Robati R M, Abdollahimajd F, Robati A M
Skin Research Center, Shahid Beheshti University of Medical Sciences, Shohada-e Tajrish Hospital, Shahrdari Sreet, Tehran 1989934148, Iran.
Department of Surgery, Bam University of Medical Sciences, Bam, Iran.
Dermatol Res Pract. 2015;2015:976153. doi: 10.1155/2015/976153. Epub 2015 Dec 16.
Background. A prominent nasolabial fold (NLF) is a cosmetic problem. Currently, numerous therapeutic modalities are available for pronounced NLFs with variable efficacy. Objective. To determine the efficacy and safety of subcision using a hypodermic needle for the correction of the prominent NLFs and its effect on skin elasticity. Methods. Sixteen patients with prominent NLFs underwent subcision. The investigators' assessment of improvement and the patients' satisfaction were both recorded 1 and 6 months after the procedure. Also, we evaluate the skin elasticity of NLFs before and after the treatment using a sensitive biometrologic device with the measurement of cutaneous resonance running time (CRRT). Results. Thirteen (81.25%) patients showed a moderate improvement at 1st month and 13 (81.25%) patients had at least a mild improvement at 6th month. There was no persistent side effect lasting more than a few days. Mean CRRT at 1 and 6 months after the treatment was significantly higher compared to the baseline. Conclusion. Subcision may be considered effective for the correction of pronounced NLFs. However, further controlled studies with larger sample size are necessary to assess the efficacy of this technique in particular with use of more objective assessment of skin biometric characteristics. This trial is registered with IRCT201108097270N1 (registered on January 27, 2012).
背景。明显的鼻唇沟是一个美容问题。目前,有多种治疗方法可用于改善明显的鼻唇沟,但其疗效各异。目的。确定使用皮下注射针进行皮下分离术矫正明显鼻唇沟的疗效和安全性及其对皮肤弹性的影响。方法。16例有明显鼻唇沟的患者接受了皮下分离术。在术后1个月和6个月记录研究者对改善情况的评估以及患者的满意度。此外,我们使用一种敏感的生物计量设备测量皮肤共振运行时间(CRRT),评估治疗前后鼻唇沟的皮肤弹性。结果。13例(81.25%)患者在第1个月时显示出中度改善,13例(81.25%)患者在第6个月时至少有轻度改善。没有持续超过几天的副作用。治疗后1个月和6个月时的平均CRRT明显高于基线水平。结论。皮下分离术对于矫正明显的鼻唇沟可能是有效的。然而,需要进一步开展更大样本量的对照研究,以评估该技术的疗效,特别是在使用更客观的皮肤生物特征评估方面。本试验已在伊朗临床试验注册中心注册,注册号为IRCT201108097270N1(于2012年1月27日注册)。