Aspiration pneumonia
Conditions
Interventions
Experimental group:Accurate assessment system for dysphagia and formulation of personalized physical therapy measures
Control group:routine assessment and diagnosis-treatment intervention
Sponsors
Aerospace Center Hospital
Eligibility
Sex/Gender
All
Age
60 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Aged >= 60 years old; 2.Diagnosed with senile neurodegenerative diseases in accordance with diagnostic criteria, such as Alzheimer's disease, Parkinson's disease, dementia with Lewy bodies, frontotemporal dementia, Huntington's disease, multiple sclerosis, etc.; 3.Having swallowing dysfunction of varying degrees or being at risk of abnormal swallowing function after preliminary screening; 4.The patient or their family members signing the informed consent form.
Exclusion criteria
Exclusion criteria: 1.Complicated with life-threatening diseases such as severe cardiopulmonary failure and hepatic-renal insufficiency; 2.Recent history of oral or pharyngeal surgery, or acute infection in these areas; 3.Presence of mental disorders that prevent cooperation with researchers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| incidence rate of aspiration pneumonia;Death event; | — |
Secondary
| Measure | Time frame |
|---|---|
| Total hospitalization days;The duration of antibiotic treatment;The number of days admitted to the intensive care unit (ICU);Adverse reaction event;Situation of withdrawal from the study; | — |
Countries
China
Contacts
Public ContactGuo Na
Aerospace Center Hospital
Outcome results
None listed