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The application of acute Normovolemic Hemodilution in cardiac surgery can effectively reduce perioperative blood transfusion, reduce postoperative complications and mortality, and is a low-cost, operable and effective blood protection measure.For the application of Acute Normovolemic Hemodilution in heart surgery, we still face an urgent problem: to what extent can Acute Normovolemic Hemodilution achieve better "blood saving effect", that is, whether a large number of Acute Normovolemic Hemodilution can reduce perioperative blood transfusion to a greater extent.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Large Volume Acute Normovolemic Hemodilution | Experimental | All the participants will undergo Large Volume Acute Normovolemic Hemodilution. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Acute Normovolemic Hemodilution | Procedure | Following induction of anesthesia, the volume of blood to be removed during Acute Normovolemic Hemodilution was calculated using an established formula:V=Weight(Kg)×12-15(mL/Kg);Blood to be removed was capped at: Vmax=EVB×(Hi-Hf)/Hav(EBV= estimated blood volume (male:70mL/Kg,female:65mL/Kg);Hi= initial hemoglobin ;Hf=target Hb( 10g/dL );Hav= the average of the initial and minimal allowable hemoglobin).Ensure the volume of removed blood does not exceed the upper limit and Hb ≥10g/dL after blood removed. |
| Measure | Description | Time Frame |
|---|---|---|
| Enrollment rate of subjects | The percentage of patients who completed the study | Through study completion,about 8 months |
| Completion rate of acute normovolemic hemodilution | The percentage of patients who complete large volume of acute normovolemic hemodilution | Through study completion,about 8 months |
| Additional blood transfusion beyond transfusion protocol | Nonstandard blood transfusion | Through study completion,about 8 months |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of perioperative blood transfusion | The percentage of red blood, fresh frozen plasma and platelet transfusion | Through study completion,about 8 months |
| Rate of postoperative cardiac complications |
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Inclusion Criteria:
Exclusion Criteria:
(1)Low body weight (male: <50 kg;Female: < 45kg);(2)preoperative shock;(3)myocardial infarction within 3 months before surgery;(4)ischemic heart disease;Left main coronary artery stenosis >70%;Severe aortic stenosis (area < 0.7cm2);Severe changes in left ventricular function (ejection fraction <30%, requiring vasoactive agents to assist circulation);(5)uncontrolled hypertension;(6) severe carotid artery stenosis (>70% or with symptoms);(7) kidney failure (blood creatinine level >442 mmol/L) or dialysis treatment;(8) serum albumin level (ALB) is less than 25 g/L.(9) international standardized ratio (INR) >1.5 or platelet count <100 103/mm3;(10)Inherited/acquired coagulation function defect;(11)preoperative preparation platelet;(12) contagious or infectious diseases;(13) patient or family members refused to participate in research;(14)refused to infusion of autologous blood or allogeneic blood products
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| Name | Affiliation | Role |
|---|---|---|
| Min Yan, Doctor | Zhejiang University | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The second affiliated hospital of Zhejiang University | Hangzhou | Zhejiang | 310000 | China |
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Including myocardial infarction, heart failure, low cardiac output, pericardial tamponade, severe arrhythmia according to physical and laboratory examination
| Through study completion,about 8 months |
| Rate of postoperative pulmonary complications | Including moderate and massive pleural effusion, respiratory failure, re-intubation according to physical and laboratory examination | Through study completion,about 8 months |
| Rate of postoperative neurological complication | Including cerebral hemorrhage, cerebral infarction according to physical and laboratory examination | Through study completion,about 8 months |
| Rate of postoperative renal complication | Need renal replacement therapy | Through study completion,about 8 months |
| Other severe complication | Including re-operation, re-admission of intensive care unit, multiple organ dysfunction, all cause death according to physical and laboratory examination and medical record | Through study completion,about 8 months |