Postoperative complications
Conditions
Interventions
Observation group:None
Sponsors
The Fourth Affiliated Hospital of Harbin Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Research participants who underwent surgery in the surgery room of the Fourth Affiliated Hospital of Harbin Medical University within the past five years; 2.The research participants themselves, their legal representatives or authorized agents agree to participate in the research and sign the informed consent form; 3.Continuous intraoperative monitoring (ECG, BIS, hemodynamics, etc.); 4.The postoperative hospital stay was >=24 hours;
Exclusion criteria
Exclusion criteria: 1.Situations such as acute and critical conditions that researchers consider unsuitable for inclusion; 2.Research participants who refused to sign the informed consent form; 3.The monitoring data is missing and the completeness is less than 80% of the cases; 4.The data recording is inaccurate, with obvious errors or contradictions;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative outcome;High-frequency monitoring parameter information during the operation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Preoperative baseline characteristics; | — |
Countries
China
Contacts
Public ContactQi Sihua
The Fourth Affiliated Hospital of Harbin Medical University
Outcome results
None listed