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Updated: Oct 1, 2025

Implantation of the Syncardia Total Artificial Heart
Published on: July 18, 2014
Anemia and outcomes following left ventricular assist device implantation
Teruhiko Imamura1,2, Nikhil Narang2,3, Stephanie Besser2
1Second Department of Internal Medicine, University of Toyama, Toyama, Japan.
Insights
Anemia is common in patients with left ventricular assist devices (LVAD) and increases their risk of heart failure readmissions and adverse events. Further research is needed to determine the best treatment for anemia after LVAD implantation.
Area of Science:
- Cardiology
- Hematology
- Medical Devices
Background:
- Concomitant anemia and congestive heart failure are associated with poor patient outcomes.
- The prevalence and clinical risks of anemia in patients with durable left ventricular assist devices (LVAD) are not well understood.
Purpose of the Study:
- To investigate the prevalence of anemia in patients receiving LVADs.
- To determine the association between hemoglobin levels at discharge and one-year adverse events in LVAD patients.
Main Methods:
- Retrospective analysis of 168 patients who underwent LVAD implantation from 2014 to 2018.
- Stratification of patients into anemia (hemoglobin <9.7 g/dL) and non-anemia groups.
- Investigation of the association between discharge hemoglobin and a composite endpoint of heart failure readmissions or hemocompatibility-related adverse events within one year.
Main Results:
- Anemia was prevalent, affecting 99 out of 168 patients.
- The anemia group showed a significantly higher one-year incidence of the composite endpoint (56% vs. 36%, p=0.013).
- Anemia was associated with an adjusted hazard ratio of 1.83 for adverse events and suboptimal bi-ventricular unloading.
Conclusions:
- Anemia is a common comorbidity in LVAD patients.
- Post-LVAD anemia is linked to increased risks of heart failure and hemocompatibility issues.
- Optimal therapeutic thresholds for post-LVAD anemia require further investigation.
Background:
Patients with concomitant anemia and congestive heart failure have poor outcomes. The prevalence and clinical risk of anemia in patients receiving durable left ventricular assist devices (LVAD) remain unknown.
Methods:
We retrospectively analyzed patients who underwent LVAD implantation between 2014 and 2018. The association between hemoglobin level at the time of index discharge and the one-year composite endpoint of heart failure readmissions or hemocompatibility-related adverse events was investigated.
Results:
A total of 168 patients (57 [48, 66] years old, 123 males) were included and stratified into a classification of anemia (hemoglobin <9.7 g/dl, N = 99) or non-anemia (N = 69). The anemia group had a higher one-year incidence of the composite endpoint (56% vs 36%, p = .013) with an adjusted hazard ratio of 1.83 (95% confidence interval 1.08-2.82). Patients with anemia also experienced suboptimal bi-ventricular unloading.
Conclusions:
Anemia was prevalent in LVAD patients and associated with a greater risk of heart failure and hemocompatibility-related adverse events. The optimal threshold for therapeutic intervention in response to post-LVAD anemia needs further investigation.
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