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超过55000名接受乳房植入手术患者的五年安全性数据:硅胶植入物与国家规范及盐水植入物罕见不良事件发生率的比较

Five-Year Safety Data for More than 55,000 Subjects following Breast Implantation: Comparison of Rare Adverse Event Rates with Silicone Implants versus National Norms and Saline Implants.

作者信息

Singh Navin, Picha George J, Hardas Bhushan, Schumacher Andrew, Murphy Diane K

机构信息

Chevy Chase, Md.; Brecksville, Ohio; and Irvine, Calif.

From Washingtonian Plastic Surgery; Applied Medical Technology, Inc.; and Allergan plc.

出版信息

Plast Reconstr Surg. 2017 Oct;140(4):666-679. doi: 10.1097/PRS.0000000000003711.

Abstract

BACKGROUND

The U.S. Food and Drug Administration has required postapproval studies of silicone breast implants to evaluate the incidence of rare adverse events over 10 years after implantation.

METHODS

The Breast Implant Follow-Up Study is a large 10-year study (>1000 U.S. sites) evaluating long-term safety following primary augmentation, revision-augmentation, primary reconstruction, or revision-reconstruction with Natrelle round silicone breast implants compared with national norms and outcomes with saline implants. Targeted adverse events in subjects followed for 5 to 8 years included connective tissue diseases, neurologic diseases, cancer, and suicide.

RESULTS

The safety population comprised 55,279 women (primary augmentation, n = 42,873; revision-augmentation, n = 6837; primary reconstruction, n = 4828; and revision-reconstruction, n = 741). No targeted adverse events occurred at significantly greater rates in silicone implant groups versus national norms across all indications. The standardized incidence rate (observed/national norm) for all indications combined was 1.4 for cervical/vulvar cancer, 0.8 for brain cancer, 0.3 for multiple sclerosis, and 0.1 for lupus/lupus-like syndrome. Silicone implants did not significantly increase the risk for any targeted adverse events compared with saline implants. The risk of death was similar with silicone versus saline implants across all indications. The suicide rate (10.6 events per 100,000 person-years) was not significantly higher than the national norm. No implant-related deaths occurred.

CONCLUSIONS

Results from 5 to 8 years of follow-up for a large number of subjects confirmed the safety of Natrelle round silicone implants, with no increased risk of systemic disease or suicide versus national norms or saline implants.

CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, II.

摘要

背景

美国食品药品监督管理局要求对硅胶乳房植入物进行批准后研究,以评估植入后10年内罕见不良事件的发生率。

方法

乳房植入物随访研究是一项为期10年的大型研究(超过1000个美国研究点),评估使用娜绮丽圆形硅胶乳房植入物进行初次隆乳、修复性隆乳、初次重建或修复性重建后的长期安全性,并与国家规范以及盐水植入物的结果进行比较。对随访5至8年的受试者的目标不良事件包括结缔组织疾病、神经系统疾病、癌症和自杀。

结果

安全人群包括55279名女性(初次隆乳,n = 42873;修复性隆乳,n = 6837;初次重建,n = 4828;修复性重建,n = 741)。在所有适应症中,硅胶植入物组的目标不良事件发生率均未显著高于国家规范。所有适应症综合的标准化发病率(观察值/国家规范),宫颈癌/外阴癌为1.4,脑癌为0.8,多发性硬化症为0.3,狼疮/狼疮样综合征为0.1。与盐水植入物相比,硅胶植入物并未显著增加任何目标不良事件的风险。在所有适应症中,硅胶植入物与盐水植入物的死亡风险相似。自杀率(每10万人年10.6例事件)并不显著高于国家规范。未发生与植入物相关的死亡。

结论

对大量受试者进行5至8年的随访结果证实了娜绮丽圆形硅胶植入物的安全性,与国家规范或盐水植入物相比,系统性疾病或自杀风险并未增加。

临床问题/证据水平:治疗性,II级。

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