Thrombolysis in young adults with stroke: Findings from Get With The Guidelines-Stroke.

Autor:	Dodds JA; From the Department of Neurology (J.A.D., Y.X.) and Duke Clinical Research Institute (Y.X., S.S., R.M., E.D.P.), Duke University Medical Center, Durham NC; Division of Cardiology (G.C.F.), University of California, Los Angeles (G.C.F.); Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School (D.L.B.), Boston, MA; Department of Neurology (L.H.S.), Massachusetts General Hospital, Boston; and Department of Clinical Neurosciences and Hotchkiss Brain Institute (E.E.S.), University of Calgary, Alberta, Canada., Xian Y; From the Department of Neurology (J.A.D., Y.X.) and Duke Clinical Research Institute (Y.X., S.S., R.M., E.D.P.), Duke University Medical Center, Durham NC; Division of Cardiology (G.C.F.), University of California, Los Angeles (G.C.F.); Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School (D.L.B.), Boston, MA; Department of Neurology (L.H.S.), Massachusetts General Hospital, Boston; and Department of Clinical Neurosciences and Hotchkiss Brain Institute (E.E.S.), University of Calgary, Alberta, Canada., Sheng S; From the Department of Neurology (J.A.D., Y.X.) and Duke Clinical Research Institute (Y.X., S.S., R.M., E.D.P.), Duke University Medical Center, Durham NC; Division of Cardiology (G.C.F.), University of California, Los Angeles (G.C.F.); Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School (D.L.B.), Boston, MA; Department of Neurology (L.H.S.), Massachusetts General Hospital, Boston; and Department of Clinical Neurosciences and Hotchkiss Brain Institute (E.E.S.), University of Calgary, Alberta, Canada., Fonarow GC; From the Department of Neurology (J.A.D., Y.X.) and Duke Clinical Research Institute (Y.X., S.S., R.M., E.D.P.), Duke University Medical Center, Durham NC; Division of Cardiology (G.C.F.), University of California, Los Angeles (G.C.F.); Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School (D.L.B.), Boston, MA; Department of Neurology (L.H.S.), Massachusetts General Hospital, Boston; and Department of Clinical Neurosciences and Hotchkiss Brain Institute (E.E.S.), University of Calgary, Alberta, Canada., Bhatt DL; From the Department of Neurology (J.A.D., Y.X.) and Duke Clinical Research Institute (Y.X., S.S., R.M., E.D.P.), Duke University Medical Center, Durham NC; Division of Cardiology (G.C.F.), University of California, Los Angeles (G.C.F.); Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School (D.L.B.), Boston, MA; Department of Neurology (L.H.S.), Massachusetts General Hospital, Boston; and Department of Clinical Neurosciences and Hotchkiss Brain Institute (E.E.S.), University of Calgary, Alberta, Canada., Matsouaka R; From the Department of Neurology (J.A.D., Y.X.) and Duke Clinical Research Institute (Y.X., S.S., R.M., E.D.P.), Duke University Medical Center, Durham NC; Division of Cardiology (G.C.F.), University of California, Los Angeles (G.C.F.); Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School (D.L.B.), Boston, MA; Department of Neurology (L.H.S.), Massachusetts General Hospital, Boston; and Department of Clinical Neurosciences and Hotchkiss Brain Institute (E.E.S.), University of Calgary, Alberta, Canada., Schwamm LH; From the Department of Neurology (J.A.D., Y.X.) and Duke Clinical Research Institute (Y.X., S.S., R.M., E.D.P.), Duke University Medical Center, Durham NC; Division of Cardiology (G.C.F.), University of California, Los Angeles (G.C.F.); Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School (D.L.B.), Boston, MA; Department of Neurology (L.H.S.), Massachusetts General Hospital, Boston; and Department of Clinical Neurosciences and Hotchkiss Brain Institute (E.E.S.), University of Calgary, Alberta, Canada., Peterson ED; From the Department of Neurology (J.A.D., Y.X.) and Duke Clinical Research Institute (Y.X., S.S., R.M., E.D.P.), Duke University Medical Center, Durham NC; Division of Cardiology (G.C.F.), University of California, Los Angeles (G.C.F.); Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School (D.L.B.), Boston, MA; Department of Neurology (L.H.S.), Massachusetts General Hospital, Boston; and Department of Clinical Neurosciences and Hotchkiss Brain Institute (E.E.S.), University of Calgary, Alberta, Canada., Smith EE; From the Department of Neurology (J.A.D., Y.X.) and Duke Clinical Research Institute (Y.X., S.S., R.M., E.D.P.), Duke University Medical Center, Durham NC; Division of Cardiology (G.C.F.), University of California, Los Angeles (G.C.F.); Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School (D.L.B.), Boston, MA; Department of Neurology (L.H.S.), Massachusetts General Hospital, Boston; and Department of Clinical Neurosciences and Hotchkiss Brain Institute (E.E.S.), University of Calgary, Alberta, Canada. eesmith@ucalgary.ca.
Jazyk:	angličtina
Zdroj:	Neurology [Neurology] 2019 Jun 11; Vol. 92 (24), pp. e2784-e2792. Date of Electronic Publication: 2019 May 15.
DOI:	10.1212/WNL.0000000000007653
Abstrakt:	Objective: To determine whether young adults (≤40 years old) with acute ischemic stroke are less likely to receive IV tissue plasminogen activator (tPA) and more likely to have longer times to brain imaging and treatment. Methods: We analyzed data from the Get With The Guidelines-Stroke registry for patients with acute ischemic stroke hospitalized between January 2009 and September 2015. We used multivariable models with generalized estimating equations to evaluate tPA treatment and outcomes between younger (age 18-40 years) and older (age >40 years) patients with acute ischemic stroke. Results: Of 1,320,965 patients with acute ischemic stroke admitted to 1,983 hospitals, 2.3% (30,448) were 18 to 40 years of age. Among these patients, 12.5% received tPA vs 8.8% of those >40 years of age (adjusted odds ratio [aOR] 1.63, 95% confidence interval [CI] 1.56-1.71). However, younger patients were less likely to receive brain imaging within 25 minutes (62.5% vs 71.5%, aOR 0.78, 95% CI 0.73-0.84) and to be treated with tPA within 60 minutes of hospital arrival (37.0% vs 42.8%, aOR 0.74, 95% CI 0.68-0.79). Compared to older patients, younger patients treated with tPA had a lower symptomatic intracranial hemorrhage rate (1.7% vs 4.5%, aOR 0.55, 95% CI 0.42-0.72) and lower in-hospital mortality (2.0% vs 4.3%, aOR 0.65, 95% CI 0.52-0.81). Conclusions: In contrast to our hypothesis, younger patients with acute ischemic stroke were more likely to be treated with tPA than older patients, but they were more likely to experience delay in evaluation and treatment. Compared with older patients, younger patients had better outcomes, including fewer intracranial hemorrhages. (© 2019 American Academy of Neurology.)
Databáze:	MEDLINE
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