Cohort study

Cardiac implantable electronic devices and bloodstream infections: management and outcomes

Eur Heart JPublished

  • Retrospective cohort study
  • single-centre

Authors' conclusion

Diagnostic workup of defibrillator patients with BSI admitted to a non-cardiology unit is often insufficient to characterize lead-related endocarditis.

Study context

Population
Consecutive implantable cardioverter defibrillator (ICD)/cardiac resynchronization therapy and defibrillator (CRT-D) patients implanted 2012–202147 bloodstream infection (BSI) episodes in 36 patients
Participants
515 patients
Exposure
BSI vs no BSI
  • BSIn = 36

Main finding

All-cause mortality · median follow-up 59 months (IQR 31-87 months)

Hazard ratio

6.7

95% CI 3.9–11.2

P < 0.001

BSI vs No BSI
HR 6.7 (95% CI 3.9–11.2); P < 0.001

As reported in the abstract

Observational data: associations, not effects.

Further findings

Management of BSI episodes

Admitted to non-cardiology units
92%
Episodes without cardiac imaging
25 (53%)
Short-term antibiotics
85%
Chronic antibiotic suppression therapy
4
System extraction
3

Original publication

Cardiac implantable electronic devices and bloodstream infections: management and outcomes. Eur Heart J. Published 28 March 2024. doi:10.1093/eurheartj/ehae127

Summarised from the published abstract; every number is checked against it