Condition 1: Acute abdomen. Condition 2: Acut peritonitis. Condition 3: Biliary peritonitis. Condition 4: Fecal peritonitis. Acute abdomen Peritonitis Peritonitis Peritonitis
Conditions
Interventions
Intervention 1: Intervention group: Patients with subcutaneous fat thickness greater than 20 mm who underwent pre-suture subcutaneous Corrugated drain implantation in emergency open midline laparotomy
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Patients diagnosed with acute peritonitis who have undergone acute midline incision surgery Patients with biliary peritonitis, fecal peritonitis, or patients with obvious pus in the peritoneal cavity Patients with subcutaneous fat thickness of more than 20 mm
Exclusion criteria
Exclusion criteria: Patients under 18 years old and over 70 years old Patients who do not consent to participate in the study Patients who undergo surgery with incisions other than midline incisions (McBurney incision, cochlear incision, paramedin incision, etc.) Pregnant patients Immune deficiency patients (patients with HIV positive serology, patients undergoing immunosuppressive therapy and patients undergoing any chemotherapy in the last 3 months) Patients for whom any other implant except drain is implanted (including meshplasty, etc.) Patients who do not visit the clinic at the appointed times for follow up Patients with a subcutaneous fat thickness of less than 20 mm Patients with other types of peritonitis (pancreatic peritonitis, etc.)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Surgical site infection. Timepoint: Evaluation of surgical site infection daily during hospitalization and also at the time of patients' visit to the hospital clinic up to 30 days after surgery. Method of measurement: Physical examination. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactIman Aminian
Tehran University of Medical Sciences
Outcome results
None listed