Patients undergoing cardiac surgery with CPB during surgery
Conditions
Interventions
No experimental products were involved, and no control group was designed:No intervention, only observation
Sponsors
Shanghai First People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Patients between the ages of 18 and 80 years (inclusive); 2. Patients undergoing cardiac surgery for CPB intraoperatively; 3. Prospective study participants or their legal representatives are able to understand the content of the study and voluntarily sign in writing Consent form. Retrospective study participants are not required to sign an informed consent form
Exclusion criteria
Exclusion criteria: 1. Patients with known hereditary or acquired coagulation disorders; 2. Patients with severe liver and kidney dysfunction, such as chronic kidney disease stage 5 or cirrhosis Child-Pugh Grade C; 3. Patients with hematopoietic malignant tumors; 4. Transplant patients; 5. Patients with left ventricular assist device implantation; 6. Patients undergoing pulmonary embolization resection; 7. Patients undergoing emergency cardiac surgery; 8. Patients with missing laboratory tests involved in this study before surgery; 9. Other medical conditions that, in the opinion of the investigator, may affect the results of the study or the safety of the patient.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| This project is an observational study with no indicators; | — |
Countries
China
Contacts
Public ContactLou Jiatao
Shanghai First People's Hospital
Outcome results
None listed