Table 4

Association of long-term clinical course of childbearing-aged patients with ARVD/C with pregnancy history

All (n=143)Pregnancy with ARVD/C* (n=26)No pregnancies while diagnosed (n=117)p Value
Demographic characteristics
 Proband (%)83 (58)13 (50)70 (60)0.36
 Mutation carrier (%)95 (67)16 (64)79 (68)0.69
 European ancestry138 (96)26 (100)112 (96)0.59
Clinical characteristics at diagnosis
 Age (median, IQR)30 (21–39)28 (25–32)31 (21–41)0.14
 Sustained VT/VF (% VA)50 (35)6 (23)44 (38)0.16
 Heart failure ≥ Class C (%)2 (1.7)0 (0)2 (1.4)1.0
 Major RV structural abnormalities by Task  Force Criteria (n=132)54/132 (41)8/25 (32)46/107 (43)0.31
Cardiac outcomes at last follow-up
 Sustained VT/ICD shock (% VA)73 (51)12 (46)61 (52)0.58
 Heart failure ≥ Class C (%)16 (11)2 (8)14 (12)0.73
 Major RV structural abnormalities (by TFC)68 (48)10 (39)58 (50)0.31
 Transplant3 (2.1)0 (0)3 (2.6)1.0
 Death4 (3)1 (4)3 (3)0.56
Follow-up duration (mean years from diagnosis)6.5±5.68.2±5.36.1±5.60.08
  • *Pregnancy proceeding beyond the first trimester. ARVD/C, arrhythmogenic right ventricular dysplasia/cardiomyopathy; ICD, implantable cardioverter defibrillator; RV, right ventricular; TFC, 2010 ARVD/C Task Force Criteria16; VA, sustained ventricular arrhythmia or appropriate ICD therapy for a ventricular arrhythmia; VF, ventricular fibrillation; VT, ventricular tachycardia.