Illustration of the ACURATE neo2 Aortic Valve System in anatomy. Supra-annular TAVI. Illustration of the ACURATE neo2 Aortic Valve System in anatomy. Supra-annular TAVI.

Pacemaker rates

“One of the unique features of ACURATE neo2 is the balanced radial force for a low PPI rate. This is a huge impact for the patient.”

- Prof. Michael Zembala

Best-in-class PPI (permanent pacemaker implantation) rates

ACURATE neo2

Real-world data indicates you can lower your patients' risk of needing a pacemaker. With top-down deployment and upper- and lower- crown anchoring, ACURATE neo2™ minimizes Left Ventricular Outflow Tract (LVOT) protrusion to:

  • Reduce the risk of new conduction disturbances
  • Lower PPI rates
  • Reduce patient length of stay

Early neo2 Registry core-lab results

Top-down deployment with upper- and lower-crown anchoring minimizes LVOT protrusion – reducing the risk of new conduction disturbances, lowering PPI rates, and reducing patient length of stay.

6%

new permanent pacemaker1

2.7%

moderate to severe PVL (Paravalvular Leak)1 

8.0mmHg

mean gradient1

Minimized conduction system injury

Persistent Left Bundle Branch Block (LBBB) is a known contributor to an increase in patient mortality rates. Minimize conduction system injury with the ACURATE neo2 Valve’s optimized radial outward force distribution.2

Minimize conduction system injury with the ACURATE neo2 Valve’s optimized radial outward force distribution.

Other self-expanding valves were associated with a 50% increase in TAVI patient conduction injury at discharge when compared to the ACURATE™ Valve Platform. 

chart, Other self-expanding valves were associated with a 50% increase in TAVI patient conduction injury at discharge when compared to the ACURATE™ Valve Platform.

1. Rück A. Early neo2 Registry: Full Core-lab Results of TAVI with the new ACURATE neo2 Valve. TVT Congress. 20 July 2021

Caution: The law restricts these devices to sale by or on the order of a physician. Indications, contraindications, warnings and instructions of use can be found in the product labeling supplied with each device. Information for the use only in countries with applicable health authority product registrations. The information presented in this document by Boston Scientific is intended for healthcare professionals in India. [The information presented in this document is intended to provide balanced, scientific, and evidence-based answers to unsolicited medical questions.] The information should not be, however, treated as comprehensive and does not intend to provide diagnosis, treatment or any medical or health advice. For full information about the product, please refer to the appropriate product labeling. Responsibility for patient care resides with the healthcare professional on the basis of his or her professional license, experience and knowledge of the patient. Healthcare professionals must rely on their judgment when deciding which treatments and procedures to use with patients.