A congenitally “poor” pulmonary artery is a major reason for exclusion from Fontan operation |
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Authors: | Makoto Nakazawa Insam Park Miho Yamada Toshio Nakanishi Kazuo Momma Shuichi Noshino Yoshinori Takanashi Yasuharu Imai |
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Affiliation: | (1) Department of Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical College, 8-1 Kawada-cho, Shinjuku-ku, 162 Tokyo, Japan;(2) Department of Pediatric Cardiac Surgery, The Heart Institute of Japan, Tokyo Women's Medical College, 8-1 Kawada-cho, Shinjuku-ku, 162 Tokyo, Japan |
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Abstract: | Summary We reviewed the clinical records of 185 patients who were possible candidates for Fontan operation. We did this to clarify whether all patients with suitable anomalies ultimately underwent a Fontan operation. Of the 152 patients with decreased pulmonary blood flow, 38 (26%) did not fulfill the criteria for Fontan operation, and 17 of the 33 patients (52%) with increased pulmonary blood flow (P<0.01) were excluded as candidates. Of 48 non-candidate survivors, 19 had high pulmonary artery (PA) pressure or resistance and small PA (which we term “poor PA”), 17 had pulmonary hypertension, 6 had a markedly distorted PA, and 6 had severe ventricular dysfunction. A significant proportion of possible candidates with a suitable anomaly ultimately did not undergo a Fontan operation, because of “poor PA”, a congenital condition that precluded Fontan operation. |
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Keywords: | Fontan candidate Pulmonary artery Palliative operation Catheterization Strategy for Fontan operation |
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