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Antithrombotic Therapy in Atrial Fibrillation: The Seventh ACCP Conference on Antithrombotic and Thrombolytic Therapy
Section snippets
Results of a systematic review of randomized trials of oral vitamin K antagonist (VKA) therapy vs no antithrombotic therapy:
Investigators from the five primary prevention trials pooled their data after standardizing clinical definitions.6 The individual studies and their results are summarized in Tables 2345.1213141516 The results of individual-subject meta-analyses of these trials and later trials with pooled data are provided in Table 6. The clinical trials included patients with chronic persistent (also known as “sustained,” and including the category “permanent”17) or, less commonly, paroxysmal AF (PAF)
Recommendations
1.1.1. In patients with persistent (also known as “sustained,” and including patients categorized as “permanent” in certain classification schemes17) or paroxysmal (intermittent) AF at high risk of stroke (ie, having any of the following features: prior ischemic stroke, TIA, or systemic embolism, age > 75 years, moderately or severely impaired left ventricular systolic function and/or congestive heart failure, history of hypertension, or diabetes mellitus), we recommend anticoagulation with an
Recommendation
1.2. For patients with atrial flutter, we suggest that antithrombotic therapy decisions follow the same risk-based recommendations as for AF (Grade 2C).
Recommendations
1.3.1. For patients with AF and mitral stenosis, we recommend anticoagulation with an oral VKA, such as warfarin (target INR, 2.5; range, 2.0 to 3.0) [Grade 1C+].
1.3.2. For patients with AF and prosthetic heart valves, we recommend anticoagulation with an oral VKA, such as warfarin (Grade 1C+).
Remark: The target intensity of anticoagulation may be INR 3.0 (range, 2.5 to 3.5), ie, higher than the usual target INR of 2.5 (range, 2.0 to 3.0), and it may be appropriate to add aspirin, depending on
Recommendation
1.4. For AF occurring shortly after open-heart surgery and lasting > 48 h, we suggest anticoagulation with an oral VKA, such as warfarin, if bleeding risks are acceptable (Grade 2C). The target INR is 2.5 (range, 2.0 to 3.0). We suggest continuing anticoagulation for several weeks following reversion to NSR, particularly if patients have risk factors for thromboembolism (Grade 2C).
2.1 Anticoagulation for elective cardioversion of AF
Four decades have passed since synchronized capacitor discharge was first introduced by Lown and coworkers152153154 for the rapid termination of atrial and ventricular tachyarrhythmias. Systemic embolism is the most serious complication of cardioversion and may follow external or internal direct current (DC), pharmacologic, and spontaneous cardioversion of AF. Evidence favoring the efficacy of anticoagulation is based on observational studies. The large reported efficacy from such studies has
Recommendations
2.1.1. For patients with AF of ≥ 48 h or of unknown duration for whom pharmacologic or electrical cardioversion is planned, we recommend anticoagulation with an oral VKA, such as warfarin (target INR, 2.5; range, 2.0 to 3.0), for 3 weeks before elective cardioversion and for at least 4 weeks after successful cardioversion (Grade 1C+).
Remark: This recommendation applies regardless of a patient's risk factor status. Continuation of anticoagulation beyond 4 weeks is based on whether the patient
1.1 Atrial fibrillation
1.1.1. In patients with persistent (also known as “sustained,” and including patients categorized as “permanent” in certain classification schemes17) or paroxysmal (intermittent) AF at high risk of stroke (ie, having any of the following features: prior ischemic stroke, TIA, or systemic embolism, age > 75 years, moderately or severely impaired left ventricular systolic function and/or congestive heart failure, history of hypertension, or diabetes mellitus), we recommend anticoagulation with an
ACKNOWLEDGMENT
We are grateful to Margaret C. Fang, MD, MPH, for help reviewing the relevant literature and for reviewing early drafts of this chapter.
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