Description
The Ready System® is a complete pre-configured system for implementing minimized cardiopulmonary bypass. The Ready System® offers clinicians a platform to drastically lower blood product usage, reduce air/blood interface, and reduce the presence of silicone from the bypass circuit. These attributes can allow clinicians to implement cardiopulmonary bypass with decreased patient morbidity as compared to traditional cardiopulmonary bypass systems. The Ready System® has been designed to accommodate the changing clinical scenarios of cardiac surgery and cardiopulmonary bypass by providing the clinician with a safe and flexible cardiopulmonary bypass platform. The Ready System® allows for reduced circuit set-up time and an increase in standardization of the cardiopulmonary bypass circuit in both routine and emergent procedures as compared to standard CPB systems.

Features
The Ready System® features an adult hollow fiber membrane oxygenator, an arterial blood filter, and a centrifugal pump. A patented, vacuum capable closed flexible reservoir is utilized as a venous blood reservoir. The components of the Ready System® are mounted on a rigid backplane that functions as a product holder as well as the packaging material of the system. The Ready System® has a priming volume of 650 ml.

Benefits
The benefits of the Ready System® can be best expressed in terms of the way the device affects the safety, flexibility and convenience of implementing cardiopulmonary bypass.
Safety

• The integrated vacuum capable closed venous reservoir acts as a safety feature and helps prevent air from entering the bypass system.
• The Ready System® has an integrated one-way valve to prevent dangerous backflow through the system.
• The Ready System® has an integrated vacuum relief valve on the venous reservoir.
• The Ready System® has an integrated level and bubble sensor when utilized with the Jostra-Maquet Rotaflow pump.
• The Ready System® utilizes a standard circuit configuration.

Flexibility

• The Ready System® is adaptable to any heart lung machine or can be mounted on an IV pole
• The Ready System® is able to adapt to other cardiopulmonary products to accommodate specific clinical needs
  

Convenience

• Integrated system for quick set-up and prime.
• Standardized circuitry that can adapt to changing clinical needs.
• Enclosed receptacle for convenient disposal.
• Consolidated packaging for easy shipping and storage.
  

NovoSci R.E.S.U.L.T.
R.E.S.U.L.T. – “REady System UnconditionaL Registry Trial”


RESULT Descrition
A prospective, observational registry trial utilizing the NovoSci Ready System® for both beating or arrested heart procedures. The results from this registry trial will be comparedto on-pump and off-pump results available in the literature. The expectations are that this registry will provide important clinical outcome data in support of this new approach to minimal cardiopulmonary bypass.

RESULT Design
Prospective, non-randomized, multi-center observational registry trial.

RESULT Purpose
To complete a clinical data registry trial utilizing the NovoSci Ready System® and obtain clinical outcome results which can be compared to coronary artery bypass grafting (CABG) procedures and valve procedures with conventional cardiopulmonary bypass (CPB) and off-pump bypass results from the literature.