Morphine Post-Conditioning Effect on QT Dispersion in Patients Undergoing Primary Percutaneous Coronary Intervention on Anterior Descending Cardiac Artery

A Cohort Study

Authors

  • Mohammad Tayyebi M.D., Assistant Professor, Department of Cardiology, Atherosclerosis Prevention Research Center, Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, Iran

Keywords:

Morphine, Angioplasty, Electrocardiogram, QT-Dispersion

Abstract

Introduction: QT dispersion is the difference between the maximum and minimum QTc interval in a 12-lead electrocardiogram (ECG). Some researchers have demonstrated the effects of an increase of QT-d in STEMI and its reduction with successful therapy. The aim of this study was to investigate the morphine post-conditioning effect on the QT dispersion in patients undergoing primary percutaneous coronary intervention (PCI) on anterior descending cardiac artery.

Methods: This cohort study was conducted on STEMI patients admitted to the Hospital of Imam Reza (AS), Mashhad, Iran, from March 2015 to February 2016 who were undergoing primary angioplasty on the anterior descending cardiac artery. The patients were divided into two groups based on the intake or non-intake of morphine (5 mg morphine for the period of 30 minutes prior to PCI). Parameters, including age, gender, history of diabetes, and blood pressure as well as admission and 24 hours after PCI ejection fraction (EF) and QT-d, were recorded in all patients and compared between the two intervention and control groups. Independent and paired t-tests and chi-square test were used to compare the qualitative and quantitative data between the two groups using SPSS version 19 software.

Results: The present research was performed on 77 patients (61 males) with mean age of 58.71±11.84 years in the two groups of morphine consumption before PCI (n=46) and control (n=31). No statistical difference was found among the groups in age, gender, diabetes, hypertension, and onset of symptoms until primary PCI. Admission electrocardiogram QT-d value in the positive exposure group showed no significant difference with the control group, but QT-d value at 24 hours after PCI was lower in the positive exposure group than in the control group (morphine versus control: 40.32±6.98 versus 59.64±8.89; p=0.000). QT-d value 24 hours after PCI compared with the admission QT-d value was significantly reduced in both groups. The mean decrease of admission QT-d relative to QT-d 24 hours after PCI was higher in the positive exposure group than in the control group, and this difference was also statistically significant (morphine versus control: 48.65±9.95 versus 25.74±6.66; p=0.000).

Conclusion: The findings of the current survey demonstrated that morphine consumption before PCI can further reduce QT-d value in an electrocardiogram for PCI as compared to patients who did not take morphine before PCI.

References

Lloyd-Jones D, Adams R, Carnethon M, De Simone G, Ferguson TB, Flegal K, et al. Heart disease and

stroke statistics-2009 update a report from the American Heart Association Statistics Committee and Stroke

Statistics Subcommittee. Circulation. 2009; 119(3): e21-181. doi:

1161/CIRCULATIONAHA.108.191261. PMID: 19075105.

Schuijf JD, Kaandorp TA, Lamb HJ, van der Geest RJ, Viergever EP, van der Wall EE, et al.

Quantification of myocardial infarct size and transmurality by contrast-enhanced magnetic resonance

imaging in men. Am J Cardiol. 2004; 94(3): 284-8. doi: 10.1016/j.amjcard.2004.04.020. PMID: 15276089.

Gibbons RJ, Valeti US, Araoz PA, Jaffe AS. The quantification of infarct size. J Am Coll Cardiol. 2004;

(8): 1533-42. doi: 10.1016/j.jacc.2004.06.071. PMID: 15489082.

Stenestrand U, Wallentin L; Swedish Register of Cardiac Intensive Care (RIKS-HIA). Early statin

treatment following acute myocardial infarction and 1-year survival. Jama. 2001; 285(4): 430-6. doi:

1001/jama.285.4.430. PMID: 11242427.

Jong P, Yusuf S, Rousseau MF, Ahn SA, Bangdiwala SI. Effect of enalapril on 12-year survival and life

expectancy in patients with left ventricular systolic dysfunction: a follow-up study. Lancet. 2003;

(9372): 1843-8. doi: 10.1016/S0140-6736(03)13501-5. PMID: 12788569.

Testa L, Van Gaal WJ, Biondi Zoccai GG, Agostoni P, Latini RA, Bedogni F, et al. Myocardial infarction

after percutaneous coronary intervention: a meta-analysis of troponin elevation applying the new universal

definition. QJM. 2009; 102(6): 369-78. doi: 10.1093/qjmed/hcp005. PMID: 19286891.

Ridker PM, Rifai N, Pfeffer M, Sacks F, Lepage S, Braunwald E, et al. Elevation of tumor necrosis factor-α

and increased risk of recurrent coronary events after myocardial infarction. Circulation. 2000; 101(18):

-53. doi: 10.1161/01.CIR.101.18.2149. PMID: 10801754.

Marmor A, Sobel BE, Roberts R. Factors presaging early recurrent myocardial infarction ("extension").

The American journal of cardiology. 1981; 48(4): 603-10. doi: 10.1016/0002-9149(81)90137-5. PMID:

Yellon DM, Hausenloy DJ. Myocardial reperfusion injury. N Engl J Med. 2007; 357(11): 1121-35. doi:

1056/NEJMra071667. PMID: 17855673.

Park JL, Lucchesi BR. Mechanisms of myocardial reperfusion injury. Ann Thorac Surg. 1999; 68(5): 1905- 12. doi: 10.1016/S0003-4975(99)01073-5. PMID: 10585102.

Zhao ZQ, Corvera JS, Halkos ME, Kerendi F, Wang NP, Guyton RA, et al. Inhibition of myocardial injury

by ischemic postconditioning during reperfusion: comparison with ischemic preconditioning. Am J Physiol

Heart Circ Physiol. 2003; 285(2): H579-88. doi: 10.1152/ajpheart.01064.2002. PMID: 12860564.

Ferdinandy P, Schulz R, Baxter GF. Interaction of cardiovascular risk factors with myocardial

ischemia/reperfusion injury, preconditioning, and postconditioning. Pharmacol Rev. 2007; 59(4): 418-58.

doi: 10.1124/pr.107.06002. PMID: 18048761.

Kin H, Zhao ZQ, Sun HY, Wang NP, Corvera JS, Halkos ME, et al. Postconditioning attenuates

myocardial ischemia–reperfusion injury by inhibiting events in the early minutes of reperfusion.

Cardiovascular research. 2004; 62(1): 74-85. doi: 10.1016/j.cardiores.2004.01.006. PMID: 15023554.

Hausenloy DJ, Tsang A, Yellon DM. The reperfusion injury salvage kinase pathway: a common target for

both ischemic preconditioning and postconditioning. Trends Cardiovasc Med. 2005; 15(2): 69-75. doi:

1016/j.tcm.2005.03.001. PMID: 15885573.

Cohen MV, Yang XM, Downey JM. Acidosis, oxygen, and interference with mitochondrial permeability

transition pore formation in the early minutes of reperfusion are critical to postconditioning's success. Basic

Res Cardiol. 2008; 103(5): 464-71. doi: 10.1007/s00395-008-0737-9. PMID: 18626679, PMCID:

PMC2660166.

Huhn R, Heinen A, Weber NC, Schlack W, Preckel B, Hollmann MW. Ischaemic and morphine-induced

post-conditioning: impact of mK(Ca) channels. Br J Anaesth. 2010; 105(5): 589-95. doi:

1093/bja/aeq213. PMID: 20693178.

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; 78(6): 1100-4. doi:

1161/01.RES.78.6.1100. PMID: 8635241.

Day CP, McComb JM, Campbell RW. QT dispersion: an indication of arrhythmia risk in patients with long

QT intervals. Br Heart J. 1990; 63(6): 342-4. doi: 10.1136/hrt.63.6.342. PMID: 2375895, PMCID:

PMC1024518.

Malik M, Batchvarov VN. Measurement, interpretation and clinical potential of QT dispersion. J Am Coll

Cardiol. 2000; 36(6): 1749-66. doi: 10.1016/S0735-1097(00)00962-1. PMID: 11092641.

Shah CP, Thakur RK, Reisdorff EJ, Lane E, Aufderheide TP, Hayes OW. QT dispersion may be a useful

adjunct for detection of myocardial infarction in the chest pain center. Am Heart J. 1998; 136(3): 496-8.

doi: 10.1016/S0002-8703(98)70226-1. PMID: 9736143.

Ashikaga T, Nishizaki M, Arita M, Yamawake N, Suzuki M, Hashimoto Y, et al. Effect of dipyridamole on

QT dispersion in vasospastic angina pectoris. Am J Cardiol. 1999; 84(7): 807-10. doi: 10.1016/S0002- 9149(99)00441-5. PMID: 10513778.

Stolt A, Karila T, Viitasalo M, Mäntysaari M, Kujala UM, Karjalainen J. QT interval and QT dispersion in

endurance athletes and in power athletes using large doses of anabolic steroids. Am J Cardiol. 1999; 84(3):

-6, A9. doi: 10.1016/S0002-9149(99)00299-4. PMID: 10496458.

Brendorp B, Elming H, Jun L, Køber L, Torp ‐ Pedersen C; DIAMOND Study Group. Danish

Investigations Of Arrhythmia and Mortality On Dofetilide. Effect of dofetilide on QT dispersion and the

prognostic implications of changes in QT dispersion for patients with congestive heart failure. Eur J Heart

Fail. 2002; 4(2): 201-6. doi: 10.1016/S1388-9842(01)00235-5. PMID: 11959050.

Macfarlane, PW and on behalf of the WOSCOP Study Group. QT dispersion: lack of discriminating power.

Circulation. 1998; 98: 181.

Okin PM, Devereux RB, Howard BV, Fabsitz RR, Lee ET, Welty TK. Assessment of QT interval and QT

dispersion for prediction of all-cause and cardiovascular mortality in American Indians the Strong Heart

Study. Circulation. 2000; 101(1): 61-6. doi: 10.1161/01.CIR.101.1.61. PMID: 10618305.

de Bruyne MC, Hoes AW, Kors JA, Hofman A, van Bemmel JH, Grobbee DE. QTc dispersion predicts

cardiac mortality in the elderly the rotterdam study. Circulation. 1998; 97(5): 467-72. doi:

1161/01.CIR.97.5.467. PMID: 9490242.

Ling Ling J, Wong GT, Yao L, Xia Z, Irwin MG. Remote pharmacological post‐conditioning by

intrathecal morphine: cardiac protection from spinal opioid receptor activation. Acta Anaesthesiol Scand.

; 54(9): 1097-104. doi: 10.1111/j.1399-6576.2010.02295.x. PMID: 20887411.

Gao DP, Zhao GQ, Wang J, Gao M. Effects of Morphine Postconditioning on Myocardial Ischemia- Reperfusion Injury in Rats In Vivo. Advanced Materials Research. Trans Tech Publ. 2013; 680(8): 617-9.

doi: 10.4028/www.scientific.net/AMR.680.617.

Zhang R, Shen L, Xie Y, Gen L, Li X, Ji Q. Effect of morphine-induced postconditioning in corrections of

tetralogy of fallot. J Cardiothorac Surg. 2013; 8: 76. doi: 10.1186/1749-8090-8-76. PMID: 23577699,

PMCID: PMC3666925.

Published

2022-01-18