Abstract
BackgroundPatients undergoing elective electrical cardioversion (ECV) for atrial fibrillation have a temporarily increased risk of thromboembolism. Current guidelines recommend adequate anticoagulation for ≥3 consecutive weeks precardioversion, i.e. consecutive INR values 2.0–3.0 in patients with vitamin K antagonists (VKA). We aimed to evaluate the occurrence and impact of subtherapeutic INRs precardioversion and to study factors associated with these unwanted fluctuations. MethodsWe recruited 346 consecutive patients undergoing elective ECV in the Maastricht University Medical Centre between 2008 and 2013. Predictors of subtherapeutic INR values were identified and incorporated into a logistic regression model. ResultsA subtherapeutic INR precardioversion occurred in 55.2% of patients. The only statistically significant predictor was VKA-naivety (Odds Ratio (OR) 4.78, 95% Confidence Interval (CI) 2.67–8.58, p<0.001). In patients with ≥1 subtherapeutic INR precardioversion, time from referral until cardioversion was 91.1±42.8days, compared to 41.7±26.6days (p<0.001) in patients without subtherapeutic INRs.No thromboembolic events occurred <30days after the ECV. Independent predictors for the combined endpoint of cardiovascular death, ischemic stroke and the need of blood transfusion (n=30, median follow-up of 374days) were coronary artery disease in the history (OR 3.35, 95%CI 1.54–7.25, p=0.002) and subtherapeutic INR precardioversion (OR 3.64, 95%CI 1.43–9.24, p=0.007). ConclusionsThe use of VKA often results in subtherapeutic INRs precardioversion and is associated with a significant delay until cardioversion, especially in patients with recent initiation of VKA therapy. Furthermore, subtherapeutic INR levels prior to ECV are associated with the combined endpoint of cardiovascular death, ischemic stroke and the need of blood transfusion.
Highlights
Patients undergoing elective electrical cardioversion (ECV) for atrial fibrillation have a temporarily increased risk of thromboembolism
The objective of this study is to evaluate the occurrence, extent and impact of subtherapeutic INR values prior to and following elective electrical cardioversion (ECV) and to study factors associated with these unwanted fluctuations
This implies that vitamin K antagonists (VKA) dose adjustments should be made with precaution in patients on the waiting list for elective cardioversion, since one subtherapeutic INR value means a delay of cardioversion of at least 4 weeks
Summary
Patients undergoing elective electrical cardioversion (ECV) for atrial fibrillation have a temporarily increased risk of thromboembolism. Independent predictors for the combined endpoint of cardiovascular death, ischemic stroke and the need of blood transfusion (n = 30, median follow-up of 374 days) were coronary artery disease in the history (OR 3.35, 95%CI 1.54–7.25, p = 0.002) and subtherapeutic INR precardioversion (OR 3.64, 95%CI 1.43–9.24, p = 0.007). Conclusions: The use of VKA often results in subtherapeutic INRs precardioversion and is associated with a significant delay until cardioversion, especially in patients with recent initiation of VKA therapy. Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia It is a major health problem, not merely due to its vastness and because of the associated risks, in particular of thromboembolism (TE). Pericardioversion oral anticoagulation is warranted to significantly decrease the rate of thromboembolic complications from 5.3% to 0.8– 1.0% [4,5]
Published Version (Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.