Evidence map›Paper›PMID 37668620›Full record

Trial reportJAMA2023

Blood Pressure Management After Endovascular Therapy for Acute Ischemic Stroke: The BEST-II Randomized Clinical Trial.

Eva A Mistry, Kimberly W Hart, Larry T Davis, Yue Gao, Charles J Prestigiacomo, Shilpi Mittal, Tapan Mehta, Hayden LaFever, Pablo Harker, Hilary E Wilson-Perez and 19 more

2 registry-linked trialsAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 67 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 7 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04116112 phase2completednot on this map

Blood Pressure After Endovascular Stroke Therapy-II: A Randomized Trial

TypeinterventionalSponsorUniversity of CincinnatiRan2020 to 2022Enrolled120ConditionsAcute Stroke, Endovascular ThrombectomyArmsNicardipine, Labetalol, Hydralazine
NCT07527013 phase3not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Stratified Blood Pressure Management After Endovascular Treatment for Acute Ischemic Stroke (RESCUE-BP)

TypeinterventionalSponsorBeijing Tiantan HospitalRan2026 to 2028Enrolled544ConditionsEndovascular Therapy, Acute Ischaemic Stroke, Collateral Circulation, Blood Pressure ManagementArmsStratified Blood Pressure Management
3 · Its place in the literature

Who cites it

67 citing papers in PubMed, 7 syntheses or guidelines pooled it.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Blood pressure targets after successful reperfusion in mechanical thrombectomy for acute ischemic stroke: an updated systematic review and meta-analysis of randomized clinical trials.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Pooled it
  7. Pooled it
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Systolic blood pressure targets after successful endovascular thrombectomy: a network meta-analysis of randomized controlled trials.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Observational
  19. Mid-term systolic BP variability beyond 24 h after successful recanalization predicts poor outcomes following ischemic stroke.Hypertension research : official journal of the Japanese Society of Hypertension · 2026
    Article
  20. Article

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors.

Eva A MistryDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati, Cincinnati, Ohio.
Kimberly W HartDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Larry T DavisDepartment of Radiology, Vanderbilt University Medical Center, Nashville, Tennessee.
Yue GaoDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Charles J PrestigiacomoDepartment of Neurosurgery, University of Cincinnati, Cincinnati, Ohio.
Shilpi MittalDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee.
Tapan MehtaAyer Neuroscience Institute, Department of Neurology, Hartford Hospital, Hartford, Connecticut.
Hayden LaFeverDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee.
Pablo HarkerDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati, Cincinnati, Ohio.
Hilary E Wilson-PerezDepartment of Neurosurgery, University of Cincinnati, Cincinnati, Ohio.
Kalli A BeasleyDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati, Cincinnati, Ohio.
Neeharika KrothapalliAyer Neuroscience Institute, Department of Neurology, Hartford Hospital, Hartford, Connecticut.
Emily LippincottDepartment of Radiology, Vanderbilt University Medical Center, Nashville, Tennessee.
Heather StefekDepartment of Radiology, Vanderbilt University Medical Center, Nashville, Tennessee.
Michael FroehlerDepartment of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee.
Rohan ChitaleDepartment of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Matthew FuscoDepartment of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Aaron GrossmanDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati, Cincinnati, Ohio.
Peyman ShiraniDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati, Cincinnati, Ohio.
Matthew SmithDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati, Cincinnati, Ohio.
Matthew N JaffaAyer Neuroscience Institute, Department of Neurology, Hartford Hospital, Hartford, Connecticut.
Sharon D YeattsDepartment of Public Health Sciences, Medical University of South Carolina, Charleston.
Gregory W AlbersDepartment of Neurology, Stanford University, Palo Alto, California.
Jonathan P WandererDepartment of Anesthesiology, Vanderbilt University Medical Center, Nashville, Tennessee.
Juliana TollesDepartment of Emergency Medicine, Harbor-UCLA Medical Center, Los Angeles, California.
Christopher J LindsellDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.
Roger J LewisDepartment of Emergency Medicine, Harbor-UCLA Medical Center, Los Angeles, California.
Gordon R BernardDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Pooja KhatriDepartment of Neurology and Rehabilitation Medicine, University of Cincinnati, Cincinnati, Ohio.

Funding

Blood Pressure after Endovascular Stroke Therapy-II: A Randomized TrialK23NS113858 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MISTRY, EVA · 2019 to 2023
$901k
NINDS NIH HHS K23 NS113858
6 · The paper itself

Abstract

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.

Indexed as

Antihypertensive AgentsBlood PressureBrain InfarctionEndovascular ProceduresHypertensionIschemic StrokeAcute DiseaseAgedAged, 80 and overFemaleHumansHypotensionInfarctionMaleMiddle AgedStrokeAntihypertensive Agents

Identifiers

PMID37668620
PMCPMC10481231

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.