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- Publisher Website: 10.1152/ajpheart.00048.2003
- Scopus: eid_2-s2.0-0141788691
- PMID: 12763744
- WOS: WOS:000185249900049
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Article: Right ventricular volume measurement by conductance catheter
Title | Right ventricular volume measurement by conductance catheter |
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Authors | |
Keywords | Conductance catheter Magnetic resonance imaging |
Issue Date | 2003 |
Citation | American Journal of Physiology - Heart and Circulatory Physiology, 2003, v. 285 n. 4 54-4, p. H1774-H1785 How to Cite? |
Abstract | Continuous ventricular volume measurement by the conductance method assumes a homogeneous electrical field dispersed throughout and contained within the ventricle. Because of dense trabeculation and complex geometry, right ventricular (RV) volume description by this method may be seriously compromised. This study sought to determine the accuracy and limitations of RV volume measurement by conductance, with magnetic resonance (MR) imaging (MRI) used as a reference, in the porcine RV. Anesthetized pigs (n = 5, 45-55 kg) were placed in a 1.5-T magnet, and ECG-gated transverse MR images (5-mm slices) were acquired during the complete cardiac cycle. RV cavity volumes were subsequently determined by Simpson's technique. Animals were then instrumented with an RV conductance catheter and an ultrasonic pulmonary artery flow probe. Conductance catheter signals were recorded using single- and dual-field (SF and DF) excitation, and the saline-dilution technique was used to correct volumes for parallel conductance. The gain factor (α) was calculated as the ratio of conductance- to MRI-derived stroke volume (α sv). Variation of α during the cardiac cycle was computed by comparing RV conductance volumes with 1) MRI volumes at isochronal time points within the cardiac cycle [α(t)] and 2) the pulmonary flow integral during ejection. After calibration, the conductance-MRI volume relation was modeled lin-early with good correlation [r = 0.96 (SF) and r = 0.94 (DF)], close to the line of identity. Individual conductance-MRI plots displayed a slight curvilinear relation that was concave toward the MRI axis. Consistent with this finding, α(t) varied significantly during the cardiac cycle (0.49 and 0.39 by SF for end systole and end diastole, respectively, P = 0.011). DF excitation resulted in improved volume measurement [α sv = 0.41 (SF) and 0.96 (DF)], with less variation in α(t) (1.0 and 0.92 by DF for end systole and end diastole, respectively, P = 0.66). These results indicate that, with calibration, the conductance method can measure absolute RV volume under steady-state conditions. However, the curvilinearity and α(t) variation would indicate the potential for nonlinearity when RV volumes are varied over a wider range. |
Persistent Identifier | http://hdl.handle.net/10722/192660 |
ISSN | 2023 Impact Factor: 4.1 2023 SCImago Journal Rankings: 1.452 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Danton, MHD | en_US |
dc.contributor.author | Greil, GF | en_US |
dc.contributor.author | Byrne, JG | en_US |
dc.contributor.author | Hsin, M | en_US |
dc.contributor.author | Cohn, L | en_US |
dc.contributor.author | Maier, SE | en_US |
dc.date.accessioned | 2013-11-20T04:54:56Z | - |
dc.date.available | 2013-11-20T04:54:56Z | - |
dc.date.issued | 2003 | en_US |
dc.identifier.citation | American Journal of Physiology - Heart and Circulatory Physiology, 2003, v. 285 n. 4 54-4, p. H1774-H1785 | en_US |
dc.identifier.issn | 0363-6135 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/192660 | - |
dc.description.abstract | Continuous ventricular volume measurement by the conductance method assumes a homogeneous electrical field dispersed throughout and contained within the ventricle. Because of dense trabeculation and complex geometry, right ventricular (RV) volume description by this method may be seriously compromised. This study sought to determine the accuracy and limitations of RV volume measurement by conductance, with magnetic resonance (MR) imaging (MRI) used as a reference, in the porcine RV. Anesthetized pigs (n = 5, 45-55 kg) were placed in a 1.5-T magnet, and ECG-gated transverse MR images (5-mm slices) were acquired during the complete cardiac cycle. RV cavity volumes were subsequently determined by Simpson's technique. Animals were then instrumented with an RV conductance catheter and an ultrasonic pulmonary artery flow probe. Conductance catheter signals were recorded using single- and dual-field (SF and DF) excitation, and the saline-dilution technique was used to correct volumes for parallel conductance. The gain factor (α) was calculated as the ratio of conductance- to MRI-derived stroke volume (α sv). Variation of α during the cardiac cycle was computed by comparing RV conductance volumes with 1) MRI volumes at isochronal time points within the cardiac cycle [α(t)] and 2) the pulmonary flow integral during ejection. After calibration, the conductance-MRI volume relation was modeled lin-early with good correlation [r = 0.96 (SF) and r = 0.94 (DF)], close to the line of identity. Individual conductance-MRI plots displayed a slight curvilinear relation that was concave toward the MRI axis. Consistent with this finding, α(t) varied significantly during the cardiac cycle (0.49 and 0.39 by SF for end systole and end diastole, respectively, P = 0.011). DF excitation resulted in improved volume measurement [α sv = 0.41 (SF) and 0.96 (DF)], with less variation in α(t) (1.0 and 0.92 by DF for end systole and end diastole, respectively, P = 0.66). These results indicate that, with calibration, the conductance method can measure absolute RV volume under steady-state conditions. However, the curvilinearity and α(t) variation would indicate the potential for nonlinearity when RV volumes are varied over a wider range. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | American Journal of Physiology - Heart and Circulatory Physiology | en_US |
dc.subject | Conductance catheter | - |
dc.subject | Magnetic resonance imaging | - |
dc.title | Right ventricular volume measurement by conductance catheter | en_US |
dc.type | Article | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1152/ajpheart.00048.2003 | - |
dc.identifier.pmid | 12763744 | - |
dc.identifier.scopus | eid_2-s2.0-0141788691 | en_US |
dc.identifier.volume | 285 | en_US |
dc.identifier.issue | 4 54-4 | en_US |
dc.identifier.spage | H1774 | en_US |
dc.identifier.epage | H1785 | en_US |
dc.identifier.isi | WOS:000185249900049 | - |
dc.identifier.issnl | 0363-6135 | - |