TY - JOUR
T1 - Ultrasound current source density imaging
AU - Olafsson, Ragnar
AU - Witte, Russell S.
AU - Huang, Sheng Wen
AU - O'Donnell, Matthew
N1 - Funding Information:
Manuscript received June 29, 2007. This work was supported in part by the National Institutes of Health under Grant HL67647, Grant EB003451, and Grant HL082640, in part by the Department of Biomedical Engineering at the University of Michigan, and in part by the Fulbright Fellowship Program, U.S. Department of State. Asterisk indicates corresponding author. *R. Olafsson is with the Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109 USA (e-mail: [email protected]). R. S. Witte is with the University of Arizona, Tucson, AZ 85724 USA (e-mail: [email protected]). S.-W. Huang is with the Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109 USA (e-mail: [email protected]). M. O’Donnell is with the Department of Bioengineering, University of Washington, Seattle, WA 98195 USA (e-mail: [email protected]). Color versions of one or more of the figures in this paper are available online at http://ieeexplore.ieee.org. Digital Object Identifier 10.1109/TBME.2008.919115
PY - 2008/7
Y1 - 2008/7
N2 - Surgery to correct severe heart arrhythmias usually requires detailed maps of the cardiac activation wave prior to ablation. The pinpoint electrical mapping procedure is laborious and limited by its spatial resolution (5-10 mm). We propose ultrasound current source density imaging (UCSDI), a direct 3-D imaging technique that potentially facilitates existing mapping procedures with superior spatial resolution. The technique is based on a pressure-induced change in resistivity known as the acoustoelectric (AE) effect, which is spatially confined to the ultrasound focus. AE-modulated voltage recordings are used to map and reconstruct current densities. In this preliminary study, we tested UCSDI under controlled conditions and compared it with conventional electrical mapping techniques. A 2-D dipole field was produced by a pair of electrodes in a bath of 0.9% NaCl solution. Boundary electrodes detected the AE signal while a 7.5-MHz focused ultrasound transducer was scanned across the bath. UCSDI located the current source and sink to within 1 mm of their actual positions. A future UCSDI system potentially provides real-time 3-D images of the cardiac activation wave coregistered with anatomical ultrasound and would greatly facilitate corrective procedures for heart abnormalities.
AB - Surgery to correct severe heart arrhythmias usually requires detailed maps of the cardiac activation wave prior to ablation. The pinpoint electrical mapping procedure is laborious and limited by its spatial resolution (5-10 mm). We propose ultrasound current source density imaging (UCSDI), a direct 3-D imaging technique that potentially facilitates existing mapping procedures with superior spatial resolution. The technique is based on a pressure-induced change in resistivity known as the acoustoelectric (AE) effect, which is spatially confined to the ultrasound focus. AE-modulated voltage recordings are used to map and reconstruct current densities. In this preliminary study, we tested UCSDI under controlled conditions and compared it with conventional electrical mapping techniques. A 2-D dipole field was produced by a pair of electrodes in a bath of 0.9% NaCl solution. Boundary electrodes detected the AE signal while a 7.5-MHz focused ultrasound transducer was scanned across the bath. UCSDI located the current source and sink to within 1 mm of their actual positions. A future UCSDI system potentially provides real-time 3-D images of the cardiac activation wave coregistered with anatomical ultrasound and would greatly facilitate corrective procedures for heart abnormalities.
KW - Acoustics
KW - Acoustoelectric effect
KW - Bioelectric phenomena
KW - Electrocardiography
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U2 - 10.1109/TBME.2008.919115
DO - 10.1109/TBME.2008.919115
M3 - Article
C2 - 18595802
AN - SCOPUS:45749095469
SN - 0018-9294
VL - 55
SP - 1840
EP - 1848
JO - IEEE Transactions on Biomedical Engineering
JF - IEEE Transactions on Biomedical Engineering
IS - 7
ER -