Seizures and epilepsy

744,851views

Seizures and epilepsy

PGreen

PGreen

Cell-cell junctions
Marfan syndrome
Cellular structure and function
Development of the renal system
Mitosis and meiosis
Colorectal polyps and cancer: Pathology review
Endometrial hyperplasia and cancer: Clinical
Lung cancer
Metaplasia and dysplasia
Oral cancer
Testicular cancer
Apnea, hypoventilation and pulmonary hypertension: Pathology review
Acute respiratory distress syndrome
Arterial disease
Asthma
Atrial septal defect
Bronchiectasis
Chronic bronchitis
Chronic venous insufficiency
Angina pectoris
Aortic valve disease
Coarctation of the aorta
Heart failure
Pneumonia
Tetralogy of Fallot
Shock
Mitral valve disease
Pericarditis and pericardial effusion
Pleural effusion
Dementia: Pathology review
Dementia: Pathology review
Dementia: Pathology review
Dementia: Pathology review
Dementia: Pathology review
Anxiety disorders: Clinical
Arteriovenous malformation
Bipolar and related disorders
Cauda equina syndrome
Seizures and epilepsy
Generalized anxiety disorder
Headaches: Pathology review
Huntington disease
Ischemic stroke
Major depressive disorder
Meningitis
Migraine
Multiple sclerosis
Panic disorder
Parkinson disease
Stroke: Clinical
Alzheimer disease
Diabetes mellitus: Pathology review
Adrenocorticotropic hormone
Chlamydia trachomatis
Cortisol
Cushing syndrome
Endometriosis
Glucagon
Glucocorticoids
Herpes simplex virus
HIV (AIDS)
Hyperthyroidism: Pathology review
Hypothyroidism: Pathology review
Hypothyroidism
Insulin
Pelvic inflammatory disease
Testosterone
Polycystic ovary syndrome
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Thyroid hormones
Anemia of chronic disease
Chronic leukemia
Coagulation disorders: Pathology review
Disseminated intravascular coagulation
Factor V Leiden
Hemophilia
Non-Hodgkin lymphoma
Hypocalcemia
Hypokalemia
Inflammation
Innate immune system
Introduction to the immune system
Iron deficiency anemia
Leukemias: Pathology review
Platelet disorders: Pathology review
Sickle cell disease (NORD)
Type IV hypersensitivity
Acute cholecystitis
Acute pancreatitis
Acute pyelonephritis
Alcohol-associated liver disease
Appendicitis
Autoimmune hepatitis
Biliary colic
Bowel obstruction
Chronic cholecystitis
Chronic pyelonephritis
Chronic pancreatitis
Cirrhosis
Congenital disorders: Clinical
Crohn disease
Gastroesophageal reflux disease (GERD)
Irritable bowel syndrome
Lower urinary tract infection
Nephrotic syndromes: Pathology review
Peptic ulcer
Renal failure: Pathology review
Ulcerative colitis
Urinary tract infections: Pathology review
Viral hepatitis
Acne vulgaris
Atopic dermatitis
Back pain: Pathology review
Bone disorders: Pathology review
Burns
Osteoarthritis
Osteoporosis
Paget disease of bone
Psoriasis
Rheumatoid arthritis
Skin cancer
Varicella zoster virus
Down syndrome (Trisomy 21)
Inheritance patterns
DNA damage and repair
DNA replication
Selective permeability of the cell membrane
Cell cycle
Free radicals and cellular injury
Autosomal trisomies: Pathology review
Breast cancer: Pathology review
Hypertension: Pathology review
Deep vein thrombosis
Emphysema
Endocarditis
Gas exchange in the lungs, blood and tissues
Peripheral artery disease
Pulmonary edema
Restrictive lung diseases
Stroke volume, ejection fraction, and cardiac output
Ventilation-perfusion ratios and V/Q mismatch
Cranial nerves
Migraine
Myasthenia gravis
Abnormal uterine bleeding: Clinical
Neisseria gonorrhoeae
Primary adrenal insufficiency
Benign prostatic hyperplasia
Hodgkin lymphoma
Introduction to the immune system
Celiac disease
Introduction to pharmacology
Drug administration and dosing regimens
Enzyme function
Pharmacokinetics: Drug metabolism
Pharmacokinetics: Drug elimination and clearance
Pharmacokinetics: Drug absorption and distribution
Pharmacodynamics: Drug-receptor interactions
Pharmacodynamics: Desensitization and tolerance
Pharmacodynamics: Agonist, partial agonist and antagonist
Opioid antagonists
Opioid agonists, mixed agonist-antagonists and partial agonists
Opioid use disorder
Acetaminophen (Paracetamol)
Non-steroidal anti-inflammatory drugs
Anticoagulants: Direct factor inhibitors
Anticoagulants: Heparin
Anticoagulants: Warfarin
Antiplatelet medications
Thrombolytics
Hematopoietic medications
Role of Vitamin K in coagulation
Vitamin B12 deficiency
Loop diuretics
Miscellaneous lipid-lowering medications
Potassium sparing diuretics
Adrenergic antagonists: Alpha blockers
Calcium channel blockers
Lipid-lowering medications: Fibrates
Lipid-lowering medications: Statins
Adrenergic antagonists: Beta blockers
Class II antiarrhythmics: Beta blockers
Class IV antiarrhythmics: Calcium channel blockers and others
Class III antiarrhythmics: Potassium channel blockers
Class I antiarrhythmics: Sodium channel blockers
Thiazide and thiazide-like diuretics
ACE inhibitors, ARBs and direct renin inhibitors
Positive inotropic medications
Vaccinations
Anthelmintic medications
Anti-mite and louse medications
Antimalarials
Hepatitis medications
Integrase and entry inhibitors
Antimetabolites: Sulfonamides and trimethoprim
Azoles
Cell wall synthesis inhibitors: Cephalosporins
Cell wall synthesis inhibitors: Penicillins
DNA synthesis inhibitors: Metronidazole
DNA synthesis inhibitors: Fluoroquinolones
Echinocandins
Herpesvirus medications
Mechanisms of antibiotic resistance
Miscellaneous cell wall synthesis inhibitors
Miscellaneous protein synthesis inhibitors
Neuraminidase inhibitors
Non-nucleoside reverse transcriptase inhibitors (NNRTIs)
Nucleoside reverse transcriptase inhibitors (NRTIs)
Protease inhibitors
Protein synthesis inhibitors: Aminoglycosides
Protein synthesis inhibitors: Tetracyclines
Antihistamines for allergies
Miscellaneous antifungal medications
Androgens and antiandrogens
Aromatase inhibitors
Estrogens and antiestrogens
PDE5 inhibitors
Progestins and antiprogestins
Uterine stimulants and relaxants
Acid reducing medications
Antidiarrheals
Laxatives and cathartics
Non-corticosteroid immunosuppressants and immunotherapies
Hyperthyroidism medications
Hypoglycemics: Insulin secretagogues
Hypothyroidism medications
Insulins
Miscellaneous hypoglycemics
Mineralocorticoids and mineralocorticoid antagonists
Sympatholytics: Alpha-2 agonists
Anticonvulsants and anxiolytics: Barbiturates
Anticonvulsants and anxiolytics: Benzodiazepines
Nonbenzodiazepine anticonvulsants
Atypical antipsychotics
Atypical antidepressants
Typical antipsychotics
Lithium
Monoamine oxidase inhibitors
Selective serotonin reuptake inhibitors
Serotonin and norepinephrine reuptake inhibitors
Tricyclic antidepressants
Anti-parkinson medications
Cholinomimetics: Direct agonists
Cholinomimetics: Indirect agonists (anticholinesterases)
Muscarinic antagonists
Headaches: Clinical
Migraine medications
Bronchodilators: Beta 2-agonists and muscarinic antagonists
Bronchodilators: Leukotriene antagonists and methylxanthines
Antigout medications
Folate (Vitamin B9) deficiency
Vitamin D
Fat-soluble vitamin deficiency and toxicity: Pathology review
Mumps virus
Measles virus
Rubella virus
Bordetella pertussis (Whooping cough)
Poliovirus
Pediatric infectious rashes: Clinical

Transcript

Watch video only

A seizure refers to a one-time event caused by abnormal, excessive, and synchronous electrical activity in the brain that can result in autonomic, sensory, and motor symptoms. When seizures specifically involve motor activity, like jerking, we call them convulsions. Most seizures last less than 5 minutes, but if the seizure continues for 5 minutes or more, it’s called status epilepticus.

Keep in mind that seizures are a symptom, not a diagnosis, meaning they can occur due to various underlying causes, such as trauma, infections, and metabolic imbalances. However, when seizures arise without a clear cause, they are considered unprovoked. And if someone experiences two or more unprovoked seizures, at least twenty-four hours apart, think epilepsy.

Normally, the brain and its neurons rely on a balance between excitatory and inhibitory neurotransmitters. Think of excitatory neurotransmitters like green traffic lights that speed things up, encouraging the neuron to pass electrical impulses to the next one. On the other hand, inhibitory neurotransmitters act like red traffic lights that slow traffic down, stopping the further propagation of electrical impulses.

Now, whether there’s too much excitation or not enough inhibition, neurons can begin firing impulses simultaneously. This leads to abnormal, excessive, and synchronous electrical activity in the brain, which results in a seizure.

Now, there are various causes of seizures, and you can remember the most important ones using the mnemonic “VITTAMINS”. “V” stands for Vascular conditions, like strokes and intracranial hemorrhage, and “I” covers Infection, including meningitis, encephalitis, and brain abscess. Next, the first “T” refers to head Trauma, while the second “T” refers to Toxins, such as cocaine or amphetamine overdose, but also alcohol withdrawal. “A” is for Autoimmune conditions, such as CNS vasculitis and lupus; and “M” is for Metabolic conditions, including hepatic- and uremic encephalopathy, as well as electrolyte disturbances, such as hyponatremia. The second “I” is for Idiopathic, meaning no identifiable cause, which refers to epilepsy. Finally, “N” is for neoplasm or brain tumors, and “S” covers differential diagnoses like Syncope, pSychogenic seizures, and migraineS.

Now, based on where the abnormal activity starts, seizures are broadly classified into generalized and focal seizures.

Generalized seizures arise from both cerebral hemispheres and almost always cause a sudden impairment of consciousness. This type of seizure can be further subdivided into generalized motor- and non-motor seizures.

Generalized motor seizures, as their name implies, involve muscle activity and include several types. First, tonic seizures are characterized by a significant increase in muscle tone that results in stiffness and rigidity. Next, clonic seizures are associated with repeated, rapid, rhythmic jerking movements, usually of arms and legs. These episodes can last from several seconds to a couple of minutes.

Also, there’s a combination of the two patterns, called tonic-clonic seizures, which combine muscle stiffening with muscle jerking. During tonic-clonic seizures, a person may experience a sudden contraction of their vocal cord muscles, resulting in an involuntary scream or cry. Also, the eye muscles can contract, causing the eyes to roll back, while the contraction of the oropharyngeal muscles can impair swallowing, causing saliva to pool in the oropharynx. On top of that, the jaw muscles can contract and result in tongue biting. In this case, a person might also lose control of their bladder or bowels during the seizure, resulting in urinary and fecal incontinence.

Next, we have atonic seizures, which basically mean seizures with “no muscle tone”. In this type, there's a sudden loss of postural muscle tone lasting 1 to 2 seconds, causing the individual to collapse to the ground. On the flip side, myoclonic seizures involve sudden, brief, rapid muscle twitches that last only a fraction of a second. Finally, there’s a combination of the previous two, called myoclonic-atonic seizure, marked by rapid muscle twitches followed by a brief loss of muscle tone and collapse.

Alright, moving on to generalized non-motor seizures, also known as absence seizures, which are most common in children and adolescents. These seizures cause a brief loss of consciousness, particularly awareness, without any change in the postural muscle tone. It’s like the brain hits the “pause” button for a moment, then quickly presses “play” again. For example, a student might be sitting in a class, listening to a lecture, and suddenly zone out, only to snap back to reality several moments later. Unfortunately, these episodes can occur hundreds of times per day, and parents and teachers often think the child is just stareing off into space or not paying attention.

Furthermore, absence seizures are subdivided into typical- and atypical absence seizures. Typical absence seizures come on quickly, usually last up to 20 seconds, and have a fast recovery. On the other hand, atypical absence seizures are slower in onset, last more than 20 seconds, and take more time to recover from. After atypical absence seizures, individuals often appear confused or dazed.

Sources

  1. "Davidson's Principles and Practice of Medicine. Available from: ClinicalKey Student, (24th Edition). Page 1152 – 1157 " Elsevier Limited (UK), (2022)
  2. "Conn's Current Therapy 2024. Available from: ClinicalKey Student, Page 803 – 812 " Elsevier Limited (UK) (2023)
  3. "Netter's Neurology. Available from: ClinicalKey Student, (3rd Edition). Page 278 – 292 " Elsevier Health Sciences (US)
  4. "USMLE Step 1 Secrets in Color. Available from: ClinicalKey Student, (5th Edition). Page 437 " Elsevier Limited (UK) (2022)