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Classification of sleep disorders and parasomniasEnoch R G
Sleep is made up of two physiological states: non-rapid eye movement (NREM) sleep and rapid eye movement (REM) sleep. There are several brain regions and neurotransmitters that regulate the sleep-wake cycle, including serotonin, norepinephrine, acetylcholine, melatonin, and dopamine. Sleep disorders are classified in the DSM-5 and ICSD-2 and include insomnia, sleep-related breathing disorders, hypersomnias, circadian rhythm sleep-wake disorders, parasomnias, and other sleep-related movement disorders.
Approach to temporal lobe anatomy,function,epilepsy MRI findingDr Surendra Khosya
A 40-year-old lawyer experienced seizures and was found to have a left temporal lobe tumor. After the tumor was removed, he had word-finding difficulties but was able to return to work. The temporal lobe is located at the side of the head and is involved in functions like auditory and visual processing, memory, emotion, and language. It contains areas important for these functions and connects to other brain regions. Disorders of the temporal lobe can cause issues with perception, attention, memory, personality, and behavior.
A 52-year-old woman suffered a subarachnoid hemorrhage that caused ischemia in the right parietal and frontal lobes. She developed non-fluent aphasia characterized by reduced speech, word-finding difficulties, and paraphasias. Testing revealed crossed Wernicke's aphasia. Her language deficits gradually improved as her cerebral blood flow returned to normal levels with treatment. The document then discusses approaches to evaluating language and speech disorders like aphasia, including classification systems, assessment tools, and the clinical features of different aphasia subtypes and related conditions.
This document discusses the anatomy, functions, and clinical presentations of lesions involving the frontal lobe, including the motor cortex, prefrontal cortex, and their roles in executive function, social behavior, language, and more. Specific tests are described to evaluate functions like motor control, language, problem-solving, and emotional regulation that are mediated by the frontal lobe. A variety of clinical syndromes can result from frontal lobe lesions depending on the location and extent of the damage.
The document discusses parasomnias, which are abnormal behaviors or movements that occur during sleep or sleep transitions. It describes the different stages of sleep based on EEG patterns. It then discusses various parasomnias like sleepwalking, sleep terrors, confusional arousals, REM sleep behavior disorder, nightmares, and sleep paralysis. It provides details on characteristics, typical age of onset, precipitating factors, treatment options. It also discusses disorders like sleep talking, catathrenia, hypnic jerks, and excessive fragmentary myoclonus that are common and clinically insignificant. The document outlines investigations like polysomnography and neurological imaging that can help evaluate parasomnias.
EEG is a non-invasive method to measure electrical activity in the brain. It can help in psychiatry by ruling out physical causes for psychiatric symptoms, aiding in differential diagnosis and treatment selection, and predicting prognosis. EEG findings can provide clues to underlying conditions in disorders like schizophrenia, mood disorders, OCD, panic attacks, dementia, delirium, and substance abuse. However, EEG findings in psychiatry are often nonspecific and EEG has limitations due to only recording cortical activity from the scalp. It currently has no definitive role in diagnosing Axis I or II psychiatric disorders.
The document discusses auditory brainstem response (ABR) testing, which is used to evaluate hearing in newborns. ABR testing uses electrodes to measure electrical activity in the brainstem in response to auditory clicks or tones. It is an effective screening tool for detecting hearing loss, with a high sensitivity and specificity. ABR testing can identify abnormalities in the auditory nerve or brainstem that may indicate conditions like acoustic neuromas. It provides objective information about hearing thresholds and neural conduction in the auditory pathway.
This document discusses sleep, sleep disorders, and their diagnosis and treatment. It covers:
- The stages and functions of normal sleep
- Tools used in sleep medicine like polysomnography
- Common sleep disorders like insomnia, hypersomnia, narcolepsy, sleep apnea
- Treatment approaches including behavioral therapies, pharmacological options, and management of specific disorders.
Classification of sleep disorders and parasomniasEnoch R G
Sleep is made up of two physiological states: non-rapid eye movement (NREM) sleep and rapid eye movement (REM) sleep. There are several brain regions and neurotransmitters that regulate the sleep-wake cycle, including serotonin, norepinephrine, acetylcholine, melatonin, and dopamine. Sleep disorders are classified in the DSM-5 and ICSD-2 and include insomnia, sleep-related breathing disorders, hypersomnias, circadian rhythm sleep-wake disorders, parasomnias, and other sleep-related movement disorders.
Approach to temporal lobe anatomy,function,epilepsy MRI findingDr Surendra Khosya
A 40-year-old lawyer experienced seizures and was found to have a left temporal lobe tumor. After the tumor was removed, he had word-finding difficulties but was able to return to work. The temporal lobe is located at the side of the head and is involved in functions like auditory and visual processing, memory, emotion, and language. It contains areas important for these functions and connects to other brain regions. Disorders of the temporal lobe can cause issues with perception, attention, memory, personality, and behavior.
A 52-year-old woman suffered a subarachnoid hemorrhage that caused ischemia in the right parietal and frontal lobes. She developed non-fluent aphasia characterized by reduced speech, word-finding difficulties, and paraphasias. Testing revealed crossed Wernicke's aphasia. Her language deficits gradually improved as her cerebral blood flow returned to normal levels with treatment. The document then discusses approaches to evaluating language and speech disorders like aphasia, including classification systems, assessment tools, and the clinical features of different aphasia subtypes and related conditions.
This document discusses the anatomy, functions, and clinical presentations of lesions involving the frontal lobe, including the motor cortex, prefrontal cortex, and their roles in executive function, social behavior, language, and more. Specific tests are described to evaluate functions like motor control, language, problem-solving, and emotional regulation that are mediated by the frontal lobe. A variety of clinical syndromes can result from frontal lobe lesions depending on the location and extent of the damage.
The document discusses parasomnias, which are abnormal behaviors or movements that occur during sleep or sleep transitions. It describes the different stages of sleep based on EEG patterns. It then discusses various parasomnias like sleepwalking, sleep terrors, confusional arousals, REM sleep behavior disorder, nightmares, and sleep paralysis. It provides details on characteristics, typical age of onset, precipitating factors, treatment options. It also discusses disorders like sleep talking, catathrenia, hypnic jerks, and excessive fragmentary myoclonus that are common and clinically insignificant. The document outlines investigations like polysomnography and neurological imaging that can help evaluate parasomnias.
EEG is a non-invasive method to measure electrical activity in the brain. It can help in psychiatry by ruling out physical causes for psychiatric symptoms, aiding in differential diagnosis and treatment selection, and predicting prognosis. EEG findings can provide clues to underlying conditions in disorders like schizophrenia, mood disorders, OCD, panic attacks, dementia, delirium, and substance abuse. However, EEG findings in psychiatry are often nonspecific and EEG has limitations due to only recording cortical activity from the scalp. It currently has no definitive role in diagnosing Axis I or II psychiatric disorders.
The document discusses auditory brainstem response (ABR) testing, which is used to evaluate hearing in newborns. ABR testing uses electrodes to measure electrical activity in the brainstem in response to auditory clicks or tones. It is an effective screening tool for detecting hearing loss, with a high sensitivity and specificity. ABR testing can identify abnormalities in the auditory nerve or brainstem that may indicate conditions like acoustic neuromas. It provides objective information about hearing thresholds and neural conduction in the auditory pathway.
This document discusses sleep, sleep disorders, and their diagnosis and treatment. It covers:
- The stages and functions of normal sleep
- Tools used in sleep medicine like polysomnography
- Common sleep disorders like insomnia, hypersomnia, narcolepsy, sleep apnea
- Treatment approaches including behavioral therapies, pharmacological options, and management of specific disorders.
The QEEG is a non-invasive brain imaging procedure that measures brain wave activity through electrodes placed on the scalp. Brain waves are recorded both at rest and during tasks to analyze characteristics like frequency, amplitude, and distribution. These characteristics are then compared to a normal database to evaluate metrics like relative power, asymmetry, coherence, and phase which provide information about brain performance and efficiency. The QEEG can be used to assess conditions like traumatic brain injury, learning disabilities, and neurological or psychological disorders.
This document defines hypnosis and provides an overview of its history, techniques, and applications. Hypnosis is described as an altered state of consciousness where people become deeply relaxed and highly suggestible. The history outlines early pioneers like Braid who coined the term and Mesmer who used magnetic forces. Characteristics include suggestibility, dissociation, enhanced memory, and posthypnotic suggestion. Applications include using hypnosis for pain control, treatment of issues like smoking, and controlling undesired behaviors or symptoms. The document aims to educate about hypnosis while dispelling common misconceptions.
The document discusses traumatic brain injury (TBI) and its relationship to domestic violence. It notes that every 23 seconds someone in the US sustains a TBI, and over 90% of domestic violence injuries occur to the head, face or neck. Living with TBI can make it difficult for abused women to safely leave their partners or care for themselves and their families. The document outlines common cognitive, physical and psychosocial effects of TBI and resources for treatment and support.
The temporal lobe is involved in several important functions:
1) It processes auditory and visual information through distinct cortical areas.
2) The medial temporal lobe structures including the hippocampus and amygdala are critical for forming memories and regulating emotions.
3) Disorders of the temporal lobe can cause problems with memory, language processing, perception and personality changes depending on the area affected.
The document provides an overview of neuroimaging techniques used in psychiatry such as MRI, CT, PET, SPECT, fMRI, DTI, and MRS. It discusses the basic principles, milestones in development, and applications of these techniques. Specifically, it summarizes research using these neuroimaging methods that have found abnormalities in brain structure and function in patients with obsessive-compulsive disorder (OCD), such as reduced serotonin transporter binding in fronto-striatal circuits and differences in brain activity in regions like the thalamus and orbitofrontal cortex.
The temporal lobe is involved in processing sensory input, memory formation, language comprehension, and emotional processing. It contains structures like the hippocampus and amygdala that are important for memory and emotional associations. Disorders of the temporal lobe can cause problems like epilepsy, memory deficits, language issues like aphasia, and behavioral changes. Temporal lobe epilepsy is a common type of seizure originating in structures of the anteromedial temporal lobe. Bilateral damage to the amygdala and inferior temporal cortex can cause Klüver-Bucy syndrome characterized by changes in behavior and cognition. The temporal lobe also plays a key role in conditions like Alzheimer's disease, frontotemporal dementia, and traumatic brain injury.
Narcolepsy is a sleeping disorder characterized by excessive daytime sleepiness and frequent sleep attacks. Symptoms include cataplexy (loss of muscle control triggered by emotions), sleep paralysis, microsleep (brief sleep episodes with no memory), nighttime wakefulness, and hallucinations when falling asleep or waking up. There is no cure for narcolepsy, but treatment aims to control symptoms through lifestyle changes like scheduled naps and light meals, as well as prescription medications to promote wakefulness. Narcolepsy can develop at any age but often first appears in teenagers and young adults.
Epileptic encephalopathies are a group of heterogeneous brain disorders occurring during brain development that cause frequent abnormal EEG activity leading to cognitive and motor regression. West syndrome presents as infantile spasms, developmental arrest, and the hypsarrhythmia EEG pattern. Lennox-Gastaut syndrome presents between 1-7 years with multiple seizure types and cognitive impairment. Dravet syndrome presents before 1 year with early febrile seizures and later myoclonic seizures. Landau-Kleffner syndrome presents between 2-8 years with acquired aphasia. Panayiotopoulos syndrome presents between 1-14 years with autonomic seizures during sleep. Epilepsy with myoclonic-
1. The document describes several benign pediatric epileptic syndromes including benign familial neonatal seizures, benign idiopathic neonatal seizures, benign infantile seizures, childhood absence epilepsy, benign epilepsy of childhood with centrotemporal spikes, and idiopathic childhood occipital epilepsy of Gastaut.
2. Key features of these syndromes are provided such as typical age of onset, seizure semiology, EEG patterns, treatment approaches, and prognosis. Genetic mutations associated with some of these syndromes are also mentioned.
3. Distinguishing features between benign familial neonatal convulsions and benign idiopathic neonatal convulsions are outlined as well as diagnostic criteria and exclusion criteria for childhood absence
Temporal lobe epilepsy is characterized by seizures originating in the temporal lobe. It is the most common localization-related epilepsy, accounting for around 60% of such cases. Mesial temporal lobe epilepsy is the most frequent form, often caused by hippocampal sclerosis. Auras are common and can include epigastric sensations, cephalic sensations, anxiety, hallucinations and more. Automatisms like lip smacking or gesturing often occur during seizures. Around 60% of temporal lobe epilepsy patients respond well to antiepileptic drug treatment, while the remaining 40% have drug-resistant epilepsy and may require surgery.
Amotivational syndrome is a psychiatric disorder characterized by a lack of motivation and reduced cognitive functioning. It was first described in the 1960s among long-term cannabis users. Chronic use of psychoactive substances like cannabis, cocaine, and medications like SSRIs can potentially cause changes in the brain's frontal lobe and serotonin/dopamine activity linked to symptoms of amotivational syndrome. These include reduced energy, passivity, introversion, apathy, poor concentration, and decreased desire for social interaction and work. Treatment involves medication to address neurological imbalances, counseling, lifestyle changes, and abstaining from psychoactive substance use. With treatment and abstinence, symptoms are potentially reversible within months.
neuromyelitis optica spectrum disorder Dr. Musa AtarzadehMusa Atazadeh
1. The document discusses the diagnosis and diagnostic criteria for Neuromyelitis Optica Spectrum Disorder (NMOSD) according to the 2015 AAN criteria.
2. The diagnosis involves assessing for core clinical characteristics, compatible neuroimaging findings, and testing for AQP4-IgG antibodies.
3. Certain clinical presentations and neuroimaging patterns can raise red flags and suggest alternative diagnoses rather than NMOSD. Repeating AQP4-IgG testing over time or in the CSF may also be considered in some cases.
The document summarizes EEG patterns seen in various encephalopathies. It describes diffuse slowing, triphasic waves, burst suppression, periodic epileptiform discharges (PLEDs, BIPLEDs, GPEDs), alpha coma, spindle coma and beta coma patterns. Specific patterns are seen in hepatic encephalopathy, uremia, Hashimoto's encephalopathy, NMDAR encephalitis, Creutzfeldt-Jakob disease, subacute sclerosing panencephalitis. Criteria for periodic discharges and electrocerebral inactivity seen in brain death are also outlined.
Lennox-Gastaut syndrome is a severe childhood epilepsy syndrome characterized by multiple seizure types, cognitive impairment, and a specific EEG pattern of slow spike-and-wave discharges. It commonly causes seizures, especially during sleep, and is associated with high mortality. Polysomnography can identify comorbid sleep disorders like sleep apnea and assess seizure activity during sleep. Treatment involves antiepileptic drugs and management of sleep issues and comorbidities.
Neurobiology of sleep_disorders_lattova(5280ab0cb6099)Hena Jawaid
This document provides an overview of neurobiology of sleep and sleep disorders. It defines normal sleep, describes the circadian rhythm and two-process model that regulate sleep-wake cycles. It outlines the reticular activating system and flip-flop switch that control transitions between wake and sleep states. Non-REM and REM sleep are characterized based on EEG patterns. Polysomnography and other tools for measuring sleep are discussed. Common sleep disorders like insomnia are introduced.
Transcranial magnetic stimulation (TMS) is a noninvasive procedure that uses magnetic fields to stimulate nerve cells in the brain and has shown positive results in treating depression. Repetitive transcranial magnetic stimulation (rTMS) involves placing an electromagnet against the patient's head to deliver magnetic bursts and stimulate the brain region involved in mood control. rTMS has evolved as a tool for improving various neurological and psychiatric disorders beyond just depression.
The document discusses the control of gaze and eye movements through six neuronal control systems that keep the fovea on target. These include systems for saccadic, pursuit, and vergence eye movements, as well as vestibulo-ocular and optokinetic movements. It describes the neural pathways and brain structures involved in generating different types of eye movements like saccades, smooth pursuit, and vestibular-ocular reflexes. It also discusses how lesions in different parts of the brain can affect eye movement control and coordination.
The document discusses executive functions and provides definitions from various studies. It describes executive functions as a set of cognitive processes that regulate other cognitive processes such as planning, working memory, attention, problem solving and inhibition. Executive functions are controlled by the frontal lobes of the brain and are responsible for self-regulation and goal-directed behavior. The document summarizes several models of executive functions including models by Norman and Shallice, Barkley, Lezak and others. It discusses areas executive functions are involved in and factors that influence executive functions. Common disorders associated with executive dysfunction are also listed.
Supranuclear disorders of ocular motilitySSSIHMS-PG
This document summarizes various disorders of ocular motility involving the supranuclear and internuclear pathways. It describes the different types of eye movements and their neural pathways/control centers in the brainstem. Key supranuclear disorders discussed include saccadic palsy, slowing of saccades in conditions like progressive supranuclear palsy, unwanted saccades like square wave jerks. Internuclear disorders summarized are internuclear ophthalmoplegia and skew deviation. Clinical features and localization of various vertical gaze palsies are also outlined.
The document discusses the anatomy and physiology of the consciousness system in the brain. It describes how the ascending reticular activating system (ARAS) originating in the brainstem projects to the thalamus and cortex, enabling conscious awareness. Damage to either the ARAS or diffuse bilateral cortical regions can cause coma. The document outlines how coma is evaluated by assessing respiratory patterns, pupil reaction, motor response and other signs. Potential causes of coma include supratentorial mass lesions, infratentorial lesions, metabolic disturbances and others.
The QEEG is a non-invasive brain imaging procedure that measures brain wave activity through electrodes placed on the scalp. Brain waves are recorded both at rest and during tasks to analyze characteristics like frequency, amplitude, and distribution. These characteristics are then compared to a normal database to evaluate metrics like relative power, asymmetry, coherence, and phase which provide information about brain performance and efficiency. The QEEG can be used to assess conditions like traumatic brain injury, learning disabilities, and neurological or psychological disorders.
This document defines hypnosis and provides an overview of its history, techniques, and applications. Hypnosis is described as an altered state of consciousness where people become deeply relaxed and highly suggestible. The history outlines early pioneers like Braid who coined the term and Mesmer who used magnetic forces. Characteristics include suggestibility, dissociation, enhanced memory, and posthypnotic suggestion. Applications include using hypnosis for pain control, treatment of issues like smoking, and controlling undesired behaviors or symptoms. The document aims to educate about hypnosis while dispelling common misconceptions.
The document discusses traumatic brain injury (TBI) and its relationship to domestic violence. It notes that every 23 seconds someone in the US sustains a TBI, and over 90% of domestic violence injuries occur to the head, face or neck. Living with TBI can make it difficult for abused women to safely leave their partners or care for themselves and their families. The document outlines common cognitive, physical and psychosocial effects of TBI and resources for treatment and support.
The temporal lobe is involved in several important functions:
1) It processes auditory and visual information through distinct cortical areas.
2) The medial temporal lobe structures including the hippocampus and amygdala are critical for forming memories and regulating emotions.
3) Disorders of the temporal lobe can cause problems with memory, language processing, perception and personality changes depending on the area affected.
The document provides an overview of neuroimaging techniques used in psychiatry such as MRI, CT, PET, SPECT, fMRI, DTI, and MRS. It discusses the basic principles, milestones in development, and applications of these techniques. Specifically, it summarizes research using these neuroimaging methods that have found abnormalities in brain structure and function in patients with obsessive-compulsive disorder (OCD), such as reduced serotonin transporter binding in fronto-striatal circuits and differences in brain activity in regions like the thalamus and orbitofrontal cortex.
The temporal lobe is involved in processing sensory input, memory formation, language comprehension, and emotional processing. It contains structures like the hippocampus and amygdala that are important for memory and emotional associations. Disorders of the temporal lobe can cause problems like epilepsy, memory deficits, language issues like aphasia, and behavioral changes. Temporal lobe epilepsy is a common type of seizure originating in structures of the anteromedial temporal lobe. Bilateral damage to the amygdala and inferior temporal cortex can cause Klüver-Bucy syndrome characterized by changes in behavior and cognition. The temporal lobe also plays a key role in conditions like Alzheimer's disease, frontotemporal dementia, and traumatic brain injury.
Narcolepsy is a sleeping disorder characterized by excessive daytime sleepiness and frequent sleep attacks. Symptoms include cataplexy (loss of muscle control triggered by emotions), sleep paralysis, microsleep (brief sleep episodes with no memory), nighttime wakefulness, and hallucinations when falling asleep or waking up. There is no cure for narcolepsy, but treatment aims to control symptoms through lifestyle changes like scheduled naps and light meals, as well as prescription medications to promote wakefulness. Narcolepsy can develop at any age but often first appears in teenagers and young adults.
Epileptic encephalopathies are a group of heterogeneous brain disorders occurring during brain development that cause frequent abnormal EEG activity leading to cognitive and motor regression. West syndrome presents as infantile spasms, developmental arrest, and the hypsarrhythmia EEG pattern. Lennox-Gastaut syndrome presents between 1-7 years with multiple seizure types and cognitive impairment. Dravet syndrome presents before 1 year with early febrile seizures and later myoclonic seizures. Landau-Kleffner syndrome presents between 2-8 years with acquired aphasia. Panayiotopoulos syndrome presents between 1-14 years with autonomic seizures during sleep. Epilepsy with myoclonic-
1. The document describes several benign pediatric epileptic syndromes including benign familial neonatal seizures, benign idiopathic neonatal seizures, benign infantile seizures, childhood absence epilepsy, benign epilepsy of childhood with centrotemporal spikes, and idiopathic childhood occipital epilepsy of Gastaut.
2. Key features of these syndromes are provided such as typical age of onset, seizure semiology, EEG patterns, treatment approaches, and prognosis. Genetic mutations associated with some of these syndromes are also mentioned.
3. Distinguishing features between benign familial neonatal convulsions and benign idiopathic neonatal convulsions are outlined as well as diagnostic criteria and exclusion criteria for childhood absence
Temporal lobe epilepsy is characterized by seizures originating in the temporal lobe. It is the most common localization-related epilepsy, accounting for around 60% of such cases. Mesial temporal lobe epilepsy is the most frequent form, often caused by hippocampal sclerosis. Auras are common and can include epigastric sensations, cephalic sensations, anxiety, hallucinations and more. Automatisms like lip smacking or gesturing often occur during seizures. Around 60% of temporal lobe epilepsy patients respond well to antiepileptic drug treatment, while the remaining 40% have drug-resistant epilepsy and may require surgery.
Amotivational syndrome is a psychiatric disorder characterized by a lack of motivation and reduced cognitive functioning. It was first described in the 1960s among long-term cannabis users. Chronic use of psychoactive substances like cannabis, cocaine, and medications like SSRIs can potentially cause changes in the brain's frontal lobe and serotonin/dopamine activity linked to symptoms of amotivational syndrome. These include reduced energy, passivity, introversion, apathy, poor concentration, and decreased desire for social interaction and work. Treatment involves medication to address neurological imbalances, counseling, lifestyle changes, and abstaining from psychoactive substance use. With treatment and abstinence, symptoms are potentially reversible within months.
neuromyelitis optica spectrum disorder Dr. Musa AtarzadehMusa Atazadeh
1. The document discusses the diagnosis and diagnostic criteria for Neuromyelitis Optica Spectrum Disorder (NMOSD) according to the 2015 AAN criteria.
2. The diagnosis involves assessing for core clinical characteristics, compatible neuroimaging findings, and testing for AQP4-IgG antibodies.
3. Certain clinical presentations and neuroimaging patterns can raise red flags and suggest alternative diagnoses rather than NMOSD. Repeating AQP4-IgG testing over time or in the CSF may also be considered in some cases.
The document summarizes EEG patterns seen in various encephalopathies. It describes diffuse slowing, triphasic waves, burst suppression, periodic epileptiform discharges (PLEDs, BIPLEDs, GPEDs), alpha coma, spindle coma and beta coma patterns. Specific patterns are seen in hepatic encephalopathy, uremia, Hashimoto's encephalopathy, NMDAR encephalitis, Creutzfeldt-Jakob disease, subacute sclerosing panencephalitis. Criteria for periodic discharges and electrocerebral inactivity seen in brain death are also outlined.
Lennox-Gastaut syndrome is a severe childhood epilepsy syndrome characterized by multiple seizure types, cognitive impairment, and a specific EEG pattern of slow spike-and-wave discharges. It commonly causes seizures, especially during sleep, and is associated with high mortality. Polysomnography can identify comorbid sleep disorders like sleep apnea and assess seizure activity during sleep. Treatment involves antiepileptic drugs and management of sleep issues and comorbidities.
Neurobiology of sleep_disorders_lattova(5280ab0cb6099)Hena Jawaid
This document provides an overview of neurobiology of sleep and sleep disorders. It defines normal sleep, describes the circadian rhythm and two-process model that regulate sleep-wake cycles. It outlines the reticular activating system and flip-flop switch that control transitions between wake and sleep states. Non-REM and REM sleep are characterized based on EEG patterns. Polysomnography and other tools for measuring sleep are discussed. Common sleep disorders like insomnia are introduced.
Transcranial magnetic stimulation (TMS) is a noninvasive procedure that uses magnetic fields to stimulate nerve cells in the brain and has shown positive results in treating depression. Repetitive transcranial magnetic stimulation (rTMS) involves placing an electromagnet against the patient's head to deliver magnetic bursts and stimulate the brain region involved in mood control. rTMS has evolved as a tool for improving various neurological and psychiatric disorders beyond just depression.
The document discusses the control of gaze and eye movements through six neuronal control systems that keep the fovea on target. These include systems for saccadic, pursuit, and vergence eye movements, as well as vestibulo-ocular and optokinetic movements. It describes the neural pathways and brain structures involved in generating different types of eye movements like saccades, smooth pursuit, and vestibular-ocular reflexes. It also discusses how lesions in different parts of the brain can affect eye movement control and coordination.
The document discusses executive functions and provides definitions from various studies. It describes executive functions as a set of cognitive processes that regulate other cognitive processes such as planning, working memory, attention, problem solving and inhibition. Executive functions are controlled by the frontal lobes of the brain and are responsible for self-regulation and goal-directed behavior. The document summarizes several models of executive functions including models by Norman and Shallice, Barkley, Lezak and others. It discusses areas executive functions are involved in and factors that influence executive functions. Common disorders associated with executive dysfunction are also listed.
Supranuclear disorders of ocular motilitySSSIHMS-PG
This document summarizes various disorders of ocular motility involving the supranuclear and internuclear pathways. It describes the different types of eye movements and their neural pathways/control centers in the brainstem. Key supranuclear disorders discussed include saccadic palsy, slowing of saccades in conditions like progressive supranuclear palsy, unwanted saccades like square wave jerks. Internuclear disorders summarized are internuclear ophthalmoplegia and skew deviation. Clinical features and localization of various vertical gaze palsies are also outlined.
The document discusses the anatomy and physiology of the consciousness system in the brain. It describes how the ascending reticular activating system (ARAS) originating in the brainstem projects to the thalamus and cortex, enabling conscious awareness. Damage to either the ARAS or diffuse bilateral cortical regions can cause coma. The document outlines how coma is evaluated by assessing respiratory patterns, pupil reaction, motor response and other signs. Potential causes of coma include supratentorial mass lesions, infratentorial lesions, metabolic disturbances and others.
Session 10_ Performing Central Nervous System Examination.pptRamadhaniKitwana3
This document provides guidance on examining the central nervous system. It outlines common neurological complaints, guidelines for examination, and techniques for assessing different parts of the nervous system including mental status, cranial nerves, motor skills, reflexes, and sensation. The examination is designed to be comprehensive yet efficient, following a logical sequence and utilizing basic tests like strength, coordination, reflexes, and sensory response to identify potential nervous system abnormalities.
The document provides statistics and information about different types of headaches. Some key points:
- Migraines are the 7th highest cause of disability worldwide and are highly debilitating. Over half of migraine sufferers have at least one attack per month.
- Tension headaches and migraines are among the most common health conditions globally. Nearly 5.2 million emergency room visits in the US each year are due to headaches.
- Headaches can have various causes like migraines, tension, cluster, sinus, or cervical issues. Migraines involve intense pulsing pain often on one side of the head plus nausea and sensitivity to light and sound.
- Poor posture from technology use
This document provides an overview of peripheral vestibular disorders (PVDs). It defines PVDs as pathologies of the inner ear vestibular structures and vestibular nerve that diminish sensory information about head movement. The peripheral vestibular system is described, including the semi-circular canals, otolith organs, and vestibular nerve. Clinical classifications, etiologies, pathophysiology, diagnosis, and treatment approaches for various PVDs are discussed at a high level. Diagnostic tests include electronystagmography and imaging, while treatment may involve vestibular suppressants, rehabilitation exercises, or ablative procedures depending on the specific disorder.
This document provides information about strabismus (squinting):
- It affects 7.5 million people in the US and an estimated 130-260 million worldwide. Strabismus occurs when the eyes are not properly aligned on the point of focus.
- The anatomy of the extraocular muscles that control eye movement is described, including the actions of the six muscles and their nerve supply.
- Paralytic squints can be caused by neurogenic or myogenic factors. The document discusses third and fourth nerve palsies as examples. Treatment options for strabismus include optical devices, botulinum toxin injections, orthoptic exercises, and surgery.
1. The neurological history and examination are the most important parts of the evaluation. The history should be comprehensive and determine the progression of symptoms over time.
2. The examination includes assessing mental status, cranial nerves, motor function, reflexes, sensation, coordination and gait. Abnormalities in these areas can provide clues to the underlying neurological condition.
3. Key aspects of the history include the present illness, past medical history, drug history, family history, and social history to identify risk factors and hereditary conditions.
This document discusses congenital nystagmus, including its pathophysiology, classification, evaluation, and treatment. There are three main mechanisms that help maintain clear vision: ocular fixation, the vestibulo-ocular reflex, and the central nervous system. Nystagmus is classified based on characteristics like direction, amplitude, frequency, and whether it is conjugate or disjunctive. Evaluation involves assessing visual acuity, eye movements, and neuroimaging in some cases. Treatment may include optical corrections, medications, botulinum toxin injections, or strabismus surgery to modify eye position and reduce nystagmus intensity.
Dr. Reshma's presentation covered the clinical evaluation of squint, including taking a thorough patient history, assessing visual acuity and refraction under cycloplegia, and evaluating motor and sensory status. Key parts of the evaluation include measuring any ocular deviation using cover tests, evaluating versions and vergences, and testing binocular vision functions like suppression and stereopsis. A thorough exam is important for establishing the cause of strabismus and diagnosing amblyopia or other issues.
Supranuclear disorders of ocular motilityerameshita
This document discusses supranuclear disorders of ocular motility. It begins by outlining the hierarchy of ocular motor control, with the cerebral cortex, cerebellum, and basal ganglia at the highest level 1. Level 2 includes brainstem nuclei and cranial nerve nuclei, and level 3 includes the ocular motor nerves and extraocular muscles. The document then discusses various types of eye movements including fast eye movements like saccades, as well as gaze palsies and vertical gaze palsies. It also covers disorders like internuclear ophthalmoplegia, one-and-a-half syndrome, the ocular tilt reaction, and disorders of pursuit movements and optokinetic nystagmus
This document provides information about infantile esotropia, including its definition, clinical features, etiology, differential diagnosis, and management. Infantile esotropia is defined as a large-angle esotropia present before 6 months of age. It is the most common form of strabismus. Clinical features include alternating or crossed fixation, apparent limitation of abduction, and associated motor abnormalities like inferior oblique overaction and dissociated vertical deviation. Treatment involves correcting refractive errors, amblyopia therapy, observation for small angles, and early surgical correction typically between 6 months to 2 years of age.
This document provides an overview of vestibular function tests. It discusses the six semicircular canal planes and their roles in detecting head rotation and translation. It describes eye movements like saccades, smooth pursuit, and vestibulo-ocular reflex that stabilize vision. Common vestibular tests are discussed like head thrust, head shaking, and dynamic visual acuity. Features of nystagmus seen with peripheral and central lesions are summarized. A history should inquire about triggers, associated symptoms, and risk factors to localize the cause of dizziness.
This document provides an overview of ocular motility disorders, including:
1. The anatomy and function of the extraocular muscles and neural control centers.
2. Classification of abnormal eye movements including types (e.g. saccades, smooth pursuit) and causes (e.g. myopathies, nerve palsies).
3. Specific disorders are described in detail such as internuclear ophthalmoplegia, Parinaud's syndrome, and progressive supranuclear palsy.
4. Nystagmus is classified and mechanisms are discussed.
This document provides an overview of neuro-ophthalmology and discusses various topics including vision loss, visual field defects, diplopia, supranuclear ocular motility disorders, and abnormal eye movements. It defines neuro-ophthalmology as diseases of the eye and related neurological structures. It describes the anatomy and pathways involved in various eye movements like saccades, smooth pursuit, and vestibulo-ocular reflex. It also discusses lesions that can cause abnormalities in these eye movements.
The nervous system has several key functions including sensation, perception, proprioception, motor control, integration of sensory information, sleep, learning, memory, and plasticity. Sensory receptors detect changes and stimuli which are transmitted as nerve impulses to the central nervous system. The motor system then coordinates muscle movements through upper and lower motor neurons. Integration involves processing sensory information to make decisions and engage in complex behaviors and states like arousal, learning, memory and sleep.
This document discusses three key mechanisms involved in maintaining foveal centration of an object of interest: fixation, the vestibulo-ocular reflex, and the neural integrator. Fixation involves the visual system detecting drift and signaling a corrective eye movement. The vestibulo-ocular reflex maintains foveation during head movements through neural connections between the vestibular system and oculomotor system. The neural integrator, which includes the cerebellum and oculomotor nuclei, generates signals to avoid backward drift and maintains constant innervation of the extraocular muscles. Deficits in the neural integrator can cause gaze-evoked nystagmus and oscillopsia.
This document discusses primary glaucoma, including primary open angle glaucoma. It defines primary glaucoma as optic neuropathy with characteristic changes to the optic disc and visual field, mostly associated with increased intraocular pressure. It describes the classification, epidemiology, physiology, clinical manifestations, diagnosis and management of primary open angle glaucoma. It also discusses ocular hypertension and defines it as increased intraocular pressure without optic disc or visual field changes, noting those with high risk factors should be carefully monitored.
The document provides an overview of approaches to diagnosing and classifying ataxia. It begins by defining ataxia and discussing tests to differentiate various causes, including cerebellar ataxia, sensory ataxia, cortical ataxia, labyrinthine ataxia, and others. It then discusses the approach to cerebellar ataxia in adults, including considering mode of onset, progression, focal/symmetric involvement, and localizing the lesion. Acquired causes like infection, autoimmune, nutritional deficiencies and more are discussed. Inherited ataxias like autosomal dominant SCA types 1-3 and others are also summarized.
This document summarizes a lecture on attention. It discusses the different types of attention, including alertness, vigilance, and selective attention. It also describes the neurophysiology of attention, including the roles of the reticular activating system, superior colliculus, thalamus, parietal lobe, frontal lobe, and cingulate cortex. Additionally, it covers the topic of neglect, or hemineglect, including its clinical features, sensory-representational, motor-exploratory, and motivational aspects. It concludes with a discussion of the right hemisphere's dominance for spatial attention.
این پاورپوینت در اولین کارگاه از سیر تا پیاز اوتیسم توسط دکتر هاشم فرهنگ دوست ارائه شده است.
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این پاورپوینت در کارگاه توانبخشی هوش دکتر میثم محمدی ارائه شده است. برای مشاهده فایلهای بیشتر در این زمینه، به وب سایت فروردین مراجعه کنید.
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این پاورپوینت در کارگاه توانبخشی هوش دکتر محمدی ارائه شده است.
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این پاورپوینت در کارگاه توانبخشی هوش توسط دکتر میثم محمدی ارائه شده است. برای مطالعه مطالب بیشتر در این زمینه به وب سایت فروردین مراجعه کنید.
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این پاورپوینت در کارگاه رویکرد ادراکی حرکتی در کودکان مبتلا به فلج مغزی توسط دکتر ابراهیم پیشیاره ارائه شده است.
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این پاورپوینت در کارگاه رویکرد ادراکی حرکتی در کودکان مبتلا به فلج مغزی توسط دکتر پیشیاره ارائه شده است. برای مشاهده مطالب بیشتر در این زمینه به وب سایت فروردین مراجعه نمایید.
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این پاورپوینت در کارگاه ارزیابی و توانبخشی مشکلات راه رفتن در کودکان فلج مغزی توسط دکتر محمد خیاط زاده ارائه شده است.
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این پاورپوینت در کارگاه ارزیابی و توانبخشی مشکلات راه رفتن در کودکان مبتلا به فلج مغزی توسط دکتر محمد خیاط زاده ارائه شده است.
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این پاورپوینت توسط دکتر محمد خیاط زاده در کارگاه ارزیابی و توانبخشی مشکلات راه رفتن در کودکان مبتلا به فلج مغزی ارائه شده است.
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This document summarizes gait abnormalities in children with cerebral palsy. It begins by defining cerebral palsy and describing the three main types: spastic, dyskinetic, and ataxic. For each type, it outlines the characteristic neuromuscular deficits that affect gait. It then describes normal gait cycle and determinants. Key factors that influence gait in CP are weaknesses, shortened muscles, spasticity, and bone deformities from altered forces. Gait abnormalities range from mild toe-walking to severe crouched gait. Prognosis for walking depends on CP type, severity, and age of independent walking. Over time, walking ability tends to decline in adolescents and adults with CP
این پاورپوینت در کارگاه مداخلات ادراکی حرکتی در کودکان با فلج مغزی توسط دکتر جانمحمدی ارائه شده است.
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این پاورپوینت در کارگاه معاینات عصبی در توانبخشی کودکان توسط دکتر محمدی ارائه شده است.
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این پاورپوینت در کارگاه معاینات عصبی در توانبخشی کودکان توسط دکتر میثم محمدی ارائه شده است.
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این ارائه در کارگاه تخصصی تقلید و آپراکسی سرنخ هایی برای مداخلات مبتنی بر شواهد توسط دکتر هاشم فرهنگ دوست تدریس شده است.
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این پاورپوینت در کارگاه ارزیابی و توانبخشی کودکان مبتلا به فلج مغزی توسط کاردرمانگر مهدی بیغم ارائه شده است.
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این فایل متنی توسط دکتر میثم محمدی در کارگاه تخصصی آگاهی، توجه، عصب شناسی و توانبخشی ارائه شده است.
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این پاورپوینت در کارگاه تخصصی توانبخشی شناختی در اختلالات یادگیری توسط دکتر هاشم فرهنگ دوست ارائه شده است.
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این پاورپوینت در کارگاه تخصصی رویکرد جدید بوبات در توانبخشی کودکان مبتلا به فلج مغزی ارائه شده است.
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این پاورپوینت در کارگاه تخصصی آگاهی، توجه، عصب شناسی و توانبخشی توسط دکتر میثم محمدی، دکترای کاردرمانی تدریس شده است. برای مشاهده مطالب بیشتر در این زمینه به وب سایت فروردین مراجعه نمایید.
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این پاورپوینت توسط دکتر محمدی در کارگاه آگاهی، توجه، عصب شناسی و توانبخشی ارائه شده است.
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More from Farvardin Neuro-Cognitive Training Group (20)
Nano-gold for Cancer Therapy chemistry investigatory projectSIVAVINAYAKPK
chemistry investigatory project
The development of nanogold-based cancer therapy could revolutionize oncology by providing a more targeted, less invasive treatment option. This project contributes to the growing body of research aimed at harnessing nanotechnology for medical applications, paving the way for future clinical trials and potential commercial applications.
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Histololgy of Female Reproductive System.pptxAyeshaZaid1
Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
Computer in pharmaceutical research and development-Mpharm(Pharmaceutics)MuskanShingari
Statistics- Statistics is the science of collecting, organizing, presenting, analyzing and interpreting numerical data to assist in making more effective decisions.
A statistics is a measure which is used to estimate the population parameter
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Osvaldo Bernardo Muchanga-GASTROINTESTINAL INFECTIONS AND GASTRITIS-2024.pdfOsvaldo Bernardo Muchanga
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GASTROINTESTINAL INFECTIONS result from the ingestion of pathogens that cause infections at the level of this tract, generally being transmitted by food, water and hands contaminated by microorganisms such as E. coli, Salmonella, Shigella, Vibrio cholerae, Campylobacter, Staphylococcus, Rotavirus among others that are generally contained in feces, thus configuring a FECAL-ORAL type of transmission.
Among the factors that lead to the occurrence of gastrointestinal infections are the hygienic and sanitary deficiencies that characterize our markets and other places where raw or cooked food is sold, poor environmental sanitation in communities, deficiencies in water treatment (or in the process of its plumbing), risky hygienic-sanitary habits (not washing hands after major and/or minor needs), among others.
These are generally consequences (signs and symptoms) resulting from gastrointestinal infections: diarrhea, vomiting, fever and malaise, among others.
The treatment consists of replacing lost liquids and electrolytes (drinking drinking water and other recommended liquids, including consumption of juicy fruits such as papayas, apples, pears, among others that contain water in their composition).
To prevent this, it is necessary to promote health education, improve the hygienic-sanitary conditions of markets and communities in general as a way of promoting, preserving and prolonging PUBLIC HEALTH.
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In addition to bacterial infections, gastritis and gastric ulcers are associated with several factors, with emphasis on prolonged fasting, chemical substances including drugs, alcohol, foods with strong seasonings including chilli, which ends up causing inflammation of the stomach walls and/or corrosion. of the same, resulting in the appearance of wounds and consequent gastritis or ulcers, respectively.
Among patients with gastritis and/or ulcers, one of the dilemmas is associated with the foods to consume in order to minimize the sensation of pain and discomfort.
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These lecture slides, by Dr Sidra Arshad, offer a simplified look into the mechanisms involved in the regulation of respiration:
Learning objectives:
1. Describe the organisation of respiratory center
2. Describe the nervous control of inspiration and respiratory rhythm
3. Describe the functions of the dorsal and respiratory groups of neurons
4. Describe the influences of the Pneumotaxic and Apneustic centers
5. Explain the role of Hering-Breur inflation reflex in regulation of inspiration
6. Explain the role of central chemoreceptors in regulation of respiration
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2. Chapter 36, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 13, Human Physiology by Lauralee Sherwood, 9th edition
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2. ATTENTION
WILLIAM JAMES (1907)
“EVERYONE KNOWS WHAT ATTENTION IS. IT IS
THE TAKING POSSESSION BY THE MIND IN CLEAR
AND VIVID FORM OF ONE OUT OF WHAT SEEM
SEVERAL SIMULTANEOUS OBJECTS OR TRAINS OF
THOUGHT”.
3. ATTENTION REQUIRED!
• SEARCH FOR A BLUE THING.
• FEEL THE SEAT AGAINST YOUR BACK.
• LISTEN TO EXTRANEOUS NOISE
• PREPARE TO TAP THE DESK NEXT TIME YOU HEAR A
COUGH.
• ALL REQUIRE “ATTENTION” TO DIFFERENT INTERNAL OR
ENVIRONMENTAL INFORMATION AND “SETTING UP”.
4. OUTLINE
• WHAT IS ATTENTION?
• NEUROANATOMICAL STRUCTURES OF ATTENTION
• MODELS OF ATTENTION: POSNER & PETERSEN
• ORIENTING
• APPLICATION: NEGLECT
• ALERTING
• APPLICATION: NEGLECT
• EXECUTIVE
• APPLICATION: NEGLECT
• ATTENTIONAL IMPAIRMENTS
5. “ATTENTION CAN BE
LIKENED TO A
SPOTLIGHT THAT
ENHANCES THE
EFFICIENCY OF THE
DETECTION OF EVENTS
WITHIN ITS BEAM”
POSNER ET AL (1980).
6. UNDERSTANDING ATTENTION
• ATTENTION IS REQUIRED TO LIMIT ENTRY TO A FINITE
CAPACITY PROCESSING SYSTEM BY SELECTING ONLY A SUBSET
OF ALL AVAILABLE INFORMATION.
• ATTENTION ITSELF IS A RESOURCE OF LIMITED CAPACITY
WHICH CAN BE DIVIDED BETWEEN TASKS.
• ATTENTION IS RESPONSIBLE FOR VIGILANCE OVER TIME
• PROCESSING AND ATTENTIONAL CAPACITY IS LINKED TO
AROUSAL AND ALERTNESS.
14. MODELS OF ATTENTION:
POSNER & PETERSEN (1990)
• ATTENTION SYSTEM ANATOMICALLY SEPARATE
• ATTENTION CARRIED OUT BY A NETWORK OF ANATOMICAL
AREAS
• AREAS INVOLVED CARRY OUT DIFFERENT FUNCTIONS THAT
CAN BE SPECIFIED IN COGNITIVE TERMS
15. POSNER & PETERSEN’S MODEL OF
ATTENTION
• ORIENTING:
• DIRECTED ATTENTION
• DISENGAGE AND SHIFT ATTENTION
• ALERTNESS: (SUSTAINED ATTENTION/ AROUSAL/
VIGILANCE)
• MAINTAINING FOCUS OVER A PERIOD OF TIME
• EXECUTIVE: TARGET DETECTION; SUPERVISORY
CONTROL
16. ANATOMY
• ORIENTING:
• POSTERIOR ATTENTIONAL SYSTEM
• ALERTNESS: (SUSTAINED ATTENTION/
AROUSAL/ VIGILANCE)
• RIGHT LATERALIZED, FRONTAL-PARIETAL-THALAMIC
NETWORK
• EXECUTIVE:
• ANTERIOR ATTENTIONAL SYSTEM
17. ORIENTING: POSTERIOR
ATTENTION SYSTEM
• ORIENTING
• VISUAL LOCATIONS
• OVERT
• COVERT
• THREE COGNITIVE OPERATIONS OF ORIENTING
• DISENGAGING
• SHIFTING
• RE-ENGAGING/READING
19. ANATOMY OF POSTERIOR
ATTENTION SYSTEM
• DISENGAGING POSTERIOR PARIETAL LOBE
• SHIFTING SUPERIOR COLLICULUS
• RE-ENGAGING/READING LATERAL PULVINAR NUCLEUS
OF THE POSTEREOLATERAL THALAMUS
20.
21. LESION EFFECTS
• DAMAGE TO POSTERIOR PARIETAL
• INABILITY TO DISENGAGE FROM ATTENTIONAL FOCUS TO A
TARGET LOCATED IN A DIRECTION CONTRALATERAL TO
LESION SITE
• NEGLECT/BEHAVIOURAL INATTENTION
• DAMAGE TO SUPERIOR COLLICULUS
• INABILITY TO SHIFT ATTENTION REGARDLESS OF WHETHER
ATTENTION IS DIRECTED ELSEWHERE INITIALLY
• SUPRANUCLEAR PALSY
• DAMAGE TO PULVINAR
• SLOWED RESPONSE TO A VALID OR INVALID CUED TARGET
ON SIDE CONTRALATERAL TO LESION
• LABERGE & BUCHSBAUM (1990)
22. PULVINAR & GATING FUNCTION
Right Visual Field Left Visual Field
LaBerge & Buchsbaum (1990)
N O Q W
M R A S
O
23. HEMI-NEGLECT
• ASSOCIATED WITH RIGHT POSTERIOR PARIETAL LESIONS.
• PATIENTS TESTED ON POSNER’S ORIENTING TASKS HAVE
DIFFICULTY ORIENTING ATTENTION TO THE NEGLECTED
SIDE.
• DEFICIT IN ATTENTIONAL PROCESSING
30. HEMI-NEGLECT
• PROBLEM IN UNILATERAL VISUAL NEGLECT IS IN
DISENGAGING FROM NON-NEGLECTED SIDE TO SHIFT TO
NEGLECTED SIDE?
31. SIMULTANAGNOSIA AND VISUAL
EXTINCTION
• OFTEN EXHIBITED BY INDIVIDUALS WITH VISUAL NEGLECT.
• SIMULTANAGNOSIA, CHARACTERISED BY INABILITY TO “SEE”
MORE THAN ONE OBJECT CONCURRENTLY.
32. NEGLECT OF OTHER “SPACES”
• REPRESENTATIONAL SPACE (BISIACH AND LUZZATTI(1978).
• SENSORY SPACE (BISIACH 1988).
• OBJECT CENTRED SPACE.( E.G. DRIVER AND HALLIGAN
1991).
• PERSONAL SPACE
• SUGGESTS A VERY COMPLEX VARIETY OF “SPATIAL”
SYSTEMS WITHIN WHICH ATTENTION CAN OPERATE.
33. SPATIAL VS. OBJECT BASED
ATTENTION
• MOST OF THE EVIDENCE FOR THE POSTERIOR
ATTENTIONAL SYSTEM DERIVED FROM SPATIAL TASKS
• SPACE-BASED THEORIES
• WHAT ABOUT OBJECTS? CAN ATTENTION BE OBJECT-
BASED?
• IS THE SAME POSTERIOR PARIETAL ATTENTIONAL NETWORK
ENGAGED IN OBJECT-BASED BOTTOM-UP ATTENTIONAL
TASKS?
34. OBJECT-BASED ATTENTIONAL
PROCESSING
• OVERLAPPING FACES AND HOUSES (ALL IN SAME
LOCATION), ONE STIMULUS MOVING
• ATTEND TO: FACES, HOUSE, OR DIRECTION OF MOTION
• ACTIVITY GREATER WHEN ATTENDING TO PREFERRED
STIMULUS (EG. FUSIFORM FACE AREA GREATER DURING
FACES)--OBJECT-BASED ATTENTIONAL MODULATION
SINCE ALL STIMULI IN SAME LOCATION.
O’CRAVEN ET AL. (1999)
35. POSNER & PETERSEN’S MODEL OF
ATTENTION
• ORIENTING:
• DIRECTED ATTENTION
• DISENGAGE AND SHIFT ATTENTION
• ALERTNESS: (SUSTAINED ATTENTION/ AROUSAL/
VIGILANCE)
• MAINTAINING FOCUS OVER A PERIOD OF TIME
• EXECUTIVE: TARGET DETECTION; SUPERVISORY
CONTROL
36. ALERTING: VIGILANCE &
SUSTAINED ATTENTION
• VIGILANCE REQUIRES CONSTANT MONITORING FOR SIGNAL
OCCURRENCE.
• SUSTAINED ATTENTION IS REQUIRED ONCE SELECTION HAS
OCCURRED AND FURTHER PROCESSING IS NECESSARY TO
COMPLETE TASK.
• BOTH INVOLVE GOAL MAINTENANCE OVER TIME. (MORE AN
ISSUE OF EXECUTIVE CONTROL.)
• RELATED TO AROUSAL LEVELS.
37. Neuroanatomy of
Sustained Attention
•Evidence from lesion
& neuroimaging
studies (i.e. Sturm et al., 1999)
•R-lateralized network
•DLPFC, posterior
parietal cortex,
subcortical (thalamic)
RDLPFC
PPC
MD Thalamus
39. ROLE OF SUSTAINED ATTENTION
• ROBERTSON AND MANLY (1999) SUGGEST
UNILATERAL NEGLECT ASSOCIATED WITH
NON-LATERALISED ATTENTIONAL DEFICITS.
• RIGHT HEMISPHERE (PARTICULARLY
DORSOLATERAL PREFRONTAL) IS MORE
IMPORTANT FOR SUSTAINING ATTENTION
THAN SHIFTING IT.
• CONTRIBUTIONS TO NEGLECT, EXTINCTION
AND SIMULTANAGNOSIA MAY RESULT FROM
A MORE GENERAL EFFECT OF REDUCED
AROUSAL, IMPAIRED SPATIAL ATTENTION
AND REDUCED ATTENTIONAL CAPACITY.
40. POSNER & PETERSEN’S MODEL OF
ATTENTION
• ORIENTING:
• DIRECTED ATTENTION
• DISENGAGE AND SHIFT ATTENTION
• ALERTNESS: (SUSTAINED ATTENTION/ AROUSAL/
VIGILANCE)
• MAINTAINING FOCUS OVER A PERIOD OF TIME
• EXECUTIVE: TARGET DETECTION; SUPERVISORY
CONTROL
41. ANTERIOR ATTENTIONAL SYSTEM
• EXECUTIVE CONTROL OF DIRECTED ATTENTION
• TOP-DOWN PROCESSING
• OVERT, INTENTIONALLY CONTROLLED ORIENTING SYSTEM
• INVOLVES FRONTAL AREAS
• E.G. DIVIDED ATTENTION
• ALLOCATION OF ATTENTIONAL RESOURCES
42. ANTERIOR ATTENTIONAL SYSTEM
• EXECUTIVE CONTROL OF DIRECTED ATTENTION: INVOLVED
IN BOTH SELECTIVE AND SUSTAINED ATTENTION
• TOP-DOWN PROCESSING
• COMPONENTS OF THE ANTERIOR
ATTENTIONAL/SUPERVISORY SYSTEM:
• CONCENTRATION OF ATTENTION
• SHARING ATTENTION (DIVIDED ATTENTION)
• SUPPRESSING ATTENTION
• SHIFTING ATTENTION
• PREPARATORY ATTENTION
• SETTING ATTENTION
• SUSTAINING ATTENTION
(STUSS ET AL., 1995)
45. Impairments of Attention
Cerebral Vascular Accident (stroke) - diverse
impairments, dependent on site, hemi-neglect
Alzheimers- impairments in control over focused
and divided attention, progressive
Brain Injury - slowness of information processing,
in some individuals impaired control as well. Some
recovery in slowness.
46. Complaints of subjects two years after
severe brain injury, in percentages:
- forgetfulness 54
- mental slowness 33
- poor concentration 33
- mental fatigue 30
- unable to do 2 things 21
- intolerance of bustle 19
47. Leclercq and Azouvi (2002):
“Impairments in control processes may be
demonstrated, apart from slowed processing,
- in more complex situations
- under time pressure
- under high working memory load
- in the more severely injured patients”.
49. ATTENTION DEFICIT AND
HYPERACTIVITY DISORDER
• SYMPTOMS: DISTRACTIBILITY, IMPULSIVITY AND
OVERACTIVITY
• POOR AT CONTINUOUS PERFORMANCE TASKS
• PROBLEMS WITH SUSTAINED ATTENTION AND SHIFTING
ATTENTION (BREWER ET AL., 2001)
• POORER PERFORMANCE ON SUSTAINED ATTENTION
RELATED TO SMALLER VOLUME OF WHITE MATTER IN
RIGHT HEMISPHERE (SIMRUD-CLIKEMAN ET AL.,
2000)
50. CONCLUSIONS
• “….ATTENTIONAL COMPUTATIONS ARE CARRIED OUT BY A
COMPLEX BUT SPECIFIABLE ANATOMICAL NETWORK AND ...
EACH AREA OF THE NETWORK HAS ITS OWN
COMPUTATIONS.
FARAH AND RATCLIFF (1998).
• ..ATTENTION ... A WIDELY DISTRIBUTED STATE IN WHICH
SEVERAL BRAIN SYSTEMS WORK ON THE DIFFERENT
PROPERTIES AND ACTION IMPLICATIONS OF THE SAME
SELECTED OBJECT.”
DUNCAN (1999).
51. CONCLUSIONS
• A MAJOR CHALLENGE FOR THE FUTURE IS TO DETERMINE
HOW THESE MULTIPLE ATTENTIONAL MECHANISMS
OPERATE IN A COORDINATED MANNER TO MAINTAIN
UNITY OF BEHAVIOUR. (POSNER AND PETERSEN 1990).