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贝克尔假体乳房重建效果的多中心研究。

Multicenter study on breast reconstruction outcome using Becker implants.

机构信息

Department of Plastic Surgery, University La Sapienza, Rome, Italy.

出版信息

Aesthetic Plast Surg. 2011 Feb;35(1):66-72. doi: 10.1007/s00266-010-9559-x. Epub 2010 Jul 30.

Abstract

The use of tissue expanders and implants is the simplest option for breast reconstruction following mastectomy. In the 1980s, Hilton Becker introduced a round, inflatable breast implant that could be used as a permanent implant. Since then, the original implant has been improved in both design and architecture. The new Becker device consists of an anatomical implant composed of 35% cohesive silicone gel in the outer chamber and 65% normal saline in the inner chamber. This multicenter study describes our experience with the new anatomical Becker implants in a large series of patients, in both immediate and delayed breast reconstruction. We reviewed the clinical records of 204 patients who underwent a breast reconstruction with an anatomical Becker-type implant in the sub-muscular position between November 2004 and December 2006. Data on the patients' characteristics, indications for reconstruction, operative technique, device size used, complications, and need for further operations were collected and analyzed. A total of 248 breast reconstructions were performed in 204 patients. One hundred forty-three patients (70%) underwent an immediate reconstruction; in the remaining 61 cases (30%), the breast reconstruction was performed later. The patients' age ranged from 26 to 66 years, with a median age of 47.5 years. The implant was placed unilaterally in 160 women (78.5%) and bilaterally in the remaining 44 (21.5%). Complications occurred in 85 cases (34.2%), in both the immediate and delayed reconstruction groups, and were related to wound healing, bleeding, seroma, and problems with the inflatable expanders. Iatrogenic implant rupture was documented in one case (0.4%). Inflation was impossible in 7 cases (2.8%) as a result of valve obstruction (3 cases, 1.2%) and valve displacement (4 cases, 1.6%). Implant malposition was the most troublesome complication; indeed, 34 patients (13.7%) complained of device malposition. Capsular contracture was assessed in all the patients. Significant capsular contracture (Baker grade III and IV) was detected in 6 cases (2.4%) at the follow-up approximately 1 year after surgery. Breast reconstruction with permanent inflatable expanders is widely acknowledged as a useful technique for breast cancer patients undergoing simple or modified radical mastectomy. The use of this device eliminates the need to replace a temporary tissue expander with a breast implant, thus avoiding a second operation. Although we believe autologous tissues afford the best method of reconstruction in the majority of patients, the results of our study show that expander implant placement may yield a reasonable reconstruction.

摘要

乳房切除术之后,使用组织扩张器和植入物进行乳房重建是最简单的选择。20 世纪 80 年代,希尔顿·贝克尔(Hilton Becker)引入了一种圆形、可充气的乳房植入物,可用作永久性植入物。从那时起,原始植入物在设计和结构上都得到了改进。新型贝克尔(Becker)装置由一个解剖型植入物组成,外部腔室为 35%的粘性硅胶凝胶,内部腔室为 65%的生理盐水。这项多中心研究描述了我们在大量患者中使用新型解剖型贝克尔(Becker)植入物进行即刻和延迟乳房重建的经验。我们回顾了 2004 年 11 月至 2006 年 12 月期间 204 例接受肌肉下解剖型贝克尔(Becker)型植入物乳房重建的患者的临床记录。收集并分析了患者特征、重建指征、手术技术、使用的器械尺寸、并发症以及是否需要进一步手术的数据。204 例患者共进行了 248 例乳房重建。143 例患者(70%)接受了即刻重建;在其余 61 例(30%)中,乳房重建是在以后进行的。患者年龄为 26-66 岁,中位年龄为 47.5 岁。160 名女性(78.5%)接受了单侧植入物,44 名女性(21.5%)接受了双侧植入物。即刻和延迟重建组均有 85 例(34.2%)发生并发症,与伤口愈合、出血、血清肿和充气扩张器问题有关。1 例(0.4%)记录到医源性植入物破裂。由于瓣膜阻塞(3 例,1.2%)和瓣膜移位(4 例,1.6%),7 例(2.8%)无法充气。植入物位置不当是最麻烦的并发症;实际上,34 例患者(13.7%)抱怨装置位置不当。对所有患者进行了包膜挛缩评估。术后约 1 年随访时,发现 6 例(2.4%)有明显包膜挛缩(贝克 3 级和 4 级)。永久性充气扩张器用于接受单纯或改良根治性乳房切除术的乳腺癌患者的乳房重建被广泛认为是一种有用的技术。使用该装置可避免在第二次手术中用乳房植入物替代临时组织扩张器。尽管我们认为自体组织为大多数患者提供了最佳的重建方法,但我们的研究结果表明,扩张器植入物的放置可以获得合理的重建效果。

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