RSS-Feed abonnieren
DOI: 10.1055/s-0040-1721692
Intrapartum Basal Ganglia–Thalamic Pattern Injury and Radiologically Termed “Acute Profound Hypoxic–Ischemic Brain Injury” Are Not Synonymous
Abstract
Objective Human cases of acute profound hypoxic-ischemic (HI) injury (HII), in which the insult duration timed with precision had been identified, remains rare, and there is often uncertainty of the prior state of fetal health.
Study Design A retrospective analysis of 10 medicolegal cases of neonatal encephalopathy-cerebral palsy survivors who sustained intrapartum HI basal ganglia-thalamic (BGT) pattern injury in the absence of an obstetric sentinel event.
Results Cardiotocography (CTG) admission status was reassuring in six and suspicious in four of the cases. The median time from assessment by admission CTG or auscultation to birth was 687.5 minutes (interquartile range [IQR]: 373.5–817.5 minutes), while the median time interval between first pathological CTG and delivery of the infant was 179 minutes (IQR: 137–199.25 minutes). The mode of delivery in the majority of infants (60%) was by unassisted vaginal birth; four were delivered by delayed caesarean section. The median (IQR) interval between the decision to perform a caesarean section and delivery was 169 minutes (range: 124–192.5 minutes).
Conclusion The study shows that if a nonreassuring fetal status develops during labor and is prolonged, a BGT pattern HI injury may result, in the absence of a perinatal sentinel event. Intrapartum BGT pattern injury and radiologically termed “acute profound HI brain injury” are not necessarily synonymous. A visualized magnetic resonance imaging (MRI) pattern should preferably solely reflect the patterns description and severity, rather than a causative mechanism of injury.
Key Points
-
BGT HI injury pattern on MRI may develop in the absence of a perinatal sentinel event.
-
BGT pattern injury may not be synonymous with “acute profound HI brain injury.”
-
MRI pattern and severity thereof should be described rather than a causative mechanism of injury.
Keywords
hypoxic–ischemic encephalopathy - acute profound - basal ganglia thalamus injury pattern - cerebral palsyAuthors' Contribution
J.S., R.S., and R.v.T. contributed to conceptualization, data collection, data analysis and/or data interpretation, drafting, revision, and approval of the final manuscript. L.V., S.A., and J.A. contributed to data collection, data analysis and/or data interpretation, drafting, revision, and approval of the final manuscript. E.J.L. and J.W.L. contributed to data collection, data analysis and/or data interpretation, revision, and approval of the final manuscript.
Note
The study was approved by the Health Research Ethics Committee of Stellenbosch University (HREC no.: C20/02/005).
Publikationsverlauf
Eingereicht: 21. September 2020
Angenommen: 04. November 2020
Artikel online veröffentlicht:
15. Dezember 2020
© 2020. Thieme. All rights reserved.
Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA
-
References
- 1 Lawn JE, Cousens S, Zupan J. Neonatal Survival Steering Team. 4 million neonatal deaths: when? Where? Why?. Lancet 2005; 365 (9462): 891-900
- 2 Lee ACC, Kozuki N, Blencowe H. et al. Intrapartum-related neonatal encephalopathy incidence and impairment at regional and global levels for 2010 with trends from 1990. Pediatr Res 2013; 74 (Suppl. 01) 50-72
- 3 Buchmann EJ, Pattinson RC, Nyathikazi N. Intrapartum-related birth asphyxia in South Africa - Lessons from the first national perinatal care survey. S Afr J Obstet Gynaecol 2003; 9 (01) 12-15
- 4 Grass B, El Shahed A, Ly LG. et al. Therapeutic hypothermia for hypoxic-ischemic encephalopathy after perinatal sentinel events: less brain injury on MRI and improved neurodevelopmental outcome at 18-36 months. J Perinatol 2020; 40 (04) 633-639
- 5 de Vries LS, Groenendaal F. Patterns of neonatal hypoxic-ischaemic brain injury. Neuroradiology 2010; 52 (06) 555-566
- 6 Shankaran S, Laptook AR, McDonald SA. et al. Eunice Kennedy Shriver National Institute of Child Health, and Human Development Neonatal Research Network. Acute perinatal sentinel events, neonatal brain injury pattern, and outcome of infants undergoing a trial of hypothermia for neonatal hypoxic-ischemic encephalopathy. J Pediatr 2017; 180: 275-278.e2
- 7 Okereafor A, Allsop J, Counsell SJ. et al. Patterns of brain injury in neonates exposed to perinatal sentinel events. Pediatrics 2008; 121 (05) 906-914
- 8 Pasternak JF, Gorey MT. The syndrome of acute near-total intrauterine asphyxia in the term infant. Pediatr Neurol 1998; 18 (05) 391-398
- 9 Okumura A, Hayakawa F, Kato T, Kuno K, Watanabe K. Bilateral basal ganglia-thalamic lesions subsequent to prolonged fetal bradycardia. Early Hum Dev 2000; 58 (02) 111-118
- 10 Naeye RL, Lin HM. Determination of the timing of fetal brain damage from hypoxemia-ischemia. Am J Obstet Gynecol 2001; 184 (02) 217-224
- 11 Rennie J, Rosenbloom L. How long have we got to get the baby out? A review of the effects of acute and profound intrapartum hypoxia and ischaemia. Obstet Gynaecol 2011; 13 (03) 169-174
- 12 Pettker CM. Systematic approaches to adverse events in obstetrics, Part II: Event analysis and response. Semin Perinatol 2017; 41 (03) 156-160
- 13 Ranck Jr JB, Windle WF. Brain damage in the monkey, macaca mulatta, by asphyxia neonatorum. Exp Neurol 1959; 1 (02) 130-154
- 14 Myers RE. Four patterns of perinatal brain damage and their conditions of occurrence in primates. Adv Neurol 1975; 10: 223-234
- 15 Gunn AJ, Parer JT, Mallard EC, Williams CE, Gluckman PD. Cerebral histologic and electrocorticographic changes after asphyxia in fetal sheep. Pediatr Res 1992; 31 (05) 486-491
- 16 Mallard EC, Gunn AJ, Williams CE, Johnston BM, Gluckman PD. Transient umbilical cord occlusion causes hippocampal damage in the fetal sheep. Am J Obstet Gynecol 1992; 167 (05) 1423-1430
- 17 Mallard EC, Williams CE, Gunn AJ, Gunning MI, Gluckman PD. Frequent episodes of brief ischemia sensitize the fetal sheep brain to neuronal loss and induce striatal injury. Pediatr Res 1993; 33 (01) 61-65
- 18 Mallard EC, Williams CE, Johnston BM, Gunning MI, Davis S, Gluckman PD. Repeated episodes of umbilical cord occlusion in fetal sheep lead to preferential damage to the striatum and sensitize the heart to further insults. Pediatr Res 1995; 37 (06) 707-713
- 19 Juul SE, Aylward E, Richards T, McPherson RJ, Kuratani J, Burbacher TM. Prenatal cord clamping in newborn Macaca nemestrina: A model of perinatal asphyxia. Dev Neurosci 2007; 29 (4–5): 311-320
- 20 Volpe JJ, Inder T, Darras B. eds. Volpe's Neurology of the Newborn. 6th ed.. Philadelphia, PA: Elsevier; 2018
- 21 Adamson SJ, Alessandri LM, Badawi N, Burton PR, Pemberton PJ, Stanley F. Predictors of neonatal encephalopathy in full-term infants. BMJ 1995; 311 (7005): 598-602
- 22 Nelson DB, Lucke AM, McIntire DD, Sánchez PJ, Leveno KJ, Chalak LF. Obstetric antecedents to body-cooling treatment of the newborn infant. Am J Obstet Gynecol 2014; 211 (02) 155.e1-155.e6
- 23 Trevathan W. Primate pelvic anatomy and implications for birth. Philos Trans R Soc B Biol Sci 1663; 2015: 370
- 24 Executive summary: neonatal encephalopathy and neurologic outcome, second edition. Report of the American College of Obstetricians and Gynecologists' Task Force on Neonatal Encephalopathy. Obstet Gynecol 2014; 123 (04) 896-901
- 25 Windle WF. Brain damage at birth. Functional and structural modifications with time. JAMA 1968; 206 (09) 1967-1972
- 26 Myers RE. Two patterns of perinatal brain damage and their conditions of occurrence. Am J Obstet Gynecol 1972; 112 (02) 246-276
- 27 Novak CM, Eke AC, Ozen M, Burd I, Graham EM. Risk factors for neonatal hypoxic-ischemic encephalopathy in the absence of sentinel events. Am J Perinatol 2019; 36 (01) 27-33
- 28 Kasdorf E, Grunebaum A, Perlman JM. Subacute hypoxia-ischemia and the timing of injury in treatment with therapeutic hypothermia. Pediatr Neurol 2015; 53 (05) 417-421
- 29 MacLennan A. Acute near-total intrauterine asphyxia. Pediatr Neurol 1999; 20 (01) 81-82
- 30 Murray DM, O'Riordan MN, Horgan R, Boylan G, Higgins JR, Ryan CA. Fetal heart rate patterns in neonatal hypoxic-ischemic encephalopathy: relationship with early cerebral activity and neurodevelopmental outcome. Am J Perinatol 2009; 26 (08) 605-612
- 31 Ayres-de-Campos D, Spong CY, Chandraharan E. FIGO Intrapartum Fetal Monitoring Expert Consensus Panel. FIGO consensus guidelines on intrapartum fetal monitoring: cardiotocography. Int J Gynaecol Obstet 2015; 131 (01) 13-24
- 32 Leung AS, Leung EK, Paul RH. Uterine rupture after previous cesarean delivery: maternal and fetal consequences. Am J Obstet Gynecol 1993; 169 (04) 945-950
- 33 Westgate JA, Wibbens B, Bennet L, Wassink G, Parer JT, Gunn AJ. The intrapartum deceleration in center stage: a physiologic approach to the interpretation of fetal heart rate changes in labor. Am J Obstet Gynecol 2007; 197 (03) 236.e1-236.e11
- 34 Peebles DM, Spencer JAD, Edwards AD. et al. Relation between frequency of uterine contractions and human fetal cerebral oxygen saturation studied during labour by near infrared spectroscopy. Br J Obstet Gynaecol 1994; 101 (01) 44-48