Evidence map›Paper›PMID 35268383›Full record

ArticleJournal of clinical medicine2022

Functional Aplasia of the Contralateral A1 Segment Influences Clinical Outcome in Patients with Occlusion of the Distal Internal Carotid Artery.

Sebastian Fischer, Lukas Goertz, Charlotte S Weyland, Ali Khanafer, Christoph J Maurer, Hanna Zimmermann, Thomas David Fischer, Hanna Styczen, Benjamin Tan, Maria Alexandrou and 15 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

25 authors.

Sebastian FischerInstitute of Diagnostic and Interventional Radiology, Neuroradiology and Nuclear Medicine, Knappschaftskrankenhaus Bochum, Ruhr-University Bochum, 44892 Bochum, Germany.
Lukas GoertzDepartment of Diagnostic and Interventional Radiology, University Hospital Cologne, 50937 Cologne, Germany.
Charlotte S WeylandDepartment of Diagnostic and Interventional Neuroradiology, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-1374-7854
Ali KhanaferNeuroradiological Clinic, Klinikum Stuttgart, 70174 Stuttgart, Germany.ORCID 0000-0002-9482-0151
Christoph J MaurerDepartment of Diagnostic and Interventional Neuroradiology, University Hospital Augsburg, 86156 Augsburg, Germany.ORCID 0000-0002-0305-0797
Hanna ZimmermannInstitute for Diagnostic and Interventional Neuroradiology, University Hospital München-Großhadern, 81377 Munich, Germany.
Thomas David FischerInstitute for Diagnostic and Interventional Neuroradiology, University Hospital München-Großhadern, 81377 Munich, Germany.
Hanna StyczenInstitute for Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, 45147 Essen, Germany.
Benjamin TanDivision of Neurology, Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, National University Health System, Singapore 119077, Singapore.ORCID 0000-0003-1824-9077
Maria AlexandrouDepartment of Diagnostic and Interventional Neuroradiology, Klinikum Bremen-Mitte, 28211 Bremen, Germany.
Donald LobsienDepartment of Diagnostic and Interventional Radiology and Neuroradiology, Helios General Hospital Erfurt, 99089 Erfurt, Germany.
Elmar LobsienDepartment of Neurology, Helios General Hospital Erfurt, 99089 Erfurt, Germany.
Maximilian ThormannDepartment of Diagnostic and Interventional Radiology, University Hospital Magdeburg, 39120 Magdeburg, Germany.
Lukas MeyerDepartment of Diagnostic and Interventional Neuroradiology, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.
Nuran AbdullayevDepartment of Diagnostic and Interventional Radiology, University Hospital Cologne, 50937 Cologne, Germany.
Jens FiehlerDepartment of Diagnostic and Interventional Neuroradiology, University Hospital Hamburg-Eppendorf, 20246 Hamburg, Germany.
Anastasios MpotsarisDepartment of Diagnostic and Interventional Radiology, University Hospital Magdeburg, 39120 Magdeburg, Germany.
Panagiotis PapanagiotouDepartment of Diagnostic and Interventional Neuroradiology, Klinikum Bremen-Mitte, 28211 Bremen, Germany.ORCID 0000-0002-3124-1398
Leonard YeoDivision of Neurology, Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, National University Health System, Singapore 119077, Singapore.ORCID 0000-0002-4249-0402
Cornelius DeuschlInstitute for Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, 45147 Essen, Germany.
Thomas LiebigInstitute for Diagnostic and Interventional Neuroradiology, University Hospital München-Großhadern, 81377 Munich, Germany.
Ansgar BerlisDepartment of Diagnostic and Interventional Neuroradiology, University Hospital Augsburg, 86156 Augsburg, Germany.
Hans HenkesNeuroradiological Clinic, Klinikum Stuttgart, 70174 Stuttgart, Germany.
Markus MöhlenbruchDepartment of Diagnostic and Interventional Neuroradiology, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Volker MausInstitute of Diagnostic and Interventional Radiology, Neuroradiology and Nuclear Medicine, Knappschaftskrankenhaus Bochum, Ruhr-University Bochum, 44892 Bochum, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The importance of an A1 aplasia remains unclear in stroke patients. In this work, we analyze the impact of an A1 aplasia contralateral to an acute occlusion of the distal internal carotid artery (ICA) on clinical outcomes. Methods: We conducted a retrospective study of consecutive stroke patients treated with mechanical thrombectomy at 12 tertiary care centers between January 2015 and February 2021 due to an occlusion of the distal ICA. Functional A1 aplasia was defined as the absence of A1 or hypoplastic A1 (>50% reduction to the contralateral site). Functional independence was measured by the modified Rankin Scale (mRS ≤ 2). Results: In total, 81 out of 1068 (8%) patients had functional A1 aplasia contralateral to distal ICA occlusion. Patients with functional contralateral A1 aplasia were more severely affected on admission (median NIHSS 18, IQR 15−23 vs. 17, IQR 13−21; aOR: 0.672, 95% CI: 0.448−1.007, p = 0.054) and post-interventional ischemic damage was larger (median ASPECTS 5, IQR 1−7, vs. 6, IQR 3−8; aOR: 1.817, 95% CI: 1.184−2.789, p = 0.006). Infarction occurred more often within the ipsilateral ACA territory (20/76, 26% vs. 110/961, 11%; aOR: 2.482, 95% CI: 1.389−4.437, p = 0.002) and both ACA territories (8/76, 11% vs. 5/961, 1%; aOR: 17.968, 95% CI: 4.979−64.847, p ≤ 0.001). Functional contralateral A1 aplasia was associated with a lower rate of functional independence at discharge (6/81, 8% vs. 194/965, 20%; aOR: 2.579, 95% CI: 1.086−6.122, p = 0.032) and after 90 days (5/55, 9% vs. 170/723, 24%; aOR: 2.664, 95% CI: 1.031−6.883, p = 0.043). Conclusions: A functional A1 aplasia contralateral to a distal ICA occlusion is associated with a poorer clinical outcome.

Indexed as

acute ischemic strokeICA occlusionmechanical thrombectomy

Identifiers

PMID35268383
PMCPMC8911253

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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.