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 volunteersQualifiers
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
Parallel
Treatments tested in this trial
Red Blood Cell transfusion
Other interventionWhen 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
Trial outcomes
Primary outcomes
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.
Secondary outcomes
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.
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.
Red blood cell transfusion exposure
The proportion of patients on ECMO who receive allogeneic red blood cell (RBC) transfusions.
Adherence
The number of adherence and non-adherence transfusion events.
Other outcomes
In-ICU morbidity
All in-ICU morbidity, including neurological, cardiac, hemorrhagic, abdominal, renal, infection, peripheral, and transfusion-related complications.
Transfusion reasons
To evaluate the reasons for RBC transfusion beyond solely using hemoglobin (Hb) levels as the trigger.
Exposure to other transfusion products
The number of transfusions of other blood-derived products or coagulation factors, such as platelet concentrates.
Supportive therapy duration
The duration of supportive therapies, including invasive mechanical ventilation and renal replacement therapy, measured in both days and hours.
Sponsors and contacts
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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