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. 2011 Dec 14;20(1):16–23. doi: 10.1007/s12471-011-0224-z

Table 3.

Adverse events beyond 30 days after TAVI, AVR and medical treatment

TAVIa AVRa Medicala
All (n = 106) Fatal (n = 40) All (n = 10) Fatal (n = 5) Fatal (n = 59)
Cardiac 46 (43) 19 (48) 5 (50) 1 (20) 31 (53)
Heart failure 13 (12) 4 (10) 4 (40) 1 (20) 19 (32)
Sudden death 8 (8) 8 (20) 0 0 9 (15)
Myocardial infarction 2 (2) 2 (5) 1 (20) 0 1 (2)
Cardiac re-intervention 3 (3)1 0 0 0 0
Stroke or TIA 11 (10)2 4 (10) 0 0 2 (3)
Pacemaker implantation 9 (9) 1 (3)3 0 0 0
Non-cardiac 56 (53) 21 (52) 5 (50) 4 (80) 9 (15)
Infection 17 (16) 8 (20) 1 (10) 1 (20) 5 (8)
Renal failure 7 (7) 4 (10) 2 (20) 2 (40) 0
Vascular 3 (3) 0 0 0 0
Bleeding (non-cranial) 3 (3) 1 (3) 1 (10) 0 0
Neoplasm 9 (8) 4 (10) 0 0 1 (2)
Metabolic disease 2 (2) 2 (5) 0 0 0
Other 15 (14) 2 (5)4 1 (10) 1 (20)5 3 (5)6
Unknown 4 (4) 0 0 0 19 (32)

aMedian follow-up was 298 (IQR: 107–688) days in the TAVI group, 836 (IQR: 327–1269) days in the AVR group and 456 (IQR: 187–869) days in the medical group

1Re-interventions before discharge included AVR (n = 1) and post-implantation balloon aortic valvuloplasty (n = 2)

2Including TIA (n = 4); of the 11 events, 9 were ischaemic of which 2 fatal and 2 were haemorrhagic, both of which fatal

3Pneumothorax following pacemaker implantation (n = 1)

4Blood transfusion reaction (n = 1), euthanasia (n = 1)

5Delirium (n = 1)

6Obstructive pulmonary disease (n = 2), lung emboli (n = 1)