Preview

Messenger of ANESTHESIOLOGY AND RESUSCITATION

Advanced search

Dynamics of laboratory markers of systemic inflammation in neurosurgical operations using α-2-adrenoagonists

https://doi.org/10.24884/2078-5658-2023-20-6-19-27

Abstract

The objective was to study the degree of deviations of laboratory parameters of the systemic inflammatory response syndrome (SIRS) under the conditions of modulation of the reactions of the sympathetic nervous system by various α-2-adrenergic receptors during neurosurgical interventions for the removal of the brain tumor of subtentorial localization

Materials and methods. The laboratory data of 179 patients operated for the brain tumor of subtentorial localization were analyzed. The operations were performed under conditions of total intravenous anesthesia. The patients were divided into two groups depending on the α-2-adrenergic agonist used in the structure of the anesthetic aid: clonidine was used in the first group, dexmedetomidine was used in the second group. Laboratory tests included analysis of the levels of cytokines (IL-8, IL-6, IL-10, TNF-α), CRP, fibrinogen. Blood sampling for the study was carried out in five stages: 1 – one day before the operation, 2 – on the day of the operation before the introductory anesthesia, 3 – after the induction anesthesia, 4 – after removal of the tumor (at the stage of hemostasis); 5 – on the first day after surgery.

Results. The dynamics of laboratory parameters were similar in both study groups and reflected the manifestations of the systemic inflammatory response of the body to intracranial intervention. The levels of pro-inflammatory cytokines IL-6, IL-8, TNF-α, and C-reactive protein (CRP) increased in the fourth and fifth stages of the study. The increase in the level of IL-6 and fibrinogen in the fifth stage of the study in the second group was more significant, which was explained by the less pronounced anti-inflammatory effect of dexmedetomidine compared to clonidine.

Conclusions. Changes in laboratory parameters of SIRS as the reaction to surgical intervention on the brain were transient. Under conditions of total intravenous anesthesia with the use of α-2-adrenergic agonists, modulation of the inflammatory response was demonstrated, which ensured adequate consistency of the inflammatory process.

About the Authors

N. A. Lesteva
Polenov Neurosurgical Institute, the branch of the Almazov National Medical Research Centre
Russian Federation

Lesteva Nataliya A. – Cand. of Sci. (Med.), Anesthesiologist-Intensivist, Head of the Department of Anesthesiology and Intensive Care, Leading Research Fellow, Research Laboratory of Neuroprotection and Neurometabolic Disorders

tel.: 702-37-49 ext. 001632

12, Mayakovsky str., Saint Petersburg, 191014



N. V. Dryagina
Polenov Neurosurgical Institute, the branch of the Almazov National Medical Research Centre
Russian Federation

Dryagina Nataliya V. – Cand. of Sci. (Med.), Head of the Clinical and Diagnostic Laboratory with Express Group, Senior Research Fellow of the Group for the Study of Minimal Consciousness

tel.: 702-37-49 ext. 001704

12, Mayakovsky str., Saint Petersburg, 191014



A. N. Kondratiev
Polenov Neurosurgical Institute, the branch of the Almazov National Medical Research Centre
Russian Federation

Kondratiev Anatoli N. – Dr. of Sci. (Med.), Professor, Anesthesiologist-Intensivist, Head of the Research Laboratory of Neuroprotection and Neurometabolic Disorders

tel.: 702-37-49 ext. 001632

12, Mayakovsky str., Saint Petersburg, 191014



References

1. Adzhigaliev R.R., Вautin А.E., Рasyuga V.V. The influence of anesthesia components on systemic inflammatory response during cardiac surgery with cardiopulmonary bypass. Annals of Critical Care, 2019, no. 4, pp. 73–80. (In Russ.) DOI: 10.21320/1818-474X-2019-4-73-80.

2. Arefiev A.M., Kulikov A.S., Kurnosov A.B., Gadzhieva O.A., Lubnin A.Yu.. Dexmedetomidine infusion for prevention of hypertension and agitation during awakening after transsphenoidal resection of pituitary adenoma. Russian Journal of Anaesthesiology and Reanimatology, 2020, no. 6, pp. 30–36. (In Russ.) DOI: 10.17116/anaesthesiology202006130.

3. Balandina E.V., Volchkov V.A., Boyarkin A.A., Nefedov A.V, Kovalev S.V. Intraoperative use of clonidine and dexmedetomidine for prevention of early postoperative neurocognitive disorders after coronary artery bypass surgery. Russian Journal of Anaesthesiology and Reanimatology, 2020, no. 4, pp. 42–47. (In Russ.) DOI: 10.17116/anaesthesiology202004142.

4. Berikashvili L.B., Kadantseva K.K., Ermokhina N.V. et al. Postoperative neurocognitive disorders: the legacy of almost 400 years of history (review). General Reanimatology, 2023, vol. 19, no. 4, pp. 29–42. (In Russ.) DOI: 10.15360/1813-9779-2023-4-29-42.

5. Berlinskiy V.V., Naleev A.A., Kuznetsova O.V. Peculiarities of the course of the postoperative period depending on the method of general аnesthesia. Anaesthesiology and reanimatology, 2012, no. 1, pp. 24–27. (In Russ.)

6. Borisov K.Yu., Moroz V.V., Grebenchikov O.A. et al. Effect of propofol on sevoflurane-induced myocardial preconditioning in the experiment. General Reanimatology, 2013, vol. 9, no. 4, pp. 30–35. (In Russ.) DOI: 10.15360/1813-9779-2013-4-30.

7. Vitik A.A., Shen N.P. Organoprotective effects of the α2-adrenoreceptor agonist dexmedetomidine (literature review). Alexander Saltanov Intensive Care Herald, 2018, no. 4, pp. 74–79. (In Russ.) DOI: 10.21320/1818-474X-2018-4-74-79.

8. Gorbachev V.I., Bragina N.V. Blood-brain barrier from the point of view of anesthesiologist. Review. Part 2. Annals of Critical Care, 2020, no. 3, pp. 46–55. (In Russ.) DOI: 10.21320/1818-474X-2020-3-46-55.

9. Grechko A.V., Kiryachkov Yu.Yu., Petrova M.V. Modern aspects of the relationship between the functional state of the autonomic nervous system and clinical and laboratory indices of the body’s homeostasis in brain injuries. Alexander Saltanov Intensive Care Herald, 2018, no. 2, pp. 79–86. (In Russ.) DOI: 10.21320/1818-474X-2018-2-79-86.

10. Kondratiev A.N. Reader for anesthesiologists-resuscitators. St. Petersburg, SpetsLit, 2023, pp. 422. (In Russ.)

11. Koryachkin V.A., Zabolotsky D.V. Eponyms in anesthesiology and intensive care: Dictionary – reference book. St. Petersburg, IP Makov M.Yu., 2020, 120 p. (In Russ.)

12. Likhvantsev V.V., Landoni G., Subbotin V.V. et al. Impact of anesthesia method on immune response in patients undergoing radical surgery for breast cancer (a meta-analysis of comparative clinical studies). General Reanimatology, 2022, vol. 18, no. 4, pp. 20–28. (In Russ.) DOI: 10.15360/1813-9779-2022-4-20-28.

13. Polushin Yu.S., Polushin А.Yu., Yukina G.Yu., Kozhemyakina M.V. Postoperative cognitive dysfunction – what we know and where we go. Messenger of Anesthesiology and Resuscitation, 2019, vol. 16, no. 1, pp. 19–28. (In Russ.) DOI: 10.21292/2078-5658-2019-16-1-19-28.

14. Savelyev V.S. Sepsis: classification, clinical and diagnostic concept and treatment: a practical guide. 3rd ed., add. and rev. Savelyev V.S., Gelfand B.R, eds. Moscow, Medical Information Agency, 2013, 360 p. (In Russ.)

15. Blum F., Zuo Z. Volatile anesthetics-induced neuroinflammatory and antiinflammatory responses. Medical Gas Research, 2013, vol. 3, no. 1, pp. 16. DOI: 10.1186/2045-9912-3-16.

16. Farag E., Argalious M., Sessler D.I. et al. Use of α(2)-Agonists in Neuroanesthesia: An Overview. Ochsner J., 2011, vol. 11, no. 1, pp. 57–69. PMID: 21603337.

17. Chen Y., Zhang X., Zhang B. et al. Dexmedetomidine reduces the neuronal apoptosis related to cardiopulmonary bypass by inhibiting activation of the JAK2-STAT3 pathway. Drug Des Devel Ther, 2017, vol. 11, pp. 2787–2799. DOI: 10.2147/DDDT.S140644.

18. Cheng X.Q., Mei B., Zuo Y.M. et al. POCD Study Group. A multicentre randomised controlled trial of the effect of intra-operative dexmedetomidine on cognitive decline after surgery. Anaesthesia, 2019, vol. 74, no. 6, pp. 741–750. DOI: 10.1111/anae.14606.

19. Jia L., Jianli Goh S.J., Ying Lei Tng P. et al. Systemic inflammatory response following acute traumatic brain injury. Front. Biosci. (Landmark Ed), 2009, vol. 14, no. 10, pp. 3795–3813. DOI: 10.2741/3489.

20. Jiang L., Hu M., Lu Y. et al. The protective effects of dexmedetomidine on ischemic brain injury: A meta-analysis. J Clin Anesth, 2017, vol. 40, pp. 25–32. DOI: 10.1016/j.jclinane.2017.04.003.

21. Klimek M., Hol J.W., Wens S. et al. Inflammatory profile of awake function-controlled craniotomy and craniotomy under general anesthesia. Mediators Inflamm, 2009, vol. 2009, pp. 670480. DOI: 10.1155/2009/670480.

22. Konsman J. P., Luheshi G. N., Bluthe R. M. et al. The vagus nerve mediates behavioural depression, but not fever, in response to peripheral immune signals; functional anatomical analysis // Eur. J. Neurosci. – 2000. – Vol. 12. – P. 4434–4446. DOI: 10.1046/j.0953-816x.2000.01319.x.

23. Lee J. R., Joseph B., Hofacer R. D. et al. Effect of dexmedetomidine on sevoflurane-induced neurodegeneration in neonatal rats // Br J Anaesth. – 2021. – Vol. 126, № 5. – P. 1009–1021. DOI: 10.1016/j.bja.2021.01.033.

24. Lei D., Sha Y., Wen S. et al. Dexmedetomidine may reduce IL-6 level and the risk of postoperative cognitive dysfunction in patients after surgery: a meta-analysis // Dose Response. – 2020. – Vol. 18, № 1. – P. 1559325820902345. DOI: 10.1177/1559325820902345.

25. Liu X., Jing J., Guo-Qing Z. General anesthesia affecting on developing brain: evidence from animal to clinical research // Int. J. Anesthetics and Anesthesiology. – 2019. – Vol. 7, № 1. – P. 101. DOI: 10.23937/2377-4630/1410101.

26. Markovic-Bozic J., Karpe B., Potocnik I. et al. Effect of propofol and sevoflurane on the inflammatory response of patients undergoing craniotomy // BMC Anesthesiol. – 2016. – Vol. 16. – P. 18. DOI: 10.1186/s12871-016-0182-5.

27. Mellergård P., Aneman O., Sjögren F. et al. Changes in extracellular concentrations of some cytokines, chemokines, and neurotrophic factors after insertion of intracerebral microdialysis catheters in neurosurgical patients // Neurosurgery. – 2008. – Vol. 62, № 1. – P. 151–157. DOI: 10.1227/01.NEU.0000311072.33615.3A.

28. Schneemilch C., Schilling T., Bank U. Effects of general anesthesia on inflammation // Best Pract Res Clin Anaesthesiol. – 2004. – Vol. 18, № 5. – P. 493–507.

29. Tasbihgou S. R., Barends C. R. M., Absalom A. R. The role of dexmedetomidine in neurosurgery // Best Pract Res Clin Anaesthesiol. – 2021. – Vol. 35, № 2. – P. 221–229. DOI: 10.1016/j.bpa.2020.10.002. PMID: 34030806.

30. Tracey K. J. The inflammatory reflex // Nature. – 2002. – Vol. 420. – P. 853–859. DOI: 10.1038/nature01321.

31. Vacas S., Degos V., Feng X. et al. The neuroinflammatoryresponse of postoperative cognitive decline // Br Med Bull. – 2013. – Vol. 106. – P. 161–178. DOI: 10.1093/bmb/ldt006.

32. Wu X., Lu Y., Dong Y. et al. The inhalation anesthetic isofluraneincreases levels of proinflammatory TNF-alpha, IL-6, and IL1beta // Neurobiol Aging. – 2012. – Vol. 33, № 7. – P. 1364–1378. DOI: 10.1016/j.neurobiolaging.2010.11.002.

33. Xianbao L., Hong Z., Xu Z. et al. Dexmedetomidine reduced cytokine release during postpartum bleedinginduced multiple organ dysfunction syndrome in rats // MediatorsInflamm. – 2013. – Vol. 2013. – P. 627831. DOI: 10.1155/2013/627831.


Review

For citations:


Lesteva N.A., Dryagina N.V., Kondratiev A.N. Dynamics of laboratory markers of systemic inflammation in neurosurgical operations using α-2-adrenoagonists. Messenger of ANESTHESIOLOGY AND RESUSCITATION. 2023;20(6):19-27. (In Russ.) https://doi.org/10.24884/2078-5658-2023-20-6-19-27



Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2078-5658 (Print)
ISSN 2541-8653 (Online)