675-nm Diode Laser as Adjuvant Therapy for Telogen Effluvium: A Retrospective Case Series
This retrospective case series included 13 patients diagnosed with telogen effluvium at a Dermatologic Laser Center in Mexico. All patients received adjuvant treatment with a 675-nm diode laser; no comparator group was included. Follow-up duration was not reported.
Among the 13 patients, 72% had a positive baseline pull test that became negative after treatment. Pruritus improved in 83% of symptomatic patients, and trichodynia resolved in 75%. No adverse events occurred, and the therapy was described as well-tolerated.
Key limitations include the retrospective design, small sample size (n=13), lack of a control group, and single-center setting. The primary outcome was not reported, and no statistical measures (p-values or confidence intervals) were provided. Causality cannot be inferred due to the absence of a comparator.
In practice, 675-nm diode laser appears to be a safe, well-tolerated adjuvant option for telogen effluvium, but controlled studies are needed to confirm efficacy. These findings should be interpreted with low certainty.