Congenital: Fontan
Progression in Fontan conduit stenosis and hemodynamic impact during childhood and adolescence

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Abstract

Objective

To characterize changes in Fontan conduit size over time and determine if cross-sectional area (CSA) affects cardiac output, pulmonary artery growth, and exercise capacity.

Methods

We conducted a retrospective cross-sectional study of patients with Fontan physiology who underwent cardiac magnetic resonance imaging or cardiac catheterization between January 2013 and October 2019. We collected Fontan and pulmonary artery measurements, hemodynamic data, and cardiopulmonary exercise test data. We identified 158 patients with an extracardiac Fontan. We measured minimum and mean Fontan conduit CSA and assessed whether these correlated with Nakata index, cardiac index, or exercise capacity.

Results

Minimum Fontan CSA decreased by a median of 33% (24%, 40%) during a mean follow-up of 9.6 years. Median percentage decrease in Fontan CSA did not differ among 16-, 18-, and 20-mm conduits (P = .29). There was a significant decrease in the minimum Fontan CSA (33% [25%, 41%]) starting less than 1-year post-Fontan. Median Nakata index was 177.6 mm2/m2 (149.1, 210.8) and was not associated with Fontan CSA/BSA (ρ = 0.09, P = .29). Fontan CSA/BSA was not associated with cardiac index (ρ = –0.003, P = .97). A larger Fontan CSA/BSA had a modest correlation with % predicted oxygen consumption (ρ = 0.31, P = .013).

Conclusions

Fontan conduit CSA decreases as early as 6 months post-Fontan. The minimum Fontan CSA/BSA was not associated with cardiac index or pulmonary artery size but did correlate with % predicted peak oxygen consumption.

Key Words

congenital heart surgery
Fontan
magnetic resonance imaging
cardiac catheterization
exercise capacity

Abbreviations

BSA
body surface area
CHLA
Children's Hospital Los Angeles
CPET
cardiopulmonary exercise test
CSA
cross-sectional area
IVC
inferior vena cava
LPA
left pulmonary artery
MRI
magnetic resonance imaging
Qp:Qs
ratio of pulmonary blood flow to systemic blood flow
RPA
right pulmonary artery
SVC
superior vena cava
VO2
oxygen consumption

Cited by (0)

A. L. Cheng was supported by intramural grants from Children's Hospital Los Angeles (The Saban Research Institute Research Career Development Award) and University of Southern California (Wright Foundation Pilot Grant).