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Abstract Details

Increased Frequency and Mortality in Persons with Neurological Disorders During COVID-19
Infectious Disease
P2 - Poster Session 2 (2:45 PM-3:45 PM)
060

To perform a population-based comparative study assessing the mortality in those with premorbid neurological syndromes and the incidence, types, and outcomes of new neurological sequalae after developing COVID-19 infection.

Defining the mortality, incidence, specific disorders, and outcomes of neurological complication(s) of COVID-19 are imperative for understanding risk status as well as recognition of emerging neurological syndromes that may influence healthcare needs. Moreover, a fuller grasp of this neurological disease burden enables better planning for clinical management.

Using health service data collected from March 1, 2020, to June 30, 2021, we constructed a cohort of SARS-CoV-2 RNA-positive (n=177,892) and -negative (n=177,800) adults who were age-, sex-, and comorbidity-matched, not yet vaccinated, and underwent RT- PCR testing at similar times. COVID-19 associated mortality rates were examined within the cohort. Neurological sequelae were analyzed during the acute (less than three months) and the post-acute (three to nine months) phases post-infection. 

The risk of death was significantly greater in the SARS-CoV-2 RNA-positive (2,140 per 100,000 person years) compared to RNA-negative (922 per 100,000 person years) over a follow-up of 9 months, particularly amongst those with premorbid neurological disorders: adjusted odds ratios (aOR, 95% CI) in persons with a history of parkinsonism (1·65, 1·15-2·37), dementia (1·30, 1·11-1·52), seizures (1·91, 1·26-2·87), encephalopathy (1·82, 1·02-3·23), and stroke (1·74, 1·05-2·86). There was a significantly increased risk of new onset neurological sequelae during the acute time phase after COVID-19 including encephalopathy (2·0, 1·10-3·64), dementia (1·36, 1·07-1·73), seizure (1·77, 1·22-2·56), and brain fog (1·96, 1·20-3·20). These risks persisted into the post-acute time phase after COVID-19 during which inflammatory myopathy (2·57, 1·07-6·15) and coma (1·87, 1·22-2·87) also became significantly increased.

Persons with SARS-CoV-2 infection and premorbid neurological disorders are at greater risk of death while SARS-CoV-2 infection was complicated by increased risk of new onset neurological disorders following COVID-19. 

Authors/Disclosures
Candace Marsters, MD
PRESENTER
Dr. Marsters has nothing to disclose.
Jeffrey Bakal Jeffrey Bakal has received personal compensation in the range of $5,000-$9,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for American Heart Association.
Grace Lam (University of Alberta) No disclosure on file
Finlay McAlister (University of Alberta) No disclosure on file
Christopher Power, MD Dr. Power has nothing to disclose.