Table 1.
Condition | Clinical Clues | Additional Investigations |
---|---|---|
1. Initial Diagnosis Correct | ||
Intrinsic feature of GBS illness |
|
MRI Brain normal EMG/NCS may be suggestive CSF albuminocytologic dissociation |
Intrinsic feature of GBS variant | ||
Anti‐Gq1b disease |
|
Serum anti‐Gq1b antibody positivity Brain MRI usually normal |
Complications of disease | ||
Metabolic derangement | ||
Hyponatremia (SIADH) |
|
Serum sodium, Serum Osmolality, Urine Osmolality. |
Hypercarbia (respiratory muscle weakness) |
|
Arterial blood gas ‐ CO2 levels |
Infections | Signs of pulmonary, urinary or skin infection especially | Elevated WCC, CRP; Abnormal CXR or urinalysis |
Autonomic instability | ||
Posterior reversible encephalopathy syndrome (PRES) |
|
T2 and FLAIR hyperintensities predominantly in posterior brain regions |
Complication of treatment | ||
IVIG‐relatesd | ||
Hypercoagulability(also rarely encountered with plasmapheresis) | Focal neurological deficits(arterial/venous)+/‐seizures, headache, papilloedema(venous) | MRI Brain: Diffusion restriction; vascular imaging help define cause and extent of thrombosis |
PRES | as above | as above |
Aseptic meningitis |
|
Culture‐negative CSF pleocytosis |
Medications
|
|
Medication administration review |
CNS, Central Nervous System; CRP, c‐reactive protein; CO2, carbon dioxide; CSF, cerebrospinal fluid; CXR, chest X‐ray; EMG, Electromyography; FLAIR, fluid‐attenuated inversion recovery; GBS, Guillain‐Barré Syndrome; IVIG, intravenous immunoglobulin; MRI, magnetic resonance imaging; NCS, nerve conduction studies; PRES, posterior reversible encephalopathy syndrome; SIADH, syndrome of inappropriate ADH secretion; WCC, white cell count