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SOPs for management of common acute neurological problems.

Department of Neurology, JIPMER; 2014

Acute Flaccid Paralysis in Adults


Acute Quadriparesis/plegia

1. General measures

 Ensure protection of airway and adequate ventilation


(Especially if there is respiratory muscle weakness,
shallow respiration, dysphagia, weak gag)
 Check and support: BP and Heart Rate
 Immobilize neck if history of neck/head trauma
 Send electrolytes and get an ECG- to look for hypokalaemia

2. Examination and classification into pattern for example,


SOPs for management of common acute neurological problems.
Department of Neurology, JIPMER; 2014

 Flaccid quadriparesis with sensory level (early bladder dysfunction)-


Transverse myelitis, compressive myelopathy
 Flaccid afebrile symmetric Para/quadriparesis (+/− bulbar and
Respiratory involvement) with areflexia and minimal sensory loss (but
often sensory symptoms): Acute neuropathy or polyradiculopathy (esp.,
Guillain Barre Syndrome)
 Flaccid, febrile, pure motor, asymmetric, paralysis (no bladder
involvement) often with meningismus: Enteroviral, polio, or vaccine
associated poliomyelitis
 Flaccid motor-sensory lower limb monoparesis after IM injection:
Injection neuritis
 Ophthalmoplegia, ptosis, bulbar weakness with motor weakness: Miller-
Fischer variant of Guillain Barre Syndrome, Botulism, Myasthenia Gravis
 Proximal muscle weakness, muscle tenderness without sensory symptoms
or signs and with preserved reflexes: Viral myositis, inflammatory
myopathy (e.g., dermatomyositis)

3. Investigations (according to the suspected site of lesion and cause of


paralysis)

 Neuroimaging (spinal cord) MRI indicated in all cases of myelopathy,


suspected transverse myelitis
 X- ray spine: suspected atlantoaxial dislocation, vertebral tuberculosis
 Electrophysiological testing (NCV & electromyography/ RNST):
Guillain Barre Syndrome, Myasthenic Crisis, Inflammatory Myopathy,
Periodic Paralysis (Dyskalemic), acute neuromyositis
 Lumbar puncture (CSF): Guillain Barre syndrome, suspicion of viral
myelitis
 Biochemistry: Creatine Kinase, Potassium, Magnesium, Phosphate
SOPs for management of common acute neurological problems.
Department of Neurology, JIPMER; 2014

 ECG: Hypokalemia
 Urine for porpho-bilinogens, toxins: arsenic, lead etc.,

4. Management (depends on the underlying aetiology identified)

1) Meticulous supportive care, anticipate and identify

 Respiratory, bulbar weakness (except in injection neuritis), shock due to


reduced vascular tone (spinal cord disease), Autonomic instability,
complications of immobilization and prevention of nosocomial infections.

2) Specific therapy:

 Guillain Barre syndrome: IVIG, 2 g/kg over 2–5 d


 Transverse myelitis: IV methyl-prednisolone 10–30 mg/kg, daily (max-1
g) for 3–5 d
 Compressive myelopathy: spinal immobilization, surgical intervention,
steroids (acute traumatic myelopathy)
 Dermatomyositis, Myasthenia Gravis: Immunomodulation
 Hypokalaemia: Intravenous potassium correction
SOPs for management of common acute neurological problems.
Department of Neurology, JIPMER; 2014

References

1. Marx A, Glass JD, Sutter RW. Differential diagnosis of acute


Flaccid paralysis and its role in poliomyelitis surveillance. Epidemiology
Rev. 2000; 22:298–316.
2. Hughes RAC, Rees JH. Clinical and epidemiological features of
Guillain-Barre syndrome. J Infect Dis. 1997; 176:S92–8.
3. Paradiso G, Tripoli J, Galicchio S, Fejerman N. Epidemiological,
Clinical and electrodiagnostic findings in childhood Guillain-Barre
Syndrome: a reappraisal. Ann Neurol. 1999; 46:701–7.
4. Kalra V, Sankhyan N, Sharma S, Gulati S, Choudhry R, Dhawan
B. Outcome in childhood Guillain-Barre syndrome. Indian J
Pediatr. 2009; 76:795–9.
5. Rantala H, Uhari M, Cherry J, Shields WB. Risk factors of respiratory
Failure in children with Guillain Barre Syndrome. Pediatr
Neurol. 1995; 13:289–92.
6. Melnick J. Enteroviruses: polioviruses, coxsackieviruses, echoviruses,
and newer enteroviruses. In: Field’s BN, Knipe DM,
Chanock RM, eds. Field’s virology. Philadelphia: Lippincott-
Raven Publishers; 1996. pp. 655–712.
7. Wadia NH, Wadia PN, Katrak SM, Misra VP. A study of the
Neurologic disorder associated with acute haemorrhagic conjunctivitis
due to enterovirus 70. J Neurol Neurosurg Psychiatry.
1983; 46:599–610.
8. Gadre G, Satishchandra P, Mahadevan A, et al. Rabies viral
Encephalitis: clinical determinants in diagnosis with special
Reference to paralytic form. J Neurol Neurosurg Psychiatry.
SOPs for management of common acute neurological problems.
Department of Neurology, JIPMER; 2014

2010; 81:812–20.
9. Tyler KL. Herpes simplex virus infections of the central nervous
System: encephalitis and meningitis, including Mollaret’s. Herpes.
2004; 11:57A–64A.
10. Misra UK, Kalita J. Anterior horn cells are also involved in
Japanese encephalitis. Acta Neurol Scand. 1997;96:114–7.
11. Frohman EM, Wingerchuk DM. Clinical practice. Transverse myelitis.
N Engl J Med. 2010;363:564–72.

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