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Patient #5: Andrew Patient #5: Andrew

Patient #5: Andrew - PowerPoint Presentation

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Uploaded On 2016-07-15

Patient #5: Andrew - PPT Presentation

Ashton Crowe Rayvin Ewers Miranda McCormick Andrews Case Andrew a 45 yearold single father of two comes to you in confidence Hes noticed that the muscles in his hands and feet have gotten progressively weaker lately and from time to time he sees these muscles twitch He used to l ID: 405078

muscles als andrew therapist als muscles therapist andrew speech diagnosis time symptoms disease neurons trouble ability brain physical motor

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Presentation Transcript

Slide1

Patient #5: Andrew

Ashton Crowe

Rayvin

Ewers

Miranda McCormickSlide2

Andrew’s Case

Andrew, a 45 year-old single father of two, comes to you in confidence. He’s noticed that the muscles in his hands and feet have gotten progressively weaker lately, and from time to time, he sees these muscles twitch. He used to lift weights at the gym quite a bit, but he now has trouble lifting the bar. His daughter noticed that he seems to be tripping and stumbling quite often and commented that it took him quite a long time to get the key in the door the other day. Andrew claims that mentally he feels fine, but it’s almost like his muscles are slowly giving out on him. You don’t see any twitches going on right now, but you are having a hard time hearing him. He seems to be having trouble projecting his voice and his speech is slightly slurred at timesSlide3

Signs of Disease

Hands and feet muscles are getting weaker and sometimes twitch

Used to work out, but now he has trouble lifting the bar

Has been tripping and stumbling

Had trouble putting the key in the door

Muscles are slowly giving out on him

Trouble projecting his voice

Heard slightly slurring his wordsSlide4

symptoms

Weakening of hand and feet muscles

Muscle twitching

Trouble lifting heavy things

Tripping and stumbling

Bad coordination

Trouble projecting his voice

Slurred speechSlide5

Differential Diagnosis

There was an option that he may have a brain tumor in the frontal lobe. This was ruled out because usually, when there is a brain tumor in the frontal lobe, there is usually behavioral changes along with other symptoms.

There was also an option for tremors. This diagnosis was ruled out because in this case, there would be many tremors in many parts of the body and that is unusual.

Our last differential diagnosis was Rhabdomyolysis. This was ruled out because it only affects the muscles such as in the hands or feet, it usually doesn’t affect speech.Slide6

Accurate Diagnosis

The accurate diagnosis for Andrew is Amyotrophic Lateral Sclerosis (ALS)/ Lou Gehrig’s Disease. His feelings of weakness, tripping and stumbling, and slurred speech led us to this diagnosis.

ALS can have many symptoms. For most people, muscle weakness and muscle twitching are the first signs. For more progressed diagnoses, slurred speech can be a symptom.

With symptoms most like other ALS cases, ALS was the most accurate diagnosis

.Slide7

Example of Symptoms Video

https://

www.youtube.com/watch?v=uDAKAPR-b1E

(1:47-2:08)Slide8

Test to Determine Diagnosis

Electromyogram (EMG)

During this test, a doctor inserts a needle electrode through your skin. It tests the electrical activity in your muscles when they are contracted and at rest. If electrical activity is low, it can be used to diagnose ALS.

Magnetic resonance imaging (MRI

)

Uses radio waves and a powerful magnetic field to produce detailed images of your brain and spinal cord. This can be used to eliminate other factors that may be causing the symptoms.

Nerve Conduction Study

This study measures your nerves' ability to send impulses to muscles in different areas of your

body. This study can be used to determine nerve damage or muscle diseases.Slide9

Errors in Communication

In ALS, the immune system damage the axon and dendrites of motor neurons. This will ultimately destroy the neurons ability to transport messages from one neuron to another. This can be dangerous because eventually, messages can no longer be sent from the brain because of damage to motor neurons.Slide10
Slide11

What is the cause

Although the true cause is unknown there are many theories as to how the motor neurons are damaged, such as during the process of RNA there is a protein that becomes a mutation due to an incorrect amino acid. This mutation then leads to the shriveling and degeneration of the motor neurons. Other believed

causes are genetic

mutation (inherited

from a

parents), chemical

in

balance (normally have higher levels of glutamate, a liquid surrounding the brain and nerve cells, that can be toxic if too much is present), or disorganized immune system (attacks the body’s own nerve cells, or any cell in general).Slide12
Slide13
Slide14
Slide15

Prognosis

Many people with ALS die of respiratory failure within 3-5 years of being diagnosed.

Individuals have increasing problems with moving, swallowing, and speaking/forming words.

Eventually people with ALS will no longer be able to stand or walk, get in or out of bed, or use their hands and arms.

In the later stages of this disease certain individuals will have difficulty breathing due to the muscles of the respiratory system weakening.

10% of individuals may be able to survive 10 or more years.Slide16

treatment

There is no cure

There is a drug known as

R

iluzole

and it is the only drug for ALS that is FDA approved. It can prolong life for about 2-3 months. It does not relieve the symptoms though.

NeuRx

Diaphragm Pacing System uses implanted electrodes and a battery pack to cause the diaphragm to contract. It can work for about 16 months before the onset of severe respiratory failure. This is also FDA approved.Drugs are available for spasticity, pain, panic attacks, and depression.

Physical Therapy, Occupational Therapy, and rehabilitation may help with joint immobility.

Some patients may agree to forms of mechanical ventilations. Slide17

Where it all started

Lou Gehrig was a baseball player in the 1920s-1930s who was diagnosed with ALS and brought a lot of light on the disease. He played major league baseball for over 13 years of his life on first base for the New York Yankees. He became very popular and competed against Babe Ruth for major titles. Lou was also given a spot in the hall of fame. He was first diagnosed with a bladder condition, but the treatment only made him weaker. This lead the doctors to ALS, or later called Lou Gehrig’s Disease.Slide18
Slide19

Caretaker

Andrew will need may need a caretaker in the later stages of ALS. This caretaker may help with feeding him and helping him perform every day activities. Also, he may need breathing care.Slide20

Physical therapist

A physical therapist can help him with exercising muscles to help prolong muscle

function. Andrew will only need a physical therapist for the time that he can use his muscles. Once he loses all ability to move his muscles, he will not need a physical therapist any longer.Slide21

Occupational therapist

An occupational therapist may help Andrew perform everyday activities for a longer amount of time

. Over time, the need of an occupational therapist will be less and less because he will eventually lose all ability to perform all every day activities.Slide22

Speech therapist

A

speech therapist can help with the communication abilities of Andrew over

time. He will eventually not need a speech therapist once his speech ability is lost.Slide23

Psychiatrist

Andrew may need psychological and social support to help deal with the understanding and acceptance of his disease

.Slide24

Social Worker

A social worker may be needed to help decide who Andrew’s children will go after his passing. This can help with some of the psychological stress of Andrew and his children.Slide25

ALS Story

www.Youtube.com/watch?v=hNISt4fja9U