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This is a prospective, single-center, non-randomized study of immediate breast reconstruction (IBR) using a pre- or retro-pectoral technique in patients with breast cancer who have undergone total mastectomy.
The technique used is chosen according to the characteristics of the breast, the morphology of the patient and her wishes after informed information on the different techniques. The aim is not to compare the two techniques but rather to evaluate the early functional results of these two methods in order to better understand them and to propose a management adapted to each.
The main objective will be to evaluate the postoperative pain by BPI questionnaire.
The investigators also wish to observe the functional results of the homolateral upper limb by DASH questionnaire, the quality of life by BREAST Q questionnaire and the occurrence of complications.
describe the occurrence of complications between pre-pectoral and retro-pectoral technique in patients with breast cancer who have total mastectomy.
evaluate the postoperative pain by Brief Pain Inventory (BPI) self assesment observe the functional results of the homolateral upper limb by Disabilities of the Arm, Shoulder and Hand (DASH) self assesment observe quality of life by BREAST Q questionary
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| pre-pectoral prosthesis | breast cancer patients with an indication for total mastectomy + immediate breast reconstruction (IBR) by prosthesis using a pre-pectoral technique |
| |
| retropectoral prosthesis | breast cancer patients with an indication for total mastectomy + immediate breast reconstruction (IBR) by prosthesis using the retropectoral technique |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| mastectomy + immediate breast reconstruction | Procedure | pre- or retro pectoral prosthesis |
|
| Measure | Description | Time Frame |
|---|---|---|
| Describe postoperative pain and functional results | Brief Pain Inventory (BPI) short form - 4 scales from 1 (No pain) to 10 (max pain) + 7 scales from 1 (no discomfort) to 10 (max discomfort) to determine if the pain interfered with activities of daily living | 6 month |
| Measure | Description | Time Frame |
|---|---|---|
| Assessing quality of life and aesthetic satisfaction | breast questionary pre-post operative reconstruction module | 6 months |
| Evaluate the function of the homolateral upper limb | Disabilities of the Arm, Shoulder and Hand self-assessment |
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Inclusion Criteria:
Exclusion Criteria:
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Major patients followed for breast cancer with indication of mastectomy with immediate breast reconstruction by prosthesis.
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| Name | Affiliation | Role |
|---|---|---|
| Céline RENAUDEAU, MD | celine.renaudeau@ico.unicancer.fr | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Institut de Cancerologie de L'Ouest | Saint-Herblain | 44805 | France |
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| ID | Term |
|---|---|
| D008408 | Mastectomy |
| ID | Term |
|---|---|
| D013514 | Surgical Procedures, Operative |
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| 6 months |
| Describe the occurrence of postoperative complications | postoperative complications | 3 months |
| Describe the length of operative stay (for the initial reconstruction), for all patients and according to the methods of reconstruction performed | duration of hospitalization | 3 months |
| Describe the duration of drainage for all patients and according to the methods of reconstruction performed | duration of drainage in the breast and back, number of punctures and total volume of seroma punctures (classification <2) | 3 months |
| Describe the number of surgery(s) required to obtain a good aesthetic result | number of surgery(s) | 3 months |
| Describe the number of consultations for seroma punctures, for all patients and according to the methods of reconstruction performed | number of punctures and total volume of seroma punctures (classification <2) | 3 months |