National, Multicenter PMS Study "Patient Reported Outcome" in Breast Reconstruction Following Mastectomy With TiLOOP Bra

Inclusion Criteria

• •The TiLOOP®Bra is designed to assist oncologically indexed skin sparing mastectomy or subcutaneous mastectomy with preservation of the nipple-areola-complex during primary breast reconstruction, secondary breast reconstruction or corrective breast surgery. Patients shall be included if they meet all of the following criteria:
• •Clinical Criteria (reason):
• •women with indication of prophylactic operation or oncoplastic operation with support of a mesh implant
• •women with histologically confirmed breast cancer or precancerosis or genetic pre-existing conditions with increased risk of breast cancer or with a family history
• •the health of women must comply with ECOG (Eastern Cooperative Oncology Group) performance status 0-2
• •Patient is mentally able to understand the nature, aims, or possible consequences of the clinical investigation
• •Patient information has been handed out and all written consents are at hand.
• •Patient is between 18 and 70 years old.