Effect of Anesthesia in the Ante- and Intranatal Periods of Development on the Cognitive Status of Children Aged from 0 to 3 Years
- Authors: Aleksandrovich Y.S.1, Gorkovaya I.A.1, Miklyaeva A.V.2
-
Affiliations:
- Saint Petersburg State Pediatric Medical University
- Herzen State Pedagogical University of Russia
- Issue: Vol 75, No 5 (2020)
- Pages: 532-540
- Section: PEDIATRICS: CURRENT ISSUES
- URL: https://ogarev-online.ru/vramn/article/view/125715
- DOI: https://doi.org/10.15690/vramn1391
- ID: 125715
Cite item
Full Text
Abstract
The article presents the results of a systematic review of publications aimed at analizing the effects of anesthesia during ante- and intranatal periods of development on the cognitive status of infants and young children. The search for publications was carried out by analyzing electronic bibliographic databases Web of Science and PubMed. The analysis revealed five factors, which determine the effects of ante- and intranatal anesthesia on the cognitive development of children: the type of anesthesia, the type of anesthetic, the period of child’s development, the frequency and duration of exposure as well as the dosage and concentration of the substance. Such cognitive functions as memory, learning ability, speech, perceptual processes and motor activity as a predictor for intelligence formation in early childhood are the most vulnerable to the effects of ante- and intranatal anesthesia. The analysis led to the conclusion that regional anesthesia is the safest option of analgesia for operative delivery and non-surgical operations in pregnant women (in terms of the risks of neurocognitive development disorders in children). In the case of general anesthesia, the lowest risks of negative consequences for cognitive status of a child during early childhood are associated with the exposure of sevoflurane.
Keywords
Full Text
##article.viewOnOriginalSite##About the authors
Yury S. Aleksandrovich
Saint Petersburg State Pediatric Medical University
Author for correspondence.
Email: jalex1963@mail.ru
ORCID iD: 0000-0002-2131-4813
SPIN-code: 2225-1630
MD, PhD, Professor
Russian Federation, Saint PetersburgIrina A. Gorkovaya
Saint Petersburg State Pediatric Medical University
Email: iralgork@mail.ru
ORCID iD: 0000-0002-1488-4746
SPIN-code: 1604-2157
PhD in Psychological Sciences, Professor
Russian Federation, Saint PetersburgAnastasia V. Miklyaeva
Herzen State Pedagogical University of Russia
Email: a.miklyaeva@gmail.com
ORCID iD: 0000-0001-8389-2275
SPIN-code: 9471-8985
PhD in Psychological Sciences, Associate Professor
Russian Federation, Saint PetersburgReferences
- Белов А.В., Пырегов А.В., Хапчаев И.Ю. Неакушерские операции в акушерстве. Анестезия, принципы ведения, риски // Тольяттинский медицинский консилиум. — 2017. — № 5–6. — С. 59–62. [Belov AV, Pyregov AV, Hapchaev IYu. Neakusherskie operacii v akusherstve. Anesteziya, principy vedeniya, riski. Tol’yattinskij medicinskij konsilium. 2017;(5–6):59–62. (In Russ.)]
- Loftis GK, Collins SB, McDowell M. Anesthesia-induced neuronal apoptosis during synaptogenesis: a review of the literature. AANA J. 2012;80(4):291–298.
- Satomoto M. Postoperative Cognitive Function Following General Anesthesia in Children. In: Cascella M. (ed.) General Anesthesia Research. Neuromethods. 2020;150:159–166. doi: https://doi.org/10.1007/978-1-4939-9891-3_10
- Perna RB, Loughan AR, Le JA, Hertza J. Prenatal and Perinatal Anesthesia and the Long-Term Cognitive Sequelae: A Review. Applied Neuropsychology: Child. 2015;4(1):65–71. doi: https://doi.org/10.1080/21622965.2013.779275
- Ikonomidou C, Bosch F, Miksa M, et al. Blockade of NMDA Receptors and Apoptotic Neurodegeneration in the Developing Brain. Science. 1999;283(5398):70–74. doi: https://doi.org/10.1126/science.283.5398.70
- Andropoulos DB. Effect of Anesthesia on the Developing Brain: Infant and Fetus. Fetal Diagn Ther. 2018;43(1):1–11. doi: https://doi.org/10.1159/000475928
- Ikonomidou C, Bittigau P, Koch C, et al. Neurotransmitters and apoptosis in the developing brain. Biochem Pharmacol. 2001;62:401–405. doi: https://doi.org/10.1016/s0006-2952(01)00696-7
- Sun L. Early childhood general anaesthesia exposure and neurocognitive development. Br J Anaesth. 2010;105:i61–i68. doi: https://doi.org/10.1093/bja/aeq302
- Disma N, Clunies-Ross N, Chalkiadis GA. Is spinal anaesthesia in young infants really safer and better than general anaesthesia? Curr Opin Anaesthesiol. 2018;31(3):302–307. doi: https://doi.org/10.1097/ACO.0000000000000578
- Пантелеева М.В., Овезов А.М., Котов А.С., и др. Послеоперационная когнитивная дисфункция у детей (обзор литературы) // Русский медицинский журнал. — 2018. — № 9. — С. 52–56. [Panteleeva MV, Ovezov AM, Kotov AS, et al. Postoperative cognitive dysfunction in children (Literature review). Russian Medical Journal. 2018;9:52–56. (In Russ.)]
- Коттрелл Д.Е. Этот хрупкий мозг — очень юный и старый // Анестезиология и реаниматология. — 2012. — № 4. — С. 5–12. [Cottrell DE. Fragile brain — the very young and the old. Russian Journal of Anaesthesiology and Reanimatology. 2012;4:5–12. (In Russ.)]
- Mandim BLS. Review of Anesthesia for Non-Obstetrical Surgery during Pregnancy. J Community Med Health Educ. 2015;5:346. doi: https://doi.org/10.4172/2161-0711.1000346
- Diana P, Joksimovic SM, Faisant A, Jevtovic-Todorovic V. Early exposure to general anesthesia impairs social and emotional development in rats. Mol Neurobiol. 2020;57(1):41–50. doi: https://doi.org/10.1007/s12035-019-01755-x
- Zou X, Patterson TA, Divine RL, et al. Prolonged exposure to ketamine increases neurodegeneration in the developing monkey brain. International Journal of Developmental Neuroscience. 2009;27:727–731. doi: https://doi.org/10.1016/j.ijdevneu.2009.06.010
- Рязанова О.В., Александрович Ю.С., Пшениснов К.В. Влияние анестезии при оперативном родоразрешении на неврологический статус новорожденного // Регионарная анестезия и лечение острой боли. — 2012. — Т. 6. — № 3. — С. 38–43. [Ryazanova OV, Aleksandrovich YuS, Pshenisnov KV. Effect of anesthesia on neurological status of newborn in abdominal delivery. Regional Anesthesia and Acute Pain Management Journal. 2012;6(3):38–43. (In Russ.)]
- Александрович Ю.С., Рязанова О.В., Муриева Э.А., и др. Влияние анестезии при абдоминальном родоразрешении на неврологический статус новорожденного в раннем неонатальном периоде // Анестезиология и реаниматология. — 2011. — № 1. — С. 15–18. [Aleksandrovich YuS, Ryazanova OV, Murieva EA, et al. Vliyanie anestezii pri abdominal’nom rodorazreshenii na nevrologicheskij status novorozhdennogo v rannem neonatal’nom periode. Anesteziologiya i Reanimatologiya. 2011;1:15–18. (In Russ.)]
- Sprung J, Flick RP, Wilder RT, et al. Anesthesia for cesarean delivery and learning disabilities in a population-based birth cohort. Anesthesiology. 2009;111(2):302–310. doi: https://doi.org/10.1097/ALN.0b013e3181adf481
- Algert CS, Bowen JR, Warwick BG, et al. Regional block versus general anaesthesia for caesarean section and neonatal outcomes: a population-based. Study. BMC Medicine. 2009;7:20. doi: https://doi.org/10.1186/1741-7015-7-20
- Yahalom B, Athiraman U, Soriano SG, et al. Spinal anesthesia in infant rats: development of a model and assessment of neurologic outcomes. Anesthesiology. 2011;114(6):1325–1335. doi: https://doi.org/10.1097/ALN.0b013e31821b5729
- Golub MS, Germann SL. Perinatal bupivacaine and infant behavior in rhesus monkeys. Neurotoxicol Teratol. 1998;20(1):29–41. doi: https://doi.org/10.1016/s0892-0362(97)00068-8
- Sepkoski CM, Lester BM, Ostheimer GW, Brazelton TB. The effects of maternal epidural anesthesia on neonatal behavior during the first month. Dev Med Child Neurol. 1992;34(12):1072–1080. doi: https://doi.org/10.1111/j.1469-8749.1992.tb11419.x
- Abd-Elsayed AA, Díaz-gómez J, Barett G, et al. A case series discussing the anaesthetic management of pregnant patients with brain tumours. F1000Research. 2013;2:92. doi: https://doi.org/10.12688/f1000research.2-92.v2
- Bacon RC, Razis PA. The effect of propofol sedation in pregnancy on neonatal condition. Anaesthesia. 1994;49(12):1058–1060. doi: https://doi.org/10.1111/j.1365-2044.1994.tb04356.x
- Aydin GB, Coskun F, Sahin A, Aypar U. Influence of sevoflurane and desflurane on neurological and adaptive capacity scores in newborns. Saudi Med J. 2008;29(6):841–846
- Xiong M, Li J, Alhashem HM, et al. Propofol exposure in pregnant rats induces neurotoxicity and persistent learning deficit in the offspring. Brain Sci. 2014;4(2):356–375. doi: https://doi.org/10.3390/brainsci4020356
- Zhong L, Luo F, Zhao W, et al. Propofol exposure during late stages of pregnancy impairs learning and memory in rat offspring via the BDNF-TrkB signalling pathway. J Cell Mol Med. 2016;20(10):1920–1931. doi: https://doi.org/10.1111/jcmm.12884
- Chen D, Qi X, Zhuang R, et al. Prenatal propofol exposure downregulates NMDA receptor expression and causes cognitive and emotional disorders in rats. Eur J Pharmacol. 2019;843:268–276. doi: https://doi.org/10.1016/j.ejphar.2018.11.032
- Song R, Xiaomin L, Mengyuan P, et al. Maternal Sevoflurane Exposure Causes Abnormal Development of Fetal Prefrontal Cortex and Induces Cognitive Dysfunction in Offspring. Stem Cells International. 2017;2017:11. doi: https://doi.org/10.1155/2017/6158468
- Chai D, Yan J, Li C, et al. Sevoflurane inhibits neuronal migration and axon growth in the developing mouse cerebral cortex. Aging (Albany NY). 2020;12(7):6436–6455. doi: https://doi.org/10.18632/aging.103041
- Xu L, Xu Q, Xu F, et al. MicroRNA-325-3p prevents sevoflurane-induced learning and memory impairment by inhibiting Nupr1 and C/EBPβ/IGFBP5 signaling in rats. Aging (Albany NY). 2020;12(6):5209–5220. doi: https://doi.org/10.18632/aging.102942
- Chung W, Yoon S, Shin YS. Multiple exposures of sevoflurane during pregnancy induces memory impairment in young female offspring mice. Korean J Anesthesiol. 2017;70(6):642–647. doi: https://doi.org/10.4097/kjae.2017.70.6.642
- Yang T, Zhuang L, Rei Fidalgo AM, et al. Xenon and sevoflurane provide analgesia during labor and fetal brain protection in a perinatal rat model of hypoxia-ischemia. PLoS One. 2012;7(5):e37020. doi: https://doi.org/10.1371/journal.pone.0037020
- Velly LJ, Canas PT, Guillet BA, et al. Early anesthetic preconditioning in mixed cortical neuronal-glial cell cultures subjected to oxygen-glucose deprivation: the role of adenosine triphosphate dependent potassium channels and reactive oxygen species in sevoflurane-induced neuroprotection. Anesth Analg. 2009;108(3):955–963. doi: https://doi.org/10.1213/ane.0b013e318193fee7
- Luo F, Hu Y, Zhao W, et al. Maternal Exposure of Rats to Isoflurane during Late Pregnancy Impairs Spatial Learning and Memory in the Offspring by Up-Regulating the Expression of Histone Deacetylase 2. PLoS One. 2016;11(8):e0160826. doi: https://doi.org/10.1371/journal.pone.0160826
- Rizzi S, Carter LB, Ori C, Jevtovic-Todorovic V. Clinical anesthesia causes permanent damage to the fetal guinea pig brain. Brain Pathol. 2008;18(2):198–210. doi: https://doi.org/10.1111/j.1750-3639.2007.00116.x
- Li Y, Lianga G, Wangab S, et al. Effects of fetal exposure to isoflurane on postnatal memory and learning in rats. Neuropharmacology. 2007;53(8):942–950. doi: https://doi.org/10.1016/j.neuropharm.2007.09.005
- Zou S, Wei ZZ, Yue Y, et al. Desflurane and Surgery Exposure During Pregnancy Decrease Synaptic Integrity and Induce Functional Deficits in Juvenile Offspring Mice. Neurochem Res. 2020;45 (2):418–427. doi: https://doi.org/10.1007/s11064-019-02932-z
- Paule MG, Li M, Allen RR, et al. Ketamine anesthesia during the first week of life can cause long-lasting cognitive deficits in rhesus monkeys. Neurotoxicology and Teratology. 2011;33:220–230. doi: https://doi.org/10.1016/j.ntt.2011.01.001
- Zhao T, Li C, Wei W, et al. Prenatal ketamine exposure causes abnormal development of prefrontal cortex in rat. Sci Rep. 2016;6:26865. doi: https://doi.org/10.1038/srep26865
- Fujinaga M, Baden JM. Methionine prevents nitrous-oxide induced teratogenicity in rat embryos grown in culture. Anesthesiology. 1994;81:184–189. doi: https://doi.org/10.1097/00000542-199407000-00025
- Vallejo MC, Zakowski MI. Pro-Con Debate: Nitrous Oxide for Labor Analgesia. Biomed Res Int. 2019;2019:4618798. doi: https://doi.org/10.1155/2019/4618798
- Liu J, Zhao Y, Yang J, et al. Neonatal repeated exposure to isoflurane not sevoflurane in mice reversibly impaired spatial cognition at juvenile-age. Neurochemical Research. 2017;42(2):595–605. doi: https://doi.org/10.1007/s11064-016-2114-7
- Kodama M, Satoh Y, Otsubo Y, et al. Neonatal desflurane exposure induces more robust neuroapoptosis than do isoflurane and sevoflurane and impairs working memory. Anesthesiology. 2011;115:979–991. doi: https://doi.org/10.1097/ALN.0b013e318234228b
- Satomoto M, Satoh Y, Terui K, et al. Neonatal exposure to sevoflurane induces abnormal social behaviors and deficits in fear conditioning in mice. Anesthesiology. 009;110:628–637. doi: https://doi.org/10.1097/ALN.0b013e3181974fa2
- Block R, Magnotta V, Bayman E, et al. Are Anesthesia and Surgery During Infancy Associated with Decreased White Matter Integrity and Volume During Childhood? Anesthesiology. 2017;127(5):788–799. doi: https://doi.org/10.1097/ALN.0000000000001808
- Stratmann G, Lee J, Sall JW, et al. Effect of general anesthesia in infancy on long-term recognition memory in humans and rats. Neuropsychopharmacology. 2014;39:2275–2287. doi: https://doi.org/10.1038/npp.2014.134
- Vutskits L, Davidson A. Update on developmental anesthesia neurotoxicity. Curr Opin Anaesthesiol. 2017;30(3):337–342. doi: https://doi.org/10.1097/ACO.0000000000000461
- Block RI, Thomas JJ, Bayman EO, et al. Are anesthesia and surgery during infancy associated with altered academic performance during childhood? Anesthesiology. 2012;117(3):494–503. doi: https://doi.org/10.1097/ALN.0b013e3182644684
- Bartels M, Althoff RR, Boomsma DI. Anesthesia and cognitive performance in children: no evidence for a causal relationship. Twin. Res. Hum. Genet. 2009;12(3):246–253. doi: https://doi.org/10.1375/twin.12.3.246
- Sun LS, Li G, Miller TL, et al. Association between a single general anesthesia exposure before age 36 months and neurocognitive outcomes in later childhood. JAMA. 2016;315:2312–2320. doi: https://doi.org/10.1001/jama.2016.6967
- Kalkman CJ, Peelen L, Moons KG, et al. Behavior and development in children and age at the time of first anesthetic exposure. Anesthesiology. 2009;110(4):805–812. doi: https://doi.org/10.1097/ALN.0b013e31819c7124
- Jevtovic-Todorovic V. Exposure of Developing Brain to General Anesthesia: What Is the Animal Evidence? Anesthesiology. 2018;128(4):832–839. doi: https://doi.org/10.1097/ALN.0000000000002047
- Creeley C., Dikranian G., Dissen L. et al. Propofol-induced apoptosis of neurones and oligodendrocytes in fetal and neonatal rhesus macaque brain. British Journal of Anaesthesia. 2013;110(1):i29–i38. doi: https://doi.org/10.1093/bja/aet173
- Van der Veeken L, Van der Merwe J, Devroe S, et al. Maternal surgery during pregnancy has a transient adverse effect on the developing fetal rabbit brain. Am J Obstet Gynecol. 2019;221(4):355.e1–355.e19. doi: https://doi.org/10.1016/j.ajog.2019.07.029
- Davidson AJ, Disma N, de Graaff JC, et al. Neurodevelopmental outcome at 2 years of age after general anaesthesia and awake-regional anaesthesia in infancy (GAS): an international multicentre, randomised controlled trial. Lancet. 2016;387:239–250. doi: https://doi.org/10.1016/S0140-6736(15)00608-X
- Diana P, Joksimovic SM, Faisant A, Jevtovic-Todorovic V. Early exposure to general anesthesia impairs social and emotional development in rats. Mol Neurobiol. 2020;57(1):41–50. doi: https://doi.org/10.1007/s12035-019-01755-x
- Zhang Q, Luo F, Zhao W. et al. Effect of prolonged anesthesia with propofol during early pregnancy on cognitive function of offspring rats. Chinese Journal of Anesthesiology. 2014;34(9):1051–1053. doi: https://doi.org/10.1111/jcmm.13524
- Brambrink AM, Evers AS, Avidan MS, et al. Ketamine-induced neuroapoptosis in the fetal and neonatal rhesus macaque brain. Anesthesiology. 2012;116(2):372–384. doi: https://doi.org/10.1097/ALN.0b013e318242b2cd
- Yu Z, Wang J, Wang H, et al. Effects of Sevoflurane Exposure During Late Pregnancy on Brain Development and Beneficial Effects of Enriched Environment on Offspring Cognition. Cell Mol Neurobiol. 2020:1–14. doi: https://doi.org/10.1007/s10571-020-00821-6
- Lu Y, Huang Y, Jiang J, et al. Neuronal apoptosis may not contribute to the long-term cognitive dysfunction induced by a brief exposure to 2% sevoflurane in developing rats. Biomed Pharmacother. 2016;78:322–328. doi: https://doi.org/10.1016/j.biopha.2016.01.034
- Wu Z, Zhang Y, Yang X, Zhao P. Maternal Treadmill Exercise Reduces the Neurotoxicity of Prenatal Sevoflurane Exposure in Rats via Activation of p300 Histone Acetyltransferase. Neurochem Res. 2020;45(7):1626–1635. doi: https://doi.org/10.1007/s11064-020-03023-0
- Noguchi KK, Johnson SA, Dissen GA, et al. Isoflurane exposure for three hours triggers apoptotic cell death in neonatal macaque brain. British Journal of Anaesthesia. 2017;119(3):524–531. doi: https://doi.org/10.1093/bja/aex123
- Wang S, Peretich K, Zhao Y, et al. Anesthesia-Induced Neurodegeneration in Fetal Rat Brains. Pediatr Res. 2009;66:435–440. doi: https://doi.org/10.1203/PDR.0b013e3181b3381b
- Suehara T, Morishita J, Ueki M, et al. Effects of sevoflurane exposure during late pregnancy on brain development of offspring mice. Pediatric Anaesthesia. 2016;26:52–59. doi: https://doi.org/10.1111/pan.12785
- Wilder RT, Flick RP, Sprung J, et al. Early exposure to anesthesia and learning disabilities in a population-based birth cohort. Anesthesiology. 2009;110(4):796–804. doi: https://doi.org/10.1097/01.anes.0000344728.34332.5d
- Sprung J, Flick RP, Katusic SK, et al. Attention-deficit/hyperactivity disorder after early exposure to procedures requiring general anesthesia. Mayo Clin Proc. 2012;87(2):120–129. doi: https://doi.org/10.1016/j.mayocp.2011.11.008
- Flick RP, Katusic SK, Colligan RC, et al. Cognitive and behavioral outcomes after early exposure to anesthesia and surgery Pediatrics. 2011;128(5):e1053–e1061. doi: https://doi.org/10.1542/peds.2011-0351
- Wu Z, Li X, Zhang Y, et al. Effects of Sevoflurane Exposure During Mid-Pregnancy on Learning and Memory in Offspring Rats: Beneficial Effects of Maternal Exercise. Frontiers in Cellular Neuroscience. 2018;12:122. doi: https://doi.org/10.3389/fncel.2018.00122
- Shen F-Y, Song Y-C, Guo F, et al. Cognitive Impairment and Endoplasmic Reticulum Stress Induced by Repeated Short-Term Sevoflurane Exposure in Early Life of Rats. Front. Psychiatry. 2018;9:332. doi: https://doi.org/10.3389/fpsyt.2018.00332
- Fang F, Song R, Ling X, et al. Multiple sevoflurane anesthesia in pregnant mice inhibits neurogenesis of fetal hippocampus via repressing transcription factor Pax6. Life Sciences. 2017;175:16–22. doi: https://doi.org/10.1016/j.lfs.2017.03.003
- Bellinger DC. What is an adverse effect? A possible resolution of clinical and epidemiological perspectives on neurobehavioral toxicity. Environ Res. 2004;95(3):394–405. doi: https://doi.org/10.1016/j.envres.2003.07.013
Supplementary files
