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DOI: 10.1055/a-1877-6569
Intrapartum Basal Ganglia–Thalamic Pattern Injury
The comments and criticisms with regard to Smith et al have reference (Buchmann and Bhorat). Buchmann and Bhorat stated that Smith et al “disputes the current belief that the basal ganglia-thalamic (BGT) pattern injury is almost always caused by an often unexpected severe hypoxic–ischemic insult of sudden (or acute) onset lasting more than 10minutes in a previously normoxic foetus and submits that the conclusions drawn by Smith et al rely on faulty interpretation of the literature and deficient research methodology.”[1]
Publikationsverlauf
Eingereicht: 08. März 2022
Angenommen: 03. Juni 2022
Accepted Manuscript online:
16. Juni 2022
Artikel online veröffentlicht:
08. September 2022
© 2022. Thieme. All rights reserved.
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References
- 1 Smith J, Solomons R, Vollmer L. et al. Intrapartum basal ganglia-thalamic pattern injury and radiologically termed “acute profound hypoxic-ischemic brain injury” are not synonymous. Am J Perinatol 2020; (e-pub ahead of print) DOI: 10.1055/s-0040-1721692.
- 2 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
- 3 Janbu T, Nesheim BI. Uterine artery blood velocities during contractions in pregnancy and labour related to intrauterine pressure. Br J Obstet Gynaecol 1987; 94 (12) 1150-1155
- 4 Oosterhof H, Dijkstra K, Aarnoudse JG. Uteroplacental Doppler velocimetry during Braxton Hicks' contractions. Gynecol Obstet Invest 1992; 34 (03) 155-158
- 5 Li H, Gudmundsson S, Olofsson P. Acute increase of umbilical artery vascular flow resistance in compromised fetuses provoked by uterine contractions. Early Hum Dev 2003; 74 (01) 47-56
- 6 Tchirikov M, Eisermann K, Rybakowski C, Schröder HJ. Doppler ultrasound evaluation of ductus venosus blood flow during acute hypoxemia in fetal lambs. Ultrasound Obstet Gynecol 1998; 11 (06) 426-431
- 7 Volpe JJ. Neonatal encephalopathy: an inadequate term for hypoxic-ischemic encephalopathy. Ann Neurol 2012; 72 (02) 156-166
- 8 Gunn AJ, Bennet L. Fetal hypoxia insults and patterns of brain injury: insights from animal models. Clin Perinatol 2009; 36 (03) 579-593
- 9 De Haan HH, Gunn AJ, Williams CE, Gluckman PD. Brief repeated umbilical cord occlusions cause sustained cytotoxic cerebral edema and focal infarcts in near-term fetal lambs. Pediatr Res 1997; 41 (01) 96-104
- 10 McNamara H, Johnson N. The effect of uterine contractions on fetal oxygen saturation. Br J Obstet Gynaecol 1995; 102 (08) 644-647
- 11 Peebles DM, Spencer JA, 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
- 12 Dildy GA, van den Berg PP, Katz M. et al. Intrapartum fetal pulse oximetry: fetal oxygen saturation trends during labor and relation to delivery outcome. Am J Obstet Gynecol 1994; 171 (03) 679-684
- 13 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
- 14 Robertson NJ, Lewis RH, Cowan FM. et al. Early increases in brain myo-inositol measured by proton magnetic resonance spectroscopy in term infants with neonatal encephalopathy. Pediatr Res 2001; 50 (06) 692-700
- 15 Ranck Jr. JB, Windle WF. Brain damage in the monkey, Macaca mulatta, by asphyxia neonatorum. Exp Neurol 1959; 1 (02) 130-154
- 16 Myers RE. Four patterns of perinatal brain damage and their conditions of occurrence in primates. Adv Neurol 1975; 10: 223-234
- 17 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
- 18 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
- 19 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
- 20 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
- 21 Volpe JJ. Hypoxic-ischemic injury in the term infant: pathophysiology. Volpe JJ, Inder TE, Darras BT, de Vries LS, du Plessis AJ, Neil JJ. eds. Volpe's Neurology of the Newborn. Philadelphia, PA: Elsevier; 2018: 500-509
- 22 American College of Obstetricians and Gynecologists; American Academy of Pediatrics. Neonatal Encephalopathy and Neurologic Outcome.. 2nd ed. Chicago, IL: American College of Obstetricians and Gynecologists; 2019
- 23 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
- 24 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