Neuromuscular alterations 202
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Transcript Neuromuscular alterations 202
Assessment of the Nervous System
Diane McLean RN, MSN
Nursing 202
1
Objectives
Define terms associated with selected
neuromuscular system alterations.
Describe selected neurological system alterations.
Describe legal and ethical considerations related to
providing nursing care for selected neuromuscular
system alterations.
Describe the impact of selected neuromuscular
system alterations on patients throughout the
lifespan.
2
Objectives…
Relate the pathophysiology associated with selected
neuromuscular system alterations to clinical manifestations.
Describe the role of the nurse in providing care for patients
experiencing selected neuromuscular system alterations.
Explain health promotion related to selected neuromuscular
system alterations.
Interpret selected diagnostic test for neuromuscular system
alterations.
Explain complications associated with selected
neuromuscular system alterations.
Describe the pharmacological agents and/or treatments for
selected neuromuscular system alterations.
3
Objectives…
Evaluate nutritional considerations for patients experiencing
selected neuromuscular system alterations.
Identify patient response to treatment modalities for patients
experiencing selected neuromuscular system alterations.
Evaluate psychosocial needs of patients, families, and/or
support systems.
Use critical thinking to prioritize nursing care for culturally
diverse patients experiencing selected neuromuscular
system alterations.
4
Objectives…
Describe the delegation process used to
provide nursing care for patients
experiencing selected neuromuscular
system alterations.
Evaluate outcomes of nursing care for
patients experiencing selected
neuromuscular system alterations.
5
Anatomy and Physiology
Chapter 43
Neurons
Mechanism for nerve impulse conduction
Neuroglial cells
CNS
Cerebral circulation
Spinal cord
ANS, sympathetic
and parasympathetic
6
Assessment
Family history and genetic risk
Personal history
Level of consciousness and orientation
Memory: remote or long term, recall,
immediate
Attention
Language and copying
7
Assessment …
Cognition
Cranial nerves
Sensory function
Pain and temperature
Touch
Abnormal sensory findings
8
Assessment of Motor
Function
Muscle strength
Cerebral or brainstem integrity
Abnormal motor findings
9
Assessment of Cerebellar
Function
Coordination
Gait and equilibrium
10
Assessment of Reflex
Activity
Deep tendon reflexes
Cutaneous reflexes: Babinski’s sign,
abdominal reflex
Abnormal reflex findings
11
Rapid Neurologic
Assessment
Glasgow Coma Scale
Response to painful stimuli
Level of consciousness
Decortication
Decerebration
Pupil assessment
12
Glasgow Coma Scale
Glasgow Coma Score
Eye Opening (E)
Verbal Response (V)
Motor Response (M)
4=Spontaneous
3=To voice
2=To pain
1=None
5=Normal
conversation
4=Disoriented
conversation
3=Words, but not
coherent
2=No words......only
sounds
1=None
6=Normal
5=Localizes to pain
4=Withdraws to pain
3=Decorticate
posture
2=Decerebrate
1=None
Total = E+V+M
13
Laboratory Tests
Blood cultures necessary
Skull and spine x-ray tests
Cerebral angiography
CT scan: possible use of contrast medium,
assess for allergic response, fluids
Positron emission tomography
Single-photon emission CT
14
Lumbar Puncture
Insertion of spinal needle into the
subarachnoid space (between the third and
fourth lumbar vertebrae)
Contraindicated in patients with increased
intracranial pressure
Empty bladder
Position
Spinal headache possible from spinal tap
15
Electroencephalography
(EEG)
Graphically records the electrical activity of
the cerebral hemispheres
Sleep deprivation requirement
Anticonvulsants possibly withheld
16
Interventions
for patients with
Problems of the Central
Nervous System: The Brain
Chapter 44
17
Headaches
Migraine headache
Episodic familial disorder manifested by
unilateral, frontotemporal, throbbing pain in
the head, often worse behind one eye or ear
Often accompanied by a sensitive scalp,
anorexia, photophobia, nausea
Aura: sensation that signals
the onset of a headache
18
or seizure
Drug Therapy
Abortive therapy: alleviating pain during the
early aura phase includes prescribing
ergotamine derivatives, NSAIDs, triptans,
isometheptene combinations.
Acetaminophen and NSAIDs are usually
effective for mild migraine headaches.
19
Preventive Therapy
NSAID prescription
Beta-adrenergic blocker
Calcium channel blockers
20
Complementary and
Alternative Therapies
Yoga, meditation, massage, exercise,
biofeedback, relaxation techniques
Acupuncture
21
Complementary and
Alternative Therapies…
Use of herbs and nutritional therapies with
approval
Avoidance of trigger events that may result
in migraine episodes, such as tension and
stress
22
Cluster Headache
Histamine cephalagia, uncommon type of
headache
Cause unknown; attributed to vasoreactivity
and oxyhemoglobin desaturation
Unilateral, radiating to forehead, temple, or
cheek
Ipsilateral tearing of the eye, rhinorrhea,
ptosis, and miosis
23
Therapy
Same types of drugs used for migraines
patient to wear sunglasses and avoid
sunlight
Oxygen via mask
Avoidance of precipitating factors, such as
anger, excitement
Surgical management
24
Tension Headache
Neck and shoulder muscle tenderness and
bilateral pain at the base of the skull and in
the forehead
Head pain without associated symptoms
Treatment: non-opioid analgesics, muscle
relaxants, occasional opioids
Ibuprofen plus caffeine
Prophylactic treatment similar to that used in
treating migraine headaches
25
Seizures and Epilepsy
Seizure: abnormal, sudden, excessive,
uncontrolled electrical discharge of neurons
within the brain; may result in alteration in
consciousness, motor or sensory ability,
and/or behavior
Epilepsy: chronic disorder with recurrent,
unprovoked seizures; may be caused by
abnormality in electrical neuronal activity,
and/or imbalance of neurotransmitters (such
26
as GABA
Types of Seizures
Generalized seizures
Partial seizures
Unclassified seizures
27
Types of Epilepsy
Primary or idiopathic epilepsy: not
associated with any identifiable brain lesion
Secondary epilepsy: results from an
underlying brain lesion, most commonly a
tumor or trauma
28
Seizures Risks
Seizures may result from:
Metabolic disorders
Acute alcohol withdrawal
Electrolyte disturbances
Heart disease
29
Collaborative Management
A complete description of the type of seizure
activity that occurs and events surrounding
the seizure determines the best treatment
plan.
Determine whether an aura was present
before the seizure in the preictal phase.
Diagnostic testing is performed.
30
Drug Therapy
Evaluate most current blood level of
medication, if appropriate.
Be aware of drug-drug and drug-food
interactions.
Maintain therapeutic blood levels for
maximal effectiveness.
31
DRUGS to Review
Dilantin
Topamax
Depakote
Tegretol
Klonopin
Valium
Neurotin
Keppa
Phenobarbital
Mysoline
32
Drug Therapy…
Do not administer warfarin with phenytoin.
Document and report side and adverse
effects.
33
patient and Family Education
Antiepileptic drugs (AEDs) may not be
stopped, even if seizures stop.
Refer limited-income patients to social
services.
All states prohibit discrimination against
people who have epilepsy.
34
patient and Family
Education…
Alternative employment may be needed.
Vocational rehabilitation may be subsidized.
35
Seizure Precautions
Oxygen and suctioning equipment should be
readily available.
Saline lock may be necessary.
Side rails should be up at all times.
Padded side rail use is controversial.
Place bed in lowest position.
Never insert padded tongue blades into the
patient’s mouth during a seizure.
36
Seizure Management
If simple partial seizure, observe the patient
and document the seizure.
Turn the patient on the side during a
generalized tonic-clonic seizure; if possible,
turn the patient’s head to prevent aspiration.
Cyanosis usually is self-limiting.
Do not restrain.
37
Status Epilepticus
Management
Usual causes of status epilepticus:
Prolonged seizures lasting more than 5 minutes
or repeated seizures over the course of 30
minutes
Neurologic emergency that must be treated
promptly and aggressively
Sudden withdrawal of AEDs, infections, alcohol
withdrawal, head trauma, cerebral edema, and
metabolic disturbances
38
Status EpilepticusTreatment
Establish an airway.
Administer oxygen as indicated.
Establish intravenous access.
For continuous monitoring, admit patient to
intensive care unit.
Give IV diazepam, lorazepam, phenytoin,
fosphenytoin, or general anesthesia.
39
Status
EpilepticusTreatment…
Other treatments include:
Surgical management: epileptic region in a
resectable area
Corpuscallostomy
Vagal nerve stimulation
40
Meningitis
Meningitis: inflammation of the arachnoid
and pia mater of the brain and spinal cord
and the cerebrospinal fluid
Bacterial and viral origins
most common:
fungal and protozoal meningitis
41
Meningitis…
Viral meningitis: self-limiting and patient
recovers
Bacterial meningitis: a medical emergency
with a mortality rate of approximately 25%.
42
Physical Assessment and
Clinical Manifestations
Signs and symptoms of meningitis:
headache, nausea, vomiting, and fever
Photophobia and indications of increased
intracranial pressure
Nuchal rigidity and positive Kernig’s and
Brudzinski’s signs (only present in 9% of
patients)
Seizure, decreased mental status, focal
neurologic deficits
43
Laboratory Assessment of
Meningitis
Cerebrospinal fluid analysis
Computed tomography scan
Blood cultures
Counterimmunoelectrophoresis
Polymerase chain reaction
Complete blood count
X-ray study to determine presence of
infection
44
Drug Therapy
Broad-spectrum antibiotic
Hyperosmolar agents
Anticonvulsants
Steroids (controversial)
Prophylaxis treatment for those who have
been in close contact with the meningitisinfected patient
45
Encephalitis
Inflammation of the brain parenchyma and
often the meninges; affects the cerebrum,
brainstem, and cerebellum
Viral cause, most often bacteria, fungi, or
parasites
Degeneration of neurons of the cortex
Hemorrhage, edema, necrosis, small
lacunae develop in cerebral hemispheres
46
Encephalitis…
47
Other Infections
Arboviruses
Enteroviruses
Herpes simplex virus type 1
Amebae
48
Interventions
Prompt recognition and treatment of signs of
cerebral edema, hemorrhage, and necrosis
of brain tissue
Establishment of patent airway
Assessment of vital signs
Continuous supportive care and assessment
49
Parkinson Disease
Debilitating disease affecting motor ability
characterized by tremor, rigidity, akinesia,
and postural instability
Parkinson disease is separated into stages
by degree of disability: 1, 2, 3, 4, and 5.
Exact cause unknown, possibly involving
environmental and genetic factors
50
51
Parkinson’s Disease
52
Parkinson’s Disease…
53
Assessment
Fatigue, slight tremor, problems with manual
dexterity
Rigidity, changes in facial expression,
uncontrolled drooling, dementia, changes in
voluntary movement, excessive perspiration,
orthostatic hypotension
No specific diagnostic tests
54
Drug Therapy in Parkinson
Disease
Anticholinergic drugs: amantadine, selegiline
(confer mild benefit)
Dopamine agonists in the first 3 to 5 years
Levodopa
Bromocriptine or pergolide
Amantadine
Catechol O-methyltransferase inhibitors
55
Drug Toxicity
Long-term drug therapy regimens often
cause delirium, cognitive impairment,
decreased effectiveness of the drug, or
hallucinations.
Reduce medication dose.
Change medications or frequency of
administration.
Take “drug holiday,” especially in the use of
levodopa therapy.
56
Management of Parkinson
Disease
Exercise and ambulation
Self-care
Injury prevention
Nutrition
Communication
Psychosocial support
57
Management of Parkinson
Disease…
Surgical management includes:
Stereotactic pallidotomy
Deep brain stimulation
Fetal tissue transplantation
58
Alzheimer’s Disease
Chronic, progressive, degenerative disease
that accounts for 60% of dementias
occurring in people older than 65 years of
age
Loss of memory, judgment, and visuospatial
perception, and change in personality
Increasing cognitive impairment, severe
physical deterioration, death from
complications of immobility
59
Structural Changes in the
Brain
Alzheimer’s disease creates changes that
include:
Neurofibrillary tangles
Senile or neuritic plaques
Granulovascular degeneration
Increased amounts of an abnormal protein, beta
amyloid
60
Structural Changes in the
Brain…
Significantly increased vascular degeneration a
contributor to mortality in this disorder
Abnormalities of ACH, norepinephrine,
dopamine, and serotonin
61
Alzheimer’s
62
Chemical Changes in the
Brain
Alzheimer’s disease creates changes that
include abnormalities in the
neurotransmitters:
Acetylcholine
Norepinephrine
Dopamine
Serotonin
Their exact role is not well understood.
63
Manifestations
Changes in cognition
Alterations in communication and language
abilities
Changes in behavior, personality, and
judgment
Changes in self-care skills
Psychosocial assessment, especially
patient’s reaction to changes in routine
64
Interventions in Alzheimer’s
Disease
Answer patient’s questions truthfully.
Assess and treat other medical problems.
Provide cognitive restructuring and memory
training.
Structure the environment to increase
patient’s ability to function.
Prevent overstimulation.
65
Interventions
Provide consistency, orientation, and
validation therapy.
Promote independence in activities of daily
living.
Promote bowel and bladder continence.
66
Interventions …
Assist with facial recognition as the disease
progresses to prosopagnosia, an inability to
recognize oneself and other familiar faces.
Promote communication with clear, short
sentences.
67
Drug Therapy
Cholinesterase inhibitors
Memantine
Donepezil
Antidepressants
Psychotropic drugs
Complementary and
alternative therapies
68
Risk for Injury
Interventions for the patient with Alzheimer’s
disease include:
Coping with restlessness and wandering;
ensuring patient wears identification bracelet;
registering patient in Safe Return Program;
providing frequent walks and structured activities
69
Risk for Injury…
Ensuring safety by removing all potentially
dangerous objects, particularly in case seizures
occur
Minimizing agitation by talking calmly and softly;
displaying positive affect; making calm
movements; offering diversion
70
Compromised Family Coping
Interventions for the caregiver role:
Encourage family to seek legal counsel
regarding patient’s competency, need to obtain
guardianship, or durable medical power of
attorney, when necessary.
Make caregivers and family aware of their own
health and stress resulting from new
responsibilities for care.
71
Disturbed Sleep Pattern
Difficulty sleeping at night with frequent naps
in the day
Interventions for establishing sleep pattern:
Re-establish the usual day-night pattern by
providing activity and exercise during the day.
Establish before-bedtime ritual.
72
Disturbed Sleep Pattern…
Adjust treatment and medication schedule to
provide for uninterrupted sleep.
Give mild antianxiety agent or hypnotic.
73
Huntington Disease
Hereditary disorder transmitted as an
autosomal dominant trait at the time of
conception
Gradual clinical onset of progressive mental
status changes, leading to dementia and
choreiform movements in the limbs, trunk,
and facial muscles
Three stages each lasting about 5 years
over an average 15 years of the disease
74
Management of Huntington
Disease
No known cure or treatment
Genetic counseling
Antipsychotic agents or monoaminedepleting agents used to manage movement
abnormalities that are disabling or interfere
with ADLs
Medications to treat depression, anxiety, and
obsessive-compulsive behaviors
75
Care of patients with Problems of the Central
Nervous System: The Spinal Cord
Chapter 45
76
Back Pain
Low back
Herniated nucleus pulposus
Physical assessment: continuous acute pain,
altered gait, vertebral alignment, paresthesia
Diagnostic assessment using MRI, CT, and
electromyography
77
Nonsurgical Management
Williams position, firm mattress or backboard
under soft mattress
Exercise
Drug therapy
Heat and ice therapy
Diet therapy
78
Nonsurgical Management…
Other pain relief measures
Complementary and alternative therapies
Percutaneous laser disk decompression
79
Surgical Management
Diskectomy
Laminectomy
Spinal fusion (arthrodesis)
Minimally invasive lumbar procedures, such
as percutaneous lumbar diskectomy,
microdiskectomy, laser-assisted
laparoscopic lumbar diskectomy
80
Postoperative Care
Prevention and assessment of complications
Neurologic assessment; vital signs
patient’s ability to void
Pain control
Wound care
patient positioning and mobility
81
Cervical Neck Pain
Conservative treatment is the same as
described for back pain except that the
exercises focus on shoulder and neck.
If these treatments do not work, soft collar
may be used at night for a period of no
longer than 10 days.
If conservative treatment is ineffective,
surgery such as an anterior cervical
diskectomy and fusion is commonly
performed.
82
Spinal Cord Injury
Hyperflexion injury
Hyperextension injury
Axial loading injury such as those that occur
in jumping
Rotation of the head beyond its range
Penetration injury, such as those wounds
caused by a bullet or a knife
83
Cervical Injuries
Anterior cord syndrome
Posterior cord lesion
Brown-Séquard syndrome
Central cord syndrome
84
Initial Assessment
Assessment of the respiratory pattern and
ensuring an adequate airway
Assessment for indications of intraabdominal hemorrhage or hemorrhage or
bleeding around fracture sites
Assessment of level of consciousness using
Glasgow Coma Scale
85
Initial Assessment…
Establishment of level of injury: tetraplegia,
quadraplegia, quadriparesis, paraplegia, and
paraparesis
86
Spinal Shock
This condition is characterized by the
following:
Flaccid paralysis
Loss of reflex activity below the level of the
lesion
Bradycardia
Paralytic ileus
Hypotension
87
Cardiovascular Assessment
Cardiovascular dysfunction is usually the
result of disruption of the autonomic nervous
system.
Bradycardia, hypotension, and hypothermia
result from a loss of sympathetic input and
may lead to cardiac dysrhythmias.
88
Cardiovascular
Assessment…
Systolic blood pressure lower than 90 mm
Hg requires treatment because lack of
perfusion to the spinal cord worsens the
condition.
89
Autonomic Dysreflexia
Commonly seen in patients with upper spinal
cord injury
Severe hypertension
Bradycardia
Severe headache
Nasal stuffiness
Flushing
Treatment
90
Assessments
Respiratory assessment
Gastrointestinal and genitourinary
assessment
Musculoskeletal assessment
Psychosocial assessment
Laboratory assessment
Radiographic and other diagnostic
assessments
91
Ineffective Tissue Perfusion
Interventions include:
Reduction and immobilization of the fracture to
prevent further damage to the spinal cord from
bone fragments
Nonsurgical techniques, such as traction or
external fixation, but surgery may be necessary
as well
92
Immobilization for Cervical
Injuries
Fixed skeletal traction to realign the
vertebrae, facilitate bone healing, and
prevent further injury
Halo fixation and cervical tongs
Stryker frame, rotational bed, kinetic
treatment table
Pin site care and monitoring of traction ropes
93
Immobilization of Thoracic
and Lumbosacral Injuries
For patients with thoracic injuries: bedrest
and possible immobilization with a fiberglass
or plastic body cast
For patients with lumbar and sacral injuries:
immobilization of the spine with a brace or
corset worn when the patient is out of bed;
custom-fit thoracic lumbar sacral orthoses
preferred
94
Drug Therapy
Methylprednisolone (controversial)
Dextran
Atropine sulfate
Dopamine hydrochloride
Naloxone and TRH
Sygen
95
Drug Therapy…
4-AP potassium channel blocker
Dantrolene
Baclofen
Etidronate disodium
96
Surgical Management
Emergency surgery necessary for spinal
cord decompression
Decompressive laminectomy
Spinal fusion
Harrington rods to
stabilize thoracic
spinal injuries
97
Ineffective Airway Clearance
and Breathing Pattern…
Assisted coughing, quad cough, cough assist
Use of incentive spirometer
98
Ineffective Airway Clearance
and Breathing Pattern
Interventions for the patient with spinal cord
injury:
Airway management is the priority.
patients with injuries at or above the sixth
thoracic vertebra are especially at risk for
respiratory complications.
Provide measures to maintain airway.
99
Impaired Physical Mobility;
Self-Care Deficit
Interventions include:
In patients with spinal cord injury, monitor for risk
of pressure ulcers, contractures, and deep vein
thrombosis or pulmonary emboli.
Proper positioning, skin inspection, ROM
exercises, heparin, and graduated compression
stockings.
100
Impaired Physical Mobility;
Self-Care Deficit…
Prevent orthostatic hypotension.
Promote self-care.
101
Impaired Urinary Elimination;
Constipation
Interventions include:
A bladder retraining program
Spastic bladder: manipulating external area
Flaccid bladder: Valsalva maneuver
Encouraging consumption of 2000 to 2500 mL of
fluid daily to prevent urinary tract infection
102
Impaired Urinary Elimination;
Constipation…
Long-term renal complication
Signs and symptoms of urinary tract
infection not perceived by the patient
103
Establishing a Bowel
Retraining Program
Consistent time for bowel elimination
High fluid intake for at least 200 mL/day
High-fiber diet
Rectal stimulation (with or without
suppositories)
Stool softener medications, as needed
104
Impaired Adjustment
Interventions include:
Invite patients to ask questions about significant
life changes; reply openly and honestly.
Encourage patients to discuss their perceptions
of their situation and coping strategies that can
be used.
Begin a patient education program to clarify
misconceptions.
105
Spinal Cord Tumors
Surgical management: goal of removing as
much of the tumor as possible
Nonsurgical management: radiation therapy,
chemotherapy, pain control
106
Multiple Sclerosis
Chronic autoimmune disease affecting the
myelin sheath and conduction pathway of
the CNS
Characterized by periods of remission and
exacerbation
Inflammatory response resulting in random
or patchy areas of plaque in the white matter
of the CNS
107
Major Types of Multiple
Sclerosis
Relapsing-remitting
Progressive-relapsing
Primary progressive
Secondary progressive
108
Common Physical
Assessment
Findings include:
Flexor spasms at night
Intention tremor
Dysmetria
Blurred vision, diplopia, decreased visual acuity,
scotomas, nystagmus
Hypalgesia, numbness, tingling or burning
Bowel and bladder dysfunction
109
Drug Therapy
Therapies include:
Biological response modifiers
Immunosuppressives
Steroids
Antispasmodic drugs
Adjunctive
110
Management
Promoting mobility and self-care
Managing cognitive problems
Adapting to changes in sexual functioning
Managing bladder and bowel problems
Treating visual disturbances
Complementary and alternative therapies
111
Amyotrophic Lateral
Sclerosis
Known as Lou Gehrig’s disease, a
progressive and degenerative disease that
involves the motor system
Early symptoms: fatigue while talking,
tongue atrophy, dysphagia, weakness of the
hands and arms, fasciculations, nasal quality
of speech, dysarthria
112
Interventions
No known cure, no treatment, no preventive
measures
Riluzole, only drug approved by FDA to
extend survival time
Exercise and mobility program
Management of swallowing difficulties
Respiratory support
113
Chapter 46
Care of Patients with Problems of the
Peripheral Nervous System
114
Guillain-Barré Syndrome
An acute autoimmune disorder characterized
by varying degrees of motor weakness and
paralysis
The patient’s life and ultimate potential for
rehabilitation dependent upon appropriate
interventions and effectiveness of nursing
care
Chronic inflammatory demyelinating
polyneuropathy
115
Clinical Manifestations
Muscle weakness and pain have abrupt
onset; cause remains obscure.
Cerebral function or pupillary signs are not
affected.
The most common clinical pattern is that the
immune system starts to destroy the myelin
sheath surrounding the axons.
116
Clinical Manifestations…
Weakness and paresthesia begin in the
lower extremities and progress upward
toward the trunk, arms, and cranial nerves in
ascending GBS
117
Ineffective Breathing Pattern
Interventions
Priority: maintain adequate respiratory
function; implement interdisciplinary actions
Airway management:
Elevate head of bed at least 45 degrees
Suction
118
Ineffective Breathing Pattern
Interventions…
Chest physiotherapy
Incentive spirometer
Oxygen
Monitor arterial blood gas and vital capacity
Keep equipment for endotracheal intubation at
the bedside
119
Interventions for Cardiac
Dysfunction
Can affect both the sympathetic and
parasympathetic systems
patient placed on cardiac monitor because of
the risk for arrhythmias
Hypertension treated with beta blocker or
nitroprusside
IV fluids for hypotension; patient placed in
supine position
Atropine may be used for bradycardia
120
Drug Therapy
Plasmapheresis or IV immunoglobulin
Plasma exchange
IV immunoglobulin
No corticosteroids
121
Plasmapheresis
Plasmapheresis removes the circulating
antibodies assumed to cause the disease.
Plasma is selectively separated from whole
blood; the blood cells are returned to the
patient without the plasma.
Plasma usually replaces itself, or the patient
is transfused with albumin.
122
Acute Pain Interventions
Assess pain, which is often worse at night
Pain usually only relieved with opiates
Use of analgesia pump or continuous IV drip
Frequent repositioning, massage, ice, heat,
relaxation techniques, guided imagery, and
distraction (such as music or visitors)
123
Impaired Physical Mobility
and Self-Care Deficit
Interventions include:
Assess muscle function every 2 to 4 hours.
Provide assistive devices and instructions for
their use.
Ensure safety in ambulation, position changes.
Encourage independence.
124
Impaired Physical Mobility
and Self-Care Deficit…
ROM exercises every 2 to 4 hours
Diet plan to guard against malnutrition
Prevention of pressure ulcers
Prevention of pulmonary embolic and deep vein
thrombosis
125
Impaired Verbal
Communication
Interventions include:
Develop a communication system that meets the
needs of patient.
Devise simple techniques—eye blinking and
moving a finger to indicate yes and no
responses.
Develop a board using letters of the alphabet.
126
Powerlessness
Interventions include:
Encourage patient to verbalize feelings about
the illness and its effects.
Examine patterns of decision-making, roles and
responsibilities, and usual coping mechanisms.
Refer patient to other health care professionals
as needed.
127
Myasthenia Gravis
Chronic disease characterized by weakness
primarily in muscles innervated by cranial
nerves, as well as in skeletal and respiratory
muscles
Thymoma: encapsulated
thymus gland tumor
128
Myasthenia Gravis…
Progressive paresis of affected muscle
groups that is partially resolved by resting
Most common symptoms: involvement of
eye muscles, such as ocular palsies, ptosis,
diplopia, weak or incomplete eye closure
129
Tensilon Testing
Within 30 to 60 sec after injection of
Tensilon, most myasthenic patients show
marked improvement in muscle tone that
lasts 4 to 5 minutes.
Prostigmin is also used.
Cholinergic crisis is due to overmedication.
(Continue
130
Tensilon Testing…
Myasthenic crisis is due to undermedication.
Atropine sulfate is the antidote for Tensilon
complications.
131
Diet Therapy and
Interventions
Cholinesterase-inhibitor drugs
Immunosuppressants
Corticosteroids for immunosuppression
Plasmapheresis
132
Diet Therapy and
Interventions…
Respiratory support
Nonsurgical management
Assistance with activities and
communication
133
Cholinesterase Inhibitor
Drugs
Drugs include anticholinesterase and
antimyasthenics.
Enhance neuromuscular impulse
transmission by preventing decrease of ACh
by the enzyme ChE.
Administer with food.
Observe drug interactions.
134
Emergency Crises
Myasthenic crisis: an exacerbation of the
myasthenic symptoms caused by
undermedication with anticholinesterases
Cholinergic crisis: an acute exacerbation of
muscle weakness caused by overmedication
with cholinergic (anticholinesterase) dr
135
Myasthenic Emergency
Crisis
Tensilon test is performed.
Priority for nursing management is to
maintain adequate respiratory function.
Cholinesterase-inhibiting drugs are withheld
because they increase respiratory secretions
and are usually ineffective for the first few
days after the crisis begins.
136
Cholinergic Emergency
Crisis
Anticholinergic drugs are withheld while the
patient is maintained on a ventilator.
Atropine may be given and repeated, if
necessary.
Observe for thickened secretions due to the
drugs.
Improvement is usually rapid after
appropriate drugs have been given.
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Management
Immunosuppression
Plasmapheresis
Respiratory support
Promoting self-care guidelines
Assisting with communication
Nutritional support
Eye protection
Surgical management usually involving
thymectomy
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Health Teaching
Factors in exacerbation include infection,
stress, surgery, hard physical exercise,
sedatives, enemas, and strong cathartics.
Avoid overheating, crowds, overeating,
erratic changes in sleeping habits, or
emotional extremes.
Teach warning signs.
Teach importance of compliance.
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Polyneuritis and
Polyneuropathy
Syndromes whose clinical hallmarks are
muscle weakness with or without atrophy;
pain that is stabbing, cutting, or searing;
paresthesia or loss of sensation; impaired
reflexes; autonomic manifestations
Example: diabetic neuropathy
140
Peripheral Nerve Trauma
Vehicular or sports injury or wounds to the
peripheral nerves
Degeneration and retraction of the nerve
distal to the injury within 24 hours
Perioperative and postoperative care
Rehabilitation through physiotherapy
141
Restless Legs Syndrome
Leg paresthesias associated with an
irresistible urge to move; commonly
associated with peripheral and central nerve
damage in the legs and spinal cord
Management: symptomatic, involving
treating the underlying cause or contributing
factor, if known
Nonmedical treatment
Drug therapy effective for some patients
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Trigeminal Neuralgia
Affects trigeminal or fifth cranial nerve
Nonsurgical management of facial pain: drug
therapy
Surgical management: microvascular
decompression, radiofrequency thermal
coagulation, percutaneous balloon
microcompression
Postoperative care: monitoring for
complications
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Facial Paralysis or Bell’s
Palsy
Acute paralysis of seventh cranial nerve
Medical management: prednisone,
analgesics
Protection of the eye
Nutrition
Massage; warm, moist heat; facial exercises
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