Evidence map›Paper›PMID 35126670›Full record

ArticleTherapeutic advances in neurological disorders2022

Incidence, clinical spectrum, and immunotherapy of non-ischemic cerebral enhancing lesions after endovascular therapy.

Antonios Bayas, Monika Christ, Ansgar Berlis, Markus Naumann, Michael Ertl, Felix Joachimski, Mona Müller, Julia Welzel, Lisa Ann Gerdes, Klaus Seelos and 1 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in neurological disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Antonios BayasDepartment of Neurology, University Hospital of Augsburg, Stenglinstraße 2, D-86156 Augsburg, Germany.
Monika ChristDepartment of Neurology, University Hospital of Augsburg, Augsburg, Germany.ORCID https://orcid.org/0000-0002-8071-1501
Ansgar BerlisDepartment of Neuroradiology, University Hospital of Augsburg, Augsburg, Germany.
Markus NaumannDepartment of Neurology, University Hospital of Augsburg, Augsburg, Germany.
Michael ErtlDepartment of Neurology, University Hospital of Augsburg, Augsburg, Germany.
Felix JoachimskiDepartment of Neuroradiology, University Hospital of Augsburg, Augsburg, Germany.
Mona MüllerDepartment of Neurology, University Hospital of Augsburg, Augsburg, Germany.
Julia WelzelDepartment of Dermatology, University Hospital of Augsburg, Augsburg, Germany.
Lisa Ann GerdesInstitute of Clinical Neuroimmunology, Biomedical Center and University Hospital, LMU Munich, Munich, Germany.
Klaus SeelosInstitute of Neuroradiology, University Hospital, LMU Munich, Munich, Germany.
Christoph MaurerDepartment of Neuroradiology, University Hospital of Augsburg, Augsburg, Germany.
University Hospital Augsburg · DELMU Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSymptomatic and asymptomatic delayed non-ischemic cerebral enhancing (NICE) lesions in magnetic resonance imaging (MRI) have been reported as a rare complication after endovascular therapy (EVT) in recent years with incidence rates between 0.05% and 0.9% in most studies. Information on long-term clinical course and immunotherapies is scarce or has not been reported in detail in the literature. Objective: Aims of our study were to assess the incidence of NICE lesions in patients after cerebral EVT over a period of more than 12 years, describe clinical and EVT characteristics, and immunotherapies applied.

methodsA retrospective chart review of all patients treated by endovascular therapy for symptomatic or asymptomatic aneurysms at the University Hospital of Augsburg from May 1, 2008 to December 31, 2020 was performed. Patients were identified retrospectively and followed-up prospectively where appropriate. In addition, one case treated at another institution was included.

resultsFive out of 746 patients, 0.67%, developed NICE lesions after EVT, all with non-ruptured aneurysms and all symptomatic upon detection of NICE lesions by MRI. In total, the disease course of 6 female patients is reported. Symptoms occurred after a mean time of 15 days (±13.42, SD) after EVT with headache (6/6 patients), focal neurological signs (6/6 patients), epileptic seizures (2/6 patients) and cognitive deficits (3/6 patients). All 6 patients received glucocorticosteroids (GCS), 1/6 azathioprine (AZA), 4/6 mycophenolate mofetil (MMF), 1/6 methotrexate (MTX), 1/6 rituximab (RTX), 2/6 cyclophosphamide (CYC) and 3/6 tocilizumab (TCZ). A treatment response could be observed for GCS, TCZ and MMF (in two of four cases), RTX and AZA did not result in disease stabilization.

conclusionsDelayed NICE lesions are a rare complication after EVT, requiring immunotherapies in all patients reported here. Physicians should be aware of this disorder in case of new symptoms or contrast enhancing lesions after EVT.

Indexed as

aneurysmendovascular therapyMRINICEnon-ischemic cerebral enhancing lesions

Identifiers

PMID35126670
PMCPMC8808010
OpenAlexW4210319838

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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.