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. 2024 Apr 15;5(4):416–426. doi: 10.1093/ehjdh/ztae029

Table 3.

Electrocardiogram characteristics in the hypertrophic cardiomyopathy and control groups

Patients with HCM (n = 773) Controls (n = 3867) Total (n = 4640) P-value
Normal ECG 83 (10.7%) 2203 (57%) 2286 (49.3%) <0.001
Atrial fibrillation/flutter/tachycardia 58 (7.5%) 263 (6.8%) 321 (6.9%) 0.48
Ventricular pacing 6 (0.8%) 104 (2.7%) 110 (2.4%) <0.001
LBBB 17 (2.2%) 106 (2.7%) 123 (2.7%) 0.46
RBBB 41 (5.3%) 128 (3.3%) 169 (3.6%) 0.011
LVH criteria 279 (36.1%) 170 (4.4%) 449 (9.7%) <0.001
T-wave inversions 410 (53.0%) 179 (4.6%) 589 (12.7%) <0.001
Pathologic Q waves 73 (9.4%) 56 (1.4%) 129 (2.8%) <0.001
Tracing artefact 32 (4.1%) 146 (3.8%) 178 (3.8%) 0.61

P-values result from a Wilcoxon rank-sum test (continuous variables) or Fisher’s exact test (categorical variables).

AF, atrial fibrillation; LBBB, left bundle branch block; RBBB, right bundle branch block; LVH, left ventricular hypertrophy.

Normal ECG: sinus rhythm, 50–110 b.p.m., normal intervals, sinus arrhythmia acceptable; bundle branch blocks: complete (QRS >120 ms); LVH per Sokolow–Lyon criteria: S-wave depth in V1 + tallest R-wave height in V5––V6 (whichever is larger) >35 mm; TWIs: inferior or lateral ≥0.1 mV in ≥2 contiguous leads (in those without BBB); pathologic Q waves: ≥1/3 of R-wave or ≥0.3 mV in ≥2 contiguous inferior or lateral leads; artefact: tracing distortion that could interfere with ECG interpretation in the reviewer’s opinion [high-frequency noise, baseline wander, disconnected lead(s), combinations].