4. Epilepsy
“A neurological disorder marked by sudden recurrent
episodes of sensory disturbance, loss of
consciousness, or convulsions, associated with
abnormal electrical activity in the brain.”
• A disorder of the nervous system
that can cause people to suddenly
become unconscious and to have
violent, uncontrolled movements of
the body.
8. Definitions
Basic “ State of continuing or recurring seizures in which recovery is
incomplete.”
Official “Status epilepticus is a condition resulting either from the failure of
the mechanisms responsible for seizure termination or from the initiation of
mechanisms, which lead to abnormally, prolonged seizures (after time point t1). It is a
condition, which can have long-term consequences (after time point t2) including
neuronal death, neuronal injury, and alteration of neuronal networks, depending on the
type and duration of seizures.”
Pathophysiologic “ any seizure activity lasting longer than 30 minutes”
9. Definitions
Status epilepticus occurs when….
• The active part of a tonic-clonic seizure lasts 5 minutes
or longer
• A person goes into a second seizure without recovering
consciousness from the first one
• If a person is having repeated seizures for 30 minutes or
longer
11. tions
Etiology
50% of seizures/SE are acute symptomatic
–Stroke
–Trauma
–Cerebral hypoxia
–Infection
–Tumor
AED noncompliance or use of drugs that lower seizure threshold
Substance withdrawal
Metabolic derangements
Infectious cause
Autoimmune/Paraneoplastic
13. tions
1. Generalized Convuslive SE
• Tonic-Clonic SE
• Tonic SE
• Clonic SE
• Myoclonic SE
2. Generalized Nonconvulsive SE
• Absence SE
3. Simple Partial (Focal) SE
• Somatomotor SE
I. Epilepsia Partialis Continua
• Sensory SE
I. Somatosensory
II. Special Sensory
• Aphasic SE
• Autonomic SE
4. Complex Partial (Focal) SEClassification
18. tions
Treatment
0—5 min
6-9 min
10 –
45min
46 – 60
min
1 hour
Obtain vital signs, establish airway, administer oxygen if needed.
Observe seizures briefly to ascertain that patient is really in status.
Draw baseline blood work (CBC, chemistry panel, antiepileptic
drug levels), draw ABGs (for pO2 and pH), draw toxicology screen.
Quickly assess patient for signs of cardio-respiratory compromise,
hyperpyrexia, focal neurologic signs, head trauma, CNS infection.
Vitals
19. tions
Treatment
0—5
min
6-9 min
10 –
45min
46 – 60
min
1 hour
Start IV infusion with saline solution.
Administer 100 mg thiamine, IV, if malnutrition
and alcoholism are potential Factors.
Administer 50 ml of 50% glucose solution, IV, if
blood sugar is low or unobtainable.
Do not give glucose if blood sugar is normal or
high.
Always have CPR equipment at bedside of a
patient in status.
Thiamine
Vitals
20. tions
Treatment
0—5
min
6-9 min
10 – 45min
46 – 60
min
1 hour
To rapidly suppress the seizures, we have used
diazepam intravenously at a rate of about 2 mg/min
until the seizures stop or a total of 20 mg has been given;
alternatively, lorazepam, 0 . 1 mg/kg given by intravenous
push at a rate not to exceed 2 mg/min, is now favored,
being marginally more effective than diazepam because
of its clinically longer duration of action (see Table 1 6-8) .
Thiamine
Vitals
Lorazipam
21. tions
Treatment
0—5
min
6-9 min
10 – 45min
46 – 60
min
1 hour
• Immediately thereafter, a loading dose (20 mg/kg)
of phenytoin is administered by vein at a rate of less
than 50 mg/ min. More rapid administration risks
hypotension and heart block; consequently, it is
recommended that the blood pressure and
electrocardiogram be monitored during the infusion.
• An alternative to phenytoin is fosphenytoin that can
be injected with twice the rate of phenytoin so help
to stop seizure rapidly .
Lorazipam
Thiamine
Vitals
Phenytoin
22. tions
Treatment
0—5
min
6-9 min
10 –
45min
46 – 60 min
1 hour
• If phenytoin alone is not able to control the seizures then give high doses of
midazolam (0.2 mg / kg loading dose followed by an infusion of 0 . 1 to 0.4
mg/kg/h along with phenytoin.
• Propofol given in a bolus of 2 mg/kg and then as an intravenous drip of 2 to
8 mg I kg /h is an effective alternative to midazolam, but after 24 h the
drug behaves like a high dose of barbiturate and there
may be hypotension. Prolonged use of propofol may precipitate
hypertriglyceridemia-associated pancreatitis or a
fatal shock and acidosis ("propofol syndrome") .
Lorazipam
Thiamine
Vitals
Phenytoin
23. tions
Treatment
0—5
min
6-9 min
10 –
45min
46 – 60 min
1 hour
If seizures persist, intubate and give phenobarbital, 20
mg/kg, at 100 mg/min.
Never use Valium and phenobarbital sequentially in the
treatment of status, unless the patient is intubated and in an
ICU. Their hypotensive and respiratory depressant actions
synergize. Serious and abrupt side effects can occur with these
two drugs when given together.
Lorazipam
Thiamine
Vitals
Phenytoin
Phenobarbital
24. tions
Treatment
0—5
min
6-9 min
10 –
45min
46 – 60
min
1 hour
If seizures persist, the patient should be placed in a drug induced
coma with pentobarbital, a benzodiazepine, or other anesthetic
agent to prevent life threatening lactic acidosis, hypoxia,
hyperthermia, and permanent seizure-induced neuronal damage.
The patient must be in an ICU, and outcome should be monitored
and treatment guided by EEG with the goal being suppression of
seizure activity on EEG
Phenobarbital
Lorazipam
Thiamine
Vitals
Phenytoin
Pentobarbital
25. tions
Treatment
0—5
min
6-9 min
10 –
45min
46 – 60
min
1 hour
If seizure still continues we will move further to
stop all muscle activity by pancuronium
That cause neuromuscular paralysis.
Inahalational Anesthesia (isoflurane and
halothane)
Absence status should be managed by intravenous
lorazepam, valproic acid, or both, followed by ethosuximide.
Nonconvulsive generalized status is treated along
the lines of grand mal status, usually stopping short of
using anesthetic agents (see Meierkord)
Phenobarbital
Lorazipam
Thiamine
Vitals
Phenytoin
Pentobarbital
Pancrunium
26. 0—5
min
6-9 min
10 –
45min
46 – 60
min
1 hour
tions
Treatment
Phenobarbital
Lorazipam
Thiamine
Vitals
Phenytoin
Pentobarbital
Pancrunium
34. What is an absence seizure?
An absence seizure causes a short period of “blanking out” or staring into space. Like other kinds of
seizures, they are caused by abnormal activity in a person’s brain. You may also hear people call absence
seizures petit mal (“PUH-tee mahl”) seizures, although that name is not common anymore.
There are two types of absence seizures:
Simple absence seizures: During a simple absence seizure, a person usually just stares into space for less
than 10 seconds. Because they happen so quickly, it’s very easy not to notice simple absence seizures —
or to confuse them with daydreaming or not paying attention.
Complex absence seizures: During a complex absence seizure, a person will make some kind of
movement in addition to staring into space. Movements may include blinking, chewing, or hand gestures.
A complex absence seizure can last up to 20 seconds.
Absence seizures can also happen with other kinds of seizures.
35. What is an atonic seizure?
Muscle "tone" is the muscle's normal tension. "Atonic" (a-TON-ik) means "without tone," so in an atonic
seizure, muscles suddenly lose strength. The eyelids may droop, the head may nod, and the person may
drop things and often falls to the ground. These seizures are also called "drop attacks" or "drop seizures."
The person usually remains conscious. These seizures typically last less than 15 seconds. They often start
in childhood yet last into adulthood. Many people with atonic seizures are injured when they fall, so they
may choose to use protection such as a helmet.
Another name for this type of seizure is "akinetic" (a-kin-ET-ik), which means "without movement."
36. What is a clonic seizure?
"Clonus" (KLOH-nus) means rapidly alternating contraction and relaxation of a muscle -- in other words,
repeated jerking. The movements cannot be stopped by restraining or repositioning the arms or legs.
Clonic (KLON-ik) seizures are rare. Much more common are tonic-clonic seizures, in which the jerking is
preceded by stiffening (the "tonic" part). Sometimes tonic-clonic seizures start with jerking alone. These
are called clonic-tonic-clonic seizures! These seizures tend to last for a few seconds to a minute.
Brief and infrequent clonic seizures in infants usually disappear on their own within a short time. Other
types may need prolonged treatment
37. What is a myoclonic seizure?
Myoclonic (MY-o-KLON-ik) seizures are brief, shock-like jerks of a muscle or a group of muscles. "Myo"
means muscle and "clonus" (KLOH-nus) means rapidly alternating contraction and relaxation—jerking or
twitching—of a muscle. Usually they don't last more than a second or two. There can be just one, but
sometimes many will occur within a short time.
38. What is a tonic seizure?
Muscle "tone" is the muscle's normal tension at rest. In a "tonic" seizure, the tone is greatly increased and
the body, arms, or legs make sudden stiffening movements. Consciousness is usually preserved. Tonic
seizures most often occur during sleep and usually involve all or most of the brain, affecting both sides of
the body. If the person is standing when the seizure starts, he or she often will fall. These seizures usually
last less than 20 seconds.
39. What is a tonic-clonic seizure?
This type is what most people think of when they hear the word "seizure." An older term for them is
"grand mal." As implied by the name, they combine the characteristics of tonic seizures and clonic
seizures.
The tonic phase comes first: All the muscles stiffen. Air being forced past the vocal cords causes a cry or
groan. The person loses consciousness and falls to the floor. The tongue or cheek may be bitten, so
bloody saliva may come from the mouth. The person may turn a bit blue in the face.
After the tonic phase comes the clonic phase: The arms and usually the legs begin to jerk rapidly and
rhythmically, bending and relaxing at the elbows, hips, and knees. After a few minutes, the jerking slows
and stops. Bladder or bowel control sometimes is lost as the body relaxes. Consciousness returns slowly,
and the person may be drowsy, confused, agitated, or depressed.
These seizures generally last 1 to 3 minutes.
A tonic-clonic seizure that lasts longer than 5 minutes needs medical help. A seizure that lasts more than
10 minutes, or three seizures without a normal period in between, indicates a dangerous condition called
convulsive status epilepticus. This requires emergency treatment.
40. What is a simple partial seizure?
Simple partial seizures are usually divided into categories depending on the type of symptoms the person experiences:
Motor seizures:
These cause a change in muscle activity. For example, a person may have abnormal movements such as jerking of a finger or stiffening of
part of the body.
The movements may spread, either staying on one side of the body or extending to both sides. Other examples are weakness, which can
even affect speech, and coordinated actions such as laughter or automatic hand movements.
Sensory seizures:
These cause changes in any one of the senses.
People with sensory seizures may smell or taste things that aren't there; hear clicking, ringing, or a person's voice when there is no
actual sound; or feel a sensation of "pins and needles" or numbness.
Seizures may even be painful for some patients. They may feel as if they are floating or spinning in space.
They may have visual hallucinations, seeing things that aren't there (a spot of light, a scene with people). They also may experience
illusions—distortions of true sensations. For instance, they may believe that a parked car is moving farther away, or that a person's voice
is muffled when it's actually clear.
Autonomic seizures:
These cause changes in the part of the nervous system that automatically controls bodily functions.
These common seizures may include strange or unpleasant sensations in the stomach, chest, or head; changes in the heart rate or
breathing; sweating; or goose bumps.
Psychic seizures:
These seizures change how people think, feel, or experience things.
They may have problems with memory, garbled speech, an inability to find the right word, or trouble understanding spoken or written
language.
They may suddenly feel emotions like fear, depression, or happiness with no outside reason.
Some may feel as though they are outside their body or may have feelings of déja vu ("I've been through this before") or jamais vu ("This
is new to me"— even though the setting is really familiar).
41. What is a complex partial seizure?
These seizures usually start in a small area of the temporal lobe or frontal lobe of the brain. They quickly involve other areas of the brain
that affect alertness and awareness. So even though the person's eyes are open and they may make movements that seem to have a
purpose, in reality "nobody's home." If the symptoms are subtle, other people may think the person is just daydreaming.
Some people can have seizures of this kind without realizing anything has happened. The seizure can wipe out memories of events just
before or after it.
Some of these seizures (usually ones beginning in the temporal lobe) start with a simple partial seizure.
Then the person loses awareness and stares blankly.
Most people move their mouth, pick at the air or their clothing, or perform other purposeless actions. These movements are called
"automatisms" (aw-TOM-ah-TIZ-ums).
Less often, people may repeat words or phrases, laugh, scream, or cry. Some people do things during these seizures that can be
dangerous or embarrassing, such as walking into traffic or taking their clothes off. These people need to take precautions in advance.
Complex partial seizures starting in the frontal lobe tend to be shorter than the ones from the temporal lobe. The seizures that start in
the frontal lobe are also more likely to include automatisms like bicycling movements of the legs or pelvic thrusting.
Some complex partial seizures turn into secondarily generalized seizures. They usually last between 30 seconds and 2 minutes.
Afterward, the person may be tired or confused for about 15 minutes and may not be return to normal function for hours.
As for many other kinds of seizures, the outlook depends on whether the cause is known. They may be outgrown or controlled with
medication. If medication is not effective, some can be eliminated by epilepsy surgery.
42. Epilepsia partialis continua (also called Kojevnikov's or Kozhevnikov's epilepsia) is a rare[1] type of
brain disorder in which a patient experiences recurrent motor epileptic seizures that are focal (hands
and face), and recur every few seconds or minutes for extended periods (days or years).
Notes de l'éditeur
Paraneoplastic encephalomyelitis (PEM) is a multifocal inflammatory disorder of the central nervous system (CNS) associated with remote neoplasia.[1] Frequently, the disorder is accompanied by subacute sensory neuronopathy (SSN) due to involvement of the dorsal root ganglia. Anti-Hu antibodies may be detected in both of these conditions. Although various malignancies have been reported in PEM, 80% of cases are associated with bronchial cancer, typically small cell lung carcinoma.[2]
Generalized Tonic-Clonic Seizures ( involve whole body )
In a "tonic" seizure, the tone is greatly increased and the body, arms, or legs make sudden stiffening movements. Consciousness is usually preserved. Tonic seizures most often occur during sleep and usually involve all or most of the brain, affecting both sides of the body.
Clonic seizures are very rare
Myoclonic seizures are brief shock-like jerks of a muscle or group of muscles. They occur in a variety of epilepsy syndromes that have different characteristics. During a myoclonic seizure, the person is usually awake and able to think clearly.
All partial seizures are characterized by onset in a limited area, or focus, of one cerebral hemisphere.