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Chapter 19 - Light-Based Assessment of the Brain

from Section 3 - Diagnosis of the Infant with Brain Injury

Published online by Cambridge University Press:  13 December 2017

David K. Stevenson
Affiliation:
Stanford University, California
William E. Benitz
Affiliation:
Stanford University, California
Philip Sunshine
Affiliation:
Stanford University, California
Susan R. Hintz
Affiliation:
Stanford University, California
Maurice L. Druzin
Affiliation:
Stanford University, California
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Publisher: Cambridge University Press
Print publication year: 2017

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References

Jöbsis, FF. Non-invasive, infra-red monitoring of cerebral O2 sufficiency, blood volume, HbO2-Hb shifts and bloodflow. Acta Neurol Scand Suppl 1977; 64: 452–3.Google ScholarPubMed
Andropoulos, DB, Stayer, SA, Diaz, LK, Ramamoorthy, C. Neurological monitoring for congenital heart surgery. Anesth Analg 2004; 99(5): 1365–75.Google Scholar
Hoffman, GM. Neurologic monitoring on cardiopulmonary bypass: what are we obligated to do? Ann Thorac Surg 2006; 81(6): S2373–80.Google Scholar
Meek, JH, Elwell, CE, McCormick, DC, et al. Abnormal cerebral haemodynamics in perinatally asphyxiated neonates related to outcome. Arch Child Fetal Neonatal Ed 1999; 81(2): F110–5.Google ScholarPubMed
Lemmers, PMA, Toet, M, van Schelven, LJ, van Bel, F. Cerebral oxygenation and cerebral oxygen extraction in the preterm infant: the impact of respiratory distress syndrome. Exp Brain Res Exp 2006; 173(3): 458–67.Google Scholar
Benni, PB, Chen, B, Dykes, FD, et al. Validation of the CAS neonatal NIRS system by monitoring vv-ECMO patients: preliminary results. Adv Exp Med Biol 2005; 566: 195201.Google Scholar
Jain, V, Buckley, EM, Licht, DJ, et al. Cerebral oxygen metabolism in neonates with congenital heart disease quantified by MRI and optics. J Cereb Blood Flow Metab 2014; 34(3): 380–8.Google Scholar
Bassan, H, Gauvreau, K, Newburger, JW, et al. Identification of pressure passive cerebral perfusion and its mediators after infant cardiac surgery. Pediatr Res 2005; 57(1):3541.Google Scholar
Menke, J, Voss, U, Möller, G, Jorch, G. Reproducibility of cerebral near infrared spectroscopy in neonates. Biol Neonate 2003; 83(1): 611.Google Scholar
Schneider, A, Minnich, B, Hofstätter, E, et al. Comparison of four near-infrared spectroscopy devices shows that they are only suitable for monitoring cerebral oxygenation trends in preterm infants. Acta Paediatr Oslo Nor 2014; 103(9): 934–8.Google Scholar
Dix, LML, van Bel, F, Baerts, W, Lemmers, PMA. Comparing near-infrared spectroscopy devices and their sensors for monitoring regional cerebral oxygen saturation in the neonate. Pediatr Res 2013; 74(5): 557–63.Google Scholar
McNeill, S, Gatenby, JC, McElroy, S, Engelhardt, B. Normal cerebral, renal and abdominal regional oxygen saturations using near-infrared spectroscopy in preterm infants. J Perinatol 2011; 31(1): 51–7.Google Scholar
Alderliesten, T, Dix, L, Baerts, W, et al. Reference values of regional cerebral oxygen saturation during the first 3 days of life in preterm neonates. Pediatr Res 2016; 79: 5564.CrossRefGoogle ScholarPubMed
Cohen, E, Baerts, W, Alderliesten, T, et al. Growth restriction and gender influence cerebral oxygenation in preterm neonates. Arch Dis Child Fetal Neonatal Ed 2016; 101(2): F156–61.Google Scholar
Lemmers, PM, van Bel, F. Left-to-right differences of regional cerebral oxygen saturation and oxygen extraction in preterm infants during the first days of life. Pediatr Res 2009; 65(2): 226–30.Google Scholar
Grossauer, K, Pichler, G, Schmölzer, G, et al. Comparison of peripheral and cerebral tissue oxygenation index in neonates. Arch Dis Child Fetal Neonatal Ed 2009; 94(2): F156.Google Scholar
Bernal, NP, Hoffman, GM, Ghanayem, NS, Arca, MJ. Cerebral and somatic near-infrared spectroscopy in normal newborns. J Pediatr Surg 2010; 45(6): 1306–10.Google Scholar
Hyttel-Sorensen, S, Pellicer, A, Alderliesten, T, et al. Cerebral near infrared spectroscopy oximetry in extremely preterm infants: phase II randomised clinical trial. BMJ 2015; 350: g7635.Google Scholar
Hou, X, Ding, H, Teng, Y, et al. Research on the relationship between brain anoxia at different regional oxygen saturations and brain damage using near-infrared spectroscopy. Physiol Meas 2007; 28(10): 1251–65.Google Scholar
Kurth, CD, Levy, WJ, McCann, J. Near-infrared spectroscopy cerebral oxygen saturation thresholds for hypoxia-ischemia in piglets. J Cereb Blood Flow Metab Off J Int Soc Cereb Blood Flow Metab 2002; 22(3): 335–41.CrossRefGoogle ScholarPubMed
Dent, CL, Spaeth, JP, Jones, BV, et al. Brain magnetic resonance imaging abnormalities after the Norwood procedure using regional cerebral perfusion. J Thorac Cardiovasc Surg 2005; 130(6): 1523–30.CrossRefGoogle ScholarPubMed
Verhagen, EA, Van Braeckel, KNJA, van der Veere, CN, et al. Cerebral oxygenation is associated with neurodevelopmental outcome of preterm children at age 2 to 3 years. Dev Med Child Neurol 2015; 57(5): 449–55.Google Scholar
Fuchs, H, Lindner, W, Buschko, A, et al. Brain oxygenation monitoring during neonatal resuscitation of very low birth weight infants. J Perinatol Off J Calif Perinat Assoc 2012; 32(5): 356–62.Google Scholar
Binder, C, Urlesberger, B, Avian, A, et al. Cerebral and peripheral regional oxygen saturation during postnatal transition in preterm neonates. J Pediatr 2013; 163(2): 394–9.CrossRefGoogle ScholarPubMed
Fuchs, H, Lindner, W, Buschko, A, et al. Cerebral oxygenation in very low birth weight infants supported with sustained lung inflations after birth. Pediatr Res 2011; 70(2): 176–80.Google Scholar
Brady, KM, Mytar, JO, Lee, JK, et al. Monitoring cerebral blood flow pressure autoregulation in pediatric patients during cardiac surgery. Stroke J Cereb Circ 2010; 41(9): 1957–62.CrossRefGoogle ScholarPubMed
Wong, FY, Leung, TS, Austin, T, et al. Impaired autoregulation in preterm infants identified by using spatially resolved spectroscopy. Pediatrics 2008; 121(3): e604–11.Google Scholar
Eriksen, VR, Hahn, GH, Greisen, G. Cerebral autoregulation in the preterm newborn using near-infrared spectroscopy: a comparison of time-domain and frequency-domain analyses. J Biomed Opt 2015; 20(3): 37009.Google Scholar
Tsuji, M, Saul, JP, du Plessis, A, et al. Cerebral intravascular oxygenation correlates with mean arterial pressure in critically ill premature infants. Pediatrics 2000; 106(4): 625–32.Google Scholar
O’Leary, H, Gregas, MC, Limperopoulos, C, et al. Elevated cerebral pressure passivity is associated with prematurity-related intracranial hemorrhage. Pediatrics 2009; 124(1): 302–9.Google Scholar
Soul, JS, Hammer, PE, Tsuji, M, et al. Fluctuating pressure-passivity is common in the cerebral circulation of sick premature infants. Pediatr Res 2007; 61(4): 467–73.Google Scholar
Chock, VY, Ramamoorthy, C, Van Meurs, KP. Cerebral autoregulation in neonates with a hemodynamically significant patent ductus arteriosus. J Pediatr 2012; 160: 936–42.Google Scholar
Binder-Heschl, C, Urlesberger, B, Schwaberger, B, et al. Borderline hypotension: how does it influence cerebral regional tissue oxygenation in preterm infants? J Matern-Fetal Neonatal Med Off J Eur Assoc Perinat Med Fed Asia Ocean Perinat Soc Int Soc Perinat Obstet 2016; 29(14): 2341–6.Google Scholar
Garner, RS, Burchfield, DJ. Treatment of presumed hypotension in very low birthweight neonates: effects on regional cerebral oxygenation. Arch Dis Child Fetal Neonatal Ed 2013; 98(2): F117–21.Google Scholar
Verhagen, EA, Ter Horst, HJ, Keating, P, et al. Cerebral oxygenation in preterm infants with germinal matrix-intraventricular hemorrhages. Stroke 2010; 41(12): 2901–7.Google Scholar
Sorensen, LC, Maroun, LL, Borch, K, et al. Neonatal cerebral oxygenation is not linked to foetal vasculitis and predicts intraventricular haemorrhage in preterm infants. Acta Paediatr 2008; 97(11): 1539–34.Google Scholar
Alderliesten, T, Lemmers, PMA, Smarius, JJM, et al. Cerebral oxygenation, extraction, and autoregulation in very preterm infants who develop peri-intraventricular hemorrhage. J Pediatr 2013; 162(4):698704.e2.CrossRefGoogle ScholarPubMed
Lemmers, PM, Toet, MC, van Bel, F. Impact of patent ductus arteriosus and subsequent therapy with indomethacin on cerebral oxygenation in preterm infants. Pediatrics 2008; 121(1): 142–7.Google Scholar
Chock, VY, Ramamoorthy, C, Van Meurs, KP. Cerebral oxygenation during different treatment strategies for a patent ductus arteriosus. Neonatology 2011; 100: 233–40.Google Scholar
Underwood, MA, Milstein, JM, Sherman, MP. Near-infrared spectroscopy as a screening tool for patent ductus arteriosus in extremely low birth weight infants. Neonatology 2007; 91(2): 134–9.Google Scholar
Vanderhaegen, J, De Smet, D, Meyns, B, et al. Surgical closure of the patent ductus arteriosus and its effect on the cerebral tissue oxygenation. Acta Paediatr 2008; 97(12): 1640–4.Google Scholar
Meier, SD, Eble, BK, Stapleton, GE, et al. Mesenteric oxyhemoglobin desaturation improves with patent ductus arteriosus ligation. J Perinatol 2006; 26(9): 562–4.Google Scholar
Zaramella, P, Freato, F, Quaresima, V, et al. Surgical closure of patent ductus arteriosus reduces the cerebral tissue oxygenation index in preterm infants: a near-infrared spectroscopy and Doppler study. Pediatr Int 2006; 48(3): 305–12.Google Scholar
Lemmers, PM, Molenschot, MC, Evens, J, et al. Is cerebral oxygen supply compromised in preterm infants undergoing surgical closure for patent ductus arteriosus? Arch Child Fetal Neonatal Ed 2010; 95(6):F429–34.Google Scholar
Bailey, SM, Hendricks-Muñoz, KD, Wells, JT, Mally, P. Packed red blood cell transfusion increases regional cerebral and splanchnic tissue oxygen saturation in anemic symptomatic preterm infants. Am J Perinatol 2010; 27(6): 445–53.Google Scholar
Dani, C, Pratesi, S, Fontanelli, G, et al. Blood transfusions increase cerebral, splanchnic, and renal oxygenation in anemic preterm infants. Transfusion (Paris) 2010; 50(6): 1220–6.Google Scholar
Wardle, SP, Weindling, AM. Peripheral fractional oxygen extraction and other measures of tissue oxygenation to guide blood transfusions in preterm infants. Semin Perinatol 2001; 25(2): 60–4.Google Scholar
van Hoften, JC, Verhagen, EA, Keating, P, et al. Cerebral tissue oxygen saturation and extraction in preterm infants before and after blood transfusion. Arch Child Fetal Neonatal Ed 2011; 95(5): F352–8.Google Scholar
Toet, MC, Lemmers, PM, van Schelven, LJ, van Bel, F. Cerebral oxygenation and electrical activity after birth asphyxia: their relation to outcome. Pediatrics 2006; 117(2): 333–9.Google Scholar
Ancora, G, Maranella, E, Grandi, S, et al. Early predictors of short term neurodevelopmental outcome in asphyxiated cooled infants: a combined brain amplitude integrated electroencephalography and near infrared spectroscopy study. Brain Dev 2013; 35(1): 2631.Google Scholar
Lemmers, PM, Zwanenburg, RJ, Benders, MJ, et al. Cerebral oxygenation and brain activity after perinatal asphyxia: does hypothermia change their prognostic value? Pediatr Res 2013; 74(2): 180–5.Google Scholar
Massaro, AN, Bouyssi-Kobar, M, Chang, T, et al. Brain perfusion in encephalopathic newborns after therapeutic hypothermia. AJNR Am J Neuroradiol 2013; 34(8): 1649–55.Google Scholar
Wintermark, P, Hansen, A, Warfield, SK, et al. Near-infrared spectroscopy versus magnetic resonance imaging to study brain perfusion in newborns with hypoxic-ischemic encephalopathy treated with hypothermia. NeuroImage 2014; 85(1): 287–93.Google Scholar
Peng, S, Boudes, E, Tan, X, et al. Does near-infrared spectroscopy identify asphyxiated newborns at risk of developing brain injury during hypothermia treatment? Am J Perinatol 2015; 32(6): 555–64.Google Scholar
Massaro, AN, Govindan, RB, Vezina, G, et al. Impaired cerebral autoregulation and brain injury in newborns with hypoxic-ischemic encephalopathy treated with hypothermia. J Neurophysiol 2015; 114(2): 818–24.Google Scholar
Shellhaas, RA, Thelen, BJ, Bapuraj, JR, et al. Limited short-term prognostic utility of cerebral NIRS during neonatal therapeutic hypothermia. Neurology 2013; 81(3): 249–55.Google Scholar
Austin, EH 3rd, Edmonds, HLJ, Auden, SM, et al. Benefit of neurophysiologic monitoring for pediatric cardiac surgery. J Thorac Cardiovasc Surg 1997; 114(5): 707–15, 717; discussion 715–6.CrossRefGoogle ScholarPubMed
Sood, ED, Benzaquen, JS, Davies, RR, et al. Predictive value of perioperative near-infrared spectroscopy for neurodevelopmental outcomes after cardiac surgery in infancy. J Thorac Cardiovasc Surg 2013; 145(2): 438–45.e1; discussion 444–5.Google Scholar
Hoffman, GM, Brosig, CL, Mussatto, KA, et al. Perioperative cerebral oxygen saturation in neonates with hypoplastic left heart syndrome and childhood neurodevelopmental outcome. J Thorac Cardiovasc Surg 2013; 146(5): 1153–64.Google Scholar
McQuillen, PS, Hamrick, SEG, Perez, MJ, et al. Balloon atrial septostomy is associated with preoperative stroke in neonates with transposition of the great arteries. Circulation 2006; 113(2): 280–5.Google Scholar
Toet, MC, Flinterman, A, Laar, I, et al. Cerebral oxygen saturation and electrical brain activity before, during, and up to 36 hours after arterial switch procedure in neonates without pre-existing brain damage: its relationship to neurodevelopmental outcome. Exp Brain Res 2005; 165(3): 343–50.CrossRefGoogle ScholarPubMed
Johnson, BA, Hoffman, GM, Tweddell, JS, et al. Near-infrared spectroscopy in neonates before palliation of hypoplastic left heart syndrome. Ann Thorac Surg 2009; 87(2): 571–7.Google Scholar
Papademetriou, MD, Tachtsidis, I, Elliot, MJ, et al. Multichannel near infrared spectroscopy indicates regional variations in cerebral autoregulation in infants supported on extracorporeal membrane oxygenation. J Biomed Opt 2012; 17(6): 067008.Google Scholar
Rhondali, O, Juhel, S, Mathews, S, et al. Impact of sevoflurane anesthesia on brain oxygenation in children younger than 2 years. Paediatr Anaesth 2014; 24(7): 734–40.Google Scholar
Conforti, A, Giliberti, P, Mondi, V, et al. Near infrared spectroscopy: experience on esophageal atresia infants. J Pediatr Surg 2014; 49(7): 1064–8.Google Scholar
Kawamura, T, Kakogawa, J, Takeuchi, Y, et al. Measurement of placental oxygenation by transabdominal near-infrared spectroscopy. Am J Perinatol 2007; 24(3): 161–6.Google Scholar
Arimitsu, T, Uchida-Ota, M, Yagihashi, T, et al. Functional hemispheric specialization in processing phonemic and prosodic auditory changes in neonates. Front Psychol 2011; 2: 202.Google Scholar
Bartocci, M, Bergqvist, LL, Lagercrantz, H, Anand, KJS. Pain activates cortical areas in the preterm newborn brain. Pain 2006; 122(1–2): 109–17.CrossRefGoogle ScholarPubMed
Benaron, DA, Parachikov, IH, Friedland, S, et al. Continuous, noninvasive, and localized microvascular tissue oximetry using visible light spectroscopy. Anesthesiology 2004; 100(6): 1469–75.Google Scholar
Heninger, C, Ramamoorthy, C, Amir, G, et al. Esophageal saturation during antegrade cerebral perfusion: a preliminary report using visible light spectroscopy. Paediatr Anaesth 2006; 16(11): 1133–7.CrossRefGoogle ScholarPubMed

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