Blood Pressure Management Following Endovascular Stroke Treatment: A Feasibility Trial and Meta‐Analysis of Outcomes

Author:

Katsanos Aristeidis H.12ORCID,Catanese Luciana1,Sahlas Demetrios J.1,Srivastava Abhilek1,Veroniki Areti‐Angeliki34,Perera Kanjana12,Ng Kelvin K. H.1,Joundi Raed12,Van Adel Brian5,Larrazabal Ramiro5,Hawkes Christine6,Deshmukh Aviraj7,Ratnayake Kanchana1,Palaiodimou Lina8,Tsivgoulis Georgios89,Benavente Oscar10,Hart Robert12,Sharma Mukul12,Shoamanesh Ashkan12

Affiliation:

1. Department of Medicine (Neurology) McMaster University Hamilton Ontario Canada

2. Brain Health and Stroke Research Program Population Health Research Institute Hamilton Ontario Canada

3. Knowledge Translation Program Li Ka Shing Knowledge Institute St. Michael's Hospital Toronto Ontario Canada

4. Institute of Health Policy Management and Evaluation University of Toronto Toronto Ontario Canada

5. Division of Neurology, Neurosurgery, and Diagnostic Imaging Hamilton General Hospital McMaster University Hamilton Ontario Canada

6. Department of Medicine (Division of Neurology) Hurvitz Brain Sciences Program Sunnybrook Health Sciences Centre University of Toronto Toronto Ontario Canada

7. Department of Medicine (Neurology) Northern Ontario School of Medicine Sudbury Ontario Canada

8. Second Department of Neurology Attikon University Hospital National and Kapodistrian University of Athens Athens Greece

9. Department of Neurology University of Tennessee Health Science Center Memphis Tennessee USA

10. Division of Neurology University of British Columbia Vancouver British Columbia Canada

Abstract

Background Although postprocedure blood pressure (BP) correlates with outcome in patients undergoing endovascular thrombectomy (EVT), the optimal target is unknown. Methods We performed a pilot randomized‐controlled clinical trial enrolling participants with persistently elevated BP after successful EVT. Participants were randomized within 1 hour from the end of EVT to either intensive (systolic BP target <140 mmHg) or standard BP target (systolic BP <180 mmHg) for 48 hours. The main end point was feasibility, which was assessed with the enrollment rate and adherence to allocated BP target. Exploratory end points included neurologic deterioration, functional improvement, intracranial hemorrhage, and flow dynamics detected by transcranial Doppler ultrasonography. We included the outcomes of our trial in an aggregate data meta‐analysis of randomized‐controlled clinical trials evaluating the utility of BP control after successful EVT. The primary outcome of the meta‐analysis was 3‐month good functional outcome, defined as a modified Rankin Scale score of ≤2. Results Between October 23, 2020, and February 4, 2023, 221 patients were screened and 30 were randomized (14%; average recruitment of 1.2 participants/month). Participants in the intensive BP arm had a mean±SD systolic BP of 131±18 mm Hg over 48 hours (75% of the readings were <140 mm Hg), whereas participants in the standard BP arm had a mean±SD 48‐hour systolic BP of 139±18 mm Hg (48% of the readings were between 140 and 180 mm Hg). No differences between the 2 groups were documented in any of the predefined exploratory end points. In a meta‐analysis of 5 randomized‐controlled clinical trials involving 1558 participants, intensive BP control was associated with lower probability for 3‐month good functional outcome (odds ratio, 0.66 [95% CI, 0.53–0.82]; I 2  = 8%) when compared with standard BP control. Conclusions The natural course of BP normalization following successful recanalization poses challenges to the conduct and success of randomized‐controlled clinical trials evaluating different BP thresholds after EVT. Meta‐analysis of existing trials suggests harm associated with active BP lowering.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Blood Pressure Variability in Acute Stroke: A Narrative Review;Journal of Clinical Medicine;2024-03-29

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