Basic Concepts in Normal Neurologic Function
Oxygen
supply: The brain requires 20% of
the O2 in the body
- Glucose supply: The brain requires 65 to 70% of the glucose in the body
- Blood supply: The brain requires 1/3 of the cardiac output
- Acid-base balance
Acidosis
1.
Cerebral vasodilation
2.
CNS depressant ® coma
Alkalosis
1.
Cerebral vasocontriction
2.
CNS stimulant ® seizures
§
Blood-brain barrier:
Protects the brain from certain drugs, chemicals and microorganism. It a layer of least semi-permeable
capillaries
§
CSF volume: CSF
cushions the brain; it nourishes the brain and determines the ICP. The choroids plexus in the lateral
ventricles primarily produces CSF. The
normal CSF volume is 100 to 150 mls at a time, an average of 120 mls.
Neurologic Assessment
1. Mental Status
- Orientation to three spheres : people, time and place
- Memory: Immediate recall, recent memory, remote memory
a.
Immediate recall: Ask
the client to repeat your question
b.
Recent memory: Ask
client about recent events that occurred few minutes, few hours
c.
Remote memory: Ask the
client about events in the remote past, or historical events that can be
answered by the general population
2. Level of
consciousness (LOC)
-
It is the most sensitive indicator of the changes in
the neurologic status of the client
-
The center for wakefulness is the ascending reticular
activating system ARAS/reticular formation
-
Assess both wakefulness and content of thought
-
Levels of consciousness:
§
Level I- conscious, coherent, cognitive (3 Cs)
§
Level II- confused, drowsy, lethargic, obtunded, somnolent
§
Level III- stuporous; responds only to noxious, strong
or intense stimuli. e.g. sternal
pressure, trapezius pinch, pressure at the base of the nail or supraorbital
area, very strong light or very loud sound
§
Level IV
1. Light coma; response is only by grimace or withdrawing limb from
pain; primitve and disorganized response to painful stimuli
2. Deep Coma; absence of response to even the most painful stimuli
GLASGOW COMA SCALE (GCS)
is an objective measure to describe LOC.
It is based on the client’s response in three areas : eye opening, motor response, verbal response
- Best eye-opening response
a. Spontaneously = 4
b. To speech =
3
c. To painful stimuli = 2
d. No opening = 1
- Best Motor Response
a.
Obeys verbal command = 6
b.
Localizes painful stimuli = 5
c.
Flexion: withdrawal to pain =
4
d.
Flexion: abnormal (decorticate =
3
e.
Extension:abonormal(decerebrate) =2
f.
No response to pain on any limb = 1
3. Best Verbal Response
a.
Oriented to time, place, person = 5
b. Engages in conversation, confused
in content = 4
c.
Words spoken but conversation not sustained = 3
d.
Groans on evoked pain = 2
e. No response = 1
CVA, Stroke
|
1. Anterior
cerebral stroke: lower extr emity more involved than upper extremity,
|
contralateral hemiparesis and sensory deficits
|
2. Posterior
cerebral stroke: contralateral sensory loss, transient contralateral
|
Middle cerebral artery stroke: upper extremity more
involved than the lower
|
extremity, contralateral sensory loss
|
Risk Factors
|
1. Diabetes
|
2.
Atherosclerosis
|
3.
Hypertension
|
4. Cardiac disease
|
5. Transient
ischemic attacks
|
Aneurysm Precautions
|
1. Avoid
rectal temperatures
|
2. Limit visitors
|
3. Avoid
Valsalva’s maneuver
|
4. Head of bed
should be between 30-45 degrees
|
Valsalva’s maneuver – occurs when attempting to
forcibly exhale with the glottis,
|
mouth and nose closed. It causes an increase in intrathoracic pressure with an
|
accompanying collapse of the vein of the chest wall.
The following may result:
|
1. Slowing of
the pulse
|
2. Decreased
return of blood to the heart
|
3. Increased
intrathoracic pressure
|
Elevated Intracranial Pressure
|
In most cases you should do the following:
|
1. Maintain
proper fluid volumes
|
2. Set-up
quiet environment for minimal sensory stimulation
|
3. Elevate HOB
(head of bed) to approximately 30 degrees
|
4. Limit
suctioning performed
|
Horner’s Syndrome
|
- Sympathetic innervation to the face is interrupted
by a lesion
|
in the brain stem resulting in pupillary constriction,
dry and red face with no
|
sweat, ptosis-Mueller’s muscle, problem located in
sympathetic ascending fibers
|
Autonomic Dysreflexia
|
- caused by a lesion in the high thoracic or cervical
cord.
|
Severe hypertension, sweating and headaches
noted. May occur with a
|
Parkinson’s Disease
|
-a degenerative disease with pr imary involvement of
the
|
basal ganglia; characterized by the following:
|
Signs/Symptoms
|
1. Bradykinesia
|
2. Resting tremor
|
3. Impaired
postural reflexes
|
4. Rigidity
|
5. Loss of
inhibitory dopamine
|
6. Mask like
affect
|
7. Emotional lability
|
Multiple Sclerosis
|
–progressive demyelinating disease of the central
nervous
|
system affecting mostly young adults
|
Cause unknown, most likely viral.
|
1. Fluctuating exacerbations
|
2. Demyelinating lesions limit neural transmission
|
3. Confirmed
with lumbar puncture, elevated gamma globulin, CT/MRI,
|
myelogram, EEG.
|
4. Mild to
moderate impaired cognition common
|
5. Sensory Deficits
|
6. Bowel and Bladder Deficits
|
7. Spasticity common
|
8. Ataxic gait
|
Myasthenia gravis
|
- neuromuscular disease characterized by fatigue of
skeletal
|
muscles and muscular weakness.
|
**
|
Key point
|
-Review the differentiation between MG and a
cholinergic crisis, using
|
the Tensilon Test. A cholinergic crisis may have
hypotension, bradycardia vs.
|
myasthenia gravis.
|
Signs/Symptoms
|
1. Progressive involvement
|
2. Decreased muscle membrane acetylcholine receptors
|
3. Severe
weakness (proximal more than distal muscles)
|
4. Facial,
ocular and bulbar weakness
|
5. Possible life-threatening respiratory muscle
weakness
|
6. Probable
use of anticholinesterase drugs for treatment
|
Guillain-Barre’ Syndrome
|
-polyneuropathy with progressive muscular weakness
|
Signs/Symptoms
|
1.
Demyelination of peripheral and cranial nerves
|
2. Motor
paralysis in an ascending pattern
|
3. 3%
Mortality – respiratory failure
|
4. Autonomic dysfunction-arrhythmias, blood pressure
changes, tachycardia
|
Amyotrophic lateral sclerosis
|
(Lou Gehrig’s disease) – degenerative disease
|
affecting upper and lower motor neurons
|
Signs/Symptoms
|
1. Death
typically in 2-5 yrs.
|
2. Spasticity, hyperreflexia
|
3. Dysarthria, Dysphagia
|
4. Autonomic
Dysfunction in approximately 1/3 of patients
|
5. Cognition
is normal
|
Post-polio Syndrome
|
- slowly progressive muscle weakness that occurs in
|
patients with a history of acute poliomyelitis, after
a stable period
|
Sign/Symptoms
|
1. New Weakness
|
2. Pain/Myalgia
|
3. Abnormal fatigue
|
Seizures
|
Epilepsy-recurrent seizures due to excessive and
sudden discharge of cerebral
|
cortical neurons.
|
Tonic-clonic (Grand Mal) –Pt. confused and drowsy
about the seizures, 2-5 min
|
generally
|
Absence seizures
(Petit Mal)- Brief, no convulsive contractions, may be up to
|
100X day
|
Simple Seizures- no loss of consciousness
|
Complex Seizures, brief loss of consciousness with
psychomotor changes
|
**
|
Key Point
|
- When a patient has a seizure during most
interventions, do not use
|
a tongue blade and allow free movement in a safe
environment
|
Meningitis-inflammation of the meninges of the spinal
cord and brain caused by
|
bacteria.
|
The most common bacteria are the following:
|
Neisseria meningitidis, Diploc occus
|
pneumoniae,
|
and
|
Haemophilus influenzae
|
Signs/Symptoms
|
1.
Brudzinski’s sign
|
2. Kernig’s
sign
|
3. Stiff/Tight neck
|
4. Fever
|
5. Confused
|
Anterior Cord Syndrome – damage is mainly in anterior
cord resulting in loss of
|
motor function and pain and temperature with
preservation of light touch,
|
proprioception and position sense
|
Brown-Sequard Syndrome – hemisection of SC resulting
in ipsilateral weakness
|
and loss of position and vibration sense below the
level of lesion
|
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