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The Israeli Trigger for Blood Transfusions in the ICU

A Multicenter Study of Anemia in the ICU Patient: Determination of the Israeli Trigger and Post ICU Course

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00413816
Enrollment
500
Registered
2006-12-20
Start date
2006-10-31
Completion date
2006-12-31
Last updated
2006-12-20

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

Conditions

Anemia

Keywords

Anemia, Critically ill

Brief summary

The purpose of the study is to determine the trigger for blood transfusions in Israeli ICU patients and the possible effects of anemia on the post ICU discharge course.

Detailed description

Anemia is a common problem in critically ill patients admitted to intensive care units (ICUs). The etiology is multifactorial and includes sepsis, overt or occult blood loss (including frequent blood sampling), decreased production of endogenous erythropoietin, and immune-associated functional iron deficiency. In the only large randomized trial addressing the issue of transfusion triggers in the perioperative and critical care setting, the Canadian Transfusion Requirements in Critical Care (TRICC) study documented an overall non significant trend toward decreased 30-day mortality (18.7% vs. 23.3%, P = .11) and significant decreases in mortality among patients who were less acutely ill (8.7% vs. 16.1%, P = .03) in the group treated using a transfusion trigger reflected in a hemoglobin level of 7.0 g/dL compared with a more liberal transfusion group that received 54% more red blood cell (RBC) transfusions. This data suggests that many critically ill patients can tolerate hemoglobin levels as low as 7 g/dL and that a liberal RBC transfusion strategy may in fact lead to worse clinical outcomes. Evidence-based transfusion guidelines for critically ill and perioperative patients recommend RBC transfusion when the hemoglobin concentration is less than 7 g/L and transfusion avoidance at values greater than 10 g/ L . The restrictive blood transfusion policy results in many patients being discharged anemic from the ICU. In a recent Scottish study, 87% of ICU survivors were discharged anemic (defined as a hemoglobin level \< 13g/dl in males and 11 g/dl in females), while 24% of males and 27.9% of females had a hemoglobin level \< 9 g/dl. While studies have shown that a restrictive blood transfusion policy does not adversely affect the 30- or 60-day mortality , there is no information regarding the effect of anemia on immediate and long term morbidity of ICU survivors. This may be important as anemia has been shown to decrease functional status and quality of life, while treating anemia may improve functional status and decrease morbidity. In addition, it is not known how many of these patients receive blood transfusions following ICU discharge. In Israel, there are no national guidelines for the administration of red blood cells in the ICU and the national trigger is unknown. * Study Rationale The determination of the ICU trigger will determine if the ICU is performing according to presently accepted standards. Determining the effect of anemia after ICU discharge may allow for targeted interventions in particular groups of patients which may improve recovery rates. * This study is a non-intervention, observational, multi- center study. * All ICU patients over 18 years of age will be included. * Demographic data will be collected on admission of the patient to the ICU * Daily hemoglobin levels (routine morning hemoglobin) and the hemoglobin level which triggered the blood transfusion (if different from the morning level) will be recorded and the number and indication for red blood cell transfusions noted. * Hemoglobin level will be noted on discharge from the ICU. * Hemoglobin levels, length of hospital stay and occurrence of complications in the post-ICU period will be noted.

Interventions

None listed

Sponsors

Rabin Medical Center
Lead SponsorOTHER

Study design

Observational model
DEFINED_POPULATION
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* all patients admitted to ICU

Exclusion criteria

* age \< 18 years * \> 20% full thickness burns

Countries

Israel

Contacts

Primary ContactJonathan Cohen, MD
jonatanc@clalit.org.il+972-3-9376525

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026