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Cross-Section of Neurological Manifestations Among SARS-CoV-2 Omicron Subvariants—Single-Center Study

Jachman-Kapułka et al., Brain Sciences, doi:10.3390/brainsci14111161, Nov 2024
https://c19early.org/jachmankapulka.html
Retrospective 426 hospitalized COVID-19 patients in Poland during Omicron dominance, showing increasing neurological manifestations over time across three Omicron subvariant periods despite improving overall survival. Authors hypothesize that different Omicron subvariants have varying neuropathogenicity, with later subvariants potentially causing stronger immune suppression and neurodegeneration while simultaneously becoming less systemically severe.
Jachman-Kapułka et al., 20 Nov 2024, retrospective, Poland, peer-reviewed, 4 authors. Contact: justyna.jachman@gmail.com (corresponding author), alek.zinczuk@gmail.com, krzysimon@gmail.com, marta.rorat@gmail.com.
Cross-Section of Neurological Manifestations Among SARS-CoV-2 Omicron Subvariants—Single-Center Study
Justyna Jachman-Kapułka, Aleksander Zińczuk, Krzysztof Simon, Marta Rorat
Brain Sciences, doi:10.3390/brainsci14111161
Background/Objectives: The Omicron variant of SARS-CoV-2 is undergoing constant mutation. New strains vary in neuropathogenicity and the neurological spectrum of disease. The aim of this study was to assess the frequency and clinical characteristics of neurological manifestations during the Omicron dominance among hospitalized patients, including the differences between three subsequent periods. Methods: This retrospective single-center study included 426 hospitalized adults with confirmed COVID-19 divided into three periods (O1, O2, and O3) dependent on the dominance of Omicron subvariants in Poland. Demographic and clinical data, in particular neurological manifestations, were collected and compared. Results: The median age of the group was 74, older in subsequent (later) periods. The number of patients with a history of previous SARS-CoV-2 infection or vaccination increased with the duration of the pandemic. The severity of COVID-19 became lower in successive periods. Neurological manifestations were observed in 55.4% of patients, and the most frequent were delirium, headache, myalgia, dizziness, cerebrovascular diseases, and encephalopathy. In subsequent periods of Omicron dominance, a higher frequency of neurological manifestations such as delirium, transient ischemic attack (TIA), and encephalopathy was observed. Headache or myalgia was related to a shorter hospitalization while delirium, cerebrovascular diseases, and ischemic stroke were linked with an increased risk of death. Conclusions: The Omicron variant of SARS-CoV-2 presents a wide spectrum of neurological manifestations. Although there is an improvement in the survival rate of patients with COVID-19, the frequency of neurological manifestations increases. The occurrence of delirium, cerebrovascular diseases, and ischemic stroke results in higher mortality.
Author Contributions: Conceptualization, J.J.-K. and M.R.; investigation and data collection, J.J.-K. and A.Z.; writing-original draft preparation, J.J.-K.; writing-review and editing, J.J.-K., M.R. and K.S.; supervision, K.S. and M.R.; final approval, M.R. All authors have read and agreed to the published version of the manuscript. Declaration of Helsinki, and approved by the Ethics Committee of Lower Silesian Medical Chamber (protocol code 02/BNR/2024 from 12 March 2024). Informed Consent Statement: Patient consent was waived due to the retrospective nature of this work. Conflicts of Interest: The authors declare no conflicts of interest.
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DOI record: { "DOI": "10.3390/brainsci14111161", "ISSN": [ "2076-3425" ], "URL": "http://dx.doi.org/10.3390/brainsci14111161", "abstract": "<jats:p>Background/Objectives: The Omicron variant of SARS-CoV-2 is undergoing constant mutation. New strains vary in neuropathogenicity and the neurological spectrum of disease. The aim of this study was to assess the frequency and clinical characteristics of neurological manifestations during the Omicron dominance among hospitalized patients, including the differences between three subsequent periods. Methods: This retrospective single-center study included 426 hospitalized adults with confirmed COVID-19 divided into three periods (O1, O2, and O3) dependent on the dominance of Omicron subvariants in Poland. Demographic and clinical data, in particular neurological manifestations, were collected and compared. Results: The median age of the group was 74, older in subsequent (later) periods. The number of patients with a history of previous SARS-CoV-2 infection or vaccination increased with the duration of the pandemic. The severity of COVID-19 became lower in successive periods. Neurological manifestations were observed in 55.4% of patients, and the most frequent were delirium, headache, myalgia, dizziness, cerebrovascular diseases, and encephalopathy. In subsequent periods of Omicron dominance, a higher frequency of neurological manifestations such as delirium, transient ischemic attack (TIA), and encephalopathy was observed. Headache or myalgia was related to a shorter hospitalization while delirium, cerebrovascular diseases, and ischemic stroke were linked with an increased risk of death. Conclusions: The Omicron variant of SARS-CoV-2 presents a wide spectrum of neurological manifestations. Although there is an improvement in the survival rate of patients with COVID-19, the frequency of neurological manifestations increases. 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Late treatment
is less effective
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