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A Syndrome-Based Clinical Approach for Clerkship Students General Comments 1. This Is Not an All-Inclusive “Cookbook” for Ev
A Syndrome-Based Clinical Approach for Clerkship Students General Comments 1. This is not an all-inclusive “cookbook” for every Neurology patient, but a set of guidelines to help you rationally approach patients with certain syndromes (sets of signs and symptoms which suggest a lesion in particular parts of the nervous system). 2. As you obtain a history and perform a neurological physical exam, try initially to localize all the patient’s signs and symptoms to one, single lesion in the nervous system. It may be surprising that a variety of signs and symptoms, at first glance apparently unrelated, on second thought can localize accurately to a single lesion. If this approach fails, then consider multiple, separate lesions for the patient’s signs and symptoms. 3. The tempo or rate at which signs and symptoms develop or occur often suggests the underlying pathological process. a. sudden onset---favors stroke (ischemia or hemorrhage), seizure, migraine (or other headache syndromes), and trauma b. subacute onset---favors inflammatory, infectious or immune-mediated disorders c. chronic onset---favors degenerative disorders, tumors Toximetabolic disorders, potentially treatable and reversible, may mimic lesions in the nervous system, and can evolve at variable tempos. Hereditary conditions may be congenital (present at birth) and nonprogressive or static, or develop later in life, with variable rates of progression. Family members affected by the same genetic disorder may be remarkably similar with regards to onset and clinical severity, while some genetic disorders vary widely regarding when and how severely family members are affected. 4. In the central nervous system, “positive symptoms or phenomena,” such as flashes of light, or a tingling sensation, suggest “excitation” or increased activity in the nervous system: migraine or seizure. -
Inherited Neuropathies
407 Inherited Neuropathies Vera Fridman, MD1 M. M. Reilly, MD, FRCP, FRCPI2 1 Department of Neurology, Neuromuscular Diagnostic Center, Address for correspondence Vera Fridman, MD, Neuromuscular Massachusetts General Hospital, Boston, Massachusetts Diagnostic Center, Massachusetts General Hospital, Boston, 2 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology Massachusetts, 165 Cambridge St. Boston, MA 02114 and The National Hospital for Neurology and Neurosurgery, Queen (e-mail: [email protected]). Square, London, United Kingdom Semin Neurol 2015;35:407–423. Abstract Hereditary neuropathies (HNs) are among the most common inherited neurologic Keywords disorders and are diverse both clinically and genetically. Recent genetic advances have ► hereditary contributed to a rapid expansion of identifiable causes of HN and have broadened the neuropathy phenotypic spectrum associated with many of the causative mutations. The underlying ► Charcot-Marie-Tooth molecular pathways of disease have also been better delineated, leading to the promise disease for potential treatments. This chapter reviews the clinical and biological aspects of the ► hereditary sensory common causes of HN and addresses the challenges of approaching the diagnostic and motor workup of these conditions in a rapidly evolving genetic landscape. neuropathy ► hereditary sensory and autonomic neuropathy Hereditary neuropathies (HN) are among the most common Select forms of HN also involve cranial nerves and respiratory inherited neurologic diseases, with a prevalence of 1 in 2,500 function. Nevertheless, in the majority of patients with HN individuals.1,2 They encompass a clinically heterogeneous set there is no shortening of life expectancy. of disorders and vary greatly in severity, spanning a spectrum Historically, hereditary neuropathies have been classified from mildly symptomatic forms to those resulting in severe based on the primary site of nerve pathology (myelin vs. -
7/19/2018 1 Falls and Movement Disorders
7/19/2018 Falls and Movement Disorders Victor Sung, MD AL Medical Directors Association Annual Conference July 28, 2018 Falls and Movement Disorders • Gait Disorders and Falls • Movement Disorders Primer • Hypokinetic Movement Disorders • Hyperkinetic Movement Disorders • Other Neurologic Contributors to Falls • Non‐Neurologic Contributors to Falls • Pearls/Pitfalls Physiology/Epidemiology of Gait Disorders • 3 Key Subsystems for Maintaining Balance • Visual • Vestibular • Somatosensory / Proprioception • Gait disorders are common • 15% of people age 65 • 25% of people age 85 • Increases risk of falls by 2.5‐3 X • >80% of gait disorders in patients >65 are multifactorial • Most common are orthopedic and neurologic factors 1 7/19/2018 Epidemiology of Gait Disorders Frequency of Etiologies for Patients Referred to Neurology for Gait D/O Etiology Percent Sensory deficits 18.3% Myelopathy 16.7% Multiple infarcts 15.0% Unknown 14.2% Parkinsonism 11.7% Cerebellar degeneration / ataxia 6.7% Hydrocephalus 6.7% Psychogenic 3.3% Other* 7.5% *Other = metabolic encephalopathy, sedative drugs, toxic disorders, brain tumor, subdural hematoma Evaluation of Gait Disorders • Start with history • Do they have falls? If so, what type/setting? • In general, what setting does the gait disorder occur? • What other medical problems may be contributing? • Exam • Abnormalities on motor/sensory/cerebellar exam • What does the gait look like? Anatomy of the Motor System Overview • Localize the Lesion!! • Motor Cortex • Subcortical Corticospinal tract • Modulators -
THE NEUROLOGY Exam & Clinical Pearls
THE NEUROLOGY Exam & Clinical Pearls Gaye McCafferty, RN, MS, NP-BC, MSCS, SCRN NPANYS-SPHP Education Day Troy, New York April 7, 2018 Objectives I. Describe the core elements of the neurology exam II. List clinical pearls of the neuro exam Neurology Exam . General Physical Exam . Mental Status . Cranial Nerves . Motor Exam . Reflex Examination . Sensory Exam . Coordination . Gait and Station 1 General Systemic Physical Exam Head Trauma Dysmorphism Neck Tone Thyromegaly Bruits MSOffice1 General Systemic Physical Exam .Cardiovascular . Heart rate, rhythm, murmur; peripheral pulses, JVD .Pulmonary . Breathing pattern, cyanosis, Mallampati airway .General Appearance Hygiene, grooming, weight (signs of self neglect) .Funduscopic Exam Mental Status Level of Consciousness . Awake . Drowsy . Somnolent . Comatose 2 Slide 5 MSOffice1 , 6/14/2009 Orientation & Attention . Orientation . Time . Place . Person Orientation & Attention . Attention . Digit Span-have the patient repeat a series of numbers, start with 3 or 4 in a series and increase until the patient makes several mistakes. Then explain that you want the numbers backwards. Normal-seven forward, five backward Hint; use parts of telephone numbers you know Memory Immediate recall and attention Tell the patient you want him to remember a name and address – Jim Green – 20 Woodlawn Road, Chicago Note how many errors are made in repeating it and how many times you have to repeat it before it is repeated correctly. Normal: Immediate registration 3 Memory . Short-term memory . About 5 minutes after asking the patient to remember the name and address, ask him to repeat it. Long –term memory . Test factual knowledge . Dates of WWII . Name a president who was shot dead Memory Mini-Mental State Exam – 30 items Mini-Cog – Rapid Screen for Cognitive Impairment – A Composite of 3 item recall and clock drawing – Takes about 5 minutes to administer Mini-Cog Mini-Cog Recall 0 Recall 1-2 Recall 3 Demented Non-demented Abnormal Clock Normal Clock Demented Non-demented 4 Memory . -
Vol. 13 No. 2 December 2020 Eissn 2508-1349 Vol
eISSN 2508-1349 Vol. 13 No. 2 December 2020 eISSN 2508-1349 Vol. 13 No. 2 December 2020 pages 69 - 136 I I www.e-jnc.org eISSN 2508-1349 Vol. 13, No. 2, 31 December 2020 Aims and Scope Journal of Neurocritical Care (JNC) aims to improve the quality of diagnoses and management of neurocritically ill patients by sharing practical knowledge and professional experience with our reader. Although JNC publishes papers on a variety of neurological disorders, it focuses on cerebrovascular diseases, epileptic seizures and status epilepticus, infectious and inflammatory diseases of the nervous system, neuromuscular diseases, and neurotrauma. We are also interested in research on neurological manifestations of general medical illnesses as well as general critical care of neurological diseases. Open Access This is an Open Access article distributed under the terms of the Creative Commons Attribution Non- Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non- commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Publisher The Korean Neurocritical Care Society Editor-in-Chief Sang-Beom Jeon Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, 88 Oylimpic-ro 43-gil, Songpa-gu, Seoul 05505, Korea Tel: +82-2-3010-3440, Fax: +82-2-474-4691, E-mail: [email protected] Correspondence The Korean Neurocritical Care Society Department of Neurology, The Catholic University College of Medicine, 222 Banpo-Daero, Seocho-Gu, Seoul 06591, Korea Tel: +82-2-2258-2816, Fax: +82-2-599-9686, E-mail: [email protected] Website: http://www.neurocriticalcare.or.kr Printing Office M2community Co. -
Gait Disorders in Older Adults
ISSN: 2469-5858 Nnodim et al. J Geriatr Med Gerontol 2020, 6:101 DOI: 10.23937/2469-5858/1510101 Volume 6 | Issue 4 Journal of Open Access Geriatric Medicine and Gerontology STRUCTURED REVIEW Gait Disorders in Older Adults - A Structured Review and Approach to Clinical Assessment Joseph O Nnodim, MD, PhD, FACP, AGSF1*, Chinomso V Nwagwu, MD1 and Ijeoma Nnodim Opara, MD, FAAP2 1Division of Geriatric and Palliative Medicine, Department of Internal Medicine, University of Michigan Medical School, USA Check for 2Department of Internal Medicine and Pediatrics, Wayne State University School of Medicine, USA updates *Corresponding author: Joseph O Nnodim, MD, PhD, FACP, AGSF, Division of Geriatric and Palliative Medicine, Department of Internal Medicine, University of Michigan Medical School, 4260 Plymouth Road, Ann Arbor, MI 48109, USA Abstract has occurred. Gait disorders are classified on a phenom- enological scheme and their defining clinical presentations Background: Human beings propel themselves through are described. An approach to the older adult patient with a their environment primarily by walking. This activity is a gait disorder comprising standard (history and physical ex- sensitive indicator of overall health and self-efficacy. Impair- amination) and specific gait evaluations, is presented. The ments in gait lead to loss of functional independence and specific gait assessment has qualitative and quantitative are associated with increased fall risk. components. Not only is the gait disorder recognized, it en- Purpose: This structured review examines the basic biolo- ables its characterization in terms of severity and associated gy of gait in term of its kinematic properties and control. It fall risk. describes the common gait disorders in advanced age and Conclusion: Gait is the most fundamental mobility task and proposes a scheme for their recognition and evaluation in a key requirement for independence. -
2020 Measure Value Set Colorectal Cancer Screening
PT ‐ 2020 Measure Value Set_Colorectal Cancer Screening Numerator Value Set Name Code Definition Code System FOBT Lab Test 82270 CPT FOBT Lab Test 82274 CPT Colorectal cancer screening; fecal occult blood test, immunoassay, 1‐3 FOBT Lab Test G0328 HCPCS simultaneous (G0328) FOBT Lab Test 12503‐9 Hemoglobin.gastrointestinal [Presence] in Stool ‐‐4th specimen LOINC FOBT Lab Test 12504‐7 Hemoglobin.gastrointestinal [Presence] in Stool ‐‐5th specimen LOINC FOBT Lab Test 14563‐1 Hemoglobin.gastrointestinal [Presence] in Stool ‐‐1st specimen LOINC FOBT Lab Test 14564‐9 Hemoglobin.gastrointestinal [Presence] in Stool ‐‐2nd specimen LOINC FOBT Lab Test 14565‐6 Hemoglobin.gastrointestinal [Presence] in Stool ‐‐3rd specimen LOINC FOBT Lab Test 2335‐8 Hemoglobin.gastrointestinal [Presence] in Stool LOINC FOBT Lab Test 27396‐1 Hemoglobin.gastrointestinal [Mass/mass] in Stool LOINC FOBT Lab Test 27401‐9 Hemoglobin.gastrointestinal [Presence] in Stool ‐‐6th specimen LOINC FOBT Lab Test 27925‐7 Hemoglobin.gastrointestinal [Presence] in Stool ‐‐7th specimen LOINC FOBT Lab Test 27926‐5 Hemoglobin.gastrointestinal [Presence] in Stool ‐‐8th specimen LOINC FOBT Lab Test 29771‐3 Hemoglobin.gastrointestinal.lower [Presence] in Stool by Immunoassay LOINC Hemoglobin.gastrointestinal.lower [Presence] in Stool by Immunoassay FOBT Lab Test 56490‐6 LOINC ‐‐2nd specimen Hemoglobin.gastrointestinal.lower [Presence] in Stool by Immunoassay FOBT Lab Test 56491‐4 LOINC ‐‐3rd specimen Hemoglobin.gastrointestinal.lower [Presence] in Stool by Immunoassay FOBT Lab Test 57905‐2 -
9781441967237.Pdf
The Neurologic Diagnosis wwwwwwwwww Jack N. Alpert The Neurologic Diagnosis A Practical Bedside Approach Jack N. Alpert, MD St. Luke’s Episcopal Hospital Department of Neurology University of Texas Medical School at Houston Houston, TX, USA [email protected] ISBN 978-1-4419-6723-7 e-ISBN 978-1-4419-6724-4 DOI 10.1007/978-1-4419-6724-4 Springer New York Dordrecht Heidelberg London Library of Congress Control Number: 2011941214 © Springer Science+Business Media, LLC 2012 All rights reserved. This work may not be translated or copied in whole or in part without the written permission of the publisher (Springer Science+Business Media, LLC, 233 Spring Street, New York, NY 10013, USA), except for brief excerpts in connection with reviews or scholarly analysis. Use in connection with any form of information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed is forbidden. The use in this publication of trade names, trademarks, service marks, and similar terms, even if they are not identifi ed as such, is not to be taken as an expression of opinion as to whether or not they are subject to proprietary rights. While the advice and information in this book are believed to be true and accurate at the date of going to press, neither the authors nor the editors nor the publisher can accept any legal responsibility for any errors or omissions that may be made. The publisher makes no warranty, express or implied, with respect to the material contained herein. Printed on acid-free paper Springer is part of Springer Science+Business Media (www.springer.com) In Memory of Morris B. -
Physical Therapy Practice
Physical Therapy Practice THE MAGAZINE OF THE ORTHOPAEDIC SECTION, APTA VOL. 18, NO. 2 2006 ORTHOPAEDIC CARDON REHABILITATION PRODUCTS, INC.™ Wurlitzer Industrial Park, 908 Niagara Falls Blvd. North Tonawanda, NY 14120 Telephone: 1-800-944-7868 • Fax: 716-297-0411 E-mail: [email protected] THE ACCEPTED STANDARD OF PERFORMANCE The Cardon Mobilization Table . Going beyond the third dimension . Now available with the patented option which eliminates the use of flexion and rotation levers. This allows the therapist to perform advanced manual therapy techniques with complete confidence and comfort with an ergonomically friendly design. The unique design provides more efficient and smooth setup while providing superior patient comfort. The option enhances patient care by allowing unsurpassed opportunity for more preciseness of treatment and monitoring of segments and joints. he design and concepts make this “T the best mobilization table manufactured today.” Professor Freddy Kaltenborn Autho, Int’l Lecturer in Manual Therapy he various sections have minimum flex “T allowing very accurate application of specific manual therapy techniques.” Olaf Evjenth ES! I would like to preview the Author, Int’l Lecturer in Manual Therapy Y Cardon Mobilization Table. Please rush your 15 minute VHS video (for standard model): SEE FOR Name: Title: YOURSELF Clinic/Institution: THESE Address: OUTSTANDING City: State: Zip Code: Telephone: Signature: FEATURES: CARDON REHABILITATION PRODUCTS, INC.™ • Accurate localization of the vertebral segment Wurlitzer Industrial Park, 908 Niagara Falls Blvd. • Precision and versatility of technique North Tonawanda, NY 14120 • Absolute control of the mobilization forces Telephone: 1-800-944-7868 • Fax: 716-297-0411 • Excellent stability for manipulation. E-mail: [email protected] Orthopaedic Practice Vol. -
Neurological History and Physical Examination
emedicine.medscape.com eMedicine Specialties > Clinical Procedures > none Neurological History and Physical Examination Kalarickal J Oommen, MD, FAAN, Professor and Crofoot Chair of Epilepsy, Department of Neurology, Chief, Section of Epilepsy, Texas Tech University Health Sciences Center; Medical Director, Texas Tech University Health Sciences Center (TTUHSC) Covenant Comprehensive Epilepsy Center Updated: Nov 25, 2009 Neurological History "From the brain and the brain only arise our pleasures, joys, laughter and jests, as well as our sorrows, pains, griefs, and tears.... These things we suffer all come from the brain, when it is not healthy, but becomes abnormally hot, cold, moist or dry." —Hippocrates The Sacred Disease, Section XVII Taking the patient's history is traditionally the first step in virtually every clinical encounter. A thorough neurologic history allows the clinician to define the patient's problem and, along with the result of physical examination, assists in formulating an etiologic and/or pathologic diagnosis in most cases.[1 ] Solid knowledge of the basic principles of the various disease processes is essential for obtaining a good history. As Goethe stated, "The eyes see what the mind knows." To this end, the reader is referred to the literature about the natural history of diseases. The purpose of this article is to highlight the process of the examination rather than to provide details about the clinical and pathologic features of specific diseases. The history of the presenting illness or chief complaint should -
Movement Disorders and Gait Disturbances
Movement disorders and gait disturbances Kovács Norbert PTE ÁOK Neurológiai Klinika Pécs 1 MD pathophysiology z Genetic mutation or environmental injury of basal ganglia functioning z Pallidum, thalamus, subthalamic nucleus, caudate nucleus, pedunculopintine nucleus 2 Vitek JL. Mov Disord 2002;17(Supp 3):S49-62 Phenomenology in MD Hyperkinetic Isokinetic Hypokinetic • Tremor (regular) • Ataxia • Rigidity • Chorea • Bradykinesia • Ballism • Hypokinesia • Dystonia • Athetosis • Myoclonus (jerky) • Tic (jerky) 3 Hyperkinetic movements 4 Tremor classification More or less regular, sinusoid movements Any body parts can be affected (e.g. limbs, neck, trunc, vocal cords) Classification: • Intensity (invisible, barely visible, moderate, severe) • Frequency (slow or fast) • Position – Rest tremor (e.g. Parkinsonism) – Postural tremor (e.g. hyperthyroidism) – Kinetic tremor (e.g. essential tremor) – Intention tremor (e.g. cerebellar tremor) 5 Rest tremor Cognition (e.g. counting), gait or talking about the disease 6 usually increases the amplitude Intention tremor The tremor amplitude is the highest at the target. Usually 7 caused by cerebellar problems. Postural –kinetic tremor 8 Postural –kinetic tremor 9 Essential tremor is the most frequent cause of kinetic tremor. Postural –kinetic tremor 10 Always examine water drinking, writing and tableware use -- QoL Deep brain stimulation for tremor 11 Chorea The word chorea denotes rapid irregular muscle jerks that occur involuntarily and unpredictably in different parts of the body. Most important cause is12 Parkinson’s disease Ballism Large involuntary movements involving the whole extremity. Usually accompanies the chorea. Vascular lesion e.g. in the area of subthalamic13 nucleus can produce Athetosis abnormal movements that are slow, sinuous, and writhing in character. 14 Dystonia • Not a disease, it is a syndrome • Involuntary phasic, movement and/or • Sustained, involuntary, abnormal muscle contractions. -
GAIT DISORDERS, FALLS, IMMOBILITY Mov7 (1)
GAIT DISORDERS, FALLS, IMMOBILITY Mov7 (1) Gait Disorders, Falls, Immobility Last updated: April 17, 2019 GAIT DISORDERS ..................................................................................................................................... 1 CLINICAL FEATURES .............................................................................................................................. 1 CLINICO-ANATOMICAL SYNDROMES .............................................................................................. 1 CLINICO-PHYSIOLOGICAL SYNDROMES ......................................................................................... 1 Dyssynergy Syndromes .................................................................................................................... 1 Frontal gait ............................................................................................................................ 2 Sensory Gait Syndromes .................................................................................................................. 2 Sensory ataxia ........................................................................................................................ 2 Vestibular ataxia .................................................................................................................... 2 Visual ataxia .......................................................................................................................... 2 Multisensory disequilibrium .................................................................................................