Blood Pressure Management After Endovascular Therapy for Acute Ischemic Stroke

医学 改良兰金量表 随机对照试验 冲程(发动机) 血压 临床终点 指南 血管内治疗 内科学 缺血性中风 心脏病学 外科 缺血 动脉瘤 机械工程 病理 工程类
作者
Eva Mistry,Kimberly W. Hart,L. Taylor Davis,Yue Gao,Charles J. Prestigiacomo,Shilpi Mittal,Tapan Mehta,Hayden LaFever,Pablo Harker,Hilary Wilson,Kalli A. Beasley,Neeharika Krothapalli,Emily Lippincott,Heather Stefek,Michael T. Froehler,Rohan Chitale,Matthew R. Fusco,Aaron W. Grossman,Peyman Shirani,Michael B. Smith,Matthew Jaffa,Sharon D. Yeatts,Gregory W. Albers,Jonathan D. Casey,Juliana Tolles,Christopher J. Lindsell,Roger Lewis,Gordon R. Bernard,Pooja Khatri
出处
期刊:JAMA [American Medical Association]
卷期号:330 (9): 821-821 被引量:30
标识
DOI:10.1001/jama.2023.14330
摘要

Importance The effects of moderate systolic blood pressure (SBP) lowering after successful recanalization with endovascular therapy for acute ischemic stroke are uncertain. Objective To determine the futility of lower SBP targets after endovascular therapy (<140 mm Hg or 160 mm Hg) compared with a higher target (≤180 mm Hg). Design, Setting, and Participants Randomized, open-label, blinded end point, phase 2, futility clinical trial that enrolled 120 patients with acute ischemic stroke who had undergone successful endovascular therapy at 3 US comprehensive stroke centers from January 2020 to March 2022 (final follow-up, June 2022). Intervention After undergoing endovascular therapy, participants were randomized to 1 of 3 SBP targets: 40 to less than 140 mm Hg, 40 to less than 160 mm Hg, and 40 to 180 mm Hg or less (guideline recommended) group, initiated within 60 minutes of recanalization and maintained for 24 hours. Main Outcomes and Measures Prespecified multiple primary outcomes for the primary futility analysis were follow-up infarct volume measured at 36 (±12) hours and utility-weighted modified Rankin Scale (mRS) score (range, 0 [worst] to 1 [best]) at 90 (±14) days. Linear regression models were used to test the harm-futility boundaries of a 10-mL increase (slope of 0.5) in the follow-up infarct volume or a 0.10 decrease (slope of −0.005) in the utility-weighted mRS score with each 20-mm Hg SBP target reduction after endovascular therapy (1-sided α = .05). Additional prespecified futility criterion was a less than 25% predicted probability of success for a future 2-group, superiority trial comparing SBP targets of the low- and mid-thresholds with the high-threshold (maximum sample size, 1500 with respect to the utility-weighted mRS score outcome). Results Among 120 patients randomized (mean [SD] age, 69.6 [14.5] years; 69 females [58%]), 113 (94.2%) completed the trial. The mean follow-up infarct volume was 32.4 mL (95% CI, 18.0 to 46.7 mL) for the less than 140–mm Hg group, 50.7 mL (95% CI, 33.7 to 67.7 mL), for the less than 160–mm Hg group, and 46.4 mL (95% CI, 24.5 to 68.2 mL) for the 180–mm Hg or less group. The mean utility-weighted mRS score was 0.51 (95% CI, 0.38 to 0.63) for the less than 140–mm Hg group, 0.47 (95% CI, 0.35 to 0.60) for the less than 160–mm Hg group, and 0.58 (95% CI, 0.46 to 0.71) for the high-target group. The slope of the follow-up infarct volume for each mm Hg decrease in the SBP target, adjusted for the baseline Alberta Stroke Program Early CT score, was −0.29 (95% CI, −0.81 to ∞; futility P = .99). The slope of the utility-weighted mRS score for each mm Hg decrease in the SBP target after endovascular therapy, adjusted for baseline utility-weighted mRS score, was −0.0019 (95% CI, −∞ to 0.0017; futility P = .93). Comparing the high-target SBP group with the lower-target groups, the predicted probability of success for a future trial was 25% for the less than 140–mm Hg group and 14% for the 160–mm Hg group. Conclusions and Relevance Among patients with acute ischemic stroke, lower SBP targets less than either 140 mm Hg or 160 mm Hg after successful endovascular therapy did not meet prespecified criteria for futility compared with an SBP target of 180 mm Hg or less. However, the findings suggested a low probability of benefit from lower SBP targets after endovascular therapy if tested in a future larger trial. Trial Registration ClinicalTrials.gov Identifier: NCT04116112
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
呼呼哈哈完成签到,获得积分10
刚刚
1秒前
lm0703完成签到,获得积分10
1秒前
1秒前
找文献呢完成签到,获得积分10
2秒前
2秒前
小灰灰完成签到,获得积分10
3秒前
可靠的电源完成签到,获得积分10
3秒前
一步一步完成签到,获得积分10
3秒前
咕咕风完成签到,获得积分10
4秒前
大强完成签到,获得积分10
5秒前
月夙应助青思采纳,获得10
5秒前
yhmi0809完成签到,获得积分10
6秒前
mito完成签到,获得积分10
6秒前
枝兮旅人完成签到,获得积分10
6秒前
pura卷卷完成签到 ,获得积分10
7秒前
科研通AI2S应助Joy采纳,获得10
7秒前
人生苦短完成签到,获得积分10
7秒前
qing_he完成签到 ,获得积分10
8秒前
闪闪山水应助大强采纳,获得10
8秒前
王新一完成签到,获得积分10
9秒前
nanan发布了新的文献求助10
10秒前
LGH完成签到,获得积分10
10秒前
君莫笑完成签到,获得积分10
10秒前
caiqinghua888888完成签到,获得积分10
11秒前
kk完成签到 ,获得积分10
11秒前
11秒前
12秒前
风景的谷建芬完成签到,获得积分10
13秒前
滴滴滴发布了新的文献求助10
15秒前
tuanheqi应助jeffrey采纳,获得150
16秒前
John不想上班完成签到 ,获得积分10
16秒前
CodeCraft应助和敬清寂采纳,获得10
16秒前
Atlantis完成签到,获得积分10
16秒前
英姑应助ellen采纳,获得10
16秒前
Yihua发布了新的文献求助10
17秒前
17秒前
郭囯完成签到,获得积分10
17秒前
LLRO完成签到,获得积分10
17秒前
19秒前
高分求助中
Handbook of Fuel Cells, 6 Volume Set 1666
Floxuridine; Third Edition 1000
Tracking and Data Fusion: A Handbook of Algorithms 1000
Sustainable Land Management: Strategies to Cope with the Marginalisation of Agriculture 800
消化器内視鏡関連の偶発症に関する第7回全国調査報告2019〜2021年までの3年間 500
One Man Talking: Selected Essays of Shao Xunmei, 1929–1939 500
Framing China: Media Images and Political Debates in Britain, the USA and Switzerland, 1900-1950 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 内科学 物理 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 冶金 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 2860802
求助须知:如何正确求助?哪些是违规求助? 2465871
关于积分的说明 6684494
捐赠科研通 2157114
什么是DOI,文献DOI怎么找? 1145935
版权声明 585087
科研通“疑难数据库(出版商)”最低求助积分说明 563114