None listed
Conditions
Interventions
Experimental group:Transcutaneous electrical acupoint stimulation
Sponsors
Xuzhou Central Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Aged between 18 and 60 years; 2. Undergo elective endoscopic nasal surgery; 3. ASA Assessment System level 1-2; 4. Education level at least primary school level or above, mainly able to fully understand and answer the questions in QoR-15 scale; 5. Agree to participate in this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Contraindications to TEAS (scars or skin lesions at the site of irritation, infection, electronic devices such as cardiac pacemakers or other implanted medical electronic devices); 2. Cognitive dysfunction and poor compliance; 3. Severe hearing or vision impairment and inability to read or aphasia; 4. The patient has neuropsychiatric abnormalities, confusion and inability to communicate normally; 5. Abnormal blood coagulation, liver and renal function; 6. Patients with severe cardiovascular disease, sinus bradycardia, atrioventricular block of degree II or higher, and severe arrhythmia; 7. Severe respiratory insufficiency; 8. Those who are not willing to take TEAS and cannot cooperate to complete the questionnaire.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Recovery-15(QoR-15);Inflammatory factor levels; | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual analogue scale (VAS);Intraoperative blood pressure and heart rate;Ramsay Sedation Scale;Analgesic pump usage;Nausea and vomiting; | — |
Countries
China
Contacts
Public ContactWang Liwei
Xuzhou Central Hospital
Outcome results
None listed