Shridharani Sachin M, Ogilvie Patricia, Couvillion Megan, Pavicic Tatjana, Lain Edward, Jierjian Edward, Lee Elisabeth, Park Grace S, Shimoga Sandhya, Tong Warren, Hopfinger René
Aesthet Surg J. 2025 Jan 16;45(2):194-201. doi: 10.1093/asj/sjae220.
Platysma prominence (PP) describes the noticeable appearance of the platysma muscle upon contraction, causing a less defined jawline contour and vertical neck bands.
The objective of this study was to assess the safety and efficacy of onabotulinumtoxinA for improvement of PP in adults.
Participants with moderate to severe (Grade 3 to 4) PP at maximum contraction received onabotulinumtoxinA or placebo on Day 1 and were monitored for 120 days. OnabotulinumtoxinA dosage (26, 31, or 36 U) was customized based on baseline PP severity on each side of the neck.
Efficacy analyses were conducted in the intent-to-treat (ITT) population (all randomized participants), and modified ITT population (mITT; psychosocially impacted by PP appearance). Results from ITT and mITT populations were comparable. As assessed by investigators, 76.7% of onabotulinumtoxinA mITT participants achieved ≥1-grade improvement vs 21.2% in the placebo group, and 41.0% vs 2.2% (P < .0001) achieved ≥2-grade improvement at Day 14. As assessed by participants, 79.9% of onabotulinumtoxinA mITT participants vs 21.8% in the placebo group and 40.8% vs 3.9% (P < .0001) achieved ≥1- or ≥2-grade improvement, respectively, at Day 14. OnabotulinumtoxinA responder rates remained higher than placebo through Day 120, gradually declining over time. OnabotulinumtoxinA participants reported significantly higher satisfaction with treatment effect, less bother from jawline and vertical neck bands, and lower psychosocial impact from PP than placebo at Day 14 (P < .0001). OnabotulinumtoxinA effectively improved self-perceived jawline definition and was well tolerated.
OnabotulinumtoxinA was well tolerated and effective at improving moderate to severe PP, including neck bands and jawline definition.
颈阔肌突出(PP)是指颈阔肌收缩时明显可见,导致下颌轮廓不清晰和颈部出现垂直条纹。
本研究旨在评估A型肉毒毒素改善成人PP的安全性和有效性。
最大收缩时患有中度至重度(3至4级)PP的参与者在第1天接受A型肉毒毒素或安慰剂治疗,并监测120天。A型肉毒毒素剂量(26、31或36 U)根据颈部两侧的基线PP严重程度进行定制。
在意向性治疗(ITT)人群(所有随机分组的参与者)和改良ITT人群(mITT;受PP外观心理社会影响者)中进行了疗效分析。ITT人群和mITT人群的结果具有可比性。根据研究者评估,在第14天,76.7%的A型肉毒毒素mITT参与者实现了≥1级改善,而安慰剂组为21.2%;实现≥2级改善的比例分别为41.0%和2.2%(P <.0001)。根据参与者评估,在第14天,79.9%的A型肉毒毒素mITT参与者和21.8%的安慰剂组参与者分别实现了≥1级或≥2级改善,比例分别为40.8%和3.9%(P <.0001)。直到第120天,A型肉毒毒素的反应率一直高于安慰剂组,且随时间逐渐下降。在第14天,与安慰剂组相比,A型肉毒毒素治疗的参与者对治疗效果的满意度显著更高,下颌轮廓和颈部垂直条纹带来的困扰更少,PP对心理社会的影响更低(P <.0001)。A型肉毒毒素有效改善了自我感知的下颌轮廓清晰度,且耐受性良好。
A型肉毒毒素耐受性良好,在改善中度至重度PP方面有效,包括颈部条纹和下颌轮廓清晰度。