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DOI 10.1002/mrm.10201

Медицинская библиотека · Magnetic resonance in medicine · 2002

Mapping myocardial perfusion with an intravascular MR contrast agent: robustness of deconvolution methods at various blood flows.

Neyran Bruno, Janier Marc F, Casali Cendrine, Revel Didier, Canet Soulas Emmanuelle P

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Evaluation of quantitative parameters such as regional myocardial blood flow (rMBF), blood volume (rMBV), and mean transit time (rMTT) by MRI is gaining acceptance for clinical applications, but still lacks robust postprocessing methods for map generation. Moreover, robustness should be preserved over the full range of myocardial flows and volumes. Using experimental data from an isolated pig heart preparation, synthetic MR kinetics were generated and four deconvolution approaches were evaluated. These methods were then applied to the first-pass T(1) images of the isolated pig heart using an intravascular contrast agent and rMBF, rMBV and rMTT maps were generated. In both synthetic and experimental data, the fit between calculated and original data reached equally good results with the four techniques. rMBV was the only parameter estimated correctly in numerical experiments. Moreover, using the algebraic method ARMA, abnormal regions were well delineated on rMBV maps. At high flows, rMBF was underestimated at the experimental noise level. Finally, rMTT maps appeared noisy and highly unreliable, especially at high flows. In conclusion, over the myocardial flow range, i.e., 0-400 ml/min/100g, rMBF identification was biased in presence of noise, whereas rMBV was correctly identified. Thus, rMBV mapping could be a fast and robust way to detect abnormal myocardial regions.

Для цитирования: Neyran Bruno, Janier Marc F, Casali Cendrine, Revel Didier, Canet Soulas Emmanuelle P. Mapping myocardial perfusion with an intravascular MR contrast agent: robustness of deconvolution methods at various blood flows.. Magnetic resonance in medicine. 2002. DOI: 10.1002/mrm.10201.

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