原发性唇裂修复和翻修术后唇部疤痕的外观是肉毒杆菌素更佳还是 Dermabond 更佳?系统回顾与元分析

FACE Pub Date : 2024-01-25 DOI:10.1177/27325016231226300
Paul F. Martinez, Theresa K. Webster, Thomas A. Imahiyerobo
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引用次数: 0

摘要

唇裂疤痕的形成是唇裂修复术(CLR)不可避免的后果,并因面部中部的动态运动而加剧。目前已有多种方法可纠正或预防这些畸形,包括硅胶薄片、手术修整、激光治疗,以及最近的 A 型肉毒杆菌毒素(Botox)和 Dermabond。本研究旨在分析和比较肉毒杆菌毒素和 Dermabond 对 CLR 后疤痕外观的影响。根据 PRISMA 指南,我们使用以下关键词在 Medline、Embase、Cochrane 和 CINAHL 上进行了系统性综述:"Dermabond"、"肉毒素 "和 "唇裂"。研究结果包括疤痕肥大率、疤痕宽度、温哥华疤痕量表(VSS)、视觉模拟量表(VAS)、霍兰德伤口评估量表(HWES)和并发症。共纳入了 9 项研究,其中 4 篇分析了肉毒杆菌毒素,5 篇分析了 Dermabond。第一和第二个时间点的疤痕宽度森林图显示,使用肉毒杆菌毒素可使疤痕宽度变小,P < .0001(95% CI:-1.09 [-1.56 to -0.63]和 95% CI:-0.94 [-1.37 to -0.50])。肉毒杆菌毒素可使 VAS 明显增加(95% CI:1.66 [1.27-2.05],P 值<.0001),而 VSS 则无明显增加。在分析 Dermabond 的文章中,疤痕外观与传统缝合组相当。两种干预方法均未出现进食并发症。比较肉毒杆菌毒素和 Dermabond 的 VAS 汇总森林图显示,与 Dermabond 相比,使用肉毒杆菌毒素可改善 VAS(95% CI:1.66 [1.27-2.05],P < .0001)(95% CI:0.07 [ -0.48 至 0.61],P = .80)。目前的文献支持使用肉毒杆菌毒素来改善 CLR 或翻修后的疤痕。然而,支持 Dermabond 用于改善 CLR 后疤痕的数据很有限,这就凸显了进一步研究的必要性。
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Is Botox or Dermabond Superior in the Appearance of the Lip Scar After Primary Cleft Lip Repair and Revision? A Systematic Review and Meta-Analysis
Cleft lip scar formation is an inevitable consequence of cleft lip repair (CLR) and is exacerbated by the dynamic movement of the middle face. Various methods to correct or prevent these deformities have been described including silicone sheeting, surgical revisions, laser therapy, and more recently, Botulinum toxin-A (Botox) and Dermabond. This study aims to analyze and compare the impact of Botox versus Dermabond on scar appearance after CLR. Following PRISMA guidelines, a systematic review was performed on Medline, Embase, Cochrane, and CINAHL using the following keywords: “Dermabond,” “botulinum toxin,” and “cleft lip.” Outcomes of interest were the rates of scar hypertrophy, scar width, Vancouver scar scale (VSS), visual analog scale (VAS), Hollander wound evaluation scale (HWES), and complications. Nine studies were included of which 4 articles analyzed Botox and 5 analyzed Dermabond. Forest plots for scar width at the first and second time point supported the use of Botox to achieve a smaller scar width with P < .0001 (95% CI: −1.09 [−1.56 to −0.63] and 95% CI: −0.94 [−1.37 to −0.50], respectively). A significant increase in VAS was observed with Botox (95% CI: 1.66 [1.27-2.05], P value < .0001) and VSS was insignificant. Of the articles that analyzed Dermabond, scar appearance was comparable to the traditional suture closure group. There were no feeding complications for either intervention. Pooled forest plots for VAS comparing Botox and Dermabond supported the use of Botox with improved VAS (95% CI: 1.66 [1.27-2.05], P < .0001) compared to Dermabond (95% CI: 0.07 [ −0.48 to 0.61], P = .80). The current literature supports the use of Botox for scar improvement following CLR or revision. However, there is limited data to support Dermabond’s utility in improving scars in CLR, which highlights the need for further studies.
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