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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
Use of the TandemHeart percutaneous ventricular assist device to support patients undergoing high-risk percutaneous
Biswajit Kar1, Matthew Forrester, Courtney Gemmato
1Cardiovascular Transplant Service and the Cardiovascular Research Laboratories of the Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, Texas, USA.
Insights
The TandemHeart percutaneous ventricular assist device (pVAD) offers hemodynamic support during high-risk percutaneous coronary intervention (PCI) for patients unsuitable for surgery. This device shows promise in improving outcomes and expanding treatment options for complex cardiac cases.
Area of Science:
- Cardiology
- Interventional Cardiology
- Medical Devices
Background:
- Coronary artery bypass grafting (CABG) is standard for unprotected left main coronary artery disease.
- Severe comorbidities can make CABG unsuitable, necessitating alternative treatments like percutaneous coronary intervention (PCI).
- High-risk PCI often requires hemodynamic support for patient safety.
Purpose of the Study:
- To evaluate the use of the TandemHeart percutaneous ventricular assist device (pVAD) in high-risk PCI procedures.
- To assess the safety and efficacy of pVAD for hemodynamic support during complex PCI.
- To determine the role of pVAD in managing patients ineligible for CABG.
Main Methods:
- The study involved 5 consecutive patients with severe comorbidities who were not candidates for CABG.
- The TandemHeart pVAD was utilized for hemodynamic support during high-risk PCI in these patients.
- Device insertion and initiation of circulatory support were performed, followed by percutaneous revascularization.
Main Results:
- The pVAD was successfully inserted and initiated support in all 5 cases without immediate complications.
- Percutaneous revascularization was completed successfully with pVAD support, providing approximately 3 L/min of flow.
- Four patients recovered uneventfully after short-term pVAD support; one patient died 10 days post-withdrawal due to heart failure and mitral regurgitation.
Conclusions:
- The pVAD can provide adequate hemodynamic support during high-risk PCI, potentially reducing morbidity and mortality.
- This device expands therapeutic options for patients with severe comorbidities who are not surgical candidates.
- Further research is recommended to fully explore the potential of the pVAD in complex PCI scenarios.
Objectives:
We describe our experience in using the TandemHeart percutaneous ventricular assist device (pVAD) during high-risk percutaneous coronary intervention (PCI).
Background:
Coronary artery bypass grafting (CABG) is the preferred treatment for disease in an unprotected left main coronary artery or left main equivalent. However, severe comorbidities may preclude surgery in some patients. In these cases, PCI is also often a high-risk procedure. The pVAD is designed to provide circulatory support during high-risk PCI.
Methods And Results:
We used the pVAD for hemodynamic support during PCI in 5 consecutive patients who were ineligible for CABG because of severe comorbidities. In all 5 cases, the device was inserted and support initiated without complications. Percutaneous revascularization was successfully performed with pVAD support (approximately 3 L per minute). Four patients were supported for an average of 107 minutes, the pVAD being withdrawn shortly after PCI; all 4 patients recovered uneventfully. The fifth patient required support for 48 more hours after the procedure because of poor ventricular function. He died of heart failure and severe mitral regurgitation 10 days after pVAD withdrawal.
Conclusions:
The pVAD may provide sufficient circulatory support for hemodynamic protection during high-risk PCI, thus improving morbidity and mortality and broadening the therapeutic options for high-risk patients. Further investigation of this device is warranted.
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