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. 2018 Sep 27;34(6):632–639. doi: 10.1002/joa3.12123

Table 2.

Device features and implantation characteristics

Infection (n = 54) No infection (n = 108) P‐value
Cardiac device
PPM (DDD) 15 (27.8%) 33 (30.6%) <0.001
PPM (VVI) 14 (25.9%) 3 (2.8%)
AICD 18 (33.3%) 57 (52.8%)
S‐ICD 0 (0.0%) 1 (0.9%)
CRT‐P 5 (9.3%) 2 (1.9%)
CRT‐D 2 (3.7%) 12 (11.1%)
Number of lead
1 30 (56.6%) 57 (52.8%) 0.871
2 16 (30.2%) 37 (34.3%)
3 7 (13.2%) 14 (13.0%)
Type of the last procedure
Primary implantation 28 (56.0%) 60 (56.1%) 0.030
Generator change 8 (16.0%) 27 (25.2%)
Lead revision 1 (2.0%) 2 (1.9%)
Generator revision 5 (10.0%) 1 (0.9%)
Device upgrade 0 (0.0%) 6 (5.6%)
Re‐implantation 8 (16.0%) 11 (10.3%)
Duration of operation, hours 119.5 (87.0‐160.0) 90.0 (70.0‐128.0) 0.017
Perioperative antibiotics
Cefazolin + cephalexin 23 (82.1%) 99 (92.5%) 0.152
Vancomycin + clindamycin 4 (14.3%) 7 (6.5%)
Others 1 (3.6%) 1 (0.9%)
Duration of antibiotic, days 7.0 (7.0‐8.5) 7.0 (7.0‐7.0) 0.003
Hematoma 3 (10.0%) 4 (3.7%) 0.177
Temporary pacemaker 3 (10.0%) 4 (3.7%) 0.177

AICD, automatic implantable cardioverter‐defibrillators; CRT‐D, cardiac resynchronization therapy defibrillator; CRT‐P, cardiac resynchronization therapy pacemaker; PPM, permanent pacemaker; S‐ICD, subcutaneous implantable cardioverter‐defibrillators.