Assessment protocol for swallowing function after aspiration pneumonia: Retrospective cohort study
Not Applicable
- Conditions
- aspiration pneumonia
- Registration Number
- JPRN-UMIN000039492
- Lead Sponsor
- Akashi Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 101
Inclusion Criteria
Not provided
Exclusion Criteria
Those unable to eat due to severe dysphagia according to assessment by an expert nurse, patients dependent on artificial nutrition (gastrostomy or total parenteral nutrition), and patients who died during hospitalization.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method days until oral intake
- Secondary Outcome Measures
Name Time Method aspiration and/or choking the amount of nutritional intake duration of hospitalization decline in swallowing ability(assessed by differences between premorbid FOIS scores before onset and at the end of treatment)