Retrospective Data Analysis on the Application of Swan-Ganz Catheter in Cardiac Surgery
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Enrollment
- 3,000
- Primary Endpoint
- Number of participants respiratory adverse events
Study Overview
Brief Summary
The investigators aimed to investigate postoperative complications associated with Swan-Ganz Catheter based on the clinical data of Wuhan Union Hospital and Wuhan Asian heart hospital for 10 years, including major cardiovascular, respiratory adverse events, ICU time, mechanical ventilation time, length of hospital stay, in-hospital mortality, and 30-day postoperative mortality events.
Study Design
- Study Type
- Observational
- Observational Model
- Case Control
- Time Perspective
- Retrospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Over 18 years old;
- •Patients undergoing major cardiac surgery under general anesthesia;
- •Patients with complete sex, age, use of floating catheter and prognosis data
Exclusion Criteria
- •ASA grade V and above;
- •End stage renal disease requiring (or undergoing) renal replacement therapy;
- •Pregnant or lactating women
Outcomes
Primary Outcomes
Number of participants respiratory adverse events
Time Frame: one week after operation
1) Acute lung injury: Diagnosis according to Berlin diagnostic standard; 2) Atelectasis: X-ray confirmed with body temperature \>37.5c or abnormal pulmonary manifestations; 3) Pneumothorax: chest X-ray diagnosis; 4) Pneumonia: confirmed by radiology or bacteriology
Number of participants with cardiovascular events
Time Frame: one week after operation
1) Cardiac death; 2) Non fatal myocardial infarction; 3) Intra aortic balloon counterpulsation (IABP); 4) Thoracotomy exploration; 5) Heart failure.
Secondary Outcomes
No secondary outcomes reported
Investigators
Shanglong Yao
Clinical Professor
Wuhan Union Hospital, China