EvaLuating negAtive pressUre Wound theRapy in brEast coNserving Surgery

Zuyderland Medisch Centrum300 enrolled

Overview

Negative pressure wound therapy (NPWT) could improve surgical outcomes and reduce complications like SSI, wound dehiscence and seroma in closed surgical wounds. To date, NPWT was not evaluated in patients undergoing breast conserving surgery without direct reconstruction.Therefore, the aim of this trial is to evaluate the feasibility of NPWT after surgery and its effects on postoperative complications.

Rationale: Negative pressure wound therapy (NPWT) could improve surgical outcomes and reduce complications like SSI, wound dehiscence and seroma in closed surgical wounds. Complication rate after breast conserving surgery for breast cancer is 2-17%, surgical site infections (SSI) being the most common. To date, NPWT was not evaluated in patients undergoing breast conserving surgery without direct reconstruction. Therefore, in this trial, the aim is to evaluate the feasibility of NPWT after breast conserving surgery and its effects on postoperative complications. Objective and study parameters: Primary objective is to compare surgical site complications in patients with and without NPWT. Secondary objective is to assess the number of re-interventions, unplanned visits and pain scores. Study design: A prospective cohort of 150 patients will be compared to a retrospective cohort of 150 patients. Study population: Breast cancer patients undergoing breast conserving surgery with or without sentinel lymph node biopsy. Intervention (if applicable): Negative pressure wound therapy. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: When participating in this study, patients will need to pay at least one extra visit to the hospital, possibly two if this cannot be combined with the standard postoperative visits. In addition, patients will need to have a device with them for 14 days after surgery. This device is connected to the wound dressing. All wound dressings may cause irritation or an allergic reaction. This risk is not higher than when receiving standard wound dressing, but it is something to take into consideration. Patients participating in this study may benefit from NPWT regarding the postoperative complication rate.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

300

Conditions

Breast Cancer Seroma Wound Complication

Interventions

Negative pressure wound therapyDEVICE

Negative pressure wound therapy using PICO14.

Eligibility

Sex: FEMALEMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Eighteen years or older. * Female sex. * Indication for breast conserving surgery, with or without sentinel lymph node biopsy. Exclusion Criteria: * Undergoing mastectomy or modified radical mastectomy. * Undergoing direct breast reconstruction. * Patients with a pacemaker, intra cardiac defibrillator (ICD) or other medical device in the proximity of the wound area, due to the magnet in the PICO® device. * Unable to comprehend implications and extent of the study and/or unable to sign for informed consent. * Participation in another breast cancer surgery related clinical trial.

Locations (1)

Zuyderland Medical Center

Sittard, Limburg, Netherlands

RECRUITING

Outcomes

Primary Outcomes

Surgical complications

Number of surgical complications, including clinically significant seroma, surgical site infections, wound dehiscence or wound necrosis.

Time frame: 3 months after surgery

Secondary Outcomes

Need of re-intervention

Number of patients who were in need of re-intervention(s) due to the previously mentioned surgical complications

Time frame: 3 months after surgery

Number of unscheduled visits to the emergency department or outpatient clinic

Time frame: 3 months after surgery

Pain scores during NPWT

A numeric rating score will be asked to all patients receiving NPWT.

Time frame: one week after surgery

Data from ClinicalTrials.gov

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