Effects of Perioperative Transauricular Vagus Nerve Electrical Stimulation on POD, POCD and CPSP
Postoperative Cognitive Dysfunction, Postoperative Delirium, Chronic Post Operative Pain
About this trial
This is an interventional prevention trial for Postoperative Cognitive Dysfunction
Eligibility Criteria
Inclusion Criteria:
- 50 to 80 years old.
- ASA grade I-Ⅲ.
- elective knee or hip replacement.
Exclusion Criteria:
- Mini-Mental State Examination (MMSE) score < 23.
- Education years<7.
- Peptic ulcer disease, serious cardiac-cerebral vascular disease.
- Neurological or psychiatric disorders.
- History of drug and alcohol abuse.
- Hepatic and/or kidney dysfunction.
- BMI>35.
- Patients on antidepressants.
- ASA >Ⅲ.
Sites / Locations
- Xuzhou Central Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
Experimental group
Control group
The transaricular vagus nerve stimulator was placed in the left ear trunk, which is dominated only by the auricular branch of the vagus nerve. Continuous stimulation was performed at a frequency of 25Hz with pulse width of 300 μs. The stimulation was adjusted to be higher than the perception threshold and lower than the pain threshold. Each stimulation lasted for 30 minutes, three times per day (morning, noon, evening), from 1 day before surgery to 7 days after surgery, and the treatment lasted for 9 consecutive days.
The transaricular vagus nerve stimulator was placed in the same position as the experimental group, covered with an insulating film and placed at the site of the stimulation, so that the patient could not actually receive the electrical stimulation. Continuous stimulation was performed at a frequency of 25Hz and pulse width of 300 μs, and the stimulation was adjusted to be higher than the perception threshold and lower than the pain threshold. Each stimulation lasted for 30 minutes, three times per day (morning, noon, evening), from 1 day before surgery to 7 days after surgery, for 9 consecutive days.