par Preiser, Jean-Charles
;De Backer, Daniel
;Debelle, Frédéric
;Vray, Bernard
;Vincent, Jean Louis 
Référence Journal of critical care, 13, 3, page (97-103)
Publication Publié, 1998-09





Référence Journal of critical care, 13, 3, page (97-103)
Publication Publié, 1998-09
Article révisé par les pairs
Résumé : | Purpose: The fate of inhaled nitric oxide (NO) has not been precisely defined in critically ill patients. This study aimed at defining the effects of long-term NO inhalation on circulating NO byproduct levels. Material and Methods: During NO therapy, plasma and urine from 13 critically ill patients were sampled daily for determination of the stable byproducts of NO (nitrite [NO2-] and nitrate [NO3-]. Routine monitoring data included inhaled NO concentration, hemodynamic parameters, arterial blood gases, creatinine clearance, and C-reactive protein. Results: For the first 24 hours of NO inhalation (6.3 ± 1.1 ppm), NO3- plasma concentration increased (from 13.3 ± 5.4 to 52.3 ± 17.6 μmol/L), but NO2- plasma concentration was not affected. The NO3- plasma concentration was correlated with the C-reactive protein level, the inhaled NO concentration. Renal excretion of NO metabolites was unaltered by NO inhalation. The NO3 concentrations returned to baseline when NO therapy was discontinued. Conclusion: Long-term NO inhalation was associated with a consistent increase in the NO3- plasma concentration. NO byproducts may be implicated in the systemic effects associated with this treatment. |