Hepatic failure, renal failure, heart failure, respiratory failure, sepsis, death, syncope, asphyxia
Conditions
Interventions
Sponsors
Department of Anaesthesiology, The First Affiliated Hospital, Army Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Part One (data collection) Inclusion criteria (Data type A): (1) patients are over 65 years old, regardless of gender; (2) ability to comply with the research protocol; (3) voluntarily participate in the study and sign the informed consent (Data type B): (1) patients aged 16-65 years old, regardless of gender; (2) ability to comply with the research protocol; (3) voluntarily participate in the study and sign the informed consent. Part Two (Evaluating) Inclusion criteria (type A) (1) patients are over 65 years old, regardless of gender (2) ability to comply with the research protocol; (3) voluntarily participate in the study and sign the informed consent type B: (1) patients aged 16-65 years old, regardless of gender; (2) ability to comply with the research protocol; (3) voluntarily participate in the study and sign the informed consent.
Exclusion criteria
Exclusion criteria: (1) incomplete preoperative examination results; (2) unable to cooperate in mental state; (3) those who are participating in other clinical trials; (4) other reasons considered by the researchers are not suitable for this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| ACC, SEN, SPE, AUC of ROC; | — |
Countries
China
Contacts
Public ContactKaizhi Lu
Department of Anaesthesiology, The First Affiliated Hospital, Army Medical University
Outcome results
None listed