TECHNIQUE FOR DETERMINING SIGNAL QUALITY IN A PHYSIOLOGIC SENSING SYSTEM USING HIGH FREQUENCY SAMPLING

• US 20100217143A1
• Filed: 02/23/2009
• Published: 08/26/2010
• Est. Priority Date: 02/23/2009
• Status: Active Grant

• Current Assignee: Biotronik SE & Company KG
• Original Assignee: Biotronik VI Patent AG (Biotronik SE & Company KG)
• Inventors: Whittington, Hollis, Lang, Volker, Muessig, Dirk
• Granted Patent: US 8,265,741 B2
• Time in Patent Office: Days
• US Class Current: 600/523
• CPC Class Codes: A61B 5/283 Invasive
• CPC Class Codes: A61B 5/30 Input circuits therefor
• CPC Class Codes: A61B 5/7207 of noise induced by motion artifacts
• CPC Class Codes: A61B 5/7221 Determining signal validity, reliability or quality A61B5/7207 and A61B5/7217 take precedence
• CPC Class Codes: A61N 1/3684 for stimulating the heart at multiple sites of the ventricle or the atrium

Abstract

A medical device for processing physiological signals such as electrocardiograms. The processing includes: sampling a physiologic signal in a first channel with a first sampling rate, simultaneously sampling the physiologic signal in a second channel with a higher sampling rate to thus generate pairs of sampling values, forming the difference between two sampling values of each pair, comparing said difference with a threshold, and generating a noise detection indicator whenever said threshold is exceeded.

Claims

1. A heart monitor comprising:

an electric signal acquisition and processing stage;

two implantable electrodes configured to pick up myocardial electric signals;

said electric signal acquisition and processing stage connected or being connectable to the two implantable electrodes;

said electric signal acquisition and processing stage comprising a first channel and a second channel that are utilized as signal processing channels;

said first channel comprising

a first sampling stage configured to sample picked-up myocardial electric signals at a first sampling rate, said first channel adapted to process the picked-up myocardial electric signals and generate an electrogram signal;

said second channel comprising

a high frequency sampling stage configured to sample at least portions of said picked-up myocardial electric signals at a second sampling rate, wherein said second sampling rate is higher than said first sampling rate;

a differential stage adapted to generate a high frequency sampled output signal that represents a difference between two consecutive high frequency sampled myocardial electric signal values; and

,

a comparator that is adapted to compare said high frequency sampled output signal with a threshold and to generate a noise detection indicator whenever said threshold is exceeded.

2. The heart monitor according to claim 1, wherein said second channel is adapted to generate pairs of high frequency sampled myocardial electric signal values with a repetition rate that is different than said second sampling rate.

3. The heart monitor according to claim 1, wherein said second channel is adapted to generate pairs of high frequency sampled myocardial electric signal values with a repetition rate that corresponds to said first sampling rate, so that one pair of high frequency sampled myocardial electric signal values is generated for each sampled myocardial electric signal value generated by the first channel.

4. The heart monitor according to claim 1 further comprising a timer that is triggered whenever the high frequency sampled signal exceeds the threshold.

5. The heart monitor according to claim 4, wherein said timer times a preset noise detection period, during which an ECG signal generated in said first channel is evaluated differently than otherwise.

6. The heart monitor according to claim 1 wherein said first sampling rate is between 200 and 300 Hz.

7. The heart monitor according to claim 1, wherein said second sampling rate is between 4 to 30 kHz.

8. A method for processing electric signals representing a time course of myocardial potentials comprising:

sampling a physiologic signal in a first channel with a first sampling rate;

simultaneously sampling the physiologic signal in a second channel with a second sampling rate that is higher than said first sampling rate;

forming a difference between two sampling values taken from said second channel;

comparing said difference with a threshold; and

,

generating a noise detection indicator whenever said threshold is exceeded.

9. The method according to claim 8, wherein the physiologic signal comprises at least one sampled myocardial electric signal value and for each sampled myocardial electric signal value generated in the first channel, a pair of high frequency sampled myocardial electric signal values is generated in the second channel

10. The method according to claim 8 wherein a noise detection period is started whenever said difference exceeds said threshold.