Restrictive Versus Liberal Thresholds for RBC Transfusion in ECMO

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

About this trial

Rationale: In patients supported with extracorporeal membrane oxygenation (ECMO), transfusion of red blood cells (RBC) is very common. This is possibly due to the application of liberal thresholds and the lack of evidence-based guidelines. Although RBC transfusion can be lifesaving, it is also a risk-bearing intervention with substantial risk for morbidity and mortality in this critically ill population. Also, with increasing scarcity, RBC transfusions are becoming more expensive. Furthermore, in the past decades it has been shown in several critically ill patient populations - not on ECMO - that maintaining a restrictive hemoglobin (Hb) threshold for RBC transfusion is non-inferior, including in cardiothoracic surgery, acute myocardial infarction and septic shock. Therefore, the investigators hypothesize that a restrictive transfusion threshold for RBC is safe to apply in patients on ECMO in comparison with a liberal transfusion threshold.

Objective: The primary objective of this trial is to study in a prospective randomized comparison whether a restrictive RBC transfusions strategy is non-inferior compared to a liberal strategy in patients on ECMO with respect to 90-day mortality.

Study design: Prospective multi-center randomized controlled non-inferiority trial.

Study population: Patients, 18 years or older, receiving ECMO.

Intervention: Restrictive RBC transfusion threshold: in case the Hb transfusion trigger of 7.0 g/dL (4.3 mmol/L) is reached, 1 RBC unit at a time will be transfused. The aimed Hb target range of the restrictive/intervention group will be 7.1 - 9.0 g/dL (4.3 - 5.6 mmol/L). Liberal RBC transfusion threshold: in case the Hb transfusion trigger of 9.0 g/dL (5.6 mmol/L) is reached, 1 RBC unit at a time will be transfused. Target range of the liberal group is defined as Hb 9.1 - 11.0 g/dL

Main study parameters/endpoints: The primary outcome parameter is 90-day all-cause mortality.

Secondary outcomes include: 1) proportion of patients on ECMO exposed to allogeneic RBC transfusion; 2) RBC volume infused per patient during ECMO; 3) reasons for RBC transfusion other than Hb triggers; 4) transfusion reactions; 5) time on ECMO; 6) length of hospital- and ICU-stay; 7) in-ICU morbidity; 8) quality of life (QoL), iMTA Medical Consumption Questionnaire (iMCQ) and Productivity Cost Questionnaire (iPCQ) at 3, 6, 9, and 12 months; 9) costs related to a) transfusion, b) hospital admission and c) transfusion-related sequelae.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient is aged 18 years or older;

Is receiving ECMO;

(Deferred) informed consent.

Disqualifiers

Not expected to survive for 24 hours when assessed;

Inability to receive blood products;

(Known) decline to blood transfusions (e.g., Jehovah's Witnesses);

Extracorporeal carbon dioxide removal (ECCO2R) using low blood flow devices or pumpless devices (i.e., MINILUNG ®, PrismaLung+);

Trial design

Design model

Parallel

Treatments tested in this trial

  • Red Blood Cell transfusion

    Other intervention

    When the appropriate Hb threshold is reached, patients in each group will have one unit of RBC administered at a time. Within 3 hours after the transfusion, a repeat Hb concentration will be measured. Each group will only be transfused when their Hb level falls below the transfusion threshold. In case of a outlier measurement, clinicians are advised to repeat the measurement. The RBC transfusion must take place within 4 hours when the Hb trigger was measured.

Treatment groups

526 Participants
are divided into 2 treatment groups
Group A: Restrictive strategyActive comparator 1 intervention
Group B: Liberal strategyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

90-day all-cause mortality

The primary outcome measure is all-cause mortality within 90 days, i.e. the proportion of patients who die from any cause during this 90-day period following ECMO support.

Time frame
90 days

Secondary outcomes

1

In-hospital mortality

All-cause mortality during the hospital stay refers to the proportion of patients who died from any cause while they were still admitted to the hospital.

Time frame
30 days
2

Duration

The duration of ECMO support, along with the length of ICU and hospital stays, are key metrics that quantify the total time a patient receives ECMO treatment, is in the intensive care unit, and remains in the hospital, measured in both days and hours.

Time frame
30 days
3

Red blood cell transfusion exposure

The proportion of patients on ECMO who receive allogeneic red blood cell (RBC) transfusions.

Time frame
30 days
4

Adherence

The number of adherence and non-adherence transfusion events.

Time frame
30 days

Other outcomes

1

In-ICU morbidity

All in-ICU morbidity, including neurological, cardiac, hemorrhagic, abdominal, renal, infection, peripheral, and transfusion-related complications.

Time frame
30 days
2

Transfusion reasons

To evaluate the reasons for RBC transfusion beyond solely using hemoglobin (Hb) levels as the trigger.

Time frame
30 days
3

Exposure to other transfusion products

The number of transfusions of other blood-derived products or coagulation factors, such as platelet concentrates.

Time frame
30 days
4

Supportive therapy duration

The duration of supportive therapies, including invasive mechanical ventilation and renal replacement therapy, measured in both days and hours.

Time frame
30 days

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Lead sponsor

Amsterdam UMC, location AMC

Sponsor institution

ZonMw: The Netherlands Organisation for Health Research and Development

Collaborator