Literature DB >> 17497125

Prolonged exposure to inhaled nitric oxide does not affect haemostasis in piglets.

Johanna Albert1, Piotr Harbut, Stanisław Zieliński, Stanisław Ryniak, Caroline Gillis-Haegerstrand, Robert Lindwall, Leszek Solski, Jon O Lundberg, Jan Svensson, Waldemar Goździk.   

Abstract

OBJECTIVE: To examine possible adverse effects on haemostasis from prolonged exposure to inhaled nitric oxide (iNO). DESIGN AND
SETTING: Blinded, randomised, experimental animal study in a university animal laboratory.
INTERVENTIONS: Anaesthetised and intubated piglets received central venous, arterial, and transabdominal urinary catheters. Twelve piglets were studied with triggered pressure support ventilation breathing with an air-oxygen mixture for 30 h with nitric oxide (NO), 40 parts per million (ppm) (n = 6) or without NO gas (n = 6) added. The tests of platelet function were assessed in a separate 1-h experiment in which 12 additional animals were blindly randomised to receive intravenous acetylsalicylic acid (ASA) (n = 7) or placebo (n = 5). MEASUREMENTS AND
RESULTS: All 12 animals were clinically stable during the study period of 30 h. Haemostasis was assessed in terms of bleeding time and platelet function by Adeplat-S, reflecting platelet adhesion. Prothrombin fragment 1 + 2, fibrin D-dimer, tissue plasminogen activator and prothrombin complex were measured to investigate whether inhaled NO (iNO) had any effects on thrombin formation, fibrin formation, fibrinolysis or coagulation. All parameters including bleeding time and Adeplat-S were unaffected by iNO. ASA significantly increased bleeding time, but did not affect Adeplat-S. Nitrate in plasma and NOx (nitrate and nitrite) in urine increased significantly in pigs receiving iNO compared with controls.
CONCLUSIONS: Prolonged exposure to iNO at 40[Symbol: see text]ppm did not affect bleeding time or coagulation parameters in healthy piglets. The findings do not support the hypothesis that iNO increases the risk of bleeding in humans.

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Year:  2007        PMID: 17497125     DOI: 10.1007/s00134-007-0666-3

Source DB:  PubMed          Journal:  Intensive Care Med        ISSN: 0342-4642            Impact factor:   17.440


  38 in total

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Review 2.  Nitrosylation. the prototypic redox-based signaling mechanism.

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3.  Inhaled nitric oxide in full-term and nearly full-term infants with hypoxic respiratory failure.

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5.  Routine template bleeding time determinations before cardiac procedures.

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6.  Bleeding time prolongation and NO inhalation.

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8.  Reduction of nitrite to nitric oxide during ischemia protects against myocardial ischemia-reperfusion damage.

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9.  Lung physiology and histopathology during cumulated exposure to nitric oxide in combination with assisted ventilation in healthy piglets.

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10.  Effects of inhaled nitric oxide compared with aspirin on platelet function in vivo in healthy subjects.

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2.  Effects of inhaled nitric oxide on hemostasis in healthy adults treated with heparin: a randomized, controlled, blinded crossover study.

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3.  A Comparative Study of Inhaled Nitric Oxide and an Intravenously Administered Nitric Oxide Donor in Acute Pulmonary Hypertension.

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4.  Organ dysfunction among piglets treated with inhaled nitric oxide and intravenous hydrocortisone during prolonged endotoxin infusion.

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