Modelling in congenital heart disease. Art or science?
被引:4
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作者:
Giannakoulas, Georgios
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Royal Brompton Hosp, Adult Congenital Heart Ctr, London SW3 6NP, England
Royal Brompton Hosp, Ctr Pulm Hypertens, London SW3 6NP, EnglandRoyal Brompton Hosp, Adult Congenital Heart Ctr, London SW3 6NP, England
Giannakoulas, Georgios
[1
,2
]
Dimopoulos, Konstantinos
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Royal Brompton Hosp, Adult Congenital Heart Ctr, London SW3 6NP, England
Royal Brompton Hosp, Ctr Pulm Hypertens, London SW3 6NP, EnglandRoyal Brompton Hosp, Adult Congenital Heart Ctr, London SW3 6NP, England
Dimopoulos, Konstantinos
[1
,2
]
Xu, X. Yun
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Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn, London SW7 2AZ, EnglandRoyal Brompton Hosp, Adult Congenital Heart Ctr, London SW3 6NP, England
Xu, X. Yun
[3
]
机构:
[1] Royal Brompton Hosp, Adult Congenital Heart Ctr, London SW3 6NP, England
[2] Royal Brompton Hosp, Ctr Pulm Hypertens, London SW3 6NP, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn, London SW7 2AZ, England
Despite the advances in imaging modalities and surgical techniques, the management of adults with congenital heart disease (ACHD) over the years has remained largely empirical rather than evidence-based. Animal models have been difficult to develop and very costly, while clinical trials are difficult to design and perform in ACHD, leaving gaps in our understanding of the pathophysiology and treatment of congenital heart disease. Disease modelling, both hypothetical and patient-specific, provides an alternative solution to many of these problems. Advances in cardiovascular imaging and diagnostics have led to the easy acquisition of large quantities of structural and functional information, which cannot be handled "intuitively". Computational modelling introduces mathematical rigour in the analysis and utilisation of these data by quantitative simulation and testing of clinically relevant hypotheses through experimentally validated models. Close multidisciplinary collaboration between bioengineers and clinicians is essential for transforming data and images derived from models of disease into clinically useful information. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
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Univ Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USAUniv Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USA
Lightdale, JR
McElhinney, DB
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Univ Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USAUniv Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USA
McElhinney, DB
Mudge, CL
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Univ Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USAUniv Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USA
Mudge, CL
Roberts, JP
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Univ Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USAUniv Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USA
Roberts, JP
Ascher, NL
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Univ Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USAUniv Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USA
Ascher, NL
Rosenthal, P
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Univ Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USAUniv Calif San Francisco, Pediat Liver Transplant Program, San Francisco, CA 94143 USA