TY - GEN
T1 - A GMSK-based conductive intracardiac communication method
AU - Zhang, Hangling
AU - Zhang, Xusheng
AU - Xu, Yong
AU - Chen, Yu
AU - Yang, Chang
AU - Fan, Xuce
AU - Song, Yong
N1 - Publisher Copyright:
© 2024 SPIE.
PY - 2024
Y1 - 2024
N2 - Conductive intracardiac communication (CIC) can be utilized for the synchronization of multi-chamber leadless pacemakers (LLPMs) to overcome complications arising from traditional pacemaker lead connections. Current CIC methods are mainly based on pulse modulation (PM) and On-Off Keying (OOK), which suffer from high power consumption and poor interference resilience, with transmitter output bit energy (Ebit) exceeding 5 pJ. Addressing these concerns, we proposed a method of conductive intracardiac communication based on Gaussian Minimum Shift Keying (GMSK). In the transmitter, a power-optimized GMSK modulation method is employed for signal transmission. In the receiver, a variable gain amplifier is utilized for CIC signal reception, and signal recovery is achieved through low-power demodulation and bit synchronization methods. A prototype transceiver was designed for measuring the bit error ratio (BER) and transmitter output Ebit of GMSK and OOK methods in in-vitro experiments using porcine hearts as channels. The transceiver was connected to the right atrium and right ventricle via stainless steel needle electrodes. At data rates of 75-500 kbps and a BER of 1e-4, the average Ebit for OOK ranged from 0.06-0.61 pJ, whereas for GMSK, it was lower, ranging from 0.02-0.35 pJ. This study demonstrates that LLPM achieving reliable CIC using GMSK at transmission powers below 35 pW is feasible in practical channel conditions. The proposed GMSK-based CIC method is more preferable to PM and OOK due to its higher reliability and lower transmission power requirements.
AB - Conductive intracardiac communication (CIC) can be utilized for the synchronization of multi-chamber leadless pacemakers (LLPMs) to overcome complications arising from traditional pacemaker lead connections. Current CIC methods are mainly based on pulse modulation (PM) and On-Off Keying (OOK), which suffer from high power consumption and poor interference resilience, with transmitter output bit energy (Ebit) exceeding 5 pJ. Addressing these concerns, we proposed a method of conductive intracardiac communication based on Gaussian Minimum Shift Keying (GMSK). In the transmitter, a power-optimized GMSK modulation method is employed for signal transmission. In the receiver, a variable gain amplifier is utilized for CIC signal reception, and signal recovery is achieved through low-power demodulation and bit synchronization methods. A prototype transceiver was designed for measuring the bit error ratio (BER) and transmitter output Ebit of GMSK and OOK methods in in-vitro experiments using porcine hearts as channels. The transceiver was connected to the right atrium and right ventricle via stainless steel needle electrodes. At data rates of 75-500 kbps and a BER of 1e-4, the average Ebit for OOK ranged from 0.06-0.61 pJ, whereas for GMSK, it was lower, ranging from 0.02-0.35 pJ. This study demonstrates that LLPM achieving reliable CIC using GMSK at transmission powers below 35 pW is feasible in practical channel conditions. The proposed GMSK-based CIC method is more preferable to PM and OOK due to its higher reliability and lower transmission power requirements.
KW - conductive intracardiac communication
KW - galvanic-coupled conductive communication
KW - GMSK
KW - intra-body communication
KW - leadless dual-chamber pacing
KW - Leadless pacemaker
KW - OOK
UR - http://www.scopus.com/inward/record.url?scp=85200448824&partnerID=8YFLogxK
U2 - 10.1117/12.3036669
DO - 10.1117/12.3036669
M3 - Conference contribution
AN - SCOPUS:85200448824
T3 - Proceedings of SPIE - The International Society for Optical Engineering
BT - Third International Conference on Biomedical and Intelligent Systems, IC-BIS 2024
A2 - Piccaluga, Pier Paolo
A2 - Baloch, Zulqarnain
PB - SPIE
T2 - 3rd International Conference on Biomedical and Intelligent Systems, IC-BIS 2024
Y2 - 26 April 2024 through 28 April 2024
ER -