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Intensive blood pressure reduction with intravenous thrombolysis therapy for acute ischaemic stroke (ENCHANTED) : an international, randomised, open-label, blinded-endpoint, phase 3 trial

Title: Intensive blood pressure reduction with intravenous thrombolysis therapy for acute ischaemic stroke (ENCHANTED) : an international, randomised, open-label, blinded-endpoint, phase 3 trial
Authors: Anderson, Craig S.; Huang, Yining; Lindley, Richard I.; Chen, Xiaoying; Arima, Hisatomi; Chen, Guofang; Li, Qiang; Billot, Laurent; Delcourt, Candice; Bath, Philip M.; Broderick, Joseph P.; Demchuk, Andrew M.; Donnan, Geoffrey A.; Durham, Alice C.; Lavados, Pablo M.; Lee, Tsong-Hai; Levi, Christopher (R19066); Martins, Sheila O.; Olavarria, Veronica V.; Pandian, Jeyaraj D.; Parsons, Mark W.; Pontes-Neto, Octavio M.; Ricci, Stefano; Sato, Shoichiro; Sharma, Vijay K.; Silva, Federico; Song, Lili; Thang, Nguyen H.; Wardlaw, Joanna M.; Wang, Ji-Guang; Wang, Xia; Woodward, Mark; Chalmers, John; Robinson, Thompson G.; Krause, M.; Priglinger, M.; Day, S.; Jala, S.; Carcel, C.; Malavera, A.; Ray, E.; Wijeratne, T.; Celestino, S.; Law, L. Y.; Ng, G.; Nagao, K.; Weiss, G.; Titton, N.; Batista, C.; Zan, D.
Publisher Information: U.K., Lancet Publishing Group
Publication Year: 2019
Collection: University of Western Sydney (UWS): Research Direct
Subject Terms: XXXXXX - Unknown
Description: Background: Systolic blood pressure of more than 185 mm Hg is a contraindication to thrombolytic treatment with intravenous alteplase in patients with acute ischaemic stroke, but the target systolic blood pressure for optimal outcome is uncertain. We assessed intensive blood pressure lowering compared with guideline-recommended blood pressure lowering in patients treated with alteplase for acute ischaemic stroke. Methods: We did an international, partial-factorial, open-label, blinded-endpoint trial of thrombolysis-eligible patients (age ≥18 years) with acute ischaemic stroke and systolic blood pressure 150 mm Hg or more, who were screened at 110 sites in 15 countries. Eligible patients were randomly assigned (1:1, by means of a central, web-based program) within 6 h of stroke onset to receive intensive (target systolic blood pressure 130–140 mm Hg within 1 h) or guideline (target systolic blood pressure
Document Type: article in journal/newspaper
File Description: print
Language: English
Relation: The Lancet--0140-6736--1474-547X Vol. 393 Issue. 10174 pp: 877-888
DOI: 10.1016/S0140-6736(19)30038-8
Availability: https://doi.org/10.1016/S0140-6736(19)30038-8; http://hdl.handle.net/1959.7/uws:66999
Accession Number: edsbas.679CC875
Database: BASE