Aspiration by inpatient
Conditions
Interventions
Experimental Group:Patients in the experimental group (EIT clinical pathway group) were evaluated by EIT before early rehabilitation intervention and before daily treatment to decide whether to carry
Control group:In the control group (routine rehabilitation group), the basic conditions at the time of enrollment were consistent with those of the experimental group, and the experimental process was
Sponsors
Suzhou Jiulong Hospital, Shanghai Jiao Tong University School of Medicine
Eligibility
Sex/Gender
All
Age
20 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. Meeting the diagnostic criteria for neurocritical care (National Institutes of Health Stroke Scale (NIHSS) >=21 points, Glasgow Scale (GCS) <=9 points), and being the first onset of the disease; The time from the onset of the disease to enrollment is 15 to 22 days. 3. Age: 20-75 years old; 4. Understand the purpose and process of this research and voluntarily participate in the research.
Exclusion criteria
Exclusion criteria: 1. Patients with severe clinical complications: liver and kidney diseases, deep vein thrombosis, decompensated heart failure, having experienced cardiac or respiratory arrest or myocardial infarction within 3 months, severe pneumonia or obstructive pulmonary disease, and unable to undergo rehabilitation treatment; 2. Those with incomplete medical records; 3. Those who are unwilling to join the group or cannot persist in completing the enrollment process.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Volume viscosity test;Videofluoroscopic Swallowing Study;Flexible Endoscopic Evaluation of Swallowing; | — |
Countries
China
Contacts
Public ContactPan Huaping
Suzhou Jiulong Hospital, Shanghai Jiao Tong University School of Medicine
Outcome results
None listed