The aim of this study is to identify risk factors for the development of incisional hernias in emergency midline laparotomies.
All patients operated with an emergency midline laparotomy and attending 1-year follow-up in our clinic is potential participants and will be screened for participation. Potential participants will be briefly informed about the project by the hospital staff. If the patients are interested, they will be thoroughly informed about the study and asked to participate by one of the trial investigators before discharge. Data will be obtained from the participants hospital files and by patient survey/interview. All data will be entered into a database using RedCap by trial investigators or their delegates. Enrolled patients will be followed for two years. The trial involves two clinical examinations and evaluations (one and two years) after surgery. Clinical examination involves interview with a standardized questionnaire and abdominal wall examination including inspection, palpation and ultrasound examination.
Study Type
OBSERVATIONAL
Enrollment
500
Department of Gastrointestinal- and Hepatic diseases, Surgical Section,
Herlev, Denmark
Risk factors of incisional hernia after emergency midline laparotomy
Multivariate analysis on selected variables evaluated for long-term complications, including sex, age, high BMI, active smoking, hernia in the midline, length of incision, rectus muscle diastasis, sarcopenia, peritonitis and multiple laparotomies
Time frame: 2 years
Rate of incisional hernias one and two years after surgery
Time frame: 2 years
30-day, 90-day, 1-year and 2-year mortality
Time frame: 2 years
Rates of asymptomatic versus symptomatic incisional hernias
Time frame: 2 years
Rate of surgery for incisional hernias 2-years post index surgery
Time frame: 2 years
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