Difference between revisions of "Seizures"
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− | { | + | ==Introduction== |
− | | | + | |
− | | | + | * '''Seizures''' are paroxysmal changes in cerebral cortex electrical activity that start abruptly, end suddenly and have a tendency to recur. |
− | | | + | * '''Epilepsy''' is the occurence of recurrent seizures. |
− | + | ||
− | | | + | ==Pathophysiology== |
+ | |||
+ | * Seizures occur when there is imbalance between exitatory and inhibitory processes. This may be due to : | ||
+ | ** Inadequate neuronal inhibition. | ||
+ | *** Major inhibitory neurotransmitters include GABA and glycine. | ||
+ | ** Excessive neuronal excitation. | ||
+ | *** Major excitatory neurotransmitters include aspartate and glutamate. | ||
+ | |||
+ | ===Proposed Mechanisms=== | ||
+ | |||
+ | * Defective feed-forward inhibition or feed-back initiation of inhibitory neurons in cortical circuits. | ||
+ | ** Recurrent excitatory collaterals may be formed. | ||
+ | * Changes in membrane properties of neurons. | ||
+ | ** These may include changes at: | ||
+ | *** Potassium, sodium, chloride and calcium ion channels | ||
+ | *** GABA receptors | ||
+ | *** Nicotinic acetyl choline receptors | ||
+ | *** NMDA receptors | ||
+ | **** Activation. | ||
+ | * Changes in the ionic microenvironment. | ||
+ | |||
+ | ===Seizure Development=== | ||
+ | |||
+ | # At the onset of a seizure, abnormal neurons undergo prolonged depolarisations. | ||
+ | #* These depolarisations are associated with the rapid firing of repeated action potentials. | ||
+ | # Depolarisation of abnormal neurons recruits adjacent neurons with which they are connected. | ||
+ | # The electrical discharges of the large number of neurons involved become linked together. | ||
+ | # A storm of electrical activity results, causing a clinical seizure. | ||
+ | # Seizures may then spread: | ||
+ | #* To adjacent areas of the brain. | ||
+ | #* Through established anatomic pathways to other distant areas. | ||
+ | |||
+ | ==Nomenclature== | ||
+ | |||
+ | * '''Status epilepticus''' is the term used to describe | ||
+ | ** A seizure lasting longer than 5 minutes, or | ||
+ | ** A collection of discrete seizures without full recovery of consciousness. | ||
+ | * '''Cluster seizures''' occur when 2 or more seizures are experienced in a brief periods, but the patient regains consciousness between them. | ||
+ | * Three classes of seizures are recognised: | ||
+ | *# Generalised seizures | ||
+ | *# Focal seizures | ||
+ | *# Focal generalising seizures | ||
+ | |||
+ | ===Generalised Seizures=== | ||
+ | |||
+ | * Generalised seizures may be: | ||
+ | ** Idiopathic | ||
+ | ** Symptomatic | ||
+ | *** Due to intracranial disease e.g. neoplasia, storage diseases etc. | ||
+ | ** Cryptogenic | ||
+ | *** There is probably an underlying cause but it cannot be identified by the diagnostic tests available. | ||
+ | ** Reactive | ||
+ | *** Due to some extracranial disorder, for example a toxin or metabolic disorder. | ||
+ | |||
+ | ====Clinical Signs==== | ||
+ | |||
+ | * Initial clinical signs show involvement of both cerebral hemispheres. | ||
+ | * Generalised seizures result in: | ||
+ | ** Change in consciousness | ||
+ | ** Motor activity | ||
+ | *** Tonic-clonic seizures are most common in dogs and cats. | ||
+ | ** Autonomic signs | ||
+ | * The body's energy utilisation can increase to around 250% of the normal value during a generalised seizure. | ||
+ | |||
+ | ====Stages==== | ||
+ | |||
+ | # Prodromal Phase | ||
+ | #* The animal experiences an indication of a forthcoming seizure. | ||
+ | #* This occurs hours to days before the event itself. | ||
+ | # Aural Phase | ||
+ | #* This is the very start of the seizure. | ||
+ | #* Behaviour changes may be apparent. | ||
+ | # Ictal Phase | ||
+ | #* The seizure "proper". | ||
+ | # Postictal phase | ||
+ | #* Consists of transient neurological and behavious changes, which can last from hours to days. | ||
+ | |||
+ | ====[[Idiopathic Epilepsy]]==== | ||
+ | |||
+ | ====Acquired Generalisd Seizures==== | ||
+ | |||
+ | * Other general seizures may be acquired. | ||
+ | * Seizures can occur at any age, but generally occur in animals younger than 2 years and older than 5 years. | ||
+ | * Causes may include: | ||
+ | ** Intracranial disease | ||
+ | *** Neoplasia | ||
+ | *** Trauma | ||
+ | *** Infection | ||
+ | *** Inflammation | ||
+ | ** Extracranial disease (also known as "reactive epilpsy"). | ||
+ | *** Electolyte disorders | ||
+ | *** Metabolic disorders | ||
+ | *** Toxicity | ||
+ | |||
+ | ===Focal Seizures=== | ||
+ | |||
+ | * Almost always an acquired disease. | ||
+ | * Active diseases often progress to become more general. | ||
+ | ** Cause generalised seizures. | ||
+ | |||
+ | ===Simple Focal Seizures=== | ||
+ | |||
+ | * Onset occurs in a limited area of one cerebral hemisphere. | ||
+ | * No impairment of consciousness. | ||
+ | |||
+ | === Complex Focal Seizures=== | ||
+ | |||
+ | * Arise in a single brain region, but cause impaired consciousness. | ||
+ | |||
+ | ==Causes of Acquired Seizures== | ||
+ | |||
+ | {| border="3" cellpadding="8" | ||
+ | !width="150"|'''<u>Cause</u>''' | ||
+ | !width="400"|'''<u>Examples</u>''' | ||
+ | |||
+ | |- | ||
+ | |Neoplasia | ||
+ | |Primary or metastatic | ||
+ | |- | ||
+ | |Inflammatory | ||
+ | |Distemper, FIP, FeLV/FIV, rabies, cryptococcosis (cats), toxoplasmosis | ||
+ | |- | ||
+ | |Traumatic | ||
+ | |Immediate or delayed | ||
+ | |- | ||
+ | |Vascular | ||
+ | |Feline ischaemic encephalopathy, thromboembolism, hypertenstion | ||
+ | |- | ||
+ | |Anomalous | ||
+ | |Hydrocephalus | ||
+ | |- | ||
+ | |Metabolic | ||
+ | |Hepatic encephalopathy, uraemia, hyperparathyroidism, hypolycaemia, hyperkalaemia, hypocalcaemia, hypoxia, acid-base disorders, hyperthermia | ||
+ | |- | ||
+ | |Toxic | ||
+ | |Lead, organophosphates, metaldehyde, strychnine | ||
+ | |} | ||
+ | [[File:Causes of Epilepsy in cats and dogs older than 6 years.pdf|alt=|thumb|Causes of Seizures in Cats and Dogs older than 6 Years]] | ||
+ | |||
+ | ==Investigation of Seizures== | ||
+ | |||
+ | * It must first be determined whether seizure activity is in fact a seizure, rather than a non-epileptic paroxysmal event, for example: | ||
+ | ** Syncope | ||
+ | ** Exercise-induced weakness | ||
+ | ** Obsessive-compulsive behaviour | ||
+ | ** Narcolepsy | ||
+ | * Idiopathic epilepsy may be differentiated from secondary or reactive seizures by considering: | ||
+ | ** Age of onset | ||
+ | ** Breed disposition | ||
+ | ** Partial seizures or asymmetrical post-ictal signs | ||
+ | *** These suggest a discrete lesion. | ||
+ | ** Older animals (>5 years) may be more likely to have an acquired aetiology. | ||
+ | ** Younger animals (<6 months) may be more likely to have toxic or metabolic causes. | ||
+ | * Useful tests include: | ||
+ | ** Metabolic screening | ||
+ | ** Haematology | ||
+ | ** Serum biochemistry | ||
+ | ** Urinalysis | ||
+ | ** Serology. | ||
+ | ** Bile acid stimulation test | ||
+ | ** Serum lead | ||
+ | ** MRI and CT scanning, and CSF analysis, help rule out cancer. | ||
+ | <br><br> | ||
+ | |||
+ | {{Template:Learning | ||
+ | |podcasts = [[Seizures podcast|RVC clinical podcast about seizures]]<br> | ||
}} | }} | ||
− | + | ||
+ | [[Category:Central Nervous System - Pathology]] |
Latest revision as of 09:59, 30 May 2021
Introduction
- Seizures are paroxysmal changes in cerebral cortex electrical activity that start abruptly, end suddenly and have a tendency to recur.
- Epilepsy is the occurence of recurrent seizures.
Pathophysiology
- Seizures occur when there is imbalance between exitatory and inhibitory processes. This may be due to :
- Inadequate neuronal inhibition.
- Major inhibitory neurotransmitters include GABA and glycine.
- Excessive neuronal excitation.
- Major excitatory neurotransmitters include aspartate and glutamate.
- Inadequate neuronal inhibition.
Proposed Mechanisms
- Defective feed-forward inhibition or feed-back initiation of inhibitory neurons in cortical circuits.
- Recurrent excitatory collaterals may be formed.
- Changes in membrane properties of neurons.
- These may include changes at:
- Potassium, sodium, chloride and calcium ion channels
- GABA receptors
- Nicotinic acetyl choline receptors
- NMDA receptors
- Activation.
- These may include changes at:
- Changes in the ionic microenvironment.
Seizure Development
- At the onset of a seizure, abnormal neurons undergo prolonged depolarisations.
- These depolarisations are associated with the rapid firing of repeated action potentials.
- Depolarisation of abnormal neurons recruits adjacent neurons with which they are connected.
- The electrical discharges of the large number of neurons involved become linked together.
- A storm of electrical activity results, causing a clinical seizure.
- Seizures may then spread:
- To adjacent areas of the brain.
- Through established anatomic pathways to other distant areas.
Nomenclature
- Status epilepticus is the term used to describe
- A seizure lasting longer than 5 minutes, or
- A collection of discrete seizures without full recovery of consciousness.
- Cluster seizures occur when 2 or more seizures are experienced in a brief periods, but the patient regains consciousness between them.
- Three classes of seizures are recognised:
- Generalised seizures
- Focal seizures
- Focal generalising seizures
Generalised Seizures
- Generalised seizures may be:
- Idiopathic
- Symptomatic
- Due to intracranial disease e.g. neoplasia, storage diseases etc.
- Cryptogenic
- There is probably an underlying cause but it cannot be identified by the diagnostic tests available.
- Reactive
- Due to some extracranial disorder, for example a toxin or metabolic disorder.
Clinical Signs
- Initial clinical signs show involvement of both cerebral hemispheres.
- Generalised seizures result in:
- Change in consciousness
- Motor activity
- Tonic-clonic seizures are most common in dogs and cats.
- Autonomic signs
- The body's energy utilisation can increase to around 250% of the normal value during a generalised seizure.
Stages
- Prodromal Phase
- The animal experiences an indication of a forthcoming seizure.
- This occurs hours to days before the event itself.
- Aural Phase
- This is the very start of the seizure.
- Behaviour changes may be apparent.
- Ictal Phase
- The seizure "proper".
- Postictal phase
- Consists of transient neurological and behavious changes, which can last from hours to days.
Idiopathic Epilepsy
Acquired Generalisd Seizures
- Other general seizures may be acquired.
- Seizures can occur at any age, but generally occur in animals younger than 2 years and older than 5 years.
- Causes may include:
- Intracranial disease
- Neoplasia
- Trauma
- Infection
- Inflammation
- Extracranial disease (also known as "reactive epilpsy").
- Electolyte disorders
- Metabolic disorders
- Toxicity
- Intracranial disease
Focal Seizures
- Almost always an acquired disease.
- Active diseases often progress to become more general.
- Cause generalised seizures.
Simple Focal Seizures
- Onset occurs in a limited area of one cerebral hemisphere.
- No impairment of consciousness.
Complex Focal Seizures
- Arise in a single brain region, but cause impaired consciousness.
Causes of Acquired Seizures
Cause | Examples |
---|---|
Neoplasia | Primary or metastatic |
Inflammatory | Distemper, FIP, FeLV/FIV, rabies, cryptococcosis (cats), toxoplasmosis |
Traumatic | Immediate or delayed |
Vascular | Feline ischaemic encephalopathy, thromboembolism, hypertenstion |
Anomalous | Hydrocephalus |
Metabolic | Hepatic encephalopathy, uraemia, hyperparathyroidism, hypolycaemia, hyperkalaemia, hypocalcaemia, hypoxia, acid-base disorders, hyperthermia |
Toxic | Lead, organophosphates, metaldehyde, strychnine |
File:Causes of Epilepsy in cats and dogs older than 6 years.pdf
Investigation of Seizures
- It must first be determined whether seizure activity is in fact a seizure, rather than a non-epileptic paroxysmal event, for example:
- Syncope
- Exercise-induced weakness
- Obsessive-compulsive behaviour
- Narcolepsy
- Idiopathic epilepsy may be differentiated from secondary or reactive seizures by considering:
- Age of onset
- Breed disposition
- Partial seizures or asymmetrical post-ictal signs
- These suggest a discrete lesion.
- Older animals (>5 years) may be more likely to have an acquired aetiology.
- Younger animals (<6 months) may be more likely to have toxic or metabolic causes.
- Useful tests include:
- Metabolic screening
- Haematology
- Serum biochemistry
- Urinalysis
- Serology.
- Bile acid stimulation test
- Serum lead
- MRI and CT scanning, and CSF analysis, help rule out cancer.
Seizures Learning Resources | |
---|---|
Podcasts Selection of relevant podcasts |
RVC clinical podcast about seizures |