Emergency Midline Laparotomy, Incisional Hernia
Conditions
Brief summary
The aim of this study is to describe the development of symptomatic and asymptomatic incisional hernias after emergency midline laparotomy over time in high-risk patients evaluated by consecutive MRI-scans.
Detailed description
All patients operated with an emergency midline laparotomy in our clinic are 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 four consecutive MRI-scans one month, three months, six months and two years after surgery. Change in quality of life, physical functioning and pain-score are also obtained by patient survey/interview at each visit. A concluding physical examination and abdominal wall ultrasound examination will be performed two years after the surgery.
Interventions
DIAGNOSTIC_TESTMagnetic resonance imaging (MRI)
MRI is a non-invasive imaging modality capable of producing precise soft-tissue images in all body areas. In contrast to CT scanning, MRI does not rely on ionizing radiation. There are no known risks associated with MRI as long as patients with contraindications such as pacemakers are identified and excluded. The MRI scans in this study will be performed without use of contrast media.
Sponsors
Herlev Hospital
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Unscheduled midline laparotomy in an emergency or subacute setting, involving perforated bowel, bowel obstruction, bowel ischemia (due to mesenteric vascular disease or incarceration), inflammatory diseases (e.g. diverticulitis, appendicitis, ulcerative colitis, cholecystitis and Crohn's disease), abscesses, non-traumatic intraabdominal bleeding or any emergency re-operation to elective surgery * Age of 18 years or above * BMI above 27 * At least one risk factor for incisional hernia i.e. earlier midline laparotomy, BMI \> 30, abdominal aortic aneurysm or prior surgery for abdominal aortic aneurysm, active smoking, liver cirrhosis, re-laparotomy, age \> 75, history of primary ventral hernia (treated or untreated before index surgery), large laparotomy involving more than 2/3 of the abdominal wall as measured from the xiphoid process to the pubic bone
Exclusion criteria
* Malign, incurable disease * Other reasons for short life expectancy \<2 year as evaluated by the investigator * Midline-incisions \<15 cm * Mesh augmentation of abdominal wall closure at index surgery or earlier mesh augmentation of the abdominal wall * Severe claustrophobia or any other mental habitus, making it impossible to perform MRI-scan without sedation * Metallic magnetic implants that serves as a contraindication for MRI-scan (including pacemakers, large tattoos, insulin pumps, etc.) * Metallic prosthetic non-magnetic implants that are suspected to create severe artefacts on the MRI-scan of the abdominal wall
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Early (30-days) MRI-diagnosed, incisional hernia development in high-risk patients after emergency midline laparotomy. | 2 years |
Secondary
| Measure | Time frame |
|---|---|
| MRI-diagnosed incisional hernia rates 3 months, 6 months and 2 years after laparotomy. | 2 years |
| Change in quality of life, physical functioning, clinical investigation and pain-score at 1 month, 3 months, 6 months and 2 years after laparotomy. | 2 years |
| Rate of MRI-verified subclinical vs. clinical detectable incisional hernias. | 2 years |
| 30-day, 90-day, and 1-year mortality. | 1 year |
Countries
Denmark
Outcome results
None listed