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| Name | Class |
|---|---|
| Second Affiliated Hospital of Third Military Medical University | OTHER |
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The aim of the study is to identify the correlation between ischaemia reperfusion injury and postoperative multiorgan damage during cardiopulmonary cardiac surgery; and to investigate biomarkers that can predict postoperative organ damage in cardiac surgery.
This study proposes to observe multi-organ functional impairment of the heart, kidney and brain after extracorporeal circulation in a prospective study of clinical patients; to obtain markers with diagnostic and predictive efficacy by collecting pre and postoperative serum and heart and ear tissue samples from patients with postoperative organ functional impairment, performing combined proteomic and metabolomic analyses, and by analysing them with detailed postoperative clinical prognostic data using machine learning algorithms.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ischemic reperfusion injury | Procedure | ischemic reperfusion injury is a pathological process in which the ischemic myocardium is restored to normal perfusion, but the tissue damage is progressively aggravated when the coronary artery supply is completely blocked after cardiopulmonary bypass surgery and then recanalised at a certain time. |
| Measure | Description | Time Frame |
|---|---|---|
| incidence of postoperative cardiac injury | troponin I will be tested before and after surgery | from the ending of surgery to 7 days after surgery |
| incidence of postoperative acute kidney injury | renal function will be tested before and after surgery | from the ending of surgery to 7 days after surgery |
| incidence of postoperative brain injury | deliriumwill be tested before and after surgery | from the ending of surgery to 7 days after surgery |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of postoperative arrhythmia events | postoperative arrhythmia events are recorded according to follow-up visits after surgery | from the ending of surgery to 72 hours after surgery |
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Inclusion Criteria:
Exclusion Criteria:
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Patients were screened from the outpatient clinics of the Second Hospital of the Army Medical University who were proposed for mitral valve replacement or mitral valve combined with aortic valve replacement, agreed to participate in this study, and signed an informed consent form.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Qiao Guo, MD | Contact | 13637870013 | guoqiao@cqmu.edu.cn | |
| Dagang Wang, MD | Contact | +86 023 63693014 | kuanrenlunli@qq.com |
| Name | Affiliation | Role |
|---|---|---|
| He Huang, MD | Chongqing Medical University, the second affiliated hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The second affiliated hospital of Chongqing medical university | Chongqing | China |
The individual participant data for this study is available from the sponsor on reasonable request through email.
Within five years
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| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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Venous blood and tissue samples be collected for biochemical testing.