med surge 2 mod 3 study guide
TRANSCRIPT
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1Module 3 Blueprint
Increased ICP
Glasgow coma scale
EYES Spontaneous 4
To voice 3
To pain 2None 1
VERBAL Oriented 5
Confused 4
Inappropriate words 3
Incomprehensible sounds 2
None 1
MOTOR Obeys command 6
Localized pain 5
Withdraws from pain 4
Flexion (decorticate) 3
Extension (decerabrate) 2
None 1
Glasgow Coma Scale pointers
15 is fully alert
7 or less is comatose book says 8 or less is generally
accepted as indicating a severe head injury
Score of 0 does not exist a dead person will score 3
MOTOR ~ be able to distinguish btw 4 & 5
MOTOR ~ 3 flexion is corticated posturing is where they bringto core; 2 extension is cerebrate posturing which is opposite of
corticated
HESI HINT
Use of the Glasgow coma scale eliminates ambiguous terms to
describe neurologic status such as lethargic, stuporous, or obtunded.
Dolls phenomenon
Tests occulocephalic reflex ~ Dr performs, not nurse; think of
eyes of baby dolls
fixed to look straight; pt will be told tofocus on something
Intact occulocephalic eyes deviate to opposite direction in
which head is turned
Abnormal eyes remain midline & move with the head
Abnormal indicates brain stem injury
If pt has cervical spine injury or even just a suspected, do not
attemptPathophysicology
3 components of brain brain tissue, blood, CSFMonroe-Kellie hypothesis - volume of any one of the 3 contents of
the skull changes the volume of the other 2 contentsCushings response is seen when cerebral blood flow significantly.
When eschemic, the vasomotor center triggers and in arterial
pressure in an effort to overcome the ICP.S/S:
Early sign is change in LOC
HA d/t pressure
N/V
Changes in VS drastic changes or significantly ICP
Cushings triad
Cushings triad systolic BP with widening of pulse
pressure, bradypnea, bradycardia,
NURSING ALERT
The earliest sign of ICP is a change in LOC. Slowing of speech and
delay in response to verbal suggestions are the other early indicators.
HESI HINT
Even subtle behavior changes, such as restlessness, irritability, or
confusion, may indicate ICP
HESI HINT
CSF leakage carries the risk of meningitis and indicates a deteriorating
condition. Because of CSF leakage, the usual signs of ICP may notoccur.
Management
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blood volume
cerebral edema
volume CSF
Done by
Restricting fluids
Controlling fever cellular metabolic demands
Administration of osmotic diuretics & corticosteroids
Draining CSF
Hyperventilating pt
HESI HINT
If temperature elevates, take quick measures to it since fever cerebral metabolism and can cerebral edema.
HESI HINT
Safety features for immobilized client:
Prevent skin breakdown with frequent turning
Maintain adequate nutrition
Prevent aspiration with slow, small feedings or NG feedings
Monitor neurological signs to detect the first signs that intracranial
pressure may be
Provide ROM exercises to prevent deformities
Prevent respiratory complications frequent turning andpositioning for optimal drainage.
HESI HINT
Restlessness may indicate a return to consciousness but can also
indicate anoxia, distended bladder, convert bleeding, or cerebralanoxia. Do notover-sedate, and report any symptoms of restlessness.
Medical management
Surgical removal of cause
clot, tumor, etc...
Osmotic diuretics ~ Manitol which removes fluid from normal
brain tissue with little effect on edematous tissue because ofblood/brain barrier (this allows more space & Lasix may be
used in conjunction), glycerol, urea cerebral edema
Steroids ~ Ex Decadron edema with tumors in areas that
are edematous around tumors complications areimmunosuppression, BS (pt on sliding scale insulin), GI
bleeding (tagment, protonix, nexium), risk of infection
CSF drainage ~ catheter in ventrical to remove CSF bur
hole in scull
Mechanical ventilation ~ controlled hyperventilation to induce
respiratory alkalosis which then causes cerebral
vasoconstriction reduces volume of blood and volume ofCSF
Temperature control ~ fever cerebral metabolism & rate that
edema occurs High dose barbiturate therapy ~ if not resolved by other
measures; cerebral resistance therefore cerebral blood flow
basically allowing less blood flow to get to head means lessvolume in head
NI
Use of narcotics are contraindicated; NEVER give morphine
to pt with ICP narcotics can ICP, Morphine affects
pupil size and accurate size cant be obtained on assessment;Codeine be prescribed for HA r/t ICP
Maintain patent airway with suctioning hyperoxygenate
prior; airway obstruction will ICP
Position ~ HOB elevated & keep head in neutral alignment
gravity enhances venous return & turned head impedes venousreturn
No straining ~ BM ICP so pt on stool softeners; NO valsalva
maneuver; Do not allow them to help repostition bc it will
cause them to push and facilitate valsalva maneuver have pt
exhale while turning or moving them up in bed to prevent
Monitor IVs to prevent fluid overload
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Passive ROM active ROM will cause I CP
HESI HINT
TRY NOT to use restraints; they only restlessness. AVOID
narcotics since they mask level of responsiveness.
HESI HINT
Almost every diagnosis in the NANDA format is applicable, as
severely neurologically impaired persons require total care.
HESI HINT
Pts with an altered state of consciousness are fed by enteral routes
since the likelihood of aspiration with oral feedings is great. Residualfeeding is the amount of previous feeding still in the stomach. The
presence of 100 mL residual in adults usually indicates poor gastric
emptying and the feeding should be held.
HESI HINT
Paralytic ileus is common in comatose clients. Gastric tube aids ingastric decompression.
HESI HINT
Any client or bedrest/immobilization must have ROM exercises oftenand very frequent position changes. Do no leave the client in any one
position for longer than 2 hours. Any positions that venous return isdangerous, i.e., sitting with dependent extremities for long periods.
NURSING ALERT
If the pt begins to emerge from unconsciousness, every measure that isavailable and appropriate for calming and quieting the pt should be
used. Any form of restraint is likely to be countered with resistance,
leading to self-injury or to a dangerous in ICP. Therefore, physicalrestraints should be avoided if possible; a written prescription must be
obtained if their use is essential for the pts well-being.
NURSING ALERT
The body temperature of an unconscious pt is never taken by mouth.
Rectal or tympanic (if not contraindicated) temperature measurementis preferred to the less accurate axillary temperature.
Posturing
Decorticate ~ abnormal flexion; arms, wrist, fingers flexed &
arms abducted; legs fully extended & internally rotated with
plantar comes to the core
Decerebrate posturing ~ stiff arms extended & adducted, hands
hyperpronated, wrist & fingers flexed, plantar flexion of feet
outward rotation from the body
Headaches
Symptom not a disease
Temporomandibular Joint Pain (TMJ) unilateral facial pain
pain can be referred to upper part of face as well as down into
neck
usually caused by malocclusion, trauma, arthritis, bruxism
(teeth grinding)
Temporal Arteritis (Cranial arteritis)
inflammation of the walls of the temporal (cranial) arteries
S/S: pain, fatigue, wt los, fever & malaise; heat, redness, &
tenderness over involved artery
specific S/S of this kind ofHA d/t the inflammation
visual disturbances or blindness may result from ischemia of
involved structures
Tx analgesics for comfort & steroids for inflammation
Migraine
Complex S/S, characterized by periodic and recurrent attacks of severHA
Caused by VASCULAR disturbance that occurs more
commonly in women and has strong familial tendency
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Onset: childhood, adolescence, puberty occurs more often
when major change in pace or schedule such as holidays,
stress, first job can have one from having time off fromwork from the let down/change in pace
Pain is unilateral
Causative factors: vasoconstriction of arteries followed by
vasodilation stretches nerve ending in vessel walls causing
pain
S/S: aura something signals the attack is coming on, lasts
about 30 min visual disturbances (light flashes, commonly
not verbalized though), N/V, photophobia, numbness &tingling in face & hands
Lasts for hours or days; until very intense
Recovery: sleep, photophobia, wet cloth on face, be alone
Precipitating factors:
o Foods tyramine, monosodium glutamate, milk
products or nitrates
Tyramine ~ cheese, chocolate, coffee, sausages,hot dogs, canned meats
Tyramine in foods with vasoactive monamine
BP ~ pickles foods, wineso Sun glare, weather changes causing sun to seem
brighter, noise, bright lights
o Birth control, Nitro vasodilator
o Mental & emotional excitement can not do welllwith certain changes in life; dont give surprise b-dayparty to
o Fatigue, hunger, smoking, alcohol
TX:
o Prevent relaxation techniques, diet (avoid foods that
cause it), quiet & dark roomso Ergotamine preps:
effective is taken early on must be taken 30-60 min prior to full blown HA (during aura)
vasoconstrictor
not used for HTN bc it is vasoconstrictor
Ergotamine tartate: acts on smooth muscle,
causing prolonged vasoconstriction of cranialblood vessels
SE:parasthesias of fingers & toes d/t
vasoconstriction; N/V, weakness in legs
d/t vasoconstriction, muscle pain in
extremities, bradycardia
contraindicated: cardiac pts, HTN, PVD,
impaired renal function, pregnancy
Cafergot: combo of ergotamine and caffeine
Imitrex: abords HA before it gets fullblown
Zomigo Meds to prevent
Inderal 40 mg tid-qid: beta blocker
remember not to abruptly dc Sansert 2 mg BID or TID: rarely used d/t SE
(blood dyscrasias) and the drug holidays that the
pt has to take q6 months for 1-2 months
prevents retroperitoneal fibrosis andpleuropulmonary and cardiac fibrosis
Cluster HA
Vascualr HA seen more during spring or fall
More frequent in men
No warning symptoms
Come in clusters one to eight per day each attack last 15
min - 3 hrs
Unilateral pain
Sudden onest & subsides abruptly
Usually localized around eye
Eyes & nose might run
Occurs mainly at night & wakes person up
This person will be up pacing floor vs migraine who wants to
be left alone
TX: eliminate the factors that cause it same as migraine
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Cluster VS Migraine
No aura Has aura
No vomiting Vomiting
Rarely nausea Nausea
Affect more men Affects more women
No menstrual relationship Menstrual cycles can trigger
Only neurological deficit is ocularsympathetic paralysis
Neurological deficits
Pt up pacing floor Dark, quiet room, alone, asleep
Frequency is greater Frequency not as often
Nocturnal attacks more frequent Waking hours normally
Serotonin does not at the onset serotonin occurs during HA
Tension HA
Muscle contraction HA
Caused by: result of sustained contraction of the mujscles ofthe neck and scalp, face & upper back
Prolonged state of contraction causes blood supply to the
muscle to become diminished and metabolic wastes begin to
accumulate
S/S: steady constant feeling of pressure in back of neck,
forehead, & temple; pt c/o feeling like a brick/wt is on head
TX: remove souce of stimuli; analgesics, Tylenol, muscle
relaxants, moist heat, massage
CVAAny functional abnormality of the CNS caused by a pathologiccondition of the individual cerebral vessels or of the cerebrovascular
system; includes any of the vessels which furnish blood to the brain
if any portion of brain has disturbed blood flow
Onset: any age; usually elderly; children with sickle cell
Risk factors: modifiable and non-modifiable
Pathological causes of CVAs
o Cerbral thrombosis
o Cerebral embolism
o Cerebral ischemia
o Cerebral hemorrhage
Epidural
Subdural
Subarachnorid
IntracerebralAnatomy of skull form outside to inside
Skin skull epidural (above dura) dura mater
subdura (below dura) arachnoid subarachnoid (below
arachnoid) pia mater brain (grey matter & white matter)
Meninges ~ fibrous connective tissue that cover the brain and
spinal cord; provide protection, support, and nourishment
Meningeal layers: dura mater arachnoid pia mater
Cerebral thrombosis
Blood clot occluding vessel that is supplying that area of the
brain with blood Slowly developing pathological process
Can occur over mins, hrs, days, or months not usually
abrupt though
May be preceded by prodromal warning such as
parasthesias Mary mentioned that migraine is preceded byprodromal warning also and also parasthesias
S/S: paresis ( strength & mobility of extremity), aphasia
(language function);
Can occur at rest or 1 hr after arising or after unusual fatigue Usually does not develop abruptly
Associated with TIA
Major causes: atherosclerosis
S/S: conciousness may or may not be lost; HA uncommon at
onset; may c/o dizziness, possible seizures
The ischemia from the clot leads to edema in that area of the
brain; since it is slowly occurring; symptoms may not be
initially d/t the thrombosis in that particular area it occurs
over time; as time goes the area of brain that is deprived of
oxygenation will start to swell edeam occurs
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Area of brain effected will give you the symptoms
HESI HINT
Atrial flutter/fibrillation has a high incidence of thrombus formation
following arrhythmia d/t turbulence of blood flow through allvalves/heart chambers.
Cerebral embolism
Can be fat or blood
Can occlude vessel totally or partially
Usually lodges in the middle cerebral artery branches of the
carotid carotid is larger so clot does not occlude and it keepsgoing until it reaches smaller vessels
Can orriginate from heart A-fib pts (from stagnant blood in
heart) or pulmonary (from infection or bedrest)
Occurs rapidly Not related to activity
Usually no prodromal signs maay have HA, but basically
have no warning sign that this is occuring
S/S & prognosis: Depends on area & how much tissue
Cerebral ischemia (TIA)
Insufficiency of blood supply to the brain
Mainly d/t [atheromatous] constriction of the arteries supplying
the brain
Most common manifestation is TIA TIA: transient impairment of blood flow comes and goes
o Temporary
o Symptoms usually resolve completely without
permanent damageo Commonly a sudden loss of motor, sensory, or visual
funciono Lasting few seconds or min or hrs, but no longer than
24 hrs
o Red flag: warning sign for impending stroke, advanced
atherosclerosis something is going on & can become
severeo TX: antiplatelet aggregation (presantine, aspirine) &
possibly anticoagulants
Cerebral hemorrhage
General info Bleed in brain
Rapid development
Occurs during activity valsalva, straining, anything that
the intrathoracic pressure that can raise the arterial pressure
S/S: result from the compression of cranial nerves or brain
tissueo Blood escaping compresses & displaces brain tissue
o Frequently asymptomatic until vessel breaks and then
o C/O severe HAo As blood escapes into brain tissue the pt will experience
nuchal rigidity (neck stiffness) the blood on thenerves or affecting the meninges is very irritating
o Dizziness; visual disturbances diplopia or loss of
vision; hemoplegia or hemoparesis; seizureso Clot will form just like in cut and blood left in tissues
will reabsorb clot will be reabsorbed/dissolved
rebleed even up to a week aftero The pt may not experience many S/S until the rebleed
then they will get severe S/S
Preceding events:
o Severe occipital HA with nuchal rigidity HA in back
of neck Mary discussed pt coming in with severe
HA and ruling out migraine d/t location and then saidthat if BP was then you know it is not good
o BP, vertigo, syncope, parasthesias in extremities,
epistaxis usually d/t BP, retinal hemorrhage
Types of cerebral hemorrhages
Epidural (extradural) hemorrhage
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7o Occurs outside dura mater
o d/t head injury (usually)
o middle meningeal artery has ruptured
o if not tx with in a few hours of incident they have little
chance of survival d/t rapid pressure on brain tissue
from the bleeding
Subdural hemmorrage
o Involves small vessels
o Acute, subacute, and chronic
o Chronic seen a lot in elderly takes a longer period of
time for a hematoma to form in this area of brain to
cause pressure on the braino Pts with chronic subdural hemorrhages may have them
for months without showing any S/So Mary gave an example of elderly pt falling a couple of
months prior Intracerebral hemorrhage
o Usually arterial BP (usually)
o S/S: depends upon the area of the brain that is involved
as well as the amount of bleeding; Rapid onset, severe
HA, nuchal rigidity, N, vertigo, loss of conciousness
o NI: Keep pt quiet and inactive it can occur with
activity
Subarachnoid hemorrhage
o Causes: trauma, hypertension, malformation of
arterial/venous system (AVM congenital)o The rupture is usually preceded by some degree of
physical straino S/S: sudden shooting pain in back of eye & sudden
shooting HA, N, nuchal rigidity, loss of conciousnesso HA is explosive
o If LP was done on this pt they would find blood in the
CSF
Diagnostic studies for CVA
Performed to differentiate btw the types/causes of the CVA
Pt hx when did it start, do they have any other problems
Neuro exam baseline to check for further deterioration;
continuously done, can predict affected areas of brain, andprognosis
Skull series (X-ray of skull/brain scan) see if there is
fx/trauma
EKG cardiac vs cerebral
LP usually not done bc can not be done if evidence of ICP
brain stem herniation or rebleeding can occur d/t the rapid
release of pressure from the ICP
MRI
CT initial diagnostic test, should be done emergently for
prompt tx (esp if candidate for tpa); differentiates type
ischemic vs hemorrhagic tx based on the typeo shows location and size of lesion; affected and/or
possibly affected areteries, veins, adjoining vessels, and
vascular branches predicts deficits pt will exhibit
PET
EEG ~ brain wave test; done with the things that stick on head
Interventions of CVA
Diuretics to edema & ICP
o Manitol osmotic diuretic; Lasix can be used as
adjunctive therapyo NI to check effectiveness of diuretics
Urinary output ~ at least 30 mL/hr should bemore
Possitive effects to neuro exam
Antiplatelet aggregates
o ASA
o Presantine 50-75 mg TID
o Ticlid
o Plavix
NURSING ALERT
Wrong pg # given but mary said When you get your pts hx duringassessment make sure you ask about herbal remedies. GINKO &
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GARLIC potentiate bleeding time. So if you give an ASA or anything
of that nature, your anticoagulants; you need to know what else the pt
is taking, like herbal remedies as well. Basically they will bleedingtime.
Anticoagulants
o Heparin & coumadin
TPA
o Criterial protocolsmust rule out active bleed
Surgical intervention for ischemic strokes
Carotid endarterectomy remove plaque/atherosclerosis/thrombus toprevent ischemia from the occlusion
Post op care from endarterectomy
Important, especially during first 24 hours
Keep head in neutral position
o Keep incision intact
o Do not want to prevent venous return HOB
Neuro assessment VS & hand grips
o VS
o Hand grips contraleteral weakness weakness on
opposite side
Monitor operative side for edema or hematoma
Nursing assessment after a sever cerebral hemorrhage
Classic picture of what you will see if somebody is having/just had a
cerebral hemorrhage Pt unconscious
Face is brick red
Difficulty in breathing
Contralateral paralysis
Cheek will blow out on paralyzed side during expiration d/t
forcefulness from the difficult respirations
BP
Slow, full, bounding pulse
The longer they are comatose the poorer the prognosisAcute care of CVA d/t cerebral hemorrhage
Complete bedrest to keep pt as quiet and inactive as
possible
Head in neutral position venous return
Prevent valsalva maneuver (straining) intrathoracic
pressure BP arterial pressure
3 main causes of death d/t hemorrhagic stroke Pneumonia
Rerupture of aneurism
Brain herniation ICP
Clinical manifestations of CVA
Baseline data: VS & neuro (Glasgow)
Perceptual Disturbances: parietal & temporal lobe (optic tract)
visual disturbanceso Homonymous hemianopsia: loss of half of visual field
(not entire eye, only half of each eye) temporary orpermanent; Loss of vision will be on SAME side of
paralysis
Neglect to one side of body
Difficulty judging distances
Eat only half of food if they only eat 50%
will be unusual looking food on the side of
visual loss will not be seen and thus ignored
turn plate around
Seizure activity: can cause seizures prophylactic
anticonvulsants Emotional lability: unpredictable; exaggerated use
distraction (change subject) when behavior becomes
exaggerated
Agnosia: incapable of importing information in various senses
o Visual identify colors
o Auditory problems identifying auditory stimuli
they can hear it, but cant identify where it is comingfrom and what it is
o
Olfactory
identifying smells
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o Tactile cant identify what they are touching hard
time identifying textures, shapes, etc
o
CRANIAL NERVE ASSESSMENT
1 Olfactory Identify smells with eyes closed
2 Optic Snellen chart; visual fields
3 Oculomotor 3,4,6 ocular rotation, conjugate
movements, nystagmus. Papillaryreflexes, inspect eyelids for ptosis
4 Trochlear
5 Trigeminal Cotton to forehead, cheeks, jaw. Rotate
btw sharp & dull in same places sensitivity to superficial pain. If
incorrect responses, test temperaturesensation.
6 Abducens
7 Facial Symmetry while smiling, whistles,
eyebrows, frowns, tightly closes eyelids
8 Acoustic Whisper or watch-tick test. Weber,
rinne
9 Glossopharyngeal Swallow, differentiate sugar vs salt
10 Vagus Gag reflex, hoarseness in voice,
swallow, AH uvula
11 Spinal accessory Shrug shoulders, head side-to-side
12 hypoglossal Stick tongue out, move it side-to-side
Type of Agnosia Affected Area
Visual Occipital
Auditory Temporal
Tactile Parietal
HESI HINTType of
Aphasia
inability to perform purposeful movements in the
absence of motor problems
Dysarthria: Difficulty articulatin
Dyshpasia: Impairment of speech and verbal comprehension
Aphasia: Loss of the ability to speak
Agraphia: Loss of the ability to write
Alexia: Loss of the ability to read
Dysphagia: Dysfunctional swallowing
Use short sentences when communicating with pt who has had a stroke dont give too many options (keep instructions & questions verysimple)
Prevention of longterm complications
Assess movement relieve pressure
Prevent external rotation of hip
Prevent clawlike contracture deformity
Prevent footdrop
Bladder control
Assess sensations Maintain Skin integrity
Speech therapy to regain communication
Brain Tumor
Biphasic age distribution peak 5-8 & 55-60
Males slightly higher risk
Children more likely to develop tumors of the cerebellum
cerebellum s/s imbalance & ataxia
90% of all tumors in adults are about tentorium
Type of Aphasia Affected Area
Auditory-Receptive Temporal
Visual-Receptive Parietal-Occipital
Expressive Speaking Frontal
Expressive writing Frontal
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Classified based on tissue origin, location, & relation to the
brain
TISSUE ORIGIN TERMINOLOGY
Neural Neuroma
Connective Glioma
Meninges MeningioBlood vessels Angio
Glands Adenoma
SUPRATENTORIAL INFRATENTORIAL
Cerebrum Cerebellum
Adults Children
HOB Supine
INTRINSIC EXTRINSIC
Originated inside brain Originated outside brain
Rapid growing Slow growing
Malignant (most) Benign (most)
Usually encapsulated
May or may not be
removed
Can be removed if too
much pressure
Most common tumor to metastasize to the brain is lung CA
followed by breast CA
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RIGHT-SIDED VS LEFT-SIDED
Left-sided paralysis Right-sided paralysis
VISIONSpatial perceptual deficits: Inability to judge distance, size, position
Inside from outside of clothing
Wheelchair running into frame of door
Buttoning clothes wrong
Lipstick crooked
One sided neglect hemianopsia
Reading left side of words can be dropped women might
be seen as men
Unable to discriminate words and lettersReading problems
Deficits in right visual field
BEHAVIORImpulsive behavior they will go too fast: teach small segments &
get them to demonstrate or repeat it back to you
If pt is getting up they might try to walk before they have theirbalance and then end up falling
When learning something new they might rush to the next stepand not learn it
Unaware of neurologic deficitsEuphoric; Distractable
Slow, cautious, & disorganized
These pts need frequent feedback
Dont give too many options (keep instructions & questions verysimple)
AnxiousQuick anger and frustration
LANGUAGEMay be alert & oriented Dysarthria: articulation muscles impaired
Aphasia may not be hard of hearing just can communicate
information; they hear, process it, but cant respond you do not have
to raise your voice
Receptive aphasia receiving
Expressive aphasia speaking
Global aphasia receptive & expressiveAgraphia
MEMORYDisoriented
Cannot recognize facesNo deficit
H
EARINGLoses ability to hear tonal variations No deficit
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Assessment
Take complete hx
o From pt
o From family they may have seen something pt cant
see personality or behavioral changes
S:S: common to all
o ICP: HA, nausea, Projectile vomiting, cushings
triad (bradycardia, BP with widening pulse pressure(systolic hypertension), braypnea)
o Focal disturbances: slight change in LOC seizure
activity
HESI info Mary pointed out as 2 classic differentiate from
Migraineo HA more severe upon awakening
o Vomiting not associated with nausea
Tumors based on tissue origination Neuroma (Acoustic)
o Involve cranial nerves
o Benign
o Intrinsic
o S/S: involves # VIII hearing & balance vertigo,
staggering, loss of coordination; as tumor grows it
compresses # V pain on same side of faceo Prognosis: can be completely removed, but because # V
is involved they can have facial paralysis; they can alsohave deafness on the side with lesion
Glioma
o Neoplasm of connective tissue
o Common brain CA
o Always intrinsic
o Infiltrating filtrates throughout brain tissue
o Can not be completely removed because it is not
ncapsulatedo Bulk can only be removed, but brain tissue comes with
o TX: surgery, chemo, radiation
o Not curable, Reoccurring
o Two main types
Astrocytomas
Graded 1-4; 4 more malignant & faster
growing 1 less malignant & slow
grawing
Medullablastomas
Rapidly growing
Children in brainstem (age 6-10)
Seeds through CSF
Most commonly in cerebellum
Meningioma
o Tumors that cover lining of brain
o Extrinsic usually encapsulated cant spread & can
be removedo Slow growing
o S/S: HA; depending on pressure put on tissue they may
have other symptoms like seizureo Prognosis: this is one you would rather have;
completely removed if needed; cured after removalo Not reoccurring
Angioma ~ Hemangioma ~ Hemangioblastoma ~
angioblasomao
Tumor of immature blood vesselso S/S: ICP HA, vertigo, nystagmus, + Rhomberg
where they tilt toward side of lesiono Prognosis is good; they can remove entire lesion
Adenoma ~ pituitary
o Can or pituitary function
o Anterior lobe GH, TSH, LSH, ACTH
o Posterior lobe ADH
o Hyperpituitarism
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Accelerates growth when GH secretion d/t
tumor children will have giantism & adults
will have acromegally
Cushings syndrome from ACTH d/t tumor
moon face, buffalo hump, BS, obesityo Hypopituitarism
Adiposity & loss of sexual function
Loss of libido, sterility, impotence, amenorrhea
Loss of vision pressure on optic nerve
Primary symptom that these pt have is when
they talk about HA they will describe it as
bifrontal HA not on one side; across entirefront of head
o TX: transphenoid hypophysectomy
Incision into maxillary gingival
Go up nasal cavity to remove tumor Postop
Mustache dressing
Mouth breathing (not nose)
No blowing nose, coughing, sneezing
ICP d/t tissue manipulation & edema
Diabetes insipidus transient
(temporary) post-op Foley, urine
looks like H20 & 3-10 L/day tx with
ADH VasopressinSymptoms according to site/location
LOBE Function S/S
Frontal Personality, mood,
language center
Impaired judgement, slowness
of thought, obscene language(never used before),
expressive aphasia
Temporal Short-term memory Hemianopsia
Parietal Sensory Parasthesias, hypoasthesias,
hyperesthesia or
sensitivity to touch
Occipital Visual Impairment, homonymous
hemianopsia
Cerebellar Balance Unstady gait, fall toward side
of lesion, intentional tremor(have tremor when reaching
for object), + Rhomberg, neg
finger to nose, nystagmus, HAin suboccipital area
Prognosis of Brain tumor
If untreated leads to death from either ICP or brain damage.
Intracranial surgery
Pre-op intracranial surgery
Tell pt what to expect post-op
o O2
o Suction
o IV
o Art lines
o Frqnt neuro check & VS
o Cranial dressing and drain
o Foley
o Transfusions
o Periorbitol edema & ecchymosis looks like they
were punched in eyes
o Leg exerciseso Deep breathing
Baseline neuro assessment to determine conditions needing
intervention post-op
Steroids brain edema
Prophylactic dilantin
Surgeries
Craniectomy
o Portion of skull removed to accomadate cerebral edema
by allowing expansions for inoperable tumor
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o Do NOT position pt on operative side no skull to
protect brain
Cranioplasty
o Repair of cranial defect d/t cosmetic defect or done to
protect braino NI
Observe dressing for bleeding & CSF leakage
Observe dressing for tightness, indicatingedema
Do NOT allow pt to lie on portion of headwhere skull has been removed
Take precausions to not accidently hit the head
Do NOT remove dressing without an orderstrict aseptic technique
Craniotomy
o Surgical opening of skull to gain access to intracranialstructures (monitors for ICP bur hole)
o Supratentorium adults, cerebrum
o Infratentorium children, cerebellum
HESI HINT
Craniotomy preoperative medications:
Corticosteroids to reduce swelling
Agents and osmotic diuretics to reduce secretions (atropine,
robinul)
Agents to reduce seizures (Dilantin)
Prophylactic antibiotics
Transphenoidal hypophysectomy approach
o Monitor for ICP d/t edema
o Pituatary surgery
o Incision in maxillary gingival upper lip btw gums
and lip; go up through the nasal passage
o Tumor is packed with muscle or fat from thigh/lower
abdomen
o Nasal cavities packed with Vaseline gauze and
ointmento Upper gums sutured
o Moustache dressing under nose to hold the packing in
placeo NI:
High fowlers
Vasopressin & steroids
No nasopharyngeal suctioning
Mouth breathing
No nose blowing, sneezing, or coughing
No tooth brusho Post-op complications
Diabetes insipidus
Hypothyroidism
Hypoglycemia CSF leak
Post-op intracranial surgery
Monitor for signs of ICP
Establish & maintain adequate airway and ventilation
Maintain body alignment after supratentorial
o HOB 30 (45)
o Position pt on side or back
o
If tumor was large do not turn on the side it was on
displacement from gravity
o Neutral head positon; no neck flexion venous
return ICP
o Pillow under head & shoulders not just neck
o When repositioning do not let pt help to prevent
valsalva have pt exhale
Maintain body alignment after infratentorial
o Supine HOB flat
o Position from side to side
o Head in neutral position esp when turning
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valsalva have pt exhale
Assess surgical dressing
o CSF leakage if clear use dextrose strip it will be +
for glucose; if bloody look for halo sign (clear/yellow)
HOB, Diamox formation of CSFo Excessive bleeding
o Do not change dressing until ordered
o Ventricular drainage
Monitor elimination avoid circulatory overload
Provide pt comfort
o HA for 24-48 d/t stretching/irritation of nerve of the
scalp
Activites to avoid bending over, coughing, sneezing;
valsalva, vomitting
Surgery complications Meningitis
o D/T
Infection
Blood in the subarachnoid space
Prolonged use of intracranial monitoring
devices 2/3d post surgeryo S/S
Headache, chills, fever, irritability, nuchal
rigidity, soreness of skin & muscles, cells inCSF, + Kernigs, + Brudzinski, delirium,
convulsiono PI
Strict aseptic technique
Prophylactic antibiotics
Seizures
o Greater risk with supratentorial
o NI: padded side rails, side rails up, dilantin prophylactic
Stress ulcers pepcid, protonix Diabetes insipidus
o Hypothalamus and pituitary gland area surgery
edema interferes with production of ADH excessiveoutput
o TX: fluid and vasopressin
Seizures
Divided into 2 major classes
Generalized
Person loses conciousness for a few sec to a min, no warning
or aura associated
Tonic-clonic (Grand Mal)
o Most common
o Loss of conciousness
o Tonic phase stiffening of body
o Clonic phase Jerking of extremities
o Excessive salivationo Bite tongue or cheeks
o Incontinence
o After seizure muscle soreness, tired, sleep for hours
o May not for normal for several hours to days after
o No memory of seizure
Petit Mal (Absent)
o Usually only children
o Rarely continues beyond adolesecence
o Brief staring spell that lasts only a few sec can gounnoticed
o Can have 100 or more episodes in a day
o May experience twitching in facial muscles
o Typical of kids that come home from school with note
from teacher saying that they are staring out into space,
they are not paying attention, and their grades areslipping
Partial
Begin in a specific region of cortex
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Confined to one side of brain and remain partial or focal in
nature or may spread to involve entire brain
Simple motor Jacksonian simple partial seizures
o Only a finger or hand may shake or mouth may jerk
uncontrollablyo May talk unintelligibly
o May be dizzy
o May experience unusual or unpleasant sights, sounds,
odors, or tasteso No loss of conciousness
o Rarely last longer than minute
Complex symptom psychomotor Complex partial
o Involves temporal lobe
o Person either remains motionless or moves
automatically (automatisms) either way it is
inappropriate movement for the time and placeo May experience emotions of fear, anger, elation, or
irritability.o Person does not remember the episode with it is over
o Lipsmacking
o Automatisms are picking at clothes, fumbling with
objects, walking away (during conversations)
Status epilepticus
Most serious
Continous
No conciousness between seizures
Problem is lack of O2 to brain brain damage can result
Severe injury or death can happen d/t trauma head injury
from falling, drowning in tub, sever burn
TX: IV Valium, Ativan, Cerebyx administered slowly to stop
seizures Dilantin, phenobarbital are administered later to
maintain seizure free state
Diagnostic Studies
Aimed at determining type, frequency, and severity, and
factors that precipitate them.
o Labs, EEG, CT, etc to determine cause of seizure
Management
Look at 2192 and picture pt on side with O2 and suctionsetup. Pads, o2, suction when pt has hx of seizures
Maintain privacy of pt
Ease pt to floor if possible
Protect head with pad
Loosen constrictive clothing
Push furniture out of way
If pt in bed, remove pillows and raise side rails
If aura precedes, insert oral airway to reduce the possibility of
pt biting tongue or cheek do not put anything in their mouth
during the seizure; can only be done prior or after Do not restrain pt
Put pt on side with head flexed forward allows tongue to fall
forward and facilitates drainage of saliva and mucua.
Use suction to clear secretion
O2
After keep pt on side
Make sure airway is patent
After grand-mal, usually a period of confusion
Short apneic period may occur during or immediately after ageneralized seizure
Pharmacological management
Maintain seizure free statemust be at a therapeutic level Periodic serum therapeutic levels taken usually every 6
months
Dilantin side effects gingival hyperplasia, drowsiness
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Meningioma Neuroma
(Acoustic)Gliomas Hemangioma
(hemangioblasoma
angioblastoma)
Adenoma
Astrocytomas Meduloblas
tomas
Location Covering of
brain
Crainial VIII
(hearing &balance)
Grows &compresses V
(Acoustic &
Facial)
Connective tissue Immature blood vessels Pitutitary
Tumor of ductless glandAdultscerebrum
Childrencerebellum
Mostcommonly
incerebellum
Originated Extrinsic Intrinsic Always intrinsic Forms a cyst
The tumor itself remains alittle nodule in the cyst wall
Benign VS
malignant
Benign Benign Usually malignant
Malignant
Grade 4 mostmalignant
Highly
malignant
Growth Slow ------------ Gades 1&2 ~slow
Grades 3&4 ~rapid
Rapid
Age 30-60 ------------ Any Frqntly inchildren
Any
Sex Femalesgreater
------------- Female to male 2:1
Prognosis Can becompletely
removed
Not recurringAfter removal
they are cured
Not curable; can neverremove all of tumor;
When removed brain tissue
comes with it d/t beinginfiltrating
Good; they can remove entirelesion
S/S Depends on
location
Vertigo,
staggering loss of
ICP HA, vetigo,
mystagmus, + rhomberg
function function
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HA usually coordination
Pain on side offace
Facial paralysis &
deafness
tilt toward side of lesion
of GHHyperpituittar
ism
Children:
gigantismAdultsacromegaly
Cushing;s
syndrome
ACTH:moon face,
buffalo hump,
BS
Encapsulated
VSInfiltrating
Encapsulated Infiltrating