• Pediatr Crit Care Me · Jul 2013

    Clinical Trial

    Sildenafil exposure and hemodynamic effect after stage II single-ventricle surgery.

    • Kevin D Hill, Robert D Tunks, Piers C A Barker, Daniel K Benjamin, Michael Cohen-Wolkowiez, Gregory A Fleming, Matthew Laughon, and Jennifer S Li.
    • Department of Pediatrics, Duke University Medical Center, Durham, NC, USA. kevin.hill@duke.edu
    • Pediatr Crit Care Me. 2013 Jul 1; 14 (6): 593600593-600.

    ObjectivesTo determine sildenafil exposure and hemodynamic effect in children after stage II single-ventricle surgery.DesignProspective, dose escalation trial.SettingSingle-center, pediatric catheterization laboratory.PatientsTwelve children poststage II single-ventricle surgical palliation and undergoing elective cardiac catheterization: median age 1.9 years (range, 0.8, 4.0), weight 11 kg (8, 13), nine females, and 10 with a single right ventricle.InterventionsCatheterization and echocardiography performed before and immediately after single-dose IV sildenafil (0.125, 0.25, 0.35, or 0.45 mg/kg over 20 min).MeasurementsPeak sildenafil and desmethyl sildenafil concentration, change in hemodynamic parameters measured by cardiac catheterization and echocardiography including indexed pulmonary vascular resistance, and myocardial performance.Main ResultsMaximum sildenafil concentrations ranged from 92 to 775 ng/mL and were above the in vitro threshold needed for 77% phosphodiesterase type 5 (PDE-5) inhibition in 80% of subjects and 90% inhibition in 80% of subjects with doses ≥0.35 mg/kg. Sildenafil lowered pulmonary vascular resistance index in all 12 subjects (median pulmonary vascular resistance index 2.2 [range, 1.6, 7.9]; decreased to 1.7 [1.2, 5.4] WU × m; p < 0.01) with no dose-response effect. Sildenafil improved pulmonary blood flow (+8% [0, 20], p = 0.04) and saturations (+2% [0, 16], p = 0.04) in those with baseline pulmonary vascular resistance index ≥ 2 WU × m (n = 7). Change in saturations correlated inversely with change in pulmonary vascular resistance index (r = 0.74, p < 0.01). Sildenafil also lowered mean blood pressure (-12% [-20, +10]; p = 0.04). There was no change in cardiac index and no effect on myocardial performance. There were no adverse events.ConclusionsSildenafil demonstrated nonlinear exposure with high interindividual variability but was well tolerated and effectively lowered pulmonary vascular resistance index in all subjects. Sildenafil did not acutely improve myocardial performance or increase cardiac index.

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