Endoscopic Transaxillary Breast Augmentation – a Case Series of 1300 Patients

Y. Sardiwalla, S. Ching
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Abstract

Abstract   Level of Evidence: V – case series  Goals/Purpose Breast augmentation is currently one of the most common aesthetic surgical procedures performed in the United States. Transaxillary breast augmentation offers an advantageous hidden scar compared with other options for implant placement. While first described as a blunt and blind approach, endoscopic technique further refined this procedure to offer surgeons complete control and visualization of dissection for precise implant placement. Despite this, breast augmentation is done far more commonly as was initially described over 60 years ago with incisions on the breast that can result in visible scarring. The purpose of this study was to report surgical outcomes on the largest published series to date in a patient cohort of 1389 endoscopic transaxillary breast augmentations. We describe the refinement of this technique and statistical analysis of patient outcomes. Methods/Technique This study included all patients with breast hypoplasia who chose endoscopic transaxillary breast augmentation from 2006 to 2022 by a single surgeon (S.C.). All patients were followed for a minimum of 3 months post procedure. All implants used were smooth, round, silicone gel implants with volumes ranging from 180 to 800cc. Implants were placed in the subfascial or submuscular plane. An incision was marked in the most prominent axillary crease. If there were no creases, an incision was marked at the highest point of the armpit along Langer’s lines. A 30 degree endoscope (Karl Storz, USA) was placed in an endoscopic breast retractor (Karl Storz, USA) and dissection proceeded either in the submuscular plane between the pectoralis major and minor, or in the subfascial plane with an angled suction cautery (Black and Black Surgical, Texas). In the case of subfascial implant placement, the pocket was dissected according to the preoperative markings. With submuscular placement, pocket dissection also followed markings, but the pectoralis muscle was divided with cautery from the level of the areola along the sternal origins of the muscle to completely divide the muscle inferiorly and laterally. The inframammary fold was lowered as necessary by cautery dissection above the level of the pectoralis fascia inferiorly. Glandular scoring was performed with cautery when needed as well. After dissection was completed, saline breast implant sizers were inserted and filled with air to estimate implant size and confirm pocket dissection in the upright position. Adjustments were made to the implant pocket with endoscopic cautery dissection as was necessary. Results/Complications A total of 1389 patients were included in our data analysis for surgeries performed between March 2006 and December 2021. Overall complication rate in our cohort was 6.69%. Malposition of implants was the most common complication at 3.64%. Contracture rate was 1.74%. There was a significant increase noted in hematoma rate in subfascial placement (3.51% increase, p-value<0.05) compared to submuscular and a decrease in implant malposition in the subfascial group (6.58% decrease, p-value<0.05) compared to the submuscular group. These complications were largely managed using endoscopic techniques. There were no significant differences noted between subfascial, subglandular and submuscular pocket placement in asymmetry, contracture and hypertrophy. Conclusion We describe a safe and effective approach to endoscopic transaxillary breast augmentation that has demonstrated long term results compared to the direct vision inframammary technique. The advantages of a hidden scar should be a consideration for surgeons to adopt this technique to improve patient outcomes.
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内窥镜经腋窝隆胸术 - 1300 例患者的病例系列
摘要 证据等级:V - 病例系列 目标/目的 隆胸是目前美国最常见的美容外科手术之一。与其他植入假体的方法相比,经腋窝隆胸具有疤痕隐蔽的优点。内窥镜技术最初被描述为一种钝性和盲目的方法,后来它进一步完善了这一手术,为外科医生提供了完全可控和可视化的剥离,以实现精确的假体植入。尽管如此,假体隆胸术仍然像 60 多年前最初描述的那样,在乳房上进行切口,可能会留下明显的疤痕。本研究的目的是报告迄今为止已发表的最大规模的内窥镜经腋窝隆胸术的手术结果,该系列共有 1389 名患者。我们描述了这项技术的改进情况以及对患者疗效的统计分析。方法/技术 这项研究包括2006年至2022年期间选择内窥镜经腋窝隆胸术的所有乳房发育不良患者,由一名外科医生(S.C.)负责。所有患者都在术后接受了至少 3 个月的随访。所有假体均为光滑的圆形硅凝胶假体,容量从 180cc 到 800cc 不等。植入物被放置在筋膜下或肌肉下平面。切口标记在最明显的腋窝皱褶处。如果没有腋窝皱褶,则在腋窝最高点沿朗格线标记切口。将 30 度内窥镜(Karl Storz,美国)置于内窥镜乳房牵引器(Karl Storz,美国)中,然后在胸大肌和胸小肌之间的肌肉下平面或筋膜下平面使用带角度的抽吸烧灼器(Black and Black Surgical,德克萨斯州)进行解剖。在筋膜下植入假体时,根据术前标记解剖袋。如果是肌肉下植入,也是按照标记解剖袋,但用烧灼器从乳晕水平沿着胸骨起源处分割胸肌,将肌肉向下和向外完全分割。必要时,在胸肌筋膜水平上方向下用烧灼器剥离乳房下皱襞。必要时还用烧灼法进行腺体扫描。剥离完成后,插入生理盐水乳房假体测量器并充入空气,以估算假体大小,并在直立位置确认假体袋剥离情况。必要时使用内窥镜烧灼法对植入袋进行调整。结果/并发症 2006年3月至2021年12月期间,共有1389名患者接受了我们的数据分析。总体并发症发生率为 6.69%。植入物错位是最常见的并发症,占 3.64%。挛缩率为 1.74%。与肌肉下植入相比,筋膜下植入的血肿率明显增加(增加 3.51%,P 值<0.05),而筋膜下植入组的植入体错位率则比肌肉下植入组有所下降(下降 6.58%,P 值<0.05)。这些并发症主要是通过内窥镜技术处理的。筋膜下、腺下和肌下口袋置入术在不对称、挛缩和肥大方面没有明显差异。结论 我们描述了一种安全有效的内窥镜经腋窝隆胸方法,与乳房下直视技术相比,这种方法的长期效果非常明显。隐蔽疤痕的优势应成为外科医生采用该技术改善患者疗效的考虑因素。
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