Evidence map›Paper›PMID 33992168›Full record

ArticleJournal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia2021

Posterior reversible encephalopathy syndrome (PRES) associated with COVID-19.

Sofía Lallana, Austin Chen, Manuel Requena, Marta Rubiera, Anna Sanchez, James E Siegler, Marián Muchada

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  11. Advances in Management of the Stroke Etiology One-Percenters.Current neurology and neuroscience reports · 2023
    Review
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  15. Early reversible leukoencephalopathy and unilateral sixth cranial nerve palsy in mild COVID-19 infection.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Article
  16. Review
  17. Correspondence concerning "Posterior reversible encephalopathy syndrome (PRES) associated with COVID-19".Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia · 2021
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  18. Article
  19. Response to correspondence concerning "Posterior reversible encephalopathy syndrome (PRES) associated with COVID-19".Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Sofía LallanaNeurology Department, Vall d'Hebron Universitary Hospital, Barcelona, Spain.
Austin ChenCooper Medical School of Rowan University, Camden, USA.
Manuel RequenaNeurology Department, Vall d'Hebron Universitary Hospital, Barcelona, Spain.
Marta RubieraNeurology Department, Vall d'Hebron Universitary Hospital, Barcelona, Spain.
Anna SanchezCritical Care Department, Vall d'Hebron Universitary Hospital, Barcelona, Spain.
James E SieglerCooper Neurologic Institute, Cooper University Hospital, Camden, USA; Cooper Medical School of Rowan University, Camden, USA. Electronic address: siegler.james@gmail.com.
Marián MuchadaNeurology Department, Vall d'Hebron Universitary Hospital, Barcelona, Spain.
Vall d'Hebron Hospital Universitari · ESCooper Medical School of Rowan University · USCooper University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The novel human coronavirus disease (COVID-19) has been associated with vascular and thrombotic complications, some of which may result from endothelial dysfunction, including the posterior reversible encephalopathy syndrome (PRES). We report a case series of 8 patients with COVID-19 and PRES diagnosed at two academic medical centers between March and July of 2020. The clinical, laboratory and radiographic data, treatment, and short-term outcomes were retrospectively analyzed. The mean age was 57.9 ± 12 years, and 50% were women. Four patients had previous vascular comorbidities. All the patients suffered from severe pneumonia, requiring intensive care unit admission. Five patients were not hypertensive at presentation (all SBP < 127 mmHg). Neurologic symptoms included seizures in 7 patients; impaired consciousness in 5 patients; focal neurological signs in 3 patients; and visual disturbances in 1 patient. All patients underwent brain magnetic resonance imaging which indicated asymmetric T2 prolongation or diffusion changes (50%), extensive fronto-parieto-occipital involvement (25%), vascular irregularities (12.5%) and intracranial hemorrhage (25%). Four patients were treated with tocilizumab. Three patients were discharged without neurologic disability, 2 patients had persistent focal neurologic deficits and 2 expired. One patient's prognosis remains guarded. Together, these data support the relationship between PRES and endothelial dysfunction associated with severe COVID-19. In patients with severe COVID-19, PRES can be triggered by uncontrolled hypertension, or occur independently in the setting of systemic illness and certain medications. Like other infectious processes, critically ill patients with COVID-19 may be at greater risk of PRES because of impaired vasoreactivity or the use of novel agents like Tocilizumab.

Indexed as

AdultAgedBrainComorbidityConsciousness DisordersCOVID-19Critical CareCritical IllnessCytokine Release SyndromeFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNervous System DiseasesPneumoniaCOVIDEndothelial dysfunctionPosterior reversible encephalopathy syndromeRESSARS-CoV-2Systemic inflammatory response syndrome

Identifiers

PMID33992168
PMCPMC7985961
OpenAlexW3137268079

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.