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Keloid and Hypertrophic Scars Treatment

  • Original Articles
  • Basic Science/Experimental
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Abstract

Background

Hypertrophic scars are contained within the site of injury and may regress over time, while keloids spread beyond the borders of the initial injury and do not regress. On histologic examination, hypertrophic scars tend to have collagen in a wavy, regular pattern, whereas keloids have no distinct pattern of collagen.

Objective

To retrospectively analyze improvement in keloid and hypertrophic scars characteristics following treatment with Ablative 10600 nm and a non-Ablative 1570 nm Hybrid Laser Device.

Methods

Treatment parameters with the ProScan Hybrid Mode were 40 W/1.3–1.5 ms for the CO2 and 12 W/4 ms for the 1570 nm in a 1:1 ratio. Outcomes were assessed based on physician scar grading as measured by the Vancouver Scar Scale and patient-reported satisfaction. Excel was used for data analysis, and a p value < 0.05 was considered statistically significant. Adverse events and patient pain were also recorded.

Results

A total of 31 hypertrophic scars and 30 keloid scars were treated. There was a significant reduction in Vancouver Scar Scale scores for both hypertrophic and keloid scars (62% ± 8% and 58% ± 7%; p = 2.6E-17 and p = 8.29E-26, respectively). In a scar-based comparison, a statistically significant difference was observed for all measures reflecting favorable outcomes for hypertrophic scars (VSS, p = 1.1E-05; satisfaction, p = 0.0112; pain, p = 0.00081). Only one adverse event was reported, a superficial burn treated with topical antibiotics.

Conclusions

The device was found to be safe and effective, with promising results for the treatment of hypertrophic and keloid scars.

Level of Evidence II

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Correspondence to Shaked Menashe.

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The authors declare that they have no conflicts of interest to disclose.

Human and Animal Rights

Retrospective data collection in this study was conducted following the approval of the ethic committee of Shamir Medical Center, Israel (approval number ASF-0092-23) and in accordance with the 1964 Declaration of Helsinki and its later amendments.

Informed Consent

This is a retrospective collection of anonymized data from previously recorded routine assessments and does not present risk of exposure of personal data of patients. Waiving informed consent will not adversely affect the rights and welfare of the subjects. Consequently, informed consent is not required, in agreement with the Israel Ministry of Health (MoH) Pharmaceutical Division Procedure 14 Part 1(02) clause 4.3.2.10.

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Menashe, S., Heller, L. Keloid and Hypertrophic Scars Treatment. Aesth Plast Surg (2024). https://doi.org/10.1007/s00266-024-03869-7

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