Skip to main content Accessibility help
×
Home
Hostname: page-component-55597f9d44-mm7gn Total loading time: 0.719 Render date: 2022-08-14T12:56:17.191Z Has data issue: true Feature Flags: { "shouldUseShareProductTool": true, "shouldUseHypothesis": true, "isUnsiloEnabled": true, "useRatesEcommerce": false, "useNewApi": true } hasContentIssue true

Chapter 2 - Developmental Cerebrovascular Physiology

Published online by Cambridge University Press:  02 November 2018

Sulpicio G. Soriano
Affiliation:
Boston Children’s Hospital
Craig D. McClain
Affiliation:
Boston Children’s Hospital
Get access

Summary

Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2018

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bruins, B, Kilbaugh, TJ, Margulies, SS, Friess, SH. The anesthetic effects on vasopressor modulation of cerebral blood flow in an immature swine model. Anesth Analg. 2013;116(4):838–44.CrossRefGoogle Scholar
Vavilala, MS, Lee, LA, Lam, AM. The lower limit of cerebral autoregulation in children during sevoflurane anesthesia. J Neurosurg Anesthesiol. 2003;15(4): 307–12.CrossRefGoogle ScholarPubMed
Brady, KM, Mytar, JO, Lee, JK, Cameron, DE, Vricella, LA, Thompson, WR, et al. Monitoring cerebral blood flow pressure autoregulation in pediatric patients during cardiac surgery. Stroke. 2010;41(9): 1957–62.CrossRefGoogle ScholarPubMed
Brady, KM, Lee, JK, Kibler, KK, Easley, RB, Koehler, RC, Czosnyka, M, et al. The lower limit of cerebral blood flow autoregulation is increased with elevated intracranial pressure. Anesth Analg. 2009;108(4): 1278–83.CrossRefGoogle ScholarPubMed
Nusbaum, D, Clark, J, Brady, K, Kibler, K, Sutton, J, Easley, RB. Alteration in the lower limit of autoregulation with elevations in cephalic venous pressure. Neurol Res. 2014;36(12): 1063–71.CrossRefGoogle ScholarPubMed
Kochanek, PM, Carney, N, Adelson, PD, Ashwal, S, Bell, MJ, Bratton, S, et al. Guidelines for the acute medical management of severe traumatic brain injury in infants, children, and adolescents—second edition. Pediatr Crit Care Med. 2012;13(suppl 1):S182.CrossRefGoogle ScholarPubMed
Armstead, WM, Riley, J, Vavilala, MS. Dopamine prevents impairment of autoregulation after traumatic brain injury in the newborn pig through inhibition of up-regulation of endothelin-1 and extracellular signal-regulated kinase mitogen-activated protein kinase. Pediatr Crit Care Med. 2013;14(2):e10311.CrossRefGoogle ScholarPubMed
Armstead, WM, Riley, J, Vavilala, MS. Preferential protection of cerebral autoregulation and reduction of hippocampal necrosis with norepinephrine after traumatic brain injury in female piglets. Pediatr Crit Care Med. 2016;17(3):e1307.CrossRefGoogle ScholarPubMed
Armstead, WM, Kiessling, JW, Riley, J, Kofke, WA, Vavilala, MS. Phenylephrine infusion prevents impairment of ATP- and calcium-sensitive potassium channel-mediated cerebrovasodilation after brain injury in female, but aggravates impairment in male, piglets through modulation of ERK MAPK upregulation. J Neurotrauma. 2011;28(1): 105–11.CrossRefGoogle ScholarPubMed
Guerra, SD, Carvalho, LF, Affonseca, CA, Ferreira, AR, Freire, HB. Factors associated with intracranial hypertension in children and teenagers who suffered severe head injuries. J Pediatr (Rio J). 2010;86(1):73–9.CrossRefGoogle ScholarPubMed
Phillips, AA, Chan, FH, Zheng, MM, Krassioukov, AV, Ainslie, PN. Neurovascular coupling in humans: physiology, methodological advances and clinical implications. J Cereb Blood Flow Metab. 2016;36(4): 647–64.CrossRefGoogle ScholarPubMed
Oshima, T, Karasawa, F, Satoh, T. Effects of propofol on cerebral blood flow and the metabolic rate of oxygen in humans. Acta Anaesthesiol Scand. 2002;46(7):831–5.CrossRefGoogle ScholarPubMed
Tasker, RC. Intracranial pressure and cerebrovascular autoregulation in pediatric critical illness. Semin Pediatr Neurol. 2014;21(4): 255–62.CrossRefGoogle ScholarPubMed
van de Ven, KC, van der Graaf, M, Tack, CJ, Heerschap, A, de Galan, BE. Steady-state brain glucose concentrations during hypoglycemia in healthy humans and patients with type 1 diabetes. Diabetes. 2012;61(8):1974–7.CrossRefGoogle ScholarPubMed
Pryds, O, Greisen, G, Friis-Hansen, B. Compensatory increase of CBF in preterm infants during hypoglycaemia. Acta Paediatr Scand. 1988;77(5): 632–7.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×