This document discusses various causes of falls, including syncope (transient loss of consciousness) and non-syncopal causes. It covers topics such as neurocardiogenic, cardiac, and neurological causes of syncope including seizures, progressive supranuclear palsy, third ventricular cysts, and more. Investigations discussed include Holter monitoring, loop recorders, tilt table testing, and imaging. Differential diagnosis and management are also covered.
Syncope is defined as a transient loss of consciousness and postural tone caused by a fall in cerebral blood flow. The document outlines the various causes of syncope including neurally-mediated, orthostatic, cardiac, metabolic, neurological/psychiatric disorders, and unexplained causes. It emphasizes obtaining a detailed history of the syncopal episode including circumstances, symptoms, age of onset, drugs, and pregnancy to help determine the underlying cause, which guides further testing and management.
Syncope is defined as a transient loss of consciousness due to decreased cerebral blood flow. It is commonly caused by neurally-mediated reflexes, orthostatic hypotension, or cardiac arrhythmias. Evaluation involves determining the cause through history, physical exam, ECG and tests like tilt table testing, echocardiogram, and cardiac monitoring. Treatment depends on the underlying cause and may include lifestyle changes, medications, pacemakers, or defibrillators.
This document provides information on intracerebral haemorrhage (ICH), including:
1) ICH is the second most common type of stroke and onset is usually smooth and progressive unlike ischemic stroke.
2) Unenhanced CT is the first investigation and volume correlates to mortality and morbidity.
3) Risk factors include hypertension, liver dysfunction, smoking, and alcohol abuse.
4) Treatment options include factor VIIa within 4 hours to limit volume and surgery may play a role.
APPROACH TO SYNCOPE ,DIAGNOSIS AND MANAGEMENTasifiqbal545
This document discusses the management of two patients presenting with syncope.
Case 1 is a 42-year-old female with a history of passing out at work. Her workup including physical exam, EKG, labs and tilt table test was normal. She was diagnosed with vasovagal syncope as her tilt table test induced syncope.
Case 2 is an 82-year-old male found unresponsive. His workup in the ER was negative but he was admitted where 2 hours later he developed nonsustained VTach on ECG monitoring. An EP study showed inducible VTach and he received an ICD. He was found to have diffuse coronary artery disease on cardiac cath.
Syncope, or transient loss of consciousness, can be caused by various cardiac and non-cardiac conditions. A thorough history, physical exam, ECG and diagnostic testing are needed to evaluate the cause. Patients found to have cardiac syncope, abnormal vital signs, ECG changes or structural heart disease have a higher risk of adverse outcomes and should be admitted. Risk stratification tools like the San Francisco Syncope Rule and Oesil Risk Score can help determine which low-risk patients can be safely discharged. High-risk features predicting serious underlying rhythm issues include age over 45, history of heart disease or abnormal ECG.
This document provides guidance on diagnosing dystonia. It begins by noting dystonia is characterized by abnormal postures and has varied presentations making diagnosis difficult. It recommends determining if the patient has primary or secondary dystonia. Primary dystonia involves dystonia as the only symptom with normal imaging and no secondary cause. Secondary dystonia has an identifiable cause. It describes classifications, red flags, investigation approaches, dystonia plus syndromes like dopa-responsive dystonia and myoclonus dystonia, and treatment options like deep brain stimulation.
This is the third presentation after approach to dystonia and approach to chorea . This one is based upon the concensus statement on tremor by MDS. The original article is a practical ready reckoner in clinical practice. Comments are welcome .
A 58-year-old female presented with sudden onset blurred vision and right-sided weakness and was found to have an acute left thalamic infarction; imaging showed no vascular abnormalities but she had an incidental finding of a possible atrial septal defect; she was treated with tPA and made a full recovery with no residual deficits.
Syncope is defined as a transient loss of consciousness and postural tone caused by a fall in cerebral blood flow. The document outlines the various causes of syncope including neurally-mediated, orthostatic, cardiac, metabolic, neurological/psychiatric disorders, and unexplained causes. It emphasizes obtaining a detailed history of the syncopal episode including circumstances, symptoms, age of onset, drugs, and pregnancy to help determine the underlying cause, which guides further testing and management.
Syncope is defined as a transient loss of consciousness due to decreased cerebral blood flow. It is commonly caused by neurally-mediated reflexes, orthostatic hypotension, or cardiac arrhythmias. Evaluation involves determining the cause through history, physical exam, ECG and tests like tilt table testing, echocardiogram, and cardiac monitoring. Treatment depends on the underlying cause and may include lifestyle changes, medications, pacemakers, or defibrillators.
This document provides information on intracerebral haemorrhage (ICH), including:
1) ICH is the second most common type of stroke and onset is usually smooth and progressive unlike ischemic stroke.
2) Unenhanced CT is the first investigation and volume correlates to mortality and morbidity.
3) Risk factors include hypertension, liver dysfunction, smoking, and alcohol abuse.
4) Treatment options include factor VIIa within 4 hours to limit volume and surgery may play a role.
APPROACH TO SYNCOPE ,DIAGNOSIS AND MANAGEMENTasifiqbal545
This document discusses the management of two patients presenting with syncope.
Case 1 is a 42-year-old female with a history of passing out at work. Her workup including physical exam, EKG, labs and tilt table test was normal. She was diagnosed with vasovagal syncope as her tilt table test induced syncope.
Case 2 is an 82-year-old male found unresponsive. His workup in the ER was negative but he was admitted where 2 hours later he developed nonsustained VTach on ECG monitoring. An EP study showed inducible VTach and he received an ICD. He was found to have diffuse coronary artery disease on cardiac cath.
Syncope, or transient loss of consciousness, can be caused by various cardiac and non-cardiac conditions. A thorough history, physical exam, ECG and diagnostic testing are needed to evaluate the cause. Patients found to have cardiac syncope, abnormal vital signs, ECG changes or structural heart disease have a higher risk of adverse outcomes and should be admitted. Risk stratification tools like the San Francisco Syncope Rule and Oesil Risk Score can help determine which low-risk patients can be safely discharged. High-risk features predicting serious underlying rhythm issues include age over 45, history of heart disease or abnormal ECG.
This document provides guidance on diagnosing dystonia. It begins by noting dystonia is characterized by abnormal postures and has varied presentations making diagnosis difficult. It recommends determining if the patient has primary or secondary dystonia. Primary dystonia involves dystonia as the only symptom with normal imaging and no secondary cause. Secondary dystonia has an identifiable cause. It describes classifications, red flags, investigation approaches, dystonia plus syndromes like dopa-responsive dystonia and myoclonus dystonia, and treatment options like deep brain stimulation.
This is the third presentation after approach to dystonia and approach to chorea . This one is based upon the concensus statement on tremor by MDS. The original article is a practical ready reckoner in clinical practice. Comments are welcome .
A 58-year-old female presented with sudden onset blurred vision and right-sided weakness and was found to have an acute left thalamic infarction; imaging showed no vascular abnormalities but she had an incidental finding of a possible atrial septal defect; she was treated with tPA and made a full recovery with no residual deficits.
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.
This document provides diagnostic criteria for chronic inflammatory demyelinating polyneuropathy (CIDP), including:
1) Clinical criteria for typical and atypical CIDP with inclusion/exclusion factors.
2) Definite, probable, and possible electrophysiological criteria involving compound muscle action potential tests.
3) Supportive diagnostic criteria including cerebrospinal fluid analysis, MRI findings, nerve conduction studies, and nerve biopsy results.
It also outlines inclusion/exclusion criteria and supportive criteria specifically for diagnosing pure sensory CIDP without motor involvement.
The document discusses dysautonomia and Postural Orthostatic Tachycardia Syndrome (POTS). It defines POTS as excessive increase in heart rate when upright, and describes its two main forms - neuropathic POTS caused by loss of vasoconstriction and hyperadrenergic POTS with increased norepinephrine. Treatment depends on the form but may include physical countermaneuvers, salt, water, medications and exercise. Postural vasovagal syncope, characterized by fainting, is the most common type of orthostatic intolerance.
Epileptic encephalopathies are a group of epileptic disorders that cause cognitive and behavioral impairments beyond what would be expected from seizures alone. They typically begin early in life and are characterized by frequent seizures and abnormal EEG patterns. Common types include early myoclonic encephalopathy, Ohtahara syndrome, West syndrome, Dravet syndrome, and Lennox-Gastaut syndrome. These disorders can cause developmental delays, intellectual disabilities, and in some cases early death. Treatment aims to control seizures, though many types are highly treatment resistant.
This document discusses convulsive status epilepticus (CSE). It notes that the worldwide incidence of CSE is highest in children and the elderly, with mortality rates ranging from 10.5-28% and neurological sequelae occurring in 11-16% of patients. The most common causes of CSE are listed as low anti-epileptic drug levels, stroke, alcohol withdrawal, anoxic brain injury, and metabolic disturbances. The document provides details on the definition, types, risk factors, complications, management, and treatment of CSE.
frontal lobe anatomy and clinical relevanceImran Rizvi
The frontal lobes are the largest lobes in the human brain. They are located at the front of the brain and are involved in motor function, problem-solving, emotion, and language. The frontal lobes contain several important areas including the primary motor cortex, premotor cortex, prefrontal cortex, and Broca's area. Damage to different parts of the frontal lobes can cause problems with movement, cognition, behavior, and speech depending on the location of the injury. The frontal lobes receive blood supply from the anterior and middle cerebral arteries and are organized into circuits that connect the cortex to the basal ganglia and thalamus.
Corticobasal degeneration is a rare progressive neurodegenerative disease typically presenting in patients' 60s with asymmetric parkinsonism and cognitive dysfunction. It is characterized by focal cortical atrophy and tau-positive lesions in the cortex and basal ganglia. Diagnosis relies on clinical features and exclusion of other conditions, while neuropathological examination confirms the diagnosis. Currently there is no cure, and treatment focuses on managing symptoms through a multimodality approach, though available therapies have limited effectiveness.
EEG Variants with patterns by Murtaza SyedMurtaza Syed
This document provides information on normal variant EEG patterns. It discusses four main types of EEG variants: rhythmic patterns, epileptiform patterns, lambda and lambdoids, and age-related variants. Six main rhythmic variant patterns are described including alpha variants, mu rhythm, rhythmic mid-temporal theta of drowsiness, subclinical rhythmic electrographic discharges in adults, midline theta rhythm, and frontal arousal rhythm. Four epileptiform variant patterns are also outlined. The document provides detailed descriptions of each variant pattern.
Periodic Lateralized Epileptiform Discharges (PLEDs) are repeating waveforms seen on EEG that occur at regular intervals and are localized to one hemisphere. They are commonly seen after acute cortical injuries like stroke and infections. PLEDs are classified based on their pattern and presence of additional rhythmic discharges. They indicate unstable brain physiology resulting from seizures, injury or metabolic disturbances. While not strictly ictal, PLEDs are associated with increased risk of clinical seizures. Prognosis depends on the underlying cause, with acute severe strokes having the worst outcomes. Treatment involves antiepileptic drugs mainly if clinical seizures are present.
1) Uncontrolled epilepsy can be due to pseudointractability or true refractory epilepsy, requiring different treatment approaches.
2) For uncontrolled epilepsy, the first step is a careful diagnosis to correctly classify the epilepsy type and exclude other conditions, followed by proper antiepileptic drug (AED) selection, dosing, and ensuring compliance.
3) Clobazam is an effective add-on treatment for both generalized and focal epilepsies due to its broad spectrum of action, and can provide long-term seizure control when used as an adjunct to other AEDs.
1. The document discusses the approach to evaluating and diagnosing ataxia. It covers the history, examination, localization, and differential diagnosis of ataxia.
2. Key points include distinguishing cerebellar ataxia from sensory ataxia and vestibular dysfunction based on examination. The approach involves a detailed history and neurological exam followed by ancillary testing which may include imaging, genetics, and labs.
3. Common causes discussed are cerebellar, sensory, and vestibular system lesions. The differential diagnosis depends on features in the history such as onset, progression, family history, and associated findings on exam.
An electroencephalogram (EEG) is a test used to evaluate the electrical activity in the brain. Brain cells communicate with each other through electrical impulses. An EEG can be used to help detect potential problems associated with this activity.
This document provides information on evaluating and managing patients presenting with syncope (transient loss of consciousness). It describes the initial assessment including ABCs, vital signs and ECG. It outlines key questions to determine if it is true syncope, identify the cause, and assess risk of serious outcomes. Causes are categorized as high, moderate or low risk. Evaluation involves establishing the diagnosis, identifying triggers, risk factors and ruling out conditions like arrhythmias. Scoring systems like SFSR and ROSE can stratify risk. Prolonged QT interval may indicate conditions like long QT syndrome or Brugada syndrome. Management involves stabilizing and monitoring patients or transferring to higher levels of care based on risk level.
The document discusses mesial temporal lobe epilepsy (MTLE), including its history, epidemiology, etiology, pathophysiology, clinical presentation, diagnosis, and treatment. MTLE is characterized by seizures originating in the mesial temporal lobe and is often associated with hippocampal sclerosis that can be identified on MRI. Diagnosis involves a combination of clinical presentation, EEG, functional imaging like PET and SPECT, and sometimes invasive monitoring to localize the seizure focus.
Approach to Neurogenic Dysphagia (1) 24_07.pptxNeurologyKota
Approach to neurogenic dysphagia GUSS Swallow test
Individuals with Subcortical Strokes have a higher incidence of dysphagia and aspiration than those with cortical damage.
Cerebral amyloid angiopathy (CAA) is characterized by cerebrovascular amyloid deposition and is a cause of cerebral hemorrhage in older individuals. It has a close association with Alzheimer's disease, with a prevalence of around 80-90% in AD patients. CAA becomes more common with age, affecting around half of elderly individuals. While there are no definitive treatments, hematoma evacuation appears relatively safe for younger patients with CAA-related hemorrhages.
This document provides an overview of normal EEG patterns in adults. It begins with a brief history of EEG and then describes the basic electrical activity generated by the brain and how EEG recordings work. It outlines the normal frequency bands seen in EEG - delta, theta, alpha, beta and gamma. Specific normal EEG patterns like the alpha rhythm, vertex waves, sleep spindles and K-complexes are described. It also discusses benign variants and activation procedures. In summary, the document serves as a reference for the typical EEG patterns seen in healthy, awake and sleeping adults.
Cerebral salt wasting syndrome (CSWS) is a condition where there is renal loss of sodium during intracranial disorders leading to hyponatremia. It is commonly caused by subarachnoid hemorrhage, brain injuries, or central nervous system infections. CSWS results from disruption of hypothalamic-renal pathways and an imbalance of sympathetic output. Patients experience hyponatremia and a decrease in extracellular fluid volume. Treatment involves slow sodium and water replacement to correct the hyponatremia while avoiding too rapid of a correction which can cause cerebral edema.
Autoregulation of cerebral blood flow part 1/2Sameep Koshti
This document summarizes several topics related to cerebral blood flow regulation, including:
1. Autoregulation allows cerebral blood flow to remain constant over a range of blood pressures through changes in cerebral vascular resistance.
2. Carbon dioxide is a potent vasodilator and changes in CO2 levels are the primary driver of physiological chemoregulation of cerebral blood flow.
3. Oxygen, neurotransmitters, astrocytes, and other vasoactive substances also play roles in regulating cerebral blood flow and coupling flow to metabolic demand.
Syncope, or fainting, is caused by insufficient blood flow to the brain. It is usually brief and self-limited. Evaluation of syncope involves obtaining a detailed history, physical exam, ECG, and testing based on risk factors. Causes are categorized as benign if due to things like vasovagal response, or dangerous if due to cardiac arrhythmias. High-risk patients warrant further cardiac workup and monitoring, while low-risk patients can often be evaluated as outpatients.
1. HIV was first described in 1981 and is caused by HIV-1 and HIV-2 viruses which deplete CD4 lymphocytes. As of 2000, 58 million people were infected globally and 21.8 million had died.
2. Cardiac manifestations are common in HIV/AIDS patients, occurring in 28-73% of patients. Prior to antiretroviral therapy, cardiac disease was usually only detected at autopsy.
3. Guidelines recommend regular echocardiograms to monitor cardiac dysfunction in HIV patients, with increased frequency if abnormalities are detected. Endocarditis prevalence is increased in HIV patients.
This document discusses coronary artery disease in HIV patients. It covers the relative magnitude of cardiovascular disease among HIV patients, current data on the association between HIV and coronary artery disease, known risk factors and how they may be modulated by HIV diagnosis, screening and prevention recommendations, and areas for future research. Key points include increased rates of myocardial infarction and atherosclerosis in HIV patients, traditional and HIV-specific risk factors, screening tools and their limitations, effects of antiretroviral therapy on risk, and lifestyle and medical interventions for prevention.
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.
This document provides diagnostic criteria for chronic inflammatory demyelinating polyneuropathy (CIDP), including:
1) Clinical criteria for typical and atypical CIDP with inclusion/exclusion factors.
2) Definite, probable, and possible electrophysiological criteria involving compound muscle action potential tests.
3) Supportive diagnostic criteria including cerebrospinal fluid analysis, MRI findings, nerve conduction studies, and nerve biopsy results.
It also outlines inclusion/exclusion criteria and supportive criteria specifically for diagnosing pure sensory CIDP without motor involvement.
The document discusses dysautonomia and Postural Orthostatic Tachycardia Syndrome (POTS). It defines POTS as excessive increase in heart rate when upright, and describes its two main forms - neuropathic POTS caused by loss of vasoconstriction and hyperadrenergic POTS with increased norepinephrine. Treatment depends on the form but may include physical countermaneuvers, salt, water, medications and exercise. Postural vasovagal syncope, characterized by fainting, is the most common type of orthostatic intolerance.
Epileptic encephalopathies are a group of epileptic disorders that cause cognitive and behavioral impairments beyond what would be expected from seizures alone. They typically begin early in life and are characterized by frequent seizures and abnormal EEG patterns. Common types include early myoclonic encephalopathy, Ohtahara syndrome, West syndrome, Dravet syndrome, and Lennox-Gastaut syndrome. These disorders can cause developmental delays, intellectual disabilities, and in some cases early death. Treatment aims to control seizures, though many types are highly treatment resistant.
This document discusses convulsive status epilepticus (CSE). It notes that the worldwide incidence of CSE is highest in children and the elderly, with mortality rates ranging from 10.5-28% and neurological sequelae occurring in 11-16% of patients. The most common causes of CSE are listed as low anti-epileptic drug levels, stroke, alcohol withdrawal, anoxic brain injury, and metabolic disturbances. The document provides details on the definition, types, risk factors, complications, management, and treatment of CSE.
frontal lobe anatomy and clinical relevanceImran Rizvi
The frontal lobes are the largest lobes in the human brain. They are located at the front of the brain and are involved in motor function, problem-solving, emotion, and language. The frontal lobes contain several important areas including the primary motor cortex, premotor cortex, prefrontal cortex, and Broca's area. Damage to different parts of the frontal lobes can cause problems with movement, cognition, behavior, and speech depending on the location of the injury. The frontal lobes receive blood supply from the anterior and middle cerebral arteries and are organized into circuits that connect the cortex to the basal ganglia and thalamus.
Corticobasal degeneration is a rare progressive neurodegenerative disease typically presenting in patients' 60s with asymmetric parkinsonism and cognitive dysfunction. It is characterized by focal cortical atrophy and tau-positive lesions in the cortex and basal ganglia. Diagnosis relies on clinical features and exclusion of other conditions, while neuropathological examination confirms the diagnosis. Currently there is no cure, and treatment focuses on managing symptoms through a multimodality approach, though available therapies have limited effectiveness.
EEG Variants with patterns by Murtaza SyedMurtaza Syed
This document provides information on normal variant EEG patterns. It discusses four main types of EEG variants: rhythmic patterns, epileptiform patterns, lambda and lambdoids, and age-related variants. Six main rhythmic variant patterns are described including alpha variants, mu rhythm, rhythmic mid-temporal theta of drowsiness, subclinical rhythmic electrographic discharges in adults, midline theta rhythm, and frontal arousal rhythm. Four epileptiform variant patterns are also outlined. The document provides detailed descriptions of each variant pattern.
Periodic Lateralized Epileptiform Discharges (PLEDs) are repeating waveforms seen on EEG that occur at regular intervals and are localized to one hemisphere. They are commonly seen after acute cortical injuries like stroke and infections. PLEDs are classified based on their pattern and presence of additional rhythmic discharges. They indicate unstable brain physiology resulting from seizures, injury or metabolic disturbances. While not strictly ictal, PLEDs are associated with increased risk of clinical seizures. Prognosis depends on the underlying cause, with acute severe strokes having the worst outcomes. Treatment involves antiepileptic drugs mainly if clinical seizures are present.
1) Uncontrolled epilepsy can be due to pseudointractability or true refractory epilepsy, requiring different treatment approaches.
2) For uncontrolled epilepsy, the first step is a careful diagnosis to correctly classify the epilepsy type and exclude other conditions, followed by proper antiepileptic drug (AED) selection, dosing, and ensuring compliance.
3) Clobazam is an effective add-on treatment for both generalized and focal epilepsies due to its broad spectrum of action, and can provide long-term seizure control when used as an adjunct to other AEDs.
1. The document discusses the approach to evaluating and diagnosing ataxia. It covers the history, examination, localization, and differential diagnosis of ataxia.
2. Key points include distinguishing cerebellar ataxia from sensory ataxia and vestibular dysfunction based on examination. The approach involves a detailed history and neurological exam followed by ancillary testing which may include imaging, genetics, and labs.
3. Common causes discussed are cerebellar, sensory, and vestibular system lesions. The differential diagnosis depends on features in the history such as onset, progression, family history, and associated findings on exam.
An electroencephalogram (EEG) is a test used to evaluate the electrical activity in the brain. Brain cells communicate with each other through electrical impulses. An EEG can be used to help detect potential problems associated with this activity.
This document provides information on evaluating and managing patients presenting with syncope (transient loss of consciousness). It describes the initial assessment including ABCs, vital signs and ECG. It outlines key questions to determine if it is true syncope, identify the cause, and assess risk of serious outcomes. Causes are categorized as high, moderate or low risk. Evaluation involves establishing the diagnosis, identifying triggers, risk factors and ruling out conditions like arrhythmias. Scoring systems like SFSR and ROSE can stratify risk. Prolonged QT interval may indicate conditions like long QT syndrome or Brugada syndrome. Management involves stabilizing and monitoring patients or transferring to higher levels of care based on risk level.
The document discusses mesial temporal lobe epilepsy (MTLE), including its history, epidemiology, etiology, pathophysiology, clinical presentation, diagnosis, and treatment. MTLE is characterized by seizures originating in the mesial temporal lobe and is often associated with hippocampal sclerosis that can be identified on MRI. Diagnosis involves a combination of clinical presentation, EEG, functional imaging like PET and SPECT, and sometimes invasive monitoring to localize the seizure focus.
Approach to Neurogenic Dysphagia (1) 24_07.pptxNeurologyKota
Approach to neurogenic dysphagia GUSS Swallow test
Individuals with Subcortical Strokes have a higher incidence of dysphagia and aspiration than those with cortical damage.
Cerebral amyloid angiopathy (CAA) is characterized by cerebrovascular amyloid deposition and is a cause of cerebral hemorrhage in older individuals. It has a close association with Alzheimer's disease, with a prevalence of around 80-90% in AD patients. CAA becomes more common with age, affecting around half of elderly individuals. While there are no definitive treatments, hematoma evacuation appears relatively safe for younger patients with CAA-related hemorrhages.
This document provides an overview of normal EEG patterns in adults. It begins with a brief history of EEG and then describes the basic electrical activity generated by the brain and how EEG recordings work. It outlines the normal frequency bands seen in EEG - delta, theta, alpha, beta and gamma. Specific normal EEG patterns like the alpha rhythm, vertex waves, sleep spindles and K-complexes are described. It also discusses benign variants and activation procedures. In summary, the document serves as a reference for the typical EEG patterns seen in healthy, awake and sleeping adults.
Cerebral salt wasting syndrome (CSWS) is a condition where there is renal loss of sodium during intracranial disorders leading to hyponatremia. It is commonly caused by subarachnoid hemorrhage, brain injuries, or central nervous system infections. CSWS results from disruption of hypothalamic-renal pathways and an imbalance of sympathetic output. Patients experience hyponatremia and a decrease in extracellular fluid volume. Treatment involves slow sodium and water replacement to correct the hyponatremia while avoiding too rapid of a correction which can cause cerebral edema.
Autoregulation of cerebral blood flow part 1/2Sameep Koshti
This document summarizes several topics related to cerebral blood flow regulation, including:
1. Autoregulation allows cerebral blood flow to remain constant over a range of blood pressures through changes in cerebral vascular resistance.
2. Carbon dioxide is a potent vasodilator and changes in CO2 levels are the primary driver of physiological chemoregulation of cerebral blood flow.
3. Oxygen, neurotransmitters, astrocytes, and other vasoactive substances also play roles in regulating cerebral blood flow and coupling flow to metabolic demand.
Syncope, or fainting, is caused by insufficient blood flow to the brain. It is usually brief and self-limited. Evaluation of syncope involves obtaining a detailed history, physical exam, ECG, and testing based on risk factors. Causes are categorized as benign if due to things like vasovagal response, or dangerous if due to cardiac arrhythmias. High-risk patients warrant further cardiac workup and monitoring, while low-risk patients can often be evaluated as outpatients.
1. HIV was first described in 1981 and is caused by HIV-1 and HIV-2 viruses which deplete CD4 lymphocytes. As of 2000, 58 million people were infected globally and 21.8 million had died.
2. Cardiac manifestations are common in HIV/AIDS patients, occurring in 28-73% of patients. Prior to antiretroviral therapy, cardiac disease was usually only detected at autopsy.
3. Guidelines recommend regular echocardiograms to monitor cardiac dysfunction in HIV patients, with increased frequency if abnormalities are detected. Endocarditis prevalence is increased in HIV patients.
This document discusses coronary artery disease in HIV patients. It covers the relative magnitude of cardiovascular disease among HIV patients, current data on the association between HIV and coronary artery disease, known risk factors and how they may be modulated by HIV diagnosis, screening and prevention recommendations, and areas for future research. Key points include increased rates of myocardial infarction and atherosclerosis in HIV patients, traditional and HIV-specific risk factors, screening tools and their limitations, effects of antiretroviral therapy on risk, and lifestyle and medical interventions for prevention.
Cardiomyopathy in HIV patients has been shown to progress faster than idiopathic Dilated Cardiomyopathy in the HIV negative population. It is therefore important to recognize this condition early in this population and manage it appropriately. Studies need to be done to validate the current therapy for cardiomyopathy in this population since it is still unclear that LV dysfunction in this population responds in a similar fashion as in HIV negative patients with Dilated Cardiomyopathy
Cardiovascular Disease in HIV-Infected Patients.Predict It and Prevent It.2015Hivlife Info
In this downloadable slideset, Priscilla Y. Hsue, MD, and David A. Wohl, MD, discuss data on using traditional and newer markers and modalities to predict and prevent cardiovascular disease in HIV-infected patients.
Format: Microsoft PowerPoint (.ppt)
File size: 3.21 MB
Date posted: 7/16/2015
This document summarizes different devices used for closing ventricular septal defects (VSDs). It describes the common complications of VSD devices which are mostly minor, including embolization, arrhythmias, and conduction defects. Three types of Amplatzer devices are outlined - the muscular VSD device, asymmetric VSD occluder, and perimembranous VSD devices. Sizes and designs of each are provided. Results of post-myocardial infarction VSD closure show high residual leak rates. Finally, it briefly mentions some VSD devices manufactured in China including by Yatai and Lifetech, and introduces the novel NitOcclud VSD coil.
This document provides information about rotablation, a technique used to treat calcified coronary lesions. It discusses the indications and contraindications for rotablation, important trials that have evaluated it, tips for performing the procedure, complications like slow-flow and perforation, and comparisons of using rotablation with bare-metal stents versus drug-eluting stents. Key points include that rotablation works via differential cutting with diamond-coated burrs, it is useful for treating heavily calcified or difficult lesions, and optimal techniques aim to minimize platelet activation and potential complications.
This document provides several tips and tricks for navigating tortuous coronary arteries during cardiac catheterization procedures:
1) Shorter and more flexible stents and balloons can be delivered through more tortuous segments. An "anchor" technique using a buddy balloon can also aid delivery.
2) Stiffer wires can cause spasm, so microcatheters, buddy balloons, and telescopic guide systems may help. The Hi-Torque Wiggle wire can deflect to pass tortuous segments.
3) While rapid-exchange devices are faster, over-the-wire devices may track and deliver better in tortuosity. Laser or rotablater should be avoided due to risk of complications
Disorder of Adrenal Gland: Adrenal insufficiencyPratap Tiwari
This document discusses adrenal insufficiency (also known as Addison's disease), which can be primary, secondary, or tertiary. Primary adrenal insufficiency is caused by damage or disease of the adrenal glands and can result from autoimmune disease, infections, tumors, or hemorrhage. Secondary adrenal insufficiency is caused by interference with ACTH production in the pituitary gland, while tertiary is caused by interference with CRH production in the hypothalamus. Symptoms include fatigue, gastrointestinal issues, electrolyte imbalances, and hyperpigmentation. Diagnosis involves tests to evaluate cortisol levels and response to ACTH stimulation. Treatment consists of replacing glucocorticoids like hydroc
This document summarizes various devices used to close atrial septal defects (ASDs), including their designs, sizes, advantages, and disadvantages. The most commonly used device is the Amplatzer Septal Occluder, which has a double disc design and is self-expanding. Other devices discussed include the Gore HELEX, Lifetech/Cera, Figulla, Cardioseal/Starflex, and newer bioabsorbable options like the Biotrek. Complication rates of ASD device closure are generally low, below 10%, with embolization and arrhythmias being the most common issues. Larger trials have shown the Amplatzer to be very effective and easy
This document summarizes information about statins, including their uses, mechanisms of action, types, interactions, and safety considerations. It discusses how statins are used to prevent heart disease by lowering LDL cholesterol and discusses their four proposed mechanisms of action, including improving endothelial function and maintaining plaque stability. It also provides comparisons of different statin medications and identifies atorvastatin and simvastatin as producing the greatest LDL reduction, as well as pravastatin and fluvastatin as having fewer drug interactions.
The document describes various hemodynamic measurements and pressure tracings obtained from right heart catheterization. It discusses normal and abnormal left ventricular pressure tracings and their components during systole and diastole. It also describes normal and abnormal right atrial, right ventricular, pulmonary artery, and pulmonary capillary wedge pressure tracings, including how different disease states can affect the pressure waveform morphology. Various concepts in hemodynamic measurements are summarized such as timing of pressure waves, effects of respiration, and identifying features of common cardiac pathologies.
This document provides an overview of hyponatremia (sodium concentration < 135 mEq/L), including its introduction, pathophysiology, symptoms, workup, treatment, and perspectives from cardiologists. Hyponatremia is usually caused by increased water retention and can be classified into four types based on volume status and cause: type 1 is hypervolemic, type 2 is hypovolemic, type 3A is euvolemic due to SIADH, and type 3B is euvolemic due to other causes. The workup involves assessing serum and urine osmolality, sodium concentration, and specific gravity to distinguish between impaired water excretion versus excess fluid intake. Treatment depends on
The document discusses guidelines for managing dyslipidemia and cardiovascular disease risk, including:
1) It provides risk levels (very high, high, moderate, low) based on calculated cardiovascular risk and clinical factors and recommends LDL-C treatment targets for each level.
2) It discusses statin treatment for different risk levels, recommending the highest tolerated dose to reach LDL-C targets.
3) It summarizes trials comparing different statins and their average LDL-C reduction, finding some are more effective than others at reducing LDL-C.
1) Several early trials evaluated lipid lowering drugs such as mevastatin and lovastatin, which were isolated from fungi and shown to inhibit HMG CoA reductase. However, mevastatin was not marketed due to toxicity in dogs. Lovastatin was first marketed as Mevacor in 1987.
2) Large primary prevention trials such as WOSCOPS, AFCAPS/TexCAPS, CARDS and JUPITER demonstrated significant reductions in cardiovascular events with statin therapy compared to placebo in various populations with and without known heart disease.
3) Secondary prevention trials in patients with stable CAD such as 4S, CARE, LIPID and TNT showed that statin therapy reduces
Hemodynamic monitoring measures factors that influence the force and flow of blood in order to aid in diagnosing, monitoring, and managing critically ill patients. It involves using pulmonary artery catheters and transducers to obtain pressures and other cardiovascular measurements that provide information on conditions like shock states and help guide treatment decisions. Potential risks and complications require careful use of these monitoring techniques in appropriate clinical situations.
The adrenal glands sit atop the kidneys and are composed of an outer cortex and inner medulla. The cortex produces cortisol and aldosterone, while the medulla produces epinephrine and norepinephrine. Adrenal gland disorders occur when the glands do not function properly, such as Cushing's syndrome which results from excess cortisol production, congenital adrenal hyperplasia where the glands do not produce enough hormones, and pituitary tumors affecting hormone regulation. Treatments include medication, surgery, radiation, or a combination depending on the specific disorder.
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 document provides an overview of syncope (transient loss of consciousness). It discusses the pathophysiology, typical presentations, differential diagnoses, evaluation and treatment of different syncope types. The main causes discussed are neurally-mediated syncope (the most common), orthostatic hypotension, and cardiac syncope. For evaluation, the document recommends a thorough history, physical exam including orthostatic vital signs and carotid sinus massage in older patients, and tests like ECG, tilt table testing and cardiac monitoring. Treatment depends on the underlying cause, including fluid supplementation, compression stockings and pharmacotherapy for orthostatic hypotension, and pacing for cardiac syncope.
Management of patient with Epilepsy involves treating acute seizures, identifying and removing underlying causes, and long-term antiepileptic drug therapy. Seizures are classified as partial or generalized based on origin in one brain region or both hemispheres. Evaluation includes thorough history, physical exam, EEG and imaging to diagnose epilepsy and guide treatment. Management focuses on controlling seizures through medications while also addressing psychosocial needs through rehabilitation. Surgery may be considered for drug-resistant epilepsy localized to one brain region.
The document provides guidelines for the management of childhood epilepsy. It discusses the classification of seizures and epilepsy syndromes. Some key seizure types include partial seizures, generalized seizures like absence seizures, myoclonic seizures, atonic seizures, and tonic-clonic seizures. It also discusses approaches to diagnosing and treating common idiopathic or genetic epilepsy syndromes in children like benign childhood epilepsy with centrotemporal spikes and childhood absence epilepsy. Treatment involves antiepileptic drugs and considering neuroimaging in some cases.
Seizures are caused by abnormal electrical activity in the brain and can cause involuntary muscle movements, sensory disturbances, and altered consciousness. There are two main types of seizures - partial seizures which affect only one part of the brain and generalized seizures which affect the whole brain. Seizures have many potential causes including birth injuries, infections, genetic factors, head trauma, tumors, and alcohol or drug withdrawal. Diagnosis involves a medical history, physical exam, EEG and sometimes CT or MRI scans. Treatment primarily involves anticonvulsant medications to control seizures.
This document discusses epilepsy and seizures. It begins by defining key terminology like seizures, epilepsy, and different seizure types. It then discusses the difference between a seizure and epilepsy. Several epilepsy syndromes are mentioned like childhood absence epilepsy, juvenile myoclonic epilepsy, and Lennox-Gastaut syndrome. Causes, pathophysiology, signs and symptoms, classifications, and treatment options for different seizure types are summarized.
1. The document discusses convulsions (seizures) in children, including their causes, types, diagnosis, and treatment. It describes different types of seizures like simple partial, complex partial, generalized absence, myoclonic, tonic-clonic, and infantile spasms.
2. Febrile seizures, which occur due to fever but are not indicative of epilepsy, are also explained. Risk factors for developing epilepsy after febrile seizures are provided.
3. Status epilepticus, defined as continuous seizure activity for over 30 minutes, is outlined as a medical emergency with potential for neurological injury and mortality. Treatment options for different seizure types and status epilepticus are summarized.
This document provides definitions and information about seizures and epilepsy. It defines a seizure as a sudden wave of synchronous electrical activity in the brain that affects how a person feels or acts for a short time. Epilepsy is defined as a condition that affects the central nervous system and requires a person to have had at least two seizures not caused by a known medical condition or extremely low blood sugar. The document discusses different types of seizures including partial and generalized seizures, as well as diagnostic testing and treatment options for epilepsy.
This document summarizes information about convulsive disorders and epilepsy, including causes, types of seizures, classification, diagnosis, treatment, and prognosis. It discusses various types of seizures including partial, generalized tonic-clonic, absence, myoclonic, atonic, and febrile seizures. It also covers epilepsy syndromes, diagnostic testing including EEG and neuroimaging, differential diagnosis, management with antiepileptic drugs, and considerations in pregnancy. The majority of people with epilepsy experience remission within 10 years if their seizures are idiopathic and onset was in childhood.
This document discusses the classification and diagnosis of seizures and epilepsy. It defines key terms like seizure, epilepsy, and types of seizures. Seizures are classified as partial or generalized. Partial seizures are further divided into simple and complex, based on effects on consciousness. Generalized seizures include absence, tonic-clonic, myoclonic, tonic, clonic, and atonic. The document also discusses evaluation methods, differential diagnosis, comorbidities, mortality risks, and treatment approaches including anti-epileptic drugs.
This document defines pediatric seizures and epilepsy, describes the different types of seizures including partial, generalized, absence, myoclonic, atonic, and tonic-clonic seizures. It discusses the epidemiology, pathophysiology, classification, and etiologies of seizures in children. Seizures are common in children, especially those under 3 years old, and have different characteristics compared to seizures in adults due to the immature nervous system in children. Febrile seizures occur in 3% of children. Genetic factors account for 20% of childhood epilepsy cases.
It contains description and salient points to diagnose various epileptic encephalopathies seen during infancy such as early myoclonic encephalopathies, Otahara syndrome, Dravet syndrome, West syndrome.
This document provides definitions and information about seizures and epilepsy. It defines a seizure as a sudden wave of electrical activity in the brain that affects how a person feels or acts for a short time. Epilepsy is defined as a condition of the central nervous system where a person has had at least two seizures not caused by a known medical condition. It describes different types of seizures including partial and generalized seizures. It also discusses evaluation, treatment and management of epilepsy including use of antiepileptic drugs and factors related to treatment resistant epilepsy.
The Shake Down: An In-Depth Look at EpilepsyAmanda Furda
This document provides an overview of epilepsy in dogs and cats. It defines seizures and describes different types including generalized tonic-clonic, focal, and primary generalized seizures. Causes of seizures include structural abnormalities, idiopathic epilepsy which may have a genetic basis, and reactive seizures caused by systemic issues. Testing is recommended to rule out underlying metabolic or structural issues. Treatment involves medications while emergency management focuses on seizure termination and postictal care.
The shake down: An in depth look at epilepsyupstatevet
This document provides an in-depth overview of epilepsy in dogs and cats. It defines seizures, describes different seizure types including focal and generalized seizures. It discusses causes of seizures including idiopathic epilepsy which has a genetic basis in some breeds, structural epilepsy caused by brain abnormalities, and reactive seizures triggered by systemic issues. The document outlines testing, treatment including common anti-seizure medications like phenobarbital, and conditions that can mimic seizures.
Nonepileptic paroxysmal events are episodes that mimic seizures but do not result from abnormal cortical electrical activity. The most common types are syncope (fainting) and psychogenic seizures. Syncope can be neurally-mediated (e.g. vasovagal) where there are vegetative prodromal symptoms before loss of consciousness, or due to orthostatic hypotension on standing. Transient ischemic attacks from cerebrovascular issues can also mimic seizures. A detailed history of the episodes is important to differentiate epileptic from nonepileptic events.
The document discusses epilepsy, including its definition, causes, classification of seizures, and treatment. Epilepsy is defined as a group of disorders that cause recurrent, unprovoked seizures. Seizures are caused by abnormal electrical discharges in the brain and can have various causes including genetic defects, brain injuries, tumors, or lack of sleep. Seizures are classified as either partial/focal or generalized depending on where they originate and spread in the brain. Treatment involves anticonvulsant drugs which work by various mechanisms to prevent neuronal overexcitation as well as surgical removal of epileptic brain regions.
- Seizures are caused by abnormal excessive neuronal activity in the brain and can be classified as either partial or generalized seizures. Partial seizures originate in a localized region of the brain while generalized seizures involve both hemispheres.
- Common types of generalized seizures include absence seizures, characterized by brief lapses of consciousness, and tonic-clonic seizures which involve tonic muscle contraction followed by clonic movements.
- Complex partial seizures originate in the temporal lobe and involve psychic experiences such as hallucinations followed by automatisms like lip smacking and confusion after the seizure.
Similar to Navin agrawal syncope presentation (20)
A review of the growth of the Israel Genealogy Research Association Database Collection for the last 12 months. Our collection is now passed the 3 million mark and still growing. See which archives have contributed the most. See the different types of records we have, and which years have had records added. You can also see what we have for the future.
বাংলাদেশের অর্থনৈতিক সমীক্ষা ২০২৪ [Bangladesh Economic Review 2024 Bangla.pdf] কম্পিউটার , ট্যাব ও স্মার্ট ফোন ভার্সন সহ সম্পূর্ণ বাংলা ই-বুক বা pdf বই " সুচিপত্র ...বুকমার্ক মেনু 🔖 ও হাইপার লিংক মেনু 📝👆 যুক্ত ..
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A workshop hosted by the South African Journal of Science aimed at postgraduate students and early career researchers with little or no experience in writing and publishing journal articles.
ISO/IEC 27001, ISO/IEC 42001, and GDPR: Best Practices for Implementation and...PECB
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Date: May 29, 2024
Tags: Information Security, ISO/IEC 27001, ISO/IEC 42001, Artificial Intelligence, GDPR
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The simplified electron and muon model, Oscillating Spacetime: The Foundation...RitikBhardwaj56
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This slide is special for master students (MIBS & MIFB) in UUM. Also useful for readers who are interested in the topic of contemporary Islamic banking.
2. A Symptom…. Not A Diagnosis
“Human beings are falliable / fallable”-quote
Falling is not an abnormal phenomenon nor a recent
phenomenon
Owsei Temkin quoted the reasons of falling in his book “THE
FALLING SICKNESS”-a history of epilepsy from the Greek era
We aim to discuss the etiology and d/d and approach to various
causes of falling
FALL is a sudden unintentional change in position causing a
individual to land on a lower level object or ground.
7. SYNCOPE
Term syncope(greek:- synkope)literally syn means ‘with’
and koptein means ‘cessation’ or ‘cutting short’ or ‘pause
DEFINITION OF SYNCOPE:-sudden transient loss of
consciousness and postural tone with spontaneous
recovery
Cessation of cerebral blood supply for 6-8 sec or decrease
of systolic BP <60 mmhg or>20% drop in cerebral blood
supply is sufficient.
Syncope accounts for 3% to 5% of emergency room visits
and 1% to 3% of hospital admissions
8. CLINICAL FEATURES OF SYNCOPE
Sense of giddiness, lightheadedness, apprehension, may
sway, headache(sometimes) Vision may dim or close in
concentrically ,tinnitus may be +nt
Patients with neuro-cardiogenic syncope experience a
typical sense of warmth associated with sweating and a
sense of `greying out`. Cardiogenic syncope may be ppt by
arrthymias or chest pain
A hurtful fall is exceptional in the young
Patient is motionless. Skeletal muscles are fully relaxed .
Sphincter control is usually maintained . Body appears pale
9. CLINICAL FEATURES contd…
After syncope:-Retrograde amnesia esp in the elderly
,muscle ache fatigue with short lasting confusion(<5min)
Convulsive syncope:-mild asynchronous clonic jerk of
limbs and trunk with face twitching , occ. flexor jerking,
rarely tongue bite and urinary incontinence
EEG shows b/l synchronous delta and theta waves esp in
frontal lobes .Flattening may occur in prolonged cardiac
arrest (>15 sec).Epileptiform activity is not seen.
11. SEIZURES
Seizures are the most common neurogenic causes of drop
attacks.
GTCS , CPS , atonic seizures and negative myoclonus and may be
causes of sudden falls
A specific aura may precede
Incontinence , hurtful falls , tongue bite , post-ictal confusion(>
5 min) and motor manifestations are imp distinguishing
features
Atonic seizures are defined as epileptic attacks chr. by a sudden
loss or diminution of muscle tone, which may be fragmentary,
confined to a segment (limb, jaw, head), or massive, leading to a
slumping to the ground
12. Negative myoclonus is defined as an interruption of tonic muscular
activity (50 to 400 msec in duration), causing “instability” or, more
often, dropping of objects from the hands, head nodding, or falls
Epileptiform EEG in the inter ictal period is diagnostic
Biochemical parameters:-Serum prolactin , serum creatine kinase ,
serum ACTH(or cortisol), serum pH, body temperature
MRI can be used to identify seizure foci.
Response to anti-convulsants can also be used for differentiation
14. OTHER NEUROLOGICAL CAUSES OF
DROP ATTACKS
cerebrovascular disoders
drop attacks
cataplexy
third ventricular cyst (colloid cyst)
otolithic crises
progressive supranuclear palsy
basilar migraine
arnold chiari malfofmation
psychogenic syncope
creudzfeldt jacob disease(variant type)
corticobasal degeneration
intermittent spinal ischemia
Hyperexplexia(`jumping frenchman of maine`)
Frontal lobe ataxia
15. FALLS IN CEREBROVASCULAR DISORDERS
Very rare manifestation
Multiple occlusions of large arteries like in Takayasu`s
disease involving carotid and vertebral arteries
Subclavian steal syndrome
Subarachnoid hemorrhage:-raised ICT causes
momentary cessation of cerebral blood
supply(equalisation of pressure),usually associated
with severe headache and neck stiffness
16. Vertebrobasilar TIA or ischemia usually associated with
other signs of brainstem dysfunction
Does not occur in ischemia confined to carotid territory.
Cervical spine abnormalities like Klippel Feil`s syndrome
and cervical spondylosis
Acute lesions of the parieto- insular vestibular cortex due
to embolisation of middle cerebral artery can cause
imbalance of vestibular stimuli and can present as falls
without hemiparesis.
17. CAUSES OF VASCULAR ORIGIN
Most common cause of syncope,>33%
Types:-
1.ORTHOSTATIC HYPOTENSION: Definition
Cause:-autonomic dysfunction , hypovolemia , drug
,vasovagal
Symptoms
Worse early in the morning and after meals or exercise
Most common cause:-drugs like diuretics ,vasodilators ,alpha
blockers ,ace inhibitors , tranquilizers
Primary autonomic failure syndromes
19. 2.REFLEX MEDIATED FALLS: Vascular effects of neural signals come from nucleus
tractus solitarius
Types:Neurally mediated hypotension:-triggers include sight of
blood ,pain ,prolonged standing , warm environment
,stressful condition , physical injury particularly to
viscera (like testicles and gut)
20. -Carotid sinus hypersensitivity: Definition:- sinus pause>3 sec , systolic BP fall of >50
mm hg
Initiated on turning head to one side while wearing a
Tight collar or while shaving
usually in standing position.
21. CARDIAC CAUSES OF FALLS
Second most common cause ,10-20%
VT is the most common tachyarrhythmia causing
syncope
Structural heart diseases like aortic stenosis,
myocardial ischemia , mitral stenosis ,atrial myxoma
22. ECG FEATURES SUGGESTIVE OF
ARRYTHMOGENIC SYNCOPE
Bifascicular block (defined as either left bundle branch block or right bundle branch block
combined with left anterior or left posterior fascicular block)
Other intraventricular conduction abnormalities (QRS duration >0.12 seconds)
Mobitz I OR type 2 second degree atrioventricular block or complete heart block
Asymptomatic sinus bradycardia (<50 beats/min), sinoatrial block, or sinus pause >3 seconds
in the absence of negatively chronotropic medications
Pre-excited QRS complexes
Prolonged QT intervals
Right bundle branch block pattern with ST-elevation in leads V1-V3 (Brugada syndrome)
Negative T waves in right precordial leads, epsilon waves and ventricular late potentials
suggestive of arrhythmogenic right ventricular dysplasia
Q waves suggesting myocardial infarction
23.
24. CATAPLEXY
Narcolepsy/Cataplexy syndrome is chr. by
excessive daytime sleepiness
cataplexy
hypnagogic hallucinations
sleep paralysis
sudden fall associated with loss of body tone precipitated by
emotional change like anger or laughter
Part of syndrome associated with narcolepsy
The cataplexy associated with narcolepsy can be managed with tricyclic
antidepressants.
The excessive sleepiness is managed with stimulants, OR newer agents,
such as modafinil,
25. PROGRESSIVE SUPRANUCLEAR PALSY
Also known as Steele-Richardson-Olszewski syndrome, is a
neurodegenerative disease that affects cognition, eye
movements, and posture
Characteristics include supranuclear, primarily vertical,
gaze dysfunction accompanied by extrapyramidal
symptoms and cognitive dysfunction
The disease usually develops after the sixth decade of life,
and the diagnosis is purely clinical.
Currently, no therapy is proven to be effective.
26. THIRD VENTRICULAR CYST
Colloid cysts are nonmalignant tumors
Almost always found in the third ventricle
Classic symptoms of intermittent obstructive
hydrocephalus with paroxysmal headache associated
with changing head position
Sudden weakness in the lower limbs associated with
falls without loss of consciousness has been reported.
27. DROP ATTACKS
Also known as ‘maladie des genoux bleus’.
usually occurs in elderly women
Usually there is sudden onset loss of body tone and
weakness of legs . people drop on their knees .no
associated symptoms.
No loss of consciousness occurs
Vision, hearing ,speech remain intact
28. OTOLITHIC CRISIS
Also known as Tumarkin`s attacks.
It occurs without warning, vertigo, nausea or vomiting,
sweating, disequilibrium, loss of consciousness, numbness
or paralysis
the feeling of being pushed to the ground
There is no loss of consciousness
Sudden increase in labyrinthine pressure is responsible for
sudden onset vertigo
29. HYPEREXPLEXIA
An autosomal dominant trait(Chromosome 5) disorder in which
babies have an exaggerated startle reflex
Hypertonia (stiffness), exaggerated startle response in some
cases, epilepsy
Acute generalized Hypertonia (sudden stiffness) causing the
person to fall like a log to the ground
Startles can be elicited by lightly touching the person's nose,
clapping or making other noises, or suddenly jolting the person's
chair.
Tendency to umbilical and inguinal hernias and congenital
dislocation of the hip.
Good response to clonazepam , valproate and phenobarbitone
30. `JUMPING FRENCHMAN OF MAINE`
Genetic mutation that prevents "exciting" signals in the nervous
system from being regulated
type of hyperexplexia
An extended, grossly exaggerated startle response from a
"jumper," including crying out, flailing limbs, twitching, and
sometimes convulsions.
sufferers are sometimes teased mercilessly by people who find
the reaction amusing, and trigger it repeatedly.
Curiously patient has an automatic reflex to obey any order that
is delivered suddenly, echolalia is present
31. IDIOPATHIC SYNCOPE
Almost one third of all syncopal attacks
Positive tilt table test suggests neuro-cardiogenic cause
Repetitive and erratically spaced syncope without a
specific predisposing factor suggests an arrthymogenic
cause and Holter and EPS study must be done
32. HYSTERICAL FAINTING
Occurs in dramatic circumstances
Esp. in young females without evidence of cardiovascular
illness
Evident lack of change in pulse , blood pressure , or color of
the skin
Outward display of anxiety
General personality and behavioral characteristics of
hysteria.
33. SUBACUTE SCLEROSING PAN-ENCEPHALITIS
A rare chronic, progressive encephalitis
Chr by a h/o of primary measles infection before the age of 2
years, f/b several asymptomatic years (6–15 on average),
gradual, progressive psycho neurological deterioration, seizures,
myoclonus, ataxia, chorioretinitis , spasticity, and coma.
EEG shows periodic(every 5-8 sec) bursts of 2 to 3/sec high
voltage waves f/b flat pattern
CSF shows increased protein esp. gamma globulin (IgG Ab)
Eosinophilic inclusions is the histopathological hallmark
34. DIFFERENTIAL DIAGNOSIS
anxiety attacks and hyperventilation syndrome
hypoglycemia
concussion
sudden vascular collapse like ruptured aortic aneurysm ,
aortic dissection , pulmonary embolism , acute blood loss
cerebellar ataxia
vestibular neuronitis
normal pressure hydrocephalus
visual deficits induced collisions and mechanical falls
sporting injury related falls
38. INVESTIGATIONS
Holter
Event monitor
Loop recorder
of
Echo
Tilt table test
EP study
(frequent syncope , suggestive
ecg,0-4% yield)
(infrequent events not with
sudden LOC)
(infrequent events in
ambulatory patients, IOC in case
bradyarrythmias)
(orthostatic,YIELD <=60%)
-50-80% yield with SHD
-5-10% yield with no SHD
-less useful for bradyarrythmias
39. EEG
(for suspected epilepsy)
CT or MRI brain(for structural abnormalities and epileptic
foci) and for hematomas.
MRI Angio for cerebrovascular diseases in cases of TIA
Carotid Doppler (for suspected TIA)
CT chest in case of suspicion of pulmonary embolus
,ruptured aneurysm and aortic dissection
42. HEAD UP TILT TABLE TEST
UNMASKS LATENT VASO VAGAL
SYNCOPE
REPRODUCES THE PATIENT
SYNCOPE
DEVELOPS BETTER PATIENT
UNDERSTANDING OF HIS ILLNESS
AND ITS SYMPTOMS
ALLOWS THE PHYSICIAN TO
PROGNOSTICATE AND COUNSEL THE
PATIENT
C/I SEVERE LVOT
OBSTRUCTION,CRITICAL MITRAL
STENOSIS,SEVERE
CEREBROVASCULAR
STENOSIS,PROXIMAL CORONARY
ARTERY STENOSIS
43. Classification of positive responses
to tilt testing
Type 1 mixed. Heart rate falls at the time of syncope but the ventricular rate does not fall
to less than 40 bpm or falls to less than 40 bpm for less than 10 s with or without asystole
of less than 3 s. Blood pressure falls before the heart rate falls.
Type 2A cardio inhibition without asystole. Heart rate falls to a ventricular rate less
than40 bpm for more than 10 s but asystole of more than 3 s does not occur. Blood
pressure falls before the heart rate falls.
Type 2B cardio inhibition with asystole. Asystole occurs for more than 3 s. Blood pressure
fall coincides with or occurs before the heart rate fall.
Type 3 vasodepressor. Heart rate does not fall more than 10% from its peak at the time o f
syncope.
Exception 1. Chronotropic incompetence. No heart rate rise during tilt testing (i.e. less
than10% from the pre tilt rate).
Exception 2. Excessive heart rate rise. An excessive heart rate rise both at the onset of the
upright position and throughout its duration before syncope (i.e. greater than 130 bpm).
44.
45. TREATMENT
MANAGEMENT OF THE CAUSE
avoiding or precautions for provocative stimuli esp those
for vasovagal syncope like prolonged standing , stress
,blood donation ,extreme emotions ,nausea ,vomiting
,micturation ,defecation
in case of syncope patient should be made to lie down
with raising of legs ,tight clothing should be loosened,
inciting stimuli if possible should be removed
46. Salt and fluid consumption may be increased ,offending drugs
should be avoided
Drugs such as beta blockers ,midodrine ,fludrocortisone ,SSRI`s
have been tried
Management of specific arrthymias with drugs or pacemakers
patient counseling regarding behavior and occupational
rehabilitation
consideration of the psychological effects of the disease
47. THANK YOU
IF BY NOW YOU`RE TIRED AND FEEL LIKE FAINTING THIS FOR
YOU IS THE CARVED ANCIENT VICTORIAN FAINTING COUCH
48. PHYSICAL EXAMINATION
GENERAL EXAMINATION FOR
PALLOR,WEAKNESS,GENERAL HEALTH
POSTURAL BLOOD PRESSURE
DETAILED CARDIAC EXAMINATION
PULSE RATE,VOLUME,REGULARITY
SYSTEMIC EXAMINATION FOR SPECIFIC DISEASES