The Study of the Safety and Effectiveness of Motiva SmoothSilk Silicone Gel-Filled Breast Implants in Patients Undergoing Primary and Revisional Breast Augmentation: Three-Year Clinical Data.

Aesthetic surgery journal 2024 Vol.44(12) p. 1273-1285

Glicksman C, Wolfe A, McGuire P

관련 도메인

Abstract

[BACKGROUND] Silicone breast implant design has evolved over the last 50 years. Regulatory bodies including the FDA require data to support the modifications designed to improve the safety, efficacy, longevity, and biocompatibility of breast implants.

[OBJECTIVES] The authors reviewed the 3-year data on the safety and effectiveness of Motiva (Establishment Labs Holdings, Inc., Alajuela, Costa Rica) SmoothSilk silicone gel-filled breast implants submitted to the FDA. The current submitted data include the primary breast augmentation and revisional augmentation cohorts.

[METHODS] The Motiva IDE is a prospective, single-arm, multicenter, 10-year pivotal study in which data are collected on breast augmentation, reconstruction, and revisional surgery. Three-year data were submitted to the FDA on adverse events, reoperations, patient and physician satisfaction, connective tissue diseases, and quality of life validated instruments. A subset of the patients underwent annual magnetic resonance imaging (MRI) at years 1, 2, and 3 to screen for implant rupture.

[RESULTS] A total of 451 patients were implanted in the primary augmentation cohort and 109 patients in the revisional augmentation cohort. There were 218 patients enrolled in the MRI cohort. Reported rates for reoperation for any reason were 6.1% in the primary augmentation cohort (92.4% follow-up) and 25.8% in the revisional augmentation cohort (88.7% follow-up).

[DISCUSSION] Motiva implants were first introduced in 2010. The 3-year Motiva data suggests that the leading cause of revisional surgery has shifted from capsular contracture and rupture to more subjective indications for reoperation such as malposition and size change.

[CONCLUSIONS] Three-year data from the primary augmentation and revisional augmentation cohorts submitted to the FDA demonstrate the safety and efficacy of the Motiva implants. There were low complication rates for implant-related complications and high surgeon and patient satisfaction.

추출된 의학 개체 (NER)

유형영어 표현한국어 / 풀이UMLS CUI출처등장
해부 breast 유방 dict 7
시술 breast augmentation 유방성형술 dict 3
해부 connective tissue scispacy 1
합병증 capsular contracture 피막구축 dict 1
합병증 implant rupture 보형물 파열 dict 1
합병증 implant-related scispacy 1
재료 silicone breast implant 실리콘 보형물 dict 1
약물 silicone C0037114
silicones
scispacy 1
약물 [BACKGROUND] Silicone breast scispacy 1
약물 FDA scispacy 1
약물 [OBJECTIVES] scispacy 1
약물 Labs scispacy 1
약물 [RESULTS] A scispacy 1
약물 [CONCLUSIONS] Three-year scispacy 1
질환 connective tissue diseases C0009782
Connective Tissue Diseases
scispacy 1
질환 rupture C3203359
Rupture
scispacy 1
질환 implant-related complications scispacy 1
질환 Breast Implants scispacy 1
기타 Patients scispacy 1
기타 patient scispacy 1
기타 capsular scispacy 1

MeSH Terms

Humans; Breast Implants; Female; Silicone Gels; Reoperation; Breast Implantation; Adult; Prospective Studies; Patient Satisfaction; Middle Aged; Prosthesis Design; Treatment Outcome; United States; Prosthesis Failure; Young Adult; Quality of Life; Magnetic Resonance Imaging; Adolescent; Time Factors; Postoperative Complications; United States Food and Drug Administration; Aged

📑 인용 관계

🔗 함께 등장하는 도메인

이 논문이 속한 카테고리와 같은 논문에서 자주 함께 다뤄지는 카테고리들

관련 논문