week 10 : mobility Flashcards
issue of mobility what could be the reason/cause ?
genetic ( inherited ) e.g duchenne muscular dystrophy
demyelination of nerve fibers
degeneration of neurons in brain
true or false. issue of mobility: one of them being is degeneration of motor neurons and injury to the bone
true
injury to spinal cord ( vertebra or edema pushing on cord ) is also seen as an issue of mobility
yes this is true
what else can bring an issue of mobility ?
impact on the pt ( mind and body ) and family
issue of mobility : impact on nursing care
true
issue of mobility : medications - treat the disease and treat problems caused by decreased mobility , is this true or false.
true
what other genetic disease can be a reason for issue in mobility ?
change of muscular dystrophy , ms , parkinson disease
what injury can be a reason/cause
spinal cord injury
higher level injury - higher impact
als and gillian burre
what is the impact on the patient ? ( mobility )
mind - fatigue, self identity, depression , independence, awareness of how they will die
recall that body is the one impacted if there is an issue with the mobiliity , what undergoes this ?
cns depression ( significant pain )
— neuropathic pain, and complex
explain how cvs system could have an impact on the patient
blood clots and pressure ulcers
what undergoes resp since this would be affected
atelectasis and pneumonia patietn can lose ability to clear their resp secretions
what undergoes GI as this would be a problem
GI ability to swallow and get good nutrition
GU problem with incontinence /can also have UTIS , is this true ?
yes this is true when it comes to mobility
how would pyschosocial be affected?
lose their sense of self and identity they have is different ( alot of significant anger ) because they lose their personal independence
impact on nursing care
resp system ( can pt clear secretions ) ?
if u have a pt who cna cough well their lungs is okay but if ot what possibilities are we looking at ?
atelectasis and secretions
impact on nursing care : body/limb alignment
what is happening
pain, muscle spasm, and perfusion
turning/repositioning – looking at the skin , how frequent are we turning ?
2 to 3 hours ( look at the pressure ulcers )
it is important to assesment the body and mind why ?
no big pressure underneath hand
thinking pressure points and what the skin looks like - help plan their future
moblity : what else are they in risk for that we should look out for ?
risk of falls ( and working hard is managing pain ) always looking for complications
what type of meds are we going to give them
prevent potential complications ( e.g dvts )
treat pain ( noiceptive, neurogenic )
treat muscle spasm
maintain general health ( breathing , nutrtion, prevent infeciton )
lets also give them the best mattress
equipment and skulls needed and used
wheelchairs, braces, canes, aspen collar
splints, pillows, roho cushions prosthetics
lifts, turning sheets/sliders , transfer board
true or false. staff to assist with mlt
teds/scds, binders, assistive devices ( feeding, writing, bathing )
communciation boars are something we utizlied as equipment and skills needed and used
true
spirometer, feeding tubes, urianry catehrs are also used.
true
what type of medications are we going to utilized ?
slow disease progression ( nerve impulses )
prevents clots
manage pain
decrease muscle spasms
antidepressants
true or false. it is important that a pt takes a med that decrese fatigue and prevent constipation and gu issues such as bladder
true
meds that prevent a lot of probelms
antidepression is big and decreasing fatigue ( make more energy ). is this true or false.
true
interprofessional
who are we working with ?
rt
social worker
rehabilitation units and ltc
sppech language therapist/patholigst
- communicating /swallowing/eating -0 swallowing assemsnet
recall that : rt
social worker
rehabilitation units and ltc
sppech language therapist/patholigst
- communicating /swallowing/eating -0 swallowing assemsnet
are interprofessional we are going to be working with , who else ?
PT
- rom , prevent contractures
-steghtening muscles
-chest physio/pulmonary toileting
OT
- wheelchairs/canes/walkers
-splints
-special cushions (roho ) to relieve pressure
-teach pt how to manage
mobility-diseases
nursing care - the pt is thinking what ?
what is the cause of this disease
curable ? any treatment?
what are the symptoms ?
how can the symptoms be managed?
will this be likely cause my death ?
how bad will it get
duchenne muscular dystrophy ( pediatris )
cannot be caught ( basically means the muscle is weakening )
this is genetic
chronic progressive and incapacitating disease
respirtory problems for duchenne msucular dystrophy
ecause their chest muscles get progressively weaker
there might be another kid that has a cough, this kid might get sick and continue on ( cannot fight it off )n
cardiac dysfunction for duchenne muscular dystrophy
cardaic rhythym abdnomalities ( encho and ekgs once a year to keep an eye on them )
obesity ( the child is not able to lose calroues. not active ) for duchenne msucular dystrophy
this is true
social isolation and pt and fmaily coping discussion s- possible transheotomy , ltc, end of life directives for duchenne muscular dystrophy
this is true
these patients die in their 20s and 30s ( shorten life despentencies )
everything gets worst
mobility gets impaired
they also get contractures
( they are a problem ) the goal is to maintain optimal functioning and prevent contractures
in terms of duchenne muscular dystrophy is this true or false
this is true
penumonia/ clearing penumonia and all of that could be seen within duchenne mucucla rdistrophy
this is true
look at slif 4 for the child walking for the musuclar dystorphy for duchenne
okym
ms describe it
chronic progerssibe remission.exacerbation
what is ms
autoimmune disorders of cns and demyelination of enrve fibers ( brain sinal cord and optic nerve )
what are the s and s for ms
motor, sensory, fatigue, pain , pt manage independence rest adn self care
dx and minotr for ms
hx, s and s
evoked repsonse testing
true or false canada has the hgihest rating for ms
true
not going to the bathroom normally
myelin is basically attack and tried to regenerate
what we see is chronic inflmmation and scaring
this is desciring ms
no discovery yet that fizes this diseases ( the cuase is unknown ) but researches have been dne in mb becauee its so high
yes this is ms
yes it is
what is ms - oerall goal and care
funtioning, independance, in daily living, mamage fatigue, mental health , adjust, reduce factors that lead to exacerbations
what is retaline for in ms
give ore energy dont ahve a ath later on teh day after a goodnight sleep lots of differnt things to do
dvt penumonia pressure ulcer atelectasis patingteaching is help these people help overal healthy life for ms
yes this si true
- Triggers/exacerbations
- Hospitalization
- Pt teaching
are needed for ms overall goal and care
yes this si tru
what is importnt for ms potarntially
learn how to straight cath themselves ( invcontinent out and about is decrease )
bladder will retain urine and habe reflex emptying , they do not have control over it
yes this is true for ms patients
bowel issues and such would what in ms overall goal an care
lactulose or peg
IF THESE PEOPLE ARE HOSPITLIZED ( DIAGNOSTIC WORKUP ) ACUTE EXACERBATIONS ( on bed rest ) fam and friedns need help
ms yes this sit rue
reduce stress/fatigue/ rest throughout the day/. extreme temperatures
very hot temp is very difficult for pts
also extreme cols
anu type of infections ( stomach flue
yes this sis true or ms ( autoimmune )
define if these are signs of duchenne muscular dystrophy ( not walking properly )
shoulders and arms are held back awkwardly
sway back
weak butt muscles ( hip straightens )
add 3 more
yes
knees may bend back to take weight
thick lower leg muscles ( the muscle is mostly fat, and not strong )
tight heel cord ( contracture ) child may walk toes
why does the belly stick out during duchenne muscula dystrophy
belly sticks out due to weak belly muscles ( child is poor at situps )
thin weak tights ( especially front part for duchenne muscle dystrophy )
yes this is true
what is the balance like for ducehnne muscle dystrophy?
poor balance : falls often , awakward clumsy if walking
weak muscles in front of leg cause foot drop, and tip toe contractures : this is true amongst duchenne muscular dystrophy
true
medications for ms
what is our goal here ?
hint** what is steroid used for ?
goal is decrease progression of disease and control symptoms
treatment acute exacerbations ( edema, inflammation at site of demyelination )
define if these medications are being utilize for MS
- Medications
– corticosteroid (methylprednisolone, prednisone)
– immunomodulator (Betaseron, Avonex)
yes this is true
recall if these meds are used for ms : * Medications :
– corticosteroid (methylprednisolone, prednisone)
– immunomodulator (Betaseron, Avonex)
– immunosuppressant (Methotrexate, Imuran, Mitoxantrone)
– anticholinergic (Ditropan) – help with bladder symptoms (tone)
– fight fatigue (Ritalin)
– antispasmodic (Baclofen)
what is ritalin for ?
we use this in ms
helping to fight fatigue ( to give more energy ) pill taken 3 times a day ( decreae muscle spasm ) getting to know their own body and how theyre body reacts ( side effects )
what is three biggest indicator of parkinson disease ?
tremors
rigidity
bradykinesia
what is parkinson disease disease process?
chronic, progressive, degenerative disease of cns
affects movement : slow to move, rigidity and tremors
what are the s & s : for parkinson disease
tremors, rigidity, slow to start moving also depression, fatigue, pain, constipation
dx & monitor : Hx and s and s
no dx test
for parkinson disease are those descriptions accurate
yes it is accurate
instead of diagnostics what are we checking for parkinsons pts ?
theres no specific diagnostic test
head to toe ( check reflexes, get checked with fam and put it together )
true or false. patients have swallowing problems because of what ?
because of the muscle weakness meds that are helpful for this disease ( dopamine receptors and transmitting neurons )
recall that remors of the hands even at rest
persistent tremors
are seen with parkinsons
what else ?
shuffling gait
unbalanced & small in steps, curved in characteristic way
if meds are late for parkinson pt what happens ?
if these meds are late — it affects their mobility
what is our goal in terms of meds for parkinsons
correct imbalance of neurotransmitters within the cns
ng care for parkinson
manage issues for mobility, communication, nutrition ( swallowing ) adapt activities
what are the different type of meds we are giving parkinson pts
dopaminergic ( L- dopa, sinemet )
beta adrenergic blocke ( inderal ) - manage tremors
*titrate dose to effect, combination of meds
*symptoms will progress, worsen
parkinson disease - overall goal and care
can have a risk of what ?
risk of falls
we want them to exercise, ( really decrease their muscle atrophy )
decrease contractures also getting exercise plan with physio therapist
what are different things we are utilizing for parkinson’s disease as an overall goal and care
physical exercise
diet
physio
sleep issues
dep and anxiety
physical exercise
diet
physio
define these in terms of PD
have trouble ingesting foods, swallowing or coughing
swllowing assesments may need , maybe diced tomake it easier to chew and swallow
safety alert for falls ( they need to adapt )
sleep issues
dep and anxiety
cognitive function change
define for PD
satin shees, and satin pajamas ( have huge impact on turning and sliding )
dep and anxiety- makes so many changes for them
cognitive function change - notice settle change in their cognitive ( even progress to full dementia )
Severe mobility issues (airway, ventilation)
what is ALS
amyotrophic lateral sclerosis
what is the descrption of ALS
progressive paralysis, mind is intanct
- no treatment , no cure, supportive care
what does als patient need eventually ?
tracheostomy and ventilator
what does medically assisted suicide mean ?
they know whats going to happen ( hard disease ) and take care of ,
upset and knows whats going to happen
what is Guillain barre syndrome
symmetrical ascending paralysis, demyelination of peripheral nerves , +++ pain peaks at week 3
what is the rate of recovery for gbs
85 percent
what is the treatment for gbs
plasmapheresis and ivig
what is ivig for gbs
intravenous immunoglobulin
infusion get from blood taken
the amount of pain for some people
for als no pain ) but for als ( pain ) tingiling , boarding lighting bols
disese peaks aorund 3 weeks meaning bad its gonna get
trueor false.
true
for gbs what happens when u have the stomach flue ?
ba stomach flue ( whole immune system goes cracy and theyhave this prolem now ) ‘alot of the time they have them sick before a resp gi problem ( not sick enough to go tot he hospital ) but then they develop this
cause and symptoms of gbs
obstruction of myelin, known as demyelination
what are the symptoms?
paralysis, including loss of breath
loss of reflexes
muscle weakness
recall that paralysis, including loss of breath
loss of reflexes
muscle weakness
are all symptoms of gbs what else?
prickly, tingling sensations in the arms and legs ( paresthesia )
mobility - injury/trauma
what type of diagnostics test are we running ?
xray, ct scan, mri
what is th neurovascular asssment are we doing for mobility - injury/trauma
color, temp, cap refull, distal pulses, edema, sensation , motor function , pain
what is the number one priority in neurovascular assesment
the number one priority is color
what do we want to prevent in mobility- injury/trauma
prevent resp complications ( db and coughing ) , spirometry, turning, ROM exercsies
what is ROM exercsies?
range of motion exercises
aside from resp complications : what else do we want to prevent ? ( for injury/trauma )
we want to prevent pressure ulcers
if they havea cast on, we need to think where is the cast hitting them
pain should improve overtime ( as the bone is healing ) if pain is not improving ( they are a complication ) is this true or false.
this is true
what is critical in our neurovascular assessment
distal pulses, edema, sensatin, motor function
what are the meds that patient is on when they have moblity issues such as injury or trauma
manage pain( baclofen, nsaids, narcotics, t3s )
phantom limb pain with amputation
prevent system complications for immobility
- cosntipation ( stool softeners ) , clots ( heparin, enoxaparin )
if someone had a rib fractures, would we encourage deep breathing and coughing ?
bruh no, this is extremely painful and it is not advisable
given this scenario , look at the mar before
fentanyl only 3 times now 4 times and pain is still there
what do u think could be happening
something is cooking up cant lie ( look further )
( pain is getting worst )
what is the general care for bone injuries
what undergoes alignment
midline, neutral position
wehat is traction in terms of geenral care for bone injuries
pulling force to keep alignment ( promtoes bone healing, dec muscle spasm , prevent furhter soft tissue and vessel injury )
true or false. it is major to assess neurovascular status for our general care for bone injureis
yest his is true
what else are we asesing for in terms of our genral care for bone injrueis
surgical site, hematoma
assess for complications such as …
for general care for bone injuries
infeciton, venous thromboemvolism, ( dvt, pe ) infection ( wound for skin or abscess )