Krzysztof Czechowicz
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Krzysztof Czechowicz has a total of 24 co-authors. Here are the top co-authors by number of shared publications:
- Andrew James Narracott
University of Sheffield
3 shared publications - David Rodney Hose
University of Sheffield
3 shared publications - Ian Halliday
Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield S10 2TN, UK
3 shared publications - Julian Gunn
Cardiovascular Research Unit, Division of Clinical Medicine, The University of Sheffield , Sheffield
2 shared publications - Paul David Morris
Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield , Beech Hill Road, Sheffield S10 2RX
2 shared publications - Abdulaziz Al Baraikan
Department of Infection, Immunity & Cardiovascular Disease, University of Sheffield, Sheffield, UK
1 shared publication
Latest Publications
- Open Access
A Digital Twin to Predict Patient Response to Valve Replacement Following Aortic Stenosis
Lack of available data, ease of clinical use and lack of evidence for prognostic benefit are arguably the key limitations to clinical uptake for any model. This paper reports the development of an image-based analysis protocol, coupling 0D left heart and systemic circulation components with a 3D aortic valve model to measure and to predict the pressure gradient across the aortic valve at rest. The model is personalized using routine clinical data available for aortic valve patients, augmented by additional image data (transesophageal echo and/or CT) to support valve characterization. Computed aortic pressure gradient both pre- and post-intervention was compared with clinical measurements based on Doppler ultrasound for a cohort of 21 patients with aortic valve disease. Correlation for the diseased state measures were adequate () for those cases for which associated image data was deemed to be of acceptable quality for segmentation to support a 3D computational fluid dynamics analysis but poor otherwise. Post treatment correlation was reasonable () for all cases. Importantly, the personalized model presented here describes the interaction between the patient’s cardiovascular system, including the heart and circulation, and the valve, rather than evaluating the valve in isolation.Open AccessA Digital Twin to Predict Patient Response to Valve Replacement Following Aortic Stenosis
Lack of available data, ease of clinical use and lack of evidence for prognostic benefit are arguably the key limitations to clinical uptake for any model. This paper reports the development of an image-based analysis protocol, coupling 0D left heart and systemic circulation components with a 3D aortic valve model to measure and to predict the pressure gradient across the aortic valve at rest. The model is personalized using routine clinical data available for aortic valve patients, augmented by additional image data (transesophageal echo and/or CT) to support valve characterization. Computed aortic pressure gradient both pre- and post-intervention was compared with clinical measurements based on Doppler ultrasound for a cohort of 21 patients with aortic valve disease. Correlation for the diseased state measures were adequate () for those cases for which associated image data was deemed to be of acceptable quality for segmentation to support a 3D computational fluid dynamics analysis but poor otherwise. Post treatment correlation was reasonable () for all cases. Importantly, the personalized model presented here describes the interaction between the patient’s cardiovascular system, including the heart and circulation, and the valve, rather than evaluating the valve in isolation. - Open Access
Modelling The Hemodynamics of Coronary Ischemia
Acting upon clinical patient data, acquired in the pathway of percutaneous intervention, we deploy hierarchical, multi-stage, data-handling protocols and interacting low- and high-order mathematical models (chamber elastance, state-space system and CFD models), to establish and then validate a framework to quantify the burden of ischaemia. Our core tool is a compartmental, zero-dimensional model of the coupled circulation with four heart chambers, systemic and pulmonary circulations and an optimally adapted windkessel model of the coronary arteries that reflects the diastolic dominance of coronary flow. We guide the parallel development of protocols and models by appealing to foundational physiological principles of cardiac energetics and a parameterisation (stenotic Bernoulli resistance and micro-vascular resistance) of patients’ coronary flow. We validate our process first with results which substantiate our protocols and, second, we demonstrate good correspondence between model operation and patient data. We conclude that our core model is capable of representing (patho)physiological states and discuss how it can potentially be deployed, on clinical data, to provide a quantitative assessment of the impact, on the individual, of coronary artery disease.
Open AccessModelling The Hemodynamics of Coronary Ischemia
Acting upon clinical patient data, acquired in the pathway of percutaneous intervention, we deploy hierarchical, multi-stage, data-handling protocols and interacting low- and high-order mathematical models (chamber elastance, state-space system and CFD models), to establish and then validate a framework to quantify the burden of ischaemia. Our core tool is a compartmental, zero-dimensional model of the coupled circulation with four heart chambers, systemic and pulmonary circulations and an optimally adapted windkessel model of the coronary arteries that reflects the diastolic dominance of coronary flow. We guide the parallel development of protocols and models by appealing to foundational physiological principles of cardiac energetics and a parameterisation (stenotic Bernoulli resistance and micro-vascular resistance) of patients’ coronary flow. We validate our process first with results which substantiate our protocols and, second, we demonstrate good correspondence between model operation and patient data. We conclude that our core model is capable of representing (patho)physiological states and discuss how it can potentially be deployed, on clinical data, to provide a quantitative assessment of the impact, on the individual, of coronary artery disease.
- Open Access
The Use of Digital Coronary Phantoms for the Validation of Arterial Geometry Reconstruction and Computation of Virtual FFR
We present computational fluid dynamics (CFD) results of virtual fractional flow reserve (vFFR) calculations, performed on reconstructed arterial geometries derived from a digital phantom (DP). The latter provides a convenient and parsimonious description of the main vessels of the left and right coronary arterial trees, which, crucially, is CFD-compatible. Using our DP, we investigate the reconstruction error in what we deem to be the most relevant way—by evaluating the change in the computed value of vFFR, which results from varying (within representative clinical bounds) the selection of the virtual angiogram pair (defined by their viewing angles) used to segment the artery, the eccentricity and severity of the stenosis, and thereby, the CFD simulation’s luminal boundary. The DP is used to quantify reconstruction and computed haemodynamic error within the VIRTUheartTM software suite. However, our method and the associated digital phantom tool are readily transferable to equivalent, clinically oriented workflows. While we are able to conclude that error within the VIRTUheartTM workflow is suitably controlled, the principal outcomes of the work reported here are the demonstration and provision of a practical tool along with an exemplar methodology for evaluating error in a coronary segmentation process.
Open AccessThe Use of Digital Coronary Phantoms for the Validation of Arterial Geometry Reconstruction and Computation of Virtual FFR
We present computational fluid dynamics (CFD) results of virtual fractional flow reserve (vFFR) calculations, performed on reconstructed arterial geometries derived from a digital phantom (DP). The latter provides a convenient and parsimonious description of the main vessels of the left and right coronary arterial trees, which, crucially, is CFD-compatible. Using our DP, we investigate the reconstruction error in what we deem to be the most relevant way—by evaluating the change in the computed value of vFFR, which results from varying (within representative clinical bounds) the selection of the virtual angiogram pair (defined by their viewing angles) used to segment the artery, the eccentricity and severity of the stenosis, and thereby, the CFD simulation’s luminal boundary. The DP is used to quantify reconstruction and computed haemodynamic error within the VIRTUheartTM software suite. However, our method and the associated digital phantom tool are readily transferable to equivalent, clinically oriented workflows. While we are able to conclude that error within the VIRTUheartTM workflow is suitably controlled, the principal outcomes of the work reported here are the demonstration and provision of a practical tool along with an exemplar methodology for evaluating error in a coronary segmentation process.