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Time in Therapeutic Range With Vitamin K Antagonists in Congenital Heart Disease: A Multicentre Study.
Basmaji, Samir; Samuel, Michelle; Shohoudi, Azadeh; Hamilton, Robert M; Aboulhosn, Jamil; Broberg, Craig S; Chaix, Marie-A; Cohen, Scott; Cook, Stephen; Dore, Annie; Fernandes, Susan M; Fortier, Annik; Fournier, Anne; Guertin, Marie-Claude; Kay, Joseph; Mondésert, Blandine; Mongeon, François-Pierre; Opotowsky, Alexander R; Proietti, Anna; Ting, Jennifer; Zaidi, Ali; Khairy, Paul.
Afiliación
  • Basmaji S; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Samuel M; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Shohoudi A; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Hamilton RM; The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
  • Aboulhosn J; University of California, Los Angeles, California, USA.
  • Broberg CS; Oregon Health and Science University, Portland, Oregon, USA.
  • Chaix MA; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Cohen S; The Wisconsin Adult Congenital Heart (WAtCH) Program, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Cook S; Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Dore A; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Fernandes SM; Stanford University, Palo Alto, California, USA.
  • Fortier A; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Fournier A; Hôpital Sainte-Justine, Université de Montréal, Montréal, Québec, Canada.
  • Guertin MC; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Kay J; University of Colorado Denver, Aurora, Colorado, USA.
  • Mondésert B; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Mongeon FP; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Opotowsky AR; Boston Adult Congenital Heart Service, Boston Children's Hospital and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Proietti A; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
  • Ting J; Milton S. Hershey Medical Center, Pennsylvania State University, Hershey, Pennsylvania, USA.
  • Zaidi A; Nationwide Children's Hospital, Ohio State University, Columbus, Ohio, USA.
  • Khairy P; Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada. Electronic address: paul.khairy@umontreal.ca.
Can J Cardiol ; 38(11): 1751-1758, 2022 11.
Article en En | MEDLINE | ID: mdl-35964887
ABSTRACT

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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrilación Atrial / Tromboembolia / Cardiopatías Congénitas Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Can J Cardiol Asunto de la revista: CARDIOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrilación Atrial / Tromboembolia / Cardiopatías Congénitas Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Can J Cardiol Asunto de la revista: CARDIOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Canadá