Patients undergoing spinal fixation surgery
Conditions
Interventions
G group:nothing
T group:Transcutaneous acupoint electrical stimulationTEAS
Sponsors
The First People's Hospital of Pinghu Zhejiang china
Eligibility
Sex/Gender
All
Age
40 Years to 70 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: 1) Willing to cooperate with the researcher and have signed informed consent; 2) The patient is mentally and mentally normal and can cooperate with relevant treatment programs; 3)American College of Anesthesiologists (ASA) Levels I to II;4) New York Heart Association (NYHA) Heart function grade I to II.
Exclusion criteria
Exclusion criteria: Exclusion criteria: 1) serious diseases of kidney and heart; 2) The patient has malignant tumor and autoimmune disease; 3) The patient did not accept this study; 4) patients with depression insomnia; 5) Patients with mental illness or expression disorders; 6) Skin infection and other related contraindications that can not be used for acupoint electrical stimulation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual analogue scaleVAS;Mini-mental state examinationMMSE; | — |
Secondary
| Measure | Time frame |
|---|---|
| Dosage of sufentanil in analgesic pump (ug) number of effective compressions (times) and number of remedies (times) 24 hours after surgery;The occurrence of postoperative adverse reactions;Anesthetic resuscitation eye opening time (min) and response time (min); | — |
Countries
China
Contacts
Public Contactwen-ping Xu
The First People's Hospital of Pinghu Zhejiang china
Outcome results
None listed