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Ischemic Stroke in Nonvalvular Atrial Fibrillation at Warfarin Initiation: Assessment via a Large Insurance Database.
Tepper, Ping G; Liu, Xianchen; Hamilton, Melissa; Mardekian, Jack; Petkun, William; Tan, Wilson; Singer, Daniel E.
Afiliación
  • Tepper PG; From the Department of Epidemiology, University of Pittsburgh, Allison Park, PA (P.G.T.); Pfizer, Inc, New York, NY (X.L., J.M., W.T.); Bristol-Myers Squibb, Princeton, NJ (M.H., W.P.); and Division of General Internal Medicine, Massachusetts General Hospital and Harvard Medical School, Boston (D.E.
  • Liu X; From the Department of Epidemiology, University of Pittsburgh, Allison Park, PA (P.G.T.); Pfizer, Inc, New York, NY (X.L., J.M., W.T.); Bristol-Myers Squibb, Princeton, NJ (M.H., W.P.); and Division of General Internal Medicine, Massachusetts General Hospital and Harvard Medical School, Boston (D.E.
  • Hamilton M; From the Department of Epidemiology, University of Pittsburgh, Allison Park, PA (P.G.T.); Pfizer, Inc, New York, NY (X.L., J.M., W.T.); Bristol-Myers Squibb, Princeton, NJ (M.H., W.P.); and Division of General Internal Medicine, Massachusetts General Hospital and Harvard Medical School, Boston (D.E.
  • Mardekian J; From the Department of Epidemiology, University of Pittsburgh, Allison Park, PA (P.G.T.); Pfizer, Inc, New York, NY (X.L., J.M., W.T.); Bristol-Myers Squibb, Princeton, NJ (M.H., W.P.); and Division of General Internal Medicine, Massachusetts General Hospital and Harvard Medical School, Boston (D.E.
  • Petkun W; From the Department of Epidemiology, University of Pittsburgh, Allison Park, PA (P.G.T.); Pfizer, Inc, New York, NY (X.L., J.M., W.T.); Bristol-Myers Squibb, Princeton, NJ (M.H., W.P.); and Division of General Internal Medicine, Massachusetts General Hospital and Harvard Medical School, Boston (D.E.
  • Tan W; From the Department of Epidemiology, University of Pittsburgh, Allison Park, PA (P.G.T.); Pfizer, Inc, New York, NY (X.L., J.M., W.T.); Bristol-Myers Squibb, Princeton, NJ (M.H., W.P.); and Division of General Internal Medicine, Massachusetts General Hospital and Harvard Medical School, Boston (D.E.
  • Singer DE; From the Department of Epidemiology, University of Pittsburgh, Allison Park, PA (P.G.T.); Pfizer, Inc, New York, NY (X.L., J.M., W.T.); Bristol-Myers Squibb, Princeton, NJ (M.H., W.P.); and Division of General Internal Medicine, Massachusetts General Hospital and Harvard Medical School, Boston (D.E.
Stroke ; 48(6): 1487-1494, 2017 06.
Article en En | MEDLINE | ID: mdl-28446621
ABSTRACT
BACKGROUND AND

PURPOSE:

Stroke risk may increase shortly after warfarin initiation in nonvalvular atrial fibrillation patients. Because of the brief period and limited number of events, large samples are needed to study this effect. We compared 30-day rates of ischemic stroke between nonvalvular atrial fibrillation patients initiating warfarin to nonwarfarin comparators using an insurance claims database.

METHODS:

We identified nonvalvular atrial fibrillation patients via 1 inpatient/2 outpatient diagnosis claims from the MarketScan database, January 1, 2009, to December 31, 2010. We studied patients initiating warfarin using prescription claims and 11 matched 22 669 initiators to comparators based on age, sex, diagnosis date, and warfarin propensity score. Follow-up began on initiation date; patients were censored at discontinuation/switch of therapy, disenrollment, or end of the study. The median follow-up was 415 days. Cox regression was used to study differences in ischemic stroke risks between warfarin initiators and comparators while controlling for important prognostic factors.

RESULTS:

Warfarin initiators were generally similar to comparators in clinical features but had higher CHADS2 scores (1.26 versus 1.19). The first 30-day ischemic stroke rate was higher among warfarin initiators than comparators (1.47%/y (27/1836) versus 0.98%/y (18/1837); P=0.18) but lower subsequently (0.81%/y [134/16 543] versus 1.09%/y [406/37 248]; P=0.002). Multivariable regression confirmed a significant interaction between follow-up and warfarin use with the adjusted hazard ratios (95% confidence intervals) for warfarin/comparator as 1.46 (0.80-2.65) in the first 30 days and 0.70 (0.57-0.85) afterward.

CONCLUSIONS:

Warfarin effect was qualitatively different in the first 30 days after initiation than subsequently. This is consistent with a modest increase in stroke risk occurring briefly after starting warfarin.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrilación Atrial / Warfarina / Isquemia Encefálica / Accidente Cerebrovascular / Anticoagulantes Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Stroke Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrilación Atrial / Warfarina / Isquemia Encefálica / Accidente Cerebrovascular / Anticoagulantes Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Stroke Año: 2017 Tipo del documento: Article