Evidence map›Paper›PMID 38000819›Full record

ArticleBMJ open2023

Early monitoring of intravenous thrombolysis in acute ischaemic stroke using wearable intelligent vital sign devices: protocol for a prospective, multicentre, observational registry cohort study.

Mengrao Liu, Jie Zhao, Suai Li, Jinming Han, Gaoting Ma, Yuxin Wang, Hong Chang

Abstract read
In one paragraph

Article in BMJ open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Mengrao Liu *Department of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China.
Jie Zhao *Department of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China.
Suai LiDepartment of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China.
Jinming HanDepartment of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China.ORCID 0000-0002-6084-3275
Gaoting MaDepartment of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China.ORCID 0000-0002-9374-7589
Yuxin WangDepartment of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China.
Hong ChangDepartment of Neurology, Xuanwu Hospital Capital Medical University, Beijing, China changhong19791111@126.com.ORCID 0000-0002-6020-2726

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionContinuous monitoring of vital signs during and after ischaemic stroke was recommended by the 'Guidelines for the Early Management of Patients with Acute Ischaemic Stroke: 2019 Update to the 2018 Guidelines for the Early Management of Acute Ischaemic Stroke'. Vital sign data can be associated with disease conditions and prognosis, while there is limited evidence regarding continuous monitoring of vital signs during and after acute ischaemic stroke. The wearable intelligent vital sign monitoring device is small and lightweight and constantly monitors the health status during daily activities. However, wearable intelligent vital sign monitoring devices have not been widely used in clinical practice so far. Therefore, we will investigate the effectiveness and safety of wearable intelligent vital sign monitoring devices in early in-hospital management and monitoring programmes for patients with acute ischaemic stroke. This paper presents the study protocol. METHODS AND

designThis study is a prospective, multicentre, observational registry study starting from 20 March 2023 to 20 March 2025. A total of 5740 patients with acute ischaemic stroke from 10 Chinese hospitals are planned to be enrolled. Continuous vital sign data, demographics, medical history, medication history, treatments, laboratory tests, imaging scans and follow-up data will be collected. Follow-up time points were 30 days after discharge, 30 days after intravenous thrombolysis, 3 months after intravenous thrombolysis and 12 months after intravenous thrombolysis (until March 2026). The primary outcome included the evaluation of the modified Rankin Scale at 3 months, as well as the assessment of the rate of symptomatic and asymptomatic intracranial haemorrhage throughout the hospitalisation period. ETHICS AND DISSEMINATION: This study has been approved by the Medical Ethics Committee of Xuanwu Hospital, Capital Medical University ([2022] 203). We plan to disseminate the research findings through publication in peer-reviewed scientific journals and presentations at international conferences. TRIAL REGISTRATION NUMBER: ChiCTR2300069512.

Indexed as

Brain IschemiaIschemic StrokeStrokeWearable Electronic DevicesCohort StudiesFibrinolytic AgentsHumansMulticenter Studies as TopicObservational Studies as TopicProspective StudiesRegistriesThrombolytic TherapyTreatment OutcomeVital SignsFibrinolytic AgentsBIOTECHNOLOGY & BIOINFORMATICSNursing CarePatient-Centered CareStroke

Identifiers

PMID38000819
PMCPMC10679986

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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.