Key result
A patient with systemic lupus erythematosus receiving a HeartWare LVAD as destination therapy experienced recurrent, diffuse spontaneous bleeding, highlighting a potential unique bleeding complication.
Why the study?
Experience with LVADs in select high-risk populations remains limited, and understanding patient and disease-specific characteristics that increase postoperative morbidity and mortality is crucial.
Case Report (n=1)
Patients with systemic lupus erythematosus may represent a high-risk cohort for unique bleeding complications following LVAD implantation.
May warrant bleeding vigilance in SLE patients evaluated for LVAD; leaves open whether lupus confers unique risk.
Continuous-flow left ventricular assist devices (LVAD) have become an increasingly utilized treatment strategy for patients with end-stage heart failure. Despite the improved outcomes evident with current generation pumps, proper patient selection remains crucial to minimize the risk of potential adverse events. The evolving use of these devices as destination therapy (DT) has led to growing numbers of patients with higher risk comorbid conditions being evaluated as potential LVAD candidates. Understanding which patient and disease-specific characteristics increase postoperative morbidity and mortality is paramount as this technology continues to expand and the experience with select populations remains limited. Presented here is a case of a patient with systemic lupus erythematosus receiving a HeartWare LVAD as DT complicated by recurrent, diffuse spontaneous bleeding. The case presented here highlights a potential unique bleeding complication in a high-risk patient cohort and underscores the need to enhance our understanding of factors influencing outcomes in high-risk populations after LVAD therapy.
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Gage et al. (2019) conducted a case report in Systemic lupus erythematosus and end-stage heart failure (n=1). HeartWare LVAD was evaluated on Recurrent, diffuse spontaneous bleeding. A patient with systemic lupus erythematosus receiving a HeartWare LVAD as destination therapy experienced recurrent, diffuse spontaneous bleeding, highlighting a potential unique bleeding complication.
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