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The impact of a reduced dose of dexamethasone on glucose control after coronary artery bypass surgery
Cardiovascular Diabetology volume 6, Article number: 39 (2007)
Intensive insulin therapy to maintain normoglycemia after cardiac surgery reduces morbidity and mortality. We investigated the magnitude and duration of hyperglycemia caused by dexamethasone administered after cardiopulmonary bypass.
A single-center before-after cohort study was performed. All consecutive patients undergoing coronary artery bypass grafting with cardiopulmonary bypass during a 6-month period were included. Insulin administration was guided by a sliding scale protocol. Halfway the observation period, the dexamethasone protocol was changed. The single dose (1D) group received a pre-operative dose of dexamethasone of 1 mg/kg. The double dose group (2D) received an additional dose of 0.5 mg/kg of dexamethasone post-operatively at ICU admission.
We included 116 patients in the 1D group and 158 patients in the 2D group. There were no significant baseline differences between the groups. Median Euroscore was 5. In univariable analysis, the glucose level was different between groups 1D and 2D at 4, 6, 9, 12 and 24 hours after ICU admission (all p < 0.001). Insulin infusion was higher in the 1D group. Corrected for insulin dose in multivariable linear analysis, the difference in glucose between the 1D and 2D groups was 1.5 mmol/L (95% confidence interval 1.0–2.0, p < 0.001) 12 hours after ICU admission.
Dexamethasone exerts a hyperglycemic effect in cardiac surgery patients. Patients receiving high-dose corticosteroid therapy should be monitored and treated more intensively for hyperglycemic episodes.
Cardiac surgery with cardiopulmonary bypass induces a strong systemic inflammatory response in previously healthy individuals . This response is characterized by changes in cardiovascular and pulmonary function [2–4]. Corticosteroids inhibit this inflammatory response and may thus ameliorate the adverse effects of cardiopulmonary bypass [1, 5, 6]. High-dose dexamethasone is one of the therapies given in some centers to reach this effect. However, corticosteroid use in cardiac surgery is controversial, because important side effects may result . One of the side effects is increased insulin resistance, which causes hyperglycemia . The emerging evidence on negative effects of dexamethasone has prompted a protocol change in our institution.
In patients with myocardial infarction, prolonged hyperglycemia after admission is associated with adverse outcome [9, 10]. Glycometabolic dysregulation is common in patients undergoing cardiac surgery . Tight glucose control with intensive insulin therapy has been shown to decrease mortality and morbidity in these patients . In patients undergoing coronary artery bypass grafting, the survival benefit persisted at 4 years follow-up . As the benefits of insulin therapy are related to the level of achieved glucose control, the impact of corticosteroids on hyperglycemia has become more relevant . We hypothesized that a reduction of dexamethasone dose would facilitate glucose control. We performed a before-after study to quantify the hyperglycemic effect of a second dose of dexamethasone administered post-operatively at the intensive care unit (ICU) in patients undergoing coronary artery bypass surgery (CABG) with cardiopulmonary bypass.
This study was performed at a 14-bed thoracic ICU in a tertiary teaching hospital. During a 6 month period (from April to October 2005) all patients undergoing CABG with the use of cardiopulmonary bypass were studied. Both patients with only CABG and CABG with additional valve repair were included. During the 6-month observation period, the treatment protocol was modified by the medical staff. Before the change, all patients were administered 1.0 mg of dexamethasone per kilogram of body weight at the induction of anesthesia and a second dose of 0.5 mg/kg at admission to the ICU. The patients in this dosing scheme were in the double-dose (2D) group. After the change, the second dose was withheld, so patients only received the initial 1.0 mg/kg dose (group 1D). The protocol change was made after a previous study, in which high-dose dexamethasone failed to provide a beneficial effect on peri-operative renal function  and review of other available evidence . The institutional review board approved this study.
At baseline, we collected demographic and clinical information, including sex, age, body mass index (BMI) and presence of diabetes before hospital admission. Operative risk stratification was done by means of the EuroSCORE model . Time on cardiopulmonary bypass and total operation time were recorded. During the ICU stay, we collected blood glucose levels, and insulin administration for the first 48 hours. Glucose levels were measured in arterial blood samples using a point-of-care blood gas analyzer present at the ICU (ABL Radiometer 700 series, Copenhagen). Insulin was administered according to a sliding-scale insulin dosing algorithm. The algorithm was designed to treat hyperglycemia defined as a glucose level over 10 mmol/L but did not aim for normoglycemia (4.4 – 6.1 mmol/L). Our protocol prescribed a 1 liter infusion of glucose 5% during the first 24 hours.
For data processing and statistical analysis SPSS version 12.0 was used. Baseline characteristics of the two groups were expressed as mean ± standard deviation (SD) for normally distributed variables or as median (interquartile range, IQR) for other variables. We compared differences between groups with the Student's t-test for normal distributed variables or the Mann-Whitney U test for other continuous variables. For categorical variables, the Chi-square test or Fisher's exact test were used when appropriate. We analyzed the blood glucose levels at 2, 4, 6, 9, 12, 24 and 48 hours after ICU admission for each patient. The glucose values at these specific times were calculated by linear interpolation. We also calculated the hyperglycemic index for the first 12 hours after admission .
The time course of glucose levels was compared with univariable analysis between groups 1D and 2D to determine if and when glucose levels diverged between the two groups. It was then determined at what time the difference in glucose was greatest between the two groups. To assess the relative contributions of patient group (1D or 2D), age, sex, diabetes, BMI and insulin administration to this maximum difference in glucose, we performed multivariable linear regression analysis. We included variables in the model that had a univariable p-value smaller than 0.15. Differences or statistical relations with a p-value of less than 0.05 were considered significant. Bonferroni's correction for multiple testing was applied where appropriate.
A total of 274 patients were included in this study, 116 in the 1D-group and 158 patients in the 2D-group. Table 1 shows the patient characteristics at baseline for both groups. The mean age of the population was 69 ± 9 years, and 70% of them were male. Median ICU length of stay was 1.0 (0.8–1.8) days and the hospital length of stay was 12 (9–16) days. Pre-operative risk scoring shows that 36% of the population was at medium risk (EuroSCORE 3–5), and 42% was at high risk (EuroSCORE > 5). Thirty-day all cause mortality was 3.3%. The operation time was slightly longer in the 1D group.
Figure 1 shows the mean and standard deviation of blood glucose levels over the first 48 hours after ICU admission. At 4, 6, 9, 12 and 24 hours after admission glucose levels were significantly lower in the 1D-group than in the 2D-group, with the greatest difference at 12 hours. The hyperglycemic index over the first 12 hours was significantly lower in the 1D group: 3.5 ± 1.4 mmol/L vs. 4.7 ± 1.7 mmol/L (p < 0.001). Performance and attention for the glucose control protocol improved during the study period. Patients in the 1D group received 26 (15 – 36) units of insulin during the first 12 hours of ICU stay, for the 2D group this was 12 (0 – 27.25, p < 0.001). The number of glucose measurements in the first 12 hours was 6 (4 – 7) in the 1D group and 4 (3 – 5) in the 2D group. Figure 2 shows the glucose level 12 hours after admission for both groups stratified for mean insulin infusion rate during the first 12 hours. In multivariable linear regression analysis, the attributable increase of glucose at 12 h after admission was 1.5 mmol/L for a second dose of dexamethasone (p < 0.001, table 2). The difference in glucose levels between the 1D and 2D groups was similar in patients with and without a history of diabetes.
In this study we found that cardiac surgical patients who received two doses of dexamethasone displayed higher blood glucose levels between 6 and 24 hours after ICU admission than patients who received one dose of dexamethasone.
High dose dexamethasone is a controversial therapy in cardiac surgery patients. Both studies that favor the use of corticosteroids  or studies that show some benefit  as well as studies that show no benefit [7, 15, 18] have been published. The effect of steroids on glucose control may be of interest, because high glucose levels are common and have been shown to be independent predictors of adverse outcome during cardiac surgery [11, 19]. Treatment of hyperglycemia by continuous insulin infusion has recently been shown to improve outcome [12, 13, 20]. The difference of 1.5 mmol/L in glucose levels we found in multivariable analysis is clinically relevant considering a post-hoc analysis found that the odds ratio for ICU mortality for every increase in glucose level of 1.1 mmol/L is 1.3 . Our study was not powered to detect a difference in mortality.
While the merit of steroids for cardiopulmonary bypass may be disputed, steroids are administered for many other indications in other critically ill patients. For instance, lower dose corticosteroids may be used to prevent atrial fibrillation after cardiac surgery . For other patient categories, effects on glucose control have recently been shown for hydrocortisone in patients with septic shock , or for dexamethasone against nausea in abdominal surgery patients .
A number of limitations of our study must be mentioned. First, we had not implemented a tight glucose control protocol at the thoracic ICU at the time of this study. Therefore, overall glucose control was not comparable to the levels achieved in intervention studies, reflected by the HGI which indicates mean glucose levels of 9.5 and 10.7 mmol/L for the groups respectively. We think this does not change our conclusion that dexamethasone induces hyperglycemia, as we hypothesize that under a tight glucose control protocol, we would have found that the 1D group would require less interventions and lower doses of insulin than the 2D group to achieve the same glucose targets. Second, although data collection was prospective, the study as a whole must be regarded as a retrospective study. Bias could have been introduced in our data in a number of ways. Inherent to the before-after design the patients were not randomly allocated to the two dosing groups. A very important variable, insulin infusion, was found to be significantly different between the two groups. The multivariable analysis incorporating this and other possible confounding factors confirmed the highly significant relation of glucose levels with the administration of one or two dexamethasone doses. This analysis may still overestimate the difference caused by dexamethasone due to unknown confounding factors and due to non-linear effects of the included variables. Not all cardiac surgery centers use dexamethasone as routine treatment in all cardiac surgery patients. This may be a limitation to the relevance of our study. However, it is unlikely that the hyperglycemic effect we measured in this study is unique to dexamethasone or cardiac surgery patients. Our findings may be extrapolated to the majority of patients receiving corticosteroids in the intensive care setting.
Although we did not study the effect of giving dexamethasone compared to no dexamethasone is this study, the first dose of dexamethasone also induced considerable insulin resistance as we have observed in a previous study . Withholding of the dose administrated upon induction of anesthesia could further improve glucose control around the time of ICU admission. This quantitative study shows that one should be prepared to administer higher doses of insulin when using dexamethasone in cardiac surgery patients. In three ICUs in our hospital, we have implemented a computerized glucose control system. We designed this system so that patients who receive steroids both get higher initial insulin doses, and are checked more frequently to promptly detect hyperglycemia . Future research on the value of corticosteroids during cardiac surgery or for other indications in the ICU should pay very close attention to the hyperglycemic effects of these drugs. If glucose control is not performed adequately, potential positive effects of steroids could be offset by iatrogenic hyperglycemia.
In summary, the administration of dexamethasone exerts a considerable hyperglycemic effect in cardiac surgery patients, interfering with glucose control.
Eagle KA, Guyton RA, Davidoff R, Edwards FH, Ewy GA, Gardner TJ, Hart JC, Herrmann HC, Hillis LD, Hutter AM, Lytle BW, Marlow RA, Nugent WC, Orszulak TA, American College of Cardiology, American Heart Association: ACC/AHA 2004 guideline update for coronary artery bypass graft surgery: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Update the 1999 Guidelines for Coronary Artery Bypass Graft Surgery). Circulation. 2004, 110 (14): e340-e437.
Murphy GJ, Angelini GD: Side effects of cardiopulmonary bypass: what is the reality?. J Card Surg. 2004, 19 (6): 481-488. 10.1111/j.0886-0440.2004.04101.x.
Kusumanto YH, Tio RA, Loef BG, Sluiter WJ, Mulder NH, Hospers GA: Systemic VEGF levels after coronary artery bypass graft surgery reflects the extent of inflammatory response. Acute Card Care. 2006, 8: 41-45.
Nathoe HM, van Dijk D, Jansen EW, Suyker WJ, Diephuis JC, van Boven WJ, De la Rivière AB, Borst C, Kalkman CJ, Grobbee DE, Buskens E, De Jaegere PP, Octopus Study Group: A comparison of on-pump and off-pump coronary bypass surgery in low-risk patients. N Engl J Med. 2003, 348 (5): 394-402. 10.1056/NEJMoa021775.
Yared JP, Starr NJ, Torres FK, Bashour CA, Bourdakos G, Piedmonte M, Michener JA, Davis JA, Rosenberger TE: Effects of single dose, postinduction dexamethasone on recovery after cardiac surgery. Ann Thorac Surg. 2000, 69 (5): 1420-1424. 10.1016/S0003-4975(00)01180-2.
Halvorsen P, Raeder J, White PF, Almdahl SM, Nordstrand K, Saatvedt K, Veel T: The effect of dexamethasone on side effects after coronary revascularization procedures. Anesth Analg. 2003, 96 (6): 1578-83. 10.1213/01.ANE.0000063922.90966.3A.
Chaney MA: Corticosteroids and cardiopulmonary bypass: a review of clinical investigations. Chest. 2002, 121 (3): 921-931. 10.1378/chest.121.3.921.
Rizza RA, Mandarino LJ, Gerich JE: Cortisol-induced insulin resistance in man: impaired suppression of glucose production and stimulation of glucose utilization due to a postreceptor detect of insulin action. J Clin Endocrinol Metab. 1982, 54: 131-138.
van der Horst IC, Nijsten MW, Vogelzang M, Zijlstra F: Persistent hyperglycemia is an independent predictor of outcome in acute myocardial infarction. Cardiovasc Diabetol. 2007, 6: 2-10.1186/1475-2840-6-2.
Vogelzang M, Zijlstra F: Glucose metabolism and acute myocardial infarction. Eur Heart J. 2006, 27 (11): 1264-1265. 10.1093/eurheartj/ehl010.
Anderson RE, Brismar K, Barr G, Ivert T: Effects of cardiopulmonary bypass on glucose homeostasis after coronary artery bypass surgery. Eur J Cardiothorac Surg. 2005, 28 (3): 425-430. 10.1016/j.ejcts.2005.05.025.
van den Berghe G, Wouters P, Weekers F, Verwaest C, Bruyninckx F, Schetz M, Vlasselaers D, Ferdinande P, Lauwers P, Bouillon R: Intensive insulin therapy in critically ill patients. N Engl J Med. 2001, 345 (19): 1359-1367. 10.1056/NEJMoa011300.
Ingels C, Debaveye Y, Milants I, Buelens E, Peeraer A, Devriendt Y, Vanhoutte T, Damme AV, Schetz M, Wouters PJ, van den Berghe G: Strict blood glucose control with insulin during intensive care after cardiac surgery: impact on 4-years survival, dependency on medical care, and quality-of-life. Eur Heart J. 2006, 27 (22): 2716-2724. 10.1093/eurheartj/ehi855.
van den Berghe G, Wouters PJ, Bouillon R, Weekers F, Verwaest C, Schetz M, Vlasselaers D, Ferdinande P, Lauwers P: Outcome benefit of intensive insulin therapy in the critically ill: Insulin dose versus glycemic control. Crit Care Med. 2003, 31 (2): 359-366. 10.1097/01.CCM.0000045568.12881.10.
Loef BG, Henning RH, Epema AH, Rietman GW, Van Oeveren W, Navis GJ, Ebels T: Effect of dexamethasone on perioperative renal function impairment during cardiac surgery with cardiopulmonary bypass. Br J Anaesth. 2004, 93 (6): 793-798. 10.1093/bja/aeh266.
Nashef SA, Roques F, Michel P, Gauducheau E, Lemeshow S, Salamon R: European system for cardiac operative risk evaluation (EuroSCORE). Eur J Cardiothorac Surg. 1999, 16: 9-13. 10.1016/S1010-7940(99)00134-7.
Vogelzang M, van der Horst IC, Nijsten MW: Hyperglycaemic index as a tool to assess glucose control: a retrospective study. Crit Care. 2004, 8 (3): R122-R127. 10.1186/cc2840.
Morariu AM, Loef BG, Aarts LP, Rietman GW, Rakhorst G, van Oeveren W, Epema AH: Dexamethasone: benefit and prejudice for patients undergoing on-pump coronary artery bypass grafting: a study on myocardial, pulmonary, renal, intestinal, and hepatic injury. Chest. 2005, 128 (4): 2677-2687. 10.1378/chest.128.4.2677.
Doenst T, Wijeysundera D, Karkouti K, Zechner C, Maganti M, Rao V, Borger MA: Hyperglycemia during cardiopulmonary bypass is an independent risk factor for mortality in patients undergoing cardiac surgery. J Thorac Cardiovasc Surg. 2005, 130 (4): 1144.
Furnary AP, Gao G, Grunkemeier GL, Wu Y, Zerr KJ, Bookin SO, Floten HS, Starr A: Continuous insulin infusion reduces mortality in patients with diabetes undergoing coronary artery bypass grafting. J Thorac Cardiovasc Surg. 2003, 125 (5): 1007-1021. 10.1067/mtc.2003.181.
Halonen J, Halonen P, Järvinen O, Taskinen P, Auvinen T, Tarkka M, Hippeläinen M, Juvonen T, Hartikainen J, Hakala T: Corticosteroids for the prevention of atrial fibrillation after cardiac surgery: a randomized controlled trial. JAMA. 2007, 297 (14): 1562-1567. 10.1001/jama.297.14.1562.
Loisa P, Parviainen I, Tenhunen J, Hovilehto S, Ruokonen E: Effect of mode of hydrocortisone administration on glycemic control in patients with septic shock: a prospective randomized trial. Crit Care. 2007, 11: R21-10.1186/cc5696.
Hans P, Vanthuyne A, Dewandre PY, Brichant JF, Bonhomme V: Blood glucose concentration profile after 10 mg dexamethasone in non-diabetic and type 2 diabetic patients undergoing abdominal surgery. Br J Anaesth. 2006, 97 (2): 164-170. 10.1093/bja/ael111.
Vogelzang M, Zijlstra F, Nijsten MW: Design and implementation of GRIP: a computerized glucose control system at a surgical intensive care unit. BMC Med Inform Decis Mak. 2005, 5: 38-10.1186/1472-6947-5-38.
The authors would like to acknowledge Dr. Wim Sluiter for expert statistical advice.
The author(s) declare that they have no competing interests.
All authors were involved in drafting the manuscript. All authors read and approved the final version. MH, JD, MJ and MN collected data. PB provided EuroSCORE data. MV, IvdH, FZ, BL and MN designed the study. MV and MN performed statistical analyses. MN coordinated the study.
Mathijs Vogelzang, Miriam Hoekstra contributed equally to this work.
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Vogelzang, M., Hoekstra, M., Drost, J.T. et al. The impact of a reduced dose of dexamethasone on glucose control after coronary artery bypass surgery. Cardiovasc Diabetol 6, 39 (2007). https://doi.org/10.1186/1475-2840-6-39
- Intensive Care Unit
- Cardiopulmonary Bypass
- Intensive Care Unit Admission
- Glucose Control