Valvular & structural heart disease

Continued non-vitamin K antagonist oral anticoagulants versus vitamin K antagonists during transcatheter aortic valve implantation

EuroInterventionPublished Prospective cohort study

Main findingResult — go to the resultOdds ratio 0.68 95% CI 0.43–1.07

Authors' conclusion

Continued NOAC compared with continued VKA during TAVI led to comparable outcomes with regard to the composite outcome measure indicating that continued OAC with both drugs is feasible.

Study context

Population
Consecutive patients on oral anticoagulation (OAC) undergoing transfemoral transcatheter aortic valve implantation (TAVI) at five European centres
Participants
584 patients
Exposure
Continued NOAC vs continued vitamin K antagonist (VKA) during TAVI
  • NOACn = 290
  • VKAn = 294reference
Outcome
Composite of:
  • Major/life-threatening bleeding
  • Stroke
  • All-cause mortality
Follow-up
30 days
Methodological detailsmulticentre, propensity-score matched
  • Multicentre
  • Propensity-score matched

Main finding

As reported in the abstract

Odds ratio

0.68

95% CI 0.43–1.07

P = 0.092

Events by group

NOAC vs VKA
OR 0.68 (95% CI 0.43–1.07); P = 0.092

Observational data: associations, not effects.

Further findings

OutcomeHR (95% CI)P value
All-cause mortality · 1 yearMultivariate Cox regression · propensity score-matched cohort revealed similar results0.61 (0.37–0.98)P = 0.043

Safety

Major/life-threatening bleeding · 30 days

Not different between groups
OR 0.87, 95% CI: 0.52-1.47; p=0.606

Stroke · 30 days

Not different between groups
OR 1.02, 95% CI: 0.29-3.59; p=0.974

Original publication

Continued non-vitamin K antagonist oral anticoagulants versus vitamin K antagonists during transcatheter aortic valve implantation. EuroIntervention. Published 6 February 2023. doi:10.4244/eij-d-22-00521

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

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