Effect of intravenous alteplase on post-stroke depression in the WAKE UP trial

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Effect of intravenous alteplase on post-stroke depression in the WAKE UP trial. / Königsberg, Alina; Sehner, Susanne; Arlt, Sönke; Cheng, Bastian; Simonsen, Claus Z; Boutitie, Florent; Serena, Joaquin; Thijs, Vincent; Ebinger, Martin; Endres, Matthias; Fiebach, Jochen B; Lemmens, Robin; Muir, Keith W; Nighoghossian, Norbert; Pedraza, Salvador; Gerloff, Christian; Thomalla, Götz; WAKE-UP Investigators.

in: EUR J NEUROL, Jahrgang 28, Nr. 6, 06.2021, S. 2017-2025.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Königsberg, A, Sehner, S, Arlt, S, Cheng, B, Simonsen, CZ, Boutitie, F, Serena, J, Thijs, V, Ebinger, M, Endres, M, Fiebach, JB, Lemmens, R, Muir, KW, Nighoghossian, N, Pedraza, S, Gerloff, C, Thomalla, G & WAKE-UP Investigators 2021, 'Effect of intravenous alteplase on post-stroke depression in the WAKE UP trial', EUR J NEUROL, Jg. 28, Nr. 6, S. 2017-2025. https://doi.org/10.1111/ene.14797

APA

Königsberg, A., Sehner, S., Arlt, S., Cheng, B., Simonsen, C. Z., Boutitie, F., Serena, J., Thijs, V., Ebinger, M., Endres, M., Fiebach, J. B., Lemmens, R., Muir, K. W., Nighoghossian, N., Pedraza, S., Gerloff, C., Thomalla, G., & WAKE-UP Investigators (2021). Effect of intravenous alteplase on post-stroke depression in the WAKE UP trial. EUR J NEUROL, 28(6), 2017-2025. https://doi.org/10.1111/ene.14797

Vancouver

Bibtex

@article{52bac4dcbd274bf9bcf9e44d41c189a9,
title = "Effect of intravenous alteplase on post-stroke depression in the WAKE UP trial",
abstract = "BACKGROUND AND PURPOSE: The aim was to study the effect of intravenous alteplase on the development of post-stroke depression (PSD) in acute stroke patients, and to identify predictors of PSD.METHODS: This post hoc analysis included patients with unknown onset stroke randomized to treatment with alteplase or placebo in the WAKE-UP trial (ClinicalTrials.gov number, NCT01525290), in whom a composite end-point of PSD was defined as a Beck Depression Inventory ≥10, medication with an antidepressant, or depression recorded as an adverse event. Multiple logistic regression was used to identify predictors of PSD at 90 days. Structural equation modelling was applied to assess the indirect effect of thrombolysis on PSD mediated by the modified Rankin Scale.RESULTS: Information on the composite end-point was available for 438 of 503 randomized patients. PSD was present in 96 of 224 (42.9%) patients in the alteplase group and 115 of 214 (53.7%) in the placebo group (odds ratio 0.63; 95% confidence interval 0.43-0.94; p = 0.022; adjusted for age and National Institutes of Health Stroke Scale at baseline). Prognostic factors associated with PSD included baseline medication with antidepressants, higher lesion volume, history of depression and assignment to placebo. While 65% of the effect of thrombolysis on PSD were caused directly, 35% were mediated by an improvement of the mRS.CONCLUSIONS: Treatment with alteplase in patients with acute stroke resulted in lower rates of depression at 90 days, which were only partially explained by reduced functional disability. Predictors of PSD including history and clinical characteristics may help in identifying patients at risk of PSD.",
author = "Alina K{\"o}nigsberg and Susanne Sehner and S{\"o}nke Arlt and Bastian Cheng and Simonsen, {Claus Z} and Florent Boutitie and Joaquin Serena and Vincent Thijs and Martin Ebinger and Matthias Endres and Fiebach, {Jochen B} and Robin Lemmens and Muir, {Keith W} and Norbert Nighoghossian and Salvador Pedraza and Christian Gerloff and G{\"o}tz Thomalla and {WAKE-UP Investigators}",
note = "{\textcopyright} 2021 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.",
year = "2021",
month = jun,
doi = "10.1111/ene.14797",
language = "English",
volume = "28",
pages = "2017--2025",
journal = "EUR J NEUROL",
issn = "1351-5101",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - Effect of intravenous alteplase on post-stroke depression in the WAKE UP trial

AU - Königsberg, Alina

AU - Sehner, Susanne

AU - Arlt, Sönke

AU - Cheng, Bastian

AU - Simonsen, Claus Z

AU - Boutitie, Florent

AU - Serena, Joaquin

AU - Thijs, Vincent

AU - Ebinger, Martin

AU - Endres, Matthias

AU - Fiebach, Jochen B

AU - Lemmens, Robin

AU - Muir, Keith W

AU - Nighoghossian, Norbert

AU - Pedraza, Salvador

AU - Gerloff, Christian

AU - Thomalla, Götz

AU - WAKE-UP Investigators

N1 - © 2021 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.

PY - 2021/6

Y1 - 2021/6

N2 - BACKGROUND AND PURPOSE: The aim was to study the effect of intravenous alteplase on the development of post-stroke depression (PSD) in acute stroke patients, and to identify predictors of PSD.METHODS: This post hoc analysis included patients with unknown onset stroke randomized to treatment with alteplase or placebo in the WAKE-UP trial (ClinicalTrials.gov number, NCT01525290), in whom a composite end-point of PSD was defined as a Beck Depression Inventory ≥10, medication with an antidepressant, or depression recorded as an adverse event. Multiple logistic regression was used to identify predictors of PSD at 90 days. Structural equation modelling was applied to assess the indirect effect of thrombolysis on PSD mediated by the modified Rankin Scale.RESULTS: Information on the composite end-point was available for 438 of 503 randomized patients. PSD was present in 96 of 224 (42.9%) patients in the alteplase group and 115 of 214 (53.7%) in the placebo group (odds ratio 0.63; 95% confidence interval 0.43-0.94; p = 0.022; adjusted for age and National Institutes of Health Stroke Scale at baseline). Prognostic factors associated with PSD included baseline medication with antidepressants, higher lesion volume, history of depression and assignment to placebo. While 65% of the effect of thrombolysis on PSD were caused directly, 35% were mediated by an improvement of the mRS.CONCLUSIONS: Treatment with alteplase in patients with acute stroke resulted in lower rates of depression at 90 days, which were only partially explained by reduced functional disability. Predictors of PSD including history and clinical characteristics may help in identifying patients at risk of PSD.

AB - BACKGROUND AND PURPOSE: The aim was to study the effect of intravenous alteplase on the development of post-stroke depression (PSD) in acute stroke patients, and to identify predictors of PSD.METHODS: This post hoc analysis included patients with unknown onset stroke randomized to treatment with alteplase or placebo in the WAKE-UP trial (ClinicalTrials.gov number, NCT01525290), in whom a composite end-point of PSD was defined as a Beck Depression Inventory ≥10, medication with an antidepressant, or depression recorded as an adverse event. Multiple logistic regression was used to identify predictors of PSD at 90 days. Structural equation modelling was applied to assess the indirect effect of thrombolysis on PSD mediated by the modified Rankin Scale.RESULTS: Information on the composite end-point was available for 438 of 503 randomized patients. PSD was present in 96 of 224 (42.9%) patients in the alteplase group and 115 of 214 (53.7%) in the placebo group (odds ratio 0.63; 95% confidence interval 0.43-0.94; p = 0.022; adjusted for age and National Institutes of Health Stroke Scale at baseline). Prognostic factors associated with PSD included baseline medication with antidepressants, higher lesion volume, history of depression and assignment to placebo. While 65% of the effect of thrombolysis on PSD were caused directly, 35% were mediated by an improvement of the mRS.CONCLUSIONS: Treatment with alteplase in patients with acute stroke resulted in lower rates of depression at 90 days, which were only partially explained by reduced functional disability. Predictors of PSD including history and clinical characteristics may help in identifying patients at risk of PSD.

U2 - 10.1111/ene.14797

DO - 10.1111/ene.14797

M3 - SCORING: Journal article

C2 - 33657675

VL - 28

SP - 2017

EP - 2025

JO - EUR J NEUROL

JF - EUR J NEUROL

SN - 1351-5101

IS - 6

ER -