About this trial
This study aims at determining whether diaphragm ultrasound examining diaphragm thickening fraction, excursion and density before and after surgery can predict respiratory complications in the postoperative period.
Patients scheduled for major elective abdominal, pelvic or vascular surgery will be included in the study and diaphragm ultrasound is performed before surgery and after surgery in the postoperative ward. Physiological parameters, laboratory parameters, data on surgery and anesthesia and comorbidities will be registered. Complications such as pneumonia, desaturation, need for intubation and other respiratory events up to 30 days will be registered and later correlated with the diaphragm measurements.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
<18 years
Underlying chronic respiratory disease
Patients not able to give informed consent
Trial population
Adults undergoing elective (study 1) or acute (study 2) abdominal, pelvic or vascular surgery
Trial design
Cohort
Prospective
Treatments tested in this trial
Diaphragm ultrasound
Diagnostic testDiaphragm ultrasound will be used pre- and postoperatively. Diaphragm dysfunction will be diagnosed using the measurements diaphragm thickening fraction, diaphragm excursion and diaphragm density.
Treatment groups
Trial outcomes
Primary outcomes
Pneumonia
Respiratory insufficiency
Need for non-invasive or invasive ventilation
Desaturation
Need for supplemental oxygen
Sponsors and contacts
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Karolinska University Hospital
Lead sponsor
Karolinska Institutet
Collaborator