https://www.selleckchem.com/products/tepp-46.html
Background Device rupture is considered a major complication associated with breast implants. The U.S. Food and Drug Administration recommends magnetic resonance imaging (MRI) surveillance 3 years after implantation and then every 2 years, but adherence to these recommendations is poor. The authors identified current practice management for breast implant rupture surveillance by surveying practicing U.S. plastic surgeons. Methods An online survey of all active members of the American Society of Plastic Surgeons was performed. Questions
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