Skip to content

Data Collection of Prepectoral Breast Reconstruction With Polyurethane Implantes

Prepectoral Breast Reconstruction With Polyurethane Implantes and Radiotherapy: a Single Center Retrospective Study Evaluating Risk and Complications

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06216106
Acronym
IBR-PPBR
Enrollment
237
Registered
2024-01-22
Start date
2020-03-18
Completion date
2023-10-05
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Reconstruction, Prepectoral Breast Reconstruction, Radiation Therapy Complication

Keywords

PPBR, POLYURETHANE, IBR, RADIOTHERAPY, BREAST IMPLANTS

Brief summary

The goal of this observational study is to learn about correct surgical indications and long-term complications in patient with immediate prepectoral breast reconstruction with polyurethane implants. The main question it aims to answer are: what are the correct indications for this type of reconstruction? what is the complications rates? are the complications affected by pre and post operative radiotherapy? It's a retrospective study of all the patients that received prepectoral breast reconstruction with polyurethane implants without any exclusion factors. Researchers will compare the non-irradiated group with the patients with pre and post radiation therapy.

Detailed description

The study is a data collection of 250 patients for a total of 317 breasts underwent prepectoral breast recosntruction with polyurethane implantes. It is a retrospective study of a single center. The investigators gave indication to that type of reconstruction only to patients with good thickness (\> 0.5 cm) and vascularity of skin flap after mastectomy. The investigators used not selective criteria regarding risk factors so to better evaluate wich of them has a negative trend on the success of the reconstruction and on the major and minor complications. In that way the investigators tried to definde clarly the correct indications for this type of reconstruction. In addition, the investigators would like to define if the postoperative radiation therapy agument the complications rate and the capsular contracture incidence. The investigators decide to perform prepectoral breast reconstruction also in 20 patientes underwent previous radiotherapy dependig on the grade of cutaneus radiodistrophy, so to propose our less invasive approach to these patients normally candidates to autologus breast reconstruction

Interventions

PROCEDUREPrepectoral breast reconstruction with polyurethane implants

Breast reconstruction in the prepectoral plane without elevate the pectoralis major muscle. We choose this type of reconstruction only in patients with mastectomy flap thickness of plus then 0.5 cm. We usally use silicone implants covered by an external layer of polyurethane so not to put directly in contact the silicone with the subcutaneus tissue.

Sponsors

European Institute of Oncology
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE

Inclusion criteria

* patients underwent prepectoral breast recosntruction with polyurethane implants after skin or nipple sparing masectomy * adequate mastectomy flap in vascularity and thickness

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
reconstruction failure12 monthsloss of implant or switch to autologus recosntruction
major complications12monthsevaluation of hematoma, infection, flap necrosis, wound dehiscence rate
minor complications12 monthsevaluation of seroma, rippling, casular contracture, asymmetry rate
risk factor12 monthsevaluation of the risk factors correlated to recostruction failure

Secondary

MeasureTime frameDescription
postoperative radiation therapy on patients underwent prepectoral breast reconstruction with polyurethane implantes12 monthsevaluation if the post operative radiation therapy is correlated with an increase of reconstruction failure and capsular contracture
patients previously irradiated (QUART) and underwent prepectoral breast reconstruction with polyurethane implantes12 monthsanalysis of clinical characteristics of pre irradiatred patients submitted to prepectoral breast recosntruction with polyurethane implantes

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026