In congenital heart defects with left to right shunting, the increased pulmonary blood flow and pulmonary hypertension leads to structural and functional changes in the pulmonary vasculature. These changes, known as pulmonary plexogenic arteriopathy, include increased muscularization, altered vasoconstrictive and impaired vasodilatatory responses in the arterial tree, and extensive extracellular matrix modulation (including increased collagen deposition and gradual occlusion of the small pulmonary arteries by intimal proliferation and fibrosis). These alterations will result in decreased compliance by the pulmonary vessels and, thus, a stiffening of the arterial wall.

Biopsy, Dye Dilution Technique, Heart Catheterization, Heart Defects, Congenital/complications/*physiopathology, Hemodynamic Processes, Humans, Hypertension, Pulmonary/complications/diagnosis/*physiopathology, Lung Diseases/diagnosis/*physiopathology, Lung/pathology, Oxygen Consumption, Pulmonary Circulation/*physiology, Thermodilution, Vascular Resistance, angiography, congenital heart disease, haemodynamics, histology, pulmonary hypertension, pulmonary vascular disease
dx.doi.org/10.1053/euhj.1999.1698, hdl.handle.net/1765/12823
European Heart Journal
Erasmus MC: University Medical Center Rotterdam

Berger, R.M.F. (2000). Possibilities and impossibilities in the evaluation of pulmonary vascular disease in congenital heart defects.. European Heart Journal (Vol. 21, pp. 17–27). doi:10.1053/euhj.1999.1698