Incidence of Neurological Manifestations in Critically Ill COVID-19 Patients: A Low-Resource Setting Experience.

Publication date: Jun 01, 2025

Introduction Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is not primarily a neurotropic virus. However, since angiotensin-converting enzyme 2 (ACE2) receptors are present in the brain, spinal cord, and nerves, the involvement of the nervous system, which could potentially influence the final outcome, cannot be ruled out. This study aimed to assess the incidence and significance of specific neurological manifestations and/or neurological disorders in critically ill COVID-19 patients treated in low-resource settings (LRS), as well as to determine their impact on the clinical outcomes of these patients. Subjects and methods The research was designed as a retrospective observational study conducted between October 2020 and February 2021, during the second wave of the COVID-19 pandemic. The incidence of specific neurological manifestations and/or neurological disorders in patients treated at the Medical Intensive Care Unit (MICU) of the University Clinical Centre (UCC) of the Republic of Srpska, Bosnia and Herzegovina, was monitored, and relevant demographic and clinical data were collected. The results were analyzed using methods from descriptive statistics and statistical testing. Results Among the 262 patients who met the inclusion criteria, 154 (58. 5%) exhibited at least one of the monitored neurological manifestations or neurological disorders. The most frequently observed were impaired consciousness (19. 5%), headache (10. 2%), myalgia (8%), loss of taste and smell (7. 6%), lower back pain (3. 4%), and ischemic cerebrovascular stroke (3. 4%). All other recorded had an incidence of less than 2%. In terms of clinical outcomes, 128 patients (48. 9%) died, 81 (30. 9%) were transferred to a step-down unit, and 53 (20. 2%) were discharged home. Using Fisher’s exact test, impaired consciousness was found to be significantly associated with a fatal outcome (p = 0. 01; OR = 0. 33; 95% CI = 0. 17-0. 64), while acute polyradiculoneuritis was associated with a favorable clinical outcome in the form of discharge home (p = 0. 04; OR = 0. 96; 95% CI = 0. 91-1. 01). Headache was more frequently reported in female patients (p = 0. 03; OR = 2. 51; 95% CI = 1. 10-5. 80). Impaired consciousness was significantly more frequent in patients aged 51-60 years (p = 0. 02; OR = 2. 61; 95% CI = 1. 12-6. 12) and those aged ≥71 years (p = 0. 01; OR = 0. 36; 95% CI = 0. 18-0. 73), while epileptic seizures were most commonly observed in the 31-40 age group (p = 0. 01; OR = 0. 36; 95% CI = 0. 18-0. 73). Conclusion The incidence and significant associations between specific neurological presentations and/or disorders and clinical outcomes, along with observed demographic variations, highlight the importance of comprehensive monitoring of extrapulmonary manifestations (including neurological) in critically ill COVID-19 patients.

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Concepts Keywords
Coronavirus covid-19 pandemic
Enzyme extrapulmonary manifestations
Epileptic

Semantics

Type Source Name
disease MESH Neurological Manifestations
disease MESH Critically Ill
disease MESH COVID-19
disease MESH neurological disorders
drug DRUGBANK Methionine
disease MESH loss of taste
disease MESH lower back pain
disease MESH cerebrovascular stroke
disease MESH fatal outcome
disease MESH polyradiculoneuritis
disease MESH epileptic seizures
pathway REACTOME Reproduction
drug DRUGBANK Coenzyme M
disease MESH Severe acute respiratory syndrome
disease IDO host
drug DRUGBANK Serine
disease IDO production
disease MESH viremia
disease MESH multiple sclerosis
disease MESH polyneuropathy
disease MESH myasthenia gravis
disease MESH coronavirus infections
disease MESH death
disease MESH uncertainty
disease MESH complications
disease MESH ischemic stroke
disease MESH dehydration
disease MESH arrhythmia
disease IDO blood
disease IDO country
disease MESH respiratory insufficiency
disease IDO intervention
disease MESH acute respiratory distress syndrome
disease MESH intracerebral hemorrhage
disease MESH encephalitis
disease MESH meningitis
disease MESH subarachnoid hemorrhage
disease MESH hemorrhage
disease MESH syndrome
disease IDO susceptibility
disease MESH infection
disease MESH pneumonia
drug DRUGBANK Etoperidone
disease MESH somnolence
disease MESH stupor
disease MESH coma
disease MESH central nervous system infection
disease MESH etiology
disease MESH cytokine storms
disease MESH brain hemorrhage
disease MESH overweight
drug DRUGBANK Tropicamide
disease IDO symptom
disease MESH hypoxia
disease MESH vertigo
disease MESH status epilepticus
disease MESH immobilization
disease MESH Anosmia
disease MESH influenza
disease MESH Guillain Barre syndrome
disease MESH Epilepsy

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