Eight-year follow-up data from the U.S. clinical trial for Sientra's FDA-approved round and shaped implants with high-strength cohesive silicone gel.

Aesthetic surgery journal 2015 Vol.35 Suppl 1() p. S3-10

Stevens WG, Harrington J, Alizadeh K, Broadway D, Zeidler K, Godinez TB

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Abstract

[BACKGROUND] On March 9, 2012, the Food and Drug Administration (FDA) approved Sientra's premarket approval application for its portfolio of silicone gel breast implants based on their review of Sientra's 3-year study data from the largest pivotal silicone gel breast implant study to date. This included the first approval of shaped breast implants in the United States.

[OBJECTIVES] The authors provide an update to the 8-year safety and effectiveness of the Sientra High-Strength silicone gel breast implants.

[METHODS] The Sientra Core study is an ongoing 10 year open-label, prospective, multi-center clinical study, which includes 1788 patients implanted with 3506 Sientra implants across four indications (Primary Augmentation, Revision Augmentation, Primary Reconstruction, and Revision Reconstruction). For the safety analysis, the incidence of post-operative complications, including all breast implant-related adverse effects (eg, infection, asymmetry), was estimated based on Kaplan-Meier risk rates. The effectiveness analyses include surgeon and patient satisfaction and changes in bra/cup size.

[RESULTS] Through 8 years, the overall risk of rupture was 4.6%, the risk of capsular contracture was 11.8% (rates were lower when using True Texture™), and the risk of reoperation was 28.3%. Out of the 580 reoperations in 456 patients, over half of all reoperations were due to cosmetic reasons (n = 299). The most common reasons for reoperation were capsular contracture (19.0%), style and/or size change (18.4%), and asymmetry (8.8%). Patient satisfaction remains high through 8 years, with 87% indicating that their breast implants make them feel more feminine than prior to enrollment.

[CONCLUSIONS] Safety data from the FDA Core study continues to support a comprehensive safety and effectiveness profile of Sientra's portfolio of round and shaped implants through 8 years.

[LEVEL OF EVIDENCE] 3 Therapeutic.

추출된 의학 개체 (NER)

유형영어 표현한국어 / 풀이UMLS CUI출처등장
해부 breast 유방 dict 6
합병증 capsular contracture 피막구축 dict 2
합병증 asymmetry 비대칭 dict 2
합병증 infection 감염 dict 1
합병증 breast implants scispacy 1
합병증 breast implant scispacy 1
약물 high-strength cohesive silicone scispacy 1
약물 silicone C0037114
silicones
scispacy 1
약물 [BACKGROUND] scispacy 1
약물 Food scispacy 1
약물 [OBJECTIVES] scispacy 1
약물 [CONCLUSIONS] scispacy 1
질환 breast implant-related C4528211
Breast Implant-Related Lesion
scispacy 1
질환 rupture C3203359
Rupture
scispacy 1
질환 contracture C0009917
Contracture
scispacy 1
기타 patients scispacy 1
기타 patient scispacy 1

MeSH Terms

Adolescent; Adult; Aged; Breast Implantation; Breast Implants; Female; Follow-Up Studies; Humans; Implant Capsular Contracture; Middle Aged; Patient Satisfaction; Prosthesis Design; Prosthesis Failure; Reoperation; Rupture; Silicone Gels; United States; Young Adult

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