Key result
Incident thrombocytopenia on DOACs is linked to ~12.8-fold higher major bleeding risk in elderly AF.
Why the study?
Bleeding risk in AF changes over time, and the impact of incident thrombocytopenia during DOAC therapy on bleeding risk had not been previously investigated.
Does incident thrombocytopenia increase the risk of major bleeding in elderly patients with nonvalvular atrial fibrillation treated with direct oral anticoagulants?
Cohort (n=957)
No
Does incident thrombocytopenia increase the risk of major bleeding in elderly patients with nonvalvular atrial fibrillation treated with direct oral anticoagulants?
Answers are grounded in this paper and cite their sources.
Dynamic monitoring of platelet counts during DOAC therapy in elderly AF patients identifies incident thrombocytopenia (3.08 per 100 person-years), which confers a nearly 13-fold increased hazard of major bleeding.
Background The bleeding risk of patients with atrial fibrillation (AF) changes over time. Most studies thus far evaluated only the baseline bleeding risk with discordant results. The impact of incident thrombocytopenia during direct oral anticoagulant (DOAC) therapy and its relation to bleeding has not been previously investigated. Objectives To investigate the incidence rate of thrombocytopenia and major bleeding (MB) risk in AF patients on DOACs. Methods Prospective ongoing ATHEROsclerosis in Atrial Fibrillation study including patients with nonvalvular AF on DOACs. Incident thrombocytopenia was defined as a platelet count <150 × 10 9 /L. MB events were recorded at each follow-up visit. Gray estimator for competing risk data was used. Estimates are expressed in terms of subdistributional hazard ratios (sHR) and relative 95% CI for MB. Results We enrolled 957 AF patients treated with DOACs (mean age, 77.3 ± 9.0 years; 49.1% women). During a follow-up (median time to censoring 1330 days; 95% CI, 1246-1443), 139 patients developed thrombocytopenia (3.08 per 100 person-years; 95% CI, 2.27-3.89) with no difference between direct thrombin and factor Xa inhibitors. Overall, 179 bleedings occurred, of which 80 were major (3.17 per 100 person-years; 95% CI, 2.34-3.99). Patients sustaining bleedings were more frequently affected by arterial hypertension, heart failure, anemia and had higher CHA 2 DS 2 -VASc and HAS-BLED scores. On multivariable Cox analysis, independent risk factors for MB were incident thrombocytopenia (sHR, 12.77; 95% CI, 8.880-18.360; P < .001), and age (sHR, 1.030 per year; 95% CI, 1.010-1.040; P = .002). Conclusion Patients developing thrombocytopenia have an increased risk of MB. Dynamic evaluation of platelet count during follow-up may provide better prognostic value than baseline assessment only.
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Menichelli et al. (2024) conducted a cohort in Nonvalvular atrial fibrillation on direct oral anticoagulants (DOACs) (n=957). Incident thrombocytopenia (platelet count <150 × 10^9/L) vs. No thrombocytopenia (platelet count >=150 × 10^9/L) was evaluated on Major bleeding (ISTH criteria) (sHR 12.77, 95% CI 8.880-18.360, p=<0.001). Incident thrombocytopenia during DOAC therapy was independently associated with an increased risk of major bleeding in elderly AF patients (sHR 12.77, 95% CI 8.880-18.360, P < .001).
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