INTRODUCTION
Melasma is a pigmentary disorder in which patients develop symmetric, hyperpigmented macules and patches most commonly on the face. Although the pathogenesis has not been completely elucidated, sun exposure and hormones are thought to contribute to the condition. It occurs most commonly in women and is more prevalent in darker skinned individuals but can occur in all skin types.1
With more than 5 million Americans affected, melasma is a common reason for dermatology appointments and can negatively impact the quality of life of patients.2,3 Despite its widespread prevalence, the treatment of melasma has proven to be difficult. The challenges of treatment are attributed to the chronicity, recurrence rate, and unclear pathogenesis. Many lasers have been used for the treatment of melasma with varying degrees of success. The aim of this study was to investigate the efficacy and safety of a novel picosecond laser for the treatment of melasma.
With more than 5 million Americans affected, melasma is a common reason for dermatology appointments and can negatively impact the quality of life of patients.2,3 Despite its widespread prevalence, the treatment of melasma has proven to be difficult. The challenges of treatment are attributed to the chronicity, recurrence rate, and unclear pathogenesis. Many lasers have been used for the treatment of melasma with varying degrees of success. The aim of this study was to investigate the efficacy and safety of a novel picosecond laser for the treatment of melasma.
MATERIALS AND METHODS
This was a randomized, controlled, split-face prospective study. A total of 10 subjects with a previous diagnosis of melasma were recruited from a dermatology office in Beverly Hills, CA. Inclusion criteria included subjects ages 18-65 with a diagnosis of melasma who were able to provide informed consent. Exclusion criteria included subjects under the age of 18 or over the age of 65, those who had used bleaching creams, chemical peels, or laser treatments within the past month prior to enrollment, those who were pregnant or breast feeding, and those who were on oral contraceptive pills.
Informed consent was obtained from subjects who fulfilled the eligibility criteria. Subjects were then randomized to laser treatment on one side of the face and underwent nine weekly picosecond laser treatments using the PiQo4 laser (Lumenis). Subjects were given and instructed to use a topical lightening cream containing .05% tretinoin/3% kojic acid/6% hydroquinone/1% hydrocortisone to their entire face daily for the duration
Informed consent was obtained from subjects who fulfilled the eligibility criteria. Subjects were then randomized to laser treatment on one side of the face and underwent nine weekly picosecond laser treatments using the PiQo4 laser (Lumenis). Subjects were given and instructed to use a topical lightening cream containing .05% tretinoin/3% kojic acid/6% hydroquinone/1% hydrocortisone to their entire face daily for the duration