Optimal achieved blood pressure in acute intracerebral hemorrhage: INTERACT2
Author
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Arima, Hisatomi
Author
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Heeley, Emma
Author
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Delcourt, Candice
Author
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Hirakawa, Yoichiro
Author
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Wang, Xia
Author
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Woodward, Mark
Author
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Robinson, Thompson
Author
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Stapf, Christian
Author
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Parsons, Mark
Author
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Lavados Germain, Pablo Manuel
Author
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Huang, Yining
Author
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Wang, Jiguang
Author
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Chalmers, John
Author
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Anderson, Craig S.
Admission date
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2019-03-18T11:52:24Z
Available date
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2019-03-18T11:52:24Z
Publication date
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2015
Cita de ítem
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Neurology 2015;84:464–471
Identifier
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1526632X
Identifier
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00283878
Identifier
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10.1212/WNL.0000000000001205
Identifier
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https://repositorio.uchile.cl/handle/2250/166508
Abstract
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Objectives: To investigate the effects of intensive blood pressure (BP) lowering according to baseline BP levels and optimal achieved BP levels in patients with acute intracerebral hemorrhage
(ICH).
Methods: INTERACT2 was an open, blinded endpoint, randomized controlled trial in 2,839 patients with ICH within 6 hours of onset and elevated systolic BP (SBP) (150–220 mm Hg) who
were allocated to receive intensive (target SBP ,140 mm Hg within 1 hour, with lower limit of
130 mm Hg for treatment cessation) or guideline-recommended (target SBP ,180 mm Hg) BPlowering treatment. Outcome was physical function across all 7 levels of the modified Rankin
Scale at 90 days.
Results: Analysis of the randomized comparisons showed that intensive BP lowering produced
comparable benefits on physical function at 90 days in 5 subgroups defined by baseline SBP
of ,160, 160–169, 170–179, 180–189, and $190 mm Hg (p homogeneity 5 0.790). Analyses
of achieved BP showed linear increases in the risk of physical dysfunction for achieved SBP above
130 mm Hg for both hyperacute (1–24 hours) and acute (2–7 days) phases while modest increases were also observed for achieved SBP below 130 mm Hg.
Conclusions: Intensive BP lowering appears beneficial across a wide range of baseline SBP levels,
and target SBP level of 130–139 mm Hg is likely to provide maximum benefit in acute ICH.