Aortic Dissection
Conditions
Interventions
Observational study component:None
Control group:Routine postoperative care for cardiac surgery
Intervention group:Intervention using interferential current therapy
Sponsors
Fujian Medical University Union Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Observational part: (1) Patients scheduled to undergo AD surgery; (2) Aged >= 18 years. Interventional part: (1) Patients scheduled to undergo AD surgery; (2) Aged >= 18 years.
Exclusion criteria
Exclusion criteria: Observational part: (1) Patients with vocal cord dysfunction, a history of neck surgery, or other conditions affecting swallowing function; (2) Patients with pre-existing respiratory diseases such as asthma or lung cancer; (3) Patients with severe psychiatric or neurological disorders. Interventional part: (1) Patients with vocal cord dysfunction, oropharyngeal malignant tumors, neck surgery, or other conditions that may affect swallowing function; (2) Patients with postoperative hemodynamic instability or active bleeding; (3) Patients with a history of respiratory diseases such as COPD, asthma, chronic bronchitis, or lung cancer; (4) Patients with a history of gastroesophageal reflux disease; (5) Patients with severe mental or neurological disorders; (6) Patients with skin damage at the electrical stimulation site or allergy to electrode pads; (7) Patients with an implanted cardiac pacemaker; (8) Patients participating in other interventional studies.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Silent aspiration; | — |
Secondary
| Measure | Time frame |
|---|---|
| Dysphagia ;Feeding status;Airway management and pneumonia status;Mechanical ventilation status;Complications and length of hospital stay; | — |
Countries
China
Contacts
Public ContactLi Sailan
Fujian Medical University Union Hospital
Outcome results
None listed