» Articles » PMID: 37875552

In Vivo Hepatic Flow Distribution by Computational Fluid Dynamics Can Predict Pulmonary Flow Distribution in Patients with Fontan Circulation

Overview
Journal Sci Rep
Specialty Science
Date 2023 Oct 24
PMID 37875552
Authors
Affiliations
Soon will be listed here.
Abstract

In Fontan patients, a lung deprived of hepatic blood may develop pulmonary arterio-venous malformations (PAVMs) resulting in shunting, reduced pulmonary vascular resistance (PVR) and decreased oxygenation. To provide guidance for corrective invasive interventions, we aimed to non-invasively determine how the hepatic to pulmonary blood flow balance correlates with pulmonary flow, PVR, and with oxygen saturation. Magnetic resonance imaging (MRI) data from eighteen Fontan patients (eight females, age 3-14 years) was used to construct patient-specific computational fluid dynamics (CFD) models to calculate the hepatic to pulmonary blood flow. This was correlated with pulmonary vein flow, simulated PVR and oxygen saturation. Clinical applicability of the findings was demonstrated with an interventional patient case. The hepatic to pulmonary blood flow balance correlated with right/left pulmonary vein flow (R = 0.50), left/right simulated PVR (R = 0.47), and oxygen saturation at rest (R = 0.56). In the interventional patient, CFD predictions agreed with post-interventional MRI measurements and with regressions in the cohort. The balance of hepatic blood to the lungs has a continuous effect on PVR and oxygen saturation, even without PAVM diagnosis. MRI combined with CFD may help in planning of surgical and interventional designs affecting the hepatic to pulmonary blood flow balance in Fontan patients.

Citing Articles

The impact of blood viscosity modeling on computational fluid dynamic simulations of pediatric patients with Fontan circulation.

Wei H, Bilgi C, Cao K, Detterich J, Pahlevan N, Cheng A Phys Fluids (1994). 2024; 36(11):111911.

PMID: 39574945 PMC: 11577338. DOI: 10.1063/5.0236095.


Biomechanics and clinical implications of Fontan upsizing.

Govindarajan V, Sahni A, Eickhoff E, Hammer P, Hoganson D, Rathod R Comput Biol Med. 2024; 183:109317.

PMID: 39471662 PMC: 11576229. DOI: 10.1016/j.compbiomed.2024.109317.


Impact of Age-Related Change in Caval Flow Ratio on Hepatic Flow Distribution in the Fontan Circulation.

Govindarajan V, Marshall L, Sahni A, Cetatoiu M, Eickhoff E, Davee J Circ Cardiovasc Imaging. 2024; 17(4):e016104.

PMID: 38567518 PMC: 11073583. DOI: 10.1161/CIRCIMAGING.123.016104.

References
1.
FONTAN F, Baudet E . Surgical repair of tricuspid atresia. Thorax. 1971; 26(3):240-8. PMC: 1019078. DOI: 10.1136/thx.26.3.240. View

2.
Gewillig M, Brown S . The Fontan circulation after 45 years: update in physiology. Heart. 2016; 102(14):1081-6. PMC: 4941188. DOI: 10.1136/heartjnl-2015-307467. View

3.
Razavi R, Hill D, Keevil S, Miquel M, Muthurangu V, Hegde S . Cardiac catheterisation guided by MRI in children and adults with congenital heart disease. Lancet. 2003; 362(9399):1877-82. DOI: 10.1016/S0140-6736(03)14956-2. View

4.
Duncan B, Desai S . Pulmonary arteriovenous malformations after cavopulmonary anastomosis. Ann Thorac Surg. 2003; 76(5):1759-66. DOI: 10.1016/s0003-4975(03)00450-8. View

5.
Srivastava D, Preminger T, Lock J, Mandell V, Keane J, Mayer Jr J . Hepatic venous blood and the development of pulmonary arteriovenous malformations in congenital heart disease. Circulation. 1995; 92(5):1217-22. DOI: 10.1161/01.cir.92.5.1217. View