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Use of a Percutaneous Ventricular Assist Device/Left Atrium to Femoral Artery Bypass System for Cardiogenic Shock
Published on: August 16, 2021
Angiotensin receptor neprilysin inhibitor use in patients with left ventricular assist devices: A single-center
Shudhanshu Alishetti1, Lorenzo Braghieri2, Douglas L Jennings2,3
1Division of Cardiology, Department of Medicine, Weill Cornell Medical Center, New York, NY, USA.
Insights
Angiotensin receptor neprilysin inhibitor (ARNi) therapy significantly reduced NT-proBNP levels in patients with left ventricular assist devices (LVADs). This study suggests ARNi is a safe and effective medical therapy for advanced heart failure patients with LVADs.
Area of Science:
- Cardiology
- Medical Devices
- Pharmacology
Background:
- Left ventricular assist devices (LVADs) are a key therapy for advanced heart failure (ACC/AHA Stage D).
- Optimal medical management for patients with LVADs remains uncertain.
- Angiotensin receptor neprilysin inhibitors (ARNi) represent a newer class of heart failure medication.
Purpose of the Study:
- To assess the safety and efficacy of ARNi therapy in patients with LVADs.
- To evaluate changes in NT-proBNP levels as a primary outcome measure.
- To examine the impact of ARNi on renal function and electrolytes.
Main Methods:
- Retrospective analysis of 30 patients implanted with LVADs between 2010 and 2019.
- Patients received ARNi therapy for at least 3 months.
- Comparison of NT-proBNP levels at initiation, 3 months, and 6 months post-ARNi initiation.
Main Results:
- A significant decrease in NT-proBNP levels was observed from baseline (1265 pg/mL) to 3 months (750 pg/mL) and 6 months (764 pg/mL) (p=0.01).
- 18 patients (60%) transitioned to ARNi from ACE inhibitors or ARBs.
- No significant changes in serum creatinine, BUN, or potassium levels were noted.
Conclusions:
- ARNi therapy is associated with significant reductions in NT-proBNP levels in LVAD patients.
- ARNi therapy appears safe regarding renal function and electrolytes in this LVAD cohort.
- Further prospective studies are warranted to confirm these findings.
Abstract:
Though left ventricular assist devices (LVADs) are an increasingly common therapy for ACC/AHA Stage D heart failure, the optimal medical therapy for patients with LVADs is not known. We sought to evaluate the safety and efficacy of angiotensin receptor neprilysin inhibitor (ARNi) therapy in our single center LVAD patient experience. We evaluated patients implanted with LVADs at Columbia University Irving Medical Center between August 2010 and May 2019, and who were treated with an ARNi for at least 3 months. Thirty patients met this criteria. Eighteen (60%) patients transitioned to an ARNi from an angiotensin-converting enzyme inhibitor (ACEi) or angiotensin receptor blocker (ARB), while all were on a beta blocker (BB) at the time of ARNi initiation. The primary outcome, NT-proBNP levels at time of initiation and 3 and 6 month follow up, significantly decreased from a median of 1265 pg/mL at initiation to 750 pg/mL at 3 months and 764 pg/mL at 6 months (p = 0.01). No significant change was seen in serum creatinine, BUN, or potassium levels.
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