An innovative technology that accurately identifies the risk of sudden cardiac death within 6 months, and benefits implantable cardiac defibrillators (ICDs).

The Vicor point correlation dimension algorithm (PD2i) is a low-cost, non-invasive, non-invasive, non-invasive or ectopic beat, and can be used for coronary artery disease (CAD) patients taking beta-blockers. . The test is based on the abnormal communication of the nervous system between the brain and the heart to determine sudden cardiac death. By analyzing the 15-minute ECG data, the PD2i CA can detect whether multiple neural work centers are working properly, from semi-coordinated to over-coordinated. The PD2i is able to detect excessive coordination of the control system, which is a clear sign that the patient may have sudden cardiac death.

The PD2i measures the degree of freedom of the patient's heart by measuring the temperature, pH, pressure receptors, etc., and the degree of cooperation. In healthy people, these cycles tend to be opposite, or work more or less independently. If this cycle begins to be highly coordinated, it indicates that the body may have a bad condition, and the brain works together to keep the body alive. This "super-coordinating" condition is unsustainable and can lead to ventricular tachycardia, ventricular fibrillation and sudden cardiac death. The PD2i CA was developed by Vicor Technologies, Fla., and has been approved by the US Food and Drug Administration (FDA) for measuring heart rate complexity.

David H. Fater, CEO of Vicor, said: "Experimental studies with the US Department of Surgery at the US Department of Texas revealed that PD2i is the only instrument with continuous and accurate diagnostic damage by using 'raw' and 'noisy' ECG data."

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