The effect of airway motion and breathing phase during imaging on CFD simulations of respiratory airflow

被引:24
作者
Gunatilaka, Chamindu C. [1 ,2 ]
Schuh, Andreas [3 ]
Higano, Nara S. [1 ,4 ]
Woods, Jason C. [1 ,2 ,4 ,5 ,6 ]
Bates, Alister J. [1 ,4 ,5 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Ctr Pulm Imaging Res, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Dept Phys, Cincinnati, OH USA
[3] Imperial Coll London, Dept Comp, London, England
[4] Cincinnati Childrens Hosp Med Ctr, Div Pulm Med, Cincinnati, OH 45229 USA
[5] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
[6] Cincinnati Childrens Hosp Med Ctr, Dept Radiol, Cincinnati, OH 45229 USA
基金
美国国家卫生研究院;
关键词
Airway CFD; Respiratory airflow; Airway motion; UTE MRI; Unsteady; Trachea; COMPUTATIONAL FLUID-DYNAMICS; ULTRASHORT ECHO TIME; MRI; CHILDREN; PRESSURE; WORK; RESISTANCE; SQUARE; VOLUME; MODEL;
D O I
10.1016/j.compbiomed.2020.104099
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Rationale: Computational fluid dynamics (CFD) simulations of respiratory airflow can quantify clinically useful information that cannot be obtained directly, such as the work of breathing (WOB), resistance to airflow, and pressure loss. However, patient-specific CFD simulations are often based on medical imaging that does not capture airway motion and thus may not represent true physiology, directly affecting those measurements. Objectives: To quantify the variation of respiratory airflow metrics obtained from static models of airway anatomy at several respiratory phases, temporally averaged airway anatomies, and dynamic models that incorporate physiological motion. Methods: Neonatal airway images were acquired during free-breathing using 3D high-resolution MRI and reconstructed at several respiratory phases in two healthy subjects and two with airway disease (tracheomalacia). For each subject, five static (end expiration, peak inspiration, end inspiration, peak expiration, averaged) and one dynamic CFD simulations were performed. WOB, airway resistance, and pressure loss across the trachea were obtained for each static simulation and compared with the dynamic simulation results. Results: Large differences were found in the airflow variables between the static simulations at various respiratory phases and the dynamic simulation. Depending on the static airway model used, WOB, resistance, and pressure loss varied up to 237%, 200%, and 94% compared to the dynamic simulation respectively. Conclusions: Changes in tracheal size and shape throughout the breathing cycle directly affect respiratory airflow dynamics and breathing effort. Simulations incorporating realistic airway wall dynamics most closely represent airway physiology; if limited to static simulations, the airway geometry must be obtained during the respiratory phase of interest for a given pathology.
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页数:11
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