Comparison of the Efficacy of Long-Pulsed Nd:YAG Laser Intervention for Treatment of Onychomycosis of Toenails or Fingernails

October 2014 | Volume 13 | Issue 10 | Original Article | 1258 | Copyright © 2014

Yan Li MD, Sisi Yu MS, Jing Xu MS, Ruina Zhang MS, and Junying Zhao BS

Department of Dermatology, Beijing Friendship Hospital, Capital Medical University, Beijing, China


BACKGROUND: Current studies have demonstrated the efficacy and safety of laser intervention in the treatment of onychomycosis. The objective of this study was to compare the efficacy of long-pulsed Nd:YAG 1064 nm laser for treatment of toenails onychomycosis with fingernails onychomycosis.
METHODS: One hundred and twelve affected fingernails or toenails in 37 patients with onychomycosis were randomized into Group 1 (22 patients with 50 affected fingernails) and Group 2 (15 patients with 62 affected toenails). These patients were further classified into three subgroups (Grade II, III, and IV) according to Scoring Clinical Index of Onychomycosis. All the affected nails were treated with long-pulse Nd:YAG 1064 nm laser intervention, once weekly, for continuous weeks, and were followed up for 24 weeks.
RESULTS: The response rates at weeks 8, 16, and 24 were 0, 0 and 52%, respectively, for Group 1, and 10, 32 and 71% for Group 2. The inter-group difference in efficacy was statistically significant (P<0.05). Even in the same subgroup, the response rate of Group 2 was higher than that of Group 1.
CONCLUSIONS: The efficacy of long-pulsed Nd:YAG 1064 nm laser intervention against affected toenails is superior to that against fingernails. It is also effective for treatment of onychomycosis with different severity.

J Drugs Dermatol. 2014;13(10):1258-1263.

Purchase Original Article

Purchase a single fully formatted PDF of the original manuscript as it was published in the JDD.

Download the original manuscript as it was published in the JDD.

Contact a member of the JDD Sales Team to request a quote or purchase bulk reprints, e-prints or international translation requests.

To get access to JDD's full-text articles and archives, upgrade here.

Save an unformatted copy of this article for on-screen viewing.

Print the full-text of article as it appears on the JDD site.

→ proceed | ↑ close


Onychomycosis is a fungal infection of the nail plate and subungual area, with a high global incidence of 2–18%.1 Most treatment is with topical or oral administration of antifungal agents. Topical antifungal agents have difficulty in penetrating the nail plate and reaching the nail bed, thus, prolonged treatment and poor efficacy might be expected.2 Oral antifungal agents may be associated with hepatorenal impairment and patient compliance is generally poor. Therefore, the treatment of onychomycosis is challenging.3 Long-pulsed Nd:YAG 1064 nm laser intervention with ClearSteps (Fotona, Germany) is approved by the US Food and Drug Administration, and its favorable efficacy and safety profiles have been thoroughly investigated.4-6 However, the regimen for laser intervention against onychomycosis has not been fully established. The course of treatment for oral antifungal agents against toenail onychomycosis is longer than that of fingernail onychomycosis.7,8 Thus, we proposed that there might be differences in the course of laser intervention and recovery between toenail and fingernail onychomycosis. To evaluate the efficacy and safety of ClearSteps for onychomycosis patients in China and improve the laser intervention regimen against onychomycosis, 37 patients with 50 fingernails, and 62 toenails affected by onychomycosis were treated with ClearSteps, and 39 patients with 118 affected nails were treated with oral itraconazole, and were followed up for 24 weeks.


Inclusion and Exclusion Criteria

Patients were included if they met the following inclusion criteria: age 18–75 years; typical clinical manifestations of onychomycosis; positive results of direct microscopic examination; and provided informed consent. They were also asked to attend follow-up as scheduled. The patients enrolled should not have received any topical antifungals within 1 month and oral antifungals within 6 months of enrollment. The Scoring Clinical Index of Onychomycosis (SCIO)9 was estimated to be 6–15 points, in response to Grade II–IV disease.

The exclusion criteria included: patients who discontinued the treatment spontaneously; had a regimen switch during the study or loss to follow-up; patients who received other antifungal drugs or other drugs that might have affected efficacy of laser treatment; patients with continuous or semicontinuous nail discoloration, including fingernail pigmentation abnormalities for therapeutic or cosmetic purposes, such as topical application of antifungal solution Castellany, Nail Stains, polishing agent (containing magnesium or iron components) or occupational exposure to dye or asphalt UML; patients receiving a photosensitizer within 6 months of enrollment; pregnant women; patients with subungual hematoma or mole-like tissue formation; and patients with nail changes concomitant with other disorders, such as nail plate psoriasis, lichen planus, and

↑ back to top

Related Articles