Burns, ulcers, wound repair
Conditions
Interventions
group TE:Percutaneous acupoint electrical stimulator was used to stimulate Baihui, Shenting, Yintang, Ershen point and other acupoints 30min before surgery, and continued to stimulate until the end of
group T:The percutaneous acupoint electrical stimulator stimulated Baihui, Shenting, Yintang, Ershen point and other acupoints until the end of the operation.
group E:Esketamine (0.4mg/kg) was injected intravenously before induction, followed by continuous pumping at 0.4mg/kg/h for 40min and then stopped.
group C:Conventional anesthesia, without acupoint electrical stimulation and esketamine intervention.
Sponsors
First Affiliated Hospital of Guangxi Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Patients receiving wound repair (burn wound, various ulcer wounds and various surgical wounds with poor healing) under general anesthesia 2. ASA grade I-III, 18-65 years old 3. The patient is conscious and the vital signs are relatively stable
Exclusion criteria
Exclusion criteria: 1. Refuse to participate in the research or quit the researcher for various reasons 2. Patients with head and face burns, shock, inhalation injuries, severe burns with more repeated combined injuries, and extremely severe burns 3. Patients with anxiety and depression scores >7 on the preoperative Hospital Anxiety Depression Scale (HADS) 4, preoperative Athens Insomnia Scale (AIS) score >4 points 5, perioperative severe hepatic and renal insufficiency, serious underlying diseases or systemic inflammatory diseases 6, have neurological and psychiatric diseases or take related drugs 7, cognitive dysfunction or inability to communicate 8, there are contraindications to the use of esketamine 9, TEAS contraindications, such as skin allergies, infections, itching, or wearing a pacemaker 10. Major organ damage or rescue occurred during perioperative period, and the patient was admitted to the intensive care unit (ICU) after surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative anxiety and depression; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative sleep status;Postoperative recovery status;Postoperative pain level; | — |
Countries
China
Contacts
Public ContactZhong Yu
First Affiliated Hospital of Guangxi Medical University
Outcome results
None listed