This document provides information on performing and interpreting nerve conduction studies. It discusses how peripheral nerves are stimulated electrically and the responses that are recorded, including compound motor action potentials, sensory nerve action potentials, and F-waves. It describes how to position electrodes and set stimulation parameters. Key aspects of the recorded waveforms like latency, amplitude, conduction velocity and abnormalities are defined. Common nerve conduction study techniques, interpretations, and limitations are also outlined.
This document discusses multiple sclerosis (MS), a chronic inflammatory demyelinating disease of the central nervous system. It defines MS and provides information on epidemiology, pathophysiology, categories of MS, and clinical features. The main types of MS are relapsing-remitting MS, primary progressive MS, and secondary progressive MS. Physiotherapy management of MS aims to address issues like sensory impairment, pain, weakness, spasticity, balance problems, and fatigue through techniques such as sensory treatment, strengthening exercises, flexibility exercises, and fatigue management.
This document provides an overview of localizing neurological lesions, including definitions of key terms like the central nervous system and peripheral nervous system. It describes various motor and sensory pathways in the brain and spinal cord. Conditions covered include the corticospinal system, stroke syndromes, multiple sclerosis, cerebellar syndrome, and motor neuron disease. For each, the causes, signs, investigations, and management are summarized. Clinical case scenarios are also provided to help localize neurological lesions.
The document provides guidance on performing a neurological examination. It outlines assessing the cranial nerves, reflexes, motor system, and sensory system. The cranial nerve examination involves testing each nerve individually. Reflex testing grades reflexes on a scale from 0 to 4. The motor exam evaluates muscle strength on a scale from 0 to 5. Finally, the sensory exam tests sensations like pain, touch, and position sense. The goal is to identify which parts of the neurological system may be affected.
This document provides an overview of approach to myopathy. It discusses types of muscle fibers, symptoms associated with myopathies including myalgia, fatigue, stiffness and others. It describes etiology such as acquired, hereditary and associated with systemic illness. Temporal evolution from onset in birth, childhood and adulthood is explained. Pattern of weakness like proximal, distal, axial and others and associated systemic symptoms are covered. Investigation approach including CK, EMG, muscle biopsy and genetic testing is summarized. Specific myopathies and their features are highlighted.
Thalamic pain syndrome is caused by a stroke in the thalamus region of the brain and results in centralized neuropathic pain that is worsened by temperature changes and often accompanied by hyperalgesia and allodynia. Recovery from a thalamic stroke focuses on restoring compromised abilities, though some side effects may not fully recover. The main cause of thalamic syndrome is a stroke, either hemorrhagic or ischemic, that occurs in the blood vessels of the thalamus region.
Cranial nerve assessment..Simple and Easy to perform for medics and Physiothe...pawan1physiotherapy
Cranial Nerve Assessment is a crucial step in neurological assessment. By following the simple theoretical aspects it can be made on your fingertips....here is an try to make the stuff easier for you....
This presentation is an introduction to the principles of Nerve Conduction Study and is entirely sourced from the book by David C Preston and Barbara E Shapiro: Electromyography and Neuromuscular disorders, 3rd Edition
This document provides information on performing and interpreting nerve conduction studies. It discusses how peripheral nerves are stimulated electrically and the responses that are recorded, including compound motor action potentials, sensory nerve action potentials, and F-waves. It describes how to position electrodes and set stimulation parameters. Key aspects of the recorded waveforms like latency, amplitude, conduction velocity and abnormalities are defined. Common nerve conduction study techniques, interpretations, and limitations are also outlined.
This document discusses multiple sclerosis (MS), a chronic inflammatory demyelinating disease of the central nervous system. It defines MS and provides information on epidemiology, pathophysiology, categories of MS, and clinical features. The main types of MS are relapsing-remitting MS, primary progressive MS, and secondary progressive MS. Physiotherapy management of MS aims to address issues like sensory impairment, pain, weakness, spasticity, balance problems, and fatigue through techniques such as sensory treatment, strengthening exercises, flexibility exercises, and fatigue management.
This document provides an overview of localizing neurological lesions, including definitions of key terms like the central nervous system and peripheral nervous system. It describes various motor and sensory pathways in the brain and spinal cord. Conditions covered include the corticospinal system, stroke syndromes, multiple sclerosis, cerebellar syndrome, and motor neuron disease. For each, the causes, signs, investigations, and management are summarized. Clinical case scenarios are also provided to help localize neurological lesions.
The document provides guidance on performing a neurological examination. It outlines assessing the cranial nerves, reflexes, motor system, and sensory system. The cranial nerve examination involves testing each nerve individually. Reflex testing grades reflexes on a scale from 0 to 4. The motor exam evaluates muscle strength on a scale from 0 to 5. Finally, the sensory exam tests sensations like pain, touch, and position sense. The goal is to identify which parts of the neurological system may be affected.
This document provides an overview of approach to myopathy. It discusses types of muscle fibers, symptoms associated with myopathies including myalgia, fatigue, stiffness and others. It describes etiology such as acquired, hereditary and associated with systemic illness. Temporal evolution from onset in birth, childhood and adulthood is explained. Pattern of weakness like proximal, distal, axial and others and associated systemic symptoms are covered. Investigation approach including CK, EMG, muscle biopsy and genetic testing is summarized. Specific myopathies and their features are highlighted.
Thalamic pain syndrome is caused by a stroke in the thalamus region of the brain and results in centralized neuropathic pain that is worsened by temperature changes and often accompanied by hyperalgesia and allodynia. Recovery from a thalamic stroke focuses on restoring compromised abilities, though some side effects may not fully recover. The main cause of thalamic syndrome is a stroke, either hemorrhagic or ischemic, that occurs in the blood vessels of the thalamus region.
Cranial nerve assessment..Simple and Easy to perform for medics and Physiothe...pawan1physiotherapy
Cranial Nerve Assessment is a crucial step in neurological assessment. By following the simple theoretical aspects it can be made on your fingertips....here is an try to make the stuff easier for you....
This presentation is an introduction to the principles of Nerve Conduction Study and is entirely sourced from the book by David C Preston and Barbara E Shapiro: Electromyography and Neuromuscular disorders, 3rd Edition
Part 1: Neurological history and physicaltschmitt2002
The document discusses assessment of the neurological system in adults. It outlines important information to gather prior to assessment, such as the location and effect of any lesions. The assessment examines level of consciousness, cranial nerves, motor function, reflexes, and more. Tests include the Glascow Coma Scale and evaluating responses of the central nervous system, peripheral nervous system, and specific areas like the cerebral cortex. The goal is to identify any abnormal signs or symptoms and select proper interventions.
Nerve conduction studies and electromyography are electrodiagnostic tests that can help diagnose neurological disorders. Nerve conduction studies measure how fast electrical signals travel through nerves, while electromyography detects electrical activity in muscles. Together these tests can identify conditions like carpal tunnel syndrome, radiculopathies, neuropathies, and myopathies. They provide information about whether a disorder affects nerve fibers or muscle, and whether damage is due to demyelination or axonal loss. Electrodiagnostic studies require specialized skills but can help diagnose common neurological problems and clarify uncertain cases seen in various medical specialties.
This document provides information about nerve conduction studies (NCS). It discusses the basic components of a NCS including compound muscle action potentials, sensory nerve action potentials, F-waves, and H-reflexes. It describes the procedure, techniques, and applications of NCS in evaluating conditions like neuropathies, radiculopathies, and neuromuscular junction disorders. Limitations include NCS only assessing the largest nerve fibers and conditions proximal to the dorsal root ganglia potentially showing normal results.
Special test for dermatomes and myotomesTafzz Sailo
The document discusses dermatomes and myotomes, which are areas of skin and muscles innervated by specific spinal nerve roots. It provides detailed instructions for testing dermatomes using pinprick and light touch tests and myotomes using resistance tests of individual muscle groups to evaluate potential nerve root injuries. Key points include identifying the spinal nerve roots that innervate specific areas of the upper and lower limbs and correlating weaknesses to the likely injured nerve roots. Diagrams depict dermatome and myotome maps to guide the clinical tests.
This document discusses current trends in the management of spasticity in hemiplegic patients. It defines spasticity as a velocity-dependent increase in muscle tone caused by damage to the central nervous system. Spasticity can range from mild muscle stiffness to severe, painful muscle spasms. If left untreated, spasticity may lead to muscle contractures, deformities, and other complications. Common treatments discussed include oral medications, botulinum toxin injections, physical therapy, and the modified Ashworth scale for assessing spasticity severity.
Nerve conduction studies are used to evaluate the function of motor and sensory nerves. They involve stimulating nerves with controlled electrical pulses and recording the responses. For motor nerve conduction studies, the compound muscle action potential is recorded from muscles. Key measurements are latency, amplitude, and conduction velocity. For sensory nerve conduction studies, the sensory nerve action potential is recorded from sensory nerves. Common sites tested include the median, ulnar, and sural nerves. The results can help diagnose various peripheral nerve and neuromuscular disorders.
Apraxia is an inability to correctly perform learned skilled movements due to a cognitive deficit in motor programming. It is broadly divided into limb apraxia and buccofacial apraxia. Limb apraxia includes ideomotor apraxia, ideational apraxia, and limb kinetic apraxia caused by lesions in the parietal lobe, frontal lobe, and connections between the two. Buccofacial apraxia involves an inability to perform skilled mouth and tongue movements and is associated with left frontal lesions. Apraxia is assessed through tasks like pantomiming tool use, imitation of gestures, and performing commands.
1) The document discusses the knee jerk reflex and stretch reflex, which are monosynaptic reflexes involving the muscle spindle.
2) The muscle spindle contains intrafusal fibers that act as proprioceptors. Primary and secondary endings in the muscle spindle sense changes in muscle length and relay signals to the spinal cord.
3) The stretch reflex arc involves muscle spindles sensing stretch and activating alpha motor neurons, causing contraction of the same muscle and opposing the stretch. This reflex helps maintain muscle tone and posture.
This document provides information about examining the motor system, including anatomy of motor pathways in the brain and spinal cord, inspection of muscles, and testing of muscle tone, power, and specific muscles. It describes how to examine muscles of the shoulder, elbow, wrist/hand, hip, and other areas, including specific tests to evaluate individual muscles like deltoid, biceps, gluteus maximus, and others. The document provides detailed instructions on posture and resistance for testing each muscle.
This document provides information about neurological examination and diseases. It begins with common neurological symptoms and then discusses commonly used terminology. It describes the goals and components of the neurological examination, including inspection of the mental state, cranial nerves, motor system, reflexes, sensation and special tests. Specific examination techniques are outlined for different parts of the body. Common neurological diseases are also listed. The document provides a thorough overview of performing and interpreting a neurological exam.
This document describes a case of Miller Fisher syndrome in a 24-year-old female patient presenting with gait instability, facial weakness, eye movement abnormalities, limb numbness, and dysphagia. Electrodiagnostic testing showed normal nerve conduction but abnormal sensory Ia afferent conduction, supporting a diagnosis of Miller Fisher syndrome. Key findings included hypotonia, areflexia, loss of the H-reflex, and decreased sensory evoked potentials attributed to increased intracranial pressure. The multiple cranial neuropathies with normal MRI and abnormal afferent conduction established a diagnosis of Miller Fisher syndrome associated with benign intracranial hypertension.
Anomalous Innervations in (EMG/NCS) by MurtazaMurtaza Syed
Anomalous Innervation.
These are the sort of normal variants which can be found in any normal subject or can concomitantly be found or superimposed in pathological cases. Identifying these anomalies helps out interpreting and making correct diagnosis and to avoid any misinterpretation.
1) The document discusses various approaches to evaluating and treating vertigo, including distinguishing between peripheral and central causes.
2) Diagnostic tests like Dix-Hallpike, VNG, and HINTS can help determine if vertigo is peripheral or central in nature and identify specific causes.
3) Treatment depends on the underlying cause but may include medications, repositioning maneuvers, vestibular rehabilitation, and in rare cases surgery.
This document discusses the Babinski sign and plantar reflex. It begins by defining the plantar reflex as the response to stimulation of the sole of the foot. It then describes Babinski's original 1896 observation of the pathological plantar reflex known as the Babinski sign, in which dorsiflexion of the toes occurs. The rest of the document covers the physiology and assessment of the plantar reflex and Babinski sign, variations, mimickers, and upper limb equivalents. It emphasizes that a positive Babinski sign indicates pyramidal tract dysfunction and underlying neurological disease.
The American Spinal Injury Association created the International Standards for Neurological Classification of Spinal Cord Injury to standardize how severity of spinal cord injuries are determined and documented. The standards provide a standardized examination of motor and sensory function to assess the extent of loss after an injury. It examines dermatomes and myotomes to determine the affected spinal cord segments. The examination involves detailed sensory and motor testing to determine sensory and motor levels, neurological level, and whether the injury is complete or incomplete.
This document provides an overview of disorders of the neuromuscular junction, including myasthenia gravis and Lambert-Eaton myasthenic syndrome. It discusses the classification, pathogenesis, clinical features, diagnosis and management of these conditions. Key points include that myasthenia gravis is caused by antibodies against acetylcholine receptors, often associated with thymoma, and presents with fatigueable muscle weakness. Lambert-Eaton syndrome involves antibodies against voltage-gated calcium channels and is commonly paraneoplastic, associated with small cell lung cancer. The document also briefly covers other acquired and congenital myasthenic syndromes, botulism, and other causes of impaired neuromuscular transmission.
The document discusses the sensory system and how it processes and transmits sensory information from peripheral receptors to the sensory cortex. It describes how different sensory modalities like pain, temperature, vibration and proprioception are carried by different nerve fiber types and pathways in the body. It provides details on testing various sensory modalities and how the patterns of sensory loss can help localize lesions to different parts of the central or peripheral nervous system.
The document describes tests that can be used to evaluate coordination, balance, gait, and posture in patients. It explains how to test for coordination by having patients perform rapidly alternating movements with their hands and point-to-point movements touching their nose and the examiner's finger. The Romberg test is described to test balance by having patients stand with their eyes closed. Gait is evaluated by having patients walk normally, heel-to-toe, on their toes, and on their heels. The wall test is provided to assess posture.
Case Review #1: 13 year old female with Scheurmanns KyphosisRobert Pashman
A 13 year old female presented with Kyphosis. She had a 75° curvature. Dr. Pashman performed a posterior spinal fusion T2-L2 and obtained a 44% reduction in her curvature.
This research report summarizes a study that collected data on four clinical tests (Six-Minute Walk Test, Berg Balance Scale, Timed Up & Go Test, and gait speeds) from 96 community-dwelling older adults aged 61-89 years. The study found:
1) The clinical tests showed high test-retest reliability.
2) Scores on the clinical tests declined with age for both male and female subjects, suggesting age-related performance changes.
3) Reference data on the tests should be used age-specifically when interpreting patient performance to account for expected age-related differences. Larger validation studies are still needed.
Part 1: Neurological history and physicaltschmitt2002
The document discusses assessment of the neurological system in adults. It outlines important information to gather prior to assessment, such as the location and effect of any lesions. The assessment examines level of consciousness, cranial nerves, motor function, reflexes, and more. Tests include the Glascow Coma Scale and evaluating responses of the central nervous system, peripheral nervous system, and specific areas like the cerebral cortex. The goal is to identify any abnormal signs or symptoms and select proper interventions.
Nerve conduction studies and electromyography are electrodiagnostic tests that can help diagnose neurological disorders. Nerve conduction studies measure how fast electrical signals travel through nerves, while electromyography detects electrical activity in muscles. Together these tests can identify conditions like carpal tunnel syndrome, radiculopathies, neuropathies, and myopathies. They provide information about whether a disorder affects nerve fibers or muscle, and whether damage is due to demyelination or axonal loss. Electrodiagnostic studies require specialized skills but can help diagnose common neurological problems and clarify uncertain cases seen in various medical specialties.
This document provides information about nerve conduction studies (NCS). It discusses the basic components of a NCS including compound muscle action potentials, sensory nerve action potentials, F-waves, and H-reflexes. It describes the procedure, techniques, and applications of NCS in evaluating conditions like neuropathies, radiculopathies, and neuromuscular junction disorders. Limitations include NCS only assessing the largest nerve fibers and conditions proximal to the dorsal root ganglia potentially showing normal results.
Special test for dermatomes and myotomesTafzz Sailo
The document discusses dermatomes and myotomes, which are areas of skin and muscles innervated by specific spinal nerve roots. It provides detailed instructions for testing dermatomes using pinprick and light touch tests and myotomes using resistance tests of individual muscle groups to evaluate potential nerve root injuries. Key points include identifying the spinal nerve roots that innervate specific areas of the upper and lower limbs and correlating weaknesses to the likely injured nerve roots. Diagrams depict dermatome and myotome maps to guide the clinical tests.
This document discusses current trends in the management of spasticity in hemiplegic patients. It defines spasticity as a velocity-dependent increase in muscle tone caused by damage to the central nervous system. Spasticity can range from mild muscle stiffness to severe, painful muscle spasms. If left untreated, spasticity may lead to muscle contractures, deformities, and other complications. Common treatments discussed include oral medications, botulinum toxin injections, physical therapy, and the modified Ashworth scale for assessing spasticity severity.
Nerve conduction studies are used to evaluate the function of motor and sensory nerves. They involve stimulating nerves with controlled electrical pulses and recording the responses. For motor nerve conduction studies, the compound muscle action potential is recorded from muscles. Key measurements are latency, amplitude, and conduction velocity. For sensory nerve conduction studies, the sensory nerve action potential is recorded from sensory nerves. Common sites tested include the median, ulnar, and sural nerves. The results can help diagnose various peripheral nerve and neuromuscular disorders.
Apraxia is an inability to correctly perform learned skilled movements due to a cognitive deficit in motor programming. It is broadly divided into limb apraxia and buccofacial apraxia. Limb apraxia includes ideomotor apraxia, ideational apraxia, and limb kinetic apraxia caused by lesions in the parietal lobe, frontal lobe, and connections between the two. Buccofacial apraxia involves an inability to perform skilled mouth and tongue movements and is associated with left frontal lesions. Apraxia is assessed through tasks like pantomiming tool use, imitation of gestures, and performing commands.
1) The document discusses the knee jerk reflex and stretch reflex, which are monosynaptic reflexes involving the muscle spindle.
2) The muscle spindle contains intrafusal fibers that act as proprioceptors. Primary and secondary endings in the muscle spindle sense changes in muscle length and relay signals to the spinal cord.
3) The stretch reflex arc involves muscle spindles sensing stretch and activating alpha motor neurons, causing contraction of the same muscle and opposing the stretch. This reflex helps maintain muscle tone and posture.
This document provides information about examining the motor system, including anatomy of motor pathways in the brain and spinal cord, inspection of muscles, and testing of muscle tone, power, and specific muscles. It describes how to examine muscles of the shoulder, elbow, wrist/hand, hip, and other areas, including specific tests to evaluate individual muscles like deltoid, biceps, gluteus maximus, and others. The document provides detailed instructions on posture and resistance for testing each muscle.
This document provides information about neurological examination and diseases. It begins with common neurological symptoms and then discusses commonly used terminology. It describes the goals and components of the neurological examination, including inspection of the mental state, cranial nerves, motor system, reflexes, sensation and special tests. Specific examination techniques are outlined for different parts of the body. Common neurological diseases are also listed. The document provides a thorough overview of performing and interpreting a neurological exam.
This document describes a case of Miller Fisher syndrome in a 24-year-old female patient presenting with gait instability, facial weakness, eye movement abnormalities, limb numbness, and dysphagia. Electrodiagnostic testing showed normal nerve conduction but abnormal sensory Ia afferent conduction, supporting a diagnosis of Miller Fisher syndrome. Key findings included hypotonia, areflexia, loss of the H-reflex, and decreased sensory evoked potentials attributed to increased intracranial pressure. The multiple cranial neuropathies with normal MRI and abnormal afferent conduction established a diagnosis of Miller Fisher syndrome associated with benign intracranial hypertension.
Anomalous Innervations in (EMG/NCS) by MurtazaMurtaza Syed
Anomalous Innervation.
These are the sort of normal variants which can be found in any normal subject or can concomitantly be found or superimposed in pathological cases. Identifying these anomalies helps out interpreting and making correct diagnosis and to avoid any misinterpretation.
1) The document discusses various approaches to evaluating and treating vertigo, including distinguishing between peripheral and central causes.
2) Diagnostic tests like Dix-Hallpike, VNG, and HINTS can help determine if vertigo is peripheral or central in nature and identify specific causes.
3) Treatment depends on the underlying cause but may include medications, repositioning maneuvers, vestibular rehabilitation, and in rare cases surgery.
This document discusses the Babinski sign and plantar reflex. It begins by defining the plantar reflex as the response to stimulation of the sole of the foot. It then describes Babinski's original 1896 observation of the pathological plantar reflex known as the Babinski sign, in which dorsiflexion of the toes occurs. The rest of the document covers the physiology and assessment of the plantar reflex and Babinski sign, variations, mimickers, and upper limb equivalents. It emphasizes that a positive Babinski sign indicates pyramidal tract dysfunction and underlying neurological disease.
The American Spinal Injury Association created the International Standards for Neurological Classification of Spinal Cord Injury to standardize how severity of spinal cord injuries are determined and documented. The standards provide a standardized examination of motor and sensory function to assess the extent of loss after an injury. It examines dermatomes and myotomes to determine the affected spinal cord segments. The examination involves detailed sensory and motor testing to determine sensory and motor levels, neurological level, and whether the injury is complete or incomplete.
This document provides an overview of disorders of the neuromuscular junction, including myasthenia gravis and Lambert-Eaton myasthenic syndrome. It discusses the classification, pathogenesis, clinical features, diagnosis and management of these conditions. Key points include that myasthenia gravis is caused by antibodies against acetylcholine receptors, often associated with thymoma, and presents with fatigueable muscle weakness. Lambert-Eaton syndrome involves antibodies against voltage-gated calcium channels and is commonly paraneoplastic, associated with small cell lung cancer. The document also briefly covers other acquired and congenital myasthenic syndromes, botulism, and other causes of impaired neuromuscular transmission.
The document discusses the sensory system and how it processes and transmits sensory information from peripheral receptors to the sensory cortex. It describes how different sensory modalities like pain, temperature, vibration and proprioception are carried by different nerve fiber types and pathways in the body. It provides details on testing various sensory modalities and how the patterns of sensory loss can help localize lesions to different parts of the central or peripheral nervous system.
The document describes tests that can be used to evaluate coordination, balance, gait, and posture in patients. It explains how to test for coordination by having patients perform rapidly alternating movements with their hands and point-to-point movements touching their nose and the examiner's finger. The Romberg test is described to test balance by having patients stand with their eyes closed. Gait is evaluated by having patients walk normally, heel-to-toe, on their toes, and on their heels. The wall test is provided to assess posture.
Case Review #1: 13 year old female with Scheurmanns KyphosisRobert Pashman
A 13 year old female presented with Kyphosis. She had a 75° curvature. Dr. Pashman performed a posterior spinal fusion T2-L2 and obtained a 44% reduction in her curvature.
This research report summarizes a study that collected data on four clinical tests (Six-Minute Walk Test, Berg Balance Scale, Timed Up & Go Test, and gait speeds) from 96 community-dwelling older adults aged 61-89 years. The study found:
1) The clinical tests showed high test-retest reliability.
2) Scores on the clinical tests declined with age for both male and female subjects, suggesting age-related performance changes.
3) Reference data on the tests should be used age-specifically when interpreting patient performance to account for expected age-related differences. Larger validation studies are still needed.
This document outlines a coordination test consisting of 13 tasks to assess finger dexterity, pronation, supination, finger-to-nose movements, rapid alternating hand movements, precision finger tapping, heel-shin sliding, overshooting a target, speech while performing rapid hand movements, tremor detection, rebound from touch, reflex checks, toe-to-finger touching, and ability to maintain a stance.
The document outlines the components of a neurological exam, including tests of mental status, cranial nerves, reflexes, motor skills, sensory function, and cerebellar function. It describes assessments of level of consciousness using the Glasgow Coma Scale and provides details on performing and grading common reflex tests. The summary should evaluate the neurological status, note any pertinent abnormalities, and list active interventions.
The document describes several ascending pathways in the spinal cord that transmit sensory information to the brain. It focuses on the dorsal column medial lemniscal pathway, which transmits information about touch, pressure, vibration and proprioception. This pathway involves three neurons: primary sensory neurons that travel through dorsal roots to the spinal cord, secondary neurons that form tracts in the spinal cord and brainstem, and tertiary neurons that connect the thalamus to the primary sensory cortex. Damage to this pathway results in the loss of discriminative touch and proprioception below the level of lesion.
This document outlines the components and purpose of a scanning examination performed in physical therapy. The scanning exam is used to ensure issues are within the scope of physical therapy and rule out serious pathology. It involves observation of gait and posture, vital signs, functional movement testing, tissue tension testing, palpation, neurological exams, and special tests. The purpose is to detect gross loss of function and movement control in order to guide further physical therapy diagnosis and treatment.
This document discusses the somatosensory system including sensory receptors, pathways, and patterns of sensory loss. It describes the different types of sensory receptors, including those that mediate touch, pain, temperature, vibration and proprioception. The pathways from receptors to the thalamus and cortex are outlined. Methods for examining sensation are provided along with different patterns of sensory loss including peripheral, segmental, conductive, cortical and functional syndromes. Potential causes of various sensory loss patterns are listed.
Dr. Donald Corenman, M.D., D.C. (http://neckandback.com), is a Vail spine surgeon specializing in all conditions of the spine and has written countless medical articles on spine related disorders including Scheuermann’s Disease—a disease marked by a curvature of the spine and a sagittal plane deformity. This presentation focuses on Scheuermann’s Disease and provides an in-depth look at the disorder. It discusses the symptoms, classifications and treatment options. It also provides a look at what a normal sagittal plane looks like vs a sagittal plane deformity. A curvature of the spine is also a symptom of scoliosis and kyphosis.
Dr. Corenman is a renowned Vail spine surgeon and also is an expert at degenerative spinal conditions including degenerative disc disease, spinal stenosis, sciatica, and spondylolythesis. He is also a sports medicine specialist and treats athletes with traumatic sports related injuries. He recently launched his own website (http://neckandback.com) to educate patients on spine disorders and to offer second opinions to physicians and colleagues who are seeking additional information on specific spine injuries and treatment options.
The document discusses planning and constructing tests to measure psychomotor skills. It provides examples of tests for different components of fitness and skill-related abilities. A sample vertical jump test is described in detail, including the test, objective, validity, equipment, procedures, scoring, and norms. The document emphasizes following proper procedures to develop valid and reliable tests that safely and accurately evaluate psychomotor abilities.
The document provides information on performing a sensory examination, including testing superficial sensations like pain, temperature, and touch. It also describes evaluating deep sensations such as proprioception, vibration, and kinesthesia. Finally, it discusses assessing combined cortical sensations including stereognosis, graphesthesia, and two-point discrimination. The examination involves testing various areas of the body using specific tools and techniques, and having the patient respond verbally or by physical demonstration to identify sensations.
The patient is a 75-year-old female who suffered a right superior and inferior pubic rami fracture from a fall at home. She has multiple medical comorbidities and is at high risk for falls. The initial physical therapy evaluation found significant impairments in gait, balance, and functional mobility. Short and long term goals were created to improve strength, range of motion, transfers, ambulation, and fall risk through a plan of care involving therapeutic exercises, gait training, and patient education.
The document provides guidance on performing a neurologic examination. It outlines examining various aspects of cerebral function, the 12 cranial nerves, motor skills, sensory function, and reflexes. For each component, it describes the tests to perform and what normal and abnormal findings may indicate, such as signs of nerve damage or increased intracranial pressure. The goal is to indirectly evaluate neurologic function through assessing specific body parts controlled by the brain and peripheral nervous system.
The document provides guidance on conducting a general physical examination in psychiatry. It outlines the importance of screening for physical disorders that may present with psychiatric symptoms. The general physical exam should evaluate overall appearance, vital signs, and specific organ systems. For psychiatric patients, the exam aims to identify any medical conditions contributing to their mental state. Neurological exams are particularly important to detect signs of focal brain lesions or diffuse cerebral dysfunction. Certain physical exam findings can help differentiate conversion disorder from organic conditions.
The document provides an overview of coordination and its assessment. It defines coordination as the ability to execute smooth, accurate movements through integration of the motor, cerebellar, vestibular and sensory systems. Coordination involves appropriate speed, direction, muscle tension and synergist influences. Coordination deficits are often related to conditions involving the cerebellum, basal ganglia or dorsal columns. Common tests of coordination include finger-to-nose, heel-to-knee, rapid alternating movements and Romberg's test. Treatment focuses on techniques like PNF, balance exercises, and Frenkel's exercises to improve coordination.
1. The document discusses examination of the cranial nerves and neurological system. Key tests described include evaluation of gait, stance, speech, mental status and cranial nerves I-XII.
2. Specific disorders are discussed such as types of dysarthria and dysphasia, optic nerve conditions seen on fundoscopy, and lesions affecting cranial nerves.
3. Examination techniques are provided for assessing conditions of the cranial nerves including testing of smell, hearing, eye movements, facial strength, and vestibular function.
Motor and sensory examination, Examination of reflexesNahry Omer
This document discusses reflexes, dividing them into superficial and deep tendon reflexes. Superficial reflexes are elicited by striking the skin or mucous membranes and include the plantar reflex elicited by stroking the sole of the foot and abdominal reflexes elicited by stroking the abdomen. Deep tendon reflexes involve tapping tendons to elicit muscle contractions and include reflexes of the biceps, triceps, patellar, and Achilles tendons. Reflexes are typically graded from 0 to 4 based on their activity level.
This neurological examination document provides details on:
1) The history, presenting complaints, family history, and review of systems to obtain for a neurological exam.
2) The components of the neurological exam including motor function, sensory function, cranial nerves, reflexes, and mental status.
3) Descriptions of how to examine each system, what abnormalities to look for, and what they may indicate. Rating scales are provided for things like strength, reflexes, and level of consciousness.
4) Common gait patterns and their potential causes are listed at the end.
This document provides a detailed outline for examining a patient with paraplegia. It begins with the history of present illness including date of onset, mode of onset, precipitating factors, and evolution of paralysis. It then discusses the patient's past medical history, family history, and sensory symptoms. The remainder of the document outlines the physical examination, including assessments of the spine, nervous system, motor functions, sensory functions, reflexes, and other body systems.
A neurological examination evaluates the functioning of the nervous system, including sensory, motor, and cognitive abilities. It involves tests of mental status, cranial nerves, motor skills, sensation, reflexes, and cerebellar function. The purposes are to identify or rule out nervous system diseases, aid diagnosis, guide treatment, and monitor changes over time. Nurses are responsible for ensuring a calm environment, accurately documenting exam findings, and informing doctors of any changes.
1. The document outlines a lesson plan for teaching nursing students about neurological assessment. It includes objectives, content, teaching methods, and an evaluation plan.
2. The content section defines neurological assessment and lists its purposes. It also describes the components of a neurological exam including vital signs, consciousness, motor function, and cranial nerve assessment.
3. The document explains how to assess various parts of the neurological exam in detail, such as the Glasgow Coma Scale for consciousness, cranial nerve examination techniques, and evaluating the motor system.
The neurological examination assesses the nervous system and consists of 8 aspects: 1) level of consciousness 2) mental status 3) special cerebral functions 4) cranial nerve function 5) motor function 6) sensory function 7) cerebellar function 8) reflexes. The exam evaluates various mental, sensory, and motor skills to detect abnormalities that could indicate neurological diseases.
This document discusses concepts and applications for knee rehabilitation. It covers several key points, including how injury affects proprioception, gait, and recovery duration. Specifically, it notes that an ACL injury can decrease proprioception for 1-3 years and alter muscle activation timing and recruitment. It also discusses developing a neuromuscular rehabilitation program with a functional focus, using exercises that provide cognitive sensory-motor challenges to facilitate motor learning. Finally, it emphasizes taking a functional approach to rehabilitation by using a patient's own movement patterns whenever possible.
The following file is about the most important procedures of neurological examination and has been taught in PBL class by MohammadSaleh Moallem.
A neurological examination is the assessment of sensory neuron and motor responses, especially reflexes, to determine whether the nervous system is impaired. This typically includes a physical examination and a review of the patient's medical history. In general, a neurological examination is focused on finding out whether there are lesions in the central and peripheral nervous systems or there is another diffuse process that is troubling the patient.
The results of the examination are taken together to anatomically identify the lesion. Finally, it is the role of the physician to find the cause for why such a problem has occurred.
Presented by: Mohammadsaleh Moallem
The document discusses the neurological examination process. It describes the various components that are assessed which include levels of consciousness, mental status, cranial nerve function, motor skills, sensation, cerebellar function, and reflexes. Nurses play an important role in conducting and documenting the neurological examination to evaluate the presence of any disease in the nervous system.
A presentation that talks about the Human Nervous System, the cranial nerves and the Neuro Assessment required to check if the nervous system is functioning properly.
The document provides an overview of performing a neurological examination, which includes obtaining a thorough health history, conducting a physical exam assessing five components (cerebral function, cranial nerves, motor system, sensory system, and reflexes), and ordering diagnostic tests. The physical exam progresses from higher levels of cortical function to lower levels and tests things like mental status, cranial nerves, muscle strength, coordination, balance, reflexes, and sensory function. Common diagnostic tests mentioned are CT, MRI, EEG, EMG, lumbar puncture, and CSF analysis.
This document summarizes the management of tremor and spasticity in multiple sclerosis. It discusses tremor, including types, assessment, and interventions like physiotherapy, oral medications, botulinum toxin injections, and deep brain stimulation. It also covers spasticity, defining it as part of the upper motor neuron syndrome and discussing its impact. Assessment of spasticity is highlighted as key to management. A multidisciplinary team approach is advocated to accurately assess issues, determine treatment goals, and provide non-pharmacological and pharmacological interventions.
In 3 sentences:
Physical therapists Gretchen Leff and Lauren Jarmusz presented on the physical therapy approach to spine care. They discussed using a movement systems framework to assess for impairments in mobility, motor control, and functional movement patterns. Treatment focuses on addressing impairments through local mobility interventions to improve neural, joint and soft tissue mobility, followed by global stability training to develop proper muscle activation, coordination and application to functional skills.
This document provides guidance on performing a neurological assessment. It defines a neurological exam and explains that it is used to evaluate a patient's brain function and motor response. The assessment includes checking the patient's level of consciousness using the Glasgow Coma Scale, pupillary response, limb movement, strength, and vital signs. It outlines how to perform each part of the exam and what to note for things like eye opening, best verbal response, motor response, and limb movement. The neurological observation form is used to record the assessment findings. Any changes in neurological status should be reported immediately to the physician.
This document provides an overview of cerebral palsy, including its definition, epidemiology, clinical manifestations, classifications, assessments, deformities, diagnostic tests, treatment goals, and treatment options. Cerebral palsy is a non-progressive brain disorder that causes motor impairments in children, including issues with movement, coordination, and muscle tone. Treatment is multidisciplinary and focuses on improving mobility and function through therapies, medications, and sometimes surgery. The goals are maximizing independence and community integration while preventing complications.
Fitness first 2012 c exa flexibility presentationMax Martin
This document discusses flexibility and movement. It explains that tightness can be caused by sedentary lifestyles, injury, poor nutrition, and age. Research shows that stretching provides flexibility gains, especially for tighter muscles, though regular stretching may provide more performance benefits than pre-exercise stretching. Myofascial release techniques like self-massage and foam rolling can improve range of motion and reduce muscle soreness. A comprehensive flexibility program incorporates assessment, exercises to address muscle imbalances, self-myofascial release, stretching, and functional movement training.
The document provides information on the anatomy and physiology of the nervous system. It discusses the three main parts of the nervous system: central nervous system (brain and spinal cord), peripheral nervous system (cranial and spinal nerves), and autonomic nervous system (sympathetic and parasympathetic). It describes the structures and lobes of the brain. It also outlines the general functions of the nervous system in controlling the body, receiving stimuli, and determining responses. The document then discusses assessment and examination of the nervous system, including consciousness, cranial nerves, motor skills, sensation, and reflexes. Finally, it covers various diagnostic tests and evaluations like CT scans, MRI, EEGs, and lumbar punctures to analyze CSF.
The document discusses various facilitation and inhibition techniques used in physical therapy, outlining the theoretical basis, principles, receptors involved, differences between the techniques, guidelines for application, and clinical implications. It provides detailed descriptions of numerous proprioceptive and cutaneous facilitation techniques including quick stretch, tapping, joint compression, as well as inhibitory techniques like maintained stretch and cooling. The techniques aim to normalize muscle tone and facilitate or inhibit motor responses depending on a patient's needs.
1. The regulation of posture and movement involves integration at multiple levels of the central nervous system, from the spinal cord to the cortex.
2. At the spinal cord level, afferent inputs produce simple reflex responses, while higher centers produce more complex responses and motor behavior.
3. Isolating centers through experimental lesions allows studying their specific influence on posture and movement.
The study aimed to determine if individuals accurately perceive aerobic exercise intensities as defined by ACSM guidelines. Five subjects completed a graded exercise test while rating perceived intensity. Actual intensity level was determined from oxygen consumption. Results showed a strong agreement between perceived and actual intensity levels, with a Cohen's Kappa of 0.722. This suggests individuals can accurately self-regulate exercise intensity using ratings of perceived exertion.
This document summarizes thalassemia, a hereditary blood disorder caused by reduced or absent production of hemoglobin A. It describes the main types (alpha and beta thalassemia), clinical features like anemia and jaundice, diagnostic testing, and management which includes lifelong blood transfusions and iron chelation therapy to prevent complications from iron overload. The most severe forms can be fatal without treatment while milder forms may cause few symptoms.
Suffocation is a general term used to indicate death due to lack of oxygen from either lack of oxygen in the breathable environment or obstruction of external air passages. Asphyxia is caused by lack of oxygen in respired air leading to hypoxaemia and hypercapnia. Smothering causes asphyxia through mechanical obstruction of the external airways (nose and mouth). Suicidal smothering often involves placing a plastic bag over the head in an attempt to cut off oxygen. Classic signs of asphyxia include petechial hemorrhages, cyanosis, congestion, and soft tissue swelling due to increased venous pressure and fluid leakage from blood vessels.
Road accidents typically cause gross musculoskeletal or organ damage, severe haemorrhaging, airway blockage from blood, or traumatic asphyxiation from chest crushing. Railway suicides often result in decapitation or extensive body disintegration from being struck by a fast-moving train. Toxicology screens should be performed to check for alcohol or drugs which may have contributed to suicidal behavior. Electrical injuries may also complicate cases where high-voltage train systems are involved.
Strangulation, hanging, suffocation, road/railway injuries, and electrocution are common methods of suicidal death. Strangulation causes asphyxia by compressing the neck and blocking blood flow and air passage to the brain. Hanging causes cerebral hypoxia by compressing the neck and jugular veins. Suffocation involves blocking external airways. Road/railway injuries typically cause severe trauma, hemorrhage or organ damage. Electrocution usually causes cardiac arrhythmias and ventricular fibrillation leading to cardiac arrest. Autopsies look for neck furrows, petechiae, internal injuries or electrical marks depending on the method.
Retinitis pigmentosa is a slow degenerative, hereditary disease of the retina that involves the rods and cones. It typically appears as a recessive trait due to consanguinity of the parents. Patients experience night blindness in childhood, tunnel vision or central visual loss in middle age, and complete blindness in advanced age. Physical examination shows black spots resembling bone corpuscles across the retina, extremely attenuated retinal blood vessels, and pale optic discs, indicating optic nerve atrophy. There is no specific treatment currently available, but cataract surgery and rehabilitation services can help manage complications.
This document discusses refractive errors of the eye, including emmetropia, myopia, and hypermetropia. Emmetropia is the normal optical condition where light focuses on the retina. Myopia, or near-sightedness, occurs when light focuses in front of the retina. Symptoms include indistinct distant vision. Hypermetropia, or far-sightedness, is when light focuses behind the retina, causing blurred near vision and eye strain. Both conditions are typically corrected with spectacles, while myopia can also be treated through surgical procedures like LASIK in some cases.
This document provides guidance on evaluating patients presenting with gradual loss of vision. It outlines taking a history to determine factors like onset, progression, associated symptoms and medical history. The physical exam involves assessing visual acuity, the red reflex, visual fields and optic nerve/macula. Common causes of gradual vision loss include glaucoma, refractive error, cataract, diabetic retinopathy and age-related macular degeneration. Treatment depends on the underlying cause but may involve prescription lenses, medical management or referral for further evaluation.
Glaucoma is a group of eye conditions that damage the optic nerve, often caused by an increase in intraocular pressure. The aqueous humour maintains pressure in the eye and normally flows through the anterior chamber, draining out of the eye. In glaucoma, the drainage pathways become blocked, increasing pressure and damaging the optic nerve. There are several types of glaucoma including open-angle glaucoma, the most common type caused by slow drainage blockage, and closed-angle glaucoma caused by physical blockage of drainage canals. Treatment aims to lower pressure through eye drops or surgery and slow progression of vision loss.
ELECTROCUTION (suicidal)
- The most common cause of death from electrocution is cardiac arrhythmias leading to ventricular fibrillation and cardiac arrest. Less commonly, respiratory arrest can occur if the current passes through the thorax, causing spasms or paralysis of intercostal muscles and the diaphragm.
- External signs include an areola of blanched skin at the contact points and possible "crocodile skin" lesions from sparking over several centimeters if voltages were in the kilovolt range. Internal autopsy findings are often absent or non-specific since the most common mode of death is cardiac arrhythmia.
Diabetic retinopathy is a complication of diabetes mellitus where changes occur in the retina. It is a leading cause of vision loss among working age adults in Malaysia. The risk of retinopathy rises with longer duration of diabetes and poor blood glucose control. Annual eye screening is recommended to detect early signs and plan treatment. Laser photocoagulation is commonly used to treat early stages while vitrectomy may be used for advanced proliferative cases with vitreous hemorrhage. Anti-VEGF drugs combined with laser can also treat diabetic macular edema.
Cataracts are a clouding of the lens of the eye that can cause gradual vision loss. They are usually caused by aging but can be caused by other factors like diabetes, smoking, or UV exposure. Cataracts are diagnosed based on a decrease in the red reflex seen during eye exams. They can be treated surgically through phacoemulsification to remove the clouded lens and replace it with an intraocular lens, improving vision. Age-related macular degeneration (AMD) is a disease of the macula that causes central vision loss. Dry AMD involves drusen buildup while wet AMD has abnormal blood vessel growth. Treatments include vitamins for dry AMD and anti-VEGF injections or photod
The document summarizes the three stages of swallowing (deglutition):
1) Buccal stage where the tongue retracts forcing the bolus into the oropharynx.
2) Pharyngeal stage is involuntary where the soft palate and larynx elevate to prevent food entering the nasal cavity and lungs. The bolus moves into the upper esophagus.
3) Esophageal stage where peristalsis propels the bolus through the esophagus and into the stomach over 8-20 seconds while the lower esophageal and stomach sphincters relax.
The document describes a case of a 26-year-old man presenting with facial swelling, lumps in his armpits, chest pain for 3 months, and weight loss over 6 months. Examination found nail clubbing and a chest X-ray showed abnormalities. Biopsy and scans confirmed stage IV lung cancer. Nail clubbing is associated with lung diseases and cancers and results from vascular changes and growth factors from the lungs. Different types of biopsies are used to diagnose cancers including needle, endoscopic, and surgical biopsies. The anatomy of the chest is also described including structures like the ribs, sternum, and thoracic skeleton that make up the rib cage.
Mr. Lim, a 47-year-old man, presented with abdominal pain and diarrhea. Endoscopy revealed a duodenal ulcer and CT scan showed a 3cm pancreatic head mass suspected to be a gastrinoma. Laboratory tests found highly elevated gastrin and basal gastric acid levels consistent with Zollinger-Ellison Syndrome. Further tests demonstrated increased gastrin response to secretin stimulation, confirming a gastrin-secreting pancreatic tumor as the cause of his symptoms. Complications of ZES include peptic ulcers, diarrhea from excess acid inactivating pancreatic enzymes, and potential malignant spread of gastrinomas. Omeprazole was prescribed to reduce gastric acid levels and treat his
Are you looking for a long-lasting solution to your missing tooth?
Dental implants are the most common type of method for replacing the missing tooth. Unlike dentures or bridges, implants are surgically placed in the jawbone. In layman’s terms, a dental implant is similar to the natural root of the tooth. It offers a stable foundation for the artificial tooth giving it the look, feel, and function similar to the natural tooth.
Spontaneous Bacterial Peritonitis - Pathogenesis , Clinical Features & Manage...Jim Jacob Roy
In this presentation , SBP ( spontaneous bacterial peritonitis ) , which is a common complication in patients with cirrhosis and ascites is described in detail.
The reference for this presentation is Sleisenger and Fordtran's Gastrointestinal and Liver Disease Textbook ( 11th edition ).
Osvaldo Bernardo Muchanga-GASTROINTESTINAL INFECTIONS AND GASTRITIS-2024.pdfOsvaldo Bernardo Muchanga
GASTROINTESTINAL INFECTIONS AND GASTRITIS
Osvaldo Bernardo Muchanga
Gastrointestinal Infections
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.
Gastritis and Gastric Health
Gastric Health is one of the most relevant concerns in human health, with gastrointestinal infections being among the main illnesses that affect humans.
Among gastric problems, we have GASTRITIS AND GASTRIC ULCERS as the main public health problems. Gastritis and gastric ulcers normally result from inflammation and corrosion of the walls of the stomach (gastric mucosa) and are generally associated (caused) by the bacterium Helicobacter pylor, which, according to the literature, this bacterium settles on these walls (of the stomach) and starts to release urease that ends up altering the normal pH of the stomach (acid), which leads to inflammation and corrosion of the mucous membranes and consequent gastritis or ulcers, respectively.
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.
- Video recording of this lecture in English language: https://youtu.be/Pt1nA32sdHQ
- Video recording of this lecture in Arabic language: https://youtu.be/uFdc9F0rlP0
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
PGx Analysis in VarSeq: A User’s PerspectiveGolden Helix
Since our release of the PGx capabilities in VarSeq, we’ve had a few months to gather some insights from various use cases. Some users approach PGx workflows by means of array genotyping or what seems to be a growing trend of adding the star allele calling to the existing NGS pipeline for whole genome data. Luckily, both approaches are supported with the VarSeq software platform. The genotyping method being used will also dictate what the scope of the tertiary analysis will be. For example, are your PGx reports a standalone pipeline or would your lab’s goal be to handle a dual-purpose workflow and report on PGx + Diagnostic findings.
The purpose of this webcast is to:
Discuss and demonstrate the approaches with array and NGS genotyping methods for star allele calling to prep for downstream analysis.
Following genotyping, explore alternative tertiary workflow concepts in VarSeq to handle PGx reporting.
Moreover, we will include insights users will need to consider when validating their PGx workflow for all possible star alleles and options you have for automating your PGx analysis for large number of samples. Please join us for a session dedicated to the application of star allele genotyping and subsequent PGx workflows in our VarSeq software.
“Psychiatry and the Humanities”: An Innovative Course at the University of Mo...Université de Montréal
“Psychiatry and the Humanities”: An Innovative Course at the University of Montreal Expanding the medical model to embrace the humanities. Link: https://www.psychiatrictimes.com/view/-psychiatry-and-the-humanities-an-innovative-course-at-the-university-of-montreal
The skin is the largest organ and its health plays a vital role among the other sense organs. The skin concerns like acne breakout, psoriasis, or anything similar along the lines, finding a qualified and experienced dermatologist becomes paramount.
Giloy in Ayurveda - Classical Categorization and SynonymsPlanet Ayurveda
Giloy, also known as Guduchi or Amrita in classical Ayurvedic texts, is a revered herb renowned for its myriad health benefits. It is categorized as a Rasayana, meaning it has rejuvenating properties that enhance vitality and longevity. Giloy is celebrated for its ability to boost the immune system, detoxify the body, and promote overall wellness. Its anti-inflammatory, antipyretic, and antioxidant properties make it a staple in managing conditions like fever, diabetes, and stress. The versatility and efficacy of Giloy in supporting health naturally highlight its importance in Ayurveda. At Planet Ayurveda, we provide a comprehensive range of health services and 100% herbal supplements that harness the power of natural ingredients like Giloy. Our products are globally available and affordable, ensuring that everyone can benefit from the ancient wisdom of Ayurveda. If you or your loved ones are dealing with health issues, contact Planet Ayurveda at 01725214040 to book an online video consultation with our professional doctors. Let us help you achieve optimal health and wellness naturally.
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
Parameters-It is used to describe the properties of an entire population.
Examples-Measures of central tendency Dispersion, Variance, Standard Deviation (SD), Absolute Error, Mean Absolute Error (MAE), Eigen Value
16. Cranial nerve mnemonics (function)
Olfactory Oh Some
Optic Oh Say
Oculomotor Oh Marry
Trochlear To Money
Trigeminal Take But
Abducent A My
Facial Family Brother
Vestibulocochlear Vacation! Says
Glossopharyngeal Go Big
Vagus Vegas Brain
Accessory And Matter
Hypoglossal Hawaii Most
18. II Optic nerve
Visual acquity
Distant
Snellen
chart(10/20
feet)
Near
Near vision
card (14inches)
Visual field
Peripheral
Wiggling
fingers
Counting
fingers
White pin
Central Red pin
fundoscopy ophthalmoscope
Pupillary light
reflex
Observe
Ptosis
irregular
Size of pupils
19. V
Trigerminal
nerve
VI VII VIII
sensory
Light touch
Cotton wisp
Corneal
reflex
Pain &
temperatur
e
P-
disposable
pin
T- cold
tuning fork
VIII Motor
Supplies
muscle of
mastication
Jaw-jerk
reflex
21. VII Vestibulocochlear
nerve
Hearing
Rinne test
perceive the
sound of the
tuning fork in
front of the ear
Hearing loss
Conductive
Bone > air
Sensorineural
Air > bone
Weber test
Hear equally
from both ears
Conductive
lateralizes the
sound to the
affected ear
Sensorineural
best heard by
the non-
involved ear.
Vestibular
Observe for
nystagmus
22. IX Glossopharyngeal
nerve
X Vagus nerve
swallowing,
phonation,
guttural and
palatal
articulation
Observe palate
movement
Palate elevate
symmetrically
Unilateral palate
weakness, palate
fails to elevate
on the weak side
23. XI Spinal Accessory Nerve
• The spinal accessory
supplies the trapezius and
sternocleidomastoid
muscles.
• observe for
– atrophy or asymmetry of the
muscles.
– quickness of shoulder shrug
XII Hypoglossal Nerve
• The hypoglossal nerve is
motor to the tongue.
• Normal Response:
– the tongue should be able to
protrude relatively straight.
Minimal degrees of deviation
(i.e. only millimeters)
affecting only the tip are
insignificant.
• Abnormal Response:
– with tongue weakness, the
tongue deviates towards the
weak side.
25. Motor examination
Abnormal Involuntary
Movements, Posture
and Bulk
Compare left to
right,proximal to distal
observe for
asymmetry, atrophy
or hypertrophy.
observe for abnormal
involuntary
movements
Tone
Spasticity
rigidity
Power
power or strength is
tested by comparing
the patient’s strength
against your own.
26. MRC Scale
Grade Description
0 no contraction
1 flicker or trace of contraction
2 active movement with gravity eliminated
3 active movement against gravity
4* active movement against gravity and resistance
5 normal power
28. Coordination
• To perform tasks of co-
ordination one requires
normal motor, sensory, and
cerebellar systems. Lesions
affecting any of these areas
could give rise to abnormal
tests of co-ordination.
• Examine
– Upper extremities
– Lower extremities
Gait
• observe the patient walk.
• if there is a subtle
abnormality this may be
made more obvious by
asking the patient to run.
• ask the patient to perform
tandem gait by walking heel
to toe (eyes open).