Sixtine Gilliot1,2, Igor Sibon3,4, Jean-Louis Mas3,5, Thierry Moulin3,6, Yannick Béjot3,7, Charlotte Cordonnier1,3, Maurice Giroud3,7, Pascal Odou2, Régis Bordet1,3, Denis Vivien3,8,9, Didier Leys10,11,12. 1. Univ. Lille, Inserm, CHU Lille, U1171 - Degenerative and Vascular Cognitive Disorders, 59000, Lille, France. 2. Univ. Lille, EA7365, CHU Lille, GRITA, 59000, Lille, France. 3. Strokavenir Network, Lille, France. 4. Bordeaux University Hospital, University of Bordeaux, Bordeaux, France. 5. University Paris Descartes, Sorbonne Paris Cité, INSERM UMR S894, Sainte-Anne Hospital, DHU NeuroVasc, Paris, France. 6. Besançon University Hospital, University of Franche-Comté, Besançon, France. 7. Dijon University Hospital, Dijon Stroke Registry (Inserm and Invs), University of Burgundi, Dijon, France. 8. Inserm, UMR-S 1237, University Caen-Normandie, GIP Cyceron, Caen, France. 9. Department of Clinical Research, CHU Caen, Caen, France. 10. Univ. Lille, Inserm, CHU Lille, U1171 - Degenerative and Vascular Cognitive Disorders, 59000, Lille, France. didier.leys@univ-lille2.fr. 11. Strokavenir Network, Lille, France. didier.leys@univ-lille2.fr. 12. Department of Neurology, Stroke Unit, Roger Salengro Hospital, Univ. Lille, CHU Lille, INSERM, U1171, 59037, Lille, France. didier.leys@univ-lille2.fr.
Abstract
BACKGROUND: Many patients who receive intravenous (i.v.) recombinant tissue-plasminogen activator (rt-PA) for acute cerebral ischemia were under angiotensin-converting enzyme inhibitors (ACE-Is) or angiotensin receptor blockers (ARBs) at stroke onset. ACE-Is and ARBs have neuroprotective properties in animal models. OBJECTIVE: To evaluate whether the 3-month outcome of patients treated with i.v. rt-PA for cerebral ischemia was influenced by on-going therapy with ACE-Is or ARBs. METHOD: This study was observational, conducted in two prospective registries of stroke patients treated with i.v. rt-PA. We evaluated outcomes with the modified Rankin scale and symptomatic intracranial hemorrhages (s-ICH) according to the ECASS2 criteria. We compared outcomes between patients with and without ACE-Is/ARBs according to the modified Rankin scale (mRS) at month 3, using logistic regression analyses adjusted on propensity scores, and propensity-matched analyses. RESULTS: Of 1803 patients, 455 (25.2%) were under ACE-Is (259), ARBs (188) or both (8). At 3 months, patients under ACE-Is or ARBs were more likely to have an mRS 0-1, but did not differ for mRS 0-2, s-ICH and death. After adjustment on propensity scores, the association between ACE-Is/ARBs and mRS 0-1 disappeared. The propensity-matched analysis, performed in 397 pairs of patients, found no difference in outcomes between patients with and without ACE-Is or ARBs. CONCLUSION: In patients treated by intravenous thrombolytic therapy for ischemic stroke, on-going treatment with ACE-Is or ARBs does not influence on outcomes after adjustment on baseline characteristics and propensity scores.
BACKGROUND: Many patients who receive intravenous (i.v.) recombinant tissue-plasminogen activator (rt-PA) for acute cerebral ischemia were under angiotensin-converting enzyme inhibitors (ACE-Is) or angiotensin receptor blockers (ARBs) at stroke onset. ACE-Is and ARBs have neuroprotective properties in animal models. OBJECTIVE: To evaluate whether the 3-month outcome of patients treated with i.v. rt-PA for cerebral ischemia was influenced by on-going therapy with ACE-Is or ARBs. METHOD: This study was observational, conducted in two prospective registries of strokepatients treated with i.v. rt-PA. We evaluated outcomes with the modified Rankin scale and symptomatic intracranial hemorrhages (s-ICH) according to the ECASS2 criteria. We compared outcomes between patients with and without ACE-Is/ARBs according to the modified Rankin scale (mRS) at month 3, using logistic regression analyses adjusted on propensity scores, and propensity-matched analyses. RESULTS: Of 1803 patients, 455 (25.2%) were under ACE-Is (259), ARBs (188) or both (8). At 3 months, patients under ACE-Is or ARBs were more likely to have an mRS 0-1, but did not differ for mRS 0-2, s-ICH and death. After adjustment on propensity scores, the association between ACE-Is/ARBs and mRS 0-1 disappeared. The propensity-matched analysis, performed in 397 pairs of patients, found no difference in outcomes between patients with and without ACE-Is or ARBs. CONCLUSION: In patients treated by intravenous thrombolytic therapy for ischemic stroke, on-going treatment with ACE-Is or ARBs does not influence on outcomes after adjustment on baseline characteristics and propensity scores.
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