Safety and Effectiveness of Two Blood Transfusion Strategies in Surgical Patients With Cardiovascular Disease

Phase 3

Completed

• Conditions: Cardiovascular Diseases; Thromboembolism; Pneumonia; Hematologic Diseases; Myocardial Infarction; Heart Diseases; Cerebrovascular Accident; Anemia
• Interventions: Biological: Liberal (10 g/dL) Transfusion Strategy; Biological: Restrictive (Symptomatic) Transfusion Strategy

• Registration Number: NCT00071032
• Lead Sponsor: Rutgers, The State University of New Jersey

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.

Study Timeline

• Study Start: 2003-07
• Study First Submitted: 2003-10-09
• Study First Submitted QC: 2003-10-10
• Study First Posted: 2003-10-13
• Primary Completion: 2009-05
• Study Completion: 2009-05
• Results First Submitted: 2014-08-14
• Results First Submitted QC: 2014-08-14
• Results First Posted: 2014-08-28
• Status Verified: 2020-10
• Last Update Submitted: 2020-10-28
• Last Update Posted: 2020-11-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 2016

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)

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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

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Liberal (10 g/dL) Transfusion Strategy	Liberal (10 g/dL) Transfusion Strategy	Transfusion strategy that maintains postoperative Hgb levels above 10 g/dL.
2	Restrictive (Symptomatic) Transfusion Strategy	Symptomatic transfusion strategy, a more conservative strategy, in which blood transfusion is withheld until the patient develops symptoms of anemia.

Primary Outcome Measures

Name	Time	Method
Inability to Walk 10 Feet or Across a Room Without Human Assistance or Death	60 days after randomization	ascertained via telephone follow-up

Secondary Outcome Measures

Name	Time	Method
Myocardial Infarction, Unstable Angina, or Death for Any Reason	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
Function - Instrumental Activities of Daily Living, at 60 Days	60 Days	Scale range 0 to 11, higher scores indicate greater dependency
Length of Stay in Hospital for United States 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
Function - Lower Extremity Activities of Daily Living. at 60 Days	60 Days	Scale range 0 to 11, higher scores indicate greater dependency
Length of Stay in Hospital for Canadian Participants	Days from randomization to discharge
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
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
Function - Fatigue/Energy, at 60 Days	60 Days	Scale ranging from 0 to 52, higher scores indicating greater level of energy
Postoperative Complications (e.g., Wound Infection, Thromboembolism, Stroke)	In hospital

Trial Locations

Locations (1)

University Medicine & Dentistry of NJ; 🇺🇸 New Brunswick, New Jersey, United States