Postoperative delirium
Conditions
Interventions
Intervention group:The intervention group received olfactory bulb stimulation during surgery (administered via nasal cannula oxygen therapy) at an oxygen flow rate of 3 L/min, with 5 mL of lavender es
Control group:The control group did not receive nasal cannula oxygen therapy during surgery.
Sponsors
Peking University Cancer Hospital
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Age >= 65 years; 2. ASA physical status classification <= III; 3. Voluntarily participating in the clinical study and having provided signed informed consent.
Exclusion criteria
Exclusion criteria: 1.Patients with a history of postoperative delirium, cognitive impairment, or dementia; 2.Patients with a history of prior nasal surgery; 3.Patients with severe preoperative neurological disorders (e.g., stroke, Parkinson’s disease); 4.Patients undergoing non-intubated general anesthesia; 5.Patients unable to comply with or complete the study procedures.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative delirium; | — |
Secondary
| Measure | Time frame |
|---|---|
| Cognitive function;Anxiety-Depression score (HADS);Pain score;Postoperative complications; | — |
Countries
China
Contacts
Public ContactTan Hongyu
Peking University Cancer Hospital
Outcome results
None listed