Use of the LightSheer Diode Laser System for Hair Reduction: Safety and Efficacy in a Large Series of Treatments



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Use of the LightSheer Diode Laser System for Hair Reduction: Safety and Efficacy in a Large Series of Treatments RUBE J. PARDO, MD, PH.D., JUDY FAHEY, RN Coral Gables Dermatology and Laser Center Department of Dermatology, University of Miami Summary Provided by Lumenis Inc. ABSTRACT. An 8 nm high-power, long-pulsed diode laser with contact cooling provides safe and effective reduction of pigmented hair in patients with a variety of skin types. This paper presents the safety and efficacy results of 8 treatments performed on 25 sites in 144 patients with Fitzpatrick skin types II-V. Over 84% of sites showed a good or excellent response following the second and subsequent treatments. Treatment responses were similar for all skin types treated, with an excellent safety profile. Side effects were noted in only two of the 8 treatments and were transient in nature. Patients were extremely or moderately satisfied with over 96% of their treatments. INTRODUCTION SEMICONDUCTOR DIODE LASERS are considered the most efficient light sources available and are particularly well suited for clinical applications including hair reduction. This paper reports the use of the LightSheer diode laser system, a high-power, long-pulsed diode laser with a wavelength of 8nm, for laser hair reduction in a large population of patients with a variety of skin and hair types. Laser hair reduction operates on the principle of selective photothermolyis. This process combines selective absorption of light energy by the melanin in hair follicles with suitable fluences and pulse durations 1. In order to achieve maximum selectivity, the laser energy is applied in a pulse duration that approximately equals the thermal relaxation time of the target. In practice, the appropriate pulse duration maximizes the temperature rise of the hair follicle and minimizes the conduction of heat to the surrounding tissue, thus sparing adjacent structures from damage. In order to achieve permanent hair reduction, sufficient light energy must be absorbed by the hair follicle. The melanin in the hair follicle absorbs 3-4 times more energy at 8 nm (the wavelength used in the LightSheer) than at 64 nm (the wavelength of Nd:YAG lasers) 2. This increased absorption means that the LightSheer laser can be used at significantly lower fluences to achieve hair reduction in contrast to the much higher fluences required for a 64 nm laser. The effectiveness of laser hair reduction depends on the patient's skin type. Laser hair reduction is typically more effective in lighter-skinned people (Fitzpatrick skin types I-III) 2. The challenge associated with laser treatment for darker-skinned patients is to avoid surface skin (epidermal and upper dermal) injury due to absorption of light in the pigmented epidermis, while still causing selective destruction of the underlying pigmented hair follicles. This study will examine almost equal numbers of treatments of light and dark skin types. Recent clinical studies have shown that longer pulse durations combined with aggressive skin cooling provide a greater margin of safety when treating darker skin by allowing higher fluences and fewer side effects 5,6. Models of skin optics and heat transfer suggest that the entire hair follicle, including the outermost follicular structures (where the stem cells are located) can be selectively damaged with longer pulse widths than those typically employed (-4 ms) 2. The LightSheer can deliver pulse durations up to ms. The thermal relaxation time for the hair follicle is dependent on its diameter; thus longer pulse durations are theoretically best suited for the treatment of medium to thick hairs 7. These longer pulse durations can be safely used with higher fluences when combined with aggressive 2 by Lumenis Inc. Published by Lumenis Inc.

2 PARDO: SAFETY AND EFFICACY February 1 skin cooling techniques to reduce epidermal damage 2. The ChillTip handpiece of the LightSheer laser contains an actively cooled convex sapphire lens. When pressed against the patient's skin before and during each laser pulse, this cooling device provides substantial thermal protection for the epidermis 8. Compression of the target area also places the hair bulb closer to upper dermis where the laser energy is the highest. The combination of longer pulse widths and the unique cooling system minimizes skin damage and allows for higher fluences to be safely used even in darker skinned patients 4. Other studies have shown that treatment efficacy is directly related to fluence levels 6. METHODS This paper reports on the safety and effectiveness of the LightSheer Diode Laser System in the reduction of pigmented hair in a large patient population with a variety of skin types and hair characteristics. The study monitored 8 hair reduction treatments at 25 sites on 144 patients. The majority of patients had Fitzpatrick skin type III or IV and medium or coarse dark brown or black hair. Almost 5% of treatments were performed on type IV and V skin. Over two-thirds of treatments were to the face or neck (Table 1). Over 9% of sites received two or more treatments. The interval between treatments ranged from 2 to 56 weeks, with an average of weeks. The most frequently used fluence was between 25 and 29 J/cm 2. Over 94% of treatments used the OptiPulse mode for pulse width, while the remaining treatments used a 3 ms pulse width (Table 2). The 3 ms pulse width was most commonly used for skin type V (29% of type V treated sites) and skin type IV (7% of type IV treated sites). Treatment success was based on apparent clearance and was assessed as no response, moderate, good, or excellent response following each treatment. Patient satisfaction with the previous treatment was assessed as dissatisfied, mildly satisfied, moderately satisfied, or very satisfied. Treatment responses were classified by skin type, hair color, hair texture, and hair density. Treated areas were visually assessed for skin responses, including edema, erythema, hypopigmentation, hyperpig- Table 1: Characteristics of Treated Sites Skin Type Number (%) of Sites II 15 (6.%) III 112 (44.8%) IV 9 (43.6%) V 14 (5.6%) Tan No 224 (89.6%) Yes 26 (.4%) Treatment Site Face/neck 172 (68.6%) Trunk 27 (.8%) Axilla 11 (4.4%) Bikini/legs 33 (13.2%) Other 7 (2.8%) Hair Color Light Brown (4.%) Dark Brown 96 (38.4%) Black 144 (57.6%) Hair Texture Fine 31 (12.4%) Medium 73 (29.2%) Coarse 146 (58.4%) Hair Density Low 46 (18.4%) Medium 116 (46.4%) Heavy 84 (33.6%) Not specified 4 (1.6%) Table 2: Treatment Parameters No. of Treatments/Site Number (%) of Sites 1 19 (7.6%) 2 74 (29.6%) 3 57 (22.8%) 4 38 (15.2%) 5 or more 62 (24.8%) Fluence (J/cm 2 ) Number (%) of Treatments < 44 (5.5%) -24 4 (13.%) 25-29 379 (47.4%) 3-34 184 (23.%) 35-39 76 (23.%) >4 13 (1.6%) Pulse Width OptiPulse mode 754 (94.3%) 3 ms 46 (5.7%)

February 1 PARDO: SAFETY AND EFFICACY 3 mentation, and textural changes following each treatment. Patients also noted their level of pain and the use of topical anesthesia was recorded. RESULTS Treatment response was rated as good or excellent for approximately 65% of all treatments. Figure 1 (A-H) illustrates several examples of treatment results. Favorable responses increased substantially after multiple treatments. Over 84% of sites showed a good or excellent response following the second and subsequent treatments (Figure 2). Multiple treatments are important for the patient to achieve the desired response. In general, the percentage of treatments that resulted in good or excellent response was similar regardless of skin type or hair color. Treatment responses for second and subsequent treatments by skin type and hair color are shown in Figures 3 and 4. The average number of treatments required for good or excellent response was similar for all body areas treated (Figure 5). Treatment satisfaction was similar for patients with different hair colors and skin types, although patients with skin type V were slightly less satisfied than those with skin types II-IV (Figures 6 and 7). The use of a ms pulse width, which was not available in this study, would likely improve the effectiveness of treatment for patients with skin type V. Overall, patients were moderately or very satisfied with 96% of their treatments (Figure 8). Safety Any untoward event at the treatment site (e.g., edema, erythema, hypopigmentation, hyperpigmentation, textural changes) that lasted 3 days or more was considered to be a side effect. Side effects were reported for only two out of 8 total treatments (.25%). These were both cases of transient hyperpigmentation. One incident of transient hyperpigmentation occurred after the second treatment of a patient with skin type IV. The patient s axilla was treated using a fluence of 28 J/cm 2 and a 3 ms pulse duration. This hyperpigmentation lasted slightly over one month. The patient underwent two further treatments at that site and no further hyperpigmentation was noted. The second incident of transient hyperpigmentation occurred following the second treatment in a patient with skin type III and black, medium texture, medium density hair. Treatment fluence was 28 J/cm 2 in Optipulse mode (pulse width of 14 ms). The patient did not undergo any further treatments at this site, but had a total of 17 other treatments on the neck, back, and cheeks with no reported side effects. The majority of patients experienced some pain during the procedure. The pain was usually mild (42% of treatments) or moderate (49% of treatments) and only 2% of treatments were associated with severe pain. Topical A B Figure 1. A female patient with Fitzpatrick Type III skin (A) before treatment of bikini line, and (B) 18 months after third treatment with the LightSheer diode laser using 26 J/cm 2 in OptiPulse mode.

4 PARDO: SAFETY AND EFFICACY February 1 C D A male patient with pseudofolliculitus barbae, Fitzpatrick Type V skin (C) before treatment of neck, and (D) 8 months after fourth treatment with the LightSheer diode laser using 15 J/cm 2 and a pulsewidth of 3 ms. E F A female patient with Fitzpatrick Type III skin (E) before treatment of axilla, and (F) months after third treatment with the LightSheer diode laser using 38 J/cm 2 in OptiPulse mode. G H A female patient with Fitzpatrick Type IV skin (G) before treatment of chin, and (H) 6 months after sixth treatment with the LightSheer diode laser using 27J/cm 2 in OptiPulse mode.

February 1 PARDO: SAFETY AND EFFICACY 5 Figure 2: Treatment Response by Treatment Number 8 7 6 5 4 3 None Moderate Good Excellent 1 2 3 4 > 4 Number of Treatments Figure 3: Treatment Response by Skin Type 7 6 5 4 3 Type II Type III Type IV Type V None Moderate Good Excellent

6 PARDO: SAFETY AND EFFICACY February 1 Figure 4: Treatment Response by Hair Color 7 6 5 4 3 Light Brown Dark Brown Black None Moderate Good Excellent 3 Figure 5: Number of Treatments for Good or Excellent Response Average Number of Treatments Required 2.5 2 Face/neck Trunk/axilla Legs/bikini

February 1 PARDO: SAFETY AND EFFICACY 7 Figure 6: Treatment Satisfaction by Skin Type 7 6 5 4 3 Type II Type III Type IV Type V Dissatisfied Mildly Moderately Very Figure 7: Treatment Satisfaction by Hair Color 6 5 4 3 Light Brown Dark Brown Black Dissatisfied Mildly Moderately Very

Figure 8: Overall Treatment Satisfaction 6 5 4 3 Dissatisfied Mildly Moderately Very anesthesia was used for only % of treatments and 6% of patients. The most commonly used topical anesthetic was EMLA (12% of treatments). CONCLUSIONS The LightSheer 8 nm high-power, long-pulsed diode laser provides effective reduction of pigmented hair in a heterogeneous population of 144 patients with 25 body sites, involving 8 treatments. Treatment was equally effective for Fitzpatrick skin types II-V and treatment response was similar for all hair colors treated (light brown, dark brown, and black). Treatment response was good or excellent in 84% of areas following the second and subsequent treatments. Patients were moderately or extremely satisfied with over 96% of their treatments. Laser hair reduction with the LightSheer Diode Laser System was very safe for all skin types treated. Side effects were noted for only two out of 8 treatments (.25%). These were transient in nature. The use of the ms pulse width, which was not available for this study, provides additional flexibility for treating skin types V-VI. The longer pulse widths and the unique cooling system available with the LightSheer Diode Laser System reduce skin damage and allow for safe and effective hair reduction even in darker skinned patients. REFERENCES 1. Anderson RR, Parish JA. Selective photothermolysis: precise microsurgery by selective absorption of pulsed radiation. Science 1983;2:524-527. 2. DiBernardo BE, Perez J, Usai H, Thompson R, Callahan L, Falleck SR. Laser hair removal: Where are we now? Plast Reconstr Surg 1999;4:247-257. 3. Dierickx CC, Anderson RR, Campos VB, Grossman MC. Effective, permanent hair reduction using a pulsed, highpower diode laser. Coherent Medical, Inc. 1999. 4. Lou WW, Quintana AT, Geronemus RG, Grossman MC. Prospective study of hair reduction by diode laser (8 nm) with long-term follow-up. Dermatol Surg ;26: 428-432. 5. Adrian RM, Tanghetti E. Clinical evaluation of a high energy long-pulse ruby laser for the treatment of unwanted body hair. Lasers Med Surg 1997; supp 9:36. 6. Battle EF. Study of very long-pulsed ( ms) highpowered diode laser for hair reduction on all skin types. Coherent Medical, Santa Clara, CA,. 7. Grossman MC, Dierckx CC, Farinelli WA, Flotte TJ, Anderson RR. Damage to hair follicles by normal-mode ruby laser pulses. J Am Acad Dematol 1996;35:889. 8. Klavuhn KG. Epidermal protection: a comparative analysis of sapphire contact and cryogen spray cooling. Laser Hair Removal Technical Note ;1:1-7.

Lumenis Inc. 24 Condensa Street Santa Clara, CA 9551 USA Tel 48 764 3 8 635 1313 Fax 48 764 3999 8 55 1133 internet: www.lumenis.com Lumenis, its logo, LightSheer, OptiPulse, ChillTip and AutoPace are trademarks or registered trademarks of the Lumenis Group of Companies. Copyright 2 the Lumenis Group of Companies. All rights reserved. Federal law restricts this device to sale by or on the order of a physician. Product specifications are subject to change without notice. email: information@lumenis.com Printed in the U.S.A. 5399-31-M PB217