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Blood Transfusion Reduction - QI Project

Blood Transfusion Reduction Quality Improvement Project

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04823273
Enrollment
1640
Registered
2021-03-30
Start date
2021-04-06
Completion date
2022-10-15
Last updated
2023-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Transfusion

Keywords

blood transfusion, EHR interventions, user-centered design, high-value care

Brief summary

Blood Banks of large medical centers have large annual budgets, typically millions of dollars. Blood product wastage results in not only in a loss of the product's cost, but also of the fees involved in transporting, handling, and administering these products. Optimal utilization of blood products requires a balance between maximizing patient clinical outcomes while avoiding unnecessary costs and risks associated with transfusions. This project will specifically focus on packed red blood cell transfusions (pRBCs). There are clear guidelines for transfusing pRBCs however these guidelines are not always followed. pRBC transfusions outside of recommended guidelines is associated with increased risk of harm to patients. Our aim is to improve adherence to guideline indicated pRBC transfusions for patient in the UCHealth system thereby decreasing inappropriate (non-guideline indicated) pRBC transfusions. We will conduct a QI project seeking to improve pRBC transfusion guideline adherence. This project will involve data review to establish baseline rates, multimodal interventions to improve adherence to pRBC transfusion guidelines including provider education, modifications to the electronic ordering interface, and changing blood back policies at participating institutions.

Interventions

BEHAVIORALGeneral improvement

Changes to interface to be more intuitive.

BEHAVIORALIn-line help text

General improvement + in-line help text

BEHAVIORALInterruptive alert

General improvement + interruptive alert

Sponsors

University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* All physicians and nurses with access to order inpatient blood transfusions through a hospital-based EMR. * All physicians and nurses ordering blood for individuals over the age of 18.

Exclusion criteria

* All physicians and nurses ordering blood transfusion ordering blood in the OR * Blood ordered through massive transfusion protocol

Design outcomes

Primary

MeasureTime frameDescription
Blood Transfusion Orders78 weeksNumber of patients who received blood transfusions during the study by arm.
Guideline Concordance Measured by Pre-Transfusion Hemoglobin Values Per Transfusion78 weeksThe American Association of Blood Banks recommends a restrictive threshold of a pre-transfusion hemoglobin level of less than 7.0g/dL for the vast majority of inpatients. Transfusions with Hemoglobin levels above 7 will be compared in arm 1 vs 2 +3 combined; arm 2 vs arm 3.
Guideline Concordance Measured by Number of Units Ordered Per Transfusion78 weeksThe American Association of Blood Banks recommends a restrictive threshold of a single unit pRBC transfusion for the vast majority of inpatients. This outcome will compare hemoglobin levels, units transfused in arm 1 verses arms 2 and 3 combined and arm 2 verses arm 3.

Other

MeasureTime frameDescription
Historical Blood Transfusion OrdersBaselineNumber of patients who received blood transfusions during the 18 months prior to study start in the EHR at the same hospital.
Historical Guideline Concordance Measured by Pre-Transfusion Hemoglobin Values Per TransfusionBaselineThe American Association of Blood Banks recommends a restrictive threshold of a pre-transfusion hemoglobin level of less than 7.0g/dL for the vast majority of inpatients. Historical data for 18 months prior to study start will be collected from EHR records for transfusions orders placed for patients with Hemoglobin levels above 7.
Guideline Concordance Measured by Number of Units Ordered Per TransfusionBaselineThe American Association of Blood Banks recommends a restrictive threshold of a single unit pRBC transfusion for the vast majority of inpatients. Historical data for 18 months prior to study start will be collected from EHR records for the number of units transfused per blood transfusion order.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026