Preventive PICO on Surgical Wounds After Large Incisional Hernia Repair

La Fe University and Polytechnic Hospital

Status

Completed

Conditions

Incisional Hernia

Treatments

Device: MEPORE dressing

Device: PICO DRESSING

Study type

Interventional

Funder types

Other

Identifiers

NCT03576222

PICO-01

Details and patient eligibility

About

To determine the efficacy on decreasing the rate of surgical wound complications in patients undergoing repair of large incisional hernias, after the prophylactic application of a single-use negative pressure therapy dressing (PICO), versus a conventional dressing.

Full description

Hypothesis The preventive use of single-use PICO dressing reduces the complications of the surgical wound (infection and dehiscence of the surgical wound) in patients after large incisional hernia repair.

Objectives

Primary:

To determine the efficacy on decreasing the rate of surgical wound complications in patients undergoing eventration surgery, after the prophylactic application of a single-use negative pressure therapy (NPT) dressing, as opposed to a conventional dressing.

Secondary:

To report the incidence of wound infection and dehiscence during the patient's admission, at 7 days, 15 days and month after surgical repair applying a conventional dressing (MEPORE) or PICO dressing.
To quantify economic costs applying a PICO dressing versus a MEPORE dressing.

Methods:

Selection of patients Collection of the sample will be made in the Abdominal Wall Surgery Unit (La Fe Hospital), according to the inclusion and exclusion criteria. The surgeon will explain to the patient the objectives of the study and will give him an informed consent and will answer all the doubts about the study.

Patients will be assigned to two groups in a 1: 1 ratio. Assignment of each patient to the different groups will be done using a randomized method according to the following distribution:

Group A, it will be applied the dressing object of study (PICO)
Group B, it will be applied the conventional dressing (MEPORE).

Data collection and Study variables

For each patient, the data collection notebook designed for this purpose must be completed, which includes the following study variables:

Dependent (study outcomes)
- Infection and dehiscence of surgical wound. These variables will be assessed throughout the admission and at 7 and 30 days from the hernia repair, during hospital stay, and at 15 days in the Unit.
- Variables related to direct costs (hospital stay, material, antibiotic use, operating room use, etc). Other variables related to indirect costs (time of cure by nursing).
Independent
- Demographic data: age, sex, BMI.
- Classification ASA (American Society of Anesthesiologists)
- Risk factors abour surgical wound complications: drainage, preoperative chemotherapy, preoperative radiotherapy, Diabetes Mellitus, cardiovascular disease, immunosuppressive treatment, active smoking, obesity, hypertension, inflammatory bowel disease.

Number of subjects 150 patients undergoing hernia repair of large incisional hernia (types W2 or W3 according to EHS classification) will be included in La Fe Hospital in Valencia from January 2017 until the recruitment of the entire sample (estimated in December 2018).

Enrollment

146 patients

Sex

All

Ages

18 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Patients over 18 years old (men and women).
To give his consent to participation in the study.
To have surgical prosthetic repair of large incisional hernia (type W2 or W3).
Patients admitted to the 6th floor, G tower (Unit of Abdominal Wall surgery).

Exclusion criteria

Patients with immediate reintervention of abdominal surgery (less than 30 days from the first surgery).
Patients after emergency surgery.
Patients with biological prosthesis.
Pregnancy and lactation.
Hepatic cirrhosis.