Neurologic Dysfunction
Neurologic Dysfunction
S SYSTEMS TO MONITOR
● Round the clock assess NeuroVitals,
Glasgow Coma Scale ● A.k. A External Ventricular Drain
● It monitors the ICP and has a
catheter inserted in the area of the
Behavior Response
lateral ventricle and drains the CSF
4- Spontaneously during increase pressure reading
3- To Speech ○ >20 mmHg call M.D
2- To pain REMEMBER THEY ARE NOT GOOD
1- No response CANDIDATES FOR LUMBAR PUNCTURE
Verbal Response 5- Oriented to time,
person, and place S STRAINING ACTIVITIES AVOIDED
4- Confused ● Vomiting
3- Inappropriate ○ antiemetic may be prescribed
words ● Sneezing
2- ● Valsalva maneuver
Incomprehensible
sounds ○ Laxative
1- No response ● Kepp environment calm anf avoid
restraint
Motor Response 6- Obeys command U UNCONSCIOUS PATIENT CARE
5- Moves to ● Avoid over sedating
localized pain ○ It can mask the early S&S of
4- Flex to withdraw
from pain increase intracranial
3- Abnormal flexion pressure
2- Abnormal ● Assess Lung sound
Extension ○ They can have pooling of
1- No response secretions
● Best Score: 15 ○ Move them every 2 hours
● Comatose: Less than 8 ○ Suction as needed (not more
● Unresponsive: 3 than 15 sec)
● Skincare for immobile Loop Diuretics and Corticosteroids
● GI Tube (protein starts leaking in a breakdown on
○ Check residual the Blood-Brain Barriers, and corticosteroids
● The risk for renal stone development can help with that)
○ Foley catheter
● Contractures
1. Select the main structures below that play a role with altering
● Eyes Care
intracranial pressure:
● Constipation A. Brain
B. Neurons
● Blood Blots (PT and INR) C. Cerebrospinal Fluid
● Treat them as a conscious patient D. Blood
E. Periosteum
Rx/MEDICATION F. Dura mater
● Barbiturates The answers are A, C, and D. Inside the skull are three structures
that can alter intracranial pressure. They are the brain, cerebrospinal
○ Decrease Brain metabolism fluid (CSF), and blood.
and Decrease BP and ICP
○ Vasopressor/IVF if they have 2. The Monro-Kellie hypothesis explains the compensatory
relationship among the structures in the skull that play a role with
too much Mannitol intracranial pressure. Which of the following are NOT compensatory
● Antihypertensive medication mechanisms performed by the body to decrease intracranial pressure
naturally? Select all that apply:
○ To decrease MAP (SBP) A. Shifting cerebrospinal fluid to other areas of the brain and spinal
● Mannitol cord
B. Vasodilation of cerebral vessels
C. Decreasing cerebrospinal fluid production
E EDEMA MANAGEMENT: D. Leaking proteins into the brain barrier
The answers are B and D. These are NOT compensatory
● Hyperosmotic Drugs mechanisms, but actions that will actually increase intracranial
pressure. Vasoconstriction (not dilation) decreases blood flow and
○ Dehydrating brain helps lower ICP. Leaking of protein actually leads to more swelling of
○ Done very carefully and the brain tissue. Remember water is attracted to protein (oncotic
pressure).
○ Monitor BP and renal
Functions
3. A patient is being treated for increased intracranial pressure.
Mannitol Which activities below should the patient avoid performing?
● Concentrated sugar A. Coughing
B. Sneezing
● Draws water that is pooling in the C. Talking
D. Valsalva maneuver
brain into the blood E. Vomiting
● Filtered through Glomerulus and Not F. Keeping the head of the bed between 30- 35 degrees
The answers are A, B, D, and E. These activities can increase ICP.
reabsorbed by the renal tubules
○ Water remove = Na+
4. A patient is experiencing hyperventilation and has a PaCO2 level
+Chloride of 52. The patient has an ICP of 20 mmHg. As the nurse you know
● The risk for Fluid Volume Overload that the PaCO2 level will?
A. cause vasoconstriction and decrease the ICP
○ The risk for Heart Failure B. promote diuresis and decrease the ICP
C. cause vasodilation and increase the ICP
○ The risk for Pulmonary D. cause vasodilation and decrease the ICP
Edema The answer is C. An elevated carbon dioxide level in the blood will
cause vasodilation (NOT constriction), which will increase ICP
● The risk for Fluid Depletion (normal ICP 5 to 15 mmHg). Therefore, many patients with severe
○ S&S: Thirst and dry ICP may need to be mechanical ventilated so PaCO2 levels can be
lowered (30-35), which will lead to vasoconstriction and decrease ICP
○ Dehydration (with constriction there is less blood volume and flow going to the
○ Monitor Renal Function, brain and this helps decrease pressure)....remember Monro-Kellie
hypothesis.
○ UOP (urinary output),
○ Electrolytes
5. You're providing education to a group of nursing students about The answer is A. LPs are avoided in patients with ICP because they
ICP. You explain that when cerebral perfusion pressure falls too low can lead to possible brain herniation.
the brain is not properly perfused and brain tissue dies. A student
asks, "What is a normal cerebral perfusion pressure level?" Your
response is: 11. You're collecting vital signs on a patient with ICP. The patient has
A. 5-15 mmHg a Glascoma Scale rating of 4. How will you assess the patient's
B. 60-100 mmHg temperature?
C. 30-45 mmHg A. Rectal
D. >160 mmHg B. Oral
The answer is B. This is a normal CPP. Option A represents a normal C. Axillary
intracranial pressure. The answer is A. This GCS rating demonstrates the patient is
unconscious. If a patient is unconscious the nurse should take the
patient’s temperature either via the rectal, tympanic, or temporal
6. Which patient below is at MOST risk for increased intracranial method. Oral and axillary are not reliable.
pressure?
A. A patient who is experiencing severe hypotension.
B. A patient who is admitted with a traumatic brain injury. 12. A patient who experienced a cerebral hemorrhage is at risk for
C. A patient who recently experienced a myocardial infarction. developing increased ICP. Which sign and symptom below is the
D. A patient post-op from eye surgery. EARLIEST indicator the patient is having this complication?
The answer is B. Remember head trauma, cerebral hemorrhage, A. Bradycardia
hematoma, hydrocephalus, tumor, encephalitis etc. can all increase B. Decerebrate posturing
ICP. C. Restlessness
D. Unequal pupil size
The answer is C. Mental status changes are the earliest indicator a
7. A patient with increased ICP has the following vital signs: blood patient is experiencing increased ICP. All the other signs and
pressure 99/60, HR 65, Temperature 101.6 'F, respirations 14, symptoms listed happen later.
oxygen saturation of 95%. ICP reading is 21 mmHg. Based on these
findings you would?
A. Administered PRN dose of a vasopressor 13. Select all the signs and symptoms that occur with increased ICP:
B. Administer 2 L of oxygen A. Decorticate posturing
C. Remove extra blankets and give the patient a cool bath B. Tachycardia
D. Perform suctioning C. Decrease in pulse pressure
The answer is C. It is important to monitor the patient for D. Cheyne-stokes
hyperthermia (a fever). A fever increases ICP and cerebral blood E. Hemiplegia
volume, and metabolic needs of the patient. The nurse can F. Decerebrate posturing
administer antipyretics per MD order, remove extra blankets, The answers are A, D, E, and F. Option B is wrong because
decrease room temperature, give a cool bath or use a cooling bradycardia (not tachycardia) happens in the late stage along with an
system. Remember it is important to prevent shivering (this also INCREASE (not decrease) in pulse pressure.
increases metabolic needs and ICP).
SECONDARY HEADACHE
PATHOPHYSIOLOGY
● It is a result of an underlying
disease/conditions
● Warning signs and symptoms
○ S Systemic Symptoms
(Illness or conditions like
cancer)
○ Their task is handling and
transmitting information and
DEFINITION: impulses
● Abnormal electrical signals in the 2 Types of Neuron
brain being fired from neurons: ● Excitatory
Two Category: ○ Whenever they are
○ Generalize (both side of the stimulated they will cause a
brain) response
○ Focal (partial seizure and ○ They will release a
only target specific parts of neurotransmitter glutamate
the brain) ● Inhibitory
PHYSIOLOGY ○ They will inhibit a response
● Neurons they will decrease it
○ They will release a ○ Hugh fever
neurotransmitter GABA ○ CNS infection
There is an equilibrium for a patient who ○ Hypoglycemia
does not have a seizure ○ EtOH withdrawal
○ Acid-base imbalances
Problem: Damage in inhibitory neuron will ○ Hypoxia
be damage then there won’t be an inhibiting ○ Brain tumor
excessive excitatory neurotransmitter ● But some patient Epilepsy frequent
release by the excitatory muscle-- seizures activity due to Chronic
overstimulation of the brain condition
● For example, the Barbituates- will ○ Traumatic brain injury (TBI)
stimulate the GABA receptors that ○ congenital birth defect
will decrease the excitatory ○ Massive Stroke
○ Idiopathic
CAUSE ○ Effects of an illness
● Affects Anyone due to an acute
illness
GUILLAIN-BARRE SYNDROME ○ It receives and transmit
signals so some type of
DEFINITION: action can occur
● Autoimmune condition ○ For sensory and motor
● The immune system attacks nerves ■ The nerve receives
in the body specifically in impulses at the
○ Peripheral Nervous system dendrites
■ Nerves located ■ Then to the stoma
outside the spinal ■ And go through the
cords Axon with Myelin
○ Cranial Nerves sheaths
● Immune system attacking ● Purpose of Myelin Sheath
○ Myelin Sheath ○ It serves as an insulator that
○ Demyelination is occurring can allow smooth passage of
● If the GBS is severe enough it can signals without being
extends to the autonomic nervous interrupted
system ○ Then allows it to reach to the
● GBS=Gradual block axon terminal
RISK FACTOR: PATHOPHYSIOLOGY
● If a defect was found in the Nerve
ANATOMY AND PHYSIOLOGY: ○ Sensory and Nerve function
● Peripheral Nervous System: will not be effective
○ Somatic: control voluntary ○ Can lead to Respiratory
functions Failure as the disease
○ Autonomic: Controls ● There is an existing condition that
involuntary functions triggers this condition
● Purpose of Nerve:
○ May ask the patient’s history ○ It is symmetrical
extensively ● This can lead to paralysation of the
● GBS can affect anyone at any age, body
any gender and any race ● The myelin sheath is destroyed and
● There is no cure to this disease won’t get any signal
If illness does exist WHY?
● The immune system usually fights ● Report illness
the illness but somewhere along the ○ 1-3 weeks of upper
way it got confuse and attacked the respiratory disease or an
Myelin sheath Gastrointestinal Disease
● Gradual Block of Sensation ■ Caused by a
Campylobacter
Different Type of Guillain Barre Jejuni
Syndrome ○ “As many as 40 percent of
❏ Miller Fisher Syndrome: GBS cases in the United
❏ MFS originates in the eyes, stated are thought to be
adversely affecting the triggered by Campylobacter
manner in which the infection” +
individual walks. It is more ○ Also link with patient with
prevalent in Asia compared Epstein Barr Virus {EBV}
to North America. ○ Also link with HIV and AIDS
❏ Acute Motor Axonal Neuropathy ○ Also link with recent
(AMAN)/Acute Motor-Sensory vaccination
Axonal Neuropathy (AMSAN): ■ Swine flu
AMSAN and AMAN ■ Influenza
❏ affect more people in Asian
countries in comparison to PATHOPHYSIOLOGY
the USA. ● If a defect was found in the Nerve
❏ Acute Inflammatory ○ Sensory and Nerve function
Demyelinating will not be effective
Polyradiculoneuropathy (AIDP): ○ Can lead to Respiratory
❏ It is the most widespread Failure as the disease
form of GBS, characterized
by muscular weakness and ● Lower extremities they felt
numbness that develops numbness and tingling and they
from the lower extremity and have trouble walking
shoots upward. Majority of ○ They reported that they have
affected Americans are severe GI illness caused by
diagnosed with the AIDP Campylobacter Jejuni
WHAT HAPPENS: ● Peripheral nerves starts
● .It tends to start in the feet demyelination downwards then
○ Feeling of paresthesia ascends
{tingling, numbness ● .After 2 weeks
● It migrates upward/ ascends
○ Work signs and symptoms ■ And patient will start
occur experiencing Difficulty
● After the worst scenario breathing
○ Remyelination occurs ○
○ The symptoms starts SIGNS AND SYMPTOMS
subsiding ● Paresthesia at the lower extremities
○ They start to get better ● Migration upward/ Ascending
● After 1 to 2 years Numbness and tingling
○ The symptoms will reoccur symmetrically
● Paralysis on the waist down
Worst case scenario ● Absent Reflexes
● Cranial: Migrates to brain stem ● Loss Muscle Time
○ Face paralysis ● Patient will complain difficulty
○ Difficulty Swallowing breathing
○ Difficulty Speaking ○ Ineffective cough
○ Vissium issue ○ So Always prepare Airway
● Severe Pain at the cramps of muscle management kit at the
○ Odd paradox bedside
● Involvement of Autonomic nervous ● Difficult swallowing
system ○ They can aspirate and can
○ Heart: develop pneumonia
■ Dysrhythmias ○ Always assess swallowing
■ Orthostatic activity
Hypotension ● They can’t speak and articulate
■ Paroxysmal words
Hypertension ○ Always provide a
● GI system: communication boards
○ Constipation ○ Always provide they
■ Feeding tube and assurance that this is
always be alerted that temporary and they can
if bowel sound is regain their sensation back
present- paralytic DIAGNOSTIC AND LABORATORY TEST
ileus ● electromyography and Nerve
■ Always check Conduction Studies
Residuals ○ Assess the demyelination of
■ the nerves by determining
○ Renal muscle’s ability to response
■ Urinary Retention to nerve stimulation
● As disease progresses and ascends ● Lumbar Puncture:
in the chest ○ Elevated Protein without
○ Muscle wall responsible for elevated white blood cell
drawing air in and out will ■ Before: Empty
start to paralyze Bladder
■ During: Position Your Grade: B
lateral recumbent with Percentage of What you Got Right: 82
knee up to abdomen
and bend chin to Go Here for More Quizzes
chest
■ After: Lie flat needs Your Answers & what you got Right &
to consume a lot of Wrong:
fluids to prevent
headache and to 1. True or False: Guillain-Barré Syndrome
replace loss CSF occurs when the body's immune system
TREATMENT attacks the myelin sheath on the nerves in
● TReatment can not CURE the central nervous system.
● They can only decrease recovery True
time and Improves Signs and False
Symptoms FALSE: Guillain-Barré Syndrome is an
○ Decrease signs and autoimmune neuro condition where the
symptoms immune system attacks the nerves (myelin
● They have to be administered 2 sheath) in the PERIPHERAL NERVOUS
weeks from the onset of symptoms SYSTEM and cranial nerves. This condition
MEDICATION does NOT occur in the central nervous
● Immunoglobulin Therapy: system (CNS).
○ IV immunoglobulin from a
donor given to the patient to
stop the antibodies that are 2. During nursing report you learn that the
damaging the nerves patient you will be caring for has Guillain-
● Plasmapheresis Barré Syndrome. As the nurse you know
○ Machine that will filter the that this disease tends to present with:
blood to remove the A. signs and symptoms that are unilateral
antibodies from the plasma and descending that start in the lower
that are attacking the myelin extremities
sheth B. signs and symptoms that are symmetrical
NURSING INTERVENTION and ascending that start in the upper
● Immobility and Paralysis can lead to extremities
Increase risk for infection, blood C. signs and symptoms that are
clots, pressure injuries UTIs, Weight asymmetrical and ascending that start in the
loss upper extremities
○ They can be Intubated D. signs and symptoms that are
○ Anticoagulants and monitor symmetrical and ascending that start in the
SCDs lower extremities
○ Turning them frequently The answer is D. GBS signs and symptoms
○ Physical therapy and will most likely start in the lower extremities
p[reventing contractures (ex: feet), be symmetrical, and will gradually
○ Maintain muscle Integrity spread upward (ascending) to the head.
○ Monitor Weights daily There are various forms of Guillain-Barré
Syndrome. Acute inflammatory C. The patient has absent reflexes in the
demyelinating polyradiculoneuropathy lower extremities.
(AIDP) is the most common type in the U.S. D. The patient reports paresthesia in the
and this is how this syndrome tends to upper extremities.
present. The answer is B. The patient’s signs and
symptoms in this scenario are typical with
Guillain-Barré Syndrome. The syndrome
3. You're assessing a patient's health tends to start in the lower extremities (with
history for risk factors associated with paresthesia that will progress to paralysis)
developing Guillain-Barré Syndrome. Select and migrate upward. The respiratory system
all the risk factors below: can be affected leading to respiratory
A. Recent upper respiratory infection failure. Therefore, the nurse should assess
B. Patient's age: 3 years old for any signs and symptoms that the
C. Positive stool culture Campylobacter respiratory system may be compromised
Jejuni (ex: weak cough, shortness of breath,
D. Hyperthermia dyspnea...patient says it is hard to breath
E. Epstein-Barr etc.). The nurse should immediately report
F. Diabetes this to the MD because the patient may
G. Myasthenia Gravis need mechanical ventilation. Absent
The answers are: A, C, and E. Risk factors reflexes is common in GBS and paresthesia
for developing Guillain-Barré Syndrome can extend to the upper extremities as the
include: experiencing upper respiratory syndrome progresses. A headache is not
infection, GI infection (especially from common.
Campylobacter Jejuni), Epstein-Barr
infection, HIV/AIDS, vaccination (flu or
swine flu) etc. 5. A patient with Guillain-Barré Syndrome
has a feeding tube for nutrition. Before
starting the scheduled feeding, it is essential
4. A 25 year-old presents to the ER with the nurse? Select all that apply:
unexplained paralysis from the hips A. Assesses for bowel sounds
downward. The patient explains that a few B. Keeps the head of bed less than 30'
days ago her feet were feeling weird and degrees
she had trouble walking and now she is C. Checks for gastric residual
unable to move her lower extremities. The D. Weighs the patient
patient reports suffering an illness about 2 The answers are A and C. Some patients
weeks ago, but has no other health history. who experience GBS will need a feeding
The physician suspects Guillain-Barré tube because they are no longer able to
Syndrome and orders some diagnostic swallow safely due to paralysis of the
tests. Which finding below during your cranial nerves that help with swallowing.
assessment requires immediate nursing GBS can lead to a decrease in gastric
action? motility and paralytic ileus. Therefore,
A. The patient reports a headache. before starting a scheduled feeding the
B. The patient has a weak cough. nurse should always assess for bowel
sounds and check gastric residual.
6. You’re educating a patient about 8. You're teaching a group of nursing
treatment options for Guillain-Barré students about Guillain-Barré Syndrome
Syndrome. Which statement by the patient and how it can affect the autonomic nervous
requires you to re-educate the patient about system. Which signs and symptoms
treatment? verbalized by the students demonstrate they
A. "Treatments available for this syndrome understood the autonomic involvement of
do not cure the condition but helps speed this syndrome? Select all that apply:
up recovery time." A. Altered body temperature regulation
B. "Plasmapheresis or immunoglobin B. Inability to move facial muscles
therapies are treatment options available for C. Cardiac dysrhythmias
this syndrome but are most effective when D. Orthostatic hypotension
given within 4 weeks of the onset of E. Bladder distension
symptoms." The answers are A, C, D, and E. All these
C. "When I start plasmapheresis treatment are some signs and symptoms that can
a machine will filter my blood to remove the present in severe cases of GBS when the
antibodies from my plasma that are autonomic nervous system is involved.
attacking the myelin sheath."
D. "Immunoglobulin therapy is where IV
immunoglobulin from a donor is given to a 9. You're about to send a patient for a
patient to stop the antibodies that are lumbar puncture to help rule out Guillain-
damaging the nerves. Barré Syndrome. Before sending the patient
The answer is B. This statement is you will have the patient?
incorrect. Plasmapheresis and A. Clean the back with antiseptic
immunoglobin therapies are treatment B. Drink contrast dye
options available for GBS, BUT they are C. Void
only really effective when given within 2 D. Wash their hair
weeks from the onset of symptoms (not 4 The answer is C. The patient will need to
weeks). void and empty the bladder before going for
a LP. This will help decrease the chances of
the bladder becoming punctured during the
7. Which tests below can be ordered to help procedure.
the physician diagnose Guillain-Barré
Syndrome? Select all that apply:
A. Edrophonium Test 10. Your patient is back from having a
B. Sweat Test lumbar puncture. Select all the correct
C. Lumbar puncture nursing interventions for this patient?
D. Electromyography A. Place the patient in lateral recumbent
E. Nerve Conduction Studies position.
The answers are C, D, and E. These are the B. Keep the patient flat.
tests that can be ordered to help the MD C. Remind the patient to refrain from eating
determine if the patient is experiencing or drinking for 4 hours.
GBS.
D. Encourage the patient to consume liquids 11. The patient's lumbar puncture results
regularly. are back. Which finding below correlates
The answers are B and D. The patient will with Guillain-Barré Syndrome?
need to stay flat after the procedure for a A. high glucose with normal white blood
prescribed amount of time to prevent a cells
headache, and the nurse will need to B. high protein with normal white blood cells
encourage the patient to drink fluids C. high protein with low white blood cells
regularly to help replace the fluid lost during D. low protein with high white blood cells
the lumbar puncture. The answer is B.
10. A patient with multiple sclerosis has 12. Which medications below can help treat
issues with completely emptying the muscle spasms in a patient with multiple
bladder. The physician orders the patient to sclerosis? Select all that apply:
take ___________, which will help with A. Propranolol
bladder emptying. B. Isoniazid
A. Bethanechol C. Baclofen
B. Oxybutynin D. Diazepam
C. Avonex E. Modafinil
D. Amantadine The answers are C and D. These
medications treat muscle spasms in patients
with MS.
MYASTHENIA GRAVIS ■ Drooping of the eyes
■ Diplopia/Lazy eyes
DEFINITION ■ Strabismus
● Autoimmune Condition ○ Throat: Another common
● Body attacks the muscle receptors signs
that controls the voluntary muscles ■ Weakens muscle on
Can lead to : throat
● Muscle weakness ■ Dysphasia
Organs Involves: ■ Hoarseness of voice
● Voluntary Muscles: ■ Chewing is an effort
○ Eyes: Most likely 1st signs ○ Arms and Legs
○ Respiratory ○ And they bind with
■ Severe case Nicotinic Acetylcholine
QUICK FACTS receptors {nAChRs}
● This disease is immune related ○ Acetylcholinesterase
● Symptoms Vary {AChE}
○ Because it can affect ■ Enzymes that Break
different Down acetylcholine
RISK FACTORS into two pieces
● This disease is immune related ● It allows the motor neuron to
● Symptoms Var transmit a signal to the muscle fiber,
ANATOMY causing muscle contraction.
● Muscles require innervation to
function—and even just to maintain
muscle tone, avoiding atrophy. In the
neuromuscular system nerves from
the central nervous system and the
peripheral nervous system are linked
and work together with muscles.
PATHOPHYSIOLOGY
● Key player:
○ Neuromuscular Junction
■ Nicotinic
● Key player: Acetylcholine
○ Neuromuscular Junction Receptors
■ Nicotinic ■ Function of Muscle
Acetylcholine Specific Kinase
Receptors ■ Acetylcholine
■ Function of Muscle ■ Immune system
Specific Kinase ● Produces
■ Acetylcholine antibodies
■ Immune system against
● Produces receptors
antibodies ● Thymus gland
against ● The Immune system build up an
receptors antibody that destroys the Nicotinic
● Thymus gland Acetylcholine receptors {nAChRs}
● A neuromuscular junction (or ● Alot of them won’t be available and
myoneural junction) is a chemical working meaning that they are not
synapse between a motor neuron functioning well
and a muscle fiber. ○ They won’t be able to receive
○ Cholinergic fibers initiates the the Acetylcholine
release of acetylcholine ○ Muscle fibers won’t be
contracting like they
should
■ WEAKNESS receptor site of
● Antiacetylcholinesterase are neuromuscular junction
administer ○ Making acetylcholine not
○ Like Pyridosestigmy reaching the tissue site
○ To prevent breakdown ■ To create voluntary
○ So more acetylcholine can contraction
be made available to these SIGNS AND SYMPTOMS
limited receptors ● ****Hallmark:
○ To increase muscle strength ○ Muscle weakness gets worse
● Thymus Gland with activity
○ Location: Anterior at the ■ Especially repetitive
upper part of the body activity
■ Behind the sternum ■ Because the
and between the receptors are very
lungs limited and remaining
○ Provides a very important acetylcholine is very
role on our immune system abundant but can be
and health destroyed later on
○ Creator or T cells when enzyme breaks
■ Fighting against them down
viruses and bacteria ○ But will improve after resting
and cell the muscle
○ This tends to be enlarge at ● “W.E.A.K.N.E.S.S”
children than an adult ○ Weakness of the neck, face,
■ By puberty the arms and legs “hemiplegia”
thymus gland has ○ Eyelid drooping “Ptosis”
usually produce a ○ Appearance mask like
lifelong supply of t ■ Very sleepy
cells that we are expression
going to need ○ Keep on choking/gagging
○ ABut as person ages usually when eating
in the older age the thymus ■ Risk for aspiration
gland will actually turn into ○ No Energy
fatty tissue ■ Do it in the morning
● People with Myasthenia Gravis the when they have
thymus gland is still enlarge enough rest
○ They are not small like they ■ When patient has
should be more energy to do
○ They have tumors stuff
○ A Lot of immune cell has ○ Extraocular Muscle
congregate together Involvement
○ The thymus is actually ■ Strabismus
erroneously creating this ■ Diplopia
antibodies to attracts the ○ Slurred speech
Shortness of breath
○ the receptors and
COMPLICATION wear them out
● Myasthenic Crisis ■ This will result a
○ Disease can go to remission decrease in the
{no signs and number of nicotinic
symptoms1]BUT can Acetylcholine
experience acute receptors available
exacerbation ■ They can be tolerant
■ THIS occurs because ○ Severe muscle weakness
they are not receiving and respiratory depression
acetylcholine like they ○ Making Acetylcholine
should abundant in the synapses
● Because LABORATORY AND DIAGNOSTIC
Cholinesteras PROCEDURE
e an enzyme ● Tensilon Test
will ○ A medication Edrophonium
continuously is given
breakdown ○ Used to diagnose and
acetylcholine differentiate myasthenic and
● Making cholinergic crisis in
acetylcholine myasthenia gravis
not available ○ It’s an anticholinesterase:
for the ■ Prevents breakdown
receptors acetylcholine more
■ Muscle can’t contract available at
○ Severe muscle weakness neuromuscular
and respiratory failure junction and makes it
■ Need for intubation more available to the
and mechanical site
ventilator Result:
○ Cause? ● Myasthenia gravis or crisis:
■ Not enough ○ They will get better
Anticholinesterase ○ Strength is improved
Medication ● Cholinergic Crisis
■ Stress ○ Strength becomes worst
■ Respiratory infection ○ Weaker
● Frequent use ○ Provide antidote:
of muscle ■ Physostigmine
■ Surgery ■ Atropine
● Cholinergic Crisis: {anticholinergic}
○ Too much medication TREATMENT and MEDICATION
■ Where a lot a ● NO CURE
acetylcholine will ● Anticholinesterase
continuously bombard “Pyridostigmine”
○Take 30 minutes to 1 hours ○ Strength of arms and legs
before meal-peak ● Determine swallowing function
● Complication: Myasthenic Crisis ○ Before eating and
{inadequate medication} and administration of PO
● Complication: Cholinergic Crisis medication
{Too much medication} ● Speech Langage pathologist must
○ Signs and Symptom: Similar be referred to patient
to over stimulation of the ● Always secure safety
parasympathetic system ○ Always assess any risk for
“Rest and digest” fall
■ Bradycardia ■ Weak arms and leg
■ Pupil constriction ■ Low rr-they might
■ Bronchospasm pass out
■ Increase salivation ■ Vission problem
and Mucous ● Aspiration
■ GI: cramping and ○ Speech Pathologist
diarrhea ○ Evaluate swallowing
■ Bladder incontinence ○ During feeding the head over
■ Muscle weakness bed mus be raised at >30
and respiratory failure degree
● Corticosteroid: ● Educating of Eating:
○ To decrease inflammatory ○ Larger meals in the morning
response because they have energy to
● IV immunoglobulins chew
● Plasmapheresis ■ Then small meal later
○ Dialysis in day
○ Blood is filtered and removes ○ Schedule medication 30 mins
antibodies to 1 hour after taking
● Thymectomy anticholinesterase
○ Improves signs and ■ It is the peak time of
symptoms the medication
NURSING INTERVENTION ○ Thicken liquid
● Note improvement, cardiac monitor, ○ Small bites, soft foods
make atropine available, have the ○ Perform most activities in the
crash cart at the bedside morning
● Monitor respiratory status: ■ Ambulating
○ Effort of breathing ■ Leg rolling
○ Respiratory rate ■ And other procedure
○ Suction must be provided to
prevent aspiration Your Grade: A
● Neuromuscular functions Percentage of What you Got Right: 90
○ Assess cranial nerves
○ Vision, sound of voice Go Here for More Quizzes
○ Speech, facial appearance
Your Answers & what you got Right & At what time should you administer this
Wrong: medication so the patient will have the
maximum benefit of this medication?
1. Myasthenia gravis occurs when A. As soon as possible
antibodies attack the __________ receptors B. 1 hour after the patient has eaten (at
at the neuromuscular junction leading to 1300)
____________. C. 1 hour before the patient eats (at 1100)
A. metabotropic; muscle weakness D. at 1200 right before the patient eats
B. nicotinic acetylcholine; muscle weakness The answer is C. Pyridostigmine is an
C. dopaminergic adrenergic; muscle anticholinesterase medication that will help
contraction improve muscle strength. It is important the
D. nicotinic adrenergic; muscle contraction patient has maximum muscle strength while
The answer is B. In myasthenia gravis, eating for the chewing and swallowing
either the nicotinic acetylcholine receptors process. Therefore, the medication should
are attacked by antibodies created by the be given 1 hour before the patient eats
immune system (hence why this disease is because this medication peaks (has the
considered autoimmune) or antibodies are maximum effect) at approximately 1 hour
inhibiting the function of muscle-specific after administration. How does the
kinase (which is a receptor tyrosine kinase medication improve muscle strength? It
that helps with maintaining and building the does this by preventing the breakdown of
neuromuscular junction). Either way this acetylcholine. Remember the nicotinic
leads to the neurotransmitter acetylcholine acetylcholine receptors are damaged and
from being able to communicate with the the patient needs as much acetylcholine as
muscle fiber to make it contract. possible to prevent muscle weakness.
Therefore, this medication will allow more
acetylcholine to be used...hence improving
2. You're educating a patient about the muscle strength.
pathophysiology of myasthenia gravis.
While explaining the involvement of the
thymus gland, the patient asks you where 4. The neurologist is conducting a Tensilon
the thymus gland is located. You state it is test (Edrophonium) at the bedside of a
located? patient who is experiencing unexplained
A. behind the thyroid gland muscle weakness, double vision, difficulty
B. within the adrenal glands breathing, and ptosis. Which findings after
C. behind the sternum in between the lungs the administration of Edrophonium would
D. anterior to the hypothalamus represent the patient has myasthenia
The answer is C. The thymus is located gravis?
anteriorly in the upper part of the chest A. The patient experiences worsening of the
behind the sternum in between the lungs. muscle weakness.
B. The patient experiences wheezing along
with facial flushing.
3. A patient with myasthenia gravis will be C. The patient reports a tingling sensation in
eating lunch at 1200. It is now 1000 and the the eyelids and sudden ringing in the ears.
patient is scheduled to take Pyridostigmine.
D. The patient experiences improved The answer is D. Remember patients who
muscle strength. experience a cholinergic crisis are most
The answer is D. During a Tensilon test likely to because they’ve received too much
Edrophonium is administered. This of their anticholinesterase medications
medication prevents the breakdown of (example Pyridostigmine). However, on the
acetylcholine, which will allow more of the other hand, patients who have received
neurotransmitter acetylcholine to be present insufficient amount of their
at the neuromuscular junction....hence anticholinesterase medication or have
IMPROVING muscle strength IF myasthenia experienced an illness/stress/surgery are
gravis is present. Therefore, if a patient with most likely to experience a myasthenia
MG is given this medication they will have crisis. Both conditions will lead to muscle
improved muscle strength. weakness and respiratory failure but from
different causes, which is why a Tensilon
test is used to help differentiate between the
5. You're preparing to help the neurologist two conditions.
with conducting a Tensilon test. Which
antidote will you have on hand in case of an
emergency? 7. Which meal option would be the most
A. Atropine appropriate for a patient with myasthenia
B. Protamine sulfate gravis?
C. Narcan A. Roasted potatoes and cubed steak
D. Leucovorin B. Hamburger with baked fries
The answer is A. Atropine will help reverse C. Clam chowder with mashed potatoes
the effects of the drug given during a D. Fresh veggie tray with sliced cheese
Tensilon test, which is Edrophonium, in cubes
case an emergency arises. Edrophonium is The answer is C. Patients with MG have
a short-acting cholinergic drug, while weak muscles and this can include the
atropine is an anticholinergic. muscles that are used for chewing and
swallowing. The patient should choose meal
options that require the least amount of
6. Which patient below is MOST at risk for chewing and that are easy to swallow.
developing a cholinergic crisis? Option C is a thick type of soup and the
A. A patient with myasthenia gravis is who mashed potatoes are soft....both are very
is not receiving sufficient amounts of their easy to eat and swallow compared to the
anticholinesterase medication. other options.
B. A patient with myasthenia gravis who
reports not taking the medication
Pyridostigmine for 2 weeks. 8. Select all the signs and symptoms below
C. A patient with myasthenia gravis who is that can present in myasthenia gravis:
experiencing a respiratory infection and A. Respiratory failure
recently had left hip surgery. B. Increased salivation
D. A patient with myasthenia gravis who C. Diplopia
reports taking too much of their D. Ptosis
anticholinesterase medication. E. Slurred speech
F. Restlessness
G. Mask-like appearance of looking sleepy 10. You're a home health nurse providing
H. Difficulty swallowing care to a patient with myasthenia gravis.
The answers are A, C, D, E, F (restlessness Today you plan on helping the patient with
from hypoxia, which is experienced with bathing and exercising. When would be the
respiratory failure), G, and H. best time to visit the patient to help these
tasks?
A. Mid-afternoon
9. You're providing teaching to a group of B. Morning
patients with myasthenia gravis. Which of C. Evening
the following is not a treatment option for D. Before bedtime
this condition? The answer is B. Patients with MG tend to
A. Plasmapheresis have the best muscle strength in the
B. Cholinesterase medications morning after sleeping or resting rather than
C. Thymectomy at the end of the day....the muscles are tired
D. Corticosteroids from being used and the muscle become
The answer is B. These medications are not weaker as the day progresses etc.
used to treat MG, but ANTIcholinesterase Therefore any rigorous activities are best
medications (like Pyridostigmine) are used performed in the morning or after the patient
to treat this condition. has rested.
● Medication ● Medication
Edrophonium= Edrophoniu
Anticholinester m=Anticholi 3. A patient is experiencing unexplained
ase nesterase muscle weakness and respiratory failure.
Medication Medication The neurologist conducts a Tensilon test to
Adds More ACh at the Adding more ACh differentiate between myasthenic crisis or
junction at the junction- cholinergic crisis. During the test the patient
experiences improved muscle strength.
Improvement of Worsening of
Based on this finding the patient has:
signs and symptoms signs and
symptoms A. Myasthenic Crisis
Positive test result B. Cholinergic Crisis
Negative test C. Neither
Treatment per MD result The answer is A. During a Tensilon test the
Order medication Edrophonium is given, which is
Anticholinesterase Treatment: an cholinesterase medication. This will
Antidote Atropine
increase the availability of acetylcholine at
hold further dose
the neuromuscular junction. If the patient
had a cholinergic crisis the problem is not
our Grade: D with the availability of acetylcholine, but
Percentage of What you Got Right: 67
because there is TOO MUCH of it at the E. Negative gag or cough reflex
receptor site. Therefore, during this test the F. Respiratory failure
patient would experience worsening of G. Bradycardia
symptoms NOT improvement. The answers are A, D, E, and F.
4. You're examining a patient’s health 7. During a Tensilon test the patient has
history and find that the patient experienced worsening of muscle weakness. The nurse
a cholinergic crisis last year. As the nurse anticipates that the physician will give the
you know that the most common cause of a following order?
cholinergic crisis is? A. Administer Atropine along with an
A. Over usage of adrenergic blocker anticholinesterase medication.
medications B. Administer Atropine and hold any further
B. Stress doses of Pyridostigmine.
C. Respiratory infections C. Administer Pyridostigmine and hold
D. Overmedication of an anticholinesterase Atropine.
medication D. Administer Edrophonium along with
The answer is D. The most common cause Atropine.
of a cholinergic crisis is overmedication of The answer is B. If a patient experiences
an anticholinesterase medication. However, worsening of muscle weakness during a
on the other hand, the cause of a Tensilon test the patient has cholinergic
myasthenic crisis is NOT enough of an crisis. Therefore, the nurse could anticipate
anticholinesterase medication or having a that the physician will order Atropine (to
respiratory infection or experiencing stress reverse the signs and symptoms...because
of some type. remember this drug is the antidote for
Edrophonium which is given during the test)
and to HOLD any further doses of
5. While assisting with a Tensilon test you Pyridostigmine (this is an anticholinesterase
will have what antidote on hand? drug).
A. Narcan
B. Atropine
C. Flumazenil 8. Select all the signs and symptoms
D. Glucagon associated with cholinergic crisis:
The answer is B. Atropine is the antidote for A. Miosis
Edrophonium, which is given during a B. Dry mouth
Tensilon test. C. Blurred vision
D. Constipation
E. Muscle fasciculation
6. Select all the signs and symptoms F. Diarrhea and abdominal cramping
associated with a myasthenic crisis: G. Respiratory failure
A. Pupil dilation The answers are A, C, E, F, and G.
B. Muscle fasciculation
C. Miosis
D. Bowel and bladder incontinence
9. You're patient is recovering from a PARKINSON'S DISEASED SYMPTOMS
myasthenic crisis and you are providing
education to the patient about the causes of
this condition. Which statement by the DEFINITION:
patient demonstrates they understood the ● Its is a neurological disease that
teaching about how to prevent this affects the movement
condition? ● Dopaminergic Neurons DIE in
A. "I will make sure I don't take too much of substantia nigra
my anticholinesterase medication because it ○ Location of Substantia Nigra
can lead to this condition." ○ This area is part of the Basal
B. "I will avoid milk products while taking ganglia which is a part of part
Pyridostigmine because it increases the of the MidBrain that overall
chances of toxicity." plays a huge role in our
C. "I will avoid taking over-the-counter movement
supplements that contain aconite." ● The substantia Nigra is black
D. "I will avoid people who are sick with ○ Dopaminergic Neurons is the
respiratory infections and be sure not to part of the brain called
miss my scheduled doses of Substantia Nigra has started
Pyridostigmine." to die
The answer is D. Myasthenic crisis is ■ They release
caused by not enough anticholinesterase Dopamine
medication (pyridostigmine) or respiratory {neurotransmitter}
infection/stress etc. The other options are ● Leading to: Less Dopamine
NOT causes of this condition. ○ Dopamine provides us an
accuracy with MOVEMENT
● The receptors are find and waiting
for the Dopamine to come
○ It involves Hands, legs, lips,
tongue
○ *Pill-Rolling*-tremors of the
finger and hand
■ Improves with
purposeful movement
● Stiffness of the extremities
○ Arms Don’t swing with gait
● Akinesia
○ Lose the ability to do
RISK FACTORS movement voluntarily
● Tends of Affects Older adults 60+ ○ Example when they’re
● Cause is Unknown walking they tend to freeze
ANATOMY up
● Dopamine provides us an ○ No voluntary movement of
accuracy with Muscle
● MOVEMENTBalance Between ■ Freeze up
○ ACh {Excitatory} ● Shuffling of gait
■ This causes ○ They won’t be able to pick up
cholinergic activity their feel very well
○ Dopamine {Inhibitory} ● Posture
What Happen when Dopamine is Less ○ Forward bent
● There is an imbalances between ● Cogwheel Rigidity
ACh and Dopamine ○ muscular rigidity in which
○ Causing Overstimulation of passive movement of the
neurons ACh to produce a limbs (as during a physical
cholinergic action: examination) elicits ratchet-
Tremors, Rigidity, etc like start-and stop
Medication involves: movements through the
● Administration of Anticholinergic range of motion of a joint (as
Medication of the elbow) and that occurs
○ Younger people are especially in individuals
common users of this affected with Parkinson's
medication disease The third major sign,
PATHOPHYSIOLOGY rigidity (sometimes called
● "cogwheel" rigidity ), is
SIGNS AND SYMPTOMS: peculiar to Parkinson's
● Subtle at 1st but it may VARY ○ The hands will just jerk back
● But as time goes on as you move them
○ May worsen-they will realize ● Bradykinesia:
the problems in movement ○ Movement is Slow
○ It may affect one side of the ○ Swallowing issue: drooling
extremities and progresses ○ Expressionless face “mask
● Tremors at Rest: like”
○ Most common
○ Chewing issue ■ Take up to 3 weeks to
○ Speech is slowed and notice decrease signs
slurred and symptoms
● Compensation for that ■ Body fluids turn dark
○ Coordination problems- color
steap to compensate ■ Long term use “weak
● Non Motor off” before next dose
○ Loss of smell ● COMT
○ Constipation inhibitors:
○ Depression Entacapone
“Comtan”
■ Entacopanoe
● Not be taken
with MAOIs
■ NO High vitamin B6
can decrease the
effects
■ Not taking food with
HIGH protein
● They compete
in the small
LABORATORY AND DIAGNOSTIC intestine
TESTING: ● Ropinirole “Requip”
● ○ Stimulates dopamine
TREATMENT receptors to increase
● There is NO CURE improvement
● But medication can be given to ○ Side Effects:
decrease the signs and symptoms ■ Drowsiness
MEDICATION ○ They might abruptly sleep
● Carbidopa with Levodopa ● Amantadine:
“sinemet” ○ Antiviral in treatment of
○ Adds more dopamine to influenza A
brain ○ Stimulates dopamine in CNS
○ Carbidopa: prevents ● Anticholinergic
levodopa from breaking ○ Benztropine “Cogentin”
down in the blood more ○ Blocks ACh
enters in the brain and turn ■ Decrease rigidity
into dopamine ■ Decrease salivation
○ Side Effects ■ Decrease signs and
■ Nausea and symptoms
involuntary movement ○ Not for glaucoma patient
○ Patient education: ○ Don't Abruptly quit
○ NO ETOH
○ They will experience Dry ○ They can use Rubber tip
mouth cane single point
● MAO inhibitors Type B ● Shoes ware: Low heel shoes without
● Rasagiline “Azilect” rubber sole
● Increase dopamine by ○ The rubber sole can stick to
stopping MAO activity the floor and end up tripping
● NO FOODS with Tyramine
○ Aged cheese Education: Freeze up
○ Smoked/cured meats ● When they are normally walking
○ Fermented food and suddenly their foot is stuck
○ Beers on the ground, can lead to
increase risk for fall
● COMT “Catechol-O- ○ Change Direction of
methyltransferase” movement
○ Used with Sinemet ■ As you move forward
○ It can decrease wearing off you’re foot suddenly
phase stops
○ Block COMT enzyme that will ■ Try to move to the
breakdown Levodopa in the side
blood to make it last longer ○ Laser patient cane or walker
NURSING INTERVENTION ○ Ass they walk and Freeze up
Areas of Intervention: happen
● Safety ■ They must
○ Cogwheel consciously make an
○ Freeze Up effort to Lift legs off
● Psychosocial the floor walking like
○ Depression their marching
○ Loss of Self Care ○ Don’t try to push through it
○ Loss of autonomy Psychosocial Part
● Medication side effects ● Autonomy problem
○ Mediation ○ Make sure that you allow
● Digestion and nutrition them to take care of
○ Constipation themselves-like feeding,
● Education dressing and etc
● Special cookware and utensils
Safety: ● Dressings: Shirt without buttons and
● Assistive Devices zipper
○ Hand rail ○ Velcros
○ Cane, walkers, ● Shoes without tie
○ Keeping rubs off the floor ○ Velcros shoes
○ Pets must be trained ● Support groups
● Balance: More slowly with position ● Exercise
changes ● Don’t try to stress them up
○ Hurrying them and etc
○ This can increase Signs and has tremors. Select the option
symptoms and might that is INCORRECT about
exacerbate symptoms tremors experienced in this
Digestion/Nutrition disease:*
● Soft easy to chew foods ○ A. The tremors are most likely
● Speech language Pathologist to occur with purposeful
● High fiber foods and 2 liter of water movements.
● Stool softer ○ B. A common term used to
● Always assess digestion describe the tremors in the
● Watch protein rich foods with hands and fingers is called
medication "pill-rolling".
○ They will compete with the ○ C. Tremors are one of the
medications most common signs and
symptoms in Parkinson's
Parkinson's Disease Disease.
○ D. Tremors in this disease can
NCLEX Questions
occur in the hands, fingers,
arms, legs and even the lips
This quiz will test your knowledge on and tongue.
Parkinson's Disease in preparation for 4. While assessing a patient
the NCLEX exam. with Parkinson's Disease, you
note the patient's arms slightly
jerk as you passively move
1. As the nurse you know that them toward the patient's
Parkinson's Disease tends to body. This is known as:*
affect the _____________ of the ○ A. Lead Pipe Rigidity
midbrain, which leads to the
○ B. Cogwheel Rigidity
depletion of the
neurotransmitter ○ C. Pronate Rigidity
________________.* ○ D. Flexor Rigidity
○ A. red nucleus, acetylcholine 5. A patient with Parkinson's
○ B. leminisci, norepinephrine Disease has slow movements
○ C. substantia nigra, dopamine that affects their swallowing,
facial expressions, and ability
○ D. tectum nigra, dopamine
to coordinate movements. As
2. True or False: Parkinson's the nurse you will document
Disease most commonly the patient has:*
affects patients in young ○ A. Akinesia
adulthood, and there is
○ B. "Freeze up" tremors
currently no cure for the
disease.* ○ C. Bradykinesia
○ A. True ○ D. Pill-rolling
○ B. False 6. You're providing free
3. You're caring for a patient education to a local community
with Parkinson's Disease that group about the signs and
symptoms of Parkinson's
Disease. Select all the signs 9. As the home health nurse
and symptoms a patient could you are helping a patient with
experience with this disease:* Parkinson's Disease get
○ A. Increased Salivation dressed. What item gathered
○ B. Loss of smell by the patient to wear should
○ C. Constipation NOT be worn?*
○ A. Velcro pants
○ D. Tremors with purposeful
○ B. Pull over sweatshirt
movement
○ E. Shuffling of gait ○ C. Non-slip socks
○ F. Freezing of extremities ○ D. Rubber sole shoes
○ G. Euphoria 10. A spouse of a husband who
has Parkinson's Disease
○ H. Coordination issues explains to you that her
7. You're providing diet husband experiences episodes
education to a patient with while walking where he freezes
Parkinson's Disease. Which and can't move. She asks what
statement below demonstrates can be done to help with these
the patient understood your types of episodes to prevent
teaching? Select all that injury. Select all the options
apply:* that are correct:*
○ A. "I will limit foods high in ○ A. Have the husband try to
fiber like fruits and vegetables change direction of movement
in my diet." by moving in the opposite
○ B. "I will be sure to drink 2 direction when the freeze ups
Liter of fluid per day." occur.
○ C. "It is very common for me ○ B. Use a cane with a laser
to experience diarrhea with point while walking.
this disease." ○ C. Have the husband try to
○ D. "I will avoid taking push through the freeze ups.
Carbidopa/Levodopa with a ○ D. Encourage the husband to
protein rich meal." consciously lift the legs while
8. A patient with Parkinson walking (as with marching).
Disease is experiencing weight 11. A patient is prescribed to
loss due to difficulty chewing take Carbidopa/Levodopa
and swallowing. Which meal (Sinemet). As the nurse you
option below is the best for know that which statement is
this patient?* incorrect about this
○ A. Scrambled eggs with a side medication:*
of cottage cheese ○ A. It can take up to 3 weeks
○ B. Grilled cheese with apple for the patient to notice a
slices decrease in signs and
○ C. Baked chicken with bacon symptoms when beginning
slices treatment with this medication.
○ D. Tacos with refried beans
○ B. Body fluids can turn a dark the patient about what side
color and stain clothes. effect?*
○ C. This medication is most ○ A. Drowsiness
commonly prescribed with a ○ B. Dry mouth
vitamin B6 supplement. ○ C. Coughing
○ D. Carbidopa helps to prevent ○ D. Dark sweat or saliva
Levodopa from being broken 14. A physician orders a
down in the blood before it patient to take Benztropine
enters the brain. Hence, (Cogentin). The patient has
levodopa is able to enter the never taken this medication
brain. before and is due to take the
12. You're patient with first dose at 1000. What
Parkinson's Disease has been statement by the patient
taking Carbidopa/Levodopa for requires you to hold the dose
several years. The patient and notify the physician?*
reports that his signs and ○ A. "I forgot to tell the doctor I
symptoms actually become take eye drops for my
worse before the next dose of glaucoma."
medication is due. As the ○ B. "I had a PET scan last
nurse, you know what week."
medication can be prescribed ○ C. "I take aspirin once day."
with this medication to help
○ D. "My hands are experiencing
decrease this for happening?*
○ A. Anticholinergic tremors at rest."
(Benztropine) 15. A patient is taking
Rasagiline "Azilect" for
○ B. Dopamine agonists
treatment of Parkinson's
(Ropinirole)
Disease. What foods do the
○ C. COMT Inhibitor patient want to limit in their
(Entacapone) diet? Select all that apply:*
○ D: Beta blockers (Metoprolol) ○ A. Liver
13. While providing discharge ○ B. Aged Cheese
teaching to a patient ○ C. Sweetbread
prescribed Ropinirole (Requip),
○ D. Beer
you make it priority to teach
○ E. Fermented foods
○ F. Shellfish
RISK FACTOR
ANATOMY
CAUSE:
● Throbbing Headache
○ Due to increase blood
pressure
● Hypertension NURSING INTERVENTION
○ Systolic 20-40 mmHg higher
than BASELINE
○ Example 106/78 to 149/92
● P-prevention
● Flushing
○ Think of the 3 Big B’s
○ Above T6 or Above injury ■ Bladder
○ Vasodilation above the injury ■ Bowel
● Pale, cool, clammy ■ Breakdown of Skin
○ Below the T6 or sight of Injury ○ Irritating response must be
eliminated
○ Vasoconstriction below the
injury
● Bradycardia
○ Below 60
● Sweating
● Dilated pupils Bladder {most common cause}
● Stuffy nose
● Anxiety
● Goosebumps ● Keep Bladder EMPTY
● Assess I and O’s
● Routine Bladder Scans
● Prevent UTIs
MEDICAL ● Foley draining
MANAGEMENTS/SURGERY/MEDICATION ○ Determine if its kink or
blocked
● Use anesthetic jelly if need
catheterized
LAST RESORT
It is a MEDICAL EMERGENCY
● Call a rapid response and get
help
Your Answers & what you got Right & 2. Your patient, who has a spinal cord
Wrong: injury at T3, states they are experiencing a
throbbing headache. What is your NEXT
nursing action?
C. A 35-year-old male patient with a spinal The answer is C. This is the nurse's NEXT
cord injury at L6. action. The patient is at risk for developing
autonomic dysreflexia because of their
spinal cord injury at T3 (remember patients
D. A 42-year-old male patient recovering who have a SCI at T6 or higher are at
from a hemorrhagic stroke. MOST risk). If a patient with this type of
injury states they have a headache, the
nurse should NEXT assess the patient's
blood pressure. If it is elevated, the nurse
The answer is B. Patients who are at MOST would take measures to check the bladder
risk for developing autonomic dysreflexia (a bladder issue is the most common
are patients who've experienced a spinal cause of AD), bowel, and skin for
cord injury at T6 or higher...this includes breakdown.
C7. L6 is below T6, and traumatic brain
injury and hemorrhagic stroke does not
increase a patient risk of AD.
3. You're performing a head-to-toe
assessment on a patient with a spinal cord
injury at T6. The patient is restless,
sweaty, and extremely flushed. You assess
the patient's blood pressure and heart rate.
The patient’s blood pressure is 140/98 and
heart rate is 52. You look at the patient's
chart and find that their baseline blood 4. You’re providing an in-service to a
pressure is 106/76 and heart rate is 72. group of new nurse graduates on the
What action should the nurse take FIRST? causes of autonomic dysreflexia. Select all
the most common causes you will discuss
during the in-service:
A. Hypoglycemia
B. Distended bladder
H. Stuffy nose
Origin Midbrain
Function * Eyeball
movement
* Pupil
Cranial Information Movement
Nerve {iris}
*{compression
I-Olfactory of III nerve
Nerves causes
Nature Sensory unilateral pupil
Nerve dilation}
{afferent} *Upper eyelid
Movement mucosa.
{levator * Muscle of
palpebrae} mastication
and sense of
IV-Trochlear lower jaw,
Nerve lower lips,
Nature Motor {efferent} chin, teeth,
hums
Origin Midbrain
Insertion Muscle of
eyeball
{superior
oblique
muscle}
Function * Eyeball
Movement
* Outward VI-Abducens
downward Nerves
Nature Motor
movement {efferent}
Insertion Accessory
Muscle of
Respiration
{Sternocleido
mastoid SCM,
scalene,
trapezius}
Function Neck
movement
CAUSES:
Management:
● Paralysis/weakness of one side
face
○ Caused by damage of lower
● Carbamazepines {Drug of choice} motor neuron of 7th cranial
○ Reduce transmission of nerve {Facial nerve}
impulses ○ Bell’s palsy usually resolves
● Oxcarbazepine on its own within six months
● Nerve Blocks {local anesthetics} ○ Physiotherapy can help
● Radiofrequency/Rhizotomy prevent muscle permanently
○ Resection of nerve roots contracting
● Glycerol injection
○ Demyelinating nerve, effective
for 3 weeks
● Avoid Cold/Hold food and fluids
Characterized by:
Cause:
● Unknown
NEURO
Risk Factors:
CNS PNS
● Diabetes
● Upper respiratory tract infection
● Some viruses Multiple Parkinso Myasthe Amyotro
○ Varicella zoster sclerosis n’s nia phic
○ Epstein Barr Virus Disease Gravis Lateral
○ Herpes zoster
Sclerosi
● Familial Inheritance
s (ALS)
SYMPTOMS:
PATHOPHYSIOLOGY OF CNS DISEASE:
● Facial exercise
Parkinson’s Disease: decrease of amount
○ It is a self limiting disease of DOPE in the PARK
○ It starts to improve generally in ● Less Dopamine
14 days and recovers in 6-15 ● Dopamine Helps Regulates
week ○ BP {when patient gets to a
● Eye Moisturizer
○ Prevent eye dryness
CODE or HYPOTENSION-
● Mouth care and eye care DOPE release to
○ Priority of Nursing care Vasoconstriction}
● Corticosteroid ○ CNS and Ability to Move
○ prednisone ■ They Move slowly
■ Shuffling Gait
● Someone barely learning how to
park a car
○ They walk so slowly, they
Neurological Disorders: Parkinson's, MS, shuffling the feet
MG, ALS ○ Pill Rolling
○ Can get you dead within 5
years
PATHOPHYSIOLOGY OF CNS DISEASE: ● Motor Neurons will get Sclerotic
and can get Stiff
PNS ○ Motor Neurons: Grip, Push,
● They are more on motor function Pull, contract and still
○ You get a prisoner of the
M.G= Disney Waltz Movie Show white body
{Sleepy} was dedicated for his friend that ■ Not dementia
has Myasthenia Gravis ■ No Loss of Sensation
● A disease that inhibits you from a ■ No Irrationality
producing a chemical called ○ You’re just in bed but you
Acetylcholine can’t just move
○ Acetylcholine- help body and ■ Very sad
neuron to contract at the ● 3 D’s of ALS
Myoneural Junction ○ Dysarthria- difficulty moving
○ If lacking it can cause severe ○ Dysphagia-Difficulty
muscle weakness Swallowing
● You have ○ Drooling
○ Ptosis “drooping eyes” ● Can get you killed with a pneumatic
○ Extremely fatigue disease
○ Severe muscle weakness ○ Because even the lung
■ Dysphagia “fail to muscles that helps your lung
swallow perfectly breath starts to fail
■ Aspiration ○ Mech vent is need
Precaution, Airway
issue and
diaphragm issue
■ Not a progressive
disease
● Myasthenia Gravis: Gravity
○ Gravity pulling down your
eyelid
○ Making you very sleepy and
TIIIIIIIRRREDDD
‘
ALS: Amyotrophic Lateral Sclerosis
(ALS).
● This is by far the worst neurological
disease you can get
○ Incurable
○ No remission