#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Association between heart rate variability and perioperative systemic inflammatory response


Authors: P. Reimer 1;  M. Káňová 1;  J. Máca 1;  P. Ševčík 1;  M. Burda 2;  M. Adamus 3
Authors‘ workplace: Klinika anesteziologie, resuscitace a intenzivní medicíny, Fakultní nemocnice Ostrava a Lékařská fakulta Ostravské univerzity 1;  Ústav pro výzkum a aplikace fuzzy modelování, Ostravská univerzita 2;  Klinika anesteziologie, resuscitace a intenzivní medicíny, Fakultní nemocnice Olomouc a Lékařská fakulta Univerzity Palackého v Olomouci 3
Published in: Anest. intenziv. Med., 29, 2018, č. 1, s. 3-13
Category: Anaesthesia - Originale paper

Overview

Objective:
Colorectal surgery significantly affects homeostasis. The aim of the study was to identify patients with high inflammatory response to surgical injury, objectivized by the levels of C-reactive protein (CRP), interleukin-6 (IL-6) and white cell count (WCC) measured within 48 hours after the beginning of surgery by pre-operative measurement of heart rate variability (HRV).

Design:
Prospective, observational study.

Setting:
Department of Anesthesiology and Intensive Care Medicine, University Hospital

Materials and methods:
HRV was measured during orthostatic load one day before surgery. The patients were divided according to the HRV results into two groups: CAR (with cardiac autonomic reactivity, n=23), and NCAR (without cardiac autonomic reactivity, n=30). Serum levels of CRP, IL-6 and WCC were obtained at 0, 12 (only IL-6), 24 and 48 hours after the beginning of surgery.

Results:
The observed CAR and NCAR were significantly different at the levels of CRP at T0 (6.5±5.1 mg/L vs. 16.4±23.2 mg/L, p<0.05), T24 (70.5±33.6 mg/L vs. 95.7±49.1 mg/L, p<0.05), T48 (103.1±42.4 mg/L vs. 159.0±63.4 mg/L, p<0.001), and IL-6 at T12 (79.3±42.2 pg/mL vs. 248.2±285.2 pg/mL, p<0.05), T24 (68.0±28.0 pg/mL vs. 239.6 ± 245.8 pg/mL, p<0.001), and T48 (39.5±18.4 pg/mL vs. 195.5±162.9 pg/mL; p<0.0001). There was no significant difference in WCC between CAR and NCAR patients.

Conclusion:
HRV is a method for identifying patients with high perioperative pro-inflammatory response. Statistical differences in CRP and IL-6 levels between the studied groups increased over time. IL-6 was statistically significantly different already at T24, thus enabled earlier identification of patients with higher pro-inflammatory response when compared to CRP.

Keywords:
heart rate variability – systemic inflammatory response – C-reactive protein – interleukin-6 – leukocytes – colorectal surgery


Sources

1. Marik PE, Flemmer M. The immune response to surgery and trauma: Implications for treatment. J Trauma Acute Care Surg. 2012;73:801–808.

2. Tracey KJ. The inflammatory reflex. Nature. 2002;420:853–859.

3. Reimer P, Máca J, Szturz P, Jor O, Kula R, Ševčík P, Burda M, Adamus M. Role of heart rate variability in preoperative assessment of physiological reserves in patients undergoing major abdominal surgery. Ther Clin Risk Manag. 2017;13:1223–1231.

4. Ernst G. Heart rate variability. 1st ed. London: Springer, 2014.

5. Metelka R. Heart rate variability – current diagnosis of the cardiac autonomic neuropathy. A review. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2014;158:327–338.

6. Vinik AI, Ziegler D. Diabetic cardiovascular autonomic neuropathy. Circulation. 2007;115:387–397.

7. Kleiger RE, Miller JP, Bigger JT, Moss AJ. Decreased heart rate variability and its association with increased mortality after acute myocardial infarction. Am J Cardiol. 1987;59:256–262.

8. Mazzeo AT, La Monaca E, Di Leo R, Vita G, Santamaria LB. Heart rate variability: a diagnostic and prognostic tool in anesthesia and intensive care. Acta Anaesthesiol Scand. 2011;55:797–811.

9. McGrane S, Atria NP, Barwise JA. Perioperative implications of the patient with autonomic dysfunction. Curr Opin Anaesthesiol. 2014;27:365–370.

10. Máca J, Burša F, Ševčík P, Sklienka P, Burda M, Holub M. Alarmins and clinical outcomes after major abdominal surgery – a prospective study. J Invest Surg. 2017;30:152–161.

11. Watt DG, Horgan PG, McMillan DC. Routine clinical markers of the magnitude of the systemic inflammatory response after elective operation: A systematic review. Surgery. 2015;157:362–380.

12. Watt DG, McSorley ST, Horgan PG, McMillan DC. Enhanced recovery after surgery: which components, if any, impact on the systemic inflammatory response following colorectal surgery? A systematic review. Medicine (Baltimore). 2015;94:e1286.

13. Gans SL, Atema JJ, van Dieren S, Groot Koerkamp B, Boermeester MA. Diagnostic value of C-reactive protein to rule out infectious complications after major abdominal surgery: a systematic review and meta-analysis. Int J Colorectal Dis. 2015;30:861–873.

14. Adamina M, Steffen T, Tarantino I, Beutner U, Schmied BM, Warschkow R. Meta-analysis of the predictive value of C-reactive protein for infectious complications in abdominal surgery. Br J Surg. 2015;102:590–598.

15. McDermott FD, Heeney A, Kelly ME, Steele RJ, Carlson GL, Winter DC. Systematic review of preoperative, intraoperative and postoperative risk factors for colorectal anastomoticleaks. Br J Surg. 2015;102:462–479.

16. Pastorino U, Morelli D, Leuzzi G, Giasabella M, Suatoni P, Taverna F, Bertocchi E, Boeri M, Sozzi G, Cantarutti A, Corrao G. Baseline and postoperative C-reactive proteinlevels predict mortality in operable lung cancer. Eur J Cancer. 2017;79:90–97.

17. Rettig TC, Verwijmeren L, Dijkstra IM, Boerma D, van de Garde EM, Noordzij PG. Postoperative interleukin-6 level and early detection of complications after elective major abdominal surgery. Ann Surg. 2016;263:1207–1212.

18. Warschkow R, Steffen T, Beutner U, Műller SA, Schmied BM, Tarantino I. Diagnostic accuracy of C-reactive protein and white blood cell counts in the early detection of inflammatory complications after open resection of colorectal cancer: a retrospective study of 1,187 patients. Int J Colorectal Dis. 2012;27:1377.

19. Haensel A, PJ Mills, Nelesen RA, Ziegler MG, Dimsdale JE. The reationship between heart rate variability and inflammatory markers in cardiovsacular disease. Psychoneuroendocrinology. 2008;33:1305–1312.

20. Papaioannou VE, Dragoumanis C, Theodorou V, Gargaretas C, Pneumatikos I. Relation of heart rate variability to serum levels of C-reactive protein, intereukin 6, and 10 in patients with sepsis and septic shock. J Crit Care. 2009;24:625.e1–7.

21. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Heart rate variability, standard of measurement, physiological interpretation, and clinical use. Eur Heart J. 1996;17:354–381.

22. Opavský J. Autonomní nervový systém a diabetická autonomní neuropatie. Klinické aspekty a diagnostika. 1. vydání. Praha: Galén, 2002.

23. Howorka K, Pumprla J, Jirkovská A, Lacigova S, Nolan J. Modified orthostatic load for spectral analysis of short-term heart rate variability improves the sensitivity of autonomic dysfunction assessment. J Diabetes Complications. 2010;24:48–54.

24. Huang CJ, Kuok CH, Kuo TB, Hsu YW, Tsai PS. Pre-operative measurement of heart rate variability predicts hypotension during general anesthesia. Acta Anaesthesiol Scand. 2006;50:542–548.

25. Esmon CT. The impact of the inflammatory response on coagulation. Thromb Res. 2004;114:321–327.

26. Nunan D, Sandercock GR, Brodie DA. A quantitative systematic review of normal values for short-term herat rate variability in healthy adults. Pacing Clin Electrophysiol. 2010;33:1407–1417.

27. Yu HP, Hseu SS, Yien HW, Teng YH, Chan KH. Oral clonidin premedication preserves heart rate variability for patients undergoing laparoscopic cholecystectomy. Acta Anaesthesiol Scand. 2003;47:185–190.

Labels
Anaesthesiology, Resuscitation and Inten Intensive Care Medicine
Login
Forgotten password

Enter the email address that you registered with. We will send you instructions on how to set a new password.

Login

Don‘t have an account?  Create new account

#ADS_BOTTOM_SCRIPTS#