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      Left ventricular blood flow kinetic energy after myocardial infarction - insights from 4D flow cardiovascular magnetic resonance

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          Abstract

          Background

          Myocardial infarction (MI) leads to complex changes in left ventricular (LV) haemodynamics that are linked to clinical outcomes. We hypothesize that LV blood flow kinetic energy (KE) is altered in MI and is associated with LV function and infarct characteristics. This study aimed to investigate the intra-cavity LV blood flow KE in controls and MI patients, using cardiovascular magnetic resonance (CMR) four-dimensional (4D) flow assessment.

          Methods

          Forty-eight patients with MI (acute-22; chronic-26) and 20 age/gender-matched healthy controls underwent CMR which included cines and whole-heart 4D flow. Patients also received late gadolinium enhancement imaging for infarct assessment. LV blood flow KE parameters were indexed to LV end-diastolic volume and include: averaged LV, minimal, systolic, diastolic, peak E-wave and peak A-wave KEi EDV. In addition, we investigated the in-plane proportion of LV KE (%) and the time difference (TD) to peak E-wave KE propagation from base to mid-ventricle was computed. Association of LV blood flow KE parameters to LV function and infarct size were investigated in all groups.

          Results

          LV KEi EDV was higher in controls than in MI patients (8.5 ± 3 μJ/ml versus 6.5 ± 3 μJ/ml, P = 0.02). Additionally, systolic, minimal and diastolic peak E-wave KEi EDV were lower in MI ( P < 0.05). In logistic-regression analysis, systolic KEi EDV (Beta = − 0.24, P < 0.01) demonstrated the strongest association with the presence of MI. In multiple-regression analysis, infarct size was most strongly associated with in-plane KE ( r = 0.5, Beta = 1.1, P < 0.01). In patients with preserved LV ejection fraction (EF), minimal and in-plane KEi EDV were reduced ( P < 0.05) and time difference to peak E-wave KE propagation during diastole increased ( P < 0.05) when compared to controls with normal EF.

          Conclusions

          Reduction in LV systolic function results in reduction in systolic flow KEi EDV. Infarct size is independently associated with the proportion of in-plane LV KE. Degree of LV impairment is associated with TD of peak E-wave KE. In patient with preserved EF post MI, LV blood flow KE mapping demonstrated significant changes in the in-plane KE, the minimal KEi EDV and the TD. These three blood flow KE parameters may offer novel methods to identify and describe this patient population.

          Electronic supplementary material

          The online version of this article (10.1186/s12968-018-0483-6) contains supplementary material, which is available to authorized users.

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          Most cited references34

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          Treatment of myocardial infarction in a coronary care unit. A two year experience with 250 patients.

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            The vortex--an early predictor of cardiovascular outcome?

            Blood motion in the heart features vortices that accompany the redirection of jet flows towards the outlet tracks. Vortices have a crucial role in fluid dynamics. The stability of cardiac vorticity is vital to the dynamic balance between rotating blood and myocardial tissue and to the development of cardiac dysfunction. Moreover, vortex dynamics immediately reflect physiological changes to the surrounding system, and can provide early indications of long-term outcome. However, the pathophysiological relevance of cardiac fluid dynamics is still unknown. We postulate that maladaptive intracardiac vortex dynamics might modulate the progressive remodelling of the left ventricle towards heart failure. The evaluation of blood flow presents a new paradigm in cardiac function analysis, with the potential for sensitive risk identification of cardiac abnormalities. Description of cardiac flow patterns after surgery or device therapy provides an intrinsic qualitative evaluation of therapeutic procedures, and could enable early risk stratification of patients vulnerable to adverse cardiac remodelling.
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              Four-dimensional blood flow-specific markers of LV dysfunction in dilated cardiomyopathy

              Aims Patients with mild heart failure (HF) who are clinically compensated may have normal left ventricular (LV) stroke volume (SV). Despite this, altered intra-ventricular flow patterns have been recognized in these subjects. We hypothesized that, compared with normal LVs, flow in myopathic LVs would demonstrate a smaller proportion of inflow volume passing directly to ejection and diminished the end-diastolic preservation of the inflow kinetic energy (KE). Methods and results In 10 patients with dilated cardiomyopathy (DCM) (49 ± 14 years, six females) and 10 healthy subjects (44 ± 17 years, four females), four-dimensional MRI velocity and morphological data were acquired. A previously validated method was used to separate the LV end-diastolic volume (EDV) into four flow components based on the blood's locations at the beginning and end of the cardiac cycle. KE was calculated over the cardiac cycle for each component. The EDV was larger (P = 0.021) and the ejection fraction smaller (P < 0.001) in DCM compared with healthy subjects; the SV was equivalent (DCM: 77 ± 19, healthy: 79 ± 16 mL). The proportion of the total LV inflow that passed directly to ejection was smaller in DCM (P = 0.000), but the end-diastolic KE/mL of the direct flow was not different in the two groups (NS). Conclusion Despite equivalent LVSVs, HF patients with mild LV remodelling demonstrate altered diastolic flow routes through the LV and impaired preservation of inflow KE at pre-systole compared with healthy subjects. These unique flow-specific changes in the flow route and energetics are detectable despite clinical compensation, and may prove useful as subclinical markers of LV dysfunction.
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                Author and article information

                Contributors
                + 441133437720 , P.Garg@leeds.ac.uk
                um16sc@leeds.ac.uk
                P.Swoboda@leeds.ac.uk
                G.J.Fent@leeds.ac.uk
                J.Foley@leeds.ac.uk
                P.G.Chew@leeds.ac.uk
                L.Brown1@leeds.ac.uk
                sethu@doctors.org.uk
                m.e.hassell@amc.uva.nl
                r.nijveldt@cardiologie-vumc.nl
                M.M.Bissell@leeds.ac.uk
                mohammed.elbaz@lumc.nl
                A.Al.Mohammad.87@googlemail.com
                J.J.M.Westenberg@lumc.nl
                J.Greenwood@leeds.ac.uk
                R.J.van_der_Geest@lumc.nl
                S.Plein@leeds.ac.uk
                E.DallArmellina@leeds.ac.uk
                Journal
                J Cardiovasc Magn Reson
                J Cardiovasc Magn Reson
                Journal of Cardiovascular Magnetic Resonance
                BioMed Central (London )
                1097-6647
                1532-429X
                30 August 2018
                30 August 2018
                2018
                : 20
                : 61
                Affiliations
                [1 ]ISNI 0000 0004 1936 8403, GRID grid.9909.9, Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM), , University of Leeds, ; Leeds, LS2 9JT UK
                [2 ]ISNI 0000000084992262, GRID grid.7177.6, Department of Cardiology, Academic Medical Center, , University of Amsterdam, ; Amsterdam, The Netherlands
                [3 ]ISNI 0000000089452978, GRID grid.10419.3d, Department of Radiology, , Leiden University Medical Center, ; Leiden, The Netherlands
                [4 ]ISNI 0000 0000 9422 8284, GRID grid.31410.37, Sheffield Teaching Hospitals NHS Foundation Trust, ; Sheffield, UK
                Author information
                http://orcid.org/0000-0002-5483-169X
                Article
                483
                10.1186/s12968-018-0483-6
                6117925
                30165869
                adbfc3d9-4123-4e85-a1a5-e10c22572bba
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 13 March 2018
                : 20 July 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000274, British Heart Foundation;
                Award ID: FS/10/62/28409
                Award Recipient :
                Funded by: Dutch ZonMw
                Award ID: 104003001
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Cardiovascular Medicine
                4d flow cmr,myocardial infarction,hemodynamics,flow quantification
                Cardiovascular Medicine
                4d flow cmr, myocardial infarction, hemodynamics, flow quantification

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