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Guillain Barré Syndrome and its variants as a manifestation of COVID-19: A systematic review of case reports and case series
- Source :
- Journal of the Neurological Sciences
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- Background The COVID-19 pandemic caused by SARS-COV-2 began in Wuhan, China in December 2019. Reports of COVID-19 with central (CNS) and peripheral nervous (PNS) system manifestations are emerging. In this systematic review, we compared and summarized the demographics, clinical features, Brighton criteria, immunological and laboratory findings with a focus on modified Erasmus GBS Outcome Score (mEGOS) in SARS-CoV-2 patients with GBS and its variants. Methods Based on PRISMA guidelines, we searched three databases (PubMed, Scopus, and Google Scholar) for studies on COVID-19 and GBS between December 1, 2019 to July 15, 2020. For descriptive analysis, we studied two groups with: 1) acute inflammatory demyelinating polyradiculoneuropathy (AIDP) variant, and 2) Non-AIDP/Other variants. We compared mEGOS scores for patients in both groups along with other key clinical features. Results Of the 50 GBS cases identified from 37 studies, 33 (66%) had acute inflammatory demyelinating polyradiculopolyneuropathy (AIDP) while 17 (34%) were of other (non-AIDP) variants. There mEGOS scores did not differ between AIDP patients and AMAN/AMSAN patients. Majority of the AIDP (66.7%) and AMAN/AMSAN (57.2%) patients belonged to Brighton level 1 indicating maximum diagnostic certainty. Conclusion To our knowledge, this is among the first reviews that includes GBS variants and the clinical prediction tool mEGOS for prognostication in COVID-19 patients. Further research is needed to assess whether IVIG is preferable over plasmapheresis in this population of GBS patients. It would also be crucial to follow these patients over time to identify the long-term disability as well as treatment outcomes.<br />Highlights • Majority of GBS variants in COVID-19 patients were AIDP. • Most AIDP, AMAN/AMSAN patients exhibited Brighton level 1-maximum diagnostic certainty. • The mean latency between COVID-19 infection and GBS ranged between 11 and 13 days.
- Subjects :
- Bickerstaff encephalitis
medicine.medical_treatment
MERS, Middle East Respiratory Syndrome
Treatment outcome
Bickerstaff brainstem encephalitis
Neural Conduction
PLEX, plasmapheresis
mEGOS, Modified Erasmus GBS Outcome Score
Review Article
COVID-19, Coronavirus infectious disease-2019
GBS, Guillain-Barre Syndrome
AIDP
SARS-CoV-2, Severe Acute Respiratory Distress Syndrome coronavirus 2
0302 clinical medicine
HCQ, Hydroxychloroquine
IL, Interleukin
030212 general & internal medicine
education.field_of_study
Guillain-Barre syndrome
AIDP, Acute inflammatory demyelinating polyneuropathy
AMAN, Acute motor axonal neuropathy
BFP, Bifacial weakness with paresthesias
HIV, Human immunodeficiency virus
Neurology
IGOS, International GBS Outcome Study
medicine.medical_specialty
Coronavirus disease 2019 (COVID-19)
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
Population
Clinical Neurology
GBS
Guillain-Barre Syndrome
AMSAN
MRC., Medical Research Council Scale for Muscle Strength
MRI, Magnetic Resonance Imaging
03 medical and health sciences
nCov, Novel Coronavirus
MFS
Internal medicine
medicine
Humans
EMG, Electromyography
WHO
World Health Organization
education
CSF, Cerebrospinal fluid
SARS-CoV-2
IDSA/ATS, Infectious Disease Society of America/American Thoracic Society
business.industry
COVID-19
MFS, Miller-Fisher syndrome
Polyradiculoneuropathy
RT-PCR, Reverse transcriptase polymerase chain reaction
medicine.disease
BBE, Bickerstaff's brainstem encephalitis
Plasmapheresis
Neurology (clinical)
business
AMSAN, Acute motor-sensory axonal neuropathy
IVIG, Intravenous immunoglobulin
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 0022510X
- Volume :
- 420
- Database :
- OpenAIRE
- Journal :
- Journal of the Neurological Sciences
- Accession number :
- edsair.doi.dedup.....e4aa3c9a9e534f6b939e9615533695f0