High-dose glucocorticoids in COVID-19 patients with acute encephalopathy: clinical and imaging findings in a retrospective cohort study.
Details
Serval ID
serval:BIB_9AA99F56A5BC
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
High-dose glucocorticoids in COVID-19 patients with acute encephalopathy: clinical and imaging findings in a retrospective cohort study.
Journal
Journal of neural transmission
ISSN
1435-1463 (Electronic)
ISSN-L
0300-9564
Publication state
Published
Issued date
04/2024
Peer-reviewed
Oui
Volume
131
Number
4
Pages
377-384
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Abstract
Acute encephalopathy (AE) has been described as a severe complication of COVID-19. Inflammation has been suggested as a pathogenic mechanism, with high-dose glucocorticoids (GC) showing a beneficial effect. Here, we retrospectively analyzed the clinical and radiological features in a group of COVID-19 AE patients who received GC treatment (GT) and in a non-treated (NT) group.
Thirty-six patients with COVID-19 AE (mean age 72.6 11 years; 86.11% men) were evaluated for GC treatment. Twelve patients (mean age 73.6 4.5 years; 66.67% men) received GC, whereas 24 patients who showed signs of spontaneous remission were not treated with GC (mean age 70.1 8.6 years; 95.83% men). Differences in clinical characteristics and correlations with imaging features were explored.
The GT group showed signs of vulnerability, with a longer hospitalization (p = 0.009) and AE duration (p = 0.012) and a higher hypertensive arteriopathy (HTNA) score (p = 0.022), when compared to NT group. At hospital discharge, the two groups were comparable in terms of clinical outcome (modified Rankin scale; p = 0.666) or mortality (p = 0.607). In our whole group analyses, AE severity was positively correlated with periventricular white matter hyperintensities (p = 0.011), deep enlarged perivascular spaces (p = 0.039) and HTNA score (p = 0.014).
This study suggests that, despite signs of radiological vulnerability and AE severity, patients treated by high-dose GC showed similar outcome at discharge, with respect to NT patients. Imaging features of cerebral small vessel disease correlated with AE severity, supporting the hypothesis that brain structural vulnerability can impact AE in COVID-19.
Thirty-six patients with COVID-19 AE (mean age 72.6 11 years; 86.11% men) were evaluated for GC treatment. Twelve patients (mean age 73.6 4.5 years; 66.67% men) received GC, whereas 24 patients who showed signs of spontaneous remission were not treated with GC (mean age 70.1 8.6 years; 95.83% men). Differences in clinical characteristics and correlations with imaging features were explored.
The GT group showed signs of vulnerability, with a longer hospitalization (p = 0.009) and AE duration (p = 0.012) and a higher hypertensive arteriopathy (HTNA) score (p = 0.022), when compared to NT group. At hospital discharge, the two groups were comparable in terms of clinical outcome (modified Rankin scale; p = 0.666) or mortality (p = 0.607). In our whole group analyses, AE severity was positively correlated with periventricular white matter hyperintensities (p = 0.011), deep enlarged perivascular spaces (p = 0.039) and HTNA score (p = 0.014).
This study suggests that, despite signs of radiological vulnerability and AE severity, patients treated by high-dose GC showed similar outcome at discharge, with respect to NT patients. Imaging features of cerebral small vessel disease correlated with AE severity, supporting the hypothesis that brain structural vulnerability can impact AE in COVID-19.
Keywords
Male, Humans, Aged, Female, Glucocorticoids/therapeutic use, Retrospective Studies, Magnetic Resonance Imaging/methods, COVID-19/complications, Cerebral Small Vessel Diseases/pathology, Acute encephalopathy, COVID-19, High-dose glucocorticoids (GC), MRI, Microbleeds, White matter hyperintensities
Pubmed
Web of science
Open Access
Yes
Create date
20/02/2024 15:31
Last modification date
23/04/2024 6:14