PediaSat Oximetry Catheter is the first and only pediatric oximetry catheter with continuous ScvO2 monitoring for proactive management of tissue hypoxia.1-3
Continuous, real-time monitoring of central venous oxygen saturation (ScvO2) offers early recognition of critical changes in oxygen delivery that may not be identified by less sensitive indicators, such as traditional vital signs or intermittent sampling.1-9
Early warning of oxygen imbalance allows early intervention.
Early indication with continuous ScvO2 monitoring offers you the clarity to detect and prevent tissue hypoxia − early− in your complex pediatric patients.4-6,8,10
Continuous ScvO2 monitoring reveals the root cause of oxygen imbalance, enabling you to proactively determine appropriate therapy.4,11 Real-time insight into the adequacy of cardiac output allows immediate assessment of your patient's clinical response to therapy − to help you stay ahead of tissue hypoxia and stages of sepsis.12
Continuous ScvO2 monitoring helps guide therapy and enables early intervention:4,5
PediaSat oximetry catheter offers the clarity of an early warning for compromised or inadequate oxygen delivery4-6,8,10
Continuous measurement of ScvO2 in combination with other surrogates of organ perfusion (vital signs, lactate, etc.) can be used as a reliable monitor of cardiocirculatory function.17
Can optimize hemodynamic management in complex pediatric patients.
Convenient, accurate and easy to use.17,22
PediaSat oximetry catheter provides:
Hemodynamic education for sustained clinical advancement
With a long-term commitment to improving the quality of care for surgical and critical care patients through education, Edwards Clinical Education meets you no matter where you are in the learning process — with a continuum of resources and tools that continuously support you as you solve the clinical challenges facing you today, and in the future.
Designed for use with Edwards' monitoring platforms, the PediaSat oximetry catheter offers the clarity of an early warning.
For a listing of indications, contraindications, precautions, warnings, and potential adverse events, please refer to the Instructions for Use (consult eifu.edwards.com where applicable).
Edwards Lifesciences devices placed on the European market meeting the essential requirements referred to in Article 3 of the Medical Device Directive 93/42/EEC bear the CE marking of conformity.
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