Effect of morphine-induced postconditioning in corrections of tetralogy of fallot
© Zhang et al.; licensee BioMed Central Ltd. 2013
Received: 10 December 2012
Accepted: 26 March 2013
Published: 11 April 2013
Results of previous reports on ischemic postconditioning in animals and humans were very encouraging. Although ischemic postconditioning possessed a wide prospect of clinical application, debates on the precise ischemic postconditioning algorithm to use in clinical settings were ongoing. In this regard, pharmacological strategies were possible alternative methods. Accumulating data demonstrated that pharmacological postconditioning with morphine conferred cardioprotection in animals. This trial aimed to evaluate the effect of morphine-induced postconditioning on protection against myocardial ischemia/reperfusion injury in patients undergoing corrections of Tetralogy of Fallot (TOF).
Eight-nine consecutive children scheduled for corrections of TOF were enrolled and randomly assigned to either a postconditioning group (patients received a dose of morphine (0.1 mg/kg) injected via a cardioplegia needle into the aortic root for direct and focused delivery to the heart within 1 minute starting at 3 min before aorta cross-clamp removal, n=44) or a control group (the same protocol was performed as in the postconditioning group except that patients received the same volume of saline instead, n=45). The peri-operative relevant data were investigated and analyzed, and the cardiac troponin I (cTnI) was assayed preoperatively, and then 4 h, 8 h, 12 h, 24 h and 48 h after reperfusion.
Morphine-induced postconditioning reduced postoperative peak cTnI release as compared to the control group (0.57 ± 0.15 versus 0.75 ± 0.20 ng/mL, p<0.0001). Morphine-induced postconditioned patients had lower peak inotropic score (5.7 ± 2.4 versus 8.4 ± 3.6, p<0.0001) and shorter duration of mechanical ventilation as well as ICU stay (20.6 ± 6.8 versus 28.5 ± 8.3 hours, p<0.0001 and 40.4 ± 10.3 versus 57.8 ± 15.2 hours, p<0.0001, respectively), while higher left ventricular ejection fraction as well as cardiac output (0.57±0.15 versus 0.51±0.13, p=0.0467 and 1.39 ± 0.25 versus 1.24 ± 0.21 L/min, p=0.0029, respectively) as compared to the control group during the first postoperative 24 hours.
Morphine-induced postconditioning may provide enhanced cardioprotection against ischemia/reperfusion injury in children undergoing corrections of TOF.
KeywordsPharmacological postconditioning Morphine Ischemia reperfusion injury Pediatric cardiac surgery Trials
Although the application of cardioplegia is an effective strategy for cardio-protection, it does not completely eradicate myocardial ischemia/reperfusion injury due to cardiac arrest during cardiac surgery. It was well-established that ischemic preconditioning, which involved a series of brief ischemia/reperfusion cycles before index ischemia, was explicitly cardioprotective strategy [1–5]. Unlike preconditioning, ischemic postconditioning, which involved brief episodes of ischemia/reperfusion during early reperfusion, did not require initiation before the ischemic event [1–8]. And hence, ischemic postconditioning was easily performed in all cardiac operations such as in those for severe aortic valve insufficiency or aortic valve stenosis where preconditioning often was difficult to be carried out before operation due to possible heart arrest and distension induced during repeated aortic clamping [1–8]. Results of previous reports on ischemic postconditioning were very encouraging in animals and humans [1–10].
Although ischemic postconditioning possessed a wide prospect of clinical application, debates on the precise ischemic postconditioning algorithm to use in clinical settings were ongoing. In this regard, pharmacological strategies [11, 12], which would avoid some adverse consequences associated with intermittent cross-clamping (such as aortic injury, left ventricular distention, and malignant arrhythmia), were possible alternative methods. Morphine, a classic opioid drug, was particularly interesting cardioprotective ligands to anesthesiologists and clinicians due to their widely used perioperatively. Schultz’s group first reported that morphine-induced preconditioning mimicked ischemic preconditioning . Accumulating data demonstrated that morphine-induced postconditioning provided powerful cardioprotective effect, which seemed to be similar to ischemic postconditioning [12, 14–17]. So far, the vast majority of previous studies assessed the impact of morphine-induced postconditioning on cardioprotection in animal experiments. However,there were few reports focused on morphine-induced postconditioning in the field of cardiac surgery, especially pediatric cardiac surgery [12, 18]. Although major advances have been made in the field of cardiac surgery for Tetralogy of Fallot (TOF), inadequate myocardial protection may remain a persistent source of mortality and morbidity associated with surgery for TOF . Whether morphine-induced postconditioning has an additive effect on cardioplegia or not in the setting of pediatric cardiac surgery for TOF remains to be determined.
The purpose of this study was to test the hypothesis that morphine-induced postconditioning could provide enhanced cardio-protection against ischemia/ reperfusion injury in children undergoing corrections of TOF.
Eligible patients were less than 18 years of age, scheduled for total correction of TOF, and cardiac function NYHA class I-III.
Exclusion criteria were as follows: TOF with pulmonary atresia, TOF with absent pulmonary artery, concomitant infective endocarditis, prior palliation with a systemic-to-pulmonary artery shunt, postoperative residual ventricular septal defect, and postoperative moderate and severe pulmonary valve regurgitation.
All selected patients underwent preoperative electrocardiogram, chest X-ray film and echocardiography. None of selected patients received preoperative inotropic support. The guardians of selected patients signed an informed consent approved by the ethics committee.
This study protocol was approved by the ethics committee of Tongji hospital affiliated to Tongji University and was consistent with the Declaration of Helsinki.
All selected patients were divided randomly into either a postconditioning group or a control group through a computer-generated randomization sequence. The randomization assignment for each patient was kept in a sealed envelope which was opened by a trial investigator at the time of patient enrollment. The hospital staff caring for postoperative patients was blinded for group allocation.
In the postconditioning group, starting at 3 min before aorta cross-clamp removal, patients received a dose of morphine (0.1 mg/kg) injected via a cardioplegia needle into the aortic root for direct and focused delivery to the heart within 1 minute. In the control group, the same protocol was performed as in the postconditioning group except that patients received the same volume of saline instead.
The pre-, intra- and post-operative relevant data of all selected patients were investigated and analyzed. Preoperative information included age, gender, weight, McGoon ratio, left ventricular end-diastolic volume index (LVEDVI), left ventricular ejection fraction (LVEF), cardiac output, hemoglobin, and saturation of arterial blood oxygen (in absence of supplemental oxygen administration). Intraoperative variables included operative type (transannular patches or not), duration of cardiopulmonary bypass (CPB) and aortic cross clamping (ACC), and resumption of cardiac activity/rhythm. Postoperative data included the first postoperative 24-hour parameters (such as urine volume, drainage volume, blood transfusion volume, peak inotropic score, creatinine, use of furosemide as well as its intravenous infusion dose), duration of mechanical ventilation and intensive care unit (ICU) stay, and in-hospital mortality. Echocardiography was performed to assess LVEF and cardiac output during the first postoperative day and before discharge. All patients were followed up for at least 30 days following surgery.
The McGoon ratio is calculated by dividing the sum of the diameter of the bilateral central pulmonary arteries by the diameter of the descending aorta at the level of the diaphragm. The first postoperative 24-hour quantitative measures of inotropes were evaluated by the inotropic score according to the following formula : ([dopamine + dobutamine] ×1) + (milrinone × 15) + ([epinephrine + norepinephrine + isoprenaline] ×100).
Management of inotropic dose was according to hemodynamic stability as reflected by such parameters as arterial blood pressure, central venous pressure, etc. Dopamine was employed as the first-line inotrope with epinephrine and/or norepinephrine as second-line inotrope for hemodynamic support in cases of hemodynamic instability as reflected by systemic blood pressure inadequacy despite maximal fluid management and dopamine use. Weaning from mechanical ventilation depended on hemodynamics, arterial blood gas analysis, etc. to assess for cardiopulmonary function; no excessive bleeding and a mandatory chest radiograph before extubation to rule out pneumothorax, pleural effusion and atelectasis. Criteria for leaving ICU included an alert, hemodynamically stable patient with an inotropic score less than 5, better pulmonary function with no metabolic acidosis, urine output more than 0.5 ml/kg/h and a mandatory chest radiograph before leaving ICU to rule out pneumothorax, pleural effusion and atelectasis. The indications that guided the use of furosemide included oliguria (urine output <0.5 ml/kg/h) and development of hypervolemia .
Blood sampling and biochemical analysis
For each patient, 2 ml blood samples were collected preoperatively, and then 4 hours, 8 hours, 12 hours, 24 hours, and 48 hours after aorta cross-clamp removal for determination of the plasma levels of cardiac troponin I (cTnI). The blood samples were transferred into dry glass tubes and stored at 4°C until centrifugation. Plasma separated after centrifugation was frozen at −80 C until assayed for cTnI using the cTnI ELISA kit which was obtained from Jidan Biotechnology Company (Nanjing, China). The cTnI values were expressed as ng/ml (normal reference value in our hospital: <0.15 ng/mL). The cTnI concentration was measured in the clinical laboratory of our hospital by individuals unaware of the group allocation.
Total cTnI release in the control and postconditioning group was represented as an area under curve (AUC) from preoperation (C0) to the last sampling time (C48). It was calculated using the equation for determining trapezoid area as follows : AUC0-48 = [(C0+C4) ×4+ (C4+C8) ×4+ (C8+C12) ×4+ (C12+C24) ×12+ (C24+C48) ×24] /2. Total cTnI release from C0 to C8 and C8 to C48 represented as AUC0-8 and AUC8-48 respectively, were calculated accordingly.
During the surgical procedure, anesthesia was induced with midazolam (0.05 mg/kg), fentanyl (4 μg/kg) and vecuronium (0.1 μg/kg), and maintained with intravenous fentanyl (total amount of fentanyl was less than 15 μg/kg during operation). All the operations were performed by the same surgical team. The operations were performed using moderate hypothermic cardiopulmonary bypass (28-31°C) with bicaval cannulation and left heart venting via the right superior pulmonary vein. The myocardium was protected using intermittent perfusion of cold blood cardioplegic solution at 4°C and in a ratio of 1:4. The cold blood cardioplegia which was composed of sodium chloride at 132 mmol/L, potassium chloride at 16 mmol/L, calcium chloride at 1.8 mmol/L, magnesium sulphate at 15 mmol/L, procaine at 0.05 mmol/L, and sodium bicarbonate at 19 mmol/L, was infused into the aortic root if there was no aortic valve regurgitation. For patients with aortic regurgitation, the aorta was opened promptly after the cross-clamp was applied, the left and right coronary artery ostia were cannulated, and the cold blood cardioplegia was delivered though a Y bifurcated catheter. The initial dose of cardioplegia infused was at 20 ml/kg; thereafter, the cardioplegia solution was re-infused every 30 min at a dose of 10 ml/kg. Modified ultrafiltration was used following separation from bypass. All patients received similar standard postoperative care in our institution.
The sample size calculations are based on a serum concentration of cTnI at post-reperfusion time points of 4 hours of 0.60 ng/mL for the postconditioning group and of 0.75 ng/mL for the control group according to results of preliminary studies. With an α level of 0.05 and a test power of 0.80, the resulting sample size was 40 patients for each group. A risk of loss of patients to follow up of 1-5% was assumed.
Statistical analysis was performed using the SPSS 13.0 statistical software package. Data are expressed as means ± standard deviation for continuous variables, and frequencies were measured for categorical variables. The unpaired t-test or t’-test according to homogeneity test for variance was used to compare measurement data and Fisher’s exact test was used to compare enumeration data. Repeated-measure analysis of variance was used to evaluate differences over time within groups for cTnI. All p values <0.05 were considered to be statistically significant.
From January 2010 to December 2011, after obtained approval by the ethic committee and written informed consent, a total of 99 consecutive patients who met the inclusion criteria were randomly divided either into a postconditioning group (n=49) or into a control group (n=50). Among them, 10 patients were excluded (infective endocarditis in 5 patients, TOF with absent left pulmonary artery in 3 patients, and postoperative residual VSD in 2 patients). Finally, the outcome analysis was conducted on 44 patients in the postconditioning group and 45 patients in the control group.
Demographic and clinical features
Cardiac output (L/min)
Operative and postoperative characteristics
Transannular patches (%)
CPB time (min)
Aortic cross-clamp time (min)
Redo surgery for bleeding
First postoperative 24 hours
Blood transfusion volume (ml/kg/24 h)
Drainage volume (ml/kg/24 h)
Peak inotropic score
Urine volume (ml/kg/24 h)
Use of furosemide
Dose of furosemide (mg/kg/24 h)
Duration of mechanical ventilation (h)
Duration of ICU stay (h)
Pre- and post-operative LVEF and cardiac output
Postoperative first day
Cardiac output (L/min)
Postoperative first day
Level of plasma cTnI
The important finding of this trial was that morphine-induced postconditioning was related to less cTnI release postoperatively. Results of this trial showed that levels of plasma cTnI at all time-points after reperfusion increased sharply and remained high for at least 48 hours in both groups, which meant myocardial injury occurred and lasted for at least 48 hours after reperfusion. Plasma cTnI levels hit their peak values at the post-reperfusion time point of 4 hours in both groups, demonstrating myocardial injury occurred mostly during the first 4 hours after reperfusion. The morphine-induced postconditioned patients showing significant reduction of cTnI levels at the time points of 4 and 8 hours, especially the AUC calculation over the first 48 hours after aortic cross-clamp removal as compared to the control patients, might imply that the morphine-induced postconditioned patients received less myocardium injury as compared to the control patients. So, morphine-induced postconditioning used in this trial was able in part to relieve myocardial injury in patients with TOF undergoing cardioplegic arrest. Since most of cTnI is eliminated in urine, urine output might significantly affect its serum level [8, 19]. Consequently, we concomitantly investigated the patients’ urine output during their first 24 hours in ICU, and found no significant difference in urine output between the two groups. Therefore, we can infer that the differences in serum cTnI levels between the two groups, particularly the cTnI AUC levels, could not be related to urine output but rather reflected release of different concentrations of cTnI by the two groups at different time points in this trial.
Two important mechanisms of cellular damage have been associated with cardioplegic arrest during open heart surgery, namely ischemic injury and reperfusion injury. In this trial, morphine-induced postconditioning reduced postoperative peak release of cTnI at the post-reperfusion time point of 4 hours by 31.6% compared to the control group and total cTnI release by 47.7% during the first postoperative 8 hours, suggesting that morphine-induced postconditioning may help to reduce myocardial injury induced by ischemia. However, cTnI release in the postconditioning group was similar to the control group at the post-reperfusion time points of 12, 24 and 48 hours, and the AUC8-48 of the two groups were alike, which might indicate that the degree of myocardial injury induced by the reperfusion was similar in the two groups and that morphine-induced postconditioning had failed to reduce myocardial injury induced by reperfusion [8, 11]. This result was consistent with ischemic postconditioning reported previously [7, 9, 19].
Another important finding of this trial was that the morphine-induced postconditioned patients received some clinical benefits. Morphine-induced postconditioning reduced the peak inotropic score as well as the use of furosemide and increased LVEF as well as cardiac output during the first postoperative day, which might imply that morphine-induced postconditioning was related to better postoperative hemodynamics. In addition, the duration of mechanical ventilation in the postconditioning group was much shorter than that in the control group, which might infer that morphine-induced postconditioning was related to better postoperative cardiopulmonary function. Less inotropic drug use, higher LVEF as well as cardiac output, and shorter duration of mechanical ventilation coincided with reduction of plasma cTnI release, which might contribute to shorter length of ICU stay in morphine-induced postconditioned patients undergoing corrections of TOF. Although its protective effects could not be translated into more obvious clinical benefits such as lower mortality, morphine-induced postconditioning really provided enhanced cardioprotection and produced some clinical benefits mentioned above.
There are several limitations of this trial. Firstly, some important clinical decisions (for example, inotropes) were decided by clinician at work instead of specific protocols, weakening the inotropic score as an important endpoint of this trial. Secondly, enrolled patients were in a low-medium risk condition with short duration of aortic cross-clamping. It remains to be determined if high-risk patients such as those with prolonged aortic cross-clamping may benefit more from morphine-induced postconditioning. Thirdly, fentanyl also is a widely used opioid along with morphine during general anesthesia, and fentanil-induced postconditioning also protects ischemia/reperfusion. The plasma concentrations of fentanil were not measured in this study. Finally, this study was only a clinical observational trial in a single centre. Effective myocardial tissue concentration of morphine was not detected in this clinical trial, and the precise mechanisms of morphine-induced postconditioning in humans were not explored. Multi-centre clinical trials involving larger sample size are needed to determine the clinical effect of morphine-induced postconditioning in pediatric cardiac surgery.
In summary, this trial showed morphine-induced postconditioning before the removal of the aortic clamp was related to less cTnI release, decreased inotropic drug use, increased LVEF as well as cardiac output, and shorter duration of mechanical ventilation as well as ICU stay. This clinical observational trial suggested morphine-induced postconditioning may provide enhanced cardioprotection against ischemia/reperfusion injury in children undergoing corrections of TOF.
Tetralogy of Fallot
Cardiac troponin I
Left ventricular end-diastolic volume index
Left ventricular ejection fraction
Aortic cross clamping
Intensive care unit
Area under curve.
- Kloner RA, Rezkalla SH: Preconditioning, postconditioning and their application to clinical cardiology. Cardiovasc Res. 2006, 70: 297-307. 10.1016/j.cardiores.2006.01.012.View ArticlePubMedGoogle Scholar
- Granfeldt A, Lefer DJ, Vinten-Johansen J: Protective ischemia in patients: preconditioning and postconditioning. Cardiovasc Res. 2009, 83: 234-246. 10.1093/cvr/cvp129.View ArticlePubMedPubMed CentralGoogle Scholar
- Crisostomo PR, Wairiuko GM, Wang M, Tsai BM, Morrell ED, Meldrum DR: Preconditioning versus postconditioning: mechanisms and therapeutic potentials. J Am Coll Surg. 2006, 202: 797-812. 10.1016/j.jamcollsurg.2005.12.002.View ArticlePubMedGoogle Scholar
- Hausenloy DJ, Yellon DM: Preconditioning and postconditioning: underlying mechanisms and clinical application. Atherosclerosis. 2009, 204: 334-341. 10.1016/j.atherosclerosis.2008.10.029.View ArticlePubMedGoogle Scholar
- Zhao ZQ, Corvera JS, Halkos ME, Kerendi F, Wang NP, Guyton RA, Vinten-Johansen J: Inhibition of myocardial injury by ischemic postconditioning during reperfusion: comparison with ischemic preconditioning. Am J Physiol Heart Circ Physiol. 2003, 285: H579-H588.View ArticlePubMedGoogle Scholar
- Zhao ZQ, Vinten-Johansen J: Postconditioning: reduction of reperfusion induced injury. Cardiovasc Res. 2006, 70: 200-211. 10.1016/j.cardiores.2006.01.024.View ArticlePubMedGoogle Scholar
- Staat P, Rioufol G, Piot C, Cottin Y, Cung TT, L’Huillier I, Aupetit JF, Bonnefoy E, Finet G, André-Fouët X, Ovize M: Postconditioning the human heart. Circulation. 2005, 112: 2143-2148. 10.1161/CIRCULATIONAHA.105.558122.View ArticlePubMedGoogle Scholar
- Ji Q, Mei Y, Wang X, Feng J, Wusha D, Cai J, Zhou Y: Effect of ischemic postconditioning in correction of tetralogy of Fallot. Int Heart J. 2011, 52: 312-317. 10.1536/ihj.52.312.View ArticlePubMedGoogle Scholar
- Garcia S, Henry TD, Wang YL, Chavez IJ, Pedersen WR, Lesser JR, Shroff GR, Moore L, Traverse JH: Long-term follow-up of patients undergoing postconditioning during ST-elevation myocardial infarction. J Cardiovasc Transl Res. 2011, 4: 92-98. 10.1007/s12265-010-9252-0.View ArticlePubMedGoogle Scholar
- Laskey WK: Brief repetitive balloon occlusions enhance reperfusion during percutaneous coronary intervention for acute myocardial infarction: a pilot study. Catheter Cardiovasc Interv. 2005, 65: 361-367. 10.1002/ccd.20397.View ArticlePubMedGoogle Scholar
- Jin ZX, Zhou JJ, Xin M, Peng DR, Wang XM, Bi SH, Wei XF, Yi DH: Postconditioning the human heart with adenosine in heart valve replacement surgery. Ann Thorac Surg. 2007, 83: 2066-2073. 10.1016/j.athoracsur.2006.12.031.View ArticlePubMedGoogle Scholar
- Kim JM, Jang YH, Kim J: Morphine and remifentanil-induced cardioprotection: its experimental and clinical outcomes. Korean J Anesthesiol. 2011, 61: 358-366. 10.4097/kjae.2011.61.5.358.View ArticlePubMedPubMed CentralGoogle Scholar
- Schultz JE, Hsu AK, Gross GJ: Morphine mimics the cardioprotective effect of ischemic preconditioning via a glibenclamide-sensitive mechanism in the rat heart. Circ Res. 1996, 8: 1100-1104.View ArticleGoogle Scholar
- Chen Z, Li T, Zhang B: Morphine postconditioning protects against reperfusion injury in the isolated rat hearts. J Surg Res. 2008, 145: 287-294. 10.1016/j.jss.2007.07.020.View ArticlePubMedGoogle Scholar
- Chang WL, Lee SS, Su MJ: Attenuation of post-ischemia reperfusion injury by thaliporphine and morphine in rat hearts. J Biomed Sci. 2005, 12: 611-619. 10.1007/s11373-005-7401-2.View ArticlePubMedGoogle Scholar
- Ling Ling J, Wong GT, Yao L, Xia Z, Irwin MG: Remote pharmacological postconditioning by intrathecal morphine: cardiac protection from spinal opioid receptor activation. Acta Anaesthesiol Scand. 2010, 54: 1097-1104. 10.1111/j.1399-6576.2010.02295.x.View ArticlePubMedGoogle Scholar
- Gong ZX, Ran K, Chang YT, Xu JM: Effect of morphine postconditioning on myocardial ischemia-reperfusion injury in rabbits. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2009, 38: 521-524.PubMedGoogle Scholar
- Jang Y, Xi J, Wang H, Mueller RA, Norfleet EA, Xu Z: Postconditioning prevents reperfusion injury by activating delta-opioid receptors. Anesthesiology. 2008, 108 (2): 243-50. 10.1097/01.anes.0000299437.93898.4a.View ArticlePubMedGoogle Scholar
- Luo WJ, Li B, Lin GQ, Huang R: Postconditioning in cardiac surgery for tetralogy of Fallot. J Thorac Cardiovasc Surg. 2007, 133: 1373-1374. 10.1016/j.jtcvs.2007.01.028.View ArticlePubMedGoogle Scholar
- Weihrauch D, Krolikowski JG, Bienengraeber M, Kersten JR, Warltier DC, Pagel PS: Morphine enhances isoflurane-induced postconditioning against myocardial infarction: the role of phosphatidylinositol-3-kinase and opioid receptors in rabbits. Anesth Analg. 2005, 101: 942-949. 10.1213/01.ane.0000171931.08371.a2.View ArticlePubMedGoogle Scholar
- Mao Z, Du X, Sun Z, Xia J: Involvement of opioid receptors in ischemic postconditioning in the isolated rat hearts. Acta Med Univ Sci Technol Huazhong. 2007, 36: 610-613.Google Scholar
- Shore S, Nelson DP, Pearl JM, Manning PB, Wong H, Shanley TP, Keyser T, Schwartz SM: Usefulness of corticosteroid therapy in decreasing epinephrine requirements in critically ill infants with congenital heart disease. Am J Cardiol. 2001, 88: 591-594. 10.1016/S0002-9149(01)01751-9.View ArticlePubMedGoogle Scholar