COVID-19-Associated Guillain-Barre Syndrome: Atypical Para-infectious Profile, Symptom Overlap, and Increased Risk of Severe Neurological Complications.
dc.contributor.author | Kajumba, Mayanja M | |
dc.contributor.author | Kolls, Brad J | |
dc.contributor.author | Koltai, Deborah C | |
dc.contributor.author | Kaddumukasa, Mark | |
dc.contributor.author | Kaddumukasa, Martin | |
dc.contributor.author | Laskowitz, Daniel T | |
dc.date.accessioned | 2021-01-01T21:49:50Z | |
dc.date.available | 2021-01-01T21:49:50Z | |
dc.date.issued | 2020-11-21 | |
dc.date.updated | 2021-01-01T21:49:48Z | |
dc.description.abstract | The concurrence of COVID-19 with Guillain-Barre syndrome (GBS) can increase the likelihood of neuromuscular respiratory failure, autonomic dysfunction, and other life-threatening symptoms. Currently, very little is known about the underlying mechanisms, clinical course, and prognostic implications of comorbid COVID-19 in patients with GBS. We reviewed COVID-19-associated GBS case reports published since the outbreak of the pandemic, with a database search up to August 2020, including a manual search of the reference lists for additional relevant cases. Fifty-one (51) case reports of COVID-19 patients (aged 23-84 years) diagnosed with GBS in 11 different countries were included in this review. The results revealed atypical manifestations of GBS, including para-infectious profiles and onset of GBS without antecedent COVID-19 symptoms. Although all tested patients had signs of neuroinflammation, none had SARS-CoV-2 in the cerebrospinal fluid (CSF), and only four (4) patients had antiganglioside antibodies. The majority had a 1- to 10-day time interval between the onset of COVID-19 and GBS symptoms, and many had a poor outcome, with 20 out of the 51 (39.2%) requiring mechanical ventilation, and two deaths within 12 to 24 h. The atypical manifestations of COVID-19-associated GBS, especially the para-infectious profile and short time interval between the onset of the COVID-19 and GBS symptoms, increase the likelihood of symptom overlap, which can complicate the treatment and result in worsened disease progression and/or higher mortality rates. Inclusion of a neurological assessment during diagnosis of COVID-19 might facilitate timely identification and effective management of the GBS symptoms and improve treatment outcome. | |
dc.identifier | 646 | |
dc.identifier.issn | 2523-8973 | |
dc.identifier.issn | 2523-8973 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Springer Science and Business Media LLC | |
dc.relation.ispartof | SN comprehensive clinical medicine | |
dc.relation.isversionof | 10.1007/s42399-020-00646-w | |
dc.subject | Atypical | |
dc.subject | COVID-19 | |
dc.subject | Guillain-Barre | |
dc.subject | Para-infectious | |
dc.subject | Prognosis | |
dc.subject | SARS-CoV-2 | |
dc.title | COVID-19-Associated Guillain-Barre Syndrome: Atypical Para-infectious Profile, Symptom Overlap, and Increased Risk of Severe Neurological Complications. | |
dc.type | Journal article | |
duke.contributor.orcid | Kolls, Brad J|0000-0002-8704-8749 | |
duke.contributor.orcid | Koltai, Deborah C|0000-0002-4254-9902 | |
duke.contributor.orcid | Laskowitz, Daniel T|0000-0003-3430-8815 | |
pubs.begin-page | 1 | |
pubs.end-page | 13 | |
pubs.issue | 12 | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Center for the Study of Aging and Human Development | |
pubs.organisational-group | Neurosurgery | |
pubs.organisational-group | Neurology, Behavioral Neurology | |
pubs.organisational-group | Psychiatry & Behavioral Sciences, Geriatric Behavioral Health | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Neurology | |
pubs.organisational-group | Psychiatry & Behavioral Sciences | |
pubs.publication-status | Published | |
pubs.volume | 2 |
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