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The Prevalence of Electrocardiographic Abnormalities in a Dilated Cardiomyopathy Cohort Characterised by Cardiovascular Magnetic Resonance Ankur Gulati, Nizar Ismail, Tevfik Ismail, Andrew Jabbour, Kishen Morajij, Carla Goncalves, Sadaf Raza, Maria Paes, Francisco Alpendurada, Dudley Pennell, Sanjay Prasad National Heart and Lung Institute, Imperial College, NIHR Cardiovascular Biomedical Research Unit and Cardiovascular Magnetic Resonance Unit, Royal Brompton Hospital, London, United Kingdom Introduction Results Conclusions The electrocardiogram (ECG) is one of the most commonly performed investigations in cardiovascular patients. Heart failure (HF) is a common condition that is associated with significant morbidity and mortality.1 Guidelines from NICE recommend that an ECG is performed in every patient suspected to have HF.2 Baseline cohort characteristics are summarised in Table 1. ECG abnormalities are displayed in Table 2. Notably, only 17% of DCM patients had a normal ECG. Common ECG abnormalities included left bundle-branch block, T-wave inversion, left axis deviation and left ventricular hypertrophy. Other prevalent abnormalities include left atrial enlargement, ventricular ectopy and atrial fibrillation. There is a high prevalence of ECG abnormalities in patients with DCM characterised by cardiovascular magnetic resonance (CMR). Patients who had a normal ECG had a significantly higher left ventricular ejection fraction (EF) (50% [8] vs. 37% [27], mean [SD]; p<0.001), a lower mean indexed end-diastolic volume (124 ml/m2 [31] vs. 142 ml/m2 [47]; p=0.003), and a lower mean indexed endsystolic volume (75 ml/m2 [33] vs. 100 ml/m2 [47]; p<0.001) than DCM patients who had an abnormal ECG. Patients with severely impaired LV systolic function were more likely to have left atrial enlargement (31% vs. 8%) and T-wave inversion (36% vs. 18%) compared to those with mild or moderate LV systolic impairment. After ischaemic heart disease, dilated cardiomyopathy (DCM) is the most common cause of HF.3 Cardiovascular magnetic resonance (CMR) imaging is the gold standard investigation for the evaluation of patients with DCM.4 It provides accurate, reproducible, quantitative assessment of ventricular volumes, mass and function and also enables detection of mid-wall fibrosis. Despite the fact that DCM is common cause of HF and the ECG is an essential screening tool for HF patients, the prevalence of ECG abnormalities in patients with DCM has not been well described. We therefore examined the nature and prevalence of ECG abnormalities in a cohort of DCM patients who were comprehensively characterised by CMR. Table 3 compares the prevalence of ECG abnormalities between DCM patients with severely impaired LV systolic function (EF≤35%) versus mild or moderate LV systolic impairment (EF>35%). Patients with severely impaired LV systolic function were more likely to have left atrial enlargement and T-wave inversion. Characteristic Methods Total number of patients Consecutive patients with suspected or known DCM who were referred for CMR evaluation between January 2009 and October 2010 were prospectively enrolled. Patients with a clinical history of previous myocardial infarction or coronary artery disease were excluded. Other exclusion criteria included significant primary valvular disease, hypertrophic cardiomyopathy or any evidence of infiltrative heart disease. The final diagnosis of DCM was corroborated by CMR findings in 157 patients. All patients had increased indexed left ventricular (LV) volumes and reduced ejection fraction (EF) normalised for age and sex, with no evidence of myocardial infarction on late gadolinium enhancement imaging. Significant coronary artery disease was additionally excluded in 137 patients by coronary angiography or non-invasive stress imaging studies. CMR (Siemens Sonata, 1.5-T, Erlangen, Germany) was performed using steady-state, free precession breath-hold cines (TE [echo time]/TR [repetition time] 1.6/3.2 ms, flip angle 60°) in long-axis planes and sequential 7-mm short-axis slices (3-mm gap) from the atrioventricular ring to the apex at the Royal Brompton Hospital. The late gadolinium enhancement (LGE) images were acquired 10 minutes after intravenous gadoliniumDTPA in identical short-axis planes using an inversion-recovery gradient echo sequence. Inversion times were adjusted to null normal myocardium. Ventricular volumes and function were measured for both ventricles using standard techniques and analysed by a cardiac imaging specialist using semi-automated software (CMRtools, Cardiovascular Imaging Solutions, London, United Kingdom). Prevalence 157 Age (years) 52 (14) Male 104 (66) Family history of DCM 18 (11) (B) (C) (D) Figure 1: CMR Images of a patient with DCM and extensive mid-wall fibrosis. (A) Four-chamber view (FCH) in enddiastole (B) FCH view in end-systole (C and D) FCH and short-axis views demonstrating mid-wall late gadolinium enhancement (arrow). A standard 12-lead ECG was performed on the same day as the CMR scan for each patient. All ECG’s were scored for any abnormality by two blinded cardiologists as per the “AHA/ACCF/HRS Recommendations for Standardization and Interpretation of the Electrocardiogram.5 Prevalence (n=157) Normal ECG 26 (17) Abnormal ECG 131 (83) Atrial fibrillation 21 (13) First degree AV block 10 (6) Left atrial enlargement 28 (18) Left axis deviation 31 (20) Left bundle-branch block 40 (25) 30 (19) Hypercholesterolaemia 46 (30) Hypertension 35 (22) Current smoker 17 (11) Left ventricular hypertrophy* History of alcohol excess 16 (10) Pathological Q waves 5 (3) Diabetes 10 (6) Right atrial enlargement 5 (3) Systolic blood pressure (mm Hg) 123 (18) Right axis deviation 7 (4) Diastolic blood pressure (mm Hg) 76 (12) Right bundle-branch block 2 (1) Heart rate (beats/min) 79 (16) ST segment depression 7 (4) NYHA functional class I 68 (42) II 46 (29) III 39 (24) IV 4 (3) Medications T-wave inversion 31 (20) Ventricular ectopy 22 (14) Our study highlights the diagnostic value of the ECG in the assessment of patients with suspected DCM. Further work is required to evaluate the prognostic significance of ECG abnormalities in the DCM population. This project was supported by the NIHR Cardiovascular Biomedical Research Unit of Royal Brompton and Harefield NHS Foundation Trust and CORDA. Dr Andrew Jabbour was supported by a Neil Hamilton Fairley Postdoctoral Research Fellowship from the National Health and Medical Research Council of Australia, the Royal Australasian College of Physicians, the St Vincent’s Clinic Foundation. References Severe LV Systolic Impairment (n=61) Mild or Moderate LV Systolic Impairment (n=96) P value ACEi 118 (75) Beta-blocker 111 (71) Atrial fibrillation 11 (18) 10 (10) 0.23 Loop diuretic 71 (45) Left atrial enlargement 19 (31) 9 (9) 0.001 Aspirin 51 (32) Left axis deviation 16 (26) 15 (16) 0.15 Statin 47 (30) Left bundle-branch block 19 (31) 21 (22) 0.25 Warfarin 35 (22) 14 (23) 16 (17) 0.41 Digoxin 21 (13) Left ventricular hypertrophy* Pathological Q waves 2 (3) 3 (3) 1.0 LV EDVi (ml/m2) 130 (38) Right atrial enlargement 4 (7) 1 (1) 0.07 LV ESVi (ml/m2) 84 (40) Right axis deviation 5 (8) 2 (2) 0.11 LV EF (%) 38 (14) 1 (2) 1 (1) 1.0 Midwall LGE 55 (35) Right bundle-branch block ST depression 6 (10) 8 (8) 0.78 T-wave inversion 22 (36) 17 (18) 0.01 Ventricular ectopy 8 (13) 22 (23) 0.15 Table 1: Baseline Cohort Characteristics. Data are n (%) or mean (SD). ACEi = angiotensin-converting enzyme inhibitor; DCM = dilated cardiomyopathy; EDVi = indexed end-diastolic volume; EF = ejection fraction; ESVi = indexed end-systolic volume; LGE = late gadolinium enhancement; LV = left ventricular; NYHA = New York Heart Association Although a small but substantial minority of patients with DCM (17%) had a normal ECG, they had a less severe DCM phenotype. Acknowledgements Table 2: ECG Findings. Data are n (%). *Left ventricular hypertrophy was defined by Sokolow-Lyon criteria.6 ECG Abnormality CMR dimensions and function (A) ECG Finding The two most common ECG abnormalities in our cohort were left bundle-branch block (25%) and T-wave inversion (20%). Table 3: ECG abnormalities of patients with severe vs. mild/moderate systolic impairment. Data are n (%). Severe LV systolic impairment was defined by an ejection fraction (EF) ≤35%. P value derived by Fisher’s exact test. 1.Bui AL, Horwich TB & Fonarow GC. Epidemiology and risk profile of heart failure. Nat Rev Cardiol. 2011;8:30-41. 2.National Institute for Health and Clinical Excellence 2010. Chronic Heart Failure: National clinical guideline for diagnosis and management in primary and secondary care. CG108. London: National Institute for Health and Clinical Excellence. 3.Cowie MR, Wood DA, Coats AJ, et al. Incidence and aetiology of heart failure; a population based study. Eur Heart J. 1999;20:421-428. 4.Alpendurada F, O'Hanlon R & Prasad SK. Cardiovascular magnetic resonance of cardiomyopathies. Curr Cardiol Rep. 2009;11:61-69. 5.Kligfield P, Gettes LS, Bailey JJ, et al. Recommendations for the standardization and interpretation of the electrocardiogram: part I: the electrocardiogram and its technology: a scientific statement from the American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; the American College of Cardiology Foundation; and the Heart Rhythm Society. J Am Coll Cardiol. 2007;49:11091127. 6.Sokolow M, Lyon TP. The ventricular complex in left ventricular hypertrophy as obtained by unipolar precordial and limb leads. Am Heart J. 1949;37:161–186. Conflicts of Interests None to declare.