ACURATE neo2™ Aortic Valve System
ACURATE neo2 PMCF Study
Presented at PCR London Valves 2022 the results of the 250 patient independent core lab assessed ACURATE neo2 PMCF study demonstrating strong performance with excellent clinical outcomes at discharge and 30 days.
SAPIEN 3 Ultra vs. ACURATE neo2
The ACURATE neo2 Valve demonstrated similar rates of PVL and superior hemodynamics when compared to the SAPIEN 3 Ultra Valve.
NEOPRO 2 Sub-Study
ACURATE neo2 Valve outcomes presented at TVT 2022
ACURATE neo2 CE-Mark Study
High procedural efficiency and low core-lab adjudicated PVL rates that improve over time.
SCOPE II Sub-Study
Assessment of PPI predictors for from the SCOPE II clinical trial.
The ACURATE neo Valve demonstrated lower permanent pacemaker rates (PPI) and superior hemodynamic performance compared to the SAPIEN 3 Valve.
Mauri, et al. Small Annulus
The ACURATE neo Valve demonstrated superior hemodynamic performance and lower risk of prosthesis-patient mismatch (PPM) in patients with small aortic annuli.
Next-Day Discharge (NDD)
The ACURATE neo Valve demonstrated higher rates of early patient discharge and lower rates of new permanent pacemaker (PPI).
The ACURATE neo CE Post-Market Registry (SAVI TF)
Strong safety and efficacy data at 30 days.
The ACURATE neo Valve demonstrated lower permanent pacemaker rates (PPI) in patients with pre-existing right bundle branch block (RBBB).
Post-Operative Length of Stay (LoS) Registry: ACURATE neo vs. Evolut R1
The ACURATE neo Valve demonstrated reduced pacemaker rates and shorter hospital lengths of stay (LoS).
Low core-lab adjudicated PVL rates that improve between discharge and 12 months.
NEOPRO Registry: ACURATE neo2 vs. Evolut PRO
The ACURATE neo Valve demonstrated comparable clinical outcomes at 30 Days.
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.