Exam 6 Flashcards

(71 cards)

1
Q

This condition is a chronic, progressive, degenerative disorder of the CNS:

A

Multiple sclerosis.

It’s considered an autoimmune disorder.

Onset: typical 20-50 years of age

Women more affected, 2-3xmore

More prevalent in temperate climates (between the tropics and the polar regions), like Colorado and Europe.

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2
Q

The pathophysiology of this disorder is not completely understood but they believe it can be triggered. What are some possible triggers of this condition?

A

Regarding multiple sclerosis:

  • Infection
  • Genetics
  • Smoking
  • Physical injury
  • Emotional stress
  • Excessive fatigue
  • Pregnancy
  • Poor state of health
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3
Q

What are the 3 pathologic processes that characterize multiple sclerosis?

A
  1. Chronic inflammation
  2. Demyelination
  3. Scarring in the CNS (seen as white plaques in the brain)
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4
Q

How does multiple sclerosis generally progress? Where does it start?

A

Starts as damage to the myelin sheath of neurons in the BRAIN and SPINAL CORD… patient may complain of noticeable impairment of function.

Ongoing inflammation leads to the myelin losing its ability to regenerate.

Finally, the nerve impulse is disrupted (bc no myelin)

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5
Q

Motor signs and symptoms of MS:

A
  • Weakness is #1
  • Diplopia (double vision)
  • Scanning speech (the tone/inflection changes during speech)
  • Muscle spasticity
  • Paralysis is when highly progressed.
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6
Q

Sensory signs and symptoms of MS:

A
  • Vision changes are often the 1st sign…
    Patchy blindness
    Blurred vision
  • Vertigo
  • Tinnitus
  • Lhermitte’s sign: an electric shock-like sensation that occurs on flexion of the neck. This sensation radiates down the spine, often into the legs, arms, and sometimes to the trunk.
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7
Q

What are some cerebellar signs and symptoms (such as ataxia)?

Note: there will be a full range of symptoms and full range of severity levels

A
  • Ataxia is the most common: lack of muscle control or coordination of voluntary movements.
  • Nystagmus: eyes make repetitive, uncontrolled movements. These movements often result in reduced vision and depth perception and can affect balance and coordination. These involuntary eye movements can occur from side to side (horizontal), up and down (vertical), or in a circular pattern (tortional).
  • Dysarthria: difficult or unclear articulation of speech
  • Fatigue: maybe don’t have energy to do anything
  • Bowel and bladder dysfunction: spastic, flaccid.
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8
Q

What do we call the difficult or unclear articulation of speech?

A

Dysarthria

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9
Q

What do we call the eye condition of uncontrolled repetitive movements?

A

Nystagmus

Horizontal: side to side
Vertical: up and down
Tortional: circular

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10
Q

What is the most common motor s/s of MS?

A

Weakness

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11
Q

What is often the first s/s of MS

A

Vision

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12
Q

What do we call the electric shock-like sensation that occurs on flexion of the neck?

A

Lhermitte’s sign. (Lar-meets)?

This often radiates down the spine, into the legs/arms and sometimes to the trunk.

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13
Q

Spastic bowel/bladder or flaccid bowel/bladder are s/s of what type of MS s/s and what can it lead to?

A

These are s/s of CEREBELLAR s/s.

These can lead to feelings of urgency or retention/incontinent.

These do not occur until later in the disease.

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14
Q

What are some emotional s/s of MS?

A

Anger

Depression

Euphoria

It can feel like an emotional roller-coaster.

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15
Q

When a patient with MS starts having cognitive s/s, what sorts of things do they begin to struggle with?

A
  • Short-term memory
  • Attention
  • Information processing
  • Planning
  • Visual perception
  • Word finding
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16
Q

How is Multiple Sclerosis characterized?

A
  1. Chronic, progressive deterioration in most
  2. Remissions and exacerbations in some
  3. Progressive deterioration in neurologic function with repeated exacerbations
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17
Q

How is MS diagnosed?

A

There are no definitive diagnostic tests…

Based on Hx, clinical manifestations, and results of certain diagnostic tests…

MRI of brain and spinal cord. This may show the presence of 
plaques
inflammation
atrophy
tissue breakdown
tissue destruction
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18
Q

Cerebellar signs are focal signs found on neurological examination that may indicate a cerebellar lesion. They can be unilateral or bilateral. The main signs can be remembered by the mnemonic DANISH:

A

Dysdiadokinesia & Dysmetria (past pointing)
inability to perform and sustain a series of rapidly alternating muscle movements (typically flipping one hand rapidly in the palm of the other). The patient overshoots when attempting to reach a point with their finger

Ataxia
gross incoordination of muscle movements. The patient may be very unsteady on their feet towards the side of the lesion. The patient may also show rebound, where pushing down on the outstretched upper limb causes it to rebound up past its original position

Nystagmus
a repetitive, involuntary oscillation of the eyes. The patient may also complain of blurred vision

Intention tremor
a wide tremor during voluntary movements, such as holding out the hands

Slurred speech
speech may be imprecise, slow and distorted

Hypotonia
patient may have muscle weakness on the side of the lesion

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19
Q

What is the criteria for a diagnosis of MS?

A
  1. Evidence on the MRI of at least 2 inflammatory demyelinating lesions in at least 2 different locations within the CNS.
  2. Damage or an attack occurring at different times (usu greater than a month apart).

** ALL other potential Dx’s must also be ruled out.

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20
Q

What do we do to slow the progression of MS?

A

Immunomodulators. “- zumab, - imab” ending drugs

These act similar to steroids… weakening the immune system.

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21
Q

What is used to manage exacerbations/relapses?

A

Corticosteroids (- isone endings)

Reminder: corticosteroids are produced in the adrenal cortex

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22
Q

What treatment options are used to manage MS symptoms?

A
  • Muscle relaxants: tx’s spasticity
  • CNS stimulants: for depression/fatigue
  • Anticholinergics: for incontinence
  • TCA’s: for depression and chronic pain
  • Anti-seizure medications: tx’s inflammation, muscle rigidity/spasms
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23
Q

What is the primary purpose of TCA medication?

A

Tricyclic antidepressants are a class of medications that are used primarily as antidepressants.

Off-label uses include: Obsessive compulsive disorder (OCD) and chronic bedwetting. In lower doses, cyclic antidepressants are used to prevent migraines and to treat chronic pain.

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24
Q

What is gabapentin used for?

A

Nerve pain and anticonvulsant…

Tx’s seizures and pain from shingles.

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25
What are some other (besides medication) treatments r/t MS spasticity?
- Surgery (removal of nerve(s) - rarely done) - Dorsal column electrical stimulation: an implanted stimulator in the spine... jolts the nerve to help with pain/spasticity - Intrathecal baclofen pump: more commonly used. Baclofen is a medication that treats muscle spasms.
26
1. Managing the disabling fatigue/quality of life 2. Maximize neuromuscular function 3. Decrease factors that precipitate exacerbations 4. Maintain independence in activities of daily living for as long as possible 5. Optimize psycho-social well-being These are all examples of which kind of management?
Nursing management. 1. CNS stimulants, having rest periods, exercise, and sleeping at night can all help with maintaining a higher quality of life. 2. In order to maximize their neuromuscular function, they need to do everything for themselves, otherwise muscular atrophy occurs 3. Stress is the big factor that precipitates exacerbation. Others include extreme temperatures, infection, and smoking.
27
This disease is from the reduction of neurons that produce dopamine:
Parkinson's Disease - There's a slow down in the initiation and execution of movement (bradykinesia) - There's an increase in muscle tone (rigidity), spasticity. - There's a tremor at rest - There's motor instability: bradykinesia, etc.
28
This disease is more common in men, affects about 2% of people over 60, and the exact cause is unknown:
Parkinson's Disease As many as 15% are younger than 50 yo, the incidence of diagnosis is increases with age...
29
Even thought the exact cause of Parkinson's is unknown, there are still some possible factors such as genetics vs. environment. What are some of these?
Family hx Exposure to toxins may trigger the dz (pesticides) Drug-induced parkinsonism: Haldol (antipsychotic/dopamine antagonist), Reglan (GERD/dopamine antagonist), meth (boosts dopamine... uses it up???)
30
What do we call the clump of proteins that aggregate inside the brain's nerve cells? The clump of dark matter (from melanin) that produce dopamine?
Lewy bodies. Substantia nigra ("black substance")
31
What does a PET scan show?
Metabolic activity. In Parkinson's there is a massive decrease in brain metabolic activity.
32
What is the classic triad of Parkinson's disease?
1. Tremor 2. Rigidity 3. Bradykinesia
33
What do we call the Parkinsonian gait exhibited by a hunched-forward posture?
Fenestration
34
What do we call the force that contributes to loss of balance in a backwards or posterior direction in Parkinson's?
Retropulsion. Retropulsion occurs due to a worsening of postural stability and an associated loss of postural reflexes.
35
What do we call the type of gait that is exhibited as a shuffling of feet and very short stride?
Parkinsonian gait. Includes a reduced arm movement.
36
What are some non-motor s/s of PD?
- Depression - Anxiety - Fatigue - Pain - Constipation - Insomnia (also could be from meds - keep in mind) - Short-term memory loss
37
Complications increase as PD progresses. Dementia occurs in 70% of patients... what are some other complications?
- Motor symptoms (falls, aspiration) - Weakness - Akinesia (no movement: leads to pneumonia, UTI's, skin breakdown and DVTs) - Neurologic problems - Neuropsychiatric problems
38
What complications can occur from dysphagia? (Parkinson's complication)
- Aspiration | - Malnutrition
39
What complications can occur from orthostatic hypotension? (Parkinson's complication)
* Falls * Injuries r/t dizziness and syncope May be from possible medications.
40
What are some diagnostic tests for Parkinson's disease?
* There are no specific tests Dx is made with Hx and clinical manifestations: - Firm dx can be made with at least 2 of 3 characteristics of the classic triad (tremors, rigidity, bradykinesia) - Confirmed dx is made with positive response to anti-parkinsonian medications.
41
How do we treat Parkinson's dz?
1. Drugs: Sinemet (carbidopa-levodopa) 2. Surgery: goal is to relieve symptoms or for those who don't respond to other treatment. 3. Deep brain stimulation, Ablation: this treats spasticity and rigidity.
42
What brain therapy is used to treat spasticity and rigidity?
Deep brain stimulation. This looks like a meat thermometer in the brain hooked up to a pulse generator down by the clavicle.
43
Nursing management may include: Maintaining nutrition Encouraging independence Increasing physical exercise Keeping safe and preventing falls
Ways to keep safe: ``` Getting rid of clutter Good lighting Bathroom aides (high toilet seat) O2 tubing Dementia concerns ``` May be challenging with dysphagia... maybe smaller more frequent meals, speech therapy, and soft foods.
44
What is the cardinal sign for myasthenia gravis?
Ptosis - a droopy eyelid
45
This condition is caused by antibodies attacking the acetylcholine receptors:
Myasthenia gravis. This condition prevents muscles from contracting. This occurs in men and women equally.
46
What can precipitate myasthenia gravis?
- Stress - Illness - Trauma - Temperature extremes - Pregnancy These are all the same triggers for MS too.
47
What are myasthenia gravis complications related to with this disease?
They are related to the weakness in muscles affecting their swallowing and breathing. Aspiration Pneumonia
48
What do we call a droopy eyelid?
Ptosis (TOE-sis)
49
This is a rare and progressive loss of motor neurons. Life expectancy is 2-6 years after dx:
Amyotrophic Lateral Sclerosis (ALS) aka Lou Gehrig's disease after the baseball player who succumbed to it.
50
Is ALS more common in men or women?
Men. No cure. Meds are given to slow progression.
51
What is the pathophysiology of Amyotrophic Lateral Sclerosis?
“amyotrophy” referring to the atrophy of muscle fibers, which are denervated as their corresponding anterior horn cells degenerate. These motor neurons are essentially "dead" and are unable to send signals.
52
What are some common symptoms of ALS?
- Limb weakness - Dysarthria: difficulty speaking - Dysphagia: difficulty swallowing. Aspiration.
53
This disease is a genetic autosomal dominant gene that results in chorea:
Huntington's disease (HD) Movements are excessive and involuntary (chorea). Chewing, swallowing and walking are severely impacted.
54
What is the life expectancy of Huntington's after diagnosis?
10 - 20 years * No cure. * Continued progression of worsening symptoms, cerebrum looks like it's atrophying. ** Patients suffer from severe depression -- high rate of suicide
55
What are some diagnostic studies given for acute neurologic conditions?
* Common: Lumbar puncture to check CSF (infection, etc) * Xrays for fractures * Used a lot: Computed Tomography (CT) - 3D images * Magnetic Resonance Imaging - soft tissue * Magnetic Resonance Angiography (MRA) - arteries/ blood flow (more for stroke) * Positron Emission Tomography (PET) - metabolic activity of the brain * Electroencephalography (EEG) - measure electrical activity.
56
Normal CSF values... Specific gravity: pH: RBCs: Presence of microorganisms:
specific gravity: 1.007 pH: 7.35 RBC's: none microorganisms: none
57
Normal CSF values... Pressure: Appearance: WBCs: Protein range: Glucose range:
Pressure: 60-150 mm H2O Appearance: Clear, odorless WBCs: 0-5 cells Protein: 15-50 mg/dL Glucose: 40 - 70 mg/dL
58
Hydrostatic force that is measured in the ventricles, subarachnoid space, epidural space, or brain tissue is commonly referred to as:
Intracranial pressure (ICP) This remains in constant balance despite changes in the body.
59
What is the normal ICP range?
5-15 mm Hg
60
What are some compensatory mechanisms that the body does to keep ICP in normal range?
1. CSF volume (absorb, produce, displace) 2. Blood volume (vasoconstriction, dilation) 3. Brain tissue (distention of dura, compression of brain tissue)
61
Our brain auto regulates blood pressure to ensure constant blood flow to meet the metabolic needs of the brain and to maintain perfusion. How is this measured?
CPP: Cerebral Perfusion Pressure CPP = MAP - ICP Normal CPP = 60 - 100 mm Hg
62
At what MAP does the cerebral blood flow begin to decrease?
Below 70 mm Hg you may begin to see signs of ischemia such as: Syncope Blurred vision
63
At what MAP do the blood vessels vasoconstrict to their maximum capability?
MAP above 150 mm Hg
64
If the CPP is less than 50, what are we concerned about?
Ischemia and neuronal death
65
If the CPP is less than 30 what are we concerned about?
Death. This perfusion pressure is incompatible with life.
66
Why is increased intracranial pressure a life-threatening condition?
It obstructs circulation to the brain, Absorption of CSF, Compresses nerves, Compresses the brainstem (respiratory center in the pons and medulla oblangata is located)
67
What is hydrocephalus?
Too much CSF. Often receive a shunt to drain off excess fluid.
68
What does an increased CO2 do to your blood volume?
Causes a vasodilation which would decrease blood volume but increase blood flow from the HR increasing to compensate.
69
First comes trauma or injury. This causes edema/swelling to injured tissues. This increased mass of tissue leads to an increase in intracranial pressure (ICP). D/T this ICP, the ventricles and blood vessels are compressed, leading to a decreased cerebral blood flow and decrease in oxygen delivery. What happens next?
This causes further swelling and edema which then leads to the compression of the brainstem and herniation into the brainstem. Pathophysiology of Increased Intracranial Pressure (IICP)
70
The following are potential clinical manifestations of what condition? * Change in LOC (lethargic to flattened affect to coma) * Vital sign changes - Cushing's triad * Ocular changes - fixed, unilateral, dilation, ptosis
Intracranial Pressure Also may show: * HA that is worse in the am and continuous * Projectile vomiting w/no warning * Seizures (d/t the connections are out of whack)
71
Irregular respirations Bradycardia Systolic hypertension (widening between systolic and diastolic BP's) Are the trifecta for which ICP condition?
Cushing's Triad Late sign of ICP, brainstem herniation is imminent.