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Efficacy of Q-Switched and picosecond lasers for acquired bilateral nevus of Ota-like macules: a systematic review and exploratory dose-response meta-analysis.

Created on 06 Aug 2026

Authors

Feng Li, Yufeng Wang, Zhaoxia Shen

Published in

Lasers in medical science. Volume 41. Issue 1. Aug 06, 2026. Epub Aug 06, 2026.

Abstract

Acquired bilateral nevus of Ota-like macules (ABNOM) is a common dermal melanocytosis predominantly affecting East Asian women. Q-switched (QS) and picosecond (PS) lasers are widely used, but their comparative efficacy and dose-response relationships have not been quantified. We conducted the first systematic review and dose-response meta-analysis to compare PS versus QS laser efficacy for isolated ABNOM. Eleven databases were searched from inception to May 27, 2026. Forty studies (50 treatment arms) of predominantly single-arm case series were included. The primary analysis used generalized linear mixed models (GLMM) for ≥ 75% clearance, complemented by dose-response meta-regression with cluster-robust standard errors. Pooled ≥ 75% clearance was 47.8% (95% CI 13.4-84.4) for PS and 53.1% (95% CI 30.3-74.6) for QS lasers (P = 0.95). Each additional treatment session was associated with a 3-fold increased odds of clearance (OR 3.2; 95% CI 2.4-4.3; P < 0.001). As an exploratory analysis, the dose-response relationship was monotonic across sessions 1-7. The PS estimate was fragile, ranging from 47.8% to 88.7% across sensitivity analyses. GRADE evidence certainty was very low. Treatment session number, rather than laser type, appeared more strongly associated with clearance. However, this dose-response finding remains hypothesis-generating due to very low certainty of evidence and requires validation in randomized trials. The absence of a statistically significant difference between laser types does not establish equivalence; PS efficacy estimates were highly fragile and based on sparse data. Wavelength may be an independent determinant of clearance and warrants further comparative study.

PMID:
42560400
Bibliographic data and abstract were imported from PubMed on 06 Aug 2026.

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