# Progressive Aortic Regurgitation After Impella Bridge-to-LVAD: A Two-Year Cohort Analysis

**Authors:** Attila Nemeth, Aron Frederik Popov, Rodrigo Sandoval Boburg, Spiros Lukas Marinos, Helene Häberle, Christoph Salewski, Volker Steger, Christian Schlensak, Medhat Radwan

PMC · DOI: 10.3390/biomedicines14030715 · Biomedicines · 2026-03-19

## TL;DR

This study shows that aortic regurgitation often develops or worsens in patients bridged from Impella to LVAD, highlighting the need for ongoing monitoring and management strategies.

## Contribution

The study provides a longitudinal analysis of aortic regurgitation progression after Impella bridge-to-LVAD, identifying its clinical implications.

## Key findings

- Aortic regurgitation ≥ mild developed in 50% at discharge, 80% at 12 months, and 87% at 24 months.
- 53% of patients progressed to moderate or severe aortic regurgitation by 24 months.
- Higher NT-proBNP levels were observed in patients with moderate-to-severe aortic regurgitation at 12 months.

## Abstract

Background/Objectives: Impella support is increasingly utilized as a crucial bridge to durable left ventricular assist device (LVAD) in patients with refractory cardiogenic shock. However, the transvalvular path of the Impella catheter raises concerns regarding mechanical trauma, potentially precipitating or accelerating aortic regurgitation (AR). We aimed to characterize the complete longitudinal trajectory of AR following Impella bridge-to-LVAD and to determine its association with clinical and hemodynamic sequelae. Methods: We conducted a single-center retrospective cohort study including all patients bridged from Impella to durable LVAD between 2013 and 2024 (n = 19). At Impella initiation, all patients met the retrospective SCAI shock stage D or worse criteria. At LVAD implantation, all patients were classified as INTERMACS 1–2 (INTERMACS 2, n = 13). The Impella models were 5.0 in 11 (axillary access), 2.5 in 5 (femoral access), and CP in 3 (femoral access); no periprocedural Impella complications were recorded. The implanted LVAD systems were HeartMate II (n = 7), HVAD (n = 3), and HeartMate III (n = 9). Patients undergoing concomitant aortic valve intervention were excluded. Transthoracic/TEE echocardiography was performed at prespecified time points (pre-Impella, pre-LVAD, post-LVAD discharge, 12 months, and 24 months) with standardized aortic regurgitation (AR) grading. Right ventricular (RV) function was assessed qualitatively when quantitative indices (TAPSE) were unavailable. Primary endpoints were new or progressive AR and AR severity at LVAD implantation. Secondary endpoints included survival, renal dysfunction, biomarkers, and rehospitalization. Univariate analyses were used to compare outcomes according to AR severity. Results: Nineteen patients (68% male, median age 57 years, IQR 47–60) underwent Impella support for 13.3 ± 9.9 days before HeartMate 3 (84%) or HVAD (16%) implantation. All patients had competent aortic valves (grade 0 AR) at the time of LVAD implantation. AR ≥ mild developed in 9/18 (50%) at discharge, 12/15 (80%) at 12 months, and 13/15 (87%) at 24 months, and 8/15 (53%) progressed to ≥ moderate AR by 24 months. Patients with moderate-to-severe AR had higher NT-proBNP levels at 12 months (median 6318 vs. 2336 pg/mL, p = 0.137). Thirty-day and 24-month survival rates were 95% and 79%, respectively. Conclusions: Aortic regurgitation frequently develops or progresses from the pre-LVAD period to follow-up in patients bridged from Impella to durable LVAD. Although limited by a small sample size and incomplete quantitative RV metrics, these observations support structured echocardiographic surveillance after Impella use and management strategies—routine valve inspection at LVAD implantation and post-LVAD speed/blood pressure targets that encourage aortic valve opening—to mitigate the risk and clinical impact of aortic regurgitation.

## Linked entities

- **Diseases:** cardiogenic shock (MONDO:0800175)

## Full-text entities

- **Diseases:** renal dysfunction (MESH:D007674), trauma (MESH:D014947), cardiogenic shock (MESH:D012770), AR (MESH:D001022), shock (MESH:D012769)
- **Chemicals:** HeartMate 3 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC13024325/full.md

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Source: https://tomesphere.com/paper/PMC13024325