Key result
Monotherapy with several antiplatelets and anticoagulants, including aspirin and rivaroxaban, as well as their combination therapies, showed significant safety signals for intraocular hemorrhage.
Why the study?
Studies evaluating the risk of intraocular hemorrhage with antiplatelet agents and anticoagulants, particularly in combination therapy, are limited due to their low frequency.
Does monotherapy or combination therapy with oral antiplatelets and anticoagulants increase the risk of intraocular hemorrhage?
Observational (n=688,467)
Does monotherapy or combination therapy with oral antiplatelets and anticoagulants increase the risk of intraocular hemorrhage?
Monotherapy and combination therapy with specific antiplatelets and anticoagulants, particularly rivaroxaban and DAPT plus warfarin, are associated with an increased risk of intraocular hemorrhage, often occurring within the first 90 days of use.
Answers are grounded in this paper and cite their sources.
Signals for intraocular hemorrhage with these antithrombotics warrant clinical awareness; leaves open causality and requires prospective validation.
Purpose: An intraocular hemorrhage is an adverse event that can lead to visual acuity impairment. Antithrombotic therapy with antiplatelet agents and anticoagulants may increase intraocular hemorrhage. However, since their frequency is low, studies on the risk of intraocular hemorrhage with these drugs, especially under combination therapy, are limited. This study aimed to investigate the occurrence of intraocular hemorrhages under monotherapy and combination therapy with antiplatelets and anticoagulants by analyzing a large pharmacovigilance database. Methods: Intraocular hemorrhage signals with oral antiplatelets and anticoagulants were evaluated by calculating reporting odds ratios and information components using the Japan Adverse Drug Reactions Report database from April 2004 to March 2022. In addition, differences in signals between younger and elderly patients, affecting factors, and time-to-onset from initial antiplatelet and anticoagulant treatments were analyzed. Results: Aspirin, clopidogrel, warfarin, apixaban, and rivaroxaban, but not ticagrelor, ticlopidine, prasugrel, dabigatran, and edoxaban showed intraocular hemorrhage signals under monotherapy. In combination therapy, dual therapy (aspirin + P2Y 12 inhibitors, warfarin, direct oral anticoagulants, and P2Y 12 inhibitors + warfarin) and triple therapy (aspirin + P2Y 12 inhibitors + warfarin) resulted in intraocular hemorrhage signals. Intraocular hemorrhage signals were observed in younger patients receiving monotherapy with aspirin and in elderly patients receiving monotherapy and combination therapy with warfarin. Affecting factors were diabetes mellitus in patients with prasugrel, use of medications for intravitreal injections, and posterior sub-Tenon injections with some antiplatelets and anticoagulants. The median period of intraocular hemorrhage occurrence after starting monotherapy with aspirin, clopidogrel, warfarin, or rivaroxaban was within 90 days. Conclusion: In addition to monotherapy with several antiplatelets and anticoagulants, combination therapy using aspirin, P2Y 12 inhibitors, and warfarin has the potential risk of intraocular hemorrhage. Particular attention should be paid to the occurrence of intraocular hemorrhages in younger patients taking aspirin, in elderly patients taking warfarin, and within the first 90 days of antiplatelet and anticoagulant use.
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Tanaka et al. (2023) conducted an observational in Patients receiving oral antiplatelets and anticoagulants (n=688,467). Antiplatelets and anticoagulants (monotherapy and combination therapy) vs. Other drugs in the database was evaluated on Intraocular hemorrhage signal (Reporting Odds Ratio) (ROR 1.40, 95% CI 1.08 to 1.80). Monotherapy with several antiplatelets and anticoagulants, including aspirin and rivaroxaban, as well as their combination therapies, showed significant safety signals for intraocular hemorrhage.
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