Impact of Anesthesia Maintenance Methods on Incidence of Postoperative Delirium
Delirium, Postoperative Complications, Postoperative Cognitive Dysfunction
About this trial
This is an interventional prevention trial for Delirium focused on measuring Sevoflurane, Propofol, Aged, Neoplasm, Surgical Procedure, Operative, Delirium, Postoperative Complications, Postoperative Cognitive Dysfunction
Eligibility Criteria
Inclusion criteria
Participants will be included if they meet all the following criteria:
- Age ≥ 65 years and < 90 years;
- Primary malignant tumor;
- Do not receive radiation therapy or chemotherapy before surgery;
- Scheduled to undergo surgery for the treatment of tumors, with an expected duration of 2 hours or more, under general anesthesia;
- Agree to participate, and give signed written informed consent.
Exclusion criteria
Patients will be excluded if they meet any of the following criteria:
- Preoperative history of schizophrenia, epilepsy, parkinsonism or myasthenia gravis;
- Inability to communicate in the preoperative period (coma, profound dementia, language barrier, or end-stage disease);
- Critical illness (preoperative American Society of Anesthesiologists physical status classification ≥ IV), severe hepatic dysfunction (Child-Pugh class C), or severe renal dysfunction (undergoing dialysis before surgery);
- Neurosurgery;
- Other reasons that are considered unsuitable for participation by the responsible surgeons or investigators (reasons must be recorded in the case report form).
Sites / Locations
- Peking University First Hospital
- Beijing Shijitan Hospital
- Peking University Cancer Hospital
- Peking University School and Hospital of Stomatology
- Cancer Hospital of Guangxi Medical University
- Shenzhen Second People's Hospital
- Guizhou Provincial People's Hospital
- Hebei Medical University Forth Hospital
- The First Affiliated Hospital of Zhengzhou University
- The Third Xiangya Hospital of Central South University
- Zhongda Hospital
- Ningxia People's Hospital
- Affiliated Hospital of Qinghai University
- Tang-Du Hospital
- Shaanxi Provincial People's Hospital
- Shanxi Province Cancer Hospital
- Tianjin Nankai Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Sevoflurane group
Propofol group
Sevoflurane will be administered by inhalation for anesthesia maintenance. The concentration of inhaled sevoflurane will be adjusted to maintain the bispectral index (BIS) value between 40 and 60. Analgesia will be supplemented with remifentanil (administered by continuous infusion), sufentanil (administered by intermittent injection/continuous infusion), or fentanyl (administered by intermittent injection). Towards the end of surgery, sevoflurane inhalational concentration will be decreased and fentanyl/sufentanil will be administered when necessary. Sevoflurane inhalation will be stopped at the end of surgery.
Propofol will be administered by intravenous infusion for anesthesia maintenance. The infusion rate of propofol will be adjusted to maintain the BIS value between 40 and 60. Analgesia will be supplemented with remifentanil (administered by continuous infusion), sufentanil (administered by intermittent injection/continuous infusion), or fentanyl (administered by intermittent injection). Towards the end of surgery, propofol infusion rate will be decreased and fentanyl/sufentanil will be administered when necessary. Propofol infusion will be stopped at the end of surgery.