytic effects. In addition, it facilitates the pene- tration of other topical agents.

Fig. 6.1. Chemical structure 50 Pearl E. Grimes

6.3 Formulations damaged of the dorsal hands and fore- arms. After pretreatment with topical and localized TCA 20%, the 50% salicylic acid A variety of formulations of salicylic acid have paste was applied to the affected area and oc- been used as peeling agents. These include 50% cluded for 48 h. Following dressing removal, ointment formulations (Table 6.1) [2, 3], as well peeling and desquamation occurred and was as 10, 20 and 30% formulations (Table relatively complete by the tenth day. Overall re- 6.2) [4, 6]. More recently, commercial formula- sults were described as excellent. Despite these tions of salicylic acid have become available results, salicylic acid peeling did not move into (BioGlan Pharmaceuticals Company, Malvern, the arena of popular peeling techniques until PA; Bionet Esthetics, Little Rock, AR). the mid 1990s. Kligman and Kligman [4] ushered salicylic acid into the current arena of superficial peeling agents. They treated 50 6 6.4 Indications women with mild to moderate photodamage, reporting improvement in pigmented lesions, The efficacy of salicylic acid peeling has been surface roughness and reduction in fine lines. assessed in several studies.Fifty percent salicyl- Grimes et al.[8] reported substantial efficacy ic acid ointment peeling was first used by Aron- and minimal side effects in 25 patients treated sohn to treat 81 patients who had freckles, pig- with 20 and 30% salicylic acid peels in darker mentation, and aging changes of the hands [3]. racial-ethnic groups. Conditions treated in- He reported excellent results. Subsequently, cluded acne vulgaris, melasma and post-in- Swinehart [7] successfully used a methyl-salic- flammatory . ylate buffered, croton oil-containing, 50% sali- Thirty-five Korean patients with facial acne cylic acid ointment paste for treatment of lenti- were treated biweekly for 12 weeks with 30% gines, pigmented keratoses and actinically salicylic acid peels [9]. Both inflammatory and non-inflammatory lesions were significantly improved. In general, the peel was well tolerat- Table 6.1 Formulations of salicylic acid: salicylic acid ed with few side effects. ointment Given these findings, indications for salicylic acid peels include acne vulgaris (inflammatory Salicylic acid powder USP 50% and non-inflammatory lesions), acne rosacea, 16 drops melasma, post-inflammatory hyperpigmenta- Aquaphor 112 g tion, freckles, lentigines, mild to moderate pho- todamage, and texturally rough skin. From Swinehart [7]

6.5 Contraindications Table 6.2 Formulations of salicylic acid: salicylic acid solutions In general, there are few contraindications to Salicylic acid Weight of Amount of salicylic acid chemical peeling. Salicylic acid peel % salicylic acid ethyl peels are well tolerated in all skin types (Fitz- powder (g) 95% (cc) patrick’s I–VI) and all racial/ethnic groups. General contraindications include salicylate 10 10 100 hypersensitivity/; unrealistic patient ex- 20 20 100 pectations; active inflammation/dermatitis or 30 30 100 infection at the salicylic acid peeling site; acute 40 40 100 viral infection; pregnancy; and 50 50 100 therapy within 3–6 months of the peeling pro- cedure. The author has performed more than From Draelos [6] 1,000 salicylic acid peels without observing any Salicylic Acid Chapter 6 51 evidence of salicylate allergy/hypersensitivity When treating acne vulgaris, topical and following a salicylic acid peel. systemic therapies (if indicated) are initiated 2 to 4 weeks prior to peeling. Topical and based products can be 6.6 Patient Preparation used daily and discontinued 1 or 2 days prior to peeling. However, unless a deeper peel is de- Peel preparation varies with the condition being sired, should be discontinued 7–10 treated. Regimens differ for photodamage, hy- days prior to salicylic acid peeling. Broad-spec- perpigmentation (melasma and post-inflamma- trum sunscreens (UVA and UVB) should be tory hyperpigmentation) and acne vulgaris [10]. worn daily (see Photodamage, Sunscreen sec- In addition there are special issues to be consid- tion). ered when treating darker racial-ethnic groups (see darker skin section). A detailed history and cutaneous examination is performed in all pa- 6.7 Peeling Technique tients prior to chemical peeling. Standardized photographs are taken of the areas to be peeled Despite some general predictable outcomes, including full-face frontal and lateral views. even superficial chemical peeling procedures Use of topical retinoids (tretinoin, tazaro- can cause hyperpigmentation and undesired tene, retinol formulations) for 2–6 weeks prior results. Popular standard salicylic acid peeling to peeling thin the stratum corneum and en- hance epidermal turnover. Such agents also re- duce the content of epidermal melanin and ex- pedite epidermal healing. Retinoids also en- hance the penetration of the peeling agent. They should be discontinued several days prior to the peeling procedure. Retinoids can be re- sumed post-operatively after all evidence of peeling and irritation subsides. In contrast to photodamage, when treating conditions such as melasma, post-inflammatory hyperpigmen- tation, and acne as well as darker skin types, retinoids should be discontinued 1 or 2 weeks before peeling or even eliminated from the prep to avoid post-peel complications such as exces- sive erythema, desquamation, and post-inflam- matory hyperpigmentation. Topical alpha hydroxy acid or polyhydroxy acid formulations can also be used to prep the skin. In general, they are less aggressive agents in impacting peel outcomes. The skin is usually prepped for 2–4 weeks with a formulation of 4% or higher compounded for- mulations (5–10%) to reduce epidermal mela- nin. This is extremely important when treating hyperpigmentation. Although less effective, other topical bleaching agents include ,kojic acid,arbutin,and licorice (see photo- aging section). Patients can also resume use of topical bleaching agents post-operatively after peeling and irritation subsides. Fig. 6.2. Salicylic acid precipitate 52 Pearl E. Grimes

techniques involve the use of 20 and 30% sali- The author always performs the initial peel cylic acid in an ethanol formulation. Salicylic with a 20% concentration to assess the patients’ acid peels are performed at 2- to 4-week inter- sensitivity and reactivity. Before treatment, the vals. Maximal results are achieved with a series face is thoroughly cleansed with alcohol and/or of three to six peels. to remove oils. The peel is then applied

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a

b

Fig. 6.3. a Frosting after salicylic acid. b Crusting 48 h later. c Resolution of crusting c in 3 to 4 days Salicylic Acid Chapter 6 53

Fig. 6.3. d Complete clearing of hypopigmentation by days 7–10. Note im- provement in acne

d with 2× 2 wedge sponges, 2 × 2 gauze sponges, or -tipped applicators. Cotton-tipped swabs can also be used to apply the peeling agent to periorbital areas.A total of two to three coats of salicylic acid is usually applied. The ac- id is first applied to the medial cheeks working laterally, followed by application to the perioral area, chin, and forehead. The peel is left on for 3–5 min. Most patients experience some mild burning and stinging during the procedure.Af- ter 1–3 min, some patients experience mild peel-related of the face. Portable handheld fans substantially mitigate the sensa- tion of burning and stinging. A white precipitate, representing crystalliza- tion of the salicylic acid, begins to form at 30 s to 1 min following peel application (Fig. 6.2). This should not be confused with frosting or whitening of the skin, which represents protein agglutination. Frosting usually indicates that the patient will observe some crusting and peeling following the procedure (Fig. 6.3a–d). This may be appropriate when treating photo- damage. However, the author prefers to have minimal to no frosting when treating other conditions. After 3–5 min the face is thoroughly rinsed with tap water,and a bland cleanser such as Cetaphil is used to remove any residual salicylic acid precipitate. A bland is applied after rinsing. My favorites are Ceta- phil, Purpose, Theraplex, and SBR Lipocream a (Figs. 6.4a, b, 6.5a, b and 6.6a, b). Fig. 6.4a. Melasma before and after a series of five sali- cylic acid peels and 4% hydroquinone 54 Pearl E. Grimes

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a

b

Fig. 6.4b. Melasma before and after a series of five sali- cylic acid peels and 4% hydroquinone

Fig. 6.5a, b. Acne vulgaris before and after four salicylic b acid peels Salicylic Acid Chapter 6 55

a b

Fig. 6.6a, b. Acne rosacea before and after three salicylic acid peels, moderate improvement

6.8 Post-peeling Care 6.9 Advantages and Complications The key benefits of salicylic acid peeling in- Bland cleansers and are continued clude: for 48 h or until all post-peel irritation sub- sides.Patients are then able to resume the use of í An established safety profile in patients their topical regimen including topi- with skin types I–VI cal bleaching agents, acne medications, and/or í An excellent peeling agent in patients retinoids. Post-peel adverse reactions such as with acne vulgaris excessive desquamation and irritation are í Given the appearance of the white treated with low to high potency topical ster- precipitate, uniformity of application oids. Topical steroids are extremely effective in is easily achieved resolving post-peel inflammation and mitigat- ing the complication of post-inflammatory hy- í After several minutes the peel can induce perpigmentation. In the author’s experience, an anesthetic effect whereby increasing any residual post-inflammatory hyperpigmen- patient tolerance tation resolves with use of topical hydroqui- none formulations following salicylic acid peeling. 56 Pearl E. Grimes

6.10 Disadvantages id peels are used to improve acne vulgaris, hy- perpigmentation (dark spots), rough texture, í Limited depth of peeling oily skin, and photodamage (sun damage). í Minimal efficacy in patients with The procedure involves first having the peel significant photodamage site prepped with alcohol, acetone or other pre-peel cleansing agents. The peeling agent is applied for 3–5 min followed by cleaning 6.11 Side Effects with tap water and a bland cleanser. In general, salicylic acid peels are extremely Side effects of salicylic acid peeling are mild well tolerated. However, the procedure can and transient. In a series of 35 Korean patients, cause swelling, redness, crusting, dryness and 6 8.8% had prolonged erythema that lasted more obvious peeling of the face which could last than 2 days [9]. Dryness occurred in 32.3%, re- for up to 7–10 days. sponding to frequent applications of moisturiz- I understand that there is a small risk of devel- ers. Intense exfoliation occurred in 17.6%,clear- oping permanent darkening after the proce- ing in 7–10 days. Crusting was noted in 11.7%. dure.There is a rare chance that the peel could There were no cases of persistent post-inflam- cause undesirable pigment loss at the treated matory hyperpigmentation or scarring. In a se- site, the condition being treated could worsen ries of 25 patients comprising 20 African Amer- after the peeling procedure,or a scar could de- icans and five Hispanics, 16% experienced mild velop.In addition,there is a small chance that a side effects [8]. One patient experienced tem- bacterial infection could develop, or the peel porary crusting and hypopigmentation that could also trigger a flare of a pre-existing Her- cleared in 7 days. Three patients had transient pes infection at the treated site. In addition, dryness and hyperpigmentation that resolved there have been uncommon cases of allergic in 7–14 days. reactions to salicylates (the active peel ingre- Salicylism, or salicylic acid toxicity, is char- dient).The benefits and side effects of the pro- acterized by rapid breathing, tinnitus, hearing cedure have been explained to me in detail.All loss, dizziness, abdominal cramps, and central of my questions have been answered. nervous system reactions. It has been reported with 20% salicylic acid applied to 50% of the í body surface,and it has also been reported with I am in stable health. use of 40 and 50% salicylic acid paste prepara- í I have not used Isotretinoin tions [7]. The author has peeled more than in the past 6 months. 1,000 patients with the current 20 and 30% í I have no to salicylic acid. marketed ethanol formulations and has ob- served no cases of salicylism. í I am not pregnant.

Outcomes are not guaranteed. 6.12 Patient’s Informed Consent Signature of Patient I, ______, hereby consent to having Date my ______(site) treated with SALICYL- Patient Name (Please Print) IC ACID CHEMICAL PEELING. The peel will be performed to improve the overall appearance Witness of the skin at the site of treatment. Salicylic ac- Date Salicylic Acid Chapter 6 57

ing with salicylic acid. Arch Dermatol 136 : 1390– References 1395 6. Draelos ZD (2000) Atlas of cosmetic dermatology. 1. Lazo ND, Meine JG, Downing DT (1995) Lipids are Churchill Livingstone, New York, pp 94–97 covalently attached to rigid corneocyte protein en- 7. Swinehart JM (1992) Salicylic acid ointment peeling velope existing predominantly as beta-sheets: a sol- of the hands and forearms. Effective nonsurgical re- id state nuclear magnetic resonance study. J Invest moval of pigmented lesions and actinic damage. Dermatol 105 : 296–300 J Dermatol Surg Oncol 18 : 495–498 2. Swinehart JM (1992) Salicylic acid ointment peeling 8. Grimes PE (1999) The safety and efficacy of salicyl- of the hands and forearms. J Dermatol Surg Oncol ic acid chemical peels in darker racial-ethnic 18 : 495–498 groups. Dermatol Surg 18–22 3. Aronsohn RB (1984) Hand chemosurgery. Am J 9. Lee HS, Kim IH (2003) Salicylic acid peels for the Cosmet Surg 24–28 treatment of acne vulgaris in Asian patients. Der- 4. Kligman D, Kligman AM (1998) Salicylic acid peels matol Surg 29 : 1196–1199 for the treatment of photoaging. Dermatol Surg 24 : 10. Brody HJ (1997) Chemical peeling, 2nd ed. Mosby, 325–328 St Louis 5. Imayama S, Ueda S, Isoda M (2000) Histologic changes in the skin of hairless mice following peel-