Related Experiment Video
Updated: Jan 17, 2026

Use of a Percutaneous Ventricular Assist Device/Left Atrium to Femoral Artery Bypass System for Cardiogenic Shock
Published on: August 16, 2021
Safety and Efficacy of the Corheart 6 Left Ventricular Assist System
Zhibing Qiu1, Xiaochun Song, Hongwei Shi
1From the Department of Cardiothoracic and Vascular Surgery, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Insights
The Corheart 6 Left Ventricular Assist System (LVAS) shows promising mid-term survival and improved cardiac function in end-stage heart failure patients. Its safety profile is manageable, with no device malfunctions reported.
Area of Science:
- Cardiology
- Medical Devices
- Mechanical Circulatory Support
Background:
- End-stage heart failure necessitates advanced therapeutic options.
- Left Ventricular Assist Systems (LVAS) offer a critical solution for patients awaiting transplant or as destination therapy.
Purpose of the Study:
- To evaluate the efficacy and safety of the Corheart 6 LVAS.
- To assess clinical outcomes, including survival and cardiac function, in patients with end-stage heart failure receiving the Corheart 6 LVAS.
Main Methods:
- Retrospective cohort study at Nanjing First Hospital (March 2022 - March 2024).
- Enrolled 28 patients with end-stage heart failure implanted with Corheart 6 LVAS.
- Primary endpoint: 6-month survival free from disabling stroke.
Main Results:
- 100% survival at 3 months, 89.3% at 6 months (3 deaths).
- Significant improvements in cardiac function observed post-implantation.
- No pump thrombosis, hemolysis, or device malfunction; stable hemolysis markers.
Conclusions:
- Corheart 6 LVAS demonstrates favorable mid-term survival and cardiac functional improvement.
- The device presents a manageable safety profile for critically ill heart failure patients.
- Further investigation into managing adverse events like infections and arrhythmias is warranted.
Abstract:
To assess the efficacy and safety of the Corheart 6 Left Ventricular Assist System (LVAS) in patients with end-stage heart failure. A retrospective cohort study was conducted at Nanjing First Hospital to evaluate the clinical outcomes of patients with end-stage heart failure who underwent implantation of the Corheart 6 LVAS between March 2022 and March 2024. A total of 28 patients were enrolled. The primary endpoint was a composite of survival free from disabling stroke at 6 months post-implantation. Statistical analyses were conducted to compare pre- and post-implantation outcomes. No intraoperative or 30 day postoperative mortality occurred. Survival rates were 100% at 3 months and 89.3% at 6 months, with three deaths attributed to cerebral hemorrhage, device alarm mismanagement, and systemic amyloidosis complications. Significant improvements in cardiac function were observed. Hemolysis markers remained stable. Adverse events included hemorrhagic cerebrovascular accident (3.6%), ventricular arrhythmias (25%), pulmonary infections (35.7%), driveline exit site infection (3.6%), renal failure (requiring dialysis) (7.1%), and right heart failure (3.6%). No pump thrombosis, hemolysis or device malfunction occurred. The Corheart 6 LVAS demonstrated favorable mid-term survival and cardiac functional improvement in critically ill heart failure patients, with a manageable safety profile.
Related Concept Videos
Heart Failure VI: Adjunct Therapies
Heart Failure V: Medical Management
Heart Failure II: Pathophysiology
Cardiomyopathy V: Interprofessional Care
Heart Failure I: Introduction
Cardiac Catheterization III: Left Heart Catheterization

