Postoperative delirium
Conditions
Interventions
Divided into oral weakness group and normal control group according to the preoperative oral weakness scale:None
Sponsors
The Second Affiliated Hospital of Nanjing Medical University
Eligibility
Sex/Gender
All
Age
65 Years to 90 Years
Inclusion criteria
Inclusion criteria: Age =65 years old, <90 years old; Accept elective/deadline non-cardiac surgery; ASA Level I-III; Voluntarily participate and sign an informed consent form; Complete clinical data, able to complete preoperative questionnaire surveys and postoperative follow-up.
Exclusion criteria
Exclusion criteria: Refuse to participate in this study; Preoperative inability to communicate due to coma, severe dementia, or language impairment; Preoperative symptoms include schizophrenia, epilepsy, Parkinson's disease, and myasthenia gravis; Severe abnormalities in heart, brain, kidney, and liver function; ASA grade IV and/or patients with expected survival = 24 hours.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative delirium;Microbial dysbiosis index; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative recovery quality;Blood routine examination;Biochemical detection;C-reactive protein; | — |
Countries
China
Contacts
Public ContactJi Muhuo
The Second Affiliated Hospital of Nanjing Medical University
Outcome results
None listed