Table 1. Characteristics of Five Patients with Guillain–Barré Syndrome after the Onset of Covid-19.*.
Patient No. | Onset of Neurologic Syndrome | Neurologic Signsand Symptoms | CSF Findings† | Antiganglioside Antibodies‡ | MRI Results | Treatment and Outcomesat Week 4 |
---|---|---|---|---|---|---|
1 | 7 Days after fever, cough, and ageusia | Flaccid areflexic tetraplegia evolving to facial weakness, upper-limb paresthesia (36 hr), and respiratory failure (day 6) |
|
Negative |
|
Received 2 cycles of IVIG; had poor outcomes, including persistence of severe upper-limb weakness, dysphagia, and lower-limb paraplegia |
2 | 10 Days after fever and pharyngitis | Facial diplegia and generalized areflexia evolving to lower-limb paresthesia with ataxia (day 2) |
|
Not tested |
|
Received IVIG; had improvements, including decrease in ataxia and mild decrease in facial weakness |
3 | 10 Days after fever and cough | Flaccid tetraparesis and facial weakness evolving to areflexia (day 2) and respiratory failure (day 5) |
|
Negative |
|
Received 2 cycles of IVIG; had poor outcomes, including ICU admission owing to neuromuscular respiratory failure and flaccid tetraplegia |
4 | 5 Days after cough and hyposmia | Flaccid areflexic tetraparesis and ataxia (day 4) |
|
Not tested |
|
Received IVIG; had mild improvement but unable to stand 1 mo after onset |
5 | 7 Days after cough, ageusia, and anosmia | Facial weakness, flaccid areflexic paraplegia (days 2–3), and respiratory failure (day 4) |
|
Negative |
|
Received IVIG and plasma exchange; had bacterial pneumonia during IVIG treatment, which delayed plasma exchange |
Covid-19 denotes coronavirus disease 2019, CSF cerebrospinal fluid, ICU intensive care unit, IVIG intravenous immune globulin, MRI magnetic resonance imaging, PCR polymerase chain reaction, and SARS-CoV-2 severe acute respiratory syndrome coronavirus 2.
On CSF analysis, all the patients had a normal glucose level and IgG index and a polyclonal pattern on electrophoresis. The normal range for the protein level is 15 to 45 mg per deciliter.
An enzyme-linked immunosorbent assay was used to test for antibodies to GM1, GQ1b, and GD1b.