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贝拉凝胶乳房植入物:一项前瞻性队列研究的4年结果。

BellaGel breast implant: 4-year results of a prospective cohort study.

作者信息

Han Jihyeon, Jeong Jae Hoon, Bang Sa Ik, Heo Chan-Yeong

机构信息

a Department of Plastic and Reconstructive Surgery Seoul National University College of Medicine, Seoul National University Bundang Hospital , Seongnam-si , Gyeonggi-do , Republic of Korea.

b Department of Plastic and Reconstructive Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine , Seoul , Republic of Korea.

出版信息

J Plast Surg Hand Surg. 2019 Aug;53(4):232-239. doi: 10.1080/2000656X.2019.1583572. Epub 2019 Mar 19.

Abstract

The demand for high-quality silicone breast implants is rising. This was the first clinical study on implantation of Asian company-made silicone breast implants into Asian women. The authors report 4-year study data for BellaGel implants. This study is an ongoing 10-year study with 103 subjects undergoing augmentation or primary reconstruction with BellaGel implants. To assess effectiveness, rupture and capsular contracture rates were measured and Kaplan-Meier analysis was performed. Paired -test was used to determine significant changes in breast dimensions. Safety assessment included evaluation of all adverse reactions. Average follow-up period was 5.9 years. Implant rupture and capsular contracture rate through 4 years were 0 percent and 2.3 percent, respectively. Capsular contracture rate was lower in the augmentation group (0.8%) than in the reconstruction group (5.6%). Among the adverse events, procedural pain was the only complication considered device-related, apart from capsular contracture. These 4-year data from the ongoing implant study support the effectiveness and safety of BellaGel implants.

摘要

对高质量硅胶乳房植入物的需求正在上升。这是首次将亚洲公司生产的硅胶乳房植入物植入亚洲女性体内的临床研究。作者报告了BellaGel植入物的4年研究数据。这项研究是一项正在进行的为期10年的研究,有103名受试者接受了BellaGel植入物的隆乳或一期重建手术。为了评估有效性,测量了破裂率和包膜挛缩率,并进行了Kaplan-Meier分析。采用配对t检验来确定乳房尺寸的显著变化。安全性评估包括对所有不良反应的评估。平均随访期为5.9年。4年的植入物破裂率和包膜挛缩率分别为0%和2.3%。隆乳组的包膜挛缩率(0.8%)低于重建组(5.6%)。在不良事件中,除了包膜挛缩外,手术疼痛是唯一被认为与器械相关的并发症。这项正在进行的植入物研究的4年数据支持了BellaGel植入物的有效性和安全性。

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