Apnea during moderate to deep sedation using either remimazolam, dexmedetomidine, propofol infusion: a retrospective cohort study
Not Applicable
Completed
- Conditions
- Injury, poisoning and certain other consequences of external causes
- Registration Number
- KCT0007492
- Lead Sponsor
- Chungnam National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 700
Inclusion Criteria
1. over 18 years old
2. ASA classification 1~3
3. Orthopedic surgery under spinal anesthesia or brachial plexus block
4. sedation performed during surgery through continuous infusion of one of the three drugs, dexmedetomidine, propol, and remimazolam
Exclusion Criteria
1. Oxygen administration during sedation and continuous end-tidal CO2 not monitored or no information exists
2. Vital Recorder record does not exist
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method end-tidal CO2;SpO2
- Secondary Outcome Measures
Name Time Method respiratory rate