Swallowing dysfunction
Conditions
Interventions
Ultra-early swallowing function training group before extubation (intervention group):Ultra-early swallowing function training
Conventional swallowing function training group (control group):Conventional swallowing function training
Sponsors
The First Affiliated Hospital of Xi'an Jiaotong University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1) Participants must voluntarily agree to take part in this study and sign the informed consent form. 2) Participants must be aged 18 years or older. 3) Eligible patients are those who have undergone invasive mechanical ventilation through endotracheal intubation or tracheostomy for a duration of 48 hours or more.
Exclusion criteria
Exclusion criteria: 1) Patients with a history of neuromuscular diseases, such as Parkinson's syndrome or stroke, as well as those with cervical spinal cord injuries; patients with impaired consciousness who are unable to follow instructions for swallowing function training. 2) Patients experiencing dysphagia prior to the establishment of an artificial airway. 3) Patients with infectious diseases that are transmitted through contact or respiratory droplets.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of dysphagia 7 days after extubation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of dysphagia 48 hours after extubation;Tracheal reintubation rate within 48 hours after extubation;Tracheal reintubation rate within 7 days after extubation;The incidence of new pneumonia within 7 days after extubation;The incidence of new pneumonia within 28 days after extubation;28 days without mechanical ventilation;ICU length of stay;Length of stay;28-day ICU hospitalization mortality.;In-hospital mortality; | — |
Countries
People’s Republic of China
Contacts
Public ContactLei Zhang;Yu Liu
The First Affiliated Hospital of Xi'an Jiaotong University
Outcome results
None listed