The Use of Post-operative NPWT Dressing in the Prevention of Infectious Complications After Ostomy Reversal Surgery
Stoma Ileostomy, Surgical Wound, Negative Pressure Wound Therapy
About this trial
This is an interventional prevention trial for Stoma Ileostomy
Eligibility Criteria
Inclusion Criteria:
- Patients aged 18 or older
- Previous colorectal resection with the formation of protective ileostomy due to cancer
- Ileostomy closure surgery as an elective procedure.
Exclusion Criteria:
- Emergency or urgent operation
- Active infection
- Other than ileostomy closure or parastomal hernioplasty operation performed.
- Patents who within 1 week after operation will be re-operated or transferred to Intensive Care Unit or other hospital word due to noninfectious complications
Sites / Locations
- Oddział kliniczny chirurgii ogólnej, endokrynologicznej i onkologii gastroenterologicznejRecruiting
- 2nd Department of General Surgery, Jagiellonian UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Standard Dressing
Postoperative NPWT dressing
In case of Control group. After Ileostomy closure skin will be closed by 6 to 8 single no absorbable Monosyn 3-0 (Ethicon, Cincinnati, Ohio., USA) sutures, and sterile standard dressing will be placed.
In case of NPWT group. After Ileostomy closure skin will be closed by 3 or 4 single no absorbable Monosyn 3-0 (Ethicon, Cincinnati, Ohio., USA) sutures. Between them small sponge "tongues" 1x 0,5x2 cm were placed and over whole incision an NANOVA (KCI USA) negative pressure dressing will be placed. In control group first dressing change was made in 48 hours after operation and then every day until suture removal at 7 postoperative day. In NPWT group NANOVA dressing was taken out at 72 hours. 3 steri-streps were placed between sutures and standard sterile dressing was placed. After it dressing was changed every 24 hours until suture removal at 7 postoperative day.