Predictors for efficient ICU use after pulmonary surgery: a retrospective multicenter study
Recruiting
- Conditions
- Pulmonary surgery, intensive care, effective intensive care use, adverse events
- Registration Number
- NL-OMON21274
- Lead Sponsor
- Amphia Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 500
Inclusion Criteria
Patients that underwent elective pulmonary surgery (pneumonectomy, (bi)(sleeve)lobectomy, segmentectomy), with a postoperative admission to the ICU are included.
Exclusion Criteria
Intraoperative death.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method -invasive mechanical ventilation (initiated on the ICU or continued from the operating theatre for at least 3 hours) <br /><br>-non-invasive mechanical ventilation (use of continuous positive airway pressure)<br /><br>-reintubation<br /><br>-use of high-flow nasal oxygen therapy Optiflow)<br /><br>-pneumothorax requiring (new) chest tube insertion or repositioning chest tube<br /><br>-need for bronchoscopy<br /><br>-bleeding requiring intervention (requiring surgery or transfusion of blood (clotting) products)<br /><br>-reoperation<br /><br>-supraventricular arrhythmia (new-onset atrial fibrillation or atrial flutter) with hemodynamic impairment<br /><br>-congestive heart failure (pleural effusion or pulmonary edema requiring diuretic therapy)<br /><br>-myocardial infarction (elevated hs-cTn in combination with clinical symptoms or electrocardiography changes)<br /><br>-hemodynamic instability requiring the use of vasopressors or inotropes<br>
- Secondary Outcome Measures
Name Time Method