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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Post-Intracranial Hemorrhage Antithrombotic Therapy in Patients With Atrial Fibrillation
Shin-Yi Lin1,2, Yu-Chen Chang3, Fang-Ju Lin1,2,3
1Department of Pharmacy National Taiwan University Hospital Taipei Taiwan.
Insights
For atrial fibrillation patients with intracranial hemorrhage, oral anticoagulants (OACs) reduce ischemic stroke risk without increasing bleeding. Non-vitamin K antagonist OACs offer survival benefits over warfarin.
Area of Science:
- Cardiology
- Neurology
- Pharmacology
Background:
- Managing antithrombotic therapy in atrial fibrillation (AF) patients post-intracranial hemorrhage (ICH) is complex.
- Balancing the risk of recurrent ischemic stroke (IS) against secondary ICH is critical.
Purpose of the Study:
- To evaluate the effectiveness and safety of withholding or restarting antithrombotic agents after ICH in AF patients.
- To compare different antithrombotic therapies, including oral anticoagulants (OACs) and antiplatelet agents, and direct oral anticoagulants (DOACs) versus warfarin.
Main Methods:
- Nationwide retrospective cohort study (2011-2017) of AF patients with ICH.
- Used inverse probability of treatment weighting and Cox proportional hazards models.
- Compared outcomes: IS, recurrent ICH, and all-cause mortality.
Main Results:
- OACs reduced IS risk (HR 0.61) without increasing ICH risk (HR 1.15) compared to no treatment.
- Antiplatelet agents showed similar IS risk (HR 1.13) but increased ICH risk (HR 1.81).
- Non-vitamin K antagonist OACs (compared to warfarin) showed similar IS risk (HR 0.92), a trend towards reduced ICH (HR 0.53), and significantly reduced all-cause mortality (HR 0.60).
Conclusions:
- Oral anticoagulants are recommended for AF patients post-ICH due to reduced IS risk and no increased ICH risk.
- Non-vitamin K antagonist OACs are preferred over warfarin for AF patients post-ICH, offering survival benefits.
Abstract:
Background To investigate the effectiveness and safety of withholding or restarting antithrombotic agents, and different antithrombotic therapies among patients with atrial fibrillation post-intracranial hemorrhage. Methods and Results This is a nationwide retrospective cohort study involving patients with atrial fibrillation receiving antithrombotic therapies who subsequently developed intracranial hemorrhage between January 1, 2011 and December 31, 2017. The risk of ischemic stroke (IS), recurrent intracerebral hemorrhage (ICH), and all-cause mortality were investigated between patients receiving no treatment versus patients reinitiating oral anticoagulants (OACs) or antiplatelet agents, and warfarin versus non-vitamin K antagonist OACs. We applied inverse probability of treatment weighting to balance the baseline characteristics and Cox proportional hazards model to estimate the hazard ratios (HRs) of different outcomes of interest. Compared with no treatment, OACs reduced the risk of IS (HR, 0.61; 0.42-0.89), without increase in the risk of ICH (1.15, 0.66-2.02); antiplatelet agent users showed a similar risk of IS (1.13, 0.81-1.56) and increased risk of ICH (1.81, 1.07-3.04). Use of OACs or antiplatelet agents did not reduce the risk of all-cause mortality (0.85, 0.72-1.01; and 0.88, 0.75-1.03, respectively). Compared with warfarin, non-vitamin K antagonist OAC users showed a similar risk of IS (0.92, 0.50-1.70), non-significantly reduced risk of ICH (0.53, 0.22-1.30), and significantly reduced all-cause mortality (0.60, 0.43-0.84). Conclusions OACs are recommended in patients with atrial fibrillation and intracranial hemorrhage because they reduced the risk of IS with no increase in the risk of subsequent ICH. Non-vitamin K antagonist OACs are recommended over warfarin owing to their survival benefits.
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