Anemia, Cardiovascular Diseases, Cerebrovascular Accident, Heart Diseases, Hematologic Diseases, Myocardial Infarction, Pneumonia, Thromboembolism
Conditions
Keywords
Blood Disease, blood transfusion
Brief summary
The purpose of this study is to compare liberal red blood cell transfusion therapy with restrictive red blood cell transfusion therapy in surgical patients with cardiovascular disease or risk factors.
Detailed description
BACKGROUND: Red blood cell transfusions are an extremely common medical intervention in both the United States and worldwide; over 14 million units of blood are transfused in the United States. Between 60 and 70 percent of all blood is transfused in the surgical setting. Despite the common use of red blood cell transfusions, the threshold for transfusion has not been adequately evaluated and is very controversial. A decade ago, the standard of care was to administer a peri-operative transfusion whenever the hemoglobin (Hgb) level fell below 10 g/dl (the 10/30 rule). Concerns about the safety of blood, especially with respect to HIV and hepatitis, and the absence of data to support a 10 g/dl threshold led to the current standard of care, which is to administer blood transfusions based on the presence of symptoms, and not a specific Hgb/hematocrit level. However, there have not been any randomized clinical trials done with surgical patients that have tested the efficacy and safety of withholding blood until the patient develops symptoms, or the 10/30 approach to transfusion. Patients with underlying cardiovascular disease are at greatest risk of adverse effects from reduced Hgb levels. DESIGN NARRATIVE: This is a multi-center randomized trial to test the effectiveness of a transfusion strategy that maintains postoperative Hgb levels above 10 g/dl (liberal transfusion) in improving patient outcome. This will be compared to the restrictive (symptomatic) transfusion strategy in which blood transfusion is withheld until the patient develops symptoms of anemia or Hgb less than 8 g/dL. Participants will be randomly assigned to one of the two transfusion strategies. The liberal (10 g/dl) threshold strategy will use enough red blood cell units to maintain Hgb levels at or above 10 g/dl through hospital discharge. Restrictive (Symptomatic) transfusion strategy patients will receive red blood cell transfusions for symptoms of anemia, although transfusion is also permitted, but not required, if the Hgb level falls below 8 g/dl. Outcomes will include functional recovery (primary outcome: ability to walk 10 feet across a room without human assistance or death 60 days post-randomization), lower extremity activities of daily living and instrumental activities of daily living, survival up to 60-days and long-term, disposition (i.e., nursing home placement), and postoperative complications (e.g., myocardial infarction, unstable angina, or death in hospital, pneumonia, wound infection, thromboembolism, stroke). Ambulation at 60 days is known to be highly predictive of ultimate functional outcome as well as of mortality at one year. Because inability to walk has such important implications for quality of life, and because it is a common problem, it far outweighs the small risk of viral infection or other complications from transfusion in elderly patients. The trial will also evaluate the effect of transfusion threshold on postoperative risk of acute cardiac ischemia. The strategy will be to enhance surveillance for ischemic events by increasing the number of EKG and serum troponin measurements beyond those already called for in the original FOCUS protocol. There is an ancillary study to the trial (R01 HL085706) to examine delirium as an outcome in a subsample of 139 patients. We will assess short-term (in hospital) and longer-term (after 30 days) severity of delirium.
Interventions
This transfusion strategy will maintains postoperative Hgb levels above 10 g/dL. This threshold strategy will use enough red blood cell units to maintain Hgb levels at or above 10 g/dL through hospital discharge or up to 30 days after randomization.
Transfusion is withheld until the patient develops symptoms from anemia (i.e., chest pain or ECG changes thought to be ischemic, congestive heart failure, unexplained tachycardia or hypotension unresponsive to fluids) or until the hemoglobin level falls below 8 g/dL. Transfusion is permitted, but is not mandatory, if the hemoglobin level falls below 8 g/dL.
Sponsors
Study design
Eligibility
Inclusion criteria
* Has undergone surgical repair for a hip fracture * Has a postoperative Hgb level below 10 g/dL within three days of surgery * Diagnosis of cardiovascular disease (e.g., coronary artery disease, congestive heart failure, stroke or transient ischemic attack, or peripheral vascular disease) or cardiovascular risk factors (e.g., diabetes mellitus, hypertension, hypercholesterolemia, tobacco use, or creatinine levels greater than 2.0 mg/dL)
Exclusion criteria
* Unable to walk prior to hip fracture * Declines blood transfusions * Suffered multiple traumas * Pathologic fracture of the hip due to malignancy * Clinically recognized acute myocardial infarction within the 30 days prior to study entry * Previously participated in the trial and fractured the other hip * Symptoms associated with anemia (e.g., ischemic chest pain) or actively bleeding at the time of randomization
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Inability to Walk 10 Feet or Across a Room Without Human Assistance or Death | 60 days after randomization | ascertained via telephone follow-up |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mortality at 30 Days | 30 days | — |
| Mortality at 60 Days | 60 Days | — |
| Composite Outcomes (a) Death, Myocardial Infarction, or Pneumonia and b) Death, Myocardial Infarction, Pneumonia, Thromboembolism, or Stroke | In-hospital | — |
| Myocardial Infarction | In-hospital | — |
| Postoperative Complications (e.g., Wound Infection, Thromboembolism, Stroke) | In hospital | — |
| Disposition Status (i.e., Nursing Home Placement) | 60 days | Nursing Home Residence |
| Function - Lower Extremity Activities of Daily Living,at 30 Days | 30 days | Using the Functional Status Index, score range 0 to 11, higher scores indicate greater dependency |
| Myocardial Infarction, Unstable Angina, or Death for Any Reason | In-hospital | — |
| Function - Fatigue/Energy, at 30 Days | 30 days | Using the Functional Assessment of Chronic Illnesses Therapy-Fatigue, score range from 0 to 52, higher scores indicating greater level of energy |
| Function - Lower Extremity Activities of Daily Living. at 60 Days | 60 Days | Scale range 0 to 11, higher scores indicate greater dependency |
| Function - Instrumental Activities of Daily Living, at 60 Days | 60 Days | Scale range 0 to 11, higher scores indicate greater dependency |
| Function - Fatigue/Energy, at 60 Days | 60 Days | Scale ranging from 0 to 52, higher scores indicating greater level of energy |
| Length of Stay in Hospital for United States Participants | Days from randomization to discharge | — |
| Length of Stay in Hospital for Canadian Participants | Days from randomization to discharge | — |
| Function - Instrumental Activities of Daily Living, at 30 Days | 30 days | Using the Older Americans Resources and Services Functional Assessment Questionnaire, score range from 0 to 4, higher scores indicating greater dependency |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Liberal (10 g/dL) Transfusion Strategy Transfusion strategy that maintains postoperative Hgb levels above 10 g/dL.
Liberal (10 g/dL) Transfusion Strategy: Maintains postoperative Hgb levels above 10 g/dL. This threshold strategy uses enough red blood cell units to maintain Hgb levels at or above 10 g/dL through hospital discharge or up to 30 days after randomization. | 1,007 |
| Restrictive Strategy Symptomatic transfusion strategy, a more conservative strategy, in which blood transfusion is withheld until the patient develops symptoms of anemia.
Restrictive (Symptomatic) Transfusion Strategy: Transfusion is withheld until the patient develops symptoms from anemia (i.e., chest pain or ECG changes thought to be ischemic, congestive heart failure, unexplained tachycardia or hypotension unresponsive to fluids) or until the hemoglobin level falls below 8 g/dL. Transfusion is permitted, but is not mandatory, if the hemoglobin level falls below 8 g/dL. | 1,009 |
| Total | 2,016 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Lost to Follow-up | 1 | 1 |
| Overall Study | Missing Primary Outcome | 0 | 1 |
| Overall Study | Withdrawal by Subject | 8 | 6 |
Baseline characteristics
| Characteristic | Restrictive Strategy | Total | Liberal (10 g/dL) Transfusion Strategy |
|---|---|---|---|
| Age, Continuous | 81.5 years STANDARD_DEVIATION 9 | 81.6 years STANDARD_DEVIATION 8.9 | 81.8 years STANDARD_DEVIATION 8.8 |
| Cardiovascular Disease History of Cardiovascular Disease | 631 participants | 1268 participants | 637 participants |
| Cardiovascular Disease No History of Cardiovascular Disease | 378 participants | 748 participants | 370 participants |
| Region of Enrollment Canada | 396 participants | 794 participants | 398 participants |
| Region of Enrollment United States | 613 participants | 1222 participants | 609 participants |
| Sex: Female, Male Female | 770 Participants | 1527 Participants | 757 Participants |
| Sex: Female, Male Male | 239 Participants | 489 Participants | 250 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 0 / 1,007 | 0 / 1,009 |
| serious Total, serious adverse events | 76 / 1,007 | 66 / 1,009 |
Outcome results
Inability to Walk 10 Feet or Across a Room Without Human Assistance or Death
ascertained via telephone follow-up
Time frame: 60 days after randomization
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Inability to Walk 10 Feet or Across a Room Without Human Assistance or Death | 351 participants |
| Restrictive Strategy | Inability to Walk 10 Feet or Across a Room Without Human Assistance or Death | 347 participants |
Composite Outcomes (a) Death, Myocardial Infarction, or Pneumonia and b) Death, Myocardial Infarction, Pneumonia, Thromboembolism, or Stroke
Time frame: In-hospital
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Composite Outcomes (a) Death, Myocardial Infarction, or Pneumonia and b) Death, Myocardial Infarction, Pneumonia, Thromboembolism, or Stroke | Death, myocardial infarction, or pneumonia | 89 Participants |
| Liberal (10 g/dL) Transfusion Strategy | Composite Outcomes (a) Death, Myocardial Infarction, or Pneumonia and b) Death, Myocardial Infarction, Pneumonia, Thromboembolism, or Stroke | Death, MI, pnuemonia, thromboembolism or stroke | 103 Participants |
| Restrictive Strategy | Composite Outcomes (a) Death, Myocardial Infarction, or Pneumonia and b) Death, Myocardial Infarction, Pneumonia, Thromboembolism, or Stroke | Death, myocardial infarction, or pneumonia | 90 Participants |
| Restrictive Strategy | Composite Outcomes (a) Death, Myocardial Infarction, or Pneumonia and b) Death, Myocardial Infarction, Pneumonia, Thromboembolism, or Stroke | Death, MI, pnuemonia, thromboembolism or stroke | 94 Participants |
Disposition Status (i.e., Nursing Home Placement)
Nursing Home Residence
Time frame: 60 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Disposition Status (i.e., Nursing Home Placement) | 137 Participants |
| Restrictive Strategy | Disposition Status (i.e., Nursing Home Placement) | 161 Participants |
Function - Fatigue/Energy, at 30 Days
Using the Functional Assessment of Chronic Illnesses Therapy-Fatigue, score range from 0 to 52, higher scores indicating greater level of energy
Time frame: 30 days
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Function - Fatigue/Energy, at 30 Days | 38.7 score on a scale | Standard Deviation 7.7 |
| Restrictive Strategy | Function - Fatigue/Energy, at 30 Days | 38.6 score on a scale | Standard Deviation 7.6 |
Function - Fatigue/Energy, at 60 Days
Scale ranging from 0 to 52, higher scores indicating greater level of energy
Time frame: 60 Days
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Function - Fatigue/Energy, at 60 Days | 41.8 score on a scale | Standard Deviation 7.3 |
| Restrictive Strategy | Function - Fatigue/Energy, at 60 Days | 42.3 score on a scale | Standard Deviation 7.4 |
Function - Instrumental Activities of Daily Living, at 30 Days
Using the Older Americans Resources and Services Functional Assessment Questionnaire, score range from 0 to 4, higher scores indicating greater dependency
Time frame: 30 days
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Function - Instrumental Activities of Daily Living, at 30 Days | 3.9 score on a scale | Standard Deviation 0.5 |
| Restrictive Strategy | Function - Instrumental Activities of Daily Living, at 30 Days | 3.9 score on a scale | Standard Deviation 0.4 |
Function - Instrumental Activities of Daily Living, at 60 Days
Scale range 0 to 11, higher scores indicate greater dependency
Time frame: 60 Days
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Function - Instrumental Activities of Daily Living, at 60 Days | 3.7 score on a scale | Standard Deviation 0.8 |
| Restrictive Strategy | Function - Instrumental Activities of Daily Living, at 60 Days | 3.7 score on a scale | Standard Deviation 0.9 |
Function - Lower Extremity Activities of Daily Living,at 30 Days
Using the Functional Status Index, score range 0 to 11, higher scores indicate greater dependency
Time frame: 30 days
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Function - Lower Extremity Activities of Daily Living,at 30 Days | 7.3 score on a scale | Standard Deviation 4 |
| Restrictive Strategy | Function - Lower Extremity Activities of Daily Living,at 30 Days | 7.4 score on a scale | Standard Deviation 5.9 |
Function - Lower Extremity Activities of Daily Living. at 60 Days
Scale range 0 to 11, higher scores indicate greater dependency
Time frame: 60 Days
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Function - Lower Extremity Activities of Daily Living. at 60 Days | 5.1 score on a scale | Standard Deviation 4.2 |
| Restrictive Strategy | Function - Lower Extremity Activities of Daily Living. at 60 Days | 5.1 score on a scale | Standard Deviation 4.3 |
Length of Stay in Hospital for Canadian Participants
Time frame: Days from randomization to discharge
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Length of Stay in Hospital for Canadian Participants | 12.03 days | Standard Deviation 9.31 |
| Restrictive Strategy | Length of Stay in Hospital for Canadian Participants | 12.70 days | Standard Deviation 9.48 |
Length of Stay in Hospital for United States Participants
Time frame: Days from randomization to discharge
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Length of Stay in Hospital for United States Participants | 3.67 days | Standard Deviation 3.38 |
| Restrictive Strategy | Length of Stay in Hospital for United States Participants | 3.97 days | Standard Deviation 3.89 |
Mortality at 30 Days
Time frame: 30 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Mortality at 30 Days | 52 Participants |
| Restrictive Strategy | Mortality at 30 Days | 43 Participants |
Mortality at 60 Days
Time frame: 60 Days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Mortality at 60 Days | 76 Participants |
| Restrictive Strategy | Mortality at 60 Days | 66 Participants |
Myocardial Infarction
Time frame: In-hospital
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Myocardial Infarction | 23 Participants |
| Restrictive Strategy | Myocardial Infarction | 38 Participants |
Myocardial Infarction, Unstable Angina, or Death for Any Reason
Time frame: In-hospital
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Myocardial Infarction, Unstable Angina, or Death for Any Reason | 43 participants |
| Restrictive Strategy | Myocardial Infarction, Unstable Angina, or Death for Any Reason | 52 participants |
Postoperative Complications (e.g., Wound Infection, Thromboembolism, Stroke)
Time frame: In hospital
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Liberal (10 g/dL) Transfusion Strategy | Postoperative Complications (e.g., Wound Infection, Thromboembolism, Stroke) | Wound Infection | 14 Participants |
| Liberal (10 g/dL) Transfusion Strategy | Postoperative Complications (e.g., Wound Infection, Thromboembolism, Stroke) | Thromboembolism | 12 Participants |
| Liberal (10 g/dL) Transfusion Strategy | Postoperative Complications (e.g., Wound Infection, Thromboembolism, Stroke) | Stroke | 8 Participants |
| Restrictive Strategy | Postoperative Complications (e.g., Wound Infection, Thromboembolism, Stroke) | Wound Infection | 8 Participants |
| Restrictive Strategy | Postoperative Complications (e.g., Wound Infection, Thromboembolism, Stroke) | Thromboembolism | 8 Participants |
| Restrictive Strategy | Postoperative Complications (e.g., Wound Infection, Thromboembolism, Stroke) | Stroke | 3 Participants |