Methods: First, ASPS members were given a validated, web-based survey of their opinions on the compatibility of FPCBTE and MRI. Second, a review of patients with FPCBTE who had undergone 1.5 Tesla (T) MRI has been performed and complications (pain, heat, migratin, skin changes, and capsule changes) were recorded. Finally, ex vivo testing of FPCBTE from each FDA-approved manufacturer (Natrelle, Sientra, and Mentor) was performed in different MRI settings (3T, shielded 1.5T, and unshielded 1.5T), measuring both torque and deflection angle.
Results: In the survey, 48% of survey respondents believe FPCBTE to be an absolute contraindication to MRI, and a full 28% reported that they would only offer delayed reconstruction if the possibility of requiring an MRI existed. Additionally, 75% would recommend non-MRI imaging or an additional anesthetic episode if a patient with FPCBTE required MRI. In the clinical series, there were no complications among 71 women with FPCBTE who underwent 1.5T MRI. In the ex vivo study, Natrelle devices had the least torque and smallest deflection angles in all 3 environments, and unshielded 1.5T MRI exerted the least ferromagnetic effect in devices from each of the 3 manufacturers.
Conclusions: Our study confirms that the compatibility of FPCBTE and MRI is largely misunderstood, it is possible for MRI to be safely performed with FPCBTE in place, and, in an experimental setting, Natrelle devices in unshielded 1.5T MRI were least affected by the magnetic force. This study defines a widespread misunderstanding that has implications for a generation of women, and works towards a better understanding of the modifiable variables that can allow women to undergo the safest, highest quality breast reconstruction.