Study of protocolized lighter sedation during open abdomen management
Not Applicable
- Conditions
- acute abdomen
- Registration Number
- JPRN-UMIN000053669
- Lead Sponsor
- Wakayama Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with abdominal compartment syndrome, patients receiving continuous muscle relaxants
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method nivariate and multivariate linear regression models will be used to evaluate the percentage of time the patient was able to maintain shallow sedation during OAM and as the amount of propofol used per body weight during OAM. In the multivariate analysis, adjustment variables will be evaluated as age, presence of dementia or institutionalization, APACHE II score, and presence of liver failure, heart failure, respiratory failure, immunodeficiency, or maintenance dialysis according to the APACHE definition. Since this is a retrospective observational study, other exploratory analyses will be performed.
- Secondary Outcome Measures
Name Time Method The duration of time to weaning from the ventilator, outcome, and sedative medication use will be discussed.