Chronic and Degenerative Neurological Disorders
Seizures
Epilepsy
chronic neurological disorder
alternation of brain function caused by an abrupt explosive, disorderly discharge of cerebral neurons
motor, sensory, autonomic, and behavior manifestations
causes
Types of Seizures
focal seizures
simple
complex
Generalized Seizures
absence
myoclonic
clonic
tonic-clonic
atonic
Unclassified epileptic seizures
Focal Seizures
motor, sensory, autonomic, or psychic symptoms
Clonic- repetitive, flexion/extension movements
EEG shows spikes in region
Seizure Stages
Aura
Prodroma
Tonic Phase
contraction
Clonic Phase
relaxation
Postictal phase
Diagnostic tests
labs
MRI
CT scan
EEG
Emergency Seizure Care
the goal is to protect the patient form injury
Do not physically restrain the patient and do not put anything in their mouth
Positioning post seizure
Treatments
do not panic
turn on their side and start timing the seizure
stay with person and do not restrain
place something soft under head
do not put anything in mouth
call 911 if seizure lasts longer than 5 minutes
Other Neurological Disorders
Parkinson’s Disease
progressive loss of dopamine-producing cells in the basal ganglia
depletion of dopamine creates an imbalance
unopposed ACH is apparent in the tremor ad abnormal spasmodic muscle movements
Signs and Symptoms
Onset usually gradual, after age 50
slow progressive
Mask-like, blank expression
pill rolling tremors
Bradykinesia
loss of normal arm swing while walking
decreased blinking
loss of ability to swallow
black expression
difficulty initiating movement
Tremor
common in hands and arms
pill rolling motion with the fingers'
occurs more often at rest
may involve diaphragm, tongue, lips, and jaw
increases with stress
Muscle Rigidity
increase resistance to passive movement
Cog wheel, jerky slow movement
Amyotrophic Lateral Sclerosis (ALS)
Loss of upper and lower motor neurons
Signs and Symptoms
painless muscle weakness
atrophy
eventually results in respiratory failure
Multiple Sclerosis (MS)
etiology unknown
damage to the myelin sheath caused by autoimmune inflammation
both sensory and motor neurons are affected
Different forms/types
Signs and Syptoms
autoimmune and usually familal
Tinnitus
decreased tearing
nystagmus
blurred vision
dysarthria
dysphagia
weakness may progress to paralysis
muscle spasticity
atoa
vertigo
urinary retention
spastic bladder
constipation
Guillan-Barre Syndrome
acquire inflammatory disease-causing demyelination of the peripheral nerves with relative sparing of axons
acute onset, ascending motor paralysis
humoral and cellular immunologic reaction
Risk factors
possible autoimmune
association with immunizations
frequently preceded by mild rserum ACH espiratory or intestinal infection
Progresses over hours to days
minimal muscle atrophy
Symmetrical paralysis
Causes problems with:
respiration
talking
swallowing
bowel and bladder function
Begins in lower extremities and ascends bilaterally
weakness
ataxia
bilateral paresthesia progressing to paralysis
Myasthenia Gravis (MG)
autoimmune disease caused by the loss of functioning ACH receptors
Signs and Symptoms
diplopia and difficult chewing, talking, and swallowing
Myasthenia crisis
cholinergic crisis
Diagnosis
edrophonium (Tensilon) testing
serum Ach receptor antibodies
EMG