Evidence map›Paper›PMID 31401075›Full record

SynthesisThe Lancet. Neurology2019

Long-term antithrombotic therapy and risk of intracranial haemorrhage from cerebral cavernous malformations: a population-based cohort study, systematic review, and meta-analysis.

Susanna M Zuurbier, Charlotte R Hickman, Christos S Tolias, Leon A Rinkel, Rebecca Leyrer, Kelly D Flemming, David Bervini, Giuseppe Lanzino, Robert J Wityk, Hans-Martin Schneble and 3 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in The Lancet. Neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 2 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.

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

46 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Susanna M ZuurbierDepartment of Neurology, Amsterdam University Medical Center, Amsterdam, Netherlands.
Charlotte R HickmanEdinburgh Medical School, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, UK.
Christos S ToliasEdinburgh Medical School, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, UK.
Leon A RinkelUniversity of Groningen, University Medical Centre Groningen, Groningen, Netherlands.
Rebecca LeyrerDepartment of Neurosurgery, University of Duisburg-Essen, Essen, Germany.
Kelly D FlemmingDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
David BerviniDepartment of Neurosurgery, Inselspital, Bern University Hospital, Bern, Switzerland.
Giuseppe LanzinoDepartment of Neurosurgery, Mayo Clinic, Rochester, MN, USA.
Robert J WitykDepartment of Neurology, Johns Hopkins Hospital, Baltimore, MD, USA.
Hans-Martin SchnebleDepartment of Neurology, Hôpital Lariboisière, Paris, France.
Ulrich SureDepartment of Neurosurgery, University of Duisburg-Essen, Essen, Germany.
Rustam Al-Shahi SalmanCentre for Clinical Brain Sciences and Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK. Electronic address: Rustam.Al-Shahi@ed.ac.uk.
Scottish Audit of Intracranial Vascular Malformations Steering Committee

Funding

Medical Research Council G1002605Medical Research Council G108/613
6 · The paper itself

Abstract

backgroundAntithrombotic (anticoagulant or antiplatelet) therapy is withheld from some patients with cerebral cavernous malformations, because of uncertainty around the safety of these drugs in such patients. We aimed to establish whether antithrombotic therapy is associated with an increased risk of intracranial haemorrhage in adults with cerebral cavernous malformations.

methodsIn this population-based, cohort study, we used data from the Scottish Audit of Intracranial Vascular Malformations, which prospectively identified individuals aged 16 years and older living in Scotland who were first diagnosed with a cerebral cavernous malformation during 1999-2003 or 2006-10. We compared the association between use of antithrombotic therapy after first presentation and the occurrence of intracranial haemorrhage or persistent or progressive focal neurological deficit due to the cerebral cavernous malformations during up to 15 years of prospective follow-up with multivariable Cox proportional hazards regression assessed in all individuals identified in the database. We also did a systematic review and meta-analysis, in which we searched Ovid MEDLINE and Embase from database inception to Feb 1, 2019, to identify comparative studies to calculate the intracranial haemorrhage incidence rate ratio according to antithrombotic therapy use. We then generated a pooled estimate using the inverse variance method and a random effects model.

findingsWe assessed 300 of 306 individuals with a cerebral cavernous malformation who were eligible for study. 61 used antithrombotic therapy (ten [16%] of 61 used anticoagulation) for a mean duration of 7·4 years (SD 5·4) during follow-up. Antithrombotic therapy use was associated with a lower risk of subsequent intracranial haemorrhage or focal neurological deficit (one [2%] of 61 vs 29 [12%] of 239, adjusted hazard ratio [HR] 0·12, 95% CI 0·02-0·88; p=0·037). In a meta-analysis of six cohort studies including 1342 patients, antithrombotic therapy use was associated with a lower risk of intracranial haemorrhage (eight [3%] of 253 vs 152 [14%] of 1089; incidence rate ratio 0·25, 95% CI 0·13-0·51; p<0·0001; I

interpretationAntithrombotic therapy use is associated with a lower risk of intracranial haemorrhage or focal neurological deficit from cerebral cavernous malformations than avoidance of antithrombotic therapy. These findings provide reassurance about safety for clinical practice and require further investigation in a randomised controlled trial.

fundingUK Medical Research Council, Chief Scientist Office of the Scottish Government, The Stroke Association, Cavernoma Alliance UK, and the Remmert Adriaan Laan Foundation.

Indexed as

AdultAgedCohort StudiesFemaleFibrinolytic AgentsHemangioma, Cavernous, Central Nervous SystemHumansIntracranial HemorrhagesLong-Term CareMaleMiddle AgedPlatelet Aggregation InhibitorsScotlandFibrinolytic AgentsPlatelet Aggregation Inhibitors

Identifiers

PMID31401075
PMCPMC6744367

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.