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. 2017 Oct 28;70(5):699–703. doi: 10.1016/j.ihj.2017.10.015

Table 1.

Demographic and etiological features of hemodynamically stable and unstable group presenting as ventricular tachycardia. ARVC; arrythmogenic right venyrticular cardiomyopathy, CAD-NoMI; coronary artery disease without acute myocardial infarction, CAD-MI; coronary artery disease with acute myocardial infarction, CMP; cardiomyopathy, HCM; hypertrophic cardiomyopathy, IdVT; idiopathic ventricular tachycardia, VTmisc; ventricular tachycardia due to miscellaneous cause, VTcong; ventricular tachycardia due to repaired or unrepaired congenital heart disease.

Hemodynamcally stable (n = 74; 69%) Hemodynamcally Unstable (n = 33; 31%) Total (n-107) Significance
Age 45 (±14) 50.3 (±15) 47 (±14.5) NS
Sex
Males 38 (51.3%) 21 (63.6%) 59 (55%) NS
Females 36 (49.7%) 12 (36.3%) 48 (45%)
Underlying Disease
ARVC 9 (12%) 6 (18%) 15 (14%) NS
CAD-NoMI 23 (31%) 5 (15%) 28 (26%) NS
CAD-MI 6 (8%) 8 (24%) 14 (13%) 0.0195*
Other CMP 19 (25.6%) 7 (21%) 26 (24%) NS
HCM 3 (4%) 1 (3%) 4 (3.7%) NS
IdVT 8 (10.8%) 2 (6%) 10 (9.3%) NS
VTmisc 4 (5.4%) 4 (1.2%) 8 (7.4%) NS
VTcong 2 (2.7%) 0 2 (1.8%) NS
LVEF 50.6 (±14.5) 48.6 (±14.5) 50 (±14.4) NS
*

significant p value.