A randomized and blinded trial of inhaled nitric oxide in a piglet model of pediatric cardiopulmonary resuscitation. (May 2021)

• Record Type: Journal Article
• Authors: Morgan, Ryan W.; Sutton, Robert M.; Himebauch, Adam S.; Roberts, Anna L.; Landis, William P.; Lin, Yuxi; Starr, Jonathan; Ranganathan, Abhay; Delso, Nile; Mavroudis, Constantine D.; Volk, Lindsay; Slovis, Julia; Marquez, Alexandra M.; Nadkarni, Vinay M.; Hefti, Marco; Berg, Robert A.; Kilbaugh, Todd J.
• Is Part Of: Resuscitation. Volume 162(2021)
• Page Start: 274
• Page End: 283
• Publication Date: 2021-05
• Subjects: In-hospital cardiac arrest -- Cardiopulmonary resuscitation -- Pediatrics -- Shock -- Pulmonary hypertension -- Inhaled nitric oxide -- Physiology -- Cerebral blood flow -- Hemodynamics -- Laboratory; Resuscitation -- Periodicals; Resuscitation -- Periodicals; Réanimation -- Périodiques; Electronic journals; 616.025
• DOI: 10.1016/j.resuscitation.2021.03.004
• Languages: English
• ISSNs: 0300-9572

Abstract

Abstract: Aim: Inhaled nitric oxide (iNO) during cardiopulmonary resuscitation (CPR) improved systemic hemodynamics and outcomes in a preclinical model of adult in-hospital cardiac arrest (IHCA) and may also have a neuroprotective role following cardiac arrest. The primary objectives of this study were to determine if iNO during CPR would improve cerebral hemodynamics and mitochondrial function in a pediatric model of lipopolysaccharide-induced shock-associated IHCA. Methods: After lipopolysaccharide infusion and ventricular fibrillation induction, 20 1-month-old piglets received hemodynamic-directed CPR and were randomized to blinded treatment with or without iNO (80 ppm) during and after CPR. Defibrillation attempts began at 10 min with a 20-min maximum CPR duration. Cerebral tissue from animals surviving 1-h post-arrest underwent high-resolution respirometry to evaluate the mitochondrial electron transport system and immunohistochemical analyses to assess neuropathology. Results: During CPR, the iNO group had higher mean aortic pressure (41.6 ± 2.0 vs. 36.0 ± 1.4 mmHg; p = 0.005); diastolic BP (32.4 ± 2.4 vs. 27.1 ± 1.7 mmHg; p = 0.03); cerebral perfusion pressure (25.0 ± 2.6 vs. 19.1 ± 1.8 mmHg; p = 0.02); and cerebral blood flow relative to baseline (rCBF: 243.2 ± 54.1 vs. 115.5 ± 37.2%; p = 0.02). Among the 8/10 survivors in each group, the iNO group had higher mitochondrial Complex I oxidative phosphorylation in the cerebral cortex (3.60 [3.56, 3.99] vs. 3.23 [2.44, 3.46] pmol O2 /s mg; p = 0.01) and hippocampus (4.79 [4.35, 5.18] vs. 3.17 [2.75, 4.58] pmol O2 /s mg; p = 0.02). There were no other differences in mitochondrial respiration or brain injury between groups. Conclusions: Treatment with iNO during CPR resulted in superior systemic hemodynamics, rCBF, and cerebral mitochondrial Complex I respiration in this pediatric cardiac arrest model.