2022
DOI: 10.1016/j.jpra.2022.02.004
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History of breast implants: Back to the future

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Cited by 31 publications
(18 citation statements)
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“…Despite our best efforts, the use of unconventional methods for calculating BI prevalence will never surpass mandatory reporting in NBIRs [ 30 ]. Therefore, we strongly support recommendations of the Scientific Committee on Health, Environmental and Emerging Risks (SCHEER)’s to implement their use [ 2 ] for obtaining a better estimate of risks related to BI complications. In Italy, despite the implementation of Law n°86 on the 5th of June 2012 [ 31 ] for the creation of regional and national breast implant registries, nearly 10 years since the law’s enactment, the country’s tracking efforts are limited to a pilot study in 2019, with 269 participating surgeons as of September 2021: [ 32 ] a number far from the required standards to generate widely applicable data.…”
Section: Discussionmentioning
confidence: 53%
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“…Despite our best efforts, the use of unconventional methods for calculating BI prevalence will never surpass mandatory reporting in NBIRs [ 30 ]. Therefore, we strongly support recommendations of the Scientific Committee on Health, Environmental and Emerging Risks (SCHEER)’s to implement their use [ 2 ] for obtaining a better estimate of risks related to BI complications. In Italy, despite the implementation of Law n°86 on the 5th of June 2012 [ 31 ] for the creation of regional and national breast implant registries, nearly 10 years since the law’s enactment, the country’s tracking efforts are limited to a pilot study in 2019, with 269 participating surgeons as of September 2021: [ 32 ] a number far from the required standards to generate widely applicable data.…”
Section: Discussionmentioning
confidence: 53%
“…The US Food and Drug Administration recently issued several orders to strengthen breast implant (BI) risk communication including restricting implant sales, boxed warnings, mandatory informed consent checklists, and updated surveillance recommendations [ 1 , 2 ]. In 2021, the scientific committee on health, emerging and environmental risks (SCHEER) of the European Commission released a detailed review of breast implant safety and updated guidance on breast implant associated-anaplastic large cell lymphoma (BIA-ALCL) [ 3 ].…”
Section: Introductionmentioning
confidence: 99%
“…Nevertheless, because of missing sales data and the lack of implant registries, it is not possible to clearly define surface-specific incidence rates. Therefore, “high-risk” implants can be considered either only those specific branded types associated with most BIA-ALCL cases, such as Allergan BIOCELL or Silimed Polyurethane-coated devices, or all the textured devices with high surface roughness, so-called macrotextured, hence including more than the previous two [ 46 ].…”
Section: Discussionmentioning
confidence: 99%
“…Nowadays, BI manufacturers recognize rupture as a potential complication [ 15 ].It is also fairly accepted that the longer the indwelling, the likelier it is for patients to experience adverse outcomes requiring surgery [ 16 ]. To strengthen BI safety, the FDA proposed black box warning that includes requesting manufacturers to improve labelling and patient information, outlining implant rupture as a relevant concern [ 17 ], as well as updating rupture screening recommendations [ 18 ]. Other means include pushing for improved reporting strategy of confirmed rupture cases, and conducting Premarket Approval (PMA) Core studies.…”
Section: Discussionmentioning
confidence: 99%