Key result
Continuous-flow left ventricular assist device support is associated with gastrointestinal bleeding primarily due to fragile arteriovenous malformations and acquired von Willebrand syndrome.
Why the study?
What are the pathophysiological mechanisms underlying gastrointestinal bleeding in patients on continuous-flow left ventricular assist device support?
What are the pathophysiological mechanisms underlying gastrointestinal bleeding in patients on continuous-flow left ventricular assist device support?
Gastrointestinal bleeding in CF-LVAD patients is primarily driven by fragile GI arteriovenous malformations or angiodysplasias associated with acquired von Willebrand syndrome.
Supports AVM/vWF evaluation in CF-LVAD bleeding; leaves open targeted prevention for prospective trials.
Continuous-flow left ventricular assist devices (CF-LVADs) are increasingly used for the management of advanced heart failure refractory to optimal medical therapy. Despite the encouraging outcomes with CF-LVADs, gastrointestinal bleeding (GIB) continues to be a rather concerning complication resulting in increased rates of readmission and increased morbidity. The exact pathophysiology of CF-LVAD-associated GIB remains poorly understood, and this lack of knowledge limits our ability to control this morbid complication. What is clear, however, is that the majority of GIB episodes in LVAD patients are due to fragile GI arteriovenous malformations or angiodysplasias, in the setting of CF-LVAD-associated acquired von Willebrand syndrome. We will, herein, appraise the proposed interactions between different pathophysiological processes thought to be causing angiodysplasias and GIB in patients on CF-LVAD support.
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Kataria et al. (2018) conducted a review in Advanced heart failure on continuous-flow left ventricular assist device support. Continuous-flow left ventricular assist devices (CF-LVADs) was evaluated. Continuous-flow left ventricular assist device support is associated with gastrointestinal bleeding primarily due to fragile arteriovenous malformations and acquired von Willebrand syndrome.
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