Neurological Disorders Flashcards
Acute autoimmune attack on peripheral nerve myelin - antibodies destroying the myelin that allows motor neuron signal - end up mostly weakness and paralysis - not interfere with pain sensation
Demyelination
Ascending paralysis (Ground to Brain) - remits same way - head to feet
Dyskinesia/paresthesias (lot weakness)
Flaccid paralysis (not interfere with pain receptors) and LOT severe pain
Resp. impairment when reaches level diaphragm - thoracic muscles that help us breathe affected first
acute/chronic
Chronic - disease process stops somewhere and not remit
3 phases - acute (1-4 weeks - active: progressing forward and have further paralysis; stays here until no further advancement); plateau (days up to two weeks - stays exactly where at; not remit or go forward); recovery (2 months to 4 yrs - get back to norm state after disease process
Aka Acute idiopathic polyneuritis
Patho - Neurological disorders - Guillain-Barre Syndrome
Viral Infections (most common)
Campylobacter jejuni 25-50%
H. influenza
Mycoplasma pneumonia
HIV
Immunization - some studies
Immune disorders - other disorders set this off
Other stresses in body cause it
Triggers - Neurological disorders - Guillain-Barre Syndrome
Begins in lower extremities
With Muscle weakness leading to paralysis
Diminished reflexes (Hypo-reflexia)
Ascending paralysis - up to head
Respiratory failure - start with thoracic muscles - not able breathe first; if progresses upward - will lose airway - often end up on ventilator
2-4-week peak severity
Can last Longer = chronic inflammatory demyelinating polyneuropathy/demyelination
CM - Neurological disorders - Guillain-Barre Syndrome
Diagnosis
CSF elevated protein - lumbar puncture for this elevated protein
Loss of nerve conduction
Critical care needed
Mechanical ventilation - often intubated
DVT/PE prophylaxis - not moving at all; no muscles help pump blood back up to heart - SCDs and heparin
IVIG-decrease circulating antibodies attacking myelin
Med treatment - Neurological disorders - Guillain-Barre Syndrome
Ineffective breathing pattern - #1 depending on where paralysis
Impaired gas exchange
Impaired physical mobility
Imbalanced nutrition: Inability to swallow - feed through PEG tube, NG tube, post-pyloric tube, TPN through central line
Impaired verbal communication
Anxiety - not affecting mental status; only motor neuron
Fear
N. diagnosis - Neurological disorders - Guillain-Barre Syndrome
Maintain respiratory function - watching and assessing as not able breathe and take action quickly - must report symp and move quickly
Enhancing physical mobility - lot passive ROM - not lose muscle mass while paralyzed
Providing good adequate nutrition - watching for infection if have central line and tolerating tube feeding
Improved communication
Decreased anxiety - med/calm enviornment
Monitoring for complications - BIG ONE
N. interventions - Neurological disorders - Guillain-Barre Syndrome
Autoimmune disorder affecting myoneural junction. - normal Ach released from muscles - antibodies onto muscle and stopping Ach from being absorbed - muscle weakness and some paralysis
Acetylcholine receptor sites impair transmission/impaired
Decreased receptor stimulation
Muscle weakness escalates with continued activity - limited amount of Ach
Women greater than Men
75% thymus gland issue - thioma and need thymus gland removed
Pathophysiology - Neurological disorders - myasthenia gravis
Diplopia/ptosis (80%) - Double vision and drooping eyelids
Face and throat muscle weakness - meds 45-60 min to prevent aspiration isues
Dysphonia - diff talking
Dysphagia - Increase risk choking/aspiration
Generalized weakness - motor involvement so lots pain
Pure motor; no sensory involvement
CM - Neurological disorders - myasthenia gravis
Acetylcholinesterase inhibitor test - only used diagnose; not work as long-term therapy; marked improvement of weakness - esp in face
WARNING: likes cause cardiac arrhythmias/arrest - if do this want know antidote (atropine) available
Lab: acetylcholine antibodies
Ice test - hold over area that has muscle weakness - allows for reabsoprtion and see symptom disappear
Repetitive nerve stimulation - weaken area
Diagnostics - Neurological disorders - myasthenia gravis
Pharmacologic therapy: Pyridostigmine; Main med; increasing concentration of available acetylcholine 4X day
Take before meals (45-60 minutes before)
Therapeutic plasma exchange - Plasmapheresis; looks like dialysis; removes offending antibodies
Surgical management
Thymectomy
Med surg treatment - Neurological disorders - myasthenia gravis
Ineffective airway clearance - weaker not able get airway open
Interrupted family process
Fatigue
Impaired physical mobility - big deal with myasthenic crisis; could also have complete resp failure and need be intubated
Imbalanced nutrition
Impaired swallowing
Hard time with getting muscles move
N. diagnosis - Neurological disorders - myasthenia gravis
Conserve energy
Consistent routines
Avoid excessive activity/stress
Avoid High environmental temp - decreased Ach ability be reabsorbed
Medication prior to meals - Prevent choking/aspiration
Tape eye closed /eye drops - crisis/relapse - Prevent corneal damage
N. interventions - Neurological disorders - myasthenia gravis
Loss of dopamine stores
Results in more excitatory neurotransmitters
Imbalance affects voluntary movement
Males greater than Women
15% early onset due to genetic mutation
Involuntary movements: tremors, walking, eating (high rate aspiration)
Patho - Neurological disorders - Parkinson’s Disease
Four cardinal signs
Tremor
Rigidity
Bradykinesia/akinesia - slow to no movement
Postural Instability
2 Types
Tremor dominate
Non-tremor dominate - a kinetic-rigid and postural instability
Diagnosis - need at least 2 of 4 cardinal symp
CM - Neurological disorders - Parkinson’s Disease
Unilateral (1) limb involvement
Minimal weakness
Hand and arm trembling
Stage 1 (Initial Stage) - Neurological disorders - Parkinson’s Disease
Bilateral limb involvement
Masklike face – flat affect and face
Slow, shuffling gain - not able walk well - gait disturbances
Stage 2 (Mild Stage) - Neurological disorders - Parkinson’s Disease
Postural instability
Increase gait disturbances
Stage 3 (Moderate Disease) - Neurological disorders - Parkinson’s Disease
Akinesia - not moving well at all and lot rigidity
Rigidity
Stage 4 (Severe Disability) - Neurological disorders - Parkinson’s Disease
As get into later stages - also psychiatric component - can have hallucinations
Stage 5 (Complete ADL Dependence) - Neurological disorders - Parkinson’s Disease
Good History
Four cardinal signs (need 2 of 4)
Diagnosis confirmed by a positive response to a levodopa trial - relieve manifestations of PD
PET – Rule out for any other disease process; not diagnostics for PD
Single-photon emission CT – Rule out for any other disease process; not diagnostics for PD
Diagnostics - Neurological disorders - Parkinson’s Disease
Pharmacotherapy
Levodopa-most effective; reuprtake
Converts to dopamine –relieves manifestations
Surgical Treatment
Deep brain stimulation (DBS)
Electrode implanted/blocks anticholinergic release
Blocks Ach allowing more dopamine to be absorbed
Medical management - Neurological disorders - Parkinson’s Disease
Impaired physical mobility
Self-care deficits
Constipation - lack good phys mobility
Impaired nutrition - high risk of aspiration
Risk for injury
Impaired verbal communication
Knowledge deficit
Family and patient
N. diagnosis - Neurological disorders - Parkinson’s Disease
Improve mobility within safety
Enhancing self care activities - providing assistive devices, built up spoons, walkers, help them be as independent
Improved bowel elimination - up walking; stool softeners
Improved nutrition - Aspiration risk; speech therapy
Enhanced swallowing
Assistive devices
Family/Pt education - lots pt and fam edu - PT, OT, speech
N. interventions - Neurological disorders - Parkinson’s Disease
Cognitive, functional, and behavioral changes eventually destroy a person’s ability to function
Phys and mental
Subtle in onset; progress slowly
Not a normal part of aging
Non-Alzheimer dementias; Vascular dementia (multiple small infarcts in the brain that eventually cause the person not be able to func)
Patho - Neurological disorders - Dementia
Specific neuropathologic and biochemical changes that interfere with neurotransmission
Neurolgoic and biochem change that affect neurotransmission
Most common disease process with dementia
Early onset (familial/genetically 40-65 years)
Late onset (greater than 65 years) - MOST COMMON
Risk factors
Alzheimer’s - Neurological disorders - Dementia
Age
Gender
Genetics
risk factors - Alzheimer’s - Neurological disorders - Dementia
Independent in ADLs - Care of self on own
Denies presence of symptoms - not deny it
Forgets names; misplaces household items
Has short-term memory loss and difficulty recalling new information - STM big one; LTM good
Shows subtle changes in personality and behavior
Loses initiative and is less engaged in social relationships
Has mild impaired cognition and problems with judgment
Demonstrates decreased performance, especially when stressed - confused easily when stress
Unable to travel alone to new destinations
Often has decreased sense of smell
Early (Mild), or Stage I (First Symptoms up to 4 Years) - CM - Neurological disorders - Dementia
Has impairment of all cognitive functions
Demonstrates problems with handling or unable to handle money and finances
Is disoriented to time, place, and event
Is possibly depressed and/or agitated - LOT AGITATION
Is increasingly dependent in ADLs
Has visuospatial deficits: has difficulty driving and gets lost - end up ditch; nothing not where think should be
Has speech and language deficits: less talkative, decreased use of vocabulary, increasingly nonfluent speech, and eventually aphasic
Incontinent
Psychotic behaviors, such as delusions, hallucinations, and paranoia
Has episodes of wandering; trouble sleeping - lots agitation at this time
Middle (Moderate), or Stage II (2 to 3 Years) - CM - Neurological disorders - Dementia
Completely incapacitated; bedridden
Totally dependent in ADLs
Has loss of mobility and verbal skills
Possibly has seizures and tremors
Has agnosia
Late (Severe), or Stage III - CM - Neurological disorders - Dementia
Clients can show manifestations from any stage at any time
Clients can have issues from any stage at anytime
Mix and Match from diff stages and can slide between stages
Health promotion - not mitigate or prevent but ward it off for slow period time
CM - Neurological disorders - Dementia
History - HUGE
Physical assessment/manifestations
Psychosocial assessment
Laboratory – Rule out
Radiological – Rule out
Diagnostics (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Behavioral management structured environment (NEED Consistency)
Cognitive stimulation - bringing up to present
Memory training
Validation therapy (Orientation) - re-orientatin - care with this because can become agitated
Redirection
Pharmacologic therapies: Donepezil (Aricept) - not cure; only Improves symptoms
Med surg treatment (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Supporting Cognitive Function
Promoting Physical Safety - locked unit - often wander off
Promoting Independence in Self-Care Activities
Reducing Anxiety and Agitation - consistency and calm enviornment
Improving Communication
Providing for Socialization and Intimacy Needs - hypersexuality often experienced
Promoting Adequate Nutrition
Promoting Balanced Activity and Rest
Home, Community and Transitional to memory Care unit
N. management (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Calm, predictable environment; Limit environmental stimuli
Quiet, pleasant manner of speaking, clear and simple explanations
Use of good memory aids; Displayed clocks and calendars
Active participation help patients maintain cognitive, functional, and social interaction abilities for a longer period
Supporting Cognitive Function - Nursing (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Simplify daily activities by organizing them into short, achievable steps
Lessen bulk ADLs into steps
Promoting Independence in Self-Care Activities - Nursing (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Remove fall risks/hazards; install hand rails - slip hazards removed
Secure doors
Wandering –gentle distraction/ persuasion/redirection
Avoid restraints - lot more agitated
Promoting Physical Safety - Nursing (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Need constant emotional support that reinforces a positive self-image
Environment should be kept familiar and noise free
Combative, agitated state: remain calm and unhurried; never force - try to redirect
Move to familiar environment; try stroking, rocking, music; Be sure pain free
Reducing Anxiety and Agitation - Nursing (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Use of clear, easy-to-understand sentences to convey messages
Tactile stimuli (hugs or hand pats) signs of affection, concern, and security.
Improving Communication - Nursing (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Encourage to participate in simple activities
Care of plants or a pet - good positive reinforcement
Providing for Socialization and Intimacy Needs - Nursing (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Keep simple and calm, without confrontations
Cueing may be necessary to encourage adequate nutrition and hydration
Food is cut into small pieces to prevent choking.
Liquids may be easier to swallow if they are thickened
temperature of the foods should be checked to prevent burns
Promoting Adequate Nutrition - Nursing (Dementia - Alzheimer’s) - Neurological disorders - Dementia
Exhibit sleep disturbances, wandering, etc.; occur when there are unmet underlying physical or psychological needs - look for sleep disturbances
Music, warm milk, or a back rub may help the patient relax
Help Participate in exercise; discourage long periods of daytime sleeping
Promoting Balanced Activity and Rest - Nursing (Dementia - Alzheimer’s) - Neurological disorders - Dementia