Erythropoietin to Improve Critical Care Patient Outcomes

• Status: Not yet recruiting
• Trial end date: 2022-12-31
• Target enrollment: 0
• Participant gender: All

Summary

Anemia is very common in intensive care patients, affecting approximately two-thirds of patients on admission, with a mean admission hemoglobin (Hb) level of 11.0 g/dl. The severity of anemia is associated with increased morbidity and mortality. Its pathophysiology is complex, involving blood loss (from repeated blood sampling, invasive procedures, surgical interventions, etc.) and inflammation. The latter is responsible for a decrease in endogenous erythropoietin (EPO) production and a decreased bone marrow response, which can be very prolonged (half of the patients discharged from ICU with anemia are still anemic at 6 months of discharge, with low levels of EPO, compared to the observed Hb levels). On this basis, several randomized clinical trials (RCTs) evaluating the effect of EPO on the transfusion rate in this population were performed in the 1990s-2000s. The authors showed a modest reduction in blood transfusion, which was not considered clinically relevant in view of the cost of EPO at that time.

Since then, meta-analyses evaluating the benefits and risks of EPO in intensive care patients suggest a positive impact of EPO on mortality. The largest, including 34 studies (and 930,470 patients) reports a reduction in the relative risk of mortality of 0.76, 95% CI [0.61 - 0.92]. Beyond the reduction in red blood cell transfusions, the benefit of EPO could be directly due to its erythropoietic effect (correction of anemia) and/or its anti-inflammatory/anti-apoptotic properties. Based on this literature, the French critical care societies have recently recommended the use of EPO. However, the European Society of Intensive Care Medicine (ESICM) recently recommended against the use of EPO, based on the same literature, but suggested that the benefit of EPO should be evaluated. Indeed, the main obstacle to recommending the use of EPO seems to be economic, whereas the arrival on the market of biosimilar molecules has significantly reduced these costs.

Most of the trials on EPO in critical care patients (and included in the meta-analyses) are quite old (about 15 years) and none of them had mortality as primary endpoint. In addition, transfusion practices and the quality of blood products have changed significantly over the years. In this context of disagreement on the recommendations for the use of EPO in these patients, but of potential benefit on mortality, there is an urgent need to evaluate whether EPO decreases mortality in adult anemic patients admitted to intensive care. However, calculation of the number of patients needed to evaluate the benefit of EPO on mortality in this population yields a number of patients to be included of the order of 1800-2000 patients.

Before considering the implementation of a multicenter study involving such a large number of patients, a pilot study evaluating the feasibility and inclusion capacity for such a study seems indispensable according to the latest CONSORT recommendations.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University Hospital, Angers
• Treatments: Epoetin Alfa

Criteria

Inclusion Criteria:

• Adult patients (age > 18 years),

• admitted to intensive care for more than 72 hours and less than 7 days

• who have received invasive ventilatory support and/or treatment with a vasoactive agent for at least one day since admission

• with an Hb level < 12 g/dl,

• with consent from the patient or patient's relative (or emergency inclusion procedure).

Exclusion Criteria:

• Moribund patient,

• Current hospitalization for acute coronary syndrome,

• Recent history of thromboembolic event (< 3 months),

• Uncontrolled hypertension despite adequate antihypertensive therapy,

• Myelodysplasia or chronic pathology requiring iterative transfusions,

• EPO treatment within the last 30 days,

• Participation in another interventional trial of an erythropoiesis-stimulating agent or anemia treatment,

• Expected discharge from the intensive care unit within 24 hours,

• Known hypersensitivity to EPO or any of its components,

• A history of erythroblastopenia following erythropoietin therapy

• Pregnant, breast-feeding or parturient woman

• Person deprived of liberty by judicial or administrative decision

• Person under forced psychiatric care

• Person under a legal protection measure.