Linz and Wels, Austria; and Munich, Germany.
From the Section of Plastic and Reconstructive Surgery, Kepler University Hospital Linz; private practice; and the Department of Plastic and Hand Surgery, Technical University Munich.
Plast Reconstr Surg. 2018 Jun;141(6):831e-842e. doi: 10.1097/PRS.0000000000004367.
BACKGROUND: Macrotextured anatomical implants are frequently used in aesthetic breast surgery; however, several safety concerns linked to this implant type have been raised recently. In an attempt to address these shortcomings, Motiva Ergonomix implants have been introduced. Here, the authors describe the current world's largest experience with these novel devices in aesthetic breast surgery and evaluate the postoperative outcome of 100 primary breast augmentations. METHODS: A retrospective assessment of 100 consecutive primary breast augmentation patients over a period of 3 years was conducted. Patients were followed for a minimum of 6 months postoperatively. Demographics, surgical data, and complications were recorded. In addition, a survey regarding the breast augmentation outcome was performed. RESULTS: The reasons for surgery were mainly hypoplasia (52 percent) and ptosis (28 percent). All implants were placed by means of an inframammary approach in a submuscular pocket, and the average implant volume was 370 cc (range, 150 to 700 cc) with mostly full projection (65 percent). The revision rate was 7 percent. The authors observed four cases of implant malpositioning, one implant rupture, one implant exchange for aesthetic reasons, and one hematoma evacuation. Nevertheless, the authors achieved a 100 percent satisfaction rate with the postsurgical outcome among both patients and surgeons. CONCLUSIONS: Motiva Ergonomix implants provide reliable and satisfying results for both patients and surgeons. They can be used safely and effectively for aesthetic breast surgery. However, like all breast prostheses, Motiva Ergonomix implants are not completely free of complications and should be used only with advanced technique to achieve optimal results. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, IV.
背景:大分子量解剖型植入物常用于美容乳房手术;然而,最近出现了与这种植入物类型相关的一些安全问题。为了应对这些缺点,Motiva Ergonomix 植入物应运而生。在此,作者描述了在美容乳房手术中使用这些新型装置的目前全球最大经验,并评估了 100 例原发性乳房增大术的术后结果。
方法:对 3 年内连续 100 例原发性乳房增大患者进行回顾性评估。患者术后至少随访 6 个月。记录患者的人口统计学、手术数据和并发症。此外,还对乳房增大的结果进行了调查。
结果:手术的主要原因是发育不良(52%)和下垂(28%)。所有植入物均通过乳晕下切口放置在胸肌下袋中,平均植入物体积为 370cc(范围为 150-700cc),大多为全突度(65%)。翻修率为 7%。作者观察到 4 例植入物位置不当、1 例植入物破裂、1 例出于美观原因更换植入物、1 例血肿清除。尽管如此,作者还是在患者和医生中实现了 100%的术后结果满意度。
结论:Motiva Ergonomix 植入物为患者和医生提供了可靠和满意的结果。它们可安全有效地用于美容乳房手术。然而,与所有乳房假体一样,Motiva Ergonomix 植入物并非完全没有并发症,应仅在使用先进技术的情况下使用,以获得最佳效果。
临床问题/证据水平:治疗性,IV。
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