Effect of Electroacupuncture on the Incidence of Postoperative Delirium in Elderly Patients Undergoing the Major Surgery
Postoperative Delirium
About this trial
This is an interventional prevention trial for Postoperative Delirium focused on measuring electroacupuncture; delirium; the elderly; surgery, major
Eligibility Criteria
Inclusion Criteria:
- Age≥65 and <90 years old;
- Planning to undergo select timed/limited surgery such as gastrointestinal tumor surgery, bile duct surgery and thoracic surgery etc under general anesthesia, and the estimated operation time is more than 2 hours;;
- Treatment without radiotherapy or chemotherapy prior to surgery;
- Agree to participate in this study and sign informed consent;
Exclusion Criteria:
- Refuse to participate in this study;
- Preoperative history of schizophrenia, epilepsy, Parkinson's disease, or myasthenia gravis;
- Inability to communicate in the preoperative period to complete preoperative evaluation because of severe dementia, coma, language barrier;
- Brain injury or neurosurgery;
- Critical condition (if the ASA grade is greater than or equal to grade IV before surgery); Severe renal impairment (dialysis treatment before surgery); Severe liver function impairment (Child-Pugh level C); Preoperative combined with severe heart disease, LVEF < 30%;
- Previous experience of acupoint stimulation therapy or non-insensitive to acupoint stimulation;
- The attending physician or researcher considers that there are other circumstances (reasons to be noted) that are not suitable for participation in this study.
Sites / Locations
- Electroacupuncture Apparatus
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
electroacupuncture treatment
sham electroacupuncture treatment
Participants in the treatment group received acupuncture (0.30mm×70mm) at bilaterally Shenmen (HT7) acupoints (0.3-0.5 inch), Neiguan (PC6) acupoints (0.5-1 inch), Baihui (DU20) acupoint (0.5-0.8 inch) and Yintang (EX-HN3) acupoint (0.3-0.5 inch) 30 minutes before anesthesia induction. After "Deqi", electroacupuncture stimulation apparatus (HANS G6805-2, Huayi Co, Shanghai, China) is connected and maintained the end of operation.
Participants in the control group received shallow needling (0.30mm×25mm) at bilateral sham HT7, PC6, DU20 and EX-HN3 (nonacupoints located 1 inch beside acupoints, about 20mm). Specifically, the depth of needle insertion into nonacupoints is 3-5mm and avoided manual stimulation and no "Deqi" without actual current output.