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Optimization of Prepectoral Breast Reconstruction

机译:Prepeteral乳房重建优化

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Introduction: Acellular dermal matrix (ADM) were introduced in the early 2000s and more recently permitted new protocols for breast reconstruction allowing a short operative time with improved outcomes until the new muscle-sparing breast reconstruction proposed in 2014 using the Braxon (R) ADM. The aim of this research is to propose a technique to improve the aesthetic outcome using Braxon ADM with prepectoral implants. Materials and Methods: The enrolled patients were submitted to a nipple skin-sparing mastectomy leaving 1 additional centimeter of subcutis on the proximal part of the upper pole of the breast (see Surgical Technique). Aesthetic outcomes were compared to those obtained with traditional breast reconstruction with prosthesis and the Braxon ADM placed in the prepectoral space. Mean values of aesthetic outcomes were analyzed using the Student t test, and the kappa test was used to analyze interobserver variability. Results: The overall aesthetic score was improved of 29.6% of the patients; in particular the most improved score was that for contour (+98.01%). Statistical significance was found for contour, upper pole definition, and total score average (p < 0.05).The kappa test showed interobserver variability with a good level of agreement on contour (kappa = 0.832). Conclusions: The proposed technique has allowed attainment of good results in terms of aesthetic outcomes. In a small sample we did not register any particular complications but we verified a better satisfaction on the evaluation of the aesthetic result (level of evidence: 3).
机译:介绍:在2000年代初推出了无细胞性皮肤基质(ADM),最近允许的乳房重建新的协议,允许短暂的操作时间,直到使用Braxon(R)ADM提出的新型肌肉备受乳房重建。本研究的目的是提出一种技术来改善使用Braxon Adm与Prephetal植入物的审美结果。材料和方法:将注册的患者提交给乳头皮肤熏蒸的乳房切除术,在乳房的上部杆的近端部分留下1厘米的亚瓣(参见手术技术)。将审美结果与用传统乳房重建获得的那些,具有假体和Braxon ADM放在Pherpeteral空间中。使用学生T检验分析审美结果的平均值,使用Kappa测试来分析Interobserver变异性。结果:整体审美评分均为29.6%的患者;特别是最改善的分数是用于轮廓(+ 98.01%)。发现轮廓,上极定义和总分平均值(P <0.05)发现统计学意义结论:拟议的技术在审美结果方面允许获得良好的效果。在一个小样本中,我们没有注册任何特定的并发症,但我们验证了对评估审美结果的更好满足(证据级别:3)。

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