Tonic-Clonic Seizures : Causes, Symptoms, Diagnosis & Treatment

Last Updated: 22/09/2022

Tonic-clonic convulsions are mixed paroxysms in which prolonged tonic spasms are replaced by rapid clonic contractions of the skeletal muscles. The causes of generalized seizures are quite extensive: epilepsy, organic pathology of the central nervous system, neuroinfections and other conditions. To verify the diagnosis, a comprehensive examination is required, including laboratory tests, tomography, and neurophysiological techniques. For the relief and therapy of convulsive syndrome, medications are used, in some cases, surgical treatment is indicated.

Causes of tonic-clonic seizures

Epilepsy

Epilepsy is the most common cause of generalized tonic-clonic seizures. The basis of classic mixed seizures is pathological activity, covering both hemispheres of the brain. Many impulses originate in the cortex of the frontal lobes as focal, but soon acquire a bilateral character. They first lead to symmetrical muscle tension, then they are converted into clonic contractions.

Separate paroxysms may begin with myoclonic jerks, but then acquire a typical three-phase course. The attack is accompanied by biting the tongue, involuntary urination. The greatest danger to patients is a sudden fall with loss of consciousness, which entails injuries with a potential threat to life. After the paroxysm, confusion, drowsiness, and transient amnesia are noted.

Cerebral pathology

Among the causes of convulsive syndrome, an important place is given to structural damage to the substance of the brain. Pathological impulses are generated in response to mechanical stimulation of motor neurons, supplemented by ischemic and metabolic shifts. Clonic and tonic convulsions are accompanied by the following conditions:

  • vascular disorders. Seizures appear with hemorrhagic or ischemic stroke, subarachnoid hemorrhage. Generalized paroxysms are characteristic of arteriovenous malformations, an epileptoid reaction accompanies the rupture of hemangiomas and saccular aneurysms.
  • Traumatic brain injury . Early post-traumatic seizures are more common in children with depressed fractures, penetrating TBI, and hematomas. The risk of developing late epileptic paroxysms increases with multiple and bilateral contusions, surgical interventions, and in old age.
  • Volumetric formations. Convulsive syndrome is a typical symptom of supratentorial brain tumors. Mixed seizures develop with medially located oligodendrogliomas, metastases of radioresistant tumors (melanoma, kidney cancer). Convulsions manifest subdural hematomas, abscesses.
  • Hypoxic-ischemic encephalopathy. Many neonatal seizures are attributed to encephalopathy due to antenatal or intranatal asphyxia. Usually, paroxysms begin on the first day after the birth of a child, are more pronounced at the onset of the disease, then turn into automatisms.

Tonic-clonic paroxysms are caused by cerebral (intracranial hypertension, edema) or focal disorders. As the pathology progresses, signs of irritation are replaced by loss of functions. In acute situations, a neurological deficit rapidly increases, damage to vital centers is associated with high mortality.

Infectious diseases

Seizures are a frequent manifestation of neuroinfections. They are based on the direct cytopathogenic effect of a microbial agent or damage involving vascular, autoimmune mechanisms. Spasms can occur against the background of fever, cerebrospinal fluid hypertension and cerebral edema, provoking ischemic changes. The most typical reasons are:

  • Meningoencephalitis. Various types of seizures are possible, but tonic-clonic ones dominate - in the form of single or multiple paroxysms. They are combined with positive meningeal signs (stiff neck muscles, symptoms of Kernig, Brudzinsky), cranial nerve paresis.
  • herpetic infection. Seizures of the type of epileptic are possible with herpetic encephalitis, which is due to damage to the limbic structures of the brain and an increase in general toxic phenomena. Mental reactions and consciousness are disturbed early.
  • Polio. The cerebral form of poliomyelitis often debuts with general convulsions in young children, but encephalitic reactions also occur in other variants of the disease. In the picture there are spastic paralysis, disorders of consciousness.

Acute infections in children manifest convulsive syndrome 2 times more often than in adults. Paroxysms are single or repeated, may indicate the development of a number of complications - subdural effusion or hematoma, heart attacks and intracerebral hemorrhages, abscesses. In the remote period after the disease, the risk of epileptic seizures is high.

 

Arterial hypertension

Convulsions in acute hypertensive encephalopathy are associated with cerebral edema, generalized spasm of arterioles. They occur in patients suffering from malignant arterial hypertension and acute kidney disease - diffuse glomerulonephritis, late toxicosis of pregnancy (severe nephropathy). In the latter case, the clinical picture is supplemented by edema, urinary syndrome with proteinuria.

The convulsive form of a hypertensive crisis and eclampsia during pregnancy debut with a severe headache, arousal. Characterized by visual disturbances, tinnitus, vomiting. Consciousness is quickly disturbed, tonic and clonic convulsions develop. The seizure begins with fibrillar twitching of the muscles of the face, then spasms of the whole body join with trismus, cyanosis. The attack ends in a coma with a gradual recovery of consciousness.

hereditary diseases

With hereditary pathology, tonic-clonic convulsions in children debut at an early age. They are often resistant to anticonvulsants and transform into various forms of epilepsy. Convulsions occur in diseases of accumulation and metabolic defects, which are characterized by a violation of metabolic processes in the structures of the central nervous system:

  • Leukodystrophy. Mixed paroxysms are accompanied by increased myelin breakdown in leukodystrophy (metachromatic, Pelizeus-Merzbacher disease, Krabbe disease). Usually they occur at the stage of pronounced manifestations in combination with progressive dementia, visual disturbances, paresis.
  • Phenylketonuria. Various convulsive attacks in phenylketonuria can pass one into another - mixed, myoclonic, infantile spasms. Early onset of paroxysms exacerbates neuropsychic development disorders, reaching a deep degree of mental retardation.
  • Leucinosis. The accumulation of leucine and other branched chain amino acids is accompanied by toxic encephalopathy. The child's condition is severe, characterized by generalized seizures, muscle hypertonicity, persistent vomiting with dehydration. Urine has an odor of maple syrup.
  • Amavrotic idiocy of Tay-Sachs. Tonic-clonic nature of convulsions are in the first year of a child's life. Attacks are accompanied by a slowdown in psychomotor development, visual and auditory disturbances, later paralysis occurs, and muscles atrophy.

intoxication

Brain damage in case of poisoning is usually due to the direct action of poisons on nerve structures with neurotransmitter, metabolic, and electrolyte disorders. Another mechanism is explained by endotoxicosis due to impaired function of internal organs (liver, kidneys). Convulsive syndrome is a clinical picture of a wide range of intoxications:

  • Drugs: cocaine, amphetamines.
  • Industrial and household poisons: organophosphorus compounds, oxalic acid, lead.
  • Plants: white hellebore, hemlock, thermopsis.
  • Nicotine.

Mixed attacks manifest an overdose of drugs from the group of alkaloids - atropine, lobelin, theophylline. Convulsions are observed with the irrational use of psychotropic (antidepressants, neuroleptics, psychostimulants), antimicrobial (β-lactam antibiotics, isoniazid, antiretroviral), painkillers.

Diagnostics

Early diagnosis is essential to determine the cause of tonic and clonic seizures. The risk of recurrence of attacks, the nature and extent of therapeutic measures, and the outcome of the disease will depend on the results obtained. The examination begins with an anamnesis and a medical examination, after which the neurologist prescribes additional procedures:

  • Laboratory tests. In a biochemical blood test, attention is paid to pH, the content of nitrogenous substances, protein levels. Diagnosis of neuroinfections is carried out by identifying specific antibodies, changes in the cerebrospinal fluid. Hereditary diseases are confirmed by molecular genetic analysis.
  • Tomography. Neuroimaging methods provide insight into structural disorders in the CNS. Brain CT data are highly informative for traumatic brain injuries, hemorrhages, and tumors. MRI better detects foci of neurodegeneration, demyelination, and ischemia.
  • Electroencephalography. EEG is considered the leading method for diagnosing paroxysmal conditions. The study determines epileptiform activity, clarifies its localization and the functional state of the brain.

Changes in the vessels are detected by neurosonography, which helps to verify ischemic damage. The displacement of the median structures of the brain can be seen on the Echo-EG, the state of the parenchymal organs (kidneys, liver) is examined by ultrasound. Mixed convulsions have to be differentiated from other paroxysmal conditions encountered in neurology and the clinic of internal diseases.

 

Treatment

Help before diagnosis

Convulsions of the tonic and clonic type are an acute situation requiring emergency care. With the onset of an attack, the victim should be protected from injury by laying on a flat surface with a pillow under his head, to ensure free access of air. With eclampsia, it is important to minimize the effect of external stimuli. A team of specialists who arrived at the call stops the ongoing attack with anticonvulsants, and conducts oxygen therapy.

Conservative therapy

A single convulsive episode is not an indication for specific therapy, but requires an active impact on the cause and mechanisms of its occurrence. In severe and life-threatening conditions, the patient is hospitalized in the resuscitation and intensive care unit, where medical correction is carried out. Among its priority areas are:

  • Anticonvulsant. Convulsions are stopped by benzodiazepines, phenobarbital, sodium oxybutyrate, and if they are ineffective, anesthetics are used. Epileptic seizures are eliminated by anticonvulsants (valproate, carbamazepine, topiramate).
  • Antimicrobial. A key role in the treatment of neuroinfections is played by etiotropic therapy with antibiotics and antiviral agents. Drugs are prescribed taking into account the sensitivity of the pathogen or empirically.
  • Hypotensive. Magnesium sulfate, methyldopa, calcium antagonists are used to eliminate hypertensive encephalopathy. Diuretics (furosemide, mannitol) help fight cerebral edema.

Children with hereditary fermentopathy are prescribed a special diet that reduces the formation of toxic substances. In case of poisoning, infusion and antidote therapy is carried out, in severe situations - extracorporeal detoxification. Vascular and degenerative diseases are treated with neuroprotectors, vasoactive, metabolic agents.

Surgery

Neurosurgical intervention helps to eliminate the cause of seizures in brain tumors, hematomas and abscesses - removal of pathological tissues, blood extraction, opening of abscesses. For the treatment of resistant epilepsy, resections (temporal, hemispherectomy), uncoupling operations, and transcranial stimulation are performed. In patients with leukodystrophies, improvement can be achieved with bone marrow transplantation.

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