Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This multi-centre study will provide sound, generalizable data on the effectiveness of a POC-based algorithm to determine to what extent this guideline can reduce blood product transfusions. Investigators will study outcomes in 7000 patients undergoing heart surgery at 10 participating hospitals. The proposed trial addresses several important research and clinical issues and has the potential to markedly improve the transfusion management and surgical care in general of cardiac surgery patients.
The intervention will be a novel POC-based algorithm that has been shown in a pilot study by us to be associated with a substantial reduction in blood product transfusions. The algorithm will employ viscoelastic and aggregometric POC-tests and an objective measure of blood loss. The primary outcome will be avoidance of red blood cell transfusion during hospitalization. The study has a 90% power to detect a 12% increase in avoidance rate. Secondary outcomes will include avoidance of red blood cell use and other blood products (plasma, platelets, and cryoprecipitate), units of blood products transfused, and adverse clinical outcomes related to transfusion (acute kidney injury, infections, and death). Data will also be collected for future health-economics analyses.
Largely due to the limitations of existing evidence, however, such algorithms are rarely used in clinical practice. The proposed trial will provide sound, generalizable data on the effectiveness of a POC-based algorithm to guide their future use. An integrated blood management algorithm that employs POC coagulation tests will reduce blood product transfusions in cardiac surgery, thereby improving clinical outcomes.
Does an integrated blood transfusion algorithm that employs POC coagulation tests applied across a network of hospitals reduce blood transfusions and associated adverse outcomes in cardiac surgery?
Despite major advances in cardiac surgery, coagulopathy continues to carry a heavy burden in cases that require the use of cardiopulmonary bypass (CPB), occurring frequently and resulting in excessive blood loss, blood product transfusions, and adverse clinical outcomes. Current management of coagulopathy is hampered by the inability of conventional laboratory tests to delineate its etiology in a timely manner, thereby precluding timely and targeted transfusion therapy. With the advent of point-of-care (POC) coagulation tests that can rapidly identify the etiology of coagulopathy, it may now be possible to reduce the burden of coagulopathy and thereby reduce transfusions and adverse outcomes. Several single-centre studies (including one by the investigator group) have found that the use of POC-based algorithms in cardiac surgery can markedly reduce blood product transfusions and by that means reduce morbidities and mortality.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Transfusion Algorithm | Other | Hospitals will be randomized to the intervention arm of the study in a stratified manner. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| POC-based transfusion algorithm | Other | A transfusion algorithm based on point-of-care coagulation testing. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Point Of Care (POC) Transfusion Algorithm Cardiac Study | The primary outcome measure will be the proportion of patients who receive any allogeneic red blood cell (RBC) transfusion from admission before surgery to end of follow-up. | 2.5 years |
| Measure | Description | Time Frame |
|---|---|---|
| Transfusion | Allogeneic blood products (platelets, plasma, cryoprecipitate) or coagulation factors (e.g., fibrinogen concentrate, factor VIIa), or undergo re-exploration; units of blood products transfused, nadir hemoglobin concentration (to identify changes in transfusion practice that may be unrelated to treatment of coagulopathy) | 7 days |
Not provided
Hospital Inclusion:
Exclusion Criteria: Hospitals not meeting inclusion.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Keyvan Karkouti, MD | University Health Network, Toronto | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Dr. Charles McAdams | Calgary | Alberta | T2N 2T9 | Canada | ||
| Blaine Achen |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27654344 | Derived | Karkouti K, Callum J, Wijeysundera DN, Rao V, Crowther M, Grocott HP, Pinto R, Scales DC; TACS Investigators. Point-of-Care Hemostatic Testing in Cardiac Surgery: A Stepped-Wedge Clustered Randomized Controlled Trial. Circulation. 2016 Oct 18;134(16):1152-1162. doi: 10.1161/CIRCULATIONAHA.116.023956. Epub 2016 Sep 21. |
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| ID | Term |
|---|---|
| D002318 | Cardiovascular Diseases |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Blood loss |
Chest-tube drainage at 6 and 24 hours after surgery |
| 24 hours |
| Ventilation and hospital stay | Duration of mechanical ventilation and length of stay in the ICU and hospital | 24 hours to 7 days |
| Kidney injury | Incidence of acute kidney injury, defined as a ≥ 2-fold in increase in creatinine or new renal replacement therapy within 48 hours after surgery | 48 hours |
| Post operative complications | Arrhythmias, sternal infection, myocardial infarction, stroke, thromboembolic events, and death | 7 days |
| Edmonton |
| Alberta |
| Canada |
| Dr. Terry Waters | Vancouver | British Columbia | V5Z 1M9 | Canada |
| Dr. Sukhpal Brar | Vancouver | British Columbia | Canada |
| Dr. H. Grocott | Winnipeg | Manitoba | R2H 2A6 | Canada |
| Dr. Summer Syed | Hamilton | Ontario | L8N 3Z5 | Canada |
| Dr. Christopher Harle | London | Ontario | N6A 5A5 | Canada |
| Dr. Daniel Kim | Newmarket | Ontario | L3Y 2P9 | Canada |
| Dr. D. Tran | Ottawa | Ontario | K1Y 4W7 | Canada |
| Dr. F. Moussa | Toronto | Ontario | M4N 3M5 | Canada |
| Dr. E. Medicis | Fleurimont | Quebec | J1H 5N4 | Canada |
| Dr. J. Bussieres | Sainte-Foy | Quebec | G1V 4G5 | Canada |