Team 2 Case Study Epilepsy
Team 2 Case Study Epilepsy
COLLEGE OF NURSING
F. Ramos St. Cebu City
Submitted by:
Delos Reyes, Jermaine
Duran, Celine Eluza
Falcone, Jasmine Mae
Federizo, Enlil Joshua
Labajo, Adreanne Dorothy
Luna, Cristoff Earl
BSN 2A
Submitted to:
Ms. Patricia Mae Gabaca, RN
Clinical Instructor
I. Introduction
Epilepsy
Definition
Epilepsy is a neurological or a central nervous system disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior,
sensations, and sometimes loss of awareness. It is a chronic disorder that causes unprovoked, recurrent seizures. A seizure is a sudden rush of electrical activity
in the brain. Epilepsy is the fourth most common neurological disorder and affects people of all ages.
Types
1. Generalized Epilepsy – Seizures produced by widespread abnormal electrical impulses present throughout the entire brain.
a. Generalized tonic-clonic (Grand Mal). Symptoms: The patient loses consciousness and usually collapses. The loss of consciousness is followed by
generalized body stiffening called the “tonic” phase of the seizure, then by violent jerking called the “clonic” phase of the seizure, after which the
patient goes into a deep sleep called the “postictal” or “after-seizure” phase. During grand-mal seizures, injuries and accidents may occur, such as
tongue biting and urinary incontinence.
b. Absence. Symptoms: Brief loss of consciousness for a few seconds with few or no symptoms. The patient typically interrupts an activity and stares
blankly. These seizures begin and end abruptly and might occur several times a day. Patients are usually not aware that they are having a seizure but
may have a feeling of “losing time.”
c. Myoclonic. Symptoms: Sporadic and brief jerking movements, usually on both sides of the body. Patients sometimes describe the jerks as brief
electrical shocks. When violent, these seizures might result in dropping or involuntarily throwing objects.
d. Clonic. Symptoms: Repetitive, rhythmic jerking movements that involve both sides of the body at the same time.
e. Tonic. Symptoms: Muscle stiffness and rigidity.
f. Atonic. Symptoms: Consist of a sudden and general loss of muscle tone, particularly in the arms and legs, which often results in a fall.
2. Focal/Partial Epilepsy – Seizures produced by electrical impulses that generate from a relatively small or “localized” part of the brain referred to as the
focus.
a. Simple partial (awareness maintained). Simple partial seizures are further divided into four groups according to the nature of their symptoms:
• Motor. Symptoms include movements such as jerking, stiffening, muscle rigidity, spasms, and head-turning.
• Sensory. Symptoms involve unusual sensations affecting any of the five senses (vision, hearing, smell, taste, or touch). The term “aura” is
used to describe sensory symptoms that are present only (and not motor symptoms).
• Autonomic. Symptoms most often involve an unusual sensation in the stomach termed “gastric uprising”.
• Psychological. Symptoms are characterized by various experiences involving memory (the sensation of déjà vu), emotions (such as fear or
pleasure), or other complex psychological phenomena.
b. Complex partial (awareness impaired). Symptoms: Impairment of awareness. Patients seem to be "out of touch," "out of it," or "staring into space"
during these seizures. Symptoms may also involve some complex symptoms called automatisms. Automatisms consist of involuntary but
coordinated movements that tend to be purposeless and repetitive. Common automatisms include lip smacking, chewing, fidgeting, and walking
around.
c. Partial seizure with secondary generalization. Symptoms: Partial seizure that evolves into a generalized seizure (typically a generalized tonic-clonic
seizure). Approximately 70% of patients with partial seizures can be controlled with medication. Partial seizures that cannot be controlled with
medication can often be treated surgically.
Clinical Manifestations
The clinical diagnosis of seizures is based on the history obtained from the patient and, most importantly, the observers.
a. An aura (unusual sensations) precedes seizures in about 20% of people who have a seizure disorder.
b. Short duration. Almost all seizures are relatively brief, lasting from a few seconds to a few minutes; most seizures last 1 to 2 minutes.
c. Postictal state. When a seizure stops, people may have a headache, sore muscles, unusual sensations, confusion, and profound fatigue; these after-
effects are called the postictal state.
d. Todd paralysis. In some people, one side of the body is weak, and the weakness lasts longer than the seizure (a disorder called Todd paralysis).
e. Visual hallucinations. Visual hallucinations (seeing unformed images) occur if the occipital lobe is affected.
f. Convulsions. A convulsion (jerking and spasms of muscles throughout the body) occurs if large areas on both sides of the brain are affected.
Risk Factors
• Age. The onset of epilepsy is most common in children and older adults, but the condition can occur at any age.
• Family history. If you have a family history of epilepsy, you may be at an increased risk of developing a seizure disorder.
• Head injuries. Head injuries are responsible for some cases of epilepsy. You can reduce your risk by wearing a seat belt while riding in a car and by
wearing a helmet while bicycling, skiing, riding a motorcycle or engaging in other activities with a high risk of head injury.
• Stroke and other vascular diseases. Stroke and other blood vessel (vascular) diseases can lead to brain damage that may trigger epilepsy. You can take a
number of steps to reduce your risk of these diseases, including limiting your intake of alcohol and avoiding cigarettes, eating a healthy diet, and
exercising regularly.
• Dementia. Dementia can increase the risk of epilepsy in older adults.
• Brain infections. Infections such as meningitis, which causes inflammation in your brain or spinal cord, can increase your risk.
• Seizures in childhood. High fevers in childhood can sometimes be associated with seizures. Children who have seizures due to high fevers generally
won’t develop epilepsy. The risk of epilepsy increases if a child has a long seizure, another nervous system condition or a family history of epilepsy.
Nursing Managements
a. History. The diagnosis of epileptic seizures is made by analyzing the patient’s detailed clinical history and by performing ancillary tests for confirmation;
someone who has observed the patient’s repeated events is usually the best person to provide an accurate history; however, the patient also provides
invaluable details about auras, preservation of consciousness, and postictal states.
b. Physical exam. A physical examination helps in the diagnosis of specific epileptic syndromes that cause abnormal findings, such as dermatologic
abnormalities (e.g., neurocutaneous syndromes such as Sturge-Weber, tuberous sclerosis, and others); also, patients who for years have had intractable
generalized tonic-clonic seizures are likely to have suffered injuries requiring stitches
Nursing interventions for a child with seizure disorder include the following:
a. Trauma/injury. Teach SO to determine and familiarize warning signs and how to care for patient during and after seizure attack; avoid using
thermometers that can cause breakage; use tympanic thermometer when necessary to take temperature; uphold strict bedrest if prodromal signs or
aura experienced; turn head to side and suction airway as indicated; support head, place on soft area, or assist to floor if out of bed; do not attempt to
restrain; monitor and document AED drug levels, corresponding side effects, and frequency of seizure activity.
b. Promote airway clearance. Maintain in lying position, flat surface; turn head to side during seizure activity; loosen clothing from neck or chest and
abdominal areas; suction as needed; supervise supplemental oxygen or bag ventilation as needed postictally.
c. Improve self-esteem. Determine individual situation related to low self-esteem in the present circumstances; refrain from over protecting the patient;
encourage activities, providing supervision and monitoring when indicated; know the attitudes or capabilities of SO; help an individual realize that his or
her feelings are normal; however, guilt and blame are not helpful.
d. Enforce education about the disease. Review pathology and prognosis of condition and lifelong need for treatments as indicated; discuss patient’s
particular trigger factors (flashing lights, hyperventilation, loud noises, video games, TV viewing); know and instill the importance of good oral hygiene
and regular dental care; review medication regimen, necessity of taking drugs as ordered, and not discontinuing therapy without physician supervision;
include directions for missed dose.
Medical and Surgical Managements
i. Monotherapy. Monotherapy is desirable because it decreases the likelihood of adverse effects and avoids drug interactions; also, monotherapy may be
less expensive than polytherapy, as many of the older anticonvulsant agents have hepatic enzyme-inducing properties that decrease the serum level of
the concomitant drug, thereby increasing the required dose of the concomitant drug.
ii. Anticonvulsant therapy. The mainstay of seizure treatment is anticonvulsant medication; the drug of choice depends on an accurate diagnosis of the
epileptic syndrome, as a response to specific anticonvulsants varies among different syndromes.
iii. Discontinuing anticonvulsant agents. After a person has been seizure free for typically 2-5 years, the physician may consider discontinuing that patient’s
medication; many patients outgrow many epileptic syndromes in childhood and do not need to take anticonvulsants.
iv. Vagal nerve stimulation. VNS is a palliative technique that involves surgical implantation of a stimulating device; VNS is FDA approved to treat medically
refractory focal-onset epilepsy in patients older than 12 years; some studies demonstrate its efficacy in focal-onset seizures and a small number of
patients with primary generalized epilepsy.
v. Implantable neurostimulator. The NeuroPace RNS System, a device that is implanted into the cranium, senses, and records electrocorticographic
patterns and delivers short trains of current pulses to interrupt ictal discharges in the brain.
vi. Lobectomy. In a randomized, controlled trial of surgery in 80 patients with temporal lobe epilepsy, 58% of patients in the group randomized to anterior
temporal lobe resective surgery were free from seizures impairing awareness at 1 year, as compared with 8% in the group that received anticonvulsant
treatment.
vii. Activity modification and restrictions. The major problem for patients with seizures is the unpredictability of the next seizure; clinicians should discuss
the following types of seizure precautions with patients who have epileptic seizures or other spells of sudden-onset seizures: driving, ascending heights,
working with fire or cooking, using power tools and other dangerous equipment, taking unsupervised baths, and swimming.
viii. Long-term monitoring. In 2018, the FDA cleared for marketing the first smartwatch for seizure tracking and epilepsy management; the Embrace smart
watch identifies convulsive seizures and sends an alert via text and phone message to caregivers; the watch also records sleep, rest, and physical activity
data; the device was tested in a study of 135 epileptic patients and found the watch’s algorithm detected 100% of patient seizures.
age family history seizures in childhood
EPILEPSY
“seizure disorder”
brain infections head injuries stroke and other vascular diseases
II. Pathophysiology
seizures are not directly caused by another medical
condition, a severe infection or an acute brain injury
Legend:
non-motor symptoms
by eyelid fluttering, mechanism/action
just stare muscles becoming weak or etc. brief muscle twitching
rapid eye blinking, or
and not jerking (clonic) limp (atonic) (myoclonus)
lip smacking
motor symptoms
non-motor symptoms
make any waves of heat or cold organ affected
motor symptoms
other tense or rigid muscles becoming tense or
movements) gastrointestinal sensations jerking (clonic)
muscles (tonic) rigid (tonic)
typical or atypical
absence seizures muscles becoming limp
unknown onset brief muscle twitching lack of movement
(staring spells) or weak (atonic)
(myoclonic) (behavior arrest)
9. Reinforce the need for adequate rest while encouraging activity and
exercise.
Rationale: To decrease dyspnea and improve quality of life.
Collaborative Interventions:
6. Educate patient and family members about the signs and symptoms of
hyperthermia and help in identifying factors related to occurrence of
fever.
Rationale: Providing health teachings to the patient and family aids in coping with
disease condition and could help prevent further complications of hyperthermia.
10. Monitor laboratory studies, such as arterial blood gas levels, electrolytes,
and cardiac and liver enzymes, glucose; urinalysis and coagulation profile.
Rationale: May reveal tissue degeneration, myoglobinuria, proteinuria, and
hemoglobinuria cam occur as products of tissue necrosis. Noting any presence of
disseminated intravascular coagulation.
Collaborative Interventions:
Epilepsy. (n.d.). Retrieved March 08, 2021, from 4. Uphold strict bedrest if prodromal signs or aura experienced. Explain the
https://www.who.int/news-room/fact- necessity for these actions.
sheets/detail/epilepsy Rationale: Patient may feel restless or need to ambulate or even defecate during
aural phase, thereby inadvertently removing self from a safe environment and
easy observation. Understanding the importance of providing for own safety needs
may enhance patient cooperation.
5. Explore and expound seizure warning signs (if appropriate) and usual
seizure pattern. Teach SO to determine and familiarize warning signs and
how to care for the patient during and after seizure attack.
Rationale: Enables patient to protect self from injury and recognize changes that
require notification of physician and further intervention. Knowing what to do
when a seizure occurs can prevent injury or complications and decreases SO’s
feelings of helplessness.
7. Turn head to side and suction airway as indicated. Insert plastic bite block
only if jaw relaxed.
Rationale: Helps maintain airway patency and reduces the risk of oral trauma but
should not be “forced” or inserted when teeth are clenched because dental and
soft-tissue damage may result. Note: Wooden tongue blades should not be used
because they may splinter and break in the patient’s mouth.
8. Support head, place on soft area or assist to the floor if out of bed. Do
not attempt to restrain.
Rationale: Supporting the extremities lessens the risk of physical injury when the
patient lacks voluntary muscle control. Note: If the attempt is made to restrain the
patient during a seizure, erratic movements may increase, and the patient may
injure self or others.
Collaborative Interventions:
Medications
• Instruct client to take prescribed medications with right dose, at the right frequency, through the right route
• Instruct client to take antiseizure medicine as directed and never stop taking them abruptly.
Environment
Treatments
Health Teaching
• Advice patient to not play computer or electronic games for long periods of time.
• Encourage the client to get enough sleep everyday.
• Encourage client to practice relaxation techniques.
• If seizure occurs, instruct SO to help the patient lie down on her side.
• Encourage SO to call emergency medical services if the client experience seizure, shortness of breath, confusion, and trouble staying awake or alert.
Diet