(Circulation. 1999;99:1215-1221.)
© 1999 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Division of Cardiology, Departments of Pediatrics (M.A.F., P.M.W., J.R.), Radiology (A.H., J.H.), and Surgery (M.J., T.L.S.), The Children's Hospital of Philadelphia, The University of Pennsylvania School of Medicine.
Correspondence to Mark A. Fogel, MD, Wyeth-Ayerst Research, 145 King of Prussia Rd, Radnor, PA 19087. E-mail fogelm{at}war.wyeth.com
BackgroundA complete understanding of fluid mechanics in Fontan physiology includes knowledge of the caval contributions to right (RPA) and left (LPA) pulmonary arterial blood flow, total systemic venous return, and relative blood flow to each lung.
Methods and ResultsTen Fontan patients underwent cine MRI. Three cine scans of the pulmonary arteries were performed: (1) no presaturation pulse, (2) a presaturation pulse labeling inferior vena cava (IVC) blood (signal void), and (3) a presaturation pulse labeling superior vena cava (SVC) blood. The relative signal decrease is proportional to the amount of blood originating from the labeled vena cava. This method was validated in a phantom. Whereas 60±6% of SVC blood flowed into the RPA, 67±12% of IVC blood flowed toward the LPA. Of the blood in the LPA and RPA, 48±14% and 31±17%, respectively, came from the IVC. IVC blood contributed 40±16% to total systemic venous return. The distributions of blood to each lung were nearly equal (RPA/LPA blood=0.94±11).
ConclusionsIn Fontan patients with total cavopulmonary connection, SVC blood is directed toward the RPA and IVC blood is directed toward the LPA. Although the right lung volume is larger than the left, an equal amount of blood flow went to both lungs. LPA blood is composed of equal amounts of IVC and SVC blood because IVC contribution to total systemic venous return is smaller than that of the SVC. This technique and these findings can help to evaluate design changes of the systemic venous pathway to improve Fontan hemodynamics.
Key Words: Fontan procedure blood flow lung magnetic resonance imaging heart defects, congenital
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