neuro bsn 3c
TRANSCRIPT
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} NEUROLOGICAL DISORDERS
Aka: Cephalgia
Classification:a. PRIMARY
is one for which no organic cause can be identified.b. SECONDARY
Is a symptom associated with an organic cause, such as in braintumor or an aneurysm.
} 2.) CLUSTER HEADACHE} have cyclical pattern of 1-3 short-lived attacks of periorbital pain} occurs more often in men} TRIGGERED BY ROH CONSUMPTION} pain described as deep, boring, intense pain of such severity that the
client has difficulty remaining still3.) MIGRAINE HEADACHE
considered as vascular h/a, vasospasm & ischemia of intracranial vesselbeing the cause of painh/a is most often unilateral, but pain may occur on alternate sides withdifferent attack
} Etiology: Idiopathic
Risk Factors:Menstrual CycleStressDepressionSleep DeprivationFatigueOveruse of MedsTyramine-rich foods
PATHOPHYSIOLOGY:Dysfunction of brainstem pathway
Abnormal metabolism of serotoninIncrease plasma serotonin level
Dilates cerebral blood vessel} 4 Phases of Migraine:
I. ProdromeII. AuraIII. Headache phaseIV. Recovery Phase
Diagnostic Tests:} Detailed History Taking} Complete Physical & Neurological Examination
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} CT-Scan} MRI} Cerebral Angiography} Medical Management} Preventive}
Abortive
Medications:1. Serotonin receptor antagonist
Sumatriptan (Imitrex)Ergotamines
Ergotamine tartrateAnti-epileptics
TopiramateGabapentin
NURSING INTERVENTIONSH-eat application or massage
E-ducate on prevention
A-nti-emetic medications
D-im or dark environment
A-dminister analgesics
C-oach on habit and lifestyle changes
H-ead elevation
E-xercise programs
INCREASED INTRACRANIAL PRESSURE
} Intracranial hypertension associated with altered states of consciousness.} Monroe-Kellie Hypothesis} Causes of Increased ICP} Cerebral edema} Brain swelling} Brain surgery} Mass lesions in the brain} Hydrocephalus} Valsalva maneuver } Clinical manifestations:} Changes in LOC} Projectile vomiting
Cushings Triad:
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} Hyperthermia} Cushings ulcer } Seizure} Papilledema} Brain Herniation
Diagnostic Tests:1. CSF Analysis with manometer 2. ICP Monitoring Device
Management
R- educing CSF & Intracranial Blood volume
E- dema decrement
D- ecrease of metabolic demand
U- pright position
C-ontrolling fever
E-nsure oxygenation
D-rug administration
SEIZURE DISORDER} Is a sudden, abnormal electrical discharge from the brain that results in
changes in sensation, behavior, movements, perception and consciousness} EPILEPSY- is a chronic disorder of recurrent seizure.
Etiology} Pathologically acquired epilepsy} Biochemical Epilepsy} Posttraumatic} Idiopathic
Clinical Findings: TYPES OF SEIZURE
I. PARTIAL SEIZURE
1.) SIMPLE-PARTIAL } Originate in themotor cortex of thefrontal lobe.
} Characterized byJACKSONIANMARCH
2. ) COMPLEX-PARTIAL
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} Originate in thetemporal lobe andlimbic system
} Characterized by AUTOMATISM.
II. Generalized Seizure
1.) GRANDMAL SEIZUREPre-ictal: Begins with an AuraIctal Phase: 2 phases:
TONIC- muscular rigidity/ extension of extremitiesCLONIC- muscular jerking.
Post-ictal Phase: Sleep2.) PETIT-MAL
Occurs to children ages 4- pubertyThe victim appears to be daydreaming.
3.) MYOCLONICInvolve a sudden uncontrollable jerking movements of either a single muscle group.
4.) ATONICAssociated with total loss of muscle tone.
5.) Febrile Seizures
Complication:
STATUS EPILEPTICUS- continuous seizure lasting for more than 30 minutes withoutfull recovery in between.
Diagnostic Tests1. EEG2. MRI3. PET Scan
Medications:} Phenytoin} Phenobarbital} Carbamazepine} Ethosuximide (Zarontin)} Valproic Acid} Diazepam
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Surgical M anagement: Cortical Resection? Corpus CallosotomyTemporal LobectomyHemispherectomyVagal nerve Stimulator Implants
NURSING Management
Seizure precautions:1. Monitor temperature & Respirations2. Note level of consciousness3. Provide a quiet, dimly lighted rooms.4. Prepare plastic airways and suction machine
NURSING Management} Safety
} Side-rails up} Ease the patient to the floor (if sitting on a chair)} Remove pillow (if in bed)} Loosen constrictive clothing} Position patient on one side if possible} Do not restraint
} Airway} Suctioning} Oxygen
Traumatic Head Injury
- a traumatic insult to the brain capable of causing physical, intellectual, emotional,social, and vocational changes
- National Head Injury Foundation
Mechanism of Brain Injury:
a. Acceleration
b. Deceleration
c. Acceleration- Deceleration
d. Rotation
e. Deformation
1. OPEN those that penetrate the skull } SCALP INJUR IES
} Laceration, hematoma, contusion and abrasion to theSKIN.
} SKULL F RACTURES
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} Caused by a force sufficient to fracture the skull} Depressed skull fractures injure the brain by bruising
it or by driving bone fragments into it} TYPES OF SKULL FRACTURE
1. Simple
2. Comminuted3. Depressed4. Basilar
CLINICAL MANIFESTATION} Battles sign} Racoons eye} Subconjunctival hemorrhage} Rhinorrhea} Otorrhea}
H
ALO S
IGN
RISK FACTORS:
2 . CLOSED -caused by blunt trauma } CONCUSS IONS
} A jarring of the brain} temporary LOC (
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} Onset of eye movement paralysis on the same side of the hematoma
} Lapses into coma} INTRACRANIAL HEMMORHAGE
2.) SUBDURAL HEM ATO M A } Rupture of VEINS in the subdural space
} Acute rapidly develop (24-48 hours)} Subacute (48hrs -
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DIAGNOSTIC TESTS1. Skull X-ray2. CT-Scan3. MRI4. Cerebral Angiography
Treatment of Increased ICPSupportive Measures:Mechanical ventilationSeizure PreventionF & E MaintenanceNutritional supportPain Management
} Surgical Management
Goal: Decompression
1.) CRANIECTOMY
- excision of the cranial bone without replacing} Surgical Management
Goal: Decompression
2.) BURR HOLE
- decompression, evacuation of clot & abscess.} Surgical Management
Goal: Decompression
3.) CRANIOTOMY
- opening of the cranium} Surgical
Approach} NURSING MANAGEMENT
Maintain Patent AirwayNeurological assessmentTreatment of ICPSupportive measuresElectrolyte & Fluid BalanceAdequate NutritionPrevention of InjuryMaintaining Skin integrity
result of trauma to the vertebral column.
CAUSES- MECHANISM OF INJURY
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A. Acceleration B. Deceleration C. Hyp erflexion D. Hyp erextension E. Axial Loading
F. Excessive Rotation
G eneral: PoikilothermiaIntegumentar y:
Warm, dry skin below level of injury
Res p irator y: Lesions at C1-C3: apnea, Inability to coughLesions at C4: poor cough, diaphragmatic breathing, hypoventilationLesions at C5-T6: decreased respiratory reserve
Cardiovascular Lesions above T5: bradycardia, hypotension, postural hypotension,absence of vasomotor tone
G astrointestinal Decrease or absent bowel sound (paralytic ileus in lesions above T5)Abdominal distentionConstipationFecal incontinenceFecal impaction
Urinar y Retention for lesions between T1 and L2Flaccid bladder (acute stage). Loss of nerve innervations causes atony of the bladder which causes urine retention.Spasticity with reflex bladder emptying (later stage)
Re p roductive Priapism (prolonged penile erection)Loss of sexual function
Neurologic i. Complete
Flaccid paralysis &anesthesia below level of injuryTetraplegiaParaplegia
ii. incompleteM usculoskeletal
Muscle atony (in flaccid state)Contractures (in spastic state)
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1. SPINAL SHOCK
Characterized by decreased reflexes, loss of sensation andflaccid paralysis below the level of injury
2. NEUROGENIC SHOCK
develops due to the loss of autonomic nervous system function below thelevel of the lesion.
Characterized by:} Bradycardia} hypotension
3. AUTONOMIC DYSREFLEXIAIs a complication with a lesion T4-T6.A hypertensive medical emergency.Caused by:
Overdistended bladder Rectal stimulationImpaction
S/Sx:PiloerectionSevere HPNHeadacheDiaphoresisNasal congestion
MANAGEMENT:1. Elevate head of the bed
2. Check the patency of catheter 3. Administer Hydralazine (Apresoline)
DIAGNOSTIC TESTSSpinal RADIOGRAPHYCT/MRIECG
EMERGENCY MANAGEMENT1. Immobilize on a spinal back board2. Avoid flexion, rotation and extension of patients neck and head3. Transport the patient to spinal injury or trauma centers4. P HARM ACOLO GI C THERAPY
} Dexamethasone (Decadron)} Anti-inflammatory and edema reducing effects
} DEXTRAN} Plasma expander to increase capillary blood flow and treat
hypotension
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} Baclofen (Lioresal)} Control muscle spasticity
1. RESP IRATORY THERAPY 2. SKELETAL TRACT ION and REDUCT ION
3. Promoting adequate breathing & airway4. Improve Mobility5. Promoting adaptation top sensory & Perceptual alterations6. Maintaining skin integrity7. Maintaining urinary elimination8. Improving bowel function9. Providing comfort measures10. Prevention of thrombophlebitis
Aneurysm} An intracranial aneurysm is the weakness in the tunica media, the middle
layer of the blood vessels.} The most common type is saccular or berry aneurysm.} Are found more often in the anterior cerebral circulation
RISK FACTORS:SmokingHypertensionAtherosclerosisAlcohol abuseStimulant drug abuseAging process
Clinical Manifestations} Asymptomatic
Ruptured Aneurysm:} Sudden onset of headache Worst headache of my life} Vomiting} Generalized seizure} Decrease LOC: confused, lethargic, coma} S/sx of Menigeal Irritation( Nuchal rigidity, photophobia)} Focal motor & Sensory Deficits
Hunt-Hess Clinical Grading ScaleI. Alert, minimal headache
II. Alert, moderate to severe headache (cranial nerve palsy allowed)III. Lethargic or confused, mild or focal deficitIV. Stuporous, moderate to severe hemiparesis, possible early decerebrate
rigidityV. Deep coma, decerebrate rigidity, moribund appearance.
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Diagnostic Tests:
} History Taking} Physical Assessment} CT Scan}
MRI} Transcranial Doppler
Medical Management1. Neurologic Assessment2. Maintain a patent Airway3. Continuous hemodynamic monitoring4. Nimodipine administration5. Morphine administration6. I & O monitoring
Surgical Management1. ANEURYSM CLIPPINGSurgical obliteration of the aneurysm with a metal clip toeliminate the risk of rebleeding.
ENDOVASCULAR THERAPY & EMBOLIZATIONInvolves obliteration of the aneurysm by means of platinum coils.
Nursing Management
A-ssess neurologic status
E-levate head at 30 degrees
U- rine output monitoring
R-espi and cardio monitoring
Y-oukeep patient & family members in a quite and comfortable environment
S -urgery preparation
M -edication administrationIs a syndrome of a group of sudden focal neurological deficit resulting frominterruption of cerebral blood flow.
Classification of Brain Attacks:
Ischemic (emboli, Thrombus)Hemorrhagic
INITIAL MANIFESTATIONS
S-evere& sudden headache
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T-trouble in speaking
R-ight or left hemiparesis
O-cular disturbances
K-onfusionE-mpairement in coordination
Changes in LOCSpatial and proprioceptive dysfunctionImpairment in memory, judgment, or problem-solving and decision-makingprocess
Decreased ability to concentrate and attend to taskAphasiaAlexiaAgraphiaAcalcula
Homonymous hemianopiaAgnosiaApraxiaHemiplegiaHemiparesisAtaxiaDysarthria
DysphagiaFlaccidity of the muscles associated with paralysis on the motor neurons.
SpasticityPtosisUnilateral neglect syndromeAmaurosisfugax
CT ScanMRICerebral AngiographyDoppler Flow studies
NSG MGT:Maintenance of a patent airway and optimal oxygenation
Control cerebral edemaControl of fluid and electrolyte balanceMaintenance of adequate cerebral blood flow and cerebral perfusionpressure
} Antihypertensive.} Platelet Aggregant
} Aspirin} Ticlodipine
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} Anticoagulant} Heparin} Warfarin
} Thrombolytics} t-PA} urokinase} streptokinase
} Calcium channel blockers} Mannitol} Dexamethasone
Surgical MGTCarotid EndarterectomyTransluminal AngioplastyStentingExtra-Intracranial (EC-IC) BypassOptimizing cerebral tissue perfusionImproving Mobility and Preventing Joint DeformityEnhancing Self-CareManaging Sensory-Perceptual DifficultiesAssisting with NutritionAttaining Bowel and Bladder ControlImproving CommunicationMaintaining Skin Integrity
Myesthenia Gravis
- an autoimmune neuromascular disorder in which there is chronic, progressivedecreased amplitude of the nerve impulse at the myoneural junction.
RISK FACTORSGender: FemaleAge: 20-40 y.oThymicTumor
} PTOSIS} Diplopia} Dysarthria} Dysphagia} Respiratory muscle weakness} Skeletal muscle weakness
CLASSIFICATIONS A. Ocular FormB. Generalized Form
Stages of generalized FormI. Mild
II. Moderate
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III. Acute FulminatingIV. Late Severe
Tensilon Testing} (+) MG; Myasthenic Crisis
} improvement in muscle strength post injection}
NEOSTIGMINE METHYLSUFATE (Prostigmin) longer duration} (-) MG; Cholinergic Crisis
} no improvement in strength} increase in severity} ATROPINE SULFATE antidote
EMG
MYASTHENIA GRAVIS1. Drug Therapy
Anticholinesterase drugs
CorticosteroidsCytotoxic and Immunosuppressive drugsPlasmapheresis
THYMECTOMY1. Promote Effective breathing pattern2. Improved Airway clearance3. Ensure adequate nutrition4. Increase activity tolerance5. Provision of optimum vision
GBS- Landry GBS, Landry-GBS-Strohl
} Is an autoimmune attack of the p eri p heral nerve m yelin .
RISK FACTORSViral infection- history of upper respiratory and GI infection
} Campylobacter jejuni most common; Gram-negative} Targets myelin sheath} Poultry, pets, raw milk and contaminated water
CMVEBVHepatitisHIVRubella &rubeolaVaricella
Clinical M anifestations } Bilateral weakness in the legs} Respiratory dysfunction} Dysphagia
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} CN VII (facial)} Horners syndrome
} ip silateral p tosis } eno p hthalmos } Anhidrosis
CSF analysis
EMG} Plasmapheresis} Steroids} Immunoglobulin infusion} Ace inhibitors} Medications: 4 AS(ANT IB IOT ICS, ANAL G ES IC, ANT ICOA G ULANTS,
AZAT HR IP INE & CYCLOP HOSP HAMI DE)} Maintaining Respiratory Function
1. Maintaining Respiratory Function2. Enhancing physical mobility3. Providing adequate nutrition4. Improving communication
5. Decreasing fear and anxiety} Progressive, degenerative disease of the CNS.Etiolog y:UNKNOWN
} Abnormalities in T-helper cells, T-suppresosr, B-lymphocytes} Viral: mumps, measles, rubella} Stress} Trauma} Pregnancy} Age: 20-45 y.o} Female
Common initial symptoms:} Tingling sensation} Numbness} Sensory symptoms: Lhermittes sign} Motor Symptoms} Charcots Triad
} Scanning of speech} Nystagmus} Tremors
} DIAGNOSTIC TESTCT-ScanCSF AnalysisMRI
PHARMACOLOGIC THERAPYSPASTICITY
Baclofen; ValiumFATIGUE
SymmetrelRitalin
Urinary frequencyAnticholinergics propantheline
Urinary retention
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Cholinergic prostigmine,bethanecol
ExacerbationsCorticosteroids, novantrone
Promoting physical mobility
1. Prevent Injury2. Enhancing bladder and bowel control3. Enhancing communication4. Manage feeding difficulties5. Improve sensory & cognitive function
BELS PALSY
- a sudden loss of motor control on one side of the face.Age: 20-60 y.oGBSGeneticsViral infection
HerpesEpstein-Barr virus
pain behind the ear 1-2 days prior to paralysis,unable to:
smile,frown,
close eyelids,puff out cheeks,
close the lips.Mouth displaced
Saliva droolsConstant tearingLoss of taste at the anterior 2/3 of the tongue.EMG
Steroids for 7 daysAnalgesicsWarm or moist applicationTENSChew on unaffected sideOral careArtificial tear Soft diet
} Tic douloureux} Idiopathic CN 5 disorder characterized by pain along one or more branches
of the CN 5.
CAUSE: UNKNOWN (compression of cerebellar artery)Age: 50 y.oGender: Female
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Compression:ArteriosclerosisAneurysmAcoustic neuromaMultiple sclerosis
Infection of the jaw and teethDIAGNOSTIC TESTS:
CT-ScanMRI
} Medical managementPharmacologic Therapy
Anti-convulsantsCarbamazepinephenytoin
Muscle relaxantsNerve block
SURGICAL MANAGEMENTPERCUTANEOUS RADIOFREQUENCY RHIZOTOMYMICROVASCULAR DECOMPRESSION/ JanettaALCOHOL/ GLYCEROL INJECTION
NURSING MANAGEMENTProvision of therapeutic environment
Room should be kept at moderate temperature and free of draftsto prevent stimulation on Trigeminal nerve.
Avoid jarring the bed or touching the patients face that cantrigger the onset of pain on the three branches of trigeminalnerve.
} Provide lukewarm water and soft cloths or cotton saturated solutions notrequiring rinsing for cleansing the face.
} Use soft-bristled toothbrush or a warm mouthwash during oral care.} Avoid extensive conversation during the acute phase because it may trigger
paroxysms of pain.} Diet must be high protein and calories and easy to chew.
Meningitis- is an inflammation of the pia mater, the arachnoid, and the cerebrospinal fluid-filled subarachnoid space.
} ETIOLOGYBacteriaVirus
RISK FACTORS:
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Head traumaOtitis mediaSinusitisMastoiditisImmunosupression
Systemic sepsisMOT:
Blood-streamDirect spread
ASSESSMENTHeadacheFever S/sx of meningeal Irritation:
Nuchal rigidity
(+) Kernigs Sign(+) Brudzinski SignPhotophobia
OpisthotonusSkin Lesions (N.menigitidis)
SeizureIncrease ICPNon-communicating hydrocephalusFriderichsen syndrome
CS F ANALYS IS CT -SCAN SKULL RAD IOG RAP H Y
Pharmacologic TreatmentPenicillinDexamethasone
PhenytoinRespiratory isolation
Im p rove of Cognitive F unction Op timizing Cerebral Tissue p erfusion Promotion of Comfort M aintenance of Normal Bod y Tem p erature Preventing Com p lications
Encephalitis- is an inflammation of the brain parenchyma (brain tissue) and often the
meninges.
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} Etiology: Viral Infection} Mumps} Measles
MOT: Direct InvasionChanges in LOCNuchal RigidityFocal neurologic deficitsMotor DysfunctionS/sx of Increased ICPLumbar PunctureMRIEEGTreatment of Increased ICPIntubation & mechanical ventilation
Pharmacologic ManagementDexamethasone
Acyclovir (Zovirax)Anti-pyreticAnalgesicsAnticonvulsants
Improve Tissue cerebral perfusionAdequate oxygenationPromotion of comfortAttain Normal Body temperature
Parkinsons DSE- Paralysis agitans
} Is a chronic, progressively degenerative disease of the basal ganglia.} Cause: Unknown
Age: >30 y.oGender: MaleGeneticsAtherosclerosisFree radicalsViral infectionsHead traumaChronic use of anti-psychotic medications
3 CARDINAL SIGNS1. Tremors2. Rigidity: Cogwheel3. Bradykinesia
} Micrographia} Masked-like facial expression} Short-shuffling steps.PET SCAN
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CSF ANALYSIS
M ED ICAT IONS:
1.) Anti-Cholinergic} Trihexyphenidyl (Artane)}
BenztropineMesylate (Cogentin)2.) Anti-histamine: Benadryl
3.) Dopaminergic Agent} Carbidopa/Levodopa (Sinemet)} Bromocriptine
4.) Anti-viral: Amantadine
5.) Anti-depressantsImproving mobilityEnhancing self-care activitiesImproving bowel eliminationImproving nutrition
Enhance swallowing 6.) Monoamine oxidase Inhibitors: Selegiline
Improving communicationSupporting coping abilities