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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 |
| | + | ** Due to an intrinsic disorder in the brain |
| | + | ** Aquired |
| | + | *** Due to some lesion in the brain |
| | + | ** Reactive |
| | + | *** Due to some extracranial disoerder, 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==== |
| | + | |
| | + | # Prodrome |
| | + | #* The animal experiences an indication of a forthcoming seizure. |
| | + | #* This occurs hours to days before the event itself. |
| | + | # Aura |
| | + | #* This is the very start of the seizure. |
| | + | #* Behaviour changes may be apparent. |
| | + | # Ictus |
| | + | #* The seizure "proper". |
| | + | # Postictal phase |
| | + | #* Consists of transient neurological and behavious changes, which can last from hours to days. |
| | + | |
| | + | ====Idiopathic Epilepsy==== |
| | + | |
| | + | * Idiopathic epilepsy is a relatively common cause of generalised seizures in the dog. |
| | + | ** NOT in the cat. |
| | + | * The onset of seizures is between 1 and 5 years of age. |
| | + | * The condition presents as recurrent, unprovoked seizures, with no specific cause. |
| | + | * There are no neurological defects between episodes. |
| | + | * Seizures tend to start as generalised seizures, with no aura. |
| | + | |
| | + | ====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 |
| | + | |} |
| | + | |
| | + | ==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. |