The reason for an improved detection and separation of pathophysiological heart function by BSPM is due to the much larger number of sampling positions of the electrodes attached to the thorax. Hence, spatially and temporally important features may be captured by BSPM but not by the 12-lead-ECG. So far, high cost and complexity have presented widespread use of BSPM in clinical settings.
Our new method requires only a standard 12-lead ECG device with digital data output providing almost identical results as BSPM. The only real difference is that not all channels are being read out simultaneously, i.e. the mapping is reconstructed from sequentially obtained ECG-Signals. A specific digital signal processing has been developed to synchronize sequentially recorded ECG signals. The resulting data is thus competitive to the “true” parallel BSPM.
IP Rights
German Patent DE 10 336 809 B4; European Patent Application EP 1653851 A1
Origin
Charité, Campus Benjamin Franklin, Berlin, Germany; Physikalisch-Technische Bundesanstalt (PTB), Berlin, Germany