A Clinical Trial Assessing the Efficacy of Intravenous Iron for the Treatment of Anemia Following Cardiac Surgery

Michael Kremke110 enrolled

Overview

BACKGROUND Anemia and iron deficiency are highly prevalent in cardiac surgery patients. Both conditions may adversely affect postoperative rehabilitation. At hospital discharge, anemia is almost invariably present due to perioperative blood loss and frequent blood sampling. Two previous analyses demonstrated a prevalence of anemia early after coronary artery bypass grafting (CABG) of 94% and 98%, respectively. Almost half of CABG patients had persistent anemia two months after surgery. Postoperative anemia may result in debilitating symptoms, like dyspnoea, fatigue and poor exercise tolerance, and is associated with an increased likelihood of cardiovascular events and death after cardiac surgery. Mild to moderate anemia is commonly corrected with oral iron supplements. Oral iron is however poorly absorbed in patients with chronic diseases, and about 40% of patients suffer from debilitating gastrointestinal side-effects. As iron stores are frequently reduced or depleted after cardiac surgery, treatment with oral iron supplements may take several months. In patients with chronic heart failure (CHF), iron deficiency is associated with reduced exercise capacity, quality of life and survival even in the absence of anemia. Several large randomised trials demonstrated that treatment with intravenous iron improved clinical symptoms, exercise capacity and quality of life of CHF patients. RATIONALE It is desirable to replenish body iron stores rapidly after cardiac surgery with the aim to effectively correct anemia, optimize exercise tolerance and improve patient wellbeing. Modern intravenous iron formulations permit fast replenishment of body iron stores and have emerged as potential alternatives to oral iron. These formulations are well-tolerated and have become an established therapeutic option in anemic patients with reduced intestinal iron absorption. Several studies have demonstrated the efficacy of intravenous iron for the treatment of anemia following major non-cardiac surgery. Data regarding the efficacy of intravenous iron in cardiac surgery, however, are conflicting. HYPOTHESIS Single-dose intravenous iron therapy with ferric derisomaltose/iron isomaltoside is superior to oral iron supplementation for the correction of anemia following cardiac surgery. Moreover, single-dose intravenous iron therapy with ferric derisomaltose/iron isomaltoside results in a greater postoperative exercise capacity, an improved quality of life and less fatigue.

Study Type

INTERVENTIONAL

Allocation

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients 18 years of age or older undergoing first-time, non-emergent cardiac surgery with cardiopulmonary bypass. Eligible procedures are A: isolated CABG surgery (+/- arrhythmia surgery), B: isolated cardiac valve surgery (+/- arrhythmia surgery), C: a combination of CABG and cardiac valve surgery (+/- arrhythmia surgery) * Moderate anaemia on the first postoperative day. According to World Health Organization-criteria defined as a haemoglobin concentration of equal to or greater than 5.0 mmol/l (8 g/dl) and less than 6.8 mmol/l (11 g/dl). Exclusion Criteria: * Known hypersensitivity to any iron formulation * Multiple drug allergies or history of previous anaphylaxis * Severe asthma, eczema or another atopic allergy * Rheumatoid arthritis or systemic lupus erythematosus * History of iron overload or disturbances in iron utilisation (e.g. haemochromatosis, hemosiderosis) * History of liver disease (e.g. cirrhosis) * Severe active infection or inflammation (e.g. endocarditis) * Porphyria cutanea tarda * Treatment with intravenous iron within 4 weeks prior to surgery. * Untreated vitamin B12 or folate deficiency. * Anticipated inability to perform a six-minute walk test. * Women of childbearing potential, pregnant and nursing women. * Anticipated postoperative length of stay in the intensive care unit (ICU) \> 48 hours. * Patients incapable of giving consent personally. * Significantly increased risk of non-adherence or loss to follow-up. * Active participation in another interventional trial with potential impact on postoperative anaemia or exercise capacity.

Outcomes

Primary Outcomes

The proportion of participants who are neither anemic nor have received allogeneic red blood cells since randomisation

Unit: percentage; anemia according to WHO criteria defined as hemoglobin \< 12 g/dl in women and \< 13 g/dl in men.

Time frame: 4-week follow-up

Secondary Outcomes

Mean change in hemoglobin level

Unit: g/dl

Time frame: From baseline to 4-week follow-up

Proportion of participants with a haemoglobin increase ≥ 1.3 mmol/l (≥ 2 g/dL)

Unit: %

Time frame: From baseline to 4-week follow-up

Mean haemoglobin level

Unit: g/dl

Time frame: 4-week follow-up

Mean reticulocyte count

Unit: 10\^9/l

Time frame: 4-week follow-up

Mean plasma iron

μmol/l

Time frame: 4-week follow-up

Mean plasma ferritin

µg/l

Time frame: 4-week follow-up

Mean transferrin saturation

Unit: %

Time frame: 4-week follow-up

Mean change in haemoglobin level

Unit: g/dl