Stanford type A aortic dissection or aortic aneurysm
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Aged 18-0 years old male and female, NYHA functional class 2 to 3; (2) surgical heart surgery is performed under conditions of CPB; (3) informed consents signed; (4) Denied disease history of esophagus and stomach, can be intraoperative TEE operation; (5) normal liver and kidney function; (6) no obvious coagulation dysfunction; (7) Denied disease history of blood system.;Inclusion criteria: (1) Aged 18-0 years old male and female, NYHA functional class 2 to 3; (2) surgical heart surgery is performed under conditions of CPB; (3) informed consents signed; (4) Denied disease history of esophagus and stomach, can be intraoperative TEE operation; (5) normal liver and kidney function; (6) no obvious coagulation dysfunction; (7) Denied disease history of blood system.;Inclusion criteria: (1) Aged 18-0 years old male and female, NYHA functional class 2 to 3; (2) surgical heart surgery is performed under conditions of CPB; (3) informed consents signed; (4) Denied disease history of esophagus and stomach, can be intraoperative TEE operation; (5) normal liver and kidney function; (6) no obvious coagulation dysfunction; (7) Denied disease history of blood system.;Inclusion criteria: (1) Aged 18-0 years old male and female, NYHA functional class 2 to 3; (2) surgical heart surgery is performed under conditions of CPB; (3) informed consents signed; (4) Denied disease history of esophagus and stomach, can be intraoperative TEE operation; (5) normal liver and kidney function; (6) no obvious coagulation dysfunction; (7) Denied disease history of blood system.;Inclusion criteria: (1) Aged 18-0 years old male and female, NYHA functional class 2 to 3; (2) surgical heart surgery is performed under conditions of CPB; (3) informed consents signed; (4) Denied disease history of esophagus and stomach, can be intraoperative TEE operation; (5) normal liver and kidney function; (6) no obvious coagulation dysfunction; (7) Denied disease history of blood system.
Exclusion criteria
Exclusion criteria: (1) Emergency surgery; (2) Hb<130g/L; (3) Who suffered allergic reactions or other serious complications during blood separation or reinfusion; (4) Due to irresistible factors caused by the separated blood can not be returned, so those who can not continue to complete the test; (5) Who claim to exit clinical trials; (6) The investigators considered that it is not advisable to continue to participate in this clinical trial.;Exclusion criteria: (1) Emergency surgery; (2) Hb<130g/L; (3) Who suffered allergic reactions or other serious complications during blood separation or reinfusion; (4) Due to irresistible factors caused by the separated blood can not be returned, so those who can not continue to complete the test; (5) Who claim to exit clinical trials; (6) The investigators considered that it is not advisable to continue to participate in this clinical trial.;Exclusion criteria: (1) Emergency surgery; (2) Hb<130g/L; (3) Who suffered allergic reactions or other serious complications during blood separation or reinfusion; (4) Due to irresistible factors caused by the separated blood can not be returned, so those who can not continue to complete the test; (5) Who claim to exit clinical trials; (6) The investigators considered that it is not advisable to continue to participate in this clinical trial.;Exclusion criteria: (1) Emergency surgery; (2) Hb<130g/L; (3) Who suffered allergic reactions or other serious complications during blood separation or reinfusion; (4) Due to irresistible factors caused by the separated blood can not be returned, so those who can not continue to complete the test; (5) Who claim to exit clinical trials; (6) The investigators considered that it is not advisable to continue to participate in this clinical trial.;Exclusion criteria: (1) Emergency surgery; (2) Hb<130g/L; (3) Who suffered allergic reactions or other serious complications during blood separation or reinfusion; (4) Due to irresistible factors caused by the separated blood can not be returned, so those who can not continue to complete the test; (5) Who claim to exit clinical trials; (6) The investigators considered that it is not advisable to continue to participate in this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| colloid osmotic pressure;Cardiac Function; | — |
Countries
China
Contacts
Department of Anesthesiology, the First Affiliated Hospital of China Medical University;Department of Anesthesiology, the First Affiliated Hospital of China Medical University;Department of Anesthesiology, the First Affiliated Hospital of China Medical University;Department of Anesthesiology, the First Affiliated Hospital of China Medical University;Department of Anesthesiology, the First Affiliated Hospital of China Medical University