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Post hoc analysis of the glutamics–trial: intravenous glutamate infusion and use of inotropic drugs after cabg

BMC Anesthesiology volume 16, Article number: 54 (2015) Cite this article

Abstract

Background

Intravenous glutamate reduced the risk of developing severe circulatory failure after isolated coronary artery bypass graft surgery (CABG) for acute coronary syndrome (ACS) in a double-blind randomised clinical trial (GLUTAMICS-ClinicalTrials.gov Identifier:NCT00489827). Here our aim was to study if glutamate was associated with reduced the use of inotropes.

Methods

Post-hoc analysis of 824 patients undergoing isolated CABG for ACS in the GLUTAMICS-trial. ICU-records were retrospectively scrutinised including hourly registration of inotropic drug infusion, dosage and total duration during the operation and postoperatively.

Results

ICU-records were found for 171 out of 177 patients who received inotropes perioperatively. Only one fourth of the patients treated with inotropes fulfilled study criteria for postoperative heart failure at weaning from cardiopulmonary bypass (CPB) or later in the ICU. Inotropes were mainly given preemptively to facilitate weaning from CPB or to treat postoperative circulatory instability (bleeding, hypovolaemia). Except for a significantly lower use of epinephrine there were only trends towards lower need of other inotropes overall in the glutamate group. In patients treated with inotropes (glutamate n = 17; placebo n = 13) who fulfilled study criteria for left ventricular failure at weaning from CPB the average duration of inotropic treatment (34 ± 20 v 80 ± 77 h; p = 0.014) and the number of inotropes used (1.35 ± 0.6 v 1.85 ± 0.7; p = 0.047) were lower in the glutamate group.

Conclusions

Intravenous glutamate was associated with a minor influence on inotrope use overall in patients undergoing CABG for ACS whereas a considerable and significant reduction was observed in patients with heart failure at weaning from CPB.

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Background

The GLUTAMICS-trial investigated if intravenous glutamate infusion given in association with surgery for acute coronary syndrome could prevent myocardial injury, postoperative heart failure and reduce mortality [1]. The study was negative with regard to the primary endpoint, which was a composite of postoperative mortality, perioperative myocardial infarction and left ventricular failure at weaning from cardiopulmonary bypass (CPB). However, intravenous glutamate reduced the relative risk of developing severe circulatory failure by more than 50 % in most high-risk groups. Patients with heart failure at weaning from CPB required markedly shorter ventilator treatment and ICU-stay if they were treated with glutamate. These results are compatible with a beneficial effect of glutamate on post-ischaemic myocardial recovery after coronary artery bypass surgery (CABG).

However, it can be argued that other factors such as differences in the use of inotropic drugs could have explained the results. If glutamate enhances myocardial recovery in post-ischaemic heart failure one would expect it to be accompanied by a reduced need for inotropic drugs. The primary aim of this study was, therefore, to investigate if intravenous glutamate infusion influenced the use of inotropic drugs in patients operated for acute coronary syndrome in the GLUTAMICS-trial. The secondary aim was to investigate if glutamate due to its suggested vasodilator properties influenced the need for vasoconstrictor therapy (noradrenaline) early postoperatively.

Methods

Patients

This study is a post hoc analysis of a double-blind prospective randomised clinical trial, the GLUTAMICS-trial [1]. Inclusion criteria were CABG for acute coronary syndrome. Patients were eligible for inclusion regardless if the procedure was done on-pump or off-pump.

Exclusion criteria were: informed consent not possible because of critical condition or other reason, age > 85 years, body weight >125 kg; food allergy known to have caused rash, flush or asthma; preoperative use of inotropic drugs or mechanical circulatory assist, preoperative dialysis, redo-procedure, unexpected intraoperative finding or event that increased the magnitude of the procedure to overshadow the originally planned procedure.

The original trial was planned for 2214 patients but the trial was terminated after 861 patients as prespecified stopping criteria per protocol were fulfilled at interim analysis as previously reported [1]. For this particular analysis a small heterogeneous group of patients having additional procedure to CABG was excluded (Fig. 1). Eight hundred twenty four patients in the GLUTAMICS-trial were operated with isolated CABG for acute coronary syndrome between October 4, 2005 and November 12, 2009 at three Swedish Cardiac Surgery Centres (University Hospital of Linköping, Örebro University Hospital and Blekinge County Hospital in Karlskrona).

Fig. 1
figure 1

Flowchart of patient selection and presentation of results at three different levels

Full size image

Patients were randomised to blinded intravenous infusion of 0.125 M glutamate or saline solution at a rate of 1.65 ml/kg body weight and hour started at the induction of anaesthesia and stopped 2.5 h after declamping the aorta or when total of 500 ml had been infused. Further details on the glutamate solution and the GLUTAMICS-trial are given in the Additional file 1.

Patients receiving inotropes were identified by the aid of the Case Report Form (CRF), the institutional database and ICU-records. Use of inotropes was registered in the CRF at weaning from CPB and on admission to ICU. Furthermore, use of inotropes exceeding 30 min was registered by the attending physicians in the institutional database. Finally the ICU records of all patients staying longer than 24 h were retrospectively investigated to identify use of inotropes that had not been recorded in the CRF or database. Complete ICU-records were found for 171 out of 177 patients who received inotropes during this period (Fig. 1). These medical records were then scrutinised by an investigator (BT) previously not involved in the GLUTAMICS-trial. Data retrieval included hourly registration of inotropic drug infusion, dosage and total duration intraoperatively and postoperatively.

Inotropic drugs used during the study period were adrenaline, milrinone (Corotrop™), levosimendan (Simdax™) and dopamine. Adrenaline and milrinone were the most used drugs whereas levosimendan and dopamine only were used in a small fraction. Therefore we present the results for inotrope use overall and separately only for adrenaline and milrinone treatment.

Noradrenaline was used liberally as a vasoconstrictor and its dosages were registered for the first 15 postoperative hours.

Definitions

Use of inotropes was defined as any use of inotropic drugs (except noradrenaline) regardless of indication, duration or dosage. Participating centres and individual clinicians were free to institute inotropic drugs according to their choice and usual practice.

Preemptive use of inotropic drugs to facilitate weaning from CPB was defined as use of inotropic drugs before weaning from CPB in patients that according to prespecified criteria were deemed, by the blinded clinical endpoints committee, not to have had heart failure at weaning. If, however, the patient fulfilled prespecified criteria for heart failure at weaning use of inotropes was considered “treatment” regardless if the drugs had been instituted before weaning or instituted because of weaning problems.

Prespecified criteria were used by a blinded endpoints committee to determine if heart failure was present. Briefly clinical and echocardiographic signs of heart failure as a cause of low mixed venous oxygen saturation (SvO2) were used to diagnose postoperative heart failure [2–4]. A surgical pulmonary artery catheter was introduced in all patients for sampling of SvO2 [2, 3]. SvO2 was measured in every patient at weaning from CPB, 5 min after protamine administration and on admission to ICU and whenever clinical condition of the patients required evaluation of the haemodynamic status. If the rare cases when a patient required more meticulous monitoring to guide haemodynamic treatment a Swan-Ganz catheter was employed. Detailed criteria are given in the Additional file 1.

Postoperative heart failure was categorised into heart failure evident at weaning from cardiopulmonary bypass or late circulatory failure presenting after apparently uncomplicated weaning. Circulatory failure was classified as late if it became evident after weaning from CPB and it was categorised as cardiac or non-cardiac in origin.

Severe circulatory failure was defined as heart failure leading to death or requiring ICU stay ≥ 48 h with intra-aortic balloon pump for ≥24 h or inotropic agents in dosages according to Additional file 1 for ≥24 h.

Postoperative mortality was defined as death within 30 days of surgery. Hospital mortality was defined as death during the first hospitalisation period including stay at the referral hospital after discharge postoperatively. Cardiac cause of death was assessed by the endpoints committee.

Statistics

Two-sided Fisher’s exact test was used was used for comparison of dichotomous variables. Two-sided Students t-test or Mann-Whitney U test as appropriate were used for comparison of continuous variables. Statistical significance was defined as p < 0.05. The data are given as percentages or means ± standard deviation.

Results

Preoperative data

Preoperative data for patients undergoing isolated CABG for acute coronary syndrome in the GLUTAMICS-trial is given in Table 1. Despite randomisation there were minor differences with significantly more patients having left main stenosis and extra-cardiac arterial disease in the glutamate group. There was also a trend toward a higher risk profile according to EuroSCORE in the glutamate group.

Table 1 Preoperative, intraoperative and postoperative data in patients undergoing isolated CABG for acute coronary syndrome in the GLUTAMICS-trial
Full size table

Intraoperative data

Intraoperative data for patients undergoing isolated CABG for acute coronary syndrome in the GLUTAMICS-trial is given in Table 1. No significant differences between the groups were observed.

Postoperative data

Postoperative data for patients undergoing isolated CABG for acute coronary syndrome in the GLUTAMICS-trial is given in Table 1. The incidence of severe circulatory failure was significantly lower in the glutamate group (1.5 % v 3.9 %; p = 0.049).

Postoperative data for all patients treated with inotropes after isolated CABG for acute coronary syndrome in the GLUTAMICS-trial is given in Table 2. The incidences of severe circulatory failure (6.2 % v 17.5 %; p = 0.03) and the need for intra-aortic balloon pump (0 % v 5.2 %; p = 0.04) were significantly lower in the glutamate group.

Table 2 Circulatory treatment and postoperative outcome in all patients treated with inotropes
Full size table

Postoperative data for patients treated with inotropes because of heart failure at weaning from CPB after isolated CABG for acute coronary syndrome in the GLUTAMICS-trial is given in Table 3. Glutamate treated patients had a significantly lower incidence of severe circulatory failure (11.8 % v 61.5 %; p = 0.007), shorter ventilator treatment and shorter stay in the ICU.

Table 3 Circulatory treatment and postoperative outcome in patients treated with inotropes because of heart failure on weaning from CPB
Full size table

Inotrope use

ICU-records were found for 171 out of 177 patients who received inotropes perioperatively. Details of inotrope use are given in Tables 1, 2 and 3. Only one fourth of patients treated with inotropes fulfilled study criteria for postoperative heart failure at weaning from CPB or later in the ICU. The other main indications to give inotropes were preemptive administration to facilitate weaning from CPB or to treat postoperative circulatory instability (bleeding, hypovolaemia). Except for a significantly lower use of adrenaline there were only trends towards lower need of other inotropes overall in the glutamate group (Tables 1 and 2).

In patients who fulfilled criteria for left ventricular failure at weaning from CPB (glutamate n = 17; placebo n = 13) the average duration of inotropic treatment (34 ± 20 v 80 ± 77 h; p = 0.014) and the number of inotropes administered (1.35 ± 0.6 v 1.85 ± 0.7; p = 0.04) were lower in the glutamate group (Table 3).

Vasoconstrictor use

Details of noradrenaline use during the first 15 postoperative hours in patients treated with inotropes are given in Tables 2 and 3. In patients treated with inotropes 71 % in the control group and 70 % in the glutamate group also received noradrenaline. The maximum dosage given did not differ significantly between the groups. Noradrenaline requirements were lower in the glutamate group among patients with heart failure at weaning from CPB (Table 3).

Discussion

This post-hoc analysis of the GLUTAMICS-trial demonstrates that glutamate treatment was associated with a reduced use of inotropes in patients with heart failure at weaning from CPB. Glutamate infusion was not associated with an increased need for vasoconstrictors suggesting that any vasodilator properties of glutamate in the dosage used is limited.

Postoperative heart failure or low cardiac output syndrome is the major cause for morbidity and mortality in cardiac surgery [5–8]. Already in the beginning of heart surgery it was noted that early death after cardiac surgery was related to low cardiac output postoperatively [9]. Although the hazards of low cardiac output syndrome have been known for a long time, there is no consensus on how to define postoperative heart failure. Furthermore, there are no generally accepted guidelines for treatment of postoperative heart failure [10–12]. Different strategies for treatment with inotropic, metabolic and mechanical support depend on local clinical practice or are up to the discretion of the individual physician [12].

Inotropic drugs improve cardiac output but this is achieved at the price of a marked increase in myocardial workload and oxygen consumption [13]. In the early postoperative period after cardiac surgery the heart is in a vulnerable state recovering from ischaemia [14, 15]. Inotropic agents can aggravate the consequences of ischaemia [16]. It has been shown that ischaemia and evolving myocardial infarction account for a large proportion of postoperative heart failure after CABG [6, 17].

The role of inotropes in cardiac surgery is therefore controversial [12]. Some authors claim that liberal use of inotropes and goal-directed haemodynamic therapy can improve outcome whereas other have reported that liberal use of inotropes was associated with increased morbidity and mortality [12, 18–20].

In clinical practice the use of inotropes in cardiac surgery varies much between different institutions and different physicians as evidence-based guidelines are lacking. In the present study only one fourth of the patients treated with inotropes fulfilled study criteria for heart failure.

Several biochemical mechanisms by which glutamate could influence outcome after myocardial ischaemia have been described [21–24]. Glutamate could enhance myocardial tolerance to ischemia by its role in the malate-aspartate shuttle transporting reducing equivalents across the mitochondrial membrane, thus facilitating anaerobic glycolysis by regulating the NAD/NADH balance in the cytosol. Glutamate also contributes to an alternative anaerobic pathway for regeneration of high-energy phosphates in the mitochondria by substrate level phosphorylation. Glutamate improves clearance of lactate and NH3 by taking part in reactions involving transamination of pyruvate to alanine and glutamate to glutamine. Glutamate could stimulate post-ischaemic recovery of myocardial oxidative metabolism and function due to its anaplerotic role; glutamate plays a key role for replenishment of Krebs cycle intermediates lost during ischaemia [21–24].

In animal in vitro and in vivo models numerous studies have shown that glutamate protects the myocardium from ischaemia and promotes recovery of oxidative metabolism after ischaemia [21, 25–27]. In humans intravenous glutamate infusion has been shown to promote metabolic and haemodynamic recovery after cardiac surgery [28, 29].

Promoting metabolic and functional recovery with metabolic support represents a novel concept in the treatment of heart failure after acute ischaemia. Intravenous glutamate improved metabolic and haemodynamic recovery early after CABG [28, 29]. Early clinical experience with intravenous metabolic support showed that the need for inotropes could almost be abolished while clinical outcomes with regard to postoperative mortality, postoperative renal dysfunction and long-term survival compared favourably with literature [4]. This encouraging experience contributed to the initiation of the GLUTAMICS-trial.

The GLUTAMICS-trial was negative with regard to the primary endpoint [1]. However, the study included a high proportion of low risk patients and furthermore the design of the primary endpoint suffered from liberal preemptive use of inotropes in patients anticipated to have weaning problems. It became evident at clinical endpoint committee meetings that preemptive use of inotropes prevented detection of weaning problems in patients who later developed severe circulatory failure. The secondary endpoint severe circulatory failure discriminated mild short-lasting heart failure at weaning from cardiopulmonary bypass from clinically significant heart failure requiring substantial circulatory support and leading to prolonged ICU stay or death. In the glutamate treated patients the relative risk of developing severe circulatory failure was reduced by more than 50 % in most risk groups undergoing isolated CABG [1]. For those who believe that inotropes are beneficial after cardiac surgery the present post-hoc analysis clearly shows that these results were not explained by more liberal use of inotropes in the glutamate group. On the contrary, glutamate infusion was associated with a reduced need for inotropes in patients fulfilling criteria for heart failure on weaning from CPB, which is compatible with the suggested mechanism of glutamate, i.e. to promote post-ischaemic recovery of the heart. These results also agree with previous clinical experience, which has showed that metabolic support can achieve excellent clinical outcomes with reduced need for inotropes [4]. The fact that glutamate had a minor impact on inotrope use overall is not unexpected given that only about one fourth of the patients treated fulfilled criteria for heart failure.

This post-hoc analysis is unique as it, to our knowledge, is the first to provide a detailed investigation on the hourly use of inotropes and vasoconstrictors postoperatively after cardiac surgery. The major limitation is the nature of the study. Post-hoc analyses should always be interpreted cautiously. The criteria used for postoperative heart failure in the GLUTAMICS-trial are inevitably debatable. Although this condition is a major cause for postoperative mortality generally accepted criteria for this diagnosis are lacking. To address this issue the investigators had based the criteria on variables documented with regard to outcome and provided the blinded clinical endpoints committee with strict prespecified criteria to minimise bias from individual clinical judgement [1–3].

A potential hazard of glutamate is that it acts as an excitotoxin, which could contribute to neurological damage under certain conditions. However, no increase in clinically evident neurological injury has been observed when glutamate enhanced cardioplegic solutions or intravenous infusions have been used in clinical practice [30, 31]. We could not detect any evidence for subclinical neurological injury associated with intravenous glutamate in the S-100B substudy of the GLUTAMICS-trial [32]. Another concern has been suggested vasodilator properties occasionally observed in association with glutamate enriched blood cardioplegia. In this post-hoc analysis no increase in the need for vasoconstrictors were observed with the dosage of glutamate used during first 15 postoperative hours when the effect of glutamate should have subsided. With the infusion rate used a decrease to normal blood levels of glutamate has been observed within 30 min after discontinuation of the infusion [33]. Thus, it appears that intravenous glutamate infusions in the dosages employed can be safely administered to patients undergoing cardiac surgery.

Conclusions

Intravenous glutamate was associated a minor effect on inotrope use overall in patients undergoing CABG for acute coronary syndrome whereas a considerable and significant reduction was observed in patients with heart failure at weaning from CPB. Only about one fourth of the patients treated with inotropes in the GLUTAMICS-trial fulfilled criteria for heart failure.

Abbreviations

ACS, acute coronary syndrome; CABG, coronary artery bypass graft surgery; CPB, cardiopulmonary bypass; CRF, case report form; GLUTAMICS, glutamate for metabolic intervention in coronary surgery; ICU, intensive care unit; NAD, nicotinamide adenine dinucleotide (oxidised form); NADH, nicotinamide adenine dinucleotide (reduced form)

References

  1. Vidlund M, Hakanson E, Friberg O, Juhl-Andersen S, Holm J, Vanky F, Sunnermalm L, Borg JO, Sharma R, Svedjeholm R. GLUTAMICS - a randomized clinical trial on glutamate infusion in 861 patients undergoing surgery for acute coronary syndrome. J Thorac Cardiovasc Surg. 2012;144(4):922–30. e927.

    Article  CAS  PubMed  Google Scholar 

  2. Svedjeholm R, Hakanson E, Szabo Z. Routine SvO2 measurement after CABG surgery with a surgically introduced pulmonary artery catheter. Eur J Cardiothorac Surg. 1999;16(4):450–7.

    Article  CAS  PubMed  Google Scholar 

  3. Holm J, Hakanson E, Vanky F, Svedjeholm R. Mixed venous oxygen saturation predicts short- and long-term outcome after coronary artery bypass grafting surgery: a retrospective cohort analysis. Br J Anaesth. 2011;107(3):344–50.

    Article  CAS  PubMed  Google Scholar 

  4. Svedjeholm R, Vidlund M, Vanhanen I, Hakanson E. A metabolic protective strategy could improve long-term survival in patients with LV-dysfunction undergoing CABG. Scand Cardiovasc J. 2010;44(1):45–58.

    Article  CAS  PubMed  Google Scholar 

  5. O’Connor GT, Birkmeyer JD, Dacey LJ, Quinton HB, Marrin CA, Birkmeyer NJ, Morton JR, Leavitt BJ, Maloney CT, Hernandez F, et al. Results of a regional study of modes of death associated with coronary artery bypass grafting. Northern New England Cardiovascular Disease Study Group. Ann Thorac Surg. 1998;66(4):1323–8.

    Article  PubMed  Google Scholar 

  6. Vanky F, Hakanson E, Maros T, Svedjeholm R. Different characteristics of postoperative heart failure after surgery for aortic stenosis and coronary disease. Scand Cardiovasc J. 2004;38(3):152–8.

    Article  PubMed  Google Scholar 

  7. Vanky FB, Hakanson E, Svedjeholm R. Long-term consequences of postoperative heart failure after surgery for aortic stenosis compared with coronary surgery. Ann Thorac Surg. 2007;83(6):2036–43.

    Article  PubMed  Google Scholar 

  8. Maganti MD, Rao V, Borger MA, Ivanov J, David TE. Predictors of low cardiac output syndrome after isolated aortic valve surgery. Circulation. 2005;112(9 Suppl):I448–52.

    PubMed  Google Scholar 

  9. Kirklin JW, Rastelli GC. Low cardiac output after open intracardiac operations. Prog Cardiovasc Dis. 1967;10(2):117–22.

    Article  CAS  PubMed  Google Scholar 

  10. Gillies M, Bellomo R, Doolan L, Buxton B. Bench-to-bedside review: Inotropic drug therapy after adult cardiac surgery - a systematic literature review. Crit Care. 2005;9(3):266–79.

    Article  PubMed  Google Scholar 

  11. Mebazaa A, Pitsis AA, Rudiger A, Toller W, Longrois D, Ricksten SE, Bobek I, De Hert S, Wieselthaler G, Schirmer U, et al. Clinical review: practical recommendations on the management of perioperative heart failure in cardiac surgery. Crit Care. 2010;14(2):201. Epub 2010 Apr 2028.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Fellahi JL, Parienti JJ, Hanouz JL, Plaud B, Riou B, Ouattara A. Perioperative use of dobutamine in cardiac surgery and adverse cardiac outcome: propensity-adjusted analyses. Anesthesiology. 2008;108(6):979–87.

    Article  CAS  PubMed  Google Scholar 

  13. Svedjeholm R, Hallhagen S, Ekroth R, Joachimsson PO, Ronquist G. Dopamine and high-dose insulin infusion (glucose-insulin-potassium) after a cardiac operation: effects on myocardial metabolism. Ann Thorac Surg. 1991;51(2):262–70.

    Article  CAS  PubMed  Google Scholar 

  14. Lazar HL, Buckberg GD, Foglia RP, Manganaro AJ, Maloney Jr JV. Detrimental effects of premature use of inotropic drugs to discontinue cardiopulmonary bypass. J Thorac Cardiovasc Surg. 1981;82(1):18–25.

    CAS  PubMed  Google Scholar 

  15. Hakanson E, Svedjeholm R, Vanhanen I. Physiologic aspects in postoperative cardiac patients. Ann Thorac Surg. 1995;59(2 Suppl):S12–4.

    Article  CAS  PubMed  Google Scholar 

  16. Maroko PR, Kjekshus JK, Sobel BE, Watanabe T, Covell JW, Ross Jr J, Braunwald E. Factors influencing infarct size following experimental coronary artery occlusions. Circulation. 1971;43(1):67–82.

    Article  CAS  PubMed  Google Scholar 

  17. Slogoff S, Keats AS. Does perioperative myocardial ischemia lead to postoperative myocardial infarction? Anesthesiology. 1985;62(2):107–14.

    Article  CAS  PubMed  Google Scholar 

  18. Aya HD, Cecconi M, Hamilton M, Rhodes A. Goal-directed therapy in cardiac surgery: a systematic review and meta-analysis. Br J Anaesth. 2013;110(4):510–7.

    Article  CAS  PubMed  Google Scholar 

  19. Giglio M, Dalfino L, Puntillo F, Rubino G, Marucci M, Brienza N. Haemodynamic goal-directed therapy in cardiac and vascular surgery. A systematic review and meta-analysis. Interact Cardiovasc Thorac Surg. 2012;15(5):878–87.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Shahin J, DeVarennes B, Tse CW, Amarica DA, Dial S. The relationship between inotrope exposure, six-hour postoperative physiological variables, hospital mortality and renal dysfunction in patients undergoing cardiac surgery. Crit Care. 2011;15(4):R162.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Rau EE, Shine KI, Gervais A, Douglas AM, Amos EC. Enhanced mechanical recovery of anoxic and ischemic myocardium by amino acid perfusion. Am J Physiol. 1979;236(6):H873–9.

    CAS  PubMed  Google Scholar 

  22. Safer B. The metabolic significance of the malate-aspartate cycle in heart. Circ Res. 1975;37(5):527–33.

    Article  CAS  PubMed  Google Scholar 

  23. Pisarenko OI. Mechanisms of myocardial protection by amino acids: facts and hypotheses. Clin Exp Pharm Physiol. 1996;23(8):627–33.

    Article  CAS  Google Scholar 

  24. Svedjeholm R, Hakanson E, Vanhanen I. Rationale for metabolic support with amino acids and glucose-insulin-potassium (GIK) in cardiac surgery. Ann Thorac Surg. 1995;59(2 Suppl):S15–22.

    Article  CAS  PubMed  Google Scholar 

  25. Lazar HL, Buckberg GD, Manganaro AJ, Becker H. Myocardial energy replenishment and reversal of ischemic damage by substrate enhancement of secondary blood cardioplegia with amino acids during reperfusion. J Thorac Cardiovasc Surg. 1980;80(3):350–9.

    CAS  PubMed  Google Scholar 

  26. Haas GS, DeBoer LW, O’Keefe DD, Bodenhamer RM, Geffin GA, Drop LJ, Teplick RS, Daggett WM. Reduction of postischemic myocardial dysfunction by substrate repletion during reperfusion. Circulation. 1984;70(3 Pt 2):I65–74.

    CAS  PubMed  Google Scholar 

  27. Engelman RM, Rousou JA, Flack JE, Iyengar J, Kimura Y, Das DK. Reduction of infarct size by systemic amino acid supplementation during reperfusion. J Thorac Cardiovasc Surg. 1991;101(5):855–9.

    CAS  PubMed  Google Scholar 

  28. Pisarenko OI, Lepilin MG, Ivanov VE. Cardiac metabolism and performance during L-glutamic acid infusion in postoperative cardiac failure. Clin Sci. 1986;70(1):7–12.

    Article  CAS  PubMed  Google Scholar 

  29. Svedjeholm R, Vanhanen I, Hakanson E, Joachimsson PO, Jorfeldt L, Nilsson L. Metabolic and hemodynamic effects of intravenous glutamate infusion early after coronary operations. J Thorac Cardiovasc Surg. 1996;112(6):1468–77.

    Article  CAS  PubMed  Google Scholar 

  30. Loop FD, Higgins TL, Panda R, Pearce G, Estafanous FG. Myocardial protection during cardiac operations. Decreased morbidity and lower cost with blood cardioplegia and coronary sinus perfusion. J Thorac Cardiovasc Surg. 1992;104(3):608–18.

    CAS  PubMed  Google Scholar 

  31. Svedjeholm R, Hakanson E, Szabo Z, Vanky F. Neurological injury after surgery for ischemic heart disease: risk factors, outcome and role of metabolic interventions. Eur J Cardiothorac Surg. 2001;19(5):611–8.

    Article  CAS  PubMed  Google Scholar 

  32. Vidlund M, Holm J, Hakanson E, Friberg O, Sunnermalm L, Vanky F, Svedjeholm R. The S-100B substudy of the GLUTAMICS trial: Glutamate infusion not associated with sustained elevation of plasma S-100B after coronary surgery. Clin Nutr. 2009;21(3):358–64.

    Google Scholar 

  33. Vanhanen I, Svedjeholm R, Hakanson E, Joachimsson PO, Jorfeldt L, Nilsson L, Vanky F. Assessment of myocardial glutamate requirements early after coronary artery bypass surgery. Scand Cardiovasc J. 1998;32(3):145–52.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We would like to acknowledge Olle Eriksson and Kalle Wahlin, Department of Computer and Information Science, Linköping University, for statistical advice. We are indebted to research nurses Inger Huljebrant, Sara Thybell, Anna Krantz and Ann-Kristin Olsson for assistance with data collection.

Funding

This work was supported by grants from The Swedish Heart-Lung Foundation [20030595]. Capio Research Foundation [2005-1021;2006-1203]. Linköping University and Östergötlands Läns Landsting.

Availability of data and materials

Data will be available for audit provided that professional secrecy applies. Due to the nature of data it will not be available for general access in order to protect the identity of individual participants.

Authors’ contributions

MV Patient recruitment, endpoint committee, study design, analysis and interpretation of data, author; BT Data collection, analysis and interpretation of data, co-author; EH Patient recruitment, endpoint committee, interpretation of data co-author; ÖF Patient recruitment, endpoint committee, interpretation of data co-author; JH; Patient recruitment, endpoint committee, interpretation of data, co-author; FV Patient recruitment, endpoint committee, interpretation of data, co-author; RS Principal investigator, study design, patient recruitment, endpoint committee, analysis and interpretation of data, senior author. All authors read and approved the final manuscript.

Authors’ information

M.V. MD, PhD, Consultant Cardiothoracic Surgeon; B.T Medical student; E.H. MD PhD Consultant Cardiothoracic Anaesthesiologist; Ö.F. MD, PhD, Consultant Cardiothoracic Surgeon; J.H; MD, PhD, Consultant Cardiothoracic Surgeon; F.V. MD, PhD, Consultant Cardiothoracic Surgeon; R.S. MD, PhD, Professor, Consultant Cardiothoracic Surgeon.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

The study was conducted in accordance with the Helsinki Declaration of Human Rights and was approved by and the Regional Ethical Review Board in Linköping (M76-05) and the Swedish Medical Products Agency (151:2003/70403). The patients were enrolled in the study after written informed consent.

Author information

Authors and Affiliations

  1. Department of Cardiothoracic Surgery and Cardiothoracic Anaesthesia, Faculty of Medicine and Health Sciences, Division of Cardiovascular Medicine, Linköping University, Linköping, Sweden

    Bashir Tajik, Erik Håkanson, Jonas Holm, Farkas Vanky & Rolf Svedjeholm

  2. Department of Cardiothoracic and Vascular Surgery, Faculty of Medicine and Health, Örebro University, Örebro, Sweden

    Mårten Vidlund & Örjan Friberg

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  1. Mårten Vidlund
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Correspondence to Rolf Svedjeholm.

Additional file

Additional file 1:

Details of intervention, study design, inclusion criteria, exclusion criteria, definition of endpoints, stopping criteria, data collection, routines for unblinding, clinical management and clinical endpoints committee. (DOC 72 kb)

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Vidlund, M., Tajik, B., Håkanson, E. et al. Post hoc analysis of the glutamics–trial: intravenous glutamate infusion and use of inotropic drugs after cabg. BMC Anesthesiol 16, 54 (2015). https://doi.org/10.1186/s12871-016-0216-z

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  • DOI: https://doi.org/10.1186/s12871-016-0216-z

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BMC Anesthesiology

ISSN: 1471-2253

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