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October 29, 2022European Stroke Journal13 citationsOpen Access

Thrombolysis after dabigatran reversal: A nation-wide Italian multicentre study, systematic review and meta-analysis

MRMichele RomoliUniversità Cattolica del Sacro CuoreEMEleonora MatteoIstituto delle Scienze Neurologiche di BolognaLMLudovica MigliaccioIstituto delle Scienze Neurologiche di Bologna

Key Result

Thrombolysis after dabigatran reversal showed comparable functional recovery and a non-significant increase in symptomatic intracranial hemorrhage (OR 1.53, 95% CI 0.67-3.50) versus controls.

Structured PICO

Does thrombolysis preceded by dabigatran-reversal with idarucizumab increase symptomatic intracranial hemorrhage in people with acute ischemic stroke?

P
Population
People with acute ischemic stroke on dabigatran. The observational cohort included 39 patients in the dabigatran-reversal group, 12 in the no-reversal group, and 300 matched controls. The meta-analysis pooled 3 studies (n=1879).
I
Intervention
Thrombolysis preceded by dabigatran-reversal with idarucizumab
C
Comparator
Age, sex, hypertension, stroke severity, and reperfusion treatment-matched controls (1:7 ratio) and people on dabigatran treated with thrombolysis without reversal
O
Outcome
Symptomatic intracranial hemorrhage (sICH)safety

Thrombolysis after dabigatran reversal with idarucizumab in acute ischemic stroke patients shows comparable functional recovery to matched controls, with a non-significant trend toward increased symptomatic intracranial hemorrhage.

Limitations

  • Further studies are needed to define treatment cost-effectiveness and potential thresholds in plasma dabigatran concentration for reversal

Abstract

Introduction: Recent anticoagulant intake represents a contraindication for thrombolysis in acute ischemic stroke. Idarucizumab reverses the anticoagulant effect of dabigatran, potentially allowing for thrombolysis. This nation-wide observational cohort study, systematic review, and meta-analysis evaluated the efficacy and safety of thrombolysis preceded by dabigatran-reversal in people with acute ischemic stroke. Patients and methods: We recruited people undergoing thrombolysis following dabigatran-reversal at 17 stroke centers in Italy (reversal-group), people on dabigatran treated with thrombolysis without reversal (no-reversal group), and age, sex, hypertension, stroke severity, and reperfusion treatment-matched controls in 1:7 ratio (control-group). We compared groups for symptomatic intracranial hemorrhage (sICH, main outcome), any brain hemorrhage, good functional outcome (mRS 0-2 at 3 months), and death. The systematic review followed a predefined protocol (CRD42017060274), and odds ratio (OR) meta-analysis was implemented to compare groups. Results: Thirty-nine patients in dabigatran-reversal group and 300 matched controls were included. Reversal was associated with a non-significant increase in sICH (10.3% vs 6%, aOR = 1.32, 95% CI = 0.39-4.52), death (17.9% vs 10%, aOR = 0.77, 95% CI = 0.12-4.93) and good functional outcome (64.1% vs 52.8%, aOR = 1.41, 95% CI = 0.63-3.19). No hemorrhagic events or deaths were registered in no-reversal group (n = 12). Pooling data from 3 studies after systematic review (n = 1879), reversal carried a non-significant trend for sICH (OR = 1.53, 95% CI = 0.67-3.50), death (OR = 1.53, 95% CI = 0.73-3.24) and good functional outcome (OR = 2.46, 95% CI = 0.85-7.16). Discussion and conclusion: People treated with reperfusion strategies after dabigatran reversal with idarucizumab seem to have a marginal increase in the risk of sICH but comparable functional recovery to matched patients with stroke. Further studies are needed to define treatment cost-effectiveness and potential thresholds in plasma dabigatran concentration for reversal.

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Cite This Study

Romoli et al. (2022) studied this question. Thrombolysis after dabigatran reversal showed comparable functional recovery and a non-significant increase in symptomatic intracranial hemorrhage (OR 1.53, 95% CI 0.67-3.50) versus controls.

synapsesocial.com/papers/6a0a596ceda9b9caed96aeb6https://doi.org/10.1177/23969873221131635
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