Changes of Electrocardiogram and Cardiac Enzymes in Acute Ischemic Stroke

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1 Changes of Electrocardiogram and Cardiac Enzymes in Acute Ischemic Stroke Yong-Seok Jang, M.D., Ji-Won Min, M.D., Bong-Goo Yoo, M.D., Kwang-Soo Kim, M.D., Kyung-Moo Yoo, M.D. Department of Neurology, Kosin University College of Medicine B a c k g r o u n d : Cardiac arrhythmias and other cardiac dysfunctions occur in relation with acute cerebral ischemia. This study was undertaken to evaluate the sequential changes of electrocardiogram and cardiac enzymes after acute ischemic stroke, and to evaluate the incidence of cardiac arrhythmias. M e t h o d s : Forty-three patients with acute ischemic stroke were recruited for this study. Electrocardiogram and cardiac enzymes were checked at 1, 3, 5, 7, 15, and 30 days after onset. Results : Heart rates were decreased acutely after ischemic stroke and showed maximal decrease at day 3 (p<0.05). Heart rates were more significantly decreased in the right-sided lesions than the left (p<0.05) and in the supratentorial lesions than the infratentorial (p<0.05). PR intervals and durations of QRS complex were prolonged at day 3 and 5 but were not significant. The prolongation of the QTc interval was found in 21 patients (48.8%) and sustained QTc prolongation at day 30 were seen in 16 patients. Compared with controls, patients showed significantly higher incidence of arrhythmias (p<0.01). Creatine phosphokinase-mb (CK-MB) was significantly increased at day 5 (p<0.01) and lactic dehydrogenase (LDH) was increased at day 7 (p<0.01). Conclusions : In our study, the incidence of neurogenic cardiac abnormalities in acute ischemic stroke was higher than that of previous studies. Abnormalities peaked at days 3 and 5 were nearly similar to control levels at day 30. These periods of peak abnormalities coincided with those of increasing brain edema. Therefore, we postulate that cardiac autonomic controls are also influenced by acute brain edema. J Korean Neurol Assoc 19(3):207~212, 2001 Key Words : Cerebral infarction, Neurogenic heart disease, Electrocardiogram, Cardiac enzymes Kyung Moo Yoo, M.D. Copyright 2001 by the Korean Neurological Association 207

2 Figure 1. Sequential changes of heart rate and comparison of heart rate between right and left hemispheric lesions. Heart rate is significantly decreased at day 3 after stroke onset (P<0.05), and then gradually increased nearly control level. Right hemspheric lesion shows significantly decreased heart rate than left one (P<0.05). 208 J Korean Neurol Assoc / Volume 19 / May, 2001

3 Table 1. The results of heart rate and PR interval in acute ischemic stroke patients Total Site (n=43) Right(n=16) Left(n=22) Heart rate 1 day day day day day day P value* PR interval 1 day day day day day day P value* *Statistical significance test is done by repeated measures ANOVA test within patients group. Table 2. Spectrum of electrocardiogram changes in acute ischemic stroke patients Patients(n=43) Control(n=44) Depolarization-repolarization abnormality Peaked P wave 11(12.3%) 0 Pathologic Q wave 15(11.6%) 0 Depressed or raised ST segment 19(44.2%) 0 Prolonged QT interval 22(51.2%) 3(6.8%) Tall or deep and inverted T wave 19(44.2%) 1(2.3%) U wave 12(14.2%) 0 Conduction abnormality First-, second-, and/or third-degree AV block 11(12.3%) 0 Intraventricular conduction defect 13(17.0%) 0 Sinus dysrhythmias Sinus bradycardia 18(41.9%) 0 Sinus tachycardia 13(30.2%) 0 Supraventricular dysrhythmias Atrial premature complexes 14(19.3%) 1(2.3%) Atrial fibrillation/flutter 11(25.6%) 1(2.3%) Supraventricular tachycardia 11(12.3%) 0 Sinus arrhythmia 11(12.3%) 0 Ventricular dysrhythmias Ventricular premature complexes 13(17.0%) 1(2.3%) AV; atrioventricular J Korean Neurol Assoc / Volume 19 / May,

4 unit is equal to 2.4 mg% CK-MB and mg% LDH. CK- Figure 2. Sequential changes of creatine phosphokinase-mb (CK-MB) and lactate dehydrogenase (LDH). Arbitrary unit, 1 MB and LDH are significantly increased at days 5 and 7 days after stroke onset, respectively (P<0.01 and P<0.01). Table 3. The results of serum cardiac enzymes in acute ischemic stroke patients Total Site Size (n=43) Right(n=16) Left(n=22) L or M(n=16) Small(n=17) CK-MB 1 day day day day day day P value* LDH 1 day day day day day day P value* AST 1 day day day day day day P value* *Statistical significance test is done by repeated measures ANOVA test within patients group. Repeated measures ANOVA used for comparison between large and small lesion during 30 day Repeated measures ANOVA used for comparison between large and small lesion during 15 day CK-MB; creatine phosphokinase-mb, LDH; lactic dehydrogenase, AST; aspartate transaminase, L or M; large or medium 210 J Korean Neurol Assoc / Volume 19 / May, 2001

5 J Korean Neurol Assoc / Volume 19 / May,

6 10. Greenhoot JH, Reichenbach DD. Cardiac injury and subarachnoid hemorrhage: a clinical, pathological, and physi- ological correlation. J Neurosurg 1969;30: Myers MG, Norris JW, Hachinski VC, Weingert ME, Sole MJ. Cardiac sequelae of acute stroke. Stroke 1982;13: Lane RD, Wallace JD, Petrosky PP, Schwartz GE, Gradman AH. Supraventricular tachycardia in patients with right hemisphere strokes. Stroke 1992;23: Oppenheimer SM, Cechetto DF, Hachinski VC. Cerebrogenic cardiac arrhythmias: cerebral electrocardiographic influences and their role in sudden death. Arch Neurol ; 4 7 : Murakawa Y, Inoue H, Nozaki A, Sugimoto T. Role of sympathovagal interaction in diuranl variation of QT interval. Am J Cardiol 1992;69: Myers MG, Norris JW, Hachinski VC, Sole MJ. Plasma norepinephrine in stroke. Stroke 1981;12: Oppenheimer SM, Wilson JX, Fuiraudon C, Cechetto DF. Insular cortex stimulation produces lethal cardiac arrhythmias: a mechamism of sudden death?. Brain Res ; : Cechetto DF. Experimental cerebral ischemic lesions and autonomic and cardiac effects in cats and rats. S t r o k e 1993;24(12 suppl): James TN, Spence CA. Distribution of cholinesterase within the sinus node and AV node of the human heart. Anat Rec 1966;155: Goldschlager N, Goldman MJ. Principles of clinical elec - t r o c a r d i o g r a p h y. 13th ed. Connecticut: Appleton & Lange, ; Kolin A, Norris JW. Myocardial damage from acute cerebral lesions. Stroke 1984;15: Rudehill A, Olsson GL, Sundqvist K, Gordon E. ECG abnormalities in patients with subarachnoid hemorrhage and intracranial tumors. J Neurol Neurosurg Psychiary 1987;50: Piscatelli RL, Fox LM. Myocardial injury from epinephrine overdosage. Am J Cardiol 1968;21: Fentz V, Gormsen J. Electrocardiographic patterns in patients with cerebrovascular accidents. C i r c u l a t i o n 1962 ; 25 : Hopkins DA, Armour JA. Medullary cells origin of physi- ologically identified cardiac nerves in the dog. Brain Res Bull 1982;8: Skinner JE. Neurocardiology: brain mechanism underlying fatal cardiac arrhythmias. Neurol Clin 1993;11: Kuo DC, Oravitz JJ, DeGroat WC. Tracing of afferent and efferent pathways in the left inferior cardiac nerve of the cat using retrograde and transganglionic transport of horseradish peroxidase. Brain Res 1984;321: Korpelainen JT, Huikuri HV, Sotaniemi KA, Myllyiä VV. Abnormal heart rate variability reflecting autonomic dysfunction in brainstem infarction. Acta Neurol Scand 1996;94: Yoon BW, Morillo CA, Cechetto DF, Hachinski V. Cerebral hemispheric lateralization in cardiac autonomic control. Arch Neurol 1997;54: Dimant J, Grob D. Electrocardiographic changes and myocardial damage in patients with acute cerebrovascular accidents. Stroke 1977;8: Hunts D, McRae C, Zapf P. Electrocardiographic and serum enzyme changes in subarachnoid hemorrhage. A m Heart J 1969;77: Fabinyi G, Hunt D, McKinley L. Myocardial creatine kinase isoenzyme in serum after subarachnoid haemorrhage. J Neurol Neurosurg Psychiatry 1977;40: Norris JW, Hachinski VC, Myers MG, Callow J, Wong T, Moore RW. Serum cardiac enzymes in stroke. S t r o k e 1979;10: Dubo H, Park DC, Pennington RJT, Kalbag RM, Walton JN. Serum creatine-kinase in case of stroke, head injury, and meaningitis. Lancet 1967;2: J Korean Neurol Assoc / Volume 19 / May, 2001

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