Evidence map›Paper›PMID 37337529›Full record

ArticleBMJ neurology open2023

Effects of blood pressure and tranexamic acid in spontaneous intracerebral haemorrhage: a secondary analysis of a large randomised controlled trial.

Jason Philip Appleton, Zhe Kang Law, Lisa Jane Woodhouse, Rustam Al-Shahi Salman, Maia Beridze, Hanne Christensen, Robert A Dineen, Juan José Egea Guerrero, Timothy J England, Michal Karlinski and 11 more

Open access · diamondAbstract read
In one paragraph

Article in BMJ neurology open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 36% of its field
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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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

21 authors at 14 institutions in 9 countries.

Jason Philip AppletonStroke, Nottingham University Hospitals NHS Trust, Nottingham, UK.ORCID 0000-0002-2604-4410
Zhe Kang LawStroke Trials Unit, Mental Health and Clinical Neurosciences, University of Nottingham, Nottingham, UK.ORCID 0000-0002-7900-9037
Lisa Jane WoodhouseStroke Trials Unit, Mental Health and Clinical Neurosciences, University of Nottingham, Nottingham, UK.ORCID 0000-0002-4472-1999
Rustam Al-Shahi SalmanCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Maia BeridzeThe First University Clinic, Tbilisi State Medical University, Tbilisi, Georgia.
Hanne ChristensenDepartment of Neurology, Copenhagen University Hospital, Bispebjerg, Denmark.
Robert A DineenRadiological Sciences, Mental Health and Clinical Neurosciences, University of Nottingham, Nottingham, UK.ORCID 0000-0002-9523-2546
Juan José Egea GuerreroNeurocritical Care Unit, Virgen del Rocio University Hospital, Sevilla, Spain.
Timothy J EnglandStroke Trials Unit, Mental Health and Clinical Neurosciences, University of Nottingham, Nottingham, UK.
Michal Karlinski2nd Department of Neurology, Institute of Psychiatry and Neurology, Warsaw, Poland.
Kailash KrishnanStroke, Nottingham University Hospitals NHS Trust, Nottingham, UK.ORCID 0000-0002-6486-3783
Ann Charlotte LaskaDepartment of Clinical Sciences, Danderyd Hospital, Karolinska Institute, Stockholm, Sweden.
Philippe LyrerNeurology and Stroke Center, University Hospital Basel, Basel, Switzerland.
Serefnur OzturkNeurology, Faculty of Medicine, Selcuk Universitesi, Konya, Turkey.
Christine RoffeStroke Research, School of Medicine, University of Keele, Stoke-on-Trent, UK.
Ian RobertsClinical Trials Unit, London School of Hygiene and Tropical Medicine, London, UK.
Thompson G RobinsonCollege of Life Sciences, University of Leicester, Leicester, UK.
Polly ScuttStroke Trials Unit, Mental Health and Clinical Neurosciences, University of Nottingham, Nottingham, UK.
David J WerringStroke Research Centre, Department of Brain Repair and Rehabilitation, UCL Queen Square Institute of Neurology, London, UK.
Philip M BathStroke, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Nikola SpriggStroke, Nottingham University Hospitals NHS Trust, Nottingham, UK.
University of Nottingham · GBNottingham University Hospitals NHS Trust · GBBispebjerg Hospital · DKInstitute of Psychiatry and Neurology · PLInstituto de Biomedicina de Sevilla · ESKarolinska Institutet · SEKeele University · GBNational Hospital for Neurology and Neurosurgery · GBSelçuk University · TRTbilisi State Medical University · GEUniversity Hospital of Basel · CHUniversity of Edinburgh · GBUniversity of Leicester · GBUniversity of London · GB

Funding

British Heart Foundation CS/18/2/33719British Heart Foundation FS/13/72/30531British Heart Foundation FS/17/53/33119British Heart Foundation SP/12/2/29422Medical Research Council G1002605Medical Research Council G108/613Medical Research Council MR/M009211/1
6 · The paper itself

Abstract

Background: Tranexamic acid reduced haematoma expansion and early death, but did not improve functional outcome in the tranexamic acid for hyperacute spontaneous intracerebral haemorrhage-2 (TICH-2) trial. In a predefined subgroup, there was a statistically significant interaction between prerandomisation baseline systolic blood pressure (SBP) and the effect of tranexamic acid on functional outcome (p=0.019). Methods: TICH-2 was an international prospective double-blind placebo-controlled randomised trial evaluating intravenous tranexamic acid in patients with acute spontaneous intracerebral haemorrhage (ICH). Prerandomisation baseline SBP was split into predefined ≤170 and >170 mm Hg groups. The primary outcome at day 90 was the modified Rankin Scale (mRS), a measure of dependency, analysed using ordinal logistic regression. Haematoma expansion was defined as an increase in haematoma volume of >33% or >6 mL from baseline to 24 hours. Data are OR or common OR (cOR) with 95% CIs, with significance at p<0.05. Results: Of 2325 participants in TICH-2, 1152 had baseline SBP≤170 mm Hg and were older, had larger lobar haematomas and were randomised later than 1173 with baseline SBP>170 mm Hg. Tranexamic acid was associated with a favourable shift in mRS at day 90 in those with baseline SBP≤170 mm Hg (cOR 0.73, 95% CI 0.59 to 0.91, p=0.005), but not in those with baseline SBP>170 mm Hg (cOR 1.05, 95% CI 0.85 to 1.30, p=0.63). In those with baseline SBP≤170 mm Hg, tranexamic acid reduced haematoma expansion (OR 0.62, 95% CI 0.47 to 0.82, p=0.001), but not in those with baseline SBP>170 mm Hg (OR 1.02, 95% CI 0.77 to 1.35, p=0.90). Conclusions: Tranexamic acid was associated with improved clinical and radiological outcomes in ICH patients with baseline SBP≤170 mm Hg. Further research is needed to establish whether certain subgroups may benefit from tranexamic acid in acute ICH. Trial registration number: ISRCTN93732214.

Indexed as

STROKE

Identifiers

PMID37337529
PMCPMC10277112
OpenAlexW4380365036

What OpenQuestion holds

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Registered trials

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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.