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Effect of Leukoreduced Blood Transfusions on Infection Following Trauma

Primary Purpose

Wounds and Injuries

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Leukoreduced blood transfusion
Sponsored by
University of Washington
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Wounds and Injuries focused on measuring transfusion-induced immunomodulation, leukoreduction, surgical site infections, nosocomial infections, transfusion, Infection, Sepsis, Hemorrhage

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Trauma patients Age > 17 Transfusion within 24 hours of injury Exclusion Criteria: Active infection at time of injury Anticipated survival of < 48 hours (e.g. gunshot wound [GSW] to head, cardiopulmonary resuscitation [CPR] in progress) Receipt of blood products for this injury event prior to randomization AB negative; B negative blood type. Positive antibody screen Prior requirement for irradiated, leukoreduced or cytomegalovirus (CMV) seronegative blood products Incarcerated Enrolled in pre-hospital trial

Sites / Locations

  • Harborview Medical Center

Outcomes

Primary Outcome Measures

Infection within 30 days of injury

Secondary Outcome Measures

Marshall organ dysfunction scores over the course of Intensive Care Unit (ICU) admission
Hospital length of stay
Duration of mechanical ventilation
Duration of ICU stay
Acute lung injury
Plasma circulating levels of inflammatory cytokines and markers of lung injury (days 2-3 and 6-8)
Measures of monocyte activation (days 2-3 and 6-8)
Measures of polymorphonuclear neutrophil (PMN) activation (days 2-3 and 6-8)
Peripheral blood mononuclear cell expression of interleukin-2 (IL-2) receptors (days 2-3 and 6-8)

Full Information

First Posted
August 23, 2005
Last Updated
January 2, 2008
Sponsor
University of Washington
Collaborators
National Institutes of Health (NIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00135291
Brief Title
Effect of Leukoreduced Blood Transfusions on Infection Following Trauma
Official Title
Effect of Leukoreduction in Infection Risk in Trauma
Study Type
Interventional

2. Study Status

Record Verification Date
January 2008
Overall Recruitment Status
Completed
Study Start Date
February 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2004 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Washington
Collaborators
National Institutes of Health (NIH)

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine if leukoreduced blood transfusions reduce the risk of infection following trauma. Specifically, the investigators intend to evaluate whether there are clinically relevant differences in the rates of infection and in the severity of multiple organ failure in critically injured trauma patients receiving leukoreduced blood products compared to those receiving standard allogeneic blood products.
Detailed Description
Many severely injured patients survive their initial resuscitation only to suffer the late sequelae of nosocomial infection and multiple organ failure. The depth of hemorrhagic shock and the severity of anatomic injury are clearly associated with these adverse outcomes, however there is clear evidence to suggest that events during the resuscitation phase also play an important role in the pathogenesis of these sequelae. Specifically, there is now substantial clinical and experimental evidence implicating blood transfusion and the transfusion of allogeneic passenger leukocytes in the immune dysregulation characteristic of the post-injury state. This immune dysregulation manifests on two fronts: an uncontrolled inflammatory response leading to organ dysfunction and a state of immunoparalysis, leading to the development of nosocomial infection. Allogeneic passenger leukocytes have been implicated in the alterations in non-specific and specific immunity that underlie this state of altered immunoresponsiveness. The importance of allogeneic leukocytes in these phenomena suggests that strategies designed to limit the exposure of patients to these cells may reduce the incidence of post-injury sequelae. Pre-storage leukoreduction, whereby donated blood is passed through a leukocyte filter prior to storage and ultimate transfusion is one such strategy. This strategy remains at the center of a national debate on a policy of universal leukoreduction in which its efficacy is unproven and its cost undisputed. Study Objectives: To evaluate whether there are clinically relevant differences in the rates of infection and in the severity of multiple organ failure in critically injured trauma patients receiving leukoreduced blood products compared to those receiving standard allogeneic blood products. To assess T-cell responsiveness and the dominant CD4 lymphocyte subset as measured by T-lymphocyte IL-2 receptor expression and cytokine profile, respectively, in critically injured subjects transfused with leukoreduced blood products compared to subjects receiving standard allogeneic blood products. To assess the activational state of the peripheral blood monocyte and the neutrophil in critically injured trauma patients receiving leukoreduced blood products compared to subjects receiving standard allogeneic blood products. To evaluate whether there are clinically relevant differences in rates of acute lung injury (ALI) and circulating markers of ALI in patients receiving leukoreduced versus standard allogeneic blood products. To evaluate rates of microchimerism in those receiving leukoreduced versus standard allogeneic transfusion

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wounds and Injuries
Keywords
transfusion-induced immunomodulation, leukoreduction, surgical site infections, nosocomial infections, transfusion, Infection, Sepsis, Hemorrhage

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
300 (false)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Leukoreduced blood transfusion
Primary Outcome Measure Information:
Title
Infection within 30 days of injury
Time Frame
30 d
Secondary Outcome Measure Information:
Title
Marshall organ dysfunction scores over the course of Intensive Care Unit (ICU) admission
Title
Hospital length of stay
Title
Duration of mechanical ventilation
Title
Duration of ICU stay
Title
Acute lung injury
Title
Plasma circulating levels of inflammatory cytokines and markers of lung injury (days 2-3 and 6-8)
Title
Measures of monocyte activation (days 2-3 and 6-8)
Title
Measures of polymorphonuclear neutrophil (PMN) activation (days 2-3 and 6-8)
Title
Peripheral blood mononuclear cell expression of interleukin-2 (IL-2) receptors (days 2-3 and 6-8)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Trauma patients Age > 17 Transfusion within 24 hours of injury Exclusion Criteria: Active infection at time of injury Anticipated survival of < 48 hours (e.g. gunshot wound [GSW] to head, cardiopulmonary resuscitation [CPR] in progress) Receipt of blood products for this injury event prior to randomization AB negative; B negative blood type. Positive antibody screen Prior requirement for irradiated, leukoreduced or cytomegalovirus (CMV) seronegative blood products Incarcerated Enrolled in pre-hospital trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Avery B Nathens, MD PhD MPH
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Harborview Medical Center
City
Seattle
State/Province
Washington
ZIP/Postal Code
98004
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16980879
Citation
Nathens AB, Nester TA, Rubenfeld GD, Nirula R, Gernsheimer TB. The effects of leukoreduced blood transfusion on infection risk following injury: a randomized controlled trial. Shock. 2006 Oct;26(4):342-7. doi: 10.1097/01.shk.0000228171.32587.a1.
Results Reference
result
PubMed Identifier
17076839
Citation
Utter GH, Nathens AB, Lee TH, Reed WF, Owings JT, Nester TA, Busch MP. Leukoreduction of blood transfusions does not diminish transfusion-associated microchimerism in trauma patients. Transfusion. 2006 Nov;46(11):1863-9. doi: 10.1111/j.1537-2995.2006.00991.x.
Results Reference
result

Learn more about this trial

Effect of Leukoreduced Blood Transfusions on Infection Following Trauma

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