Neuro-COVID-19: Neurological Complications of COVID-19
Paraules clau
Resum
Descripció
This study is a prospective observational cohort study to document prevalence and severity of neurological symptoms among patients requiring critical care admission for confirmed novel coronavirus disease (COVID-19). COVID-19 is classified as severe acute respiratory syndrome 2 (SARS-CoV-2) and shares significant structural and biological similarities with SARS-CoV, which has neuroinvasive properties and brainstem involvement. Early reports of COVID-19 progression indicate presence of severe neurological complications, including seizures, coma, encephalitis, and cerebrovascular events including ischemic stroke, intracranial hemorrhage, and cerebral venous sinus thromboses. In addition, recent data from Zika-virus and H1N1 influenza pandemics reveal a high incidence of neurological complications, including Guillain Barré syndrome and neonatal microcephaly for Zika-virus and narcolepsy with H1N1 infections. Early reports from China suggest neurological symptoms may occur in approximately 36% of SARS-CoV-2 positive patients, with increased prevalence among more severe cases, and fall into three categories: central nervous system symptoms or diseases, peripheral nervous system symptoms, and skeletal muscular symptoms. However, the exact prevalence of these conditions and impact on patient disease severity and outcomes is unknown. As the incidence and severity of COVID-19 infection continues to rapidly rise on an international level, it is imperative to capture prospective data to accurately document prevalence, severity and clinical characterization of neurological components of COVID-19, the influence of treatment regimens of neurological complications, and role of these confounders on patient and organizational outcomes.
Dates
Darrera verificació: | 05/31/2020 |
Primer enviat: | 05/27/2020 |
Inscripció estimada enviada: | 06/03/2020 |
Publicat per primera vegada: | 06/04/2020 |
Última actualització enviada: | 06/03/2020 |
Publicació de l'última actualització: | 06/04/2020 |
Data d'inici de l'estudi real: | 04/30/2020 |
Data estimada de finalització primària: | 04/29/2022 |
Data estimada de finalització de l’estudi: | 05/29/2022 |
Condició o malaltia
Intervenció / tractament
Other: further processing of health data
Fase
Criteris d'elegibilitat
Edats elegibles per estudiar | 18 Years Per a 18 Years |
Sexes elegibles per estudiar | All |
Mètode de mostreig | Non-Probability Sample |
Accepta voluntaris saludables | Sí |
Criteris | Inclusion Criteria: - Adults (age > 18 years old) treated at ICUs - Admitted with confirmed COVID-19 infection - Patient exhibiting acute neurological manifestations - General consent of the Institute of Intensive Care Medicine available from patient or legal representative Exclusion Criteria: - Pre-existing severe neurologic dysfunction |
Resultat
Mesures de resultats primaris
1. Prevalence of neurological complications [through study completion, on an average of 3 weeks]
2. Prevalence and outcome of severe neurological complications [through study completion, on an average of 3 weeks]
3. Impact of neurological complications [through study completion, on an average of 3 weeks]
4. Characteristic patterns in cerebral imaging and electroencephalography (EEG), as well as cerebrospinal fluid (CSF) [through study completion, on an average of 3 weeks]
5. Brain for pathological changes and histopathological findings (if patient dies). [through study completion, on an average of 3 weeks]