NL-OMON36531
Completed
N/A
Protective ventilation during general anesthesia for abdominal surgery * a randomized controlled trial - PROVHILO
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Ventilator associated lung injury
- Sponsor
- Academisch Medisch Centrum
- Enrollment
- 100
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Planned elective abdominal surgery
- •\- General anesthesia with intravenous medication
- •\- High or intermediate risk for postoperative pulmonary complications (ARISCAT risk score \* 26\)
Exclusion Criteria
- •\- Age \< 18 years
- •\- Body mass index \> 40 kg/m2
- •\- Laparoscopic surgery
- •\- Previous lung surgery (any)
- •\- Persistent hemodynamic instability, intractable shock (considered hemodynamic unsuitable for the study by the patient\*s managing physician)
- •\- History of previous severe chronic obstructive pulmonary disease, COPD (non\*invasive ventilation and/or oxygen therapy at home or repeated systemic corticosteroid therapy for acute exacerbations of COPD)
- •\- Recent immunosuppressive medication (patients receiving chemotherapy or radiation therapy, within the last 2 months)
- •\- Severe cardiac disease (New York Heart Association class III or IV, or acute coronary syndrome, or persistent ventricular tachyarrhythmia\*s)
- •\- Mechanical ventilation \> than 30 minutes within last 30 days
- •(e.g., in cases of general anesthesia because of surgery)
Outcomes
Primary Outcomes
Not specified
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