Patient-specific modelling of cardiac electrophysiology in heart-failure patients

被引:51
|
作者
Potse, Mark [1 ,2 ]
Krause, Dorian [3 ]
Kroon, Wilco [3 ]
Murzilli, Romina [4 ]
Muzzarelli, Stefano [4 ]
Regoli, Franc Ois [4 ]
Caiani, Enrico [5 ]
Prinzen, Frits W. [1 ,6 ]
Krause, Rolf [1 ,3 ]
Auricchio, Angelo [1 ,4 ]
机构
[1] Univ Svizzera Italiana, Fac Informat, Ctr Computat Med Cardiol, Via Giuseppe Buffi 13, CH-6904 Lugano, Switzerland
[2] Inria Bordeaux Sud Ouest, F-33405 Talence, France
[3] Univ Svizzera Italiana, Fac Informat, Inst Computat Sci, CH-6904 Lugano, Switzerland
[4] Fdn Cardioctr Ticino, Div Cardiol, CH-6904 Lugano, Switzerland
[5] Politecn Milan, Dept Elect Informat & Bioengn, I-20133 Milan, Italy
[6] Maastricht Univ, Cardiovasc Res Inst Maastricht, Dept Physiol, NL-6229 ER Maastricht, Netherlands
来源
EUROPACE | 2014年 / 16卷
关键词
Heart failure; Left bundle-branch block; Conduction disorders; Computer models;
D O I
10.1093/europace/euu257
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Left-ventricular (LV) conduction disturbances are common in heart-failure patients and a left bundle-branch block (LBBB) electrocardiogram (ECG) type is often seen. The precise cause of this pattern is uncertain and is probably variable between patients, ranging from proximal interruption of the left bundle branch to diffuse distal conduction disease in the working myocardium. Using realistic numerical simulation methods and patient-tailored model anatomies, we investigated different hypotheses to explain the observed activation order on the LV endocardium, electrogram morphologies, and ECG features in two patients with heart failure and LBBB ECG. Methods and results Ventricular electrical activity was simulated using reaction-diffusion models with patient-specific anatomies. From the simulated action potentials, ECGs and cardiac electrograms were computed by solving the bidomain equation. Model parameters such as earliest activation sites, tissue conductivity, and densities of ionic currents were tuned to reproduce the measured signals. Electrocardiogram morphology and activation order could be matched simultaneously. Local electrograms matched well at some sites, but overall the measured waveforms had deeper S-waves than the simulated waveforms. Conclusion Tuning a reaction-diffusion model of the human heart to reproduce measured ECGs and electrograms is feasible and may provide insights in individual disease characteristics that cannot be obtained by other means.
引用
收藏
页码:56 / 61
页数:6
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