[Skip to Navigation]
Sign In
Figure 1. 
Final clearance as a function of time in 34 patients receiving multiple treatments. HRE indicates hair removal efficiency.

Final clearance as a function of time in 34 patients receiving multiple treatments. HRE indicates hair removal efficiency.

Figure 2. 
Distribution of clearance values obtained at final follow-up visit (number of sites). HRE indicates hair removal efficiency.

Distribution of clearance values obtained at final follow-up visit (number of sites). HRE indicates hair removal efficiency.

Figure 3. 
Percent clearance as a function of time in 14 patients receiving multiple treatments and long-term follow-up (>12 months since the last treatment).

Percent clearance as a function of time in 14 patients receiving multiple treatments and long-term follow-up (>12 months since the last treatment).

Figure 4. 
Patient 3. Pretreatment (A) and posttreatment (B) results. Hair removal efficiency at 24 months' follow-up was 91% (skin type II, chest, 4 treatments, 615-nm filter, fluence of 40 J/cm2, pulse duration of 3.3 milliseconds, 2 pulses, pulse delay of 30 milliseconds).

Patient 3. Pretreatment (A) and posttreatment (B) results. Hair removal efficiency at 24 months' follow-up was 91% (skin type II, chest, 4 treatments, 615-nm filter, fluence of 40 J/cm2, pulse duration of 3.3 milliseconds, 2 pulses, pulse delay of 30 milliseconds).

Table 1. 
Photoepilation Protocol for Long-term Study
Photoepilation Protocol for Long-term Study
Table 2. 
Long-term Follow-up Subgroup (Follow-up >12 Months After Last Treatment)
Long-term Follow-up Subgroup (Follow-up >12 Months After Last Treatment)
Table 3. 
Potential Effects of Light-Pilosebaceous Interactions
Potential Effects of Light-Pilosebaceous Interactions
1.
Ort  RJAnderson  RR Optical hair removal.  Semin Cutan Med Surg. 1999;18149- 158Google ScholarCrossref
2.
Ross  EVLadin  ZKreindel  MDierickx  C Theoretical considerations in laser hair removal.  Dermatol Clin. 1999;17333- 355Google ScholarCrossref
3.
Liew  SHGrobbelaar  ADGault  DGreen  CLinge  C Ruby laser assisted hair removal: a preliminary report of the correlation between efficacy of treating and melanin content of hair and growth phases of hair at a specific site.  Ann Plast Surg. 1999;42255- 258Google ScholarCrossref
4.
Slominski  APaus  RPlonka  P  et al.  Melanogenesis during the anagen-catagen-telogen transformation of the murine hair cycle.  J Invest Dermatol. 1994;102862- 869Google ScholarCrossref
5.
Liew  SHGrobbelaar  AOGault  PTSander  RGreen  CLinge  C The effect of ruby laser light on ex vivo hair follicles: clinical implications.  Ann Plast Surg. 1999;42249- 254Google ScholarCrossref
6.
Sadick  NS Laser and flashlamp photoepilation: a critical review of modern concepts bridging basic science and clinical application.  J Aesthet Derm Cosmet Surg. 1999;195- 101Google Scholar
7.
Dierickx  CAlora  MBDover  JS A clinical overview of hair removal using lasers and light sources.  Dermatol Clin. 1999;17357- 366Google ScholarCrossref
8.
Tope  WDHordinsky  MK A hair's breadth closer [editorial]?  Arch Dermatol. 1998;134867- 869Google Scholar
9.
Lask  GEckhouse  SSlatkine  MWaldman  AKreindel  MGottfried  V The role of laser and intense light sources in photoepilation: a comparative evaluation.  J Cutan Laser Ther. 1999;13- 13Google ScholarCrossref
10.
Dierickx  CGrossman  MCFarinelli  WAAnderson  RR Permanent hair removal by normal mode ruby laser.  Arch Dermatol. 1998;134837- 842Google Scholar
11.
Lin  TXDMianuskiatt  WDierickx  C  et al.  Hair growth cycle affects hair follicle destruction by ruby laser pulses.  J Invest Dermatol. 1998;111107- 113Google ScholarCrossref
12.
Sommer  SRendes  CSheehan-Dare  R Facial hirsutism treated with the normal mode ruby laser: results of a 12 month follow-up study.  J Am Acad Dermatol. 1999;41974- 979Google ScholarCrossref
13.
Lask  GElman  MStatkine  MWaldman  ARosenberg  Z Laser assisted hair removal by selective photothermolysis preliminary results.  Dermatol Surg. 1997;23737- 739Google Scholar
14.
Williams  RHavoo  NJian  HIsaghollan  KMenaker  GMoy  R A clinical study of hair removal using the long pulsed ruby laser.  Dermatol Surg. 1998;24837- 842Google Scholar
15.
Grossman  MDierickx  CFarinelli  WFlotte  TAnderson  RR Damage to hair follicles by normal mode ruby laser pulses.  J Am Acad Dermatol. 1996;35889- 894Google ScholarCrossref
16.
Liew  SHGrabbelaas  AGault  DSander  PRGreen  CLinger  C Hair removal using the ruby laser: clinical efficacy in Fitzpatrick skin types I-V and histologic changes in epidermal melanocytes.  Br J Dermatol. 1999;1401105- 1109Google ScholarCrossref
17.
Nanni  CAAlster  TS Long pulsed alexandrite laser assisted hair removal at 5, 10, 20 milliseconds and pulse durations.  Lasers Surg Med. 1999;24332- 337Google ScholarCrossref
18.
McDaniel  DHLord  JAsh  KNewman  JZukowski  M Laser hair removal: a review and report on the use of the long pulsed alexandrite laser for hair removal reduction of the upper lip, leg, back and bikini region.  Dermatol Surg. 1999;25425- 430Google ScholarCrossref
19.
Goldberg  DJAhkami  R Evaluation comparing multiple treatments with a 2 msec and 10 msec alexandrite laser for hair removal.  Lasers Surg Med. 1999;25223- 228Google ScholarCrossref
20.
Williams  RMGladstone  HBMoy  RL Hair removal using an 810 nm gallium aluminum arsenide semiconductor diode laser: a preliminary study.  Dermatol Surg. 1999;25935- 937Google ScholarCrossref
21.
Rogers  CJGlaser  DASiegfried  ECWalsh  PM Hair removal using topical suspension assisted Q-switched Nd:YAG and lag pulsed alexandrite lasers: a comparative study.  Dermatol Surg. 1999;25844- 850Google ScholarCrossref
22.
Nanni  CAAlster  TA A practical review of laser assisted hair removal using the Q-switched Nd:YAG long pulsed ruby and long pulsed alexandrite lasers.  Dermatol Surg. 1998;241399- 1403Google Scholar
23.
Goldberg  DJLittler  CMWheeland  RG Topical suspension assisted Q-switched Nd:YAG laser hair removal.  Dermatol Surg. 1997;23741- 745Google Scholar
24.
Nanni  CAAlster  TA Optimizing treatment parameters for hair removal using a topical carbon based solution and 1064 nm Q-switched neodymium:YAG laser energy.  Arch Dermatol. 1997;1331546- 1549Google ScholarCrossref
25.
Littler  CM Hair removal using an Nd:YAG laser system.  Dermatol Clin. 1999;17401- 430Google ScholarCrossref
26.
Tse  V Hair removal using a pulsed-intense light source.  Dermatol Clin. 1999;17373- 380Google ScholarCrossref
27.
Sadick  NSShea  CRBurchette Jr  JLPrieto  VG High-intensity flashlamp photoepilation: a clinical, histologic and mechanistic study in human skin.  Arch Dermatol. 1999;135668- 676Google Scholar
28.
Weir  VMWoo  TY Photo-assisted epilation: review and personal observations.  J Cutan Laser Ther. 1999;1135- 143Google ScholarCrossref
29.
Gold  MHBell  MWFoster  TDStreet  S Long-term epilation using the EpiLight broad band intense pulsed light hair removal system.  Dermatol Surg. 1997;23909- 913Google Scholar
30.
Gold  MHBell  MWFoster  TDStreet  S One year follow-up using an intense pulsed light source for long-term hair removal.  J Cutan Laser Ther. 1999;1167- 171Google ScholarCrossref
31.
Schroeter  CARaulin  CThurmmann  WReineke  TDePotter  CNeumann  HAM Hair removal in 40 hirsute women with an intense laser-like light source.  Eur J Dermatol. 1999;9374- 379Google Scholar
32.
Weiss  RAWeiss  MAMorwaha  SHarrington  AC Hair removal with a non-coherent filtered flashlamp intense pulsed light source.  Lasers Surg Med. 1999;24128- 132Google ScholarCrossref
33.
Trollius  ATroillus  C Hair removal with a second-generation broad spectrum intense pulsed light source: a long-term follow-up.  J Cutan Laser Ther. 1999;1173- 178Google ScholarCrossref
34.
Stenn  KSCombates  NJEilersten  KJGordon  JSPardinas  JRParimoo  S Hair follicle growth controls.  Dermatol Clin. 1996;14543- 558Google ScholarCrossref
Study
November 2000

Long-term Photoepilation Using a Broad-spectrum Intense Pulsed Light Source

Author Affiliations

From the Department of Dermatology, Weill Medical College of Cornell University, New York, NY (Dr Sadick); the Department of Dermatology, Johns Hopkins School of Medicine, Baltimore, Md (Dr Weiss); the Departments of Pathology and Medicine (Dermatology), Duke University Medical Center, Durham, NC (Dr Shea); ESC Sharplan, Yokneam, Israel (Ms Nagel) and Norwood, Mass (Ms Nicholson); and the Departments of Pathology and Medicine (Dermatology), University of Texas–MD Anderson Cancer Center, Houston (Dr Prieto). Ms Nagel is an employee of ESC Medical Systems.

Arch Dermatol. 2000;136(11):1336-1340. doi:10.1001/archderm.136.11.1336
Abstract

Background  The goal of laser or flashlamp photoepilation is to produce long-term, cosmetically significant hair removal. We document the long-term efficacy achieved with an intense pulsed light source for photoepilation.

Design  Prospective study comparing long-term results of single vs multiple treatments, and effects of anatomic site and skin type on efficacy of photoepilation with a device emitting broad-spectrum, noncoherent (nonlaser) radiation from 550- to 1200-nm wavelengths, in macropulses divided into 2 to 5 minipulses.

Setting  Private dermatology practice.

Patients  Thirty-four patients (8 men, 26 women) with hirsutism.

Interventions  Parameters for the study were wavelength of 615 to 695 nm, pulse duration of 2.6 to 3.3 milliseconds, fluence of 34 to 42 J/cm2, 10 × 45-mm exposure field, and application of 1°C cooling gel.

Main Outcome Measures  Hair removal efficiency, calculated as percentage ratio of the number of hairs present compared with baseline counts, and patient satisfaction questionnaire completed at last follow-up.

Results  The mean hair removal efficiency achieved was 76% after a mean of 3.7 treatments. More than 94% of the sites reached mean hair removal efficiency values greater than 50%. Hair removal efficiency was not significantly related to skin type, hair color, anatomic site, or number of treatments. Side effects were mild and reversible and occurred in a minority of patients (hyperpigmentation in 3 and superficial crusting in 2).

Conclusions  Our data document the long-term clinical efficacy of intense pulsed light source–induced hair removal in light and dark skin phenotypes. Maximal photoepilation was achieved from the initial 1 to 3 treatments; only a small added benefit was seen after more treatments.

THE GOAL of laser or flashlamp photoepilation is to produce long-term, or permanent, cosmetically significant hair removal. The major proposed mechanism of action is "selective photothermolysis,"1 with follicular melanin as the major target chromophore. Wavelengths in the red and infrared range (600-1100 nm) of the electromagnetic spectrum are optimal for this goal.2 Melanization of the hair follicle has been shown to be maximal during the anagen phase.3,4 It has been proposed that efficiency of photoepilation may be optimal during this phase; since the length of the hair cycle varies among different anatomic regions, equipment settings may need to be modified accordingly to take advantage of phase-dependent melanization. However, recent studies have questioned the primary role of anagen melanization in efficacy of photoepilation.3,5 Multiple treatments may increase melanocyte synthetic activity, which may produce more beneficial results.2,3 Hair color, pilosebaceous depth, and hair follicle thickness also may influence photoepilation efficiency1-3,6; specifically, white to blond hairs, deeper pilosebaceous depth, and thicker diameter of hair follicles are associated with decreased photoepilation efficiency.3,6

Another mechanism proposed to be important in photoepilation is "thermokinetic selectivity," whereby target structures of large volume such as hair shafts are unable to transmit absorbed energy to surrounding structures, compared with smaller volume structures containing the same chromophore.6,7 By selecting the appropriate pulse length, the thermal damage may be concentrated in the target structures (follicular papilla, germinative cell layer, and bulge area).8 This is achieved by setting the duration of the impulse above the calculated thermal relaxation time of the epidermis (3-10 milliseconds) and below the thermal relaxation time of the hair follicles (40-100 milliseconds).9 Both selective photothermolysis and thermokinetic selectivity are hypothesized to mediate photoepilation via ruby,10-16 alexandrite,17-19 diode,20 and Q-switched Nd:YAG lasers,21-25 as well as intense pulsed light (IPL) source26-32 technologies.

The present report documents the long-term efficacy and permanent results achieved with an IPL source for photoepilation (EpiLight; ESC Medical Systems, Norwood, Mass/Yokheam, Israel). This device emits broad-spectrum, noncoherent (nonlaser) radiation from 550- to 1200-nm wavelengths. Unique to this technology is modulation of a pulse into a series of 2 to 5 minipulses, the duration and delay of which are customizable within the millisecond range. A footprint spot size of 10 × 45 mm or 8 × 35 mm is available. Theoretically, these options should allow deep penetration of radiation with a uniform beam, targeting deeper follicles as well as coarse or thin hair, while achieving "epidermal bypass" to minimize dyschromia. According to the specifications provided by the manufacturer, almost all skin types can be treated using these parameters.

In a previous study27 on 58 subjects, we reported mean hair loss at follow-up ranges of less than 3 months, 3 to 6 months, and 6 months or longer of 49%, 57%, and 54%, respectively, with a single treatment, and 74%, 56%, and 64%, respectively, with multiple treatments (wavelength, 590-695 nm; pulse duration, 2.9-3.0 milliseconds; fluence, 40-42 J/cm2). Herein we report on a series of 34 patients with long-term follow-up, of whom 8 were previously described with a shorter follow-up interval.27

Patients and methods
Study groups

The study group consisted of 8 men and 26 women with excess body hair, aged 16 to 68 years (mean, 38 years), who entered a multiple-treatment protocol and had long-term follow-up of 12 to 30 months since their first treatment. The 34 patients each had 1 anatomic site studied by 1 of 2 investigators (N.S.S. and R.A.W.), and were enrolled between April 1997 and September 1999. Fitzpatrick skin types ranged from II to V, and all patients had black or brown terminal hair in the areas selected for treatment. Previous modalities used on the test sites before flashlamp irradiation included waxing (14 patients), chemical depilatories (20 patients), and shaving (16 patients). Any such treatments were discontinued at least 4 weeks before IPL irradiation. Patients avoided UV-B exposure for 4 weeks before and after each treatment session.

Of the 34 total patients, a subgroup of 14 patients was available for evaluation 12 months or more after their final treatment. This subgroup was enrolled between April 1997 and August 1998, and received multiple treatments to a total of 14 anatomic sites.

Photoepilation protocol

Immediately before IPL treatment, hairs were trimmed to 1 mm and a 1°C cooling gel transparent to the irradiation wavelengths was applied to the surface. The IPL treatment was administered with surface exposure parameters related to Fitzpatrick skin type (Table 1), to a 10 × 45-mm exposure field.

All patients received 3 monthly treatments, and 13 had subsequent treatments as necessitated for further clinical improvement and/or because of partial regrowth of hair. Further treatments were administered at intervals of 1 month or more.

Clinical assessment

A 1-cm2 grid was used to count hairs at baseline and at various subsequent times (including 1, 2, 3, 4, 6, 8, 9, 12, 14, 16, 18, 20, 24, and 30 months after IPL treatment for different patients) as previously described.27 The data summarize the final clearance results observed at the last follow-up visit, accounting for different follow-up intervals after initial treatment (range, 12-30 months; mean + SD, 21.1 + 5.1 months). The treatment sites were localized with respect to defined anatomic landmarks (umbilicus, iliac crest, nipple, mandibular ramus, chin, or acromion), confirmed by reference to standardized photographs (Yashica Medical Eye II [Tokyo, Japan] with macrolens, shooting area of 24 × 360 mm, shooting distance of 15.5 cm, and consistent lighting and patient positioning). The hairs were counted with the aid of a hand lens by either of 2 investigators (N.S.S. and R.A.W.) in a nonblinded manner. The hair removal efficiency (HRE) was calculated as a percentage of the number of hairs present compared with baseline counts. Results were tabulated semiquantitively as "excellent" (HRE of 76%-100%), "good" (51%-75%), "fair" (26%-50%), or "poor" (0%-25%). Side effects, if any, were recorded at each visit. For analysis, data were stratified according to the following subsets: (1) light vs dark skin phenotypes (Fitzpatrick skin types I-III vs IV-V), (2) hair color (light-to-medium brown vs dark brown vs black), (3) anatomic location (torso vs extremities vs face), and (4) number of treatments (1-3 vs 4-7). At the end of treatment, a questionnaire was administered to determine the level of patient satisfaction: not satisfied, slightly satisfied, moderately satisfied, and greatly satisfied.

Statistical analysis

The χ2 and the paired t tests were used to compare groups. P<.05 was considered significant.

Results

Thirty-four anatomic sites in 34 patients were treated. The mean HRE achieved was 76% after a mean of 3.7 treatments (33%-100%, SD). The differences in hair count (pretreatment vs at final follow-up) were highly significant (P<10−10) (Figure 1).

Temporary hyperpigmentation ("footprinting") occurred in 3 patients (9%) and resolved within 12 weeks in all treated individuals. Superficial crusting occurred in 2 patients (6%) and resolved without scarring in 2 weeks or less. The incidence of side effects did not vary significantly as a function of skin type.

A majority of treated sites (21 of 34 sites, 62%) exhibited excellent HRE and 11 sites had good results; thus, 94% of the sites reached mean HRE values above 50%. Only 2 patients had fair results and none had poor outcome (Figure 2). Anatomic site was not a significant variable determining HRE (torso mean HRE, 78%; facial mean HRE, 72%).

Although patients with skin types I to III experienced a slightly higher HRE than types IV to V (76% vs 73%), this difference was not statistically significant. Moreover, hair color was not a significant variable affecting HRE (dark brown hair, 82%; black hair, 68%; light-to-medium brown hair, 70%). Finally, HRE was not significantly related to number of treatments (1-3 treatment mean HRE, 75%; 4-7 treatment mean HRE, 77%).

In the subgroup of 14 patients followed up for more than 12 months (mean, 20 months) after the last treatment (Table 2), a final HRE of 83% was achieved after a mean of 3.9 treatments, slightly better than the overall group results (Figure 3).

To determine any possible difference regarding short-term or long-term follow-up HRE, percentages were combined into 6 separate groups with cutoff times at 5, 10, 15, 20, 25, and 30 months of follow-up. Mean HRE values continued to improve after the last treatment, with a final HRE of 92% + 12% at 30 months' follow-up. Figure 4 demonstrates a representative patient with excellent results at long-term follow-up.

Of the 29 individuals who completed the satisfaction questionnaire at the last follow-up, only 3 (10%) were not satisfied at all. Twenty-four (83%) were moderately to greatly satisfied; of these, 15 (52%) were greatly satisfied.

Comment

Four clinical responses may ensue after the light exposure (Table 3). First, heat-induced destruction of the hair shaft without germinative area damage may lead to hair "dropout," ie, the hair shaft falls out and then regrows at the next scheduled anagen cycle as a nonaffected, terminal hair. Second, besides the hair shaft, there may be partial injury to the germinative (amplification) zone of the hair follicle, resulting in trichoregulatory dysfunction, telogen-shock response, prolonged telogen dropout, and eventual regrowth of normal hair once the anagen phase has been reinstituted. Third, partial germinative zone injury may lead to the development of dystrophic hairs (thinner and finer in texture, with variable hypopigmentation). Finally, long-term photoepilation may ensue, defined as a reduction in the number of hairs over an interval longer than the normal hair cycle (usually 1-3 months depending on the particular given anatomic region). Long-term (or potentially permanent) photoepilation most likely is a consequence of light-induced interactions with the primary "bulge" and secondary matrix germinative regions of the pilosebaceous unit.6 To induce permanent hair removal, "pan-tricho" destruction of the entire germinative areas of the hair follicle (bulge/trichoepithelium/matrix) must occur. Permanent, nonscarring hair loss has been described following a single treatment with high-fluence ruby laser pulses,7 similar to that seen with flashlamp devices.27 Miniaturization of the terminal hair follicles seems to account for this response.7

Results of this study using an IPL source for photoepilation confirm that partial, long-term hair removal may be achieved. Successful hair removal with the EpiLight has previously been reported at shorter follow-up periods. A preliminary study by Weir and Woo28 demonstrated 42% and 37% reduction of hair density using a single treatment in patients with skin types IV and V, respectively, examined over 15 months; patients with skin types IV and V were treated with a 645- and 695-nm cutoff filter, respectively, with average fluence of 37 J/cm2, 3 to 4 minipulses, a pulse duration of 2.8 to 2.9 milliseconds, and 57- to 60-millisecond delay between pulses. Gold et al29 performed a single-exposure study with an IPL system. After 12 weeks, a 60% HRE was noted. Fluences ranged from 34 to 55 J/cm2. Another study30 reported a 75% HRE 12 months after a single treatment in 24 patients with skin types I to VI and light brown to black hair; no specific treatment parameters were mentioned. In a multicenter study,21 40 women with hirsutism of the upper lip and chin achieved a 76.7% HRE after an average of 6 treatments; the average fluence was 38.7 J/cm2 and mean wavelength was 585 nm. Schroeter et al31 reported on 40 women with a median age 38.6 years, having hirsutism of the upper lip and chin. The HRE was 76.7% within 6 treatments, with an average fluence of 38.7 J/cm2 and a mean wavelength of 585 nm. Weiss et al32 treated 23 patients with an IPL source with a double-treatment protocol (cutoff filter of 615-645 nm based on Fitzpatrick skin type, pulse duration of 2.8-3.2 milliseconds, 3 pulses, and fluence of 40-42 J/cm2), and showed an HRE of 42% at 8 weeks and 33% at 6 months. Preliminary data have also been reported with a second-generation, broad-spectrum IPL source.33 Ten female patients with dark hair at the groin and of skin types II to IV were treated (600 nm) 4 times with a 1-month interval. An HRE of 74.7% at 4 and 8 months after the last treatment were 74.7% and 80.2%, respectively.

In the present study, a mean HRE of 76% was achieved after a mean of 3.7 treatment sessions, in patients followed up for a mean of 21.1 months. The long wavelengths, ability to partition high-energy fluences, and long pulse durations available with this technology may explain the similarity of our results to those described with the long-pulsed ruby laser.10

It is somewhat surprising that we demonstrated equal photoepilation efficiency in light-to-medium brown and black hair. A likely explanation is that the amount of energy delivered is sufficient to damage the hair in either subtype long-term. The similar HRE in treatments involving the face and torso is also unexpected, but should be interpreted with caution in view of the relatively small number of patients examined in this long-term study. Anagen turnover is increased in the scalp and face regions, compared with the torso and extremities, and might have been expected to favor a greater photoepilation efficiency on the former sites.34 Further studies are necessary to substantiate body site–dependent clinical photoepilation efficiency, related to relative anagen duration and pilosebaceous depth and average hair shaft diameter.

Patients in this study had the greatest HRE after 1 to 3 treatments. Although further treatments led to some increased hair removal, the added benefit was small. Possibly, the initial flashlamp treatment has sufficient energy to destroy the largest number of anagen follicles during the initial treatment session. Light-induced regression of follicles into the catagen or telogen phase may make these targets less susceptible to subsequent treatments.2,7

All treated sites in this study achieved greater than 50% HRE when evaluated more than 12 months following the last treatment; this finding correlated with the observed high level of patient satisfaction. It is unlikely that any miniaturized or damaged hairs could regrow after such a long period. The observed increasing improvement of HRE following the last treatment may be related to partial pilosebaceous injury with subsequent long-term "dropout" effect.

In conclusion, our data document the long-term clinical efficacy of IPL-induced hair removal in light and dark skin and hair phenotypes. Maximal HRE was achieved from the initial treatments. The documentation of maintenance of diminished hair counts for up to 30 months after last treatment supports the long-term value of IPL technology in the treatment of hirsutism.

Accepted for publication June 30, 2000.

This study was supported in part by ESC Sharplan, Norwood, Mass.

Reprints: Neil S. Sadick, MD, 772 Park Ave, New York, NY 10021 (e-mail: nssderm@earthlink.net).

References
1.
Ort  RJAnderson  RR Optical hair removal.  Semin Cutan Med Surg. 1999;18149- 158Google ScholarCrossref
2.
Ross  EVLadin  ZKreindel  MDierickx  C Theoretical considerations in laser hair removal.  Dermatol Clin. 1999;17333- 355Google ScholarCrossref
3.
Liew  SHGrobbelaar  ADGault  DGreen  CLinge  C Ruby laser assisted hair removal: a preliminary report of the correlation between efficacy of treating and melanin content of hair and growth phases of hair at a specific site.  Ann Plast Surg. 1999;42255- 258Google ScholarCrossref
4.
Slominski  APaus  RPlonka  P  et al.  Melanogenesis during the anagen-catagen-telogen transformation of the murine hair cycle.  J Invest Dermatol. 1994;102862- 869Google ScholarCrossref
5.
Liew  SHGrobbelaar  AOGault  PTSander  RGreen  CLinge  C The effect of ruby laser light on ex vivo hair follicles: clinical implications.  Ann Plast Surg. 1999;42249- 254Google ScholarCrossref
6.
Sadick  NS Laser and flashlamp photoepilation: a critical review of modern concepts bridging basic science and clinical application.  J Aesthet Derm Cosmet Surg. 1999;195- 101Google Scholar
7.
Dierickx  CAlora  MBDover  JS A clinical overview of hair removal using lasers and light sources.  Dermatol Clin. 1999;17357- 366Google ScholarCrossref
8.
Tope  WDHordinsky  MK A hair's breadth closer [editorial]?  Arch Dermatol. 1998;134867- 869Google Scholar
9.
Lask  GEckhouse  SSlatkine  MWaldman  AKreindel  MGottfried  V The role of laser and intense light sources in photoepilation: a comparative evaluation.  J Cutan Laser Ther. 1999;13- 13Google ScholarCrossref
10.
Dierickx  CGrossman  MCFarinelli  WAAnderson  RR Permanent hair removal by normal mode ruby laser.  Arch Dermatol. 1998;134837- 842Google Scholar
11.
Lin  TXDMianuskiatt  WDierickx  C  et al.  Hair growth cycle affects hair follicle destruction by ruby laser pulses.  J Invest Dermatol. 1998;111107- 113Google ScholarCrossref
12.
Sommer  SRendes  CSheehan-Dare  R Facial hirsutism treated with the normal mode ruby laser: results of a 12 month follow-up study.  J Am Acad Dermatol. 1999;41974- 979Google ScholarCrossref
13.
Lask  GElman  MStatkine  MWaldman  ARosenberg  Z Laser assisted hair removal by selective photothermolysis preliminary results.  Dermatol Surg. 1997;23737- 739Google Scholar
14.
Williams  RHavoo  NJian  HIsaghollan  KMenaker  GMoy  R A clinical study of hair removal using the long pulsed ruby laser.  Dermatol Surg. 1998;24837- 842Google Scholar
15.
Grossman  MDierickx  CFarinelli  WFlotte  TAnderson  RR Damage to hair follicles by normal mode ruby laser pulses.  J Am Acad Dermatol. 1996;35889- 894Google ScholarCrossref
16.
Liew  SHGrabbelaas  AGault  DSander  PRGreen  CLinger  C Hair removal using the ruby laser: clinical efficacy in Fitzpatrick skin types I-V and histologic changes in epidermal melanocytes.  Br J Dermatol. 1999;1401105- 1109Google ScholarCrossref
17.
Nanni  CAAlster  TS Long pulsed alexandrite laser assisted hair removal at 5, 10, 20 milliseconds and pulse durations.  Lasers Surg Med. 1999;24332- 337Google ScholarCrossref
18.
McDaniel  DHLord  JAsh  KNewman  JZukowski  M Laser hair removal: a review and report on the use of the long pulsed alexandrite laser for hair removal reduction of the upper lip, leg, back and bikini region.  Dermatol Surg. 1999;25425- 430Google ScholarCrossref
19.
Goldberg  DJAhkami  R Evaluation comparing multiple treatments with a 2 msec and 10 msec alexandrite laser for hair removal.  Lasers Surg Med. 1999;25223- 228Google ScholarCrossref
20.
Williams  RMGladstone  HBMoy  RL Hair removal using an 810 nm gallium aluminum arsenide semiconductor diode laser: a preliminary study.  Dermatol Surg. 1999;25935- 937Google ScholarCrossref
21.
Rogers  CJGlaser  DASiegfried  ECWalsh  PM Hair removal using topical suspension assisted Q-switched Nd:YAG and lag pulsed alexandrite lasers: a comparative study.  Dermatol Surg. 1999;25844- 850Google ScholarCrossref
22.
Nanni  CAAlster  TA A practical review of laser assisted hair removal using the Q-switched Nd:YAG long pulsed ruby and long pulsed alexandrite lasers.  Dermatol Surg. 1998;241399- 1403Google Scholar
23.
Goldberg  DJLittler  CMWheeland  RG Topical suspension assisted Q-switched Nd:YAG laser hair removal.  Dermatol Surg. 1997;23741- 745Google Scholar
24.
Nanni  CAAlster  TA Optimizing treatment parameters for hair removal using a topical carbon based solution and 1064 nm Q-switched neodymium:YAG laser energy.  Arch Dermatol. 1997;1331546- 1549Google ScholarCrossref
25.
Littler  CM Hair removal using an Nd:YAG laser system.  Dermatol Clin. 1999;17401- 430Google ScholarCrossref
26.
Tse  V Hair removal using a pulsed-intense light source.  Dermatol Clin. 1999;17373- 380Google ScholarCrossref
27.
Sadick  NSShea  CRBurchette Jr  JLPrieto  VG High-intensity flashlamp photoepilation: a clinical, histologic and mechanistic study in human skin.  Arch Dermatol. 1999;135668- 676Google Scholar
28.
Weir  VMWoo  TY Photo-assisted epilation: review and personal observations.  J Cutan Laser Ther. 1999;1135- 143Google ScholarCrossref
29.
Gold  MHBell  MWFoster  TDStreet  S Long-term epilation using the EpiLight broad band intense pulsed light hair removal system.  Dermatol Surg. 1997;23909- 913Google Scholar
30.
Gold  MHBell  MWFoster  TDStreet  S One year follow-up using an intense pulsed light source for long-term hair removal.  J Cutan Laser Ther. 1999;1167- 171Google ScholarCrossref
31.
Schroeter  CARaulin  CThurmmann  WReineke  TDePotter  CNeumann  HAM Hair removal in 40 hirsute women with an intense laser-like light source.  Eur J Dermatol. 1999;9374- 379Google Scholar
32.
Weiss  RAWeiss  MAMorwaha  SHarrington  AC Hair removal with a non-coherent filtered flashlamp intense pulsed light source.  Lasers Surg Med. 1999;24128- 132Google ScholarCrossref
33.
Trollius  ATroillus  C Hair removal with a second-generation broad spectrum intense pulsed light source: a long-term follow-up.  J Cutan Laser Ther. 1999;1173- 178Google ScholarCrossref
34.
Stenn  KSCombates  NJEilersten  KJGordon  JSPardinas  JRParimoo  S Hair follicle growth controls.  Dermatol Clin. 1996;14543- 558Google ScholarCrossref
×