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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