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Magnetocardiographic Intra‐QRS Fragmentation Analysis in the Identification of Patients with Sustained Ventricular Tachycardia after Myocardial Infarction
Author(s) -
KORHONEN PETRI,
MONTONEN JUHA,
ENDT PETER,
MÄKIJÄRVI MARKKU,
TRAHMS LUTZ,
KATILA TOIVO,
TOIVONEN LAURI
Publication year - 2001
Publication title -
pacing and clinical electrophysiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.686
H-Index - 101
eISSN - 1540-8159
pISSN - 0147-8389
DOI - 10.1046/j.1460-9592.2001.01179.x
Subject(s) - medicine , magnetocardiography , cardiology , qrs complex , ventricular tachycardia , myocardial infarction , population , signal averaged electrocardiogram , coronary artery disease , environmental health
KORHONEN, P., et al. : Magnetocardiographic Intra‐QRS Fragmentation Analysis in the Identification of Patients with Sustained Ventricular Tachycardia after Myocardial Infarction. The aim of this study was to investigate if magnetocardiographic (MCG) analysis of cardiac micropotentials within the QRS complex can identity patients prone to ventricular arrhythmias, and to compare it to MCG time‐domain, late‐field analysis. The study population consisted of 136 patients with remote MI, 53 with and 83 without a history of VT. After averaging and high pass filtering of multichannel MCG signals, time‐domain parameters describing the end‐QRS activity and fragmentation index M and score S describing the whole QRS complex were computed. Fragmentation and time‐domain parameters differed between the VT and control groups: fragmentation index M was 12 ± 3 versus 9 ± 2 ( P < 0.001 ), fragmentation score S was 83 ± 42 versus 56 ± 21 ( P < 0.001 ), and filtered QRS duration was 144 ± 32 versus 114 ± 19 ms ( P < 0.001 ) in VT and control groups, respectively. A combination of fragmentation parameters yielded 87% sensitivity and 61% specificity in VT identification. Corresponding figures for a time‐domain parameter combination were 81% and 72%. Sensitivity of time‐domain analysis was 88% and specificity was 75% in a subgroup with anterior MI. In multivariate analysis, fragmentation and time‐domain analyses discriminated VT patients from controls independently of the extent of coronary artery disease or left ventricular dysfunction. MCG in postinfarction patients reveals pathology associated with propensity to ventricular arrhythmias inside and not only at the end of the QRS complex. MCG seems most accurate in the anterior infarct location.