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A summary of the steps conducted for patient-specific computational analysis of AACOA in the current investigation included model reconstruction from cardiac magnetic resonance imaging (CMR) data, mesh generation with local refinements on the ostial region and left main coronary artery (LMCA) bifurcation, assigning multiscale boundary conditions, and postprocessing of resulting hemodynamics to visualize and quantify changes in coronary artery velocity and indices of wall shear stress (WSS). Six AAOCA patients (3 left, 3 right) status post unroofing (median = 13.5 years) underwent CMR. Timing of post-MRI ranged from 3 months-6 years (mean 2.9 years). Computational fluid dynamics (CFD) models were created from pre (n = 2) and postunroofing (n = 6) CMR data. Mesh generation was performed and locally refined until it was properly representative of the geometry. Parameters of the boundary conditions were determined so that physiologic pressure and flow waveforms were achieved. Results showed that: (1) time averaged wall shear stress (TAWSS) was higher preoperatively due to more skewed velocity profiles along the length of the angulated anomalous arteries, (2) unroofing may normalize WSS, and (3) changes in AO led to significant alterations in the local flow patterns and hemodynamics. These findings suggest that acute AO creates abnormal coronary flow patterns and hemodynamics that could leave patients more susceptible to the early onset and progression of atherosclerosis and ultimately may help explain myocardial morbidity associated with intramural AAOCA. Future studies with a larger cohort will allow for a correlation analysis between hemodynamic indices and patient outcomes to predict the patients’ future risk for ischemia or morbidity.
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Abstract   A case of aortopulmonary window associated with anomalous origin of the right coronary artery from the pulmonary artery in a four-month-old boy is reported in this paper with a different method of repair. In this patient, surgical repair was done by transferring the right coronary artery from the pulmonary artery to the aorta at the aortopulmonary window side. The defect at the pulmonary artery was repaired by a pericardial patch, so no other secondary opening was used for the aorta in order to reimplant the coronary artery .  相似文献   

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目的总结一期手术纠治主-肺动脉窗及伴发畸形的临床经验,以提高手术疗效。方法我科共收治26例主-肺动脉窗患者.男14例.女12例;年龄1.4±1.6岁;体重7.8±3.8kg。其中单纯主-肺动脉窗8例,合并主动脉弓中断、右肺动脉异常起源于主动脉、法洛四联症、房间隔缺损、室间隔缺损、二尖瓣反流和气管狭窄等18例。25例患者一期手术经主动脉切口补片关闭瘘口纠治主-肺动脉窗,同时纠治伴发的畸形;1例放弃治疗。结果全组无手术死亡。2例伴主动脉弓中断、动脉导管未闭和右肺动脉起源于升主动脉的新生儿术后3d延迟关胸;1例术后出血,3h后再次开胸止血。术后随访22例.随访时间1个月~4年。所有患者无明显的主动脉瓣上狭窄和肺动脉分支狭窄,2例残留轻度二尖瓣反流,1例残留轻至中度二尖瓣反流。结论主-肺动脉窗患者早期易发生肺动脉高压,一经诊断应立即手术。手术方式首选修补主-肺动脉窗及一期纠治伴发畸形。尽管主-肺动脉窗可合并各种心内外畸形,但早期手术纠治可获得较好的中长期疗效。  相似文献   

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