# Successful treatment of low-flow-low-gradient aortic stenosis and complex coronary artery disease in a patient with severely depressed left-ventricular function by protected percutaneous coronary intervention and transfemoral transcatheter aortic valve replacement via Y-graft vascular prosthesis: a case report

**Authors:** Yusuf Nejahsie, Samer Hakmi, Stephan Willems, Wolfgang Tigges, Eike Tigges

PMC · DOI: 10.1093/ehjcr/ytag035 · European Heart Journal. Case Reports · 2026-01-24

## TL;DR

A high-risk patient with severe heart conditions was successfully treated using a staged approach involving PCI and TAVR via a Y-graft, leading to symptom relief and improved heart function.

## Contribution

Demonstrates the feasibility and safety of Impella®-supported PCI followed by TAVR via a Y-graft in a complex clinical scenario.

## Key findings

- The patient experienced immediate symptom relief and improved ejection fraction after treatment.
- Follow-up showed improved aortic valve function and sustained clinical benefits at 3 months.
- The staged interventional approach was feasible and safe despite challenging transfemoral access.

## Abstract

Low-flow, low-gradient aortic stenosis (LFLG AS) is a subset of aortic stenosis associated with a poor prognosis and high operative risk, particularly in the presence of concomitant coronary artery disease (CAD) requiring intervention. In patients considered inoperable, minimally invasive approaches often remain the only alternative. However, there are limited data on treatment strategies and outcomes in patients with LFLG AS and severe ischaemic cardiomyopathy undergoing percutaneous coronary intervention (PCI) and transcatheter aortic valve replacement (TAVR), especially in cases with challenging transfemoral access.

An 87-year-old male presented with progressive dyspnoea and angina. Diagnostics revealed a non-ST-segment elevation myocardial infarction, acute heart failure, acute-on-chronic renal failure, LFLG AS (aortic valve area of 0.7 cm²), and a left ventricular ejection fraction of 10%. Coronary angiography showed severe CAD requiring revascularization. Due to excessive surgical risk, we planned a staged interventional treatment by Heart Team consensus. First, high-risk PCI with mechanical circulatory support was performed, followed by transfemoral TAVR using a self-expandable 29-mm bioprosthesis via a femoral Y-graft conduit. The patient reported immediate relief of symptoms. Follow-up echocardiography at discharge and at 3 months showed improvement of the aortic valve function and an increase of the ejection fraction to 35%. The patient remained asymptomatic and resumed his daily activities.

This case demonstrates that Impella®-supported PCI prior to transfemoral TAVR is feasible and safe, even in the presence of a femoral Y-graft, in a patient with LFLG AS and severely reduced ejection fraction.

## Linked entities

- **Diseases:** aortic stenosis (MONDO:0042981), coronary artery disease (MONDO:0005010), heart failure (MONDO:0005252), renal failure (MONDO:0001106)

## Full-text entities

- **Diseases:** atrioventricular conduction disturbances (MESH:D054537), chronic kidney disease (MESH:D051436), leaks (MESH:D019559), angina (MESH:D000787), induced (MESH:D000092582), aorta (MESH:D000784), atrial fibrillation (MESH:D001281), cardiogenic shock (MESH:D012770), acute myocardial infarction (MESH:D009203), hypertension (MESH:D006973), annular calcification (MESH:D016460), multivessel disease (MESH:D004194), ischaemic (MESH:D018917), aortic valve calcification (MESH:C562942), unstable angina (MESH:D000789), ostial stenosis of (MESH:D003251), pulmonary venous congestion (MESH:D006940), LFLG AS (MESH:D009800), CAD (MESH:D003324), acute-on-chronic renal failure (MESH:D058186), stroke (MESH:D020521), vascular complications (MESH:D003925), ischaemic cardiomyopathy (MESH:D009202), depressed (MESH:D003866), bleeding (MESH:D006470), AS (MESH:D001024), nephropathy (MESH:D007674), arrhythmias (MESH:D001145), heart failure (MESH:D006333), NSTEMI (MESH:D000072657), peripheral arterial disease (MESH:D058729), contrast (MESH:D005119), LV dysfunction (MESH:D018487)
- **Chemicals:** dobutamine (MESH:D004280), CP (-), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12952212/full.md

## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC12952212/full.md

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Source: https://tomesphere.com/paper/PMC12952212