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Last updated: June 16, 2026Bookmark

A seizure is defined as a sudden change in consciousness, behaviour or movement of the body, due to electrical hypersynchronization of neuronal networks in the cerebral cortex. This sudden change tends to be transient, and is characterized mainly by motor symptoms (eg. shaking) and non-motor symptoms (e.g., language, vision and sensory changes, confusion, or alterations of awareness).

Elements of a seizure

ElementDescriptionFeatures
ProdromePrecedes the seizure and last hours to days.Changes in mood or behavior
AuraA sensory experience that correlates to the epileptic eventRising epigastric sensation, gustatory/olfactory hallucination, visual changes, headache, paresthesia, or psychiatric phenomena (deja vu, jamais vu)
Post-ictal statesFollows the seizureHeadache, somnolence, aggression, confusion, cognitive impairment, temporary paralysis (Todd’s paralysis following a focal seizure in the motor cortex), or dysphasia (focal seizure in the temporal lobe)

Classification based on seizure type

ClassificationDescription
Focal onset seizuressFocal onset seizures involve one part of the brain. The patient may not lose consciousness, but may have altered awareness.
Generalised onset seizuresGeneralised seizures arise from both cerebral hemispheres.
Unkown onset seizuresThis is when the onset of a seizure has not observed. It can later be reclassified into focal or generalised when more information is available.

Types of focal onset siezures

Focal seizureDescription
Focal aware seizuresPreviously known as simple partial seizure. The patient is aware and recalls events during the seizure. It can involve sensory, motor, psychiatric, or autonomic symptoms
Focal impaired awareness seizurePreviously known as complex partial seizure. The patient has altered awareness, appearing dazed or confused. The symptoms are similar to simple focal seizures
Focal to bilateral tonic-clonic seizuresThese begin in one hemisphere then spread to involve both, producing a tonic-clonic seizure

Localising features of focal seizures

LocationFeatures
Temporal lobeAutomatisms, dysphasia, deja vu, jamais vu, emotional disturbance, elation, derealization, hallucination, delusions, and bizarre associations
Frontal lobeMotor features, Jacksonian march, motor arrest, subtle behavior disturbances, dysphasia or speech arrest, or post-ictal drowsiness
Parietal lobeSensory disturbance, or motor symptoms if it spreads to the pre-central gyrus
Occipital lobeVisual phenomena – spots, lines, and flashes

Types of generialised onset seizures

TypeDescriptionFeatures
Absence (petit mal) seizureLoss of consciousness. Non-motor. Classically seen in children. The child looks out into space for a few seconds and snaps back into realityBlank stare < 10 seconds that starts and ends abruptly, Automatisms (lip smacking, hand wringing, motor tics), 3 Hz spike and wave on EEG
Tonic-clonic (grand mal) seizureLoss of consciousness with stiffening and jerking of all limbs. There may be one without the other, i.e., stiffening only = tonic seizure, repetitive jerking only = clonic seizureLoud moan (air coming out of closed epiglottis) followed by stiffening and jerking (involving all four limbs). Tongue biting(look for tongue laceration esp. in patients who live by themselves) and Urinary incontinence. There may be post-ictal confusion and drowsiness
Myoclonic seizureNo loss of consciousness. There is a sudden jerk of a limb, face, or trunk. “My flying-saucer epilepsy”Sudden jerk of part of the body (arm or leg). They may fall over suddenly or have a violently disobedient limb
Atonic seizureSudden loss of muscle tone causing a fall.Sudden loss of muscle tone < 15 seconds, falls over. To differentiate this from syncope, an atonic seizures has haziness and confusion after loss of consciousness, while in syncope the patient will be generally OK after recovering.

Common causes of seizures

Age groupCommon causes
Neonates and infants (< 1 year)Genetic, congenital structural maldevelopment, perinatal injury, perinatal/postnatal infection (meningitis), metabolic disorder (hypoglycemia, hypocalcemia), and West syndrome
Young children (<10 y)Febrile, genetic causes, infection, traumatic Brain Injury, congenital brain malformation, metabolic disorders, and accidental poisoning
Adolescents (10-18 years)Traumatic brain injury, encephalitis, genetic disorders, and illicit substance abuse
Adults (18-60y)Alcohol withdrawal, traumatic brain injury, illicit substance use, neoplasm, infection, and metabolic acidosis
Older adults (60+ years)Traumatic brain injury, cerebrovascular disease, neoplasm, abscess, and neurodegenerative disease
  • Common triggers
  • Patient History
    • What is the frequency and duration of seizures?
    • What happened before/after the event? (pre-ictal phase and post-ictal phase)
      • Was there a preciding aura?
      • Was there residual weakness or confusion post-ictal?
    • Are there any automatisms? (Gives a clue as to the focus of origin)
      • Was there tongue-biting?
      • Was there incontinence?
    • Has there been trauma OR drug/alcohol use? (triggers)
    • Is there a Family History?
  • Differentials (VITAMIN D)
    • Vascular malformation
    • Infection, Inherited conditions
    • Trauma
    • Alzheimer’s
    • Metabolic derangement
    • Idiopathic
    • Neoplasms
    • Drugs
      • Fluoroquinolones
      • Bupropion
      • Imipramine
      • Meperidine
      • Metronidazole
      • Isoniazid
  • Investigations
    • Random blood sugar to exclude extreme hypoglycemia or hyperglycemia
    • Complete blood count to rule out systemic or CNS infections
    • U/E/Cs to rule out hyponatremia, hypernatremia, hypocalcemia and uremia
    • Urine toxicology screen to rule out cocaine, amphetamines, heroin, PCP, or GHB
    • Blood Alcohol Concentration
      • 0.06 after binge drinking
      • Alcohol withdrawal
    • Head CT or MRI for ****space occupying lesions. An MRI is the imaging modality of choice for structural lesions since it has superior resolution compared to a CT.
    • Electroencephalogram (EEG) for unprovoked first seizure
  • Treatment
    • Seizure precautions
      • DO NOT put anything in the patient’s mouth to prevent tongue biting
      • DO NOT restrain the patient
      • Gently lean the patient on their side with the head turned to the same side to prevent aspiration
      • Cushion the patients head to prevent head injury
      • Loosen or remove tight or dangerous clothing around the head and neck such as necklaces, and glasses
      • Remove dentures
      • Call for help immediately
    • Establish IV access
    • Abort the seizure using anti-epileptic drugs (see status epilepticus)
      • If the convulsion lasts more than 3 – 5 minutes consider status epilepticus or psychogenic non-epileptic seizure
Reference Intervals
Biochemistry
ACTHP: <80 ng/L
ALTP: 5–35 U/L
AlbuminP: 35–50 g/L
AldosteroneP: 100–500 pmol/L
Alk. phosphataseP: 30–130 U/L
α-AmylaseP: 0–180 IU/dL
α-FetoproteinS: <10 kU/L
Angiotensin IIP: 5–35 pmol/L
ADHP: 0.9–4.6 pmol/L
ASTP: 5–35 U/L
BicarbonateP: 24–30 mmol/L
BilirubinP: 3–17 μmol/L
BNPP: <50 ng/L
CRPP: <10 mg/L
CalcitoninP: <0.1 mcg/L
Calcium (ionized)P: 1.0–1.25 mmol/L
Calcium (total)P: 2.12–2.60 mmol/L
ChlorideP: 95–105 mmol/L
CholesterolP: <5.0 mmol/L
VLDLP: 0.128–0.645 mmol/L
LDLP: <2.0 mmol/L
HDLP: 0.9–1.93 mmol/L
Cortisol AMP: 450–700 nmol/L
Cortisol MidnightP: 80–280 nmol/L
CK ♂P: 25–195 U/L
CK ♀P: 25–170 U/L
CreatinineP: 70–100 μmol/L
FerritinP: 12–200 mcg/L
FolateS: 2.1 mcg/L
FSHP: 2–8 U/L ♂; >25 menopause
GGT ♂P: 11–51 U/L
GGT ♀P: 7–33 U/L
Glucose (fasting)P: 3.5–5.5 mmol/L
Growth hormoneP: <20 mu/L
HbA1C (DCCT)B: 4–6%
HbA1C (IFCC)B: 20–42 mmol/mol
Iron ♂S: 14–31 μmol/L
Iron ♀S: 11–30 μmol/L
Lactate (venous)P: 0.6–2.4 mmol/L
Lactate (arterial)P: 0.6–1.8 mmol/L
LDHP: 70–250 U/L
LHP: 3–16 U/L
MagnesiumP: 0.75–1.05 mmol/L
OsmolalityP: 278–305 mosmol/kg
PTHP: 0.8–8.5 pmol/L
PotassiumP: 3.5–5.3 mmol/L
Prolactin ♂P: <450 U/L
Prolactin ♀P: <600 U/L
PSAP: 0–4 mcg/mL
Protein (total)P: 60–80 g/L
Red cell folateB: 0.36–1.44 μmol/L
Renin (erect)P: 2.8–4.5 pmol/mL/h
Renin (recumbent)P: 1.1–2.7 pmol/mL/h
SodiumP: 135–145 mmol/L
TBGP: 7–17 mg/L
TSHP: 0.5–4.2 mU/L
T4P: 70–140 nmol/L
Free T4P: 9–22 pmol/L
TIBCS: 54–75 μmol/L
TriglyceridesP: 0.50–2.3 mmol/L
T3P: 1.2–3.0 nmol/L
Troponin TP: <0.1 mcg/L
Urate ♂P: 210–480 μmol/L
Urate ♀P: 150–390 μmol/L
UreaP: 2.5–6.7 mmol/L
Vitamin B12S: 0.13–0.68 nmol/L
Vitamin DS: 50 nmol/L
Arterial Blood Gases
pH7.35–7.45
PaCO₂4.7–6.0 kPa
PaO₂>10.6 kPa
Base excess±2 mmol/L
Urine
Cortisol (free)<280 nmol/24h
Hydroxyindole acetic acid16–73 μmol/24h
Hydroxymethylmandelic acid16–48 μmol/24h
Metanephrines0.03–0.69 μmol/mmol cr.
Osmolality350–1000 mosmol/kg
17-Oxogenic steroids ♂28–30 μmol/24h
17-Oxogenic steroids ♀21–66 μmol/24h
17-Oxosteroids ♂17–76 μmol/24h
17-Oxosteroids ♀14–59 μmol/24h
Phosphate (inorganic)15–50 mmol/24h
Potassium14–120 mmol/24h
Protein<150 mg/24h
Protein/creatinine ratio<3 mg/mmol
Sodium100–250 mmol/24h
Haematology
WCC4.0–11.0 ×10⁹/L
RBC ♂4.5–6.5 ×10¹²/L
RBC ♀3.9–5.6 ×10¹²/L
Hb ♂130–180 g/L
Hb ♀115–160 g/L
PCV ♂0.4–0.54 L/L
PCV ♀0.37–0.47 L/L
MCV76–96 fL
MCH27–32 pg
MCHC300–360 g/L
RDW11.6–14.6%
Neutrophils2.0–7.5 ×10⁹/L (40–75%)
Lymphocytes1.0–4.5 ×10⁹/L (20–45%)
Eosinophils0.04–0.44 ×10⁹/L (1–6%)
Basophils0–0.10 ×10⁹/L (0–1%)
Monocytes0.2–0.8 ×10⁹/L (2–10%)
Platelets150–400 ×10⁹/L
Reticulocytes0.8–2.0% / 25–100 ×10⁹/L
Prothrombin time10–14 s
APTT35–45 s
Paediatric
Pulse Rate (bpm)
Neonate140–160
Infant <1yr120–140
1–5 years110–130
5–12 years80–120
>12 years70–100
Respiratory Rate (tachypnoea)
0–2 months≥60/min
2–12 months≥50/min
1–5 years≥40/min
>5 years≥30/min
Blood Pressure (mmHg)
Term65/45
1 year75/50
4 years85/60
8 years95/65
10 years100/70
Weight Formulas
3–12 months(a + 9)/2 kg
1–6 years2a + 8 kg
>6 years(7a − 5)/2 kg
Haemoglobin (g/dL)
Term newborn13–20
1 month11–18
2 months10–15
1–2 years10–13
>2 years11–14
MUAC (6 months–5 years)
Obese>17.5 cm
Normal13.5–17.4 cm
At risk12.5–13.4 cm
Moderate malnutrition11.5–12.4 cm
Severe malnutrition<11.5 cm
Developmental Milestones
Social smile1.5 months
Head control4 months
Sits unsupported7 months
Crawls10 months
Stands unsupported10–12 months
Walks12–13 months
Talks18 months
CSF WBC (/mm³)
Term newborn0–25
>2 weeks0–5
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