Randomization to a Liberal Versus Conservative Oxygenation Target: Redox Responses in Critically Ill Children.
Journal
Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
ISSN: 1529-7535
Titre abrégé: Pediatr Crit Care Med
Pays: United States
ID NLM: 100954653
Informations de publication
Date de publication:
01 03 2023
01 03 2023
Historique:
pubmed:
3
2
2023
medline:
7
3
2023
entrez:
2
2
2023
Statut:
ppublish
Résumé
Optimal systemic oxygenation targets in pediatric critical illness are unknown. A U-shaped relationship exists between blood oxygen levels and PICU mortality. Redox stress or iatrogenic injury from intensive treatments are potential mechanisms of harm from hyperoxia. To measure biomarkers of oxidative status in children admitted to PICU and randomized to conservative (oxygen-hemoglobin saturation [Sp o2 ] 88-92%) versus liberal (Sp o2 > 94%) peripheral oxygenation targets. Mechanistic substudy nested within the Oxygen in PICU (Oxy-PICU) pilot randomized feasibility clinical trial ( ClinicalTrials.gov : NCT03040570). Three U.K. mixed medical and surgical PICUs in university hospitals. Seventy-five eligible patients randomized to the Oxy-PICU randomized feasibility clinical trial. Randomization to a conservative (Sp o2 88-92%) versus liberal (Sp o2 > 94%) peripheral oxygenation target. Blood and urine samples were collected at two timepoints: less than 24 hours and up to 72 hours from randomization in trial participants (March 2017 to July 2017). Plasma was analyzed for markers of ischemic/oxidative response, namely thiobarbituric acid-reactive substances (TBARS; lipid peroxidation marker) and ischemia-modified albumin (protein oxidation marker). Total urinary nitrate/nitrite was measured as a marker of reactive oxygen and nitrogen species (RONS). Blood hypoxia-inducible factor (HIF)-1a messenger RNA (mRNA) expression (hypoxia response gene) was measured by reverse transcription- polymerase chain reaction. Total urinary nitrate/nitrite levels were greater in the liberal compared with conservative oxygenation group at 72 hours (median difference 32.6 μmol/mmol of creatinine [95% CI 13.7-93.6]; p < 0.002, Mann-Whitney test). HIF-1a mRNA expression was increased in the conservative group compared with liberal in less than 24-hour samples (6.0-fold [95% CI 1.3-24.0]; p = 0.032). There were no significant differences in TBARS or ischemia-modified albumin. On comparing liberal with conservative oxygenation targets, we show, first, significant redox response (increase in urinary markers of RONS), but no changes in markers of lipid or protein oxidation. We also show what appears to be an early hypoxic response (increase in HIF-1a gene expression) in subjects exposed to conservative rather than liberal oxygenation targets.
Identifiants
pubmed: 36728001
doi: 10.1097/PCC.0000000000003175
pii: 00130478-202303000-00017
doi:
Substances chimiques
Biomarkers
0
Nitrates
0
Nitrites
0
Thiobarbituric Acid Reactive Substances
0
Serum Albumin
0
Oxygen
S88TT14065
Banques de données
ClinicalTrials.gov
['NCT03040570']
Types de publication
Randomized Controlled Trial
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e137-e146Subventions
Organisme : Department of Health
Pays : United Kingdom
Informations de copyright
Copyright © 2023 by the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.
Déclaration de conflit d'intérêts
The remaining authors have disclosed that they do not have any potential conflicts of interest. Drs. Jones’, Eaton’s, Ray’s, Harrison’s, and Peters’ institutions received funding from the Great Ormond Street Hospital Children’s Charity. Drs. Jones’ and Harrison’s institutions received funding from the U.K. National Institute for Health Research (NIHR). Dr. Jones was funded by the National Institute for Health Research Academic Clinical Fellowship scheme. Dr. Eaton’s institution received funding from Vitaflo; he disclosed that he is an inventor on a patent licensed to Vitaflo and University College London. Dr. Ray received support for article research from the NIHR Great Ormond Street Hospital Biomedical Research Centre; he disclosed consultancy work with La Roche Ltd. Dr. Grocott disclosed that he is a coinvestigator of the Intensive Care Unit Randomized Trial Comparing Two Approaches to OXygen Therapy (UK-ROX) in critically ill adults. Dr. Griksaitis is part funded though the National Institute for Health Research (NIHR) Senior Investigator scheme and via Southampton NIHR Biomedical Research Centre. Drs. Mouncey’s and Rowan’s institutions received funding from the U.K. NIHR Health Technology Assessment program. Dr. Mouncey received support for article research from the U.K. NIHR. Dr. Peters’ institution received funding from the Pediatric Critical Care Society; he received funding from the U.K. NIHR Health Technology Assessment Program. The remaining authors have disclosed that they do not have any potential conflicts of interest.
Références
Numa A, Aneja H, Awad J, et al.: Admission hyperoxia is a risk factor for mortality in pediatric intensive care. Pediatr Crit Care Med. 2018; 19:699–704
Raman S, Prince NJ, Hoskote A, et al.: Admission Pa o 2 and mortality in critically ill children: A cohort study and systematic review. Pediatr Crit Care Med. 2016; 17:e444–e450
Sznycer-Taub NR, Lowery R, Yu S, et al.: Hyperoxia is associated with poor outcomes in pediatric cardiac patients supported on venoarterial extracorporeal membrane oxygenation. Pediatr Crit Care Med. 2016; 17:350–358
Balcarcel DR, Coates BM, Chong G, et al.: Excessive oxygen supplementation in the first day of mechanical ventilation is associated with multiple organ dysfunction and death in critically ill children. Pediatr Crit Care Med. 2022; 23:89–98
Barrot L, Asfar P, Mauny F, et al.: Liberal or conservative oxygen therapy for acute respiratory distress syndrome. N Engl J Med. 2020; 382:999–1008
Panwar R, Hardie M, Bellomo R, et al.; CLOSE Study Investigators: Conservative versus liberal oxygenation targets for mechanically ventilated patients: A pilot multicenter randomized controlled trial. Am J Respir Crit Care Med. 2016; 193:43–51
Mackle D, Beasley R, Bellomo R, et al.: Conservative oxygen therapy during mechanical ventilation in the ICU. N Engl J Med. 2020; 382:989–998
Girardis M, Busani S, Damiani E, et al.: Effect of conservative vs conventional oxygen therapy on mortality among patients in an intensive care unit the oxygen-icu randomized clinical trial. JAMA. 2016; 316:1583–1589
Schjørring OL, Klitgaard TL, Perner A, et al.: Lower or higher oxygenation targets for acute hypoxemic respiratory failure. N Engl J Med. 2021; 384:1301–1311
Chu DK, Kim LHY, Young PJ, et al.: Mortality and morbidity in acutely ill adults treated with liberal versus conservative oxygen therapy (IOTA): A systematic review and meta-analysis. Lancet. 2018; 391:1693–1705
Valko M, Leibfritz D, Moncol J, et al.: Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol. 2007; 39:44–84
Nathan C, Cunningham-Bussel A: Beyond oxidative stress: An immunologist’s guide to reactive oxygen species. Nat Rev Immunol. 2013; 13:349–361
Zaher TE, Miller EJ, Morrow DMP, et al.: Hyperoxia-induced signal transduction pathways in pulmonary epithelial cells. Free Radic Biol Med. 2007; 42:897–908
Bar-Or D, Bar-Or R, Rael LT, et al.: Oxidative stress in severe acute illness. Redox Biol. 2015; 4:340–345
Wennmalm A, Benthin G, Edlund A, et al.: Metabolism and excretion of nitric oxide in humans: An experimental and clinical study. Circ Res. 1993; 73:1121–1127
Tsukahara H, Hiraoka M, Hori C, et al.: Age-related changes of urinary nitrite/nitrate excretion in normal children. Nephron. 1997; 76:307–309
Jalan R, Schnurr K, Mookerjee RP, et al.: Alterations in the functional capacity of albumin in patients with decompensated cirrhosis is associated with increased mortality. Hepatology. 2009; 50:555–564
Peters MJ, Jones GAL, Wiley D, et al.; Oxy-PICU Investigators for the Paediatric Intensive Care Society Study Group (PICS-SG): Conservative versus liberal oxygenation targets in critically ill children: The randomised multiple-centre pilot Oxy-PICU trial. Intensive Care Med. 2018; 44:1240–1248
Jones GAL, Ramnarayan P, Raman S, et al.; Oxy-PICU Investigators for thePaediatric Intensive Care Society-Study Group (PICS-SG): Protocol for a randomised pilot multiple centre trial of conservative versus liberal oxygenation targets in critically ill children (Oxy-PICU). BMJ Open. 2017; 7:e019253
Bar-Or D, Lau E, Winkler JV: A novel assay for cobalt-albumin binding and its potential as a marker for myocardial ischemia - A preliminary report. J Emerg Med. 2000; 19:311–315
Kikugawa K, Kojima T, Yamaki S, et al.: Interpretation of the thiobarbituric acid reactivity of rat liver and brain homogenates in the presence of ferric ion and ethylenediaminetetraacetic acid. Anal Biochem. 1992; 202:249–255
Miranda KM, Espey MG, Wink DA: A rapid, simple spectrophotometric method for simultaneous detection of nitrate and nitrite. Nitric Oxide Biol Chem. 2001; 5:62–71
R Core Team: R: A language and environment for statistical computing. Vienna, Austria, R Foundation for Statistical Computing. 2021. Available at: http://www.R-project.org . Accessed September 1, 2021
Carr AC, Spencer E, Mackle D, et al.: The effect of conservative oxygen therapy on systemic biomarkers of oxidative stress in critically ill patients. Free Radic Biol Med. 2020; 160:13–18
Parinandi NL, Kleinberg MA, Usatyuk PV, et al.: Hyperoxia-induced NAD(P)H oxidase activation and regulation by MAP kinases in human lung endothelial cells. Am J Physiol Cell Mol Physiol. 2003; 284:L26–L38
Freeman BA, Crapo JD: Hyperoxia increases oxygen radical production in rat lungs and lung mitochondria. J Biol Chem. 1981; 256:10986–10992
Ho YS, Dey MS, Crapo JD: Antioxidant enzyme expression in rat lungs during hyperoxia. Am J Physiol Cell Mol Physiol. 1996; 270:L810–L818
Bhandari V, Elias JA: Cytokines in tolerance to hyperoxia-induced injury in the developing and adult lung. Free Radic Biol Med. 2006; 41:4–18
DeMartino AW, Kim‐Shapiro DB, Patel RP, et al.: Nitrite and nitrate chemical biology and signalling. Br J Pharmacol. 2019; 176:228–245
Mas-Bargues C, Sanz-Ros J, Román-Domínguez A, et al.: Relevance of oxygen concentration in stem cell culture for regenerative medicine. Int J Mol Sci. 2019; 20:1195
Costa NA, Gut AL, Azevedo PS, et al.: Protein carbonyl, but not malondialdehyde, is associated with ICU mortality in patients with septic shock. J Intensive Care Med. 2019; 34:669–673
Bar-Or D, Winkler JV, VanBenthuysen K, et al.: Reduced albumin-cobalt binding with transient myocardial ischemia after elective percutaneous transluminal coronary angioplasty: A preliminary comparison to creatine kinase-MB, myoglobin, and troponin I. Am Heart J. 2001; 141:985–991
Ke Q, Costa M: Hypoxia-inducible factor-1 (HIF-1). Mol Pharmacol. 2006; 70:1469–1480
Weitzberg E, Hezel M, Lundberg JO: Nitrate-nitrite-nitric oxide pathway: Implications for anesthesiology and intensive care. Anesthesiology. 2010; 113:1460–1475
Nagababu E, Ramasamy S, Abernethy DR, et al.: Active nitric oxide produced in the red cell under hypoxic conditions by deoxyhemoglobin-mediated nitrite reduction. J Biol Chem. 2003; 278:46349–46356
Mitchell HH, Shonle HA, Grindley HS: The origin of the nitrates in the urine. J Biol Chem. 1916; 24:461–490
Janero DR: Malondialdehyde and thiobarbituric acid-reactivity as diagnostic indices of lipid peroxidation and peroxidative tissue injury. Free Radic Biol Med. 1990; 9:515–540
Chang I, Thomas K, O’Neill Gutierrez L, et al.: Protocol for a randomized multiple center trial of conservative versus liberal oxygenation targets in critically ill children (Oxy-PICU): Oxygen in pediatric intensive care. Pediatr Crit Care Med. 2022; 23:736–744