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POSTOPERATIVE COGNITIVE DYSFUNCTION – WHAT WE KNOW AND WHERE WE GO

https://doi.org/10.21292/2078-5658-2019-16-1-19-28

Abstract

The authors reviewed the literature and presented results of their own research of post-operative cognitive dysfunction confirming its social importance. The development of post-operative cognitive dysfunction is to be perceived as a real fact despite the differences in the published epidemiological data. Currently, there are no grounds to correlate it directly with the general anesthesia given to patients, and there is no evidence that a certain method of anesthesia or a certain drug can reduce the frequency of post-operative clinical decline. There are numerous factors within genesis of post-operative cognitive decline and they are not studied well. All suspected mechanisms (neurotoxicity of the used agents, and other factors of anesthesia and surgery; impairment of information neuro-transmission mechanisms; neuroinflammation developing as a response to trauma) can initiate the complex neuro-physiological reactions causing cognitive dysfunction.

The authors presented experimental data about morphofunctional changes in neurons and cerebellar cortex microglia after laparotomy and anesthesia with sevoflurane followed by the exposure to it in a special box for 6 hours (induction of 8 vol. % with the air flow of 2 l/min., maintaining 2 vol. % of sevoflurane with the air flow of 1 l/min.). They demonstrated that neuroinflammation was not the key factor of the detected neuronal damage. Purkinje neurons were damaged the most, since they were fairy sensitive to energy metabolic disorders, promoting the death of other neurons of the molecular layer. Neurons of the granular layer with the low level of energy metabolism were the most resistant to the impact provided by surgery/anesthesia. These data confirmed the importance of multifactorial approach when assessing the genesis of cognitive dysfunction. This research is to be continued and aimed to find out predictors of post-operative cognitive decline and to optimize anaesthesiologic support of surgery and other invasive interventions to provide a balance between their aggressiveness and effectiveness of protection, especially in senile patients who already have some cognitive dysfunctions. 

About the Authors

Yu. S. Polushin
Pavlov First Saint Petersburg State Medical University
Russian Federation

Doctor of Medical Sciences, Professor, RAS Academician, Head of Anesthesiology and Intensive Care Department, Head of Research Clinical Center of Anesthesiology and Intensive Care, Vice Rector for Research,

St. Petersburg



A. Yu. Polushin
Pavlov First Saint Petersburg State Medical University
Russian Federation

Candidate of Medical Sciences, Assistant of Neurology Department, Neurologist of Raisa Gorbacheva Memorial Research Institute of Children Oncology, Hematology and Transplantation,

St. Petersburg



G. Yu. Yukina
Pavlov First Saint Petersburg State Medical University
Russian Federation

Candidate of Biological Sciences, Head of Pathoanatomy Laboratory within Pathology Department of Research Center, Associate Professor of Histology Department,

St. Petersburg



M. V. Kozhemyakina
Pavlov First Saint Petersburg State Medical University
Russian Federation

Anesthesiologist and Intensive Physician of Anesthesiology and Intensive Care Department of Research Clinical Center of Anesthesiology and Intensive Care,

St. Petersburg



References

1. Belozertseva I.V., Dravolina O.А., Krivov V.O. et al. Postoperative behavioral changes in the rats after anesthesia with sevoflurane. Vestnik Anesteziologii I Reanimatologii, 2017, vol. 14, no. 2, pp. 55-62. (In Russ.)

2. Belozertseva I.V., Dravolina O.А., Krivov V.O. et al. Experimental simulation of post-operative cognitive dysfunctions in rats. Vestnik Anesteziologii I Reanimatologii, 2016, vol. 13, no. 5, pp. 37-49. (In Russ.)

3. Yukina G.Yu., Belozertseva I.V., Polushin Yu.S. et al. Structural and functional changes in hippocampus neurons during anesthesia with sevoflurane (experimental research). Vestnik Anesteziologii I Reanimatologii, 2017, vol. 14, no. 6, pp. 72. (In Russ.)

4. Yukina G.Yu., Belozertseva I.V., Polushin А.Yu. et al. Morpho-functional changes of pyramidal neurons of CA1 and CA4 hippocampal fields during anesthesia with sevoflurane. Morphologiya, 2018, vol. 153, no. 3, pp. 327. (In Russ.)

5. Alam A., Hana Z., Jin Z. et al. Surgery, neuroinflammation and cognitive impairment. E. BioMedicine, 2018, vol. 37, pp. 547-556.

6. Avidan M.S., Evers A.S. The fallacy of persistent postoperative cognitive decline. Anesthesiology, 2016, vol. 124, no. 2, pp. 255-258.

7. Baloyannis S.J. Dendritic and spinal pathology of the Purkinje cells from the human cerebellar vermis in Alzheimer's disease. Psychiatr. Danub., 2013, vol. 25, no. 3, pp. 221-226.

8. Bedford P.D. Adverse cerebral effects of anaesthesia on old people. Lancet, 1955, vol. 6, no. 269, pp. 259-263.

9. Block M.L., Zecca L., Hong J.S. Microglia-mediated neurotoxicity: uncovering the molecular mechanisms. Nature Reviews Neuroscience, 2007, vol. 8, no. 1, pp. 57-69.

10. Buckner R.L. The cerebellum and cognitive function: 25 years of insight from anatomy and neuroimaging. Neuron, 2013, vol. 30, no. 80 (3), pp. 807–815. doi: 10.1016/j.neuron.2013.10.044

11. Cosmo G.D., Sessa F., Fiorini F. et al. Postoperative cognitive dysfunction in elderly patients: a frequent complication. J. Anesth. Crit. Care, 2015, Open Access 2(2): 00048. doi: 10.15406/jaccoa.2015.02.00048

12. Detweiler M.B. Postoperative cognitive dysfunction: what anesthesiologists know that would benefit geriatric specialists. J. Geriatr. Med. Gerontol., 2018, vol. 4, is. 1, pp. 1-5. doi: 10.23937/2469-5858/1510038]

13. Dokkedal U., Hansen T.G., Rasmussen L.S. et al. Cognitive functioning after surgery in middle-aged and elderly danish twins. Anesthesiology, 2016, vol. 124, no. 2, pp. 312-321.

14. Ekdahl C.T., Claasen J.H., Bonde S. et al. Inflammation is detrimental for neurogenesis in adult brain. Proc. Natl. Acad. Sci., USA, 2003, vol. 11, no. 23, pp. 13632-13637.

15. Girard T.D., Jackson J.C., Pandharipande P.P. et al. Delirium as a predictor of long-term cognitive impairment in survivors of critical illness. Crit. Care Med., 2010, vol. 38, pp. 1513-1520.

16. Gonzalez H., Elgueta D., Montoya A. et al. Neuroimmune regulation of microglial activity involved in neuroinflammation and neurodegenerative diseases. J. Neuroimmunol., 2014, vol. 274, no. 1-2, pp. 1-13.

17. Graeber M.B., Streit W.J. Microglia: biology and pathology. Acta Neuropathol., 2010, vol. 119, pp. 89-105.

18. Hashem M.D., Nallagangula A., Nalamalapu S. et al. Patient outcomes after critical illness: a systematic review of qualitative studies following hospital discharge. Crit. Care, 2016, vol. 20, pp. 345, DOI 10.1186/s13054-016-1516-x.

19. Hopkins R.O., Weaver L.K., Pope D. et al. Neuropsychological sequelae and impaired health status in survivors of severe acute respiratory distress syndrome. Am. J. Respir. Crit. Care Med., 1999, vol. 160, pp. 50-56.

20. Hopkins R.O., Suchyta M.R., Snow G.L. et al. Blood glucose dysregulation and cognitive outcome in ARDS survivors. Brain Inj., 2010, vol. 24, pp. 1478-1484.

21. Iwashyna T.J., Ely E.W., Smith D M. et al. Long-term cognitive impairment and functional disability among survivors of severe sepsis. JAMA, 2010, no. 304, pp. 1787-1794.

22. Koziol L.F., Budding D., Andreasen N. et al. Consensus paper: the cerebellum's role in movement and cognition. Cerebellum, 2014, vol. 13, no. 1, pp. 151-177.

23. Lyman M., Lloyd D.G., Ji X. et al. Neuroinflammation: the role and consequences. Neurosci. Res., 2014, vol. 79, pp. 1-12.

24. Maldonado J.R. Neuropathogenesis of delirium: review of current etiologic theories and common pathways. Am. J. Geriatr. Psychiatry, 2013, vol. 21, is. 12, pp. 1190-1222.

25. Marshall S.A., McClain J.A., Kelso M.L. et al. Microglial activation is not equivalent to neuroinflammation in alcohol-induced neurodegeneration: The importance of microglia phenotype. Neurobiol. Dis., 2013, vol. 54, pp. 239-251.

26. Micha G., Tzimas P., Zalonis I. et al. Propofol vs Sevoflurane anaesthesia on postoperative cognitive dysfunction in the elderly. A randomized controlled trial. Acta Anaesthesiol. Belg., 2016, vol. 67, no. 3, pp. 129-137.

27. Miller D., Lewis S.R., Pritchard M.W., Schofield-Robinson O.J. et al. Intravenous versus inhalational maintenance of anaesthesia for postoperative cognitive outcomes in elderly people undergoing non-cardiac surgery. Cochrane Database Syst. Rev., 2018, vol. 21, CD012317. doi: 10.1002/14651858. CD012317.pub2.

28. Moller J.T., Cluitmans P., Rasmussen L.S. et al. Longterm postoperative cognitive dysfunction in the elderly ISPOCD1 study. ISPOCD investigators. International study of post-operative cognitive dysfunction. Lancet, 1998, vol. 21, no. 351 (9106), pp. 857-861.

29. Monk T.G, Weldon B.C., Garvan C.W. et al. Predictors of cognitive dysfunction after major noncardiac surgery. Anesthesiology, 2008, vol. 108, no. 1, pp. 18-30.

30. Needham D.M. Improving long-term outcomes after discharge from intensive care unit: report from a stakeholders’ conference. Crit. Care Med., 2012, vol. 40, pp. 502-509.

31. Pandharipande P.P., Girard T.D., Jackson J.C. et al. Long-term cognitive impairment after critical illness. N. Engl. J. Med., 2013, vol. 369, pp. 1306-1316.

32. Plaschke K., Muller A.K., Kopitz J. Surgery-induced changes in rat IL-1beta and acetylcholine metabolism: role of physostigmine. Clin. Exp. Pharmacol. Physiol., 2014, vol. 41, no. 9, pp. 663-670.

33. Pouzat C., Hestrin S. Developmental regulation of basket/stellate cells – Purkinje cell synapses in the cerebellum. J. Neurosci., 1997, vol. 17, no. 23, pp. 9104-9112.

34. Ratzer M., Romano E., Elklit A. Posttraumatic stress disorder in patients following intensive care unit treatment: a review of studies regarding prevalence and risk factors. J. Trauma Treat., 2014, vol. 3, is. 2. pp. 1-15.

35. Schmahmann J.D., Caplan D. Cognition, emotion and the cerebellum. Brain. 2006, vol. 129, no. 2, pp. 341-347.

36. Serhan C.N., Chiang N., Van Dyke T.E. Resolving inflammation: dual anti-inflammatory and pro-resolution lipid mediators. Nature Reviews Immunology, 2008, vol. 8, no. 5, pp. 349-361.

37. Silbert B., Evered L., Scott D.A. Cognitive decline in the elderly: is anaesthesia implicated?. Best. Pract. Res. Clin. Anaesthesiol., 2011, vol. 25, no. 3, pp. 379-393.

38. Silbert B.S., Evered L.A., Scott D.A. Incidence of postoperative cognitive dysfunction after general or spinal anaesthesia for extracorporeal shock wave lithotripsy. Br. J. Anaesth., 2014, vol. 113, no. 5, pp. 784-791.

39. Sokolov A.A., Miall R.C., Ivry R.B. The Cerebellum: adaptive prediction for movement and cognition. Trends Cogn Sci., 2017, vol. 21, no. 5, pp. 313–332. doi: 10.1016/j.tics.2017.02.005. Epub 2017 Apr 3.

40. Sprung J., Roberts R.O., Weingarten T.N. et al. Postoperative delirium in elderly patients is associated with subsequent cognitive impairment. Br. J. Anaesth., 2017, vol. 119, no. 2, pp. 316-323.

41. Szokol J.W. Postoperative cognitive dysfunction. Revista Mexicana de Anestesiología, 2010, vol. 33, suppl. 1, pp. 249-253.

42. Vizcaychipi M.P. Post-оperative сognitive dysfunction: рre-оperative risk assessment and peri-operative risk minimization: а pragmatic review of the literature. J. Intens. Crit. Care, 2016, vol. 2, no. 2, pp. 13.

43. Wake H., Moorhouse A.J., Jinno S. et al. Resting microglia directly monitor the functional state of synapses in vivo and determine the fate of ischemic terminals. J. Neurosci., 2009, vol. 29, pp. 3974-3980.

44. Wang W., Wang Y., Wu H. et al. Postoperative cognitive dysfunction: current developments in mechanism and prevention. Med. Sci. Monit., 2014, no. 20, pp. 1908-1912.

45. Weiser T.G., Haynes A.B., Molina G. et al. Estimate of the global volume of surgery in 2012: an assessment supporting improved health outcomes. Lancet, 2015, vol. 27, no. 385 (suppl. 2), pp. 11-13.

46. Yang J.J., Zuo Zh. Neuroinflammation and postoperative cognitive dysfunction: what do we know? J. Anesth. Perioper. Med., 2016, vol. 3, no. 2, pp. 53-56.

47. Zhang Y., Shan G.J., Zhang Y.X. et al. Propofol compared with sevoflurane general anaesthesia is associated with decreased delayed neurocognitive recovery in older adults. Brit. J. Anaesthesia, 2018, vol. 121, no. 3, pp. 595–604. doi: 10.1016/j.bja.2018.05.059.

48. Zhao Y., Huang L., Xu H. et al. Neuroinflammation induced by surgery does not impair the reference memory of young adult mice. Mediators of Inflammation, 2016, Article ID 3271579, 8 pages http://dx.doi.org/10.1155/2016/3271579.

49. Zhou Z., Ma D. Anaesthetics-induced neurotoxicity in developing brain: an update on preclinical evidence. Brain Sci., 2014, vol. 4, no. 1, pp. 136–149. https://doi.org/10.3390/brainsci4010136.

50. Zhu J., Jiang X., Shi E. et al. Sevoflurane preconditioning reverses impairment of hippocampal long-term potentiation induced by myocardial ischaemia-reperfusion injury. Eur. J. Anaesthesiol., 2009, vol. 26, pp. 961-968.


Review

For citations:


Polushin Yu.S., Polushin A.Yu., Yukina G.Yu., Kozhemyakina M.V. POSTOPERATIVE COGNITIVE DYSFUNCTION – WHAT WE KNOW AND WHERE WE GO. Messenger of ANESTHESIOLOGY AND RESUSCITATION. 2019;16(1):19-28. (In Russ.) https://doi.org/10.21292/2078-5658-2019-16-1-19-28



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