Time of blood pressure in target range in acute ischemic stroke

医学 冲程(发动机) 血压 内科学 心脏病学 缺血性中风 急性中风 缺血 组织纤溶酶原激活剂 机械工程 工程类
作者
Nikolaos Kakaletsis,George Ntaios,Haralampos Milionis,Athanasios Protogerou,Anastasia Karagiannaki,Ioanna Chouvarda,Vasiliki Dourliou,Ioannis Ladakis,Georgia Kaiafa,Stylianos Daios,Michael Doumas,Christos Savopoulos
出处
期刊:Journal of Hypertension [Lippincott Williams & Wilkins]
卷期号:41 (2): 303-309 被引量:1
标识
DOI:10.1097/hjh.0000000000003331
摘要

The purpose of this study was to investigate the association of blood pressure (BP) time-in-target range (TTR) derived from 24-h ambulatory BP monitoring (ABPM) during the acute phase of ischemic stroke (AIS), with the severity of stroke and its predictive value for the 3 months outcome.A total of 228 AIS patients (prospective multicenter follow-up study) underwent ABPM every 20 min within 48 h from stroke onset using an automated oscillometric device. Clinical and laboratory findings were recorded. Mean BP parameters, BP variability and TTR for SBP (90-140 mmHg), DBP (60-90 mmHg), and mean arterial pressure (MAP) were calculated. Endpoints were death and disability/death at 3 months.A total of 14 942 BP measurements were recorded (∼66 per AIS patient) within 72 h of stroke onset. Patient's 24-h TTR was 34.7 ± 29.9, 64.3 ± 24.2, and 55.3 ± 29.4% for SBP, DBP and MAP, respectively. In patients without prior hypertension, TTR was lower as stroke severity increased for both DBP (P = 0.031) and MAP (P = 0.016). In 175 patients without prior disability, increase in TTR of DBP and MAP associated significantly with a decreased risk of disability/death (hazard ratio 0.96, 95% CI 0.95-0.99, P = 0.007 and hazard ratio 0.97, 95% CI 0.96-0.99, P = 0.007). TTR of SBP in 130-180 mmHg and 110-160 mmHg ranges seems to be related with mortality and disability outcomes, respectively.TTR can be included for a more detailed description of BP course, according to stroke severity, and for the evaluation of BP predictive role, in addition to mean BP values, derived from ABPM during the acute phase of AIS.http://www.clinicaltrials.gov. Unique identifier: NCT01915862.
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