TY - JOUR
T1 - Time in Therapeutic Range With Vitamin K Antagonists in Congenital Heart Disease
T2 - A Multicentre Study
AU - Alliance for Adult Research in Congenital Cardiology (AARCC)
AU - Basmaji, Samir
AU - Samuel, Michelle
AU - Shohoudi, Azadeh
AU - Hamilton, Robert M.
AU - Aboulhosn, Jamil
AU - Broberg, Craig S.
AU - Chaix, Marie A.
AU - Cohen, Scott
AU - Cook, Stephen
AU - Dore, Annie
AU - Fernandes, Susan M.
AU - Fortier, Annik
AU - Fournier, Anne
AU - Guertin, Marie Claude
AU - Kay, Joseph
AU - Mondésert, Blandine
AU - Mongeon, François Pierre
AU - Opotowsky, Alexander R.
AU - Proietti, Anna
AU - Ting, Jennifer
AU - Zaidi, Ali
AU - Khairy, Paul
N1 - Funding Information:
The Anticoagulation Therapy in Congenital Heart Disease (TACTIC) study was funded by an investigator-initiated unrestricted grant from Boehringer Ingelheim . The sponsor had no role in the study design, data collection, analysis, interpretation, writing of the paper, and decision to submit the manuscript for publication. Dr Khairy is supported by the André Chagnon research chair in electrophysiology and congenital heart disease.
Funding Information:
The authors thank the following: Marie-Claude Villeneuve, MSc (Montreal Health Innovations Coordinating Center); Aynun Naher, MBBS, MS (Oregon Health and Science University); William R. Davidson, Jr, MD, John J. Kelleman, MD, Elizabeth E. Adams, DO, and Dena Jefferson RN, BSN, CCRC (Hershey Medical Center); Morgan Hindes (Children's Hospital of Pittsburgh); Ryan Williams and Gwen Derk (University of California, Los Angeles); Michael G. Earing, MD, Jonathan W. Cramer, MD, and Emily Reinhardt, RN (Medical College of Wisconsin); and Meena Fatah (Hospital for Sick Children, Toronto). The Anticoagulation Therapy in Congenital Heart Disease (TACTIC) study was funded by an investigator-initiated unrestricted grant from Boehringer Ingelheim. The sponsor had no role in the study design, data collection, analysis, interpretation, writing of the paper, and decision to submit the manuscript for publication. Dr Khairy is supported by the André Chagnon research chair in electrophysiology and congenital heart disease. The authors have no conflicts of interest to disclose.
Publisher Copyright:
© 2022 Canadian Cardiovascular Society
PY - 2022/11
Y1 - 2022/11
N2 - Background: Vitamin K antagonists (VKAs) are frequently prescribed to patients with congenital heart disease (CHD) for atrial arrhythmias or Fontan palliation, but there is a paucity of data regarding time spent in the therapeutic range (TTR). We sought to determine the TTR in patients with CHD and atrial arrhythmias or Fontan palliation prescribed VKAs and explore associations with thromboembolic and bleeding events. Methods: A multicentre North American cohort study was conducted on patients with CHD who received VKAs for sustained atrial arrhythmia or Fontan palliation. TTR was calculated using the Rosendaal linear interpolation method. Generalized estimating equations were used to explore factors associated with time outside the therapeutic range. Results: A total of 567 patients, aged 33 ± 17 years, 56% female, received VKAs for 11.5 ± 8.4 years for atrial arrhythmias (63.0%) or Fontan palliation (58.0%). CHD was simple, moderate, and complex in 10.8%, 20.3%, and 69.0%, respectively. Site investigators perceived good control over international normalized ratio (INR) levels in most patients (75.3%), with no or minor compliance or adherence issues (85.6%). The mean TTR was 41.9% (95% confidence interval [CI], 39.0%-44.8%). Forty-seven (8.3%) and 34 (6.0%) patients had thromboembolic and bleeding events, respectively. Thromboembolic events were associated with a higher proportion of time below the therapeutic range (31.3% vs 19.1%, P = 0.003) and bleeding complications with a higher proportion of time above the therapeutic range (32.5% vs 19.5%, P = 0.006). Conclusions: Patients with CHD who receive VKAs spend < 42% of their time with INR levels in the therapeutic range, with repercussions regarding thromboembolic and bleeding complications.
AB - Background: Vitamin K antagonists (VKAs) are frequently prescribed to patients with congenital heart disease (CHD) for atrial arrhythmias or Fontan palliation, but there is a paucity of data regarding time spent in the therapeutic range (TTR). We sought to determine the TTR in patients with CHD and atrial arrhythmias or Fontan palliation prescribed VKAs and explore associations with thromboembolic and bleeding events. Methods: A multicentre North American cohort study was conducted on patients with CHD who received VKAs for sustained atrial arrhythmia or Fontan palliation. TTR was calculated using the Rosendaal linear interpolation method. Generalized estimating equations were used to explore factors associated with time outside the therapeutic range. Results: A total of 567 patients, aged 33 ± 17 years, 56% female, received VKAs for 11.5 ± 8.4 years for atrial arrhythmias (63.0%) or Fontan palliation (58.0%). CHD was simple, moderate, and complex in 10.8%, 20.3%, and 69.0%, respectively. Site investigators perceived good control over international normalized ratio (INR) levels in most patients (75.3%), with no or minor compliance or adherence issues (85.6%). The mean TTR was 41.9% (95% confidence interval [CI], 39.0%-44.8%). Forty-seven (8.3%) and 34 (6.0%) patients had thromboembolic and bleeding events, respectively. Thromboembolic events were associated with a higher proportion of time below the therapeutic range (31.3% vs 19.1%, P = 0.003) and bleeding complications with a higher proportion of time above the therapeutic range (32.5% vs 19.5%, P = 0.006). Conclusions: Patients with CHD who receive VKAs spend < 42% of their time with INR levels in the therapeutic range, with repercussions regarding thromboembolic and bleeding complications.
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U2 - 10.1016/j.cjca.2022.08.004
DO - 10.1016/j.cjca.2022.08.004
M3 - Article
C2 - 35964887
AN - SCOPUS:85139190748
VL - 38
SP - 1751
EP - 1758
JO - Canadian Journal of Cardiology
JF - Canadian Journal of Cardiology
SN - 0828-282X
IS - 11
ER -