Assessment of adverse events for a home‐use intense pulsed light hair removal device using postmarketing surveillance

Author:

Hattersley Anne M.1,Kiernan Michael2,Goldberg David3,Dierickx Christine4,Sliney David H.5,Haedersdal Merete6,Nash J. Frank1ORCID

Affiliation:

1. Procter & Gamble Mason Ohio USA

2. CyDen Ltd. Swansea Wales UK

3. Skin Laser & Surgery Specialists of NY and NJ Hackensack New Jersey USA

4. Skinperium Clinic Luxembourg Luxembourg

5. Bloomberg School of Public Health Johns Hopkins University Baltimore Maryland USA

6. Copenhagen University Hospital Bispebjerg and Frederiksberg Copenhagen Denmark

Abstract

AbstractBackground and objectivesHome‐use intense pulsed light (IPL) hair removal devices are convenient for consumers. Consumer safety associated with home‐use IPL devices, however, remains a subject of interest. In this descriptive analysis, we assessed the most commonly reported adverse events (AEs) for a home‐use IPL device from postmarketing surveillance and qualitatively compared these with AEs from clinical studies and medical device reports of home‐use IPL treatments.Materials and methodsFor this analysis of voluntary reports, we queried a distributor′s postmarketing database for IPL devices for the period beginning January 1, 2016, to December 31, 2021. All sources of comments, for example, phone, e‐mail, company‐sponsored web sites, were included in the analysis. AE data were coded according to the Medical Dictionary for Regulatory Activities (MedDRA) terminology. Also, we conducted a PubMed search to identify AE profiles from existing literature on home‐use IPL devices and we searched the Manufacturer and User Facility Device Experience (MAUDE) database for reports on home‐use IPL devices. These results were qualitatively compared to the data in the postmarketing surveillance database.ResultsA total of 1692 cases involving IPL were identified from voluntary reports of AEs between 2016 and 2021. The shipment‐adjusted reporting rate for AE cases (number of AE cases/100,000 shipped IPL devices) was 67/100,000 during this 6‐year period. The most commonly reported AEs were pain of skin 27.8% (470/1692), “thermal burn” 18.7% (316/1692), and erythema 16.0% (271/1692). Among the top 25 AEs reported, no unexpected health events were observed. The reported AEs were qualitatively similar to the pattern seen in clinical studies and the MAUDE database associated with such home‐use IPL treatments.ConclusionThis is the first such report documenting AEs for home‐use IPL hair removal from a postmarketing surveillance program. These data are supportive of the safety of such home‐use low‐fluence IPL technology.

Publisher

Wiley

Subject

Dermatology,Surgery

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