Practical "1-2-3-4-Day" Rule for Starting Direct Oral Anticoagulants After Ischemic Stroke With Atrial Fibrillation: Combined Hospital-Based Cohort Study

被引:55
作者
Kimura, Shunsuke [1 ]
Toyoda, Kazunori [1 ]
Yoshimura, Sohei [1 ]
Minematsu, Kazuo [2 ]
Yasaka, Masahiro [3 ]
Paciaroni, Maurizio [4 ]
Werring, David J. [5 ,6 ]
Yamagami, Hiroshi [7 ]
Nagao, Takehiko [8 ]
Yoshimura, Shinichi [9 ]
Polymeris, Alexandros [10 ,11 ,12 ]
Zietz, Annaelle [10 ,11 ,12 ]
Engelter, Stefan T. [10 ,11 ,12 ]
Kallmuenzer, Bernd [13 ]
Cappellari, Manuel [14 ]
Chiba, Tetsuya [1 ]
Yoshimoto, Takeshi [15 ]
Shiozawa, Masayuki [1 ]
Kitazono, Takanari [16 ]
Koga, Masatoshi [1 ]
机构
[1] Natl Cerebral & Cardiovasc Ctr, Dept Cerebrovasc Med, 6-1 Kishibe Shimmachi, Suita, Osaka 5648565, Japan
[2] Med Corp ISEIKAI, Osaka, Japan
[3] Natl Hosp Org Kyushu Med Ctr, Clin Res Inst, Dept Cerebrovasc Med & Neurol, Fukuoka, Japan
[4] Osped San Giuseppe MultiMed IRCCS, Stroke Unit, Dept Neurol, Milan, Italy
[5] UCL Queen Sq Inst Neurol, Dept Brain Repair & Rehabil, Stroke Res Ctr, London, England
[6] Natl Hosp Neurol & Neurosurg, London, England
[7] Natl Hosp Org Osaka Natl Hosp, Dept Stroke Neurol, Osaka, Japan
[8] Tama Nagayama Hosp, Nippon Med Sch, Dept Neurol, Tokyo, Japan
[9] Hyogo Coll Med, Dept Neurosurg, Nishinomiya, Hyogo, Japan
[10] Univ Hosp Basel, Dept Neurol, Basel, Switzerland
[11] Univ Hosp Basel, Stroke Ctr, Basel, Switzerland
[12] Univ Basel, Basel, Switzerland
[13] Univ Hosp Erlangen, Dept Neurol, Erlangen, Germany
[14] Azienda Osped Univ Integrata, Stroke Unit, Dept Neurosci, Verona, Italy
[15] Natl Cerebral & Cardiovasc Ctr, Dept Neurol, Suita, Osaka, Japan
[16] Kyushu Univ, Grad Sch Med Sci, Dept Med & Clin Sci, Fukuoka, Japan
关键词
acute ischemic stroke; anticoagulation; atrial fibrillation; cardioembolism; stroke prevention; INTRACRANIAL HEMORRHAGE; EARLY INITIATION; WARFARIN; ATTACK; RIVAROXABAN; RATIONALE; DESIGN; RISK; MICROBLEEDS; CROMIS-2;
D O I
10.1161/STROKEAHA.121.036695
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The "1-3-6-12-day rule" for starting direct oral anticoagulants (DOACs) in patients with nonvalvular atrial fibrillation after acute ischemic stroke or transient ischemic attack recommends timings that may be later than used in clinical practice. We investigated more practical optimal timing of DOAC initiation according to stroke severity. Methods: The combined data of prospective registries in Japan, Stroke Acute Management with Urgent Risk-factor Assessment and Improvement-nonvalvular atrial fibrillation (September 2011 to March 2014) and RELAXED (February 2014 to April 2016) were used. Patients were divided into transient ischemic attack and 3 stroke subgroups by the National Institutes of Health Stroke Scale score: mild (0-7), moderate (8-15), and severe (>= 16). The early treatment group was defined as patients starting DOACs earlier than the median initiation day in each subgroup. Outcomes included a composite of recurrent stroke or systemic embolism, ischemic stroke, and severe bleeding within 90 days. Six European prospective registries were used for validation. Results: In the 1797 derivation cohort patients, DOACs were started at median 2 days after transient ischemic attack and 3, 4, and 5 days after mild, moderate, and severe strokes, respectively. Stroke or systemic embolism was less common in Early Group (n=785)-initiating DOACS within 1, 2, 3, and 4 days, respectively-than Late Group (n=1012) (1.9% versus 3.9%; adjusted hazard ratio, 0.50 [95% CI, 0.27-0.89]), as was ischemic stroke (1.7% versus 3.2%, 0.54 [0.27-0.999]). Major bleeding was similarly common in the 2 groups (0.8% versus 1.0%). On validation, both ischemic stroke (2.4% versus 2.2%) and intracranial hemorrhage (0.2% versus 0.6%) were similarly common in Early (n=547) and Late (n=1483) Groups defined using derivation data. Conclusions: In Japanese and European populations, early DOAC initiation within 1, 2, 3, or 4 days according to stroke severity seemed to be feasible to decrease the risk of recurrent stroke or systemic embolism and no increase in major bleeding. These findings support ongoing randomized trials to better establish the optimal timing of DOAC initiation.
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页码:1540 / 1549
页数:10
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