Iron overdose: a contributor to adverse outcomes in randomized trials of anemia correction in CKD.
Study Goal
The researchers aimed to review the potential adverse effects of overzealous use of erythropoiesis-stimulating agents (ESAs) and intravenous iron in managing anemia in CKD and ESRD patients.
Results Summary
The study found that higher hemoglobin targets with ESAs and intravenous iron were associated with more adverse outcomes, including oxidative stress, endothelial dysfunction, inflammation, impaired immunity, and renal injury. Retrospective analysis suggested higher morbidity in patients who required higher doses of ESAs and iron to achieve targets.
Population
Patients with chronic kidney disease (CKD) and end-stage renal disease (ESRD).
Effective Dosage
Not specified
Duration
Not specified
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
intravenous iron to supplement erythropoiesis stimulating agents (ESAs) | neutral | management of anemia | patients with end-stage renal disease | - | has become a common practice | #1 |
anemia correction | increase | adverse outcomes | CKD and ESRD patients assigned to the higher hemoglobin targets | - | shown more adverse outcomes | #2 |
higher doses of ESAs and iron | increase | morbidity | subjects who fail to achieve the designated hemoglobin target | - | morbidity is higher | #3 |
intravenous iron administration | neutral | natural biologic mechanisms for handling and utilization of iron | - | - | circumvents | #4 |
intravenous iron preparations | increase | oxidative stress | - | - | can cause | #5 |
intravenous iron preparations | increase | endothelial dysfunction | - | - | can cause | #6 |
intravenous iron preparations | increase | inflammation | - | - | can cause | #7 |
intravenous iron preparations | increase | impaired immunity | - | - | can cause | #8 |
intravenous iron preparations | increase | renal injury | - | - | can cause | #9 |
iron overload | increase | endothelial dysfunction | - | - | is known to promote | #10 |
iron overload | increase | cardiovascular disease | - | - | is known to promote | #11 |
iron overload | increase | immune dysfunction | - | - | is known to promote | #12 |
Administration of intravenous iron to supplement erythropoiesis stimulating agents (ESAs) has become a common practice in the management of anemia in patients with end-stage renal disease. Randomized clinical trials of anemia correction in this population have shown more adverse outcomes in CKD and ESRD patients assigned to the higher hemoglobin targets. Retrospective analysis of these trials suggests that morbidity is higher in subjects who fail to achieve the designated hemoglobin target and are typically exposed to higher doses of ESAs and iron than those that easily achieve the intended targets. Intravenous iron administration circumvents the natural biologic mechanisms for handling and utilization of iron. There is in vitro and in vivo evidence that intravenous iron preparations can cause oxidative stress, endothelial dysfunction, inflammation, impaired immunity, and renal injury. Since iron overload is known to promote endothelial dysfunction, cardiovascular disease, and immune dysfunction which are the leading causes of premature mortality in CKD and ESRD patients, it is imperative to exercise caution with the use of IV iron preparations in this population. The present review is intended to provide a brief overview of the potential adverse effects of the overzealous use of these agents.