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DOI: 10.1055/s-0038-1632368
Illness Severity Predicts Death and Brain Injury in Asphyxiated Newborns Treated with Hypothermia
Funding Pia Wintermark receives research grant funding from the FRSQ Clinical Research Scholar Career Award Junior 2, and the New Investigator Research Grant from the SickKids Foundation and the CIHR Institute of Human Development, Child and Youth Health (IHDCYH).Publication History
06 November 2017
16 January 2018
Publication Date:
16 February 2018 (online)
Abstract
Objective To determine if illness severity during the first days of life predicts adverse outcome in asphyxiated newborns treated with hypothermia.
Study Design We conducted a retrospective cohort study of asphyxiated newborns treated with hypothermia. Illness severity was calculated daily during the first 4 days of life using the Score for Neonatal Acute Physiology II (SNAP-II score). Adverse outcome (death and/or brain injury) was recorded. Differences in SNAP-II scores between the newborns with and without adverse outcome were assessed.
Result 214 newborns were treated with hypothermia. The average SNAP-II score over the first 4 days of life was significantly worse in newborns developing adverse outcome. The average SNAP-II score was an excellent predictor of death (area under the curve [AUC]: 0.93; p < 0.001) and a fair predictor of adverse outcome (AUC: 0.73; p < 0.001). The average SNAP-II score remained a significant predictor of adverse outcome (odds ratio [95% confidence interval]: 1.08 [1.04–1.12]; p < 0.001), after adjusting for baseline characteristics, degree of initial asphyxial event, and initial severity of encephalopathy.
Conclusion In asphyxiated newborns treated with hypothermia, not only the initial asphyxial event but also the illness severity during the first days of life was a significant predictor of death or brain injury.
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References
- 1 Graham EM, Ruis KA, Hartman AL, Northington FJ, Fox HE. A systematic review of the role of intrapartum hypoxia-ischemia in the causation of neonatal encephalopathy. Am J Obstet Gynecol 2008; 199 (06) 587-595
- 2 Jacobs SE, Berg M, Hunt R, Tarnow-Mordi WO, Inder TE, Davis PG. Cooling for newborns with hypoxic ischaemic encephalopathy. Cochrane Database Syst Rev 2013; 1 (01) CD003311
- 3 Shah PS, Ohlsson A, Perlman M. Hypothermia to treat neonatal hypoxic ischemic encephalopathy: systematic review. Arch Pediatr Adolesc Med 2007; 161 (10) 951-958
- 4 Richardson D, Tarnow-Mordi WO, Lee SK. Risk adjustment for quality improvement. Pediatrics 1999; 103 (1, Suppl E): 255-265
- 5 Richardson DK, Corcoran JD, Escobar GJ, Lee SK. SNAP-II and SNAPPE-II: simplified newborn illness severity and mortality risk scores. J Pediatr 2001; 138 (01) 92-100
- 6 Zupancic JA, Richardson DK, Horbar JD, Carpenter JH, Lee SK, Escobar GJ. ; Vermont Oxford Network SNAP Pilot Project Participants. Revalidation of the Score for Neonatal Acute Physiology in the Vermont Oxford Network. Pediatrics 2007; 119 (01) e156-e163
- 7 Dammann O, Naples M, Bednarek F. , et al; ELGAN Study Investigators. SNAP-II and SNAPPE-II and the risk of structural and functional brain disorders in extremely low gestational age newborns: the ELGAN study. Neonatology 2010; 97 (02) 71-82
- 8 Chien LY, Whyte R, Thiessen P, Walker R, Brabyn D, Lee SK. ; Canadian Neonatal Network. Snap-II predicts severe intraventricular hemorrhage and chronic lung disease in the neonatal intensive care unit. J Perinatol 2002; 22 (01) 26-30
- 9 Skarsgard ED, MacNab YC, Qiu Z, Little R, Lee SK. ; Canadian Neonatal Network. SNAP-II predicts mortality among infants with congenital diaphragmatic hernia. J Perinatol 2005; 25 (05) 315-319
- 10 Nakwan N, Nakwan N, Wannaro J. Predicting mortality in infants with persistent pulmonary hypertension of the newborn with the Score for Neonatal Acute Physiology-Version II (SNAP-II) in Thai neonates. J Perinat Med 2011; 39 (03) 311-315
- 11 Nasr A, Langer JC. ; Canadian Pediatric Surgery Network. Influence of location of delivery on outcome in neonates with congenital diaphragmatic hernia. J Pediatr Surg 2011; 46 (05) 814-816
- 12 Mattia FR, deRegnier RA. Chronic physiologic instability is associated with neurodevelopmental morbidity at one and two years in extremely premature infants. Pediatrics 1998; 102 (03) E35
- 13 ter Horst HJ, Jongbloed-Pereboom M, van Eykern LA, Bos AF. Amplitude-integrated electroencephalographic activity is suppressed in preterm infants with high scores on illness severity. Early Hum Dev 2011; 87 (05) 385-390
- 14 Lam JC, Claydon J, Mitton CR, Skarsgard ED. A risk-adjusted study of outcome and resource utilization for congenital diaphragmatic hernia. J Pediatr Surg 2006; 41 (05) 883-887
- 15 Logan JW, Dammann O, Allred EN. , et al; ELGAN Study Investigators. Early postnatal illness severity scores predict neurodevelopmental impairments at 10 years of age in children born extremely preterm. J Perinatol 2017; 37 (05) 606-614
- 16 Morse S, Groer M, Shelton MM, Maguire D, Ashmeade T. A systematic review: the utility of the revised version of the score for neonatal acute physiology among critically ill neonates. J Perinat Neonatal Nurs 2015; 29 (04) 315-344
- 17 Shankaran S, Laptook AR, Ehrenkranz RA. , et al; National Institute of Child Health and Human Development Neonatal Research Network. Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy. N Engl J Med 2005; 353 (15) 1574-1584
- 18 Shankaran S, Pappas A, McDonald SA. , et al; Eunice Kennedy Shriver NICHD Neonatal Research Network. Childhood outcomes after hypothermia for neonatal encephalopathy. N Engl J Med 2012; 366 (22) 2085-2092
- 19 Sarnat HB, Sarnat MS. Neonatal encephalopathy following fetal distress. A clinical and electroencephalographic study. Arch Neurol 1976; 33 (10) 696-705
- 20 al Naqeeb N, Edwards AD, Cowan FM, Azzopardi D. Assessment of neonatal encephalopathy by amplitude-integrated electroencephalography. Pediatrics 1999; 103 (6 Pt 1): 1263-1271
- 21 Gluckman PD, Wyatt JS, Azzopardi D. , et al. Selective head cooling with mild systemic hypothermia after neonatal encephalopathy: multicentre randomised trial. Lancet 2005; 365 (9460): 663-670
- 22 Barkovich AJ, Hajnal BL, Vigneron D. , et al. Prediction of neuromotor outcome in perinatal asphyxia: evaluation of MR scoring systems. Am J Neuroradiol 1998; 19 (01) 143-149
- 23 Chalak LF, Tarumi T, Zhang R. The “neurovascular unit approach” to evaluate mechanisms of dysfunctional autoregulation in asphyxiated newborns in the era of hypothermia therapy. Early Hum Dev 2014; 90 (10) 687-694
- 24 Rosenberg AA. Regulation of cerebral blood flow after asphyxia in neonatal lambs. Stroke 1988; 19 (02) 239-244
- 25 Dammann O, Allred EN, Kuban KC. , et al; Developmental Epidemiology Network. Systemic hypotension and white-matter damage in preterm infants. Dev Med Child Neurol 2002; 44 (02) 82-90
- 26 Limperopoulos C, Bassan H, Kalish LA. , et al. Current definitions of hypotension do not predict abnormal cranial ultrasound findings in preterm infants. Pediatrics 2007; 120 (05) 966-977
- 27 Perlman JM. Pathogenesis of hypoxic-ischemic brain injury. J Perinatol 2007; 27: S39-S46
- 28 Kasdorf E, Perlman JM. Strategies to prevent reperfusion injury to the brain following intrapartum hypoxia-ischemia. Semin Fetal Neonatal Med 2013; 18 (06) 379-384
- 29 Tashima L, Nakata M, Anno K, Sugino N, Kato H. Prenatal influence of ischemia-hypoxia-induced intrauterine growth retardation on brain development and behavioral activity in rats. Biol Neonate 2001; 80 (01) 81-87
- 30 Li Y, Gonzalez P, Zhang L. Fetal stress and programming of hypoxic/ischemic-sensitive phenotype in the neonatal brain: mechanisms and possible interventions. Prog Neurobiol 2012; 98 (02) 145-165
- 31 Ma Q, Zhang L. Epigenetic programming of hypoxic-ischemic encephalopathy in response to fetal hypoxia. Prog Neurobiol 2015; 124: 28-48
- 32 Phan Duy A, El Khabbaz F, Renolleau C. , et al. Intrauterine growth retardation and the developing brain [in French]. Arch Pediatr 2013; 20 (09) 1034-1038
- 33 Pollack MM, Koch MA, Bartel DA. , et al. A comparison of neonatal mortality risk prediction models in very low birth weight infants. Pediatrics 2000; 105 (05) 1051-1057
- 34 Miller SP, Ferriero DM, Leonard C. , et al. Early brain injury in premature newborns detected with magnetic resonance imaging is associated with adverse early neurodevelopmental outcome. J Pediatr 2005; 147 (05) 609-616
- 35 Boudes E, Tan X, Saint-Martin C, Shevell M, Wintermark P. MRI obtained during versus after hypothermia in asphyxiated newborns. Arch Dis Child Fetal Neonatal Ed 2015; 100 (03) F238-F242
- 36 Wintermark P, Hansen A, Soul J, Labrecque M, Robertson RL, Warfield SK. Early versus late MRI in asphyxiated newborns treated with hypothermia. Arch Dis Child Fetal Neonatal Ed 2011; 96 (01) F36-F44
- 37 van Laerhoven H, de Haan TR, Offringa M, Post B, van der Lee JH. Prognostic tests in term neonates with hypoxic-ischemic encephalopathy: a systematic review. Pediatrics 2013; 131 (01) 88-98