PEDIATRICS Vol. 102 No. 6 December 1998, pp. 1390-1393
Received Jan 8, 1998; accepted May 26, 1998.
, **,
, 
,
,
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From the Divisions of * Newborn Medicine and
Developmental
and Newborn Biology, the Departments of § Anesthesia,
Laboratory
Medicine and Pathology, ¶ Cardiology, and # Neurology, Children's
Hospital; the Departments of ** Newborn Medicine and 
Anesthesia,
Brigham and Women's Hospital, Harvard Medical School; and the
§§ Department of Biostatistics, Harvard School of Public Health,
Boston, Massachusetts.
Objective. To investigate the effect of inhaled nitric oxide (NO) treatment in newborns with persistent pulmonary hypertension on adenosine 5'-diphosphate (ADP)-dependent platelet activation.
Methods. After parental informed consent, infants with persistent pulmonary hypertension of the newborn were randomly assigned to receive conventional treatment (control group) or treatment with 40 parts per million of inhaled NO. Platelet activation was measured at time of entry and 30 minutes later by surface expression of P-selectin in response to increasing concentrations of the agonist ADP (0, 2, 5, 10, and 20 µM) using fluorescence-activated flow cytometry.
Results. We examined 11 infants in the inhaled NO group and 13 in the control group. P-selectin expression, quantified as mean fluorescence, was not significantly different in the two groups of patients at baseline. Median percent change from baseline fluorescence was assessed using the Wilcoxon matched-pairs signed-rank test. At 30 minutes after enrollment there were no statistically significant changes from baseline fluorescence in either group of patients and at all ADP concentrations.
Conclusion. Thirty minutes of exposure to 40 ppm of inhaled NO does not inhibit ADP-dependent platelet activation as measured by surface expression of P-selectin in infants with persistent pulmonary hypertension of the newborn. Key words: platelet function, bleeding, hemostasis.
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