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510 高聚型和突度型 Dual-Gel 假体隆乳术:采用一种新方法(Zenith 系统)的 75 例前瞻性研究

Breast augmentation with extra-projected and high-cohesive Dual-Gel Prosthesis 510: a prospective study of 75 consecutive cases for a new method (the Zenith system).

机构信息

Plastic and Reconstructive Surgery Unit, Fondazione IRCCS Istituto Nazionale Tumori, Via Venezian 1, 20133, Milano, Italy.

出版信息

Aesthetic Plast Surg. 2012 Aug;36(4):866-78. doi: 10.1007/s00266-012-9889-y. Epub 2012 Apr 7.

Abstract

BACKGROUND

Extra-projected Natrelle 510 belongs to a new generation of silicone breast implants. A single-surgeon prospective study set out to investigate the device's features, outcomes, and complications, and devise a proper measurement method based on the zenith system.

METHODS

From December 2004 to June 2010, 75 subjects (150 implants) were enrolled in four cohorts: primary augmentation (66.7%), primary mastopexy augmentation (17.3%), secondary implant exchange (9.3%), and secondary implant exchange+pexy (6.7%). The system used to select the implant correlated the point of maximal projection (vertex-zenith) and nipple position. The surgical approach included (1) narrow pocket, preferably dual-plane; (2) device vertex 1-2.5 cm beneath nipple (zenith range=12°-23°) related to a nipple-inframammary fold distance of 7-7.5 cm at maximal stretch and a nipple-sternum/lower-pole line distance of 4-5 cm; (3) inframammary fold lowered minimally; (4) vertex at ±1 cm from the midbreast meridian crossing the nipple; and (5) maximizing the biomechanical effects between soft-tissue dynamics, firmer gel pressure, and pectoralis major counterpressure to expand the lower skin (dynamic tension).

RESULTS

Mean follow-up was 26.5 months (range=6-72); in 20 subjects; follow-up was over 3 years (average=50 months) with a 90.8% patient satisfaction rate. This rate was lower in patients with preoperative ptosis. There was inframammary preservation with 60% of the implants and modification in 40% (0.80±0.45 cm). The overall complication rate per implant was 16.6% and included wound healing/scarring (7%), malrotation (2.6%, only 1% after primary augmentation), rippling (2%), capsular contracture (1.3%), and bottoming-out (0.6%). The revision rate was 6%, of which 3.3% were pocket revisions. Greater skills are required through the learning curve, patient education, case selection, planning using the nipple-vertex relationship (the zenith system), and improved surgical manipulation. Indications and contraindications were analyzed. Cosmetic results were compliant with different breast shapes, and excellent for the breast with poor projection, in thin subjects, and those with low BMI. Ptotic breast should require a larger amount of pexy, 510 did not lift the breast enough.

CONCLUSION

Based on vertex-nipple distance, dynamic tension, and skin extensibility, this new approach gives guidelines and methods to perform breast augmentation with extra-projected implants.

LEVEL OF EVIDENCE III

This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors at www.springer.com/00266.

摘要

背景

Extra-projected Natrelle 510 属于新一代的硅胶乳房植入物。一位外科医生开展了一项前瞻性研究,旨在调查该设备的特点、结果和并发症,并根据 zenith 系统制定适当的测量方法。

方法

从 2004 年 12 月至 2010 年 6 月,75 名患者(150 个植入物)被分为四组入组:初次隆乳术(66.7%)、初次乳房下垂矫正术+隆乳术(17.3%)、二次假体置换术(9.3%)和二次假体置换术+悬吊术(6.7%)。选择植入物的系统将最大突出点(顶点-zenith)和乳头位置相关联。手术方法包括:(1)窄口袋,最好是双平面;(2)植入物顶点位于乳头下方 1-2.5cm(zenith 范围为 12°-23°),乳头至乳晕下褶皱的最大伸展距离为 7-7.5cm,乳头至胸骨/下极线的距离为 4-5cm;(3)乳晕下皱襞最小程度降低;(4)顶点位于穿过乳头的乳房中线±1cm 处;(5)最大限度地利用软组织动力学、更坚固的凝胶压力和胸大肌反压之间的生物力学效应来扩张下皮(动态张力)。

结果

平均随访时间为 26.5 个月(范围 6-72);在 20 名患者中,随访时间超过 3 年(平均 50 个月),患者满意度为 90.8%。术前有乳房下垂的患者满意度较低。60%的患者保留了乳晕,40%的患者乳晕需要修改(0.80±0.45cm)。每个植入物的总体并发症发生率为 16.6%,包括伤口愈合/瘢痕(7%)、旋转(2.6%,仅在初次隆乳术中有 1%)、波纹(2%)、包膜挛缩(1.3%)和假体突出(0.6%)。修复率为 6%,其中 3.3%为口袋修复。需要通过学习曲线、患者教育、病例选择、使用乳头-顶点关系(zenith 系统)进行规划以及改进手术操作来提高技能。分析了适应证和禁忌证。根据不同的乳房形状,美容效果符合要求,对于乳房突出度差、体型偏瘦、BMI 较低的患者效果良好。对于乳房下垂的患者,需要进行更多的悬吊术,510 不能充分提升乳房。

结论

基于顶点-乳头距离、动态张力和皮肤延展性,这种新方法为使用外突型植入物进行乳房增大提供了指导和方法。

证据水平 III:本杂志要求作者为每篇文章分配一个证据水平。有关这些循证医学评级的完整描述,请参考目录或 www.springer.com/00266 上的在线投稿说明。

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