Prophylactic High-Flow Oxygen Nasal Cannula vs. Incentive Spirometer After Cardiac Surgery

Not Applicable

Completed

• Conditions: patients undergoing surgery with cardiopulmonary bypassmedian sternotomyno active or chronic pulmonary conditionage more than 18 years; Health Care [N]

• Registration Number: TCTR20180201001
• Lead Sponsor: Rajavithi Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-02-01
• Study Completion: 2018-06-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 67

Inclusion Criteria

- Open heart surgery with cardiopulmonary bypass
- Full median sternotomy
- age > 18 years

Exclusion Criteria

- Emergency surgery
- Active pulmonary disease
- abnormal chest imaging
- oxygen saturation of less than 95% (room air)
- PaO2/FiO2 less than 350mmHg
- Prolonged intubation more than 48 hours
- Re-operative from any cause
- patients denied participating

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Rate of Reintubation hours Absolute number of patients (percentage),Rate of pneumonia days Number of patient

Secondary Outcome Measures

Name	Time	Method
Peak flow rate days ml/min,PaO2/FiO2 days Blood gas analysis,ICU stay Days Date Count,Hospital stay Days Date count,30-day mortality Days Date count,Rate of Pneumonia hours Absolute number of patients (percentage)