Acute paralysis including hemiplegia
Patterns and definitions
- Paraparesis- partial paralysis of legs
- Paraplegia- paralysis of legs; usually implies spinal cord pathology, if spastic
(increased tone and hyperreflexic)
- Diplegia- paralysis affecting all 4 limbs, but predominantly the legs
- Quadriplegia- significant paralysis of all 4 limbs
- Hemiplegia- paralysis affecting only one side of body (asymmetrical)
- Truncal paresis- paralysis affecting the muscles of the trunk
Pathology affecting the upper motor neurone tends to produce spastic paralysis- i.e. stiff,
weak limbs with increased reflexes. However, in the early stages, the affected limbs may be flaccid.
Pathology affecting the lower motor neurone tends to produce flaccid paralysis- i.e. floppy,
weak limbs, with reduced or no reflexes. The muscles affected become atrophied, with visible loss of bulk.
Lesions in the brain are more likely to produce focal motor neurology (often a hemiplegia
paralysing the arm extensors and leg flexors on the contralateral side. There may be
associated symptoms and signs of raised intracranial pressure. Some lesions are associated
with seizures (which may be focal). Lesions in the brain are also more likely to interfere with
conscious level/ higher mental function. There may also be cranial nerve involvement.
Lesions affecting the spinal cord are more likely to produce symmetrical paralysis, usually
spastic, below the level of the lesion, with sensory loss. There also may be associated
sphincter dysfunction affecting bowel and bladder control.
In lesions affecting peripheral nerves the distal muscle groups are often affected first.
In myopathic paralysis, the pattern of paralysis is determined by affected muscles. There
may be muscle wasting, (pseudohypertrophy suggests Duchenne's muscular dystrophy) or
tenderness.
Causes of paralysis: (rare diagnoses in [brackets])
Cerebral pathology
- Head injury
- Cerebrovascular accidents: due to vascular malformations, sickle cell disease,bleeding tendency, thrombosis, emboli (e.g. rheumatic heart disease).
- Infections: meningitis, cerebral abscess, subdural empyema, sequelae of cerebral malaria, TB tuberculoma, toxoplasmosis
- HIV: encephalitis/ focal 'inflammation'; opportunistic infections (e.g. CMV, VZV, including zoster sine herpete {zoster without the rash})
- Tumour: benign or malignant
- Cerebral Palsy:'new' neurological signs appear as child develops
- Migraine
- Todd's palsy post seizure
Spinal cord pathology
- Trauma
- Transverse Myelitis, including HIV-related
- Epidural abscess
- Schistosomiasis
- TB spine
- Paravertebral tumours (e. g. Burkitt's lymphoma)
- [Cysticercosis]
- [Poliomyelitis]
- Non polio enterovirus
Peripheral Neuropathies
- Guillain-Barre Syndrome (GBS)
- HIV-related polyneuropathies: direct HIV-effect; or co-infections (e.g. CMV)
- Rabies (flaccid form)
- [Diphtheria]
- [Botulism]
- [Tick Paralysis]
Muscle pathology
- Acute viral myositis
Muscular dystrophies (and other myopathies)
- [Myasthenia Gravis crisis]
Miscellaneous
Common Causes of Non-traumatic Paraplegia in Malawi
- Burkitt's Lymphoma
- Spinal TB
- Epidural abscess
- Guillain Barre Syndrome
- Transverse Myelitis
- Schistosomiasis - often asymmetrical
- Polio - not common but must be excluded
- Non polio enteroviruses
Important points in history
Development of paralysis
- Speed of onset: recent tendency to falls/ clumsiness/ reduced activity etc
- Progressive or static
- Symetry
- Bowel and bladder function
- Swallowing or speech difficulties
- Respiratory difficulties
Current associated symptoms
- Fever
- Confusion or deterioration of consciousness; seizures
- Meningism (headache, photophobia, neck stiffness)
- Symptoms of raised intracranial pressure (headache, vomiting, visual disturbance
and in end stage bradycardia, high blood pressure and papillary edema)
- Back pain or deformity
Preceding health
- Recent ‘viral’ illness; or history of meningitic symptoms
- Past medical history (or episodes suggestive of) meningitis/ cerebral malaria/ sickle
cell disease
- Indicators of HIV infection or HIV treatment
- Birth history, developmental milestones (developmental delay or regression), learning
difficulties
Risk factors
- Trauma
- Animal scratches or bites
- Exposure to poisons, especially organophosphates
- Vaccination history esp. BCG/ polio/ diphtheria
- TB contact
- Schistosomiasis exposure risk
- Family history of similar disorder
Important points on examination
- Temperature and vital signs; BP
- Full neurological assessment
- Conscious level, orientation, meningism
- Motor (tone, power, reflexes, coordination); sensory; cranial nerves
- Fundoscopy for papilloedema
- Respiratory examination especially for hypoventilation/ associated pneumonia
- Signs of HIV infection
- Spinal gibbus or kyphoscoliosis (? TB)
- Muscle atrophy or tenderness
- Spinal tufts or pits, and head circumference (? Spina bifida; ? Hydrocephalus)
- Gower's sign, pseudohypertrophy of muscles (? Duchenne muscular dystrophy)
- Dactylitis, skull bossing (? sickle cell disease)
- Swollen extremity with decrease of pain when elevated (thrombosis) vs. cold extremity with decrease of pain when hanging down (arterial embolus) - USS for further investitation
- Evidence of valvular cardiac disease.
Investigations
- Blood culture if febrile
- LP if meningitic, reduced consciousness, or ? GBS
- Mantoux test
- Sickling test
- Urine and stool for ova/ cysts/ parasite examination
- HIV testing
- Imaging:
- USS head (infants)
- cardiac echo if hemiplegic
- spinal Xray
- CT/ MRI brain - discuss with seniors
- Muscle biopsy: may be useful if a myopathy suspected- discuss with seniors
- Stool specimen (and notification) to Ministry of Health in ALL cases of acute flaccid paralysis (please know your AFP focal person),
see acute flaccid paralysis surveillance
Indications for admission
- In general, admit all children presenting with a new-onset neurological sign
- If the child is not acutely unwell or at risk of respiratory compromise (such as in GBS,
polio) consider admission directly to Medical Bay.
Treatment
Specific treatments depend on cause identified or suspected.
- Meningitis: Broad-spectrum antibiotics, preferably after lumbar puncture (LP) (note:
there are only very few absolute contraindications for LP)
- Cerebral or spinal abscess: Ceftriaxone and seek surgical opinion
- TB spine and tuberculoma: TB treatment and orthopaedic opinion
- Schistosomiasis: Praziquantel, 40 mg/kg STAT (consider this whenever no other
cause for paralysis found and in ALL cases of paraparesis). If very probable consider treating for three days with 60 mg/kg OD.
- Consider steroids for ALL spinal cord lesions, unless evidence of bacterial infection
- Tumours: treat with surgery/ chemotherapy if appropriate. Palliative care.
- Organophosphate poisoning protocol
- Thrombotic disease: prophylactic aspirin
Supportive Care
- Relieve pain and agitation whenever possible
- Early physiotherapy; stretch tight muscles; position paralysed limbs; mobility aids
- Avoidance of bedsores, turn patient 3-hourly at least. Instruct guardian well, do not
wait for the physiotherapists to do so. Mouth care. Bladder catheterisation
- Nutritional support if required, including nasogastric feeding
- Bed rest helps in the acute stage of poliomyelitis/non polio enterovirus infection
- Blood pressure and temperature management
Monitoring
- Regular BP, vital signs, saturation (especially children with GBS), neuro signs
- Regular documentation of 'level' of disorder in ascending polyneuropathies such as
Guillain-Barre syndrome. Peak expiratory flow monitoring can be a useful way to
assess decline of respiratory function.
- Regular check for pressure sores
Complications
- Extension of lesion causing increasing neurological deficit, such as raised intracranial
pressure; involvement of respiratory muscles
- Respiratory infections
- Aspiration pneumonia
- Pressure sores
- Joint contractures
When to discharge
- Depends on cause identified, response to treatment, family wishes and social
circumstances.
- Ideally the child will be stable/ improving; the family will have knowledge of the
condition and its prognosis, and will know how they can best assist the child.
- In children with progressive or terminal conditions, or those who are likely to have
ongoing physical/ medical/ psychosocial needs, plans for follow up and community support should be made. Involve Umodzi