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. 2017 Feb 10;25(5):312–317. doi: 10.1007/s12471-017-0957-4

Table 1.

Baseline characteristics

Characteristic Patients (n = 79)
Male (n, %) 59 (74.9%)
Age, years (median, IQR) 54.0 (43.8–64.3)
Genetic arrhythmia (n, %)
DPP6 mutation
LQTS
HCM (familial)
iVF
6 (7.6%)
1 (14.3%)
1 (14.3%)
2 (28.6%)
2 (28.6%)
Ischaemic CMP (n, %) 29 (36.7%)
Non-ischaemic CMP (n, %)
Dilated CMP
Non-compaction CMP
CMP eci
Myocarditis
Peri-partum CMP
41 (51.9%)
28 (68.3%)
2 (4.8%)
2 (4.9%)
7 (17.1%)
2 (4.9%)
Wolff-Parkinson-White syndrome (n, %)
Other (n, %)
1 (1.3%)
2 (2.5%)
Previous CIED implant (n, %)
One chamber TV-ICD
Dual chamber TV-ICD
S-ICD
Pacemaker
CRT-D
26 (32.9%)
2 (7.7%)
6 (23.1%)
6 (23.1%)
1 (3.8%)
11 (42.3%)
Complication previous implant (n, %)
Infection
23 (88.5%)
23 (100%)
Indication WCD (n, %)
Newly diagnosed iCMP
Newly diagnosed non-iCMP
Bridging to implant due to infection
Bridging to implant due to other reason

12 (15.2%)
34 (43.0%)
23 (29.1%)
10 (11.9%)
Ventricular arrhythmias (n, %)
Ventricular tachycardia
Ventricular fibrillation
Non-sustained ventricular tachycardia
58 (73.4%)
16 (27.6%)
10 (17.2%)
32 (55.2%)
Supraventricular tachycardia (n, %)
Atrial fibrillation
Atrial flutter
Atrial tachycardia
AV(N)RT
16 (20.8%)
13 (81.3%)
1 (6.3%)
1 (6.3%)
1 (6.3%)
LVEF, % (median, IRQ) 25.0 (18.0–39.3)

AV(N)RT atrioventricular (nodal) re-entry tachycardia, CIED cardio implantable electronic device, CMP cardiomyopathy, iCMP ischaemic CMP, non-iCMP non-ischaemic CMP, DPP6 dipeptidylpeptidase 6, HCM hypertrophic cardiomyopathy, IQR interquartile range, LQTS long-QT syndrome, LVEF left ventricular ejection fraction, S-ICD subcutaneous implantable cardioverter-defibrillator, TV-ICD transvenous implantable cardioverter-defibrillator, WCD wearable cardioverter-defibrillator