Background:
Direct oral anticoagulant (DOAC) and warfarin treatment are associated with increased risk of intracerebral hemorrhage (ICH). Specific reversal agents only currently exist in Australia for warfarin and dabigatran; ‘reversal’ of apixaban and rivaroxaban using 3-factor Prothrombin Complex Concentrate (PCC) is included in many protocols, however data on the speed and effectiveness of these treatments is lacking.
Aims:
Our retrospective cohort study aimed to compare rates of non-dabigatran DOAC-related reversal with dabigatran/warfarin-related reversal following ICH. We also assessed the timeliness of administration of reversal agents and intravenous (IV) anti-hypertensives and their impact on mortality and functional outcomes.
Methods:
We analyzed data from electronic medical records from inception until December 2022 in South Australian Tertiary Hospitals. Patients with non-traumatic ICH and a last known well time of <24 hours were included, while those with isolated intraventricular hemorrhage or secondary causes of ICH were excluded. Outcomes analyzed included 30-day mortality and discharge modified Rankin Scale (mRS). Secondary outcomes included time to administration of reversal agent, intravenous anti-hypertensives, and time to systolic blood pressure (BP) lowering below 140 mmHg.
Results:
We included 102 patients (mean age 82 (SD 9)) of whom 74 (73%) were in the non-dabigatran DOAC group and 28 (27%) in the warfarin/dabigatran group. Reversal agent rates did not differ (46% dabigatran/warfarin vs non-dabigatran-DOAC 39% (OR, 1.4; 95% CI, 0.93-2.08). Time to reversal also did not differ (91.7 minutes (SD 137) dabigatran/warfarin vs non-dabigatran-DOAC 141 (SD 229); p=0.3). Time to first dose of IV anti-hypertensives also did not differ, nor average time from arrival to achieved BP <140. There was no difference in 30-day mortality between the two groups.
Conclusion:
In anticoagulated ICH patients, time to anticoagulation reversal and initiation of first IV anti-hypertensive was greater than 120 minutes irrespective of the pre-ICH anticoagulant. Greater effort should be made to improve time-to-treatment in both groups.