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COVID-19-Associated Guillain-Barre Syndrome: Atypical Para-infectious Profile, Symptom Overlap, and Increased Risk of Severe Neurological Complications.
Kajumba, Mayanja M; Kolls, Brad J; Koltai, Deborah C; Kaddumukasa, Mark; Kaddumukasa, Martin; Laskowitz, Daniel T.
Afiliação
  • Kajumba MM; Department of Mental Health and Community Psychology, School of Psychology, Makerere University, P. O. Box, 7062 Kampala, Uganda.
  • Kolls BJ; Duke Division of Global Neurosurgery and Neurology, Department of Neurosurgery, Duke University Medical Center, Box 3807, Durham, NC 27705 USA.
  • Koltai DC; Department of Neurology, Duke University School of Medicine, Durham, NC USA.
  • Kaddumukasa M; Neuroscience Medicine, Duke Clinical Research Institute, 300 W Morgan St, Durham, NC 27701 USA.
  • Kaddumukasa M; Duke Division of Global Neurosurgery and Neurology, Department of Neurosurgery, Duke University Medical Center, Box 3807, Durham, NC 27705 USA.
  • Laskowitz DT; Department of Neurology, Duke University School of Medicine, Durham, NC USA.
SN Compr Clin Med ; 2(12): 2702-2714, 2020.
Article em En | MEDLINE | ID: mdl-33251483
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Risk_factors_studies Idioma: En Revista: SN Compr Clin Med Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Risk_factors_studies Idioma: En Revista: SN Compr Clin Med Ano de publicação: 2020 Tipo de documento: Article