GROUP 4: EPILEPSY Nurin Syahidah Syafiqah Nadhirah Nor Anis Zullyana Nik Mohd Haziq Asyraf Hamzi Muhamad Mohd Hanif Ahmad Fais Aimi Amalina
Transcript
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GROUP 4: EPILEPSY Nurin Syahidah Syafiqah Nadhirah Nor Anis
Zullyana Nik Mohd Haziq Asyraf Hamzi Muhamad Mohd Hanif Ahmad Fais
Aimi Amalina
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DEFINITION Epilepsy is a chronic disorder of the brain that
affects people in every country of the world. It is characterized
by recurrent / two or more unprovoked seizures. Seizures are brief
episodes of involuntary shaking which may involve a part of the
body (partial) or the entire body (generalized) and sometimes
accompanied by LOC and loss control of bowel or bladder function.
Pathophysio > 1. Result of excessive electrical discharges in a
group of brain cells. 2. Different parts of the brain can be the
site of such discharges. 3. Seizures can vary from the briefest
lapses of attention or muscle jerks, to severe and prolonged
convulsions. 4. Seizures can also vary in frequency, from less than
one per year to several per day.
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EPIDEMOLOGY (BY WHO) Epilepsy is a chronic noncommunicable
disorder of the brain that affects people of all ages. Around 50
million people worldwide have epilepsy. ~ 80% of the people with
epilepsy are found in developing regions. Currently 70% - responds
to treatment, yet about 3/4 fourths of affected people in
developing countries do not get the treatment they need. Patient is
associated with stigma and discrimination in many parts of the
world
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BY NICE Incidence is estimated to be 50 per 100,000 per year
the prevalence of active epilepsy in the UK is estimated to be 510
cases per 1000. Two-thirds of people with active epilepsy have
their epilepsy controlled satisfactorily with anti-epileptic drugs
(AEDs). Other approaches may include surgery
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CAUSES (WHO) The MC type for 6/10 people with the disorder is
called idiopathic epilepsy and has no identifiable cause. In many
cases > underlying genetic basis. Secondary epilepsy/
symptomatic epilepsy > epilepsy with a known cause could be: 1.
brain damage from prenatal or perinatal injuries a loss of oxygen
or trauma during birth, low birth weight 2. congenital
abnormalities or genetic conditions with associated brain
malformations; 3. a severe blow to the head; 4. a stroke that
starves the brain of oxygen; 5. an infection of the brain such as
meningitis, encephalitis, neurocysticercosis; 6. certain genetic
syndromes; 7. a brain tumor
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CAUSESCAUSES
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CLASSIFICATION OF EPILEPSY
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TypeSub-typeMain features Generalized seizuresTonic-clonic
(Grand mal)Loss of consciousness Tonic phases Clonic phases Tongue
biting Incontinence Seizure lasts < 5 minutes Absences (Petit
mal)Brief period of unresponsiveness Episode lasts < 30 seconds
Partial seizuresSimple (Jacksonian epilepsy)Motor, sensory,
autonomic or psychic features Comples (Temporal lobe epilepsy)
Impaired consciousness Automatic repetitive acts OthersMyoclonic
Atonic
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GRAND MAL (TONIC-CLONIC) EPILEPSY Begins in the pre-school
child/occasionally at puberty Warning/aura LOC tonic & clonic
convulsions recovery Aura: Mood change Irritability Brief
hallucination Headache Sensation of strong smell (e.g burning
rubber) Initially: Face become pale Pupils dilate Opisthotonous
& glottic Respiratory muscle spasm cry & cyanosis
STATUS EPILEPTICUS Definition A seizure lasting for more than
30 min or repeated seizures over the same period without
intervening periods of consciousness dangerous: Inhalation of vomit
& saliva Brain damage d/t cerebral hypoxia Death
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PETIT MAL SEIZURES MC occur during childhood Characterized by:
Minimal/no movements : may appear like a blank stare Brief sudden
loss of awareness/consciousness (few seconds) Recur many times
Decreased learning (often thought to be daydreaming)
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SIMPLE PARTIAL (FOCAL) SEIZURES Can be motor/sensory/behavioral
Confined to one area Present as: Muscle contractions of a specific
body part Jacksonian epilepsy : spread to adjacent muscles on the
same side of the body Abnormal sensation Nausea, sweating, skin
flushing, dilated pupils
EPILEPSY : MANAGEMENT Call for help Stop treatment Lay the
patient flat on the chair, do not try to move the patient while
they are actively fitting Protect the patient from injury; Do not
attempt to put spoon or tongue depressor on between the teeth or
any other hard objects Clear the working area Do not attempt to
restrain or holding down the patient during seizure
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If patient is having difficulty to breathe or becoming
cyanosed, gently extending the neck to maintain the airway CPR or
mouth-to-mouth breathing cannot be performed during seizure and
rarely needed after seizure. Uncomplicated seizure: no other
treatment is necessary If attack continues longer than normal or
> 10 minutes, give Midazolam 10mg IM If attack does not resolve
within the next 5 minutes, call ambulance (status epilepticus)
While waiting, protect the airway with suction (remove saliva) and
administer high flow oxygen 10-15 L/min
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NICE
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MANAGEMENT The AED (anti-epileptic drug) treatment strategy
should be individualised according to the seizure type, epilepsy
syndrome, co- medication and co-morbidity, the child, young person
or adult's lifestyle, and the preferences of the person, their
family and/or carers as appropriate. [NICE 2004]epilepsy
syndrome
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EMERGENCY STOP treatment! Medication: Administer buccal
midazolam as first-line treatment in children, young people and
adults with prolonged or repeated seizures in the community.
Administer rectal diazepam if preferred or if buccal midazolam is
not available. If intravenous access is already established and
resuscitation facilities are available, administer intravenous
lorazepam. [NICE 2012]
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AAPD
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REFERENCE 1. WHO;
http://www.who.int/mediacentre/factsheets/fs999/en/ 2. NICE ;
guidance.nice.org.uk/cg137 3. Special Care in Dentistry. Churchill
Livingstone. 4. ILAE ;
Ihttp://www.ilae.org/Visitors/Centre/Definition.cfm