Evidence map›Paper›PMID 36160689›Full record

ArticleBMJ neurology open2022

Circle of Willis variation and outcome after intra-arterial treatment.

Anouk Rozeman, Hajo Hund, Jelis Boiten, Jan-Albert Vos, Wouter Schonewille, Marieke Wermer, Geert Lycklama A Nijeholt, Ale Algra

Abstract read
In one paragraph

Article in BMJ neurology open, 2022. 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
–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

2 citing papers in PubMed.

  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

8 authors.

Anouk RozemanNeurology, Albert Schweitzer Hospital, Dordrecht, The Netherlands.
Hajo HundRadiology, Haaglanden Medical Center Bronovo, Den Haag, The Netherlands.
Jelis BoitenRadiology, Haaglanden Medical Center Bronovo, Den Haag, The Netherlands.
Jan-Albert VosRadiology, Sint Antonius Ziekenhuis, Nieuwegein, The Netherlands.
Wouter SchonewilleNeurology, Sint Antonius Ziekenhuis, Nieuwegein, The Netherlands.
Marieke WermerNeurology, LUMC, Leiden, The Netherlands.
Geert Lycklama A NijeholtRadiology, Haaglanden Medical Center Bronovo, Den Haag, The Netherlands.
Ale AlgraBrain Center Rudolf Magnus, UMC Utrecht, Utrecht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Intra-arterial treatment (IAT) improves outcomes in acute ischaemic stroke. Presence of collaterals increases likelihood of good outcome. We investigated whether variations in the circle of Willis (CoW) and contributing carotid arteries influence outcome in patients who had a stroke treated with IAT. Methods: CT angiography data on patients who had an acute stroke treated with IAT were retrospectively collected. CoW was regarded complete if the contralateral A1 segment, anterior communicating artery and ipsilateral posterior communicating artery were fully developed, and the P1 segment was visible. Carotid artery contribution was studied with a self-developed carotid artery score ranging from 0 to 2 depending on the number of arteries supplying the occluded side of the CoW. Good clinical outcome was defined as modified Rankin Score ≤2 and measured at discharge and 3 months. We calculated risk ratios for the relation between completeness of the CoW, carotid score and good outcome, and performed a trend analysis for good outcome according to the carotid score. Results: 126 patients were included for analysis. Patients with a complete and incomplete CoW had a comparable risk for good outcome at discharge and 3 months. A higher carotid score was associated with a higher likelihood of good clinical outcome (p for trend 0.24 at discharge and 0.05 at 3 months). Conclusion: In patients with acute ischaemic stroke treated with IAT, chances of good clinical outcome tended to improve with number of carotid arteries supplying the cerebral circulation. Completeness of the CoW was not related to clinical outcome.

Indexed as

CEREBROVASCULAR DISEASESTROKE

Identifiers

PMID36160689
PMCPMC9490629

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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.