The document discusses seizure disorders, defining them as sudden alterations in brain activity accompanied by abnormal electrical discharges. It describes the brain activity during seizures seen on EEGs and classifies seizures into primary generalized seizures that involve both sides of the brain at once, and partial seizures that begin in one area. It lists and describes several types of primary generalized seizures including absence, atonic, tonic, tonic-clonic, and myoclonic seizures. It also covers types of partial seizures and common symptoms seen at different stages of a seizure. Causes mentioned include genetic and acquired factors like head injuries, infections, and tumors.
This document provides information on seizure disorders including definitions, classifications, etiologies, clinical features, and management. It defines a seizure as abnormal involuntary neurological discharge from the brain that can cause loss of consciousness or abnormal motor, sensory, behavioral, or autonomic functions. Seizures are classified based on etiology (primary/secondary) and type (generalized, focal/partial, unclassified). Common etiologies include infections, metabolic disturbances, trauma, tumors, and genetic or developmental conditions. Clinical diagnosis involves a detailed history and may include EEG or imaging to classify seizure type and identify underlying causes. Management primarily involves use of anticonvulsant medications.
Diabetic ketoacidosis is a serious complication of diabetes that occurs when your body produces high levels of blood acids called ketones. The condition develops when your body can't produce enough insulin.
When your cells don't get the glucose they need for energy, your body begins to burn fat for energy, which produces ketones. Ketones are chemicals that the body creates when it breaks down fat to use for energy. The body does this when it doesn’t have enough insulin to use glucose, the body’s normal source of energy. When ketones build up in the blood, they make it more acidic.
This document discusses the management of complicated alcohol withdrawal. It begins with an introduction and overview of key topics including alcohol withdrawal seizures, alcoholic hallucinosis, delirium tremens, and Wernicke's encephalopathy. It then provides more detailed information on the pathogenesis, risk factors, clinical features, investigations, and management approaches for each of these complicated alcohol withdrawal conditions. Benzodiazepines are emphasized as the primary treatment for managing withdrawal symptoms, seizures, and delirium, while thiamine supplementation is stressed for preventing and treating Wernicke's encephalopathy.
Ischemic Stroke Subclassification, An Asian ViewpointErsifa Fatimah
Pada awalnya, sistem klasifikasi stroke diderivasi dari temuan autopsi yang dikaitkan dengan klinis pasien. Seiring dengan berkembangnya modalitas imaging & investigasi vaskular, klasifikasi stroke yang pada awalnya menitikberatkan pada sindroma klinis beralih menjadi suatu proses decision-making berdasarkan data klinis-radiologis-laboratoris.
Menariknya lagi, proporsi subtipe stroke ini pun berubah, sesuai sistem & kriteria yang digunakan...
Hmmm, bagaimana dengan klasifikasi dan proporsi tipe stroke di Asia?
1) High risk factors for seizure recurrence after a first unprovoked seizure include epileptiform abnormalities on EEG, a remote symptomatic cause identified on clinical history or neuroimaging, and an abnormal neurologic examination with focal findings or mental retardation.
2) AED treatment may be considered for patients with one or more of these high risk factors. While immediate AED treatment can reduce short-term seizure recurrence rates by 30-50%, it has little impact on long-term outcome and individual patient preferences regarding adverse effects should be taken into account.
3) Other potential risk factors with uncertain significance include a history of febrile seizures, family history of epilepsy, and seizures occurring during sleep. Status epilepticus
1) The document discusses strokes (cerebrovascular accidents or CVAs), their causes, types, symptoms, diagnosis and treatment.
2) Strokes are caused by disturbances in the vascular system and can be ischemic (caused by clot or blockage) or hemorrhagic (caused by bleeding).
3) Common symptoms of strokes include weakness or numbness on one side of the body, speech problems, and visual issues. The specific symptoms depend on the area of the brain affected.
This document provides information on seizure disorders including definitions, classifications, etiologies, clinical features, and management. It defines a seizure as abnormal involuntary neurological discharge from the brain that can cause loss of consciousness or abnormal motor, sensory, behavioral, or autonomic functions. Seizures are classified based on etiology (primary/secondary) and type (generalized, focal/partial, unclassified). Common etiologies include infections, metabolic disturbances, trauma, tumors, and genetic or developmental conditions. Clinical diagnosis involves a detailed history and may include EEG or imaging to classify seizure type and identify underlying causes. Management primarily involves use of anticonvulsant medications.
Diabetic ketoacidosis is a serious complication of diabetes that occurs when your body produces high levels of blood acids called ketones. The condition develops when your body can't produce enough insulin.
When your cells don't get the glucose they need for energy, your body begins to burn fat for energy, which produces ketones. Ketones are chemicals that the body creates when it breaks down fat to use for energy. The body does this when it doesn’t have enough insulin to use glucose, the body’s normal source of energy. When ketones build up in the blood, they make it more acidic.
This document discusses the management of complicated alcohol withdrawal. It begins with an introduction and overview of key topics including alcohol withdrawal seizures, alcoholic hallucinosis, delirium tremens, and Wernicke's encephalopathy. It then provides more detailed information on the pathogenesis, risk factors, clinical features, investigations, and management approaches for each of these complicated alcohol withdrawal conditions. Benzodiazepines are emphasized as the primary treatment for managing withdrawal symptoms, seizures, and delirium, while thiamine supplementation is stressed for preventing and treating Wernicke's encephalopathy.
Ischemic Stroke Subclassification, An Asian ViewpointErsifa Fatimah
Pada awalnya, sistem klasifikasi stroke diderivasi dari temuan autopsi yang dikaitkan dengan klinis pasien. Seiring dengan berkembangnya modalitas imaging & investigasi vaskular, klasifikasi stroke yang pada awalnya menitikberatkan pada sindroma klinis beralih menjadi suatu proses decision-making berdasarkan data klinis-radiologis-laboratoris.
Menariknya lagi, proporsi subtipe stroke ini pun berubah, sesuai sistem & kriteria yang digunakan...
Hmmm, bagaimana dengan klasifikasi dan proporsi tipe stroke di Asia?
1) High risk factors for seizure recurrence after a first unprovoked seizure include epileptiform abnormalities on EEG, a remote symptomatic cause identified on clinical history or neuroimaging, and an abnormal neurologic examination with focal findings or mental retardation.
2) AED treatment may be considered for patients with one or more of these high risk factors. While immediate AED treatment can reduce short-term seizure recurrence rates by 30-50%, it has little impact on long-term outcome and individual patient preferences regarding adverse effects should be taken into account.
3) Other potential risk factors with uncertain significance include a history of febrile seizures, family history of epilepsy, and seizures occurring during sleep. Status epilepticus
1) The document discusses strokes (cerebrovascular accidents or CVAs), their causes, types, symptoms, diagnosis and treatment.
2) Strokes are caused by disturbances in the vascular system and can be ischemic (caused by clot or blockage) or hemorrhagic (caused by bleeding).
3) Common symptoms of strokes include weakness or numbness on one side of the body, speech problems, and visual issues. The specific symptoms depend on the area of the brain affected.
Guillain-Barré syndrome is an acute inflammatory polyneuropathy that causes generalized paralysis. It is usually triggered by a viral or bacterial infection and causes the immune system to damage nerve cells. Common symptoms include progressive muscle weakness, numbness, and pain. Treatment involves immunotherapy to reduce immune response and support for breathing and other vital functions until recovery. Most patients recover fully but a small percentage have permanent nerve damage or die from respiratory failure.
Guillain-Barré syndrome (GBS) can be described as a collection of clinical syndromes that manifests as an acute inflammatory polyradiculoneuropathy with resultant weakness and diminished reflexes.
Although the classic description of GBS is that of a demyelinating neuropathy with ascending weakness, many clinical variants have been well documented in the medical literature.
This document provides an overview of encephalopathy, including:
- Encephalopathy is defined as an altered mental state caused by diffuse brain dysfunction. Common symptoms include confusion, memory loss, and personality changes.
- There are many potential causes of encephalopathy including metabolic disturbances, toxins, infections, liver failure, inflammation, drugs, demyelination, and lack of oxygen to the brain.
- EEG is often abnormal in encephalopathy, with features including triphasic waves and diffuse slowing correlating to severity of symptoms and impairment of consciousness.
The document discusses intracranial pressure (ICP), providing definitions and normal values. It describes cerebrospinal fluid (CSF) and autoregulation of cerebral blood flow. It covers evaluation of raised ICP including Monro-Kellie doctrine, Cushing's triad, and changes in the cranium. It discusses types of cerebral edema and causes of raised ICP. Clinical features, investigations, and general treatment protocols are outlined. Specific conditions like normal pressure hydrocephalus and idiopathic intracranial hypertension are briefly mentioned. Prognosis is also covered.
The document provides an overview of the approach to dementia. It discusses the diagnostic criteria for dementia, epidemiology, etiology including neurodegenerative, vascular, neurological and other causes. It describes cortical vs subcortical dementia and reversible vs irreversible dementias. The document also provides details on how to diagnose a case of dementia including history, examination, investigations and differential diagnosis. Specific subtypes like Alzheimer's disease, vascular dementia, frontotemporal dementia, Lewy body dementia, Parkinson's disease, normal pressure hydrocephalus and CJD are also discussed.
1) The document discusses various syndromes that can result from lesions or occlusions in different parts of the posterior circulation arteries that supply the brainstem and cerebellum.
2) Specific syndromes are described based on the location of the lesion, including PCA, vertebral artery, and basilar artery syndromes. Onset, signs and symptoms on both sides of the lesion are outlined.
3) Midbrain, pontine, and medullary syndromes are also detailed. Bilateral lesions causing Anton's syndrome and Balint's syndrome are mentioned. A variety of resulting neurological deficits are associated with different posterior circulation artery occlusions.
This document discusses intracranial space occupying lesions, including their definition, types, clinical presentations, diagnosis, and treatment. It defines these lesions as those that expand in volume to displace normal neural structures and may increase intracranial pressure. It then describes the main types of lesions such as primary and metastatic brain tumors, traumatic injuries like hematomas, and infectious or inflammatory causes. The clinical presentations, diagnosis using imaging and other tests, and treatment approaches are outlined for each of the major lesion types. Surgical resection and other procedures are discussed as primary treatment methods depending on the specific lesion.
Febrile seizures are seizures that occur in young children between 6 months and 5 years old when they have a fever. They are classified as either simple or complex based on features like duration and recurrence. Simple febrile seizures are more common, generalized, and last less than 15 minutes. Risk factors for recurrence include age under 1, duration of fever, and family history. Causes are usually upper respiratory infections or roseola. Evaluation involves history, exam, and occasionally lumbar puncture or EEG. Treatment focuses on bringing the fever down with antipyretics and using benzodiazepines if the seizure lasts more than 5 minutes.
1. Chorea is a state of excessive, spontaneous, irregular movements that are randomly distributed and abnormal in character. It can range from mild restlessness to violent disabling movements.
2. Ballismus involves proximal, flinging, violent involuntary movements. Both chorea and ballismus are associated with basal ganglia dysfunction and abnormal neurotransmitter levels like decreased GABA and increased dopamine.
3. Causes of chorea and ballismus include infections, metabolic and endocrine disorders, drugs, trauma, vascular events, tumors, and hereditary conditions like Huntington's disease. Treatment involves reducing dopamine levels with antipsychotics or GABA agonists, as well as surgical procedures like pallidotomy or thalamotomy
Neuroleptic malignant syndrome (NMS) is a life-threatening condition caused by the use of neuroleptic drugs characterized by mental status changes, rigidity, fever, and dysautonomia. Diagnosis requires exposure to neuroleptics and two of the four cardinal symptoms. Treatment involves stopping the causative agents, supportive care, and specific treatments like dantrolene or bromocriptine. Prognosis depends on severity and medical complications, with reported mortality rates of 5-20%.
Coma is defined and the anatomy of consciousness explained. The various levels of arousal, AVPU scale and Glasgow Coma Scale described. The differential diagnosis of coma discussed are coma with & without focal deficits and the meningitis syndrome.
The various aspects of history discussed in details. The examination part includes the general examination, Brainstem reflexes, motor functions with the signs of lateralisation and meningeal irritation signs.
The basic lab investigations, Imaging and special investigations like CSF examination, EEG discussed.
Elevated intracranial pressure and its management explained.
CADASIL is caused by mutations in the NOTCH3 gene and is the most common monogenic form of cerebral small vessel disease. It is characterized clinically by recurrent strokes, cognitive decline, and mood disorders. Diagnosis involves identifying white matter changes, cerebral microbleeds, and NOTCH3 gene mutations on imaging and genetic testing. While there are currently no disease-modifying treatments, understanding the pathogenic mechanisms of CADASIL may help develop new therapeutic strategies.
Traumatic brain injury (TBI) is caused by external forces that impact or rapidly accelerate/decelerate the head. This can lead to primary injuries like contusions or hematomas from impact, or diffuse axonal injury from acceleration/deceleration forces. Secondary injuries may occur hours or days later and involve processes like cerebral edema, increased intracranial pressure, and reduced cerebral blood flow. The goals of management are to prevent secondary injuries by maintaining cerebral perfusion pressure and minimizing intracranial pressure increases through monitoring, treatment of complications, and other interventions.
Metabolic encephalopathy diagnosis and managementRobert Robinson
Overview of the diagnosis and management of metabolic encephalopathy for third year medical students in the Personalized Education Program portion of the third year curriculum at SIU Medicine
Pick's disease is a rare form of dementia that affects the frontal and temporal lobes of the brain. It causes symptoms like abnormal behavior, thinking, judgment, and memory loss. The disease is caused by abnormal tau proteins that clump together to form Pick bodies, which damage brain cells. Currently there is no cure for Pick's disease, which progressively worsens over 8-10 years as it shuts down more brain functions. Though terrifying, it remains an extremely uncommon condition.
The document discusses acute kidney injury (AKI), including its causes, diagnosis, and management. It provides details on prerenal, intrinsic, and postrenal forms of AKI. For prerenal AKI, management focuses on correcting the underlying cause, such as volume depletion, and restoring intravascular volume through fluid resuscitation. For intrinsic AKI, identifying and removing nephrotoxic agents is important. Dialysis may be needed for severe AKI with fluid/electrolyte imbalance or uremia.
The document discusses cognitive disorders and different types and stages of dementia. It defines cognition and lists different cognitive domains. It then summarizes classification systems for cognitive disorders from DSM-IV, DSM-5, and ICD-10. The stages of cognitive decline are discussed, from subjective cognitive impairment to mild cognitive impairment to dementia. The main types and causes of dementia are outlined. Assessment, risk factors, features and differentiation of different dementias like Alzheimer's and vascular dementia are summarized.
This document discusses metabolic encephalopathies, including their definition, pathophysiology, common types, diagnosis, and management. It focuses on hepatic encephalopathy caused by liver failure and uremic encephalopathy caused by kidney failure. The main mechanisms involve disruption of brain arousal centers and neurotransmitter abnormalities. Management involves treating the underlying condition, controlling seizures, reducing ammonia levels, and managing cerebral edema. Metabolic encephalopathies in critically ill patients can lead to long-term neurocognitive deficits even if the initial brain dysfunction was reversible.
The document discusses seizure disorders and epilepsy. It defines epilepsy as a brain disorder causing seizures from abnormal electrical activity in the brain. Seizures are classified as partial or generalized depending on where they originate and spread in the brain. Common causes of epilepsy include genetic factors, brain injuries, infections, and metabolic imbalances. Diagnosis involves a medical history, neurological exam, EEG, and brain imaging. Treatment focuses on medications to control seizures and sometimes surgery for refractory cases. Nursing care includes safety measures during seizures and education on epilepsy management.
Seizures are episodes of abnormal brain activity that result from excessive neuronal discharge. They can be classified as partial or generalized seizures. Partial seizures remain localized in one area of the brain while generalized seizures involve both hemispheres. Common causes include brain injuries, tumors, infections, genetic factors, and chemical imbalances. Diagnosis involves a neurological exam, EEG, and MRI. Treatment involves anti-seizure medications tailored to the individual. Generalized seizure types include tonic-clonic, absence, and atonic seizures which are characterized by muscle contractions, staring spells, and loss of muscle tone respectively. Status epilepticus is a medical emergency defined as continuous seizures lasting more than 30 minutes.
Guillain-Barré syndrome is an acute inflammatory polyneuropathy that causes generalized paralysis. It is usually triggered by a viral or bacterial infection and causes the immune system to damage nerve cells. Common symptoms include progressive muscle weakness, numbness, and pain. Treatment involves immunotherapy to reduce immune response and support for breathing and other vital functions until recovery. Most patients recover fully but a small percentage have permanent nerve damage or die from respiratory failure.
Guillain-Barré syndrome (GBS) can be described as a collection of clinical syndromes that manifests as an acute inflammatory polyradiculoneuropathy with resultant weakness and diminished reflexes.
Although the classic description of GBS is that of a demyelinating neuropathy with ascending weakness, many clinical variants have been well documented in the medical literature.
This document provides an overview of encephalopathy, including:
- Encephalopathy is defined as an altered mental state caused by diffuse brain dysfunction. Common symptoms include confusion, memory loss, and personality changes.
- There are many potential causes of encephalopathy including metabolic disturbances, toxins, infections, liver failure, inflammation, drugs, demyelination, and lack of oxygen to the brain.
- EEG is often abnormal in encephalopathy, with features including triphasic waves and diffuse slowing correlating to severity of symptoms and impairment of consciousness.
The document discusses intracranial pressure (ICP), providing definitions and normal values. It describes cerebrospinal fluid (CSF) and autoregulation of cerebral blood flow. It covers evaluation of raised ICP including Monro-Kellie doctrine, Cushing's triad, and changes in the cranium. It discusses types of cerebral edema and causes of raised ICP. Clinical features, investigations, and general treatment protocols are outlined. Specific conditions like normal pressure hydrocephalus and idiopathic intracranial hypertension are briefly mentioned. Prognosis is also covered.
The document provides an overview of the approach to dementia. It discusses the diagnostic criteria for dementia, epidemiology, etiology including neurodegenerative, vascular, neurological and other causes. It describes cortical vs subcortical dementia and reversible vs irreversible dementias. The document also provides details on how to diagnose a case of dementia including history, examination, investigations and differential diagnosis. Specific subtypes like Alzheimer's disease, vascular dementia, frontotemporal dementia, Lewy body dementia, Parkinson's disease, normal pressure hydrocephalus and CJD are also discussed.
1) The document discusses various syndromes that can result from lesions or occlusions in different parts of the posterior circulation arteries that supply the brainstem and cerebellum.
2) Specific syndromes are described based on the location of the lesion, including PCA, vertebral artery, and basilar artery syndromes. Onset, signs and symptoms on both sides of the lesion are outlined.
3) Midbrain, pontine, and medullary syndromes are also detailed. Bilateral lesions causing Anton's syndrome and Balint's syndrome are mentioned. A variety of resulting neurological deficits are associated with different posterior circulation artery occlusions.
This document discusses intracranial space occupying lesions, including their definition, types, clinical presentations, diagnosis, and treatment. It defines these lesions as those that expand in volume to displace normal neural structures and may increase intracranial pressure. It then describes the main types of lesions such as primary and metastatic brain tumors, traumatic injuries like hematomas, and infectious or inflammatory causes. The clinical presentations, diagnosis using imaging and other tests, and treatment approaches are outlined for each of the major lesion types. Surgical resection and other procedures are discussed as primary treatment methods depending on the specific lesion.
Febrile seizures are seizures that occur in young children between 6 months and 5 years old when they have a fever. They are classified as either simple or complex based on features like duration and recurrence. Simple febrile seizures are more common, generalized, and last less than 15 minutes. Risk factors for recurrence include age under 1, duration of fever, and family history. Causes are usually upper respiratory infections or roseola. Evaluation involves history, exam, and occasionally lumbar puncture or EEG. Treatment focuses on bringing the fever down with antipyretics and using benzodiazepines if the seizure lasts more than 5 minutes.
1. Chorea is a state of excessive, spontaneous, irregular movements that are randomly distributed and abnormal in character. It can range from mild restlessness to violent disabling movements.
2. Ballismus involves proximal, flinging, violent involuntary movements. Both chorea and ballismus are associated with basal ganglia dysfunction and abnormal neurotransmitter levels like decreased GABA and increased dopamine.
3. Causes of chorea and ballismus include infections, metabolic and endocrine disorders, drugs, trauma, vascular events, tumors, and hereditary conditions like Huntington's disease. Treatment involves reducing dopamine levels with antipsychotics or GABA agonists, as well as surgical procedures like pallidotomy or thalamotomy
Neuroleptic malignant syndrome (NMS) is a life-threatening condition caused by the use of neuroleptic drugs characterized by mental status changes, rigidity, fever, and dysautonomia. Diagnosis requires exposure to neuroleptics and two of the four cardinal symptoms. Treatment involves stopping the causative agents, supportive care, and specific treatments like dantrolene or bromocriptine. Prognosis depends on severity and medical complications, with reported mortality rates of 5-20%.
Coma is defined and the anatomy of consciousness explained. The various levels of arousal, AVPU scale and Glasgow Coma Scale described. The differential diagnosis of coma discussed are coma with & without focal deficits and the meningitis syndrome.
The various aspects of history discussed in details. The examination part includes the general examination, Brainstem reflexes, motor functions with the signs of lateralisation and meningeal irritation signs.
The basic lab investigations, Imaging and special investigations like CSF examination, EEG discussed.
Elevated intracranial pressure and its management explained.
CADASIL is caused by mutations in the NOTCH3 gene and is the most common monogenic form of cerebral small vessel disease. It is characterized clinically by recurrent strokes, cognitive decline, and mood disorders. Diagnosis involves identifying white matter changes, cerebral microbleeds, and NOTCH3 gene mutations on imaging and genetic testing. While there are currently no disease-modifying treatments, understanding the pathogenic mechanisms of CADASIL may help develop new therapeutic strategies.
Traumatic brain injury (TBI) is caused by external forces that impact or rapidly accelerate/decelerate the head. This can lead to primary injuries like contusions or hematomas from impact, or diffuse axonal injury from acceleration/deceleration forces. Secondary injuries may occur hours or days later and involve processes like cerebral edema, increased intracranial pressure, and reduced cerebral blood flow. The goals of management are to prevent secondary injuries by maintaining cerebral perfusion pressure and minimizing intracranial pressure increases through monitoring, treatment of complications, and other interventions.
Metabolic encephalopathy diagnosis and managementRobert Robinson
Overview of the diagnosis and management of metabolic encephalopathy for third year medical students in the Personalized Education Program portion of the third year curriculum at SIU Medicine
Pick's disease is a rare form of dementia that affects the frontal and temporal lobes of the brain. It causes symptoms like abnormal behavior, thinking, judgment, and memory loss. The disease is caused by abnormal tau proteins that clump together to form Pick bodies, which damage brain cells. Currently there is no cure for Pick's disease, which progressively worsens over 8-10 years as it shuts down more brain functions. Though terrifying, it remains an extremely uncommon condition.
The document discusses acute kidney injury (AKI), including its causes, diagnosis, and management. It provides details on prerenal, intrinsic, and postrenal forms of AKI. For prerenal AKI, management focuses on correcting the underlying cause, such as volume depletion, and restoring intravascular volume through fluid resuscitation. For intrinsic AKI, identifying and removing nephrotoxic agents is important. Dialysis may be needed for severe AKI with fluid/electrolyte imbalance or uremia.
The document discusses cognitive disorders and different types and stages of dementia. It defines cognition and lists different cognitive domains. It then summarizes classification systems for cognitive disorders from DSM-IV, DSM-5, and ICD-10. The stages of cognitive decline are discussed, from subjective cognitive impairment to mild cognitive impairment to dementia. The main types and causes of dementia are outlined. Assessment, risk factors, features and differentiation of different dementias like Alzheimer's and vascular dementia are summarized.
This document discusses metabolic encephalopathies, including their definition, pathophysiology, common types, diagnosis, and management. It focuses on hepatic encephalopathy caused by liver failure and uremic encephalopathy caused by kidney failure. The main mechanisms involve disruption of brain arousal centers and neurotransmitter abnormalities. Management involves treating the underlying condition, controlling seizures, reducing ammonia levels, and managing cerebral edema. Metabolic encephalopathies in critically ill patients can lead to long-term neurocognitive deficits even if the initial brain dysfunction was reversible.
The document discusses seizure disorders and epilepsy. It defines epilepsy as a brain disorder causing seizures from abnormal electrical activity in the brain. Seizures are classified as partial or generalized depending on where they originate and spread in the brain. Common causes of epilepsy include genetic factors, brain injuries, infections, and metabolic imbalances. Diagnosis involves a medical history, neurological exam, EEG, and brain imaging. Treatment focuses on medications to control seizures and sometimes surgery for refractory cases. Nursing care includes safety measures during seizures and education on epilepsy management.
Seizures are episodes of abnormal brain activity that result from excessive neuronal discharge. They can be classified as partial or generalized seizures. Partial seizures remain localized in one area of the brain while generalized seizures involve both hemispheres. Common causes include brain injuries, tumors, infections, genetic factors, and chemical imbalances. Diagnosis involves a neurological exam, EEG, and MRI. Treatment involves anti-seizure medications tailored to the individual. Generalized seizure types include tonic-clonic, absence, and atonic seizures which are characterized by muscle contractions, staring spells, and loss of muscle tone respectively. Status epilepticus is a medical emergency defined as continuous seizures lasting more than 30 minutes.
This document provides information about epilepsy and emergency medication management. It defines epilepsy and seizures, describes different types of seizures and their classification. It discusses general seizure management, status epilepticus, sudden unexpected death in epilepsy, risks and reducing risks. The document outlines anti-epileptic medications including diazepam and midazolam. It stresses the importance of individual seizure management plans and keeping a seizure diary.
This document summarizes information about epilepsy and seizures. It defines epilepsy as recurrent seizures and describes different types of seizures including focal-onset, generalized-onset, tonic-clonic, absence, myoclonic, atonic, and tonic seizures. Causes, pathophysiology, diagnosis and treatment options are discussed. Treatment involves antiepileptic medications as first-line treatment, with surgery, neurostimulation or dietary therapies as options for refractory cases. Potential risks and complications of treatments are also summarized.
Epilepsy is a brain disorder characterized by recurrent seizures. There are two main types of seizures - primary generalized seizures which involve both sides of the brain at once, and partial/focal seizures which begin in one area of the brain. Seizures are further classified based on symptoms such as absence, tonic, atonic, clonic, myoclonic, and tonic-clonic seizures. Epilepsy is typically diagnosed based on a patient's medical history and symptoms as well as tests like EEG, CT scan, or MRI. Common treatments include anti-seizure medications, dietary therapies, surgery, and nerve stimulation devices.
1) Seizures are temporary abnormal electrical phenomena in the brain that can manifest as alterations in mental state, movements, or other symptoms. Epilepsy is defined as recurrent unprovoked seizures.
2) Common types of seizures include generalized absence seizures, generalized tonic-clonic seizures, simple partial seizures, and complex partial seizures.
3) Evaluating and diagnosing seizure patients involves medical history, physical exam, EEG, imaging tests, and other assessments to identify potential causes and classify seizure types. Treatment often involves anti-seizure medications.
This document provides an overview of epilepsy and psychiatric aspects of epilepsy. It defines key terms like seizure, epilepsy, and status epilepticus. It describes different types of seizures including partial seizures, generalized seizures, tonic seizures, atonic seizures, myoclonic seizures, and absence seizures. Causes of epilepsy like genetic predisposition, trauma, poisoning, and tumors are discussed. The document also covers management of psychiatric patients with epilepsy and first aid for pre-ictal, ictal, and post-ictal phases of seizures.
This document provides an overview of approaches to seizure and epilepsy diagnosis and classification. It discusses the differential diagnosis of seizures and conditions that can mimic seizures like syncope. It describes focal seizures which originate in one hemisphere and can involve motor, sensory or cognitive symptoms. Generalized seizures rapidly engage both hemispheres and include absence seizures, tonic-clonic seizures and atonic seizures. Seizures are classified based on their origin and symptoms. The EEG findings for different seizure types are also outlined.
This presentation summarizes key information about epilepsy, including its definition, types of seizures, and treatment options. Epilepsy is characterized by excessive and synchronous neuronal discharge that can cause loss of consciousness or abnormal movements. Seizures are classified as partial or generalized. Partial seizures are limited to one part of the brain while generalized seizures affect both hemispheres. Common generalized seizure types include tonic-clonic, myoclonic, atonic, and absence seizures. New anti-seizure drugs discussed include vigabatrin, zonisamide, and topiramate. The presentation stresses the importance of planning and prenatal vitamin intake for women with epilepsy who are considering pregnancy.
"Navigating Epilepsy: A Holistic Approach with Dr. Ganesh"
🌟 Hello, everyone! Dr. Ganesh here, and today, we embark on a journey to explore a topic close to my heart: the comprehensive approach to epilepsy. Whether you're a patient, a caregiver, or simply curious about understanding epilepsy, this discussion is crafted with you in mind.
This document provides an overview of epilepsy, including definitions, types of seizures, causes, diagnosis, and treatment. Some key points:
- Epilepsy is defined as recurrent seizures due to an underlying neurological condition. A seizure is a brief episode caused by abnormal neuronal activity in the brain.
- Seizures are classified as either generalized or partial/focal, depending on where in the brain the abnormal activity originates. Common types include generalized tonic-clonic, absence, myoclonic, atonic, and complex partial seizures.
- Epilepsy has various causes including genetic factors, brain injury, infection, tumors, and metabolic imbalances. Diagnosis involves a neurological exam, medical history
fits and siezures deffination and its typesSalmaAzeem3
This document discusses the different types of seizures. It begins by explaining that seizures are caused by disturbances in electrical brain activity. Seizures are divided into two broad categories: generalized seizures originating across the entire brain, and partial seizures originating in a small area. Generalized seizures include grand mal, absence, myoclonic, clonic, tonic, and atonic seizures. Partial seizures are further divided into simple and complex, with simple seizures maintaining awareness and complex resulting in lost awareness. Symptoms of epilepsy include repeated seizures with symptoms like convulsions, blackouts, fainting, unresponsiveness, stiffness, falling, blinking, chewing, dazedness, repetitive movements, fear, changes in senses, and jerking
1) Seizures in children can be caused by factors like birth injuries, head trauma, infections, genetic conditions, and tumors. They are classified as generalized or partial based on where they originate in the brain.
2) Generalized seizures involve the entire brain and include tonic-clonic, absence, myoclonic, clonic, and atonic seizures. Partial seizures originate in one area of the brain and can be simple, with retained awareness, or complex, with impaired awareness.
3) Diagnosis involves medical history, physical exams, blood tests, EEGs, and brain imaging. Treatment includes medications, dietary therapies, surgery, and management of acute seizures. The prognosis depends on factors like
This document summarizes different types of epileptic seizures. It describes focal seizures, which occur in one area of the brain and may cause altered vision, muscle movements, or other localized symptoms without loss of consciousness. Generalized seizures affect both sides of the brain and cause loss of consciousness. Specific types of generalized seizures described include absence, atonic, tonic-clonic, and myoclonic seizures. The document provides brief details on the symptoms and characteristics of each seizure type.
The document provides information on seizures, convulsions, and epilepsy. It defines these terms and describes the different types of seizures including partial/focal seizures and generalized seizures. It discusses the causes, signs and symptoms, diagnostic evaluation, and management of seizures which includes anti-seizure medications, surgery, and vagus nerve stimulation. Nursing care focuses on protecting the individual during a seizure and observing/reporting seizure characteristics. Complications include prolonged seizures known as status epilepticus.
This document provides an overview of seizures and epilepsy presented by Riya Kanwalia, a third year nursing student. It defines seizures as sudden electrical disturbances in the brain that cause changes in behavior, movement and consciousness. Epilepsy is defined as two or more seizures or a tendency to have recurrent seizures. The document describes the different types of seizures including partial/focal seizures, generalized seizures, absence seizures, tonic-clonic seizures, myoclonic seizures and atonic seizures. It discusses the causes, pathophysiology, clinical manifestations, diagnosis and management of seizures and epilepsy.
Epilepsy is characterized by recurrent seizures that result from abnormal neuronal activity in the brain. Seizures can be generalized, originating simultaneously across both hemispheres of the brain, or partial, originating in a localized region of the brain. Generalized seizures include absence seizures, tonic-clonic seizures, atonic seizures, and myoclonic seizures. Partial seizures can be simple, with motor, sensory or other symptoms but no change in consciousness, or complex, with impaired consciousness. Seizures can have various causes including genetic factors, head injuries, infections, or other acquired brain abnormalities. Evaluation and treatment involve diagnostic testing, medication, and management of any underlying conditions.
EFEPA: Epilepsy at School - Training for School Nursesjgreenberger
The document provides information about Eric Marsh, an expert in epilepsy. It discusses definitions of seizures and epilepsy, prevalence statistics, common seizure types and epilepsy syndromes in children and adults. Potential causes, triggers, and treatments for epilepsy like medications, surgery, diets and vagus nerve stimulation are summarized. Risks and management of seizure emergencies are also covered.
There are two main categories of epilepsy - idiopathic (no apparent cause) and symptomatic (known cause such as brain injury). Common causes of symptomatic epilepsy include strokes, brain tumors, head injuries, infections, and birth complications. Seizures can be partial (affect small area of brain) or generalized (affect large area). Partial seizures may cause strange sensations but consciousness is retained, while complex partial seizures cause loss of awareness. Generalized seizures include absence, myoclonic, clonic, atonic, and tonic-clonic seizures which vary in their physical symptoms and effects on consciousness.
Epilepsy is characterized by recurrent seizures and is common, affecting 0.5% of the US population. Seizures can be focal, involving only part of the brain, or generalized, involving both hemispheres. Focal seizures may or may not involve impaired consciousness and can evolve to generalized seizures. Generalized seizures include absence seizures, myoclonic seizures, and tonic-clonic seizures. Epilepsy has many potential etiologies including genetic factors, structural lesions, metabolic disturbances, infections, and unknown causes. Diagnosis involves witnessing recurrent seizures and characteristic EEG changes.
10 Benefits an EPCR Software should Bring to EMS Organizations Traumasoft LLC
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2. Introduction
Normal brain function requires an orderly,
organized, coordinate d discharge of electrical
impulses.
Electrical impulses enable the brain to
communicate with the spinal cord, nerves, and
muscles as well as within itself.
Seizures may result when the brain's electrical
activity is disrupted.
3. Definition
A sudden, involuntary, time-limited alteration in
behavior, motor activity, autonomic function,
consciousness, or sensation, accompanied by an
abnormal electrical discharge in the brain.
Seizure (medicine), sudden attack or spasm, as in
epilepsy or a similar disorder. Seizures differ with
the type of condition and may consist of loss of
consciousness, convulsive jerking of parts of the
body, emotional explosions, or periods of mental
confusion.
4. Brain activity during seizures
An electroencephalogram (an EEG) is a
recording of the brain's electrical activity. The
procedure is simple and painless. About 20 small
adhesive electrodes are placed on the scalp, and
the brain's activity is recorded under normal
conditions. Then the person is exposed to various
stimuli, such as bright or flashing lights, to try to
provoke a seizure. During a seizure, electrical
activity in the brain accelerates, producing a
jagged wave pattern. Such recordings of brain
waves help identify a seizure disorder. Different
types of seizures have different wave patterns.
5. Types of seizure
A. Primary generalized seizure:
Begins with a widespread electrical discharge
Involves both sides of the brain at once
Hereditary factors are important
B. Partial Seizure:
Begins with an electrical discharge in one limited
area of the brain
Related to head injury, brain infection, stroke, or
tumor
6. Types of Primary generalized seizure
1. Absence seizures:
Brief episodes of staring
Absence seizures are considered complex absence
seizures
Include a change in muscle activity
Most common movement are eye blinks
Complex absence seizures are often more than 10
seconds long
7. Usually begin between ages 4 and 14
no warning before a seizure, and the person is
completely alert immediately afterward
Other movements include slight tasting
movements of the mouth, hand movements such
as rubbing the fingers together ,etc.
Children who get them usually have normal
development and intelligence
70% of cases, absence seizures stop by age
8. 2. Atypical absence seizure:
Atypical means unusual or not typical
Person will stare but often is somewhat responsive
Eye blinking or slight jerking movements of the lips
may occur
Hard to distinguish from the person's usual behavior,
especially in those with cognitive impairment
Generally begins at the age of 6
Most of the children affected have below-average
intelligence
9. Other types of seizures that are difficult to
control
Seizures usually continue till adulthood
Daydreaming and inattentiveness can mimic these
seizures
Diagnosis can be difficult if the behavior during
seizures is similar to the child's usual behavior
10. 3. Monoclonic seizures:
Very brief jerks, last only for 2 to 3 sec
Seizures usually cause abnormal movements on
both sides of the body at the same time
Myo means muscle and clonus means rapidly
alternating contraction and relaxation
Seizures usually begin in childhood, but the
seizures can occur at any age
11. Seizures occur in reflex epilepsies, triggered by
flashing lights or other things in the environment
Syndromes usually can be diagnosed on the basis
of the medical history and often EEG patterns
12. 4. Atonic Seizures:
Atonic means without tone
In an atonic seizure, muscles suddenly lose
strength
Eyelids may droop, the head may nod, and the
person may drop things and often falls to the
ground
Also known as drop attacks or drop seizures
The person usually remains conscious
13. Another name for this type of seizure is “akinetic”
which means without movement
Seizures often begin in childhood
Often last into adulthood
People with atonic seizures are injured when they
fall
Seizures may cause people to fall when they're
standing often have tonic seizures rather than
atonic seizures
Syndromes usually can be diagnosed on the basis of
the medical history and often EEG patterns
14. 5. Tonic Seizures:
Usually last less than 20 sec
In such seizures, the tone is greatly increased and
the body, arms, or legs make sudden stiffening
movements
Consciousness is usually preserved
Seizures most often occur during sleep
Usually involve all or most of the brain, affecting
both sides of the body
15. Common in people who have the epilepsy
syndrome called Lennox-Gastaut syndrome
Movements cannot be stopped by restraining or
repositioning the arms or legs
These seizures are rarely found
Common are tonic-clonic seizures, in which the
jerking is preceded by stiffening
16. Sometimes tonic-clonic seizures start with jerking
alone
These are called clonic-tonic-clonic seizures
Occur at various ages, including in newborns
Brief and infrequent clonic seizures in infants
usually disappear within very short period
The EEG pattern will change during a seizure, so
video- EEG is very useful for diagnosis
17. 7. Tonic-clonic seizures:
Normally last for 2 to 3 min
More than 5 min calls for immediate medical help
Seizure that lasts more than 30 minutes indicate
convulsion
Person loses consciousness and falls to the floor
Tongue or cheek may be bitten, so bloody saliva
may come from the mouth
Person may turn a bit blue in the face
18. After the tonic phase comes the clonic phase
Arms and usually the legs begin to jerk rapidly
and rhythmically
Bending and relaxing at the elbows, hips, and
knees
After a few minutes, the jerking slows and stops
Bladder or bowel control sometimes is lost as the
body relaxes
19. Consciousness returns slowly, and the person may
be drowsy, confused, agitated, or depressed
Tonic-clonic seizures can be controlled by seizure
medicines
They affect both children and adults
20. Types of Partial seizures
1. Simple partial seizures:
Different from person to person, depending on
the part of the brain where they begin
One thing they all have in common is that the
person remains alert and can remember what
happens
Usually last for less than 2 min
People who have had a head injury, brain
infection, stroke, or brain tumor likely to get
them
These seizures often can be controlled by seizure
medicines
21. 2. Complex Partial Seizures:
Usually last between 30 seconds and 2 minutes
Afterward, the person may be tired or confused for
about 15 minutes and may not be fully normal for
hours
Seizures usually start in a small area of the temporal
lobe or frontal lobe of the brain. Quickly involve
other areas of the brain that affect alertness and
awareness
These seizures (usually ones beginning in the
temporal lobe) start with a simple partial seizure
Also called an aura, this warning seizure often
includes an odd feeling in the stomach
22. Less often, people may repeat words or phrases,
laugh, scream, or cry
Some people do things during these seizures that
can be dangerous
People need to take precautions in advance
people who have had a head injury, brain
infection, stroke, or brain tumor are more likely
to get seizures
If medication is not effective, some can be
eliminated by epilepsy surgery
23. 3.Secondarily generalized seizures:
Start in one limited area of the brain
Can also spread throughout the brain becoming
generalized
Convulsive phase of these seizures usually lasts no
more than a few minutes
Preceding partial seizure is usually not very long
Happen when a burst of electrical activity in a
limited area (the partial seizure) spreads
throughout the brain
Seizures occur in more than 30% of people with
partial epilepsy
24.
25. Common Symptoms
Change in consciousness, so that you can't
remember some period of time
Change in emotion, like unexplainable fear, panic,
joy, or laughter
Change in sensation of the skin, usually spreading
over the arm, leg, or trunk
Changes in vision, including flashing lights, or
(rarely) hallucinations (seeing things that aren't
there)
Loss of muscle control and falling, often very
suddenly
26. Muscle movement such as twitching that might
spread up an arm or leg
Muscle movement such as twitching that might
spread up an arm or leg
Muscle tension/tightening that causes twisting of
the body, head, arms or leg
Tasting a bitter or metallic flavor
27. Stages
Beginning State:
This stage can be said as warning or aura
Sometimes an individual may not be aware of
such aura
In middle stage this aura is followed by other
symptoms
It may be considered as simple partial seizure
28. Middle State:
People have aura in beginning, the aura may
convert into convulsion
For those who don’t have aura, the seizure may
continue as complex partial seizure
29. End state:
This state represents a transition from seizure
back to normal state
Also referred as the “Post-ictal period”
Signifies recovery period of brain
May last from a second to minutes to hours
If a person has a convulsion, the level of
awareness gradually improves during the post-
ictal period, much like a person waking up from
anesthesia after an operation
30. Early Seizure Symptoms
Sensory/ thoughts
Smell
Sound
Taste
Visual loss or blurring
Racing thoughts
Strange feelings
Stomach feelings
Tingling feelings
Physical
Dizziness
Headache
Nausea
Numbness
No Warnings
Some times seizures come
with no feelings
Emotional
Fear/ panic
Pleasant feelings
31. Middle Seizure Symptoms
Sensory/ thoughts
Black out
Confusion
Deafness / sound
Electric shock feelings
LOC
Smell
Spacing out
Visual loss or blurring
Physical
Chewing movements
Convulsions
Eye rolling up
Falling down
Foot stomping
Inability to move
Emotional
Fear/ panic
32. Causes
Metabolic disorders
Hing fever
Brain infections
Inadequate oxygen supply to the brain
Structural damage to the brain
Abnormalities present or occurring at birth
Fluid accumulation in the brain