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Approach to a Patient with Hemiplegia and Monoplegia
CHAPTER Approach to a Patient with Hemiplegia and Monoplegia 27 Sudhir Kumar, Subhash Kaul INTRODUCTION 4. Injury to multiple cervical nerve roots. Monoplegia and hemiplegia are common neurological 5. Functional or psychogenic. symptoms in patients presenting to the emergency department as well as outpatient department. Insidious onset, gradually progressive monoplegia affecting lower limb can be caused by the following Monoplegia refers to weakness of one limb (either arm or conditions: leg) and hemiplegia refers to weakness of one arm and leg on the same side of body (either left or right side). 1. Tumor of the contralateral frontal lobe. There are a variety of underlying causes for monoplegia 2. Tumor of spinal cord at thoracic or lumbar level. and hemiplegia. The causes differ in different age groups. 3. Chronic infection of brain (frontal lobe) or spinal The causes also differ depending on the onset, progression cord (thoracic or lumbar level), such as tuberculous. and duration of weakness. Therefore, one needs to adopt a systematic approach during history taking and 4. Lumbosacral-plexopathy, due to diabetes mellitus. examination in order to arrive at the correct diagnosis. Insidious onset, gradually progressive monoplegia, Appropriate investigations after these would confirm the affecting upper limb, can be caused by one of the following diagnosis. conditions: The aim of this chapter is to systematically look at the 1. Tumor of the contralateral parietal lobe. differential diagnosis of monoplegia and hemiplegia and outline the approach needed to pinpoint the exact 2. Compressive lesion (tumor, large disc, etc) in underlying cause. cervical cord region. 3. Chronic infection of the brain (parietal lobe) or APPROACH TO THE DIAGNOSIS OF MONOPLEGIA spinal cord (cervical region), such as tuberculous. -
Myelopathy—Paresis and Paralysis in Cats
Myelopathy—Paresis and Paralysis in Cats (Disorder of the Spinal Cord Leading to Weakness and Paralysis in Cats) Basics OVERVIEW • “Myelopathy”—any disorder or disease affecting the spinal cord; a myelopathy can cause weakness or partial paralysis (known as “paresis”) or complete loss of voluntary movements (known as “paralysis”) • Paresis or paralysis may affect all four limbs (known as “tetraparesis” or “tetraplegia,” respectively), may affect only the rear legs (known as “paraparesis” or “paraplegia,” respectively), the front and rear leg on the same side (known as “hemiparesis” or “hemiplegia,” respectively) or only one limb (known as “monoparesis” or “monoplegia,” respectively) • Paresis and paralysis also can be caused by disorders of the nerves and/or muscles to the legs (known as “peripheral neuromuscular disorders”) • The spine is composed of multiple bones with disks (intervertebral disks) located in between adjacent bones (vertebrae); the disks act as shock absorbers and allow movement of the spine; the vertebrae are named according to their location—cervical vertebrae are located in the neck and are numbered as cervical vertebrae one through seven or C1–C7; thoracic vertebrae are located from the area of the shoulders to the end of the ribs and are numbered as thoracic vertebrae one through thirteen or T1–T13; lumbar vertebrae start at the end of the ribs and continue to the pelvis and are numbered as lumbar vertebrae one through seven or L1–L7; the remaining vertebrae are the sacral and coccygeal (tail) vertebrae • The brain -
Absence of Neurobehavioral Disturbance in a Focal Lesion of the Left Paracentral Lobule
Behavioural Neurology (1992), 5,189-191 ICASE REPORTI Absence of neurobehavioral disturbance in a focal lesion of the left paracentral lobule T. Imamura and K. Tsuburaya Department of Neurology, Tohoku Kohseinenkin Hospital, Sendai, Japan Correspondence to: T. Imamura, Department of Neurology, Institute of Brain Diseases, Tohoku University School of Medicine, 1-1, Seiryo-machi, Aoba-Ku, Sendai 980, Japan The case of a right-handed woman with an infarcation confined to the left paracentral lobule and sparing the supplementary motor area (SMA) is reported. She presented with a right leg monoplegia and displayed no mutism. The absence of any associ ated neurobehavioral disturbances (mutism, forced grasping, reduced spontaneous arm activity or aphasia raises the possi bility that the left SMA has discrete neurobehavioral functions. Keywords: Medial frontal lobe - Precentral gyrus - Supplementary motor area - Transcortical motor aphasia INTRODUCTION Various kinds of neurobehavioral disturbances associated medial part of the left precentral gyrus, which is adjacent with left medial frontal lesions involving the supplemen to the SMA, to evaluate its possible neurobehavioral tary motor area (SMA) have been reported. Aphasia due to functions. damage of the left medial frontal lobe is characterized by an initial period of mutism followed by a stage of CASE REPORT decreased verbal output and spontaneous initiation with normal articulation (Stuss and Benson, 1986). Forced A 73-year-old right-handed woman with a history of grasping, compulsive manipulation of tools and decreased hypertension and diabetes mellitus suddenly developed a spontaneous limb movements have also been described gait disturbance. On examination, 24 h later, she was alert (Wise, 1984; Feinberg et al., 1992). -
ICD9 & ICD10 Neuromuscular Codes
ICD-9-CM and ICD-10-CM NEUROMUSCULAR DIAGNOSIS CODES ICD-9-CM ICD-10-CM Focal Neuropathy Mononeuropathy G56.00 Carpal tunnel syndrome, unspecified Carpal tunnel syndrome 354.00 G56.00 upper limb Other lesions of median nerve, Other median nerve lesion 354.10 G56.10 unspecified upper limb Lesion of ulnar nerve, unspecified Lesion of ulnar nerve 354.20 G56.20 upper limb Lesion of radial nerve, unspecified Lesion of radial nerve 354.30 G56.30 upper limb Lesion of sciatic nerve, unspecified Sciatic nerve lesion (Piriformis syndrome) 355.00 G57.00 lower limb Meralgia paresthetica, unspecified Meralgia paresthetica 355.10 G57.10 lower limb Lesion of lateral popiteal nerve, Peroneal nerve (lesion of lateral popiteal nerve) 355.30 G57.30 unspecified lower limb Tarsal tunnel syndrome, unspecified Tarsal tunnel syndrome 355.50 G57.50 lower limb Plexus Brachial plexus lesion 353.00 Brachial plexus disorders G54.0 Brachial neuralgia (or radiculitis NOS) 723.40 Radiculopathy, cervical region M54.12 Radiculopathy, cervicothoracic region M54.13 Thoracic outlet syndrome (Thoracic root Thoracic root disorders, not elsewhere 353.00 G54.3 lesions, not elsewhere classified) classified Lumbosacral plexus lesion 353.10 Lumbosacral plexus disorders G54.1 Neuralgic amyotrophy 353.50 Neuralgic amyotrophy G54.5 Root Cervical radiculopathy (Intervertebral disc Cervical disc disorder with myelopathy, 722.71 M50.00 disorder with myelopathy, cervical region) unspecified cervical region Lumbosacral root lesions (Degeneration of Other intervertebral disc degeneration, -
Upper Extremity Function in Persons with Tetraplegia: Relationships
Neurorehabilitation and Research Articles Neural Repair Volume 23 Number 5 June 2009 413-421 © 2009 The Author(s) 10.1177/1545968308331143 Upper Extremity Function in Persons with http://nnr.sagepub.com Tetraplegia: Relationships Between Strength, Capacity, and the Spinal Cord Independence Measure Claudia Rudhe, OT, MSc, and Hubertus J. A. van Hedel, PT, PhD Objective. To quantify the relationship between the Spinal Cord Independence Measure III (SCIM III), arm and hand muscle strength, and hand function tests in persons with tetraplegia. Methods. A total of 29 individuals with tetraplegia (motor level between cervical 4 and thoracic 1; sensory-motor complete and incomplete) participated. The total score, category scores, and separate items of the SCIM III were compared to the upper extremity motor score (UEMS), an extended manual muscle test (MMT) for 11 upper extremity muscles, and 6 functional capacity tests of the hand. Spearman’s correlation coefficients (rs) and regression analyses were performed. Results. The SCIM III sum score correlated well with the sum scores of the 3 tests (rs ≥ .76). The SCIM III self-care category correlated better with the tests (rs ≥ .80) compared to the other categories (rs ≤ .72). The SCIM III self-care item “grooming” highly correlated with muscle strength and hand capacity items (rs ≥ .80). A combination of hand muscle tests and the key grasping task explained over 90% of the variability in the self-care category scores. Conclusions. The SCIM III self-care category reflects upper extremity performance as it contains especially useful and valid items that relate to upper extremity function and capacity tests. -
Cerebellar Disease in the Dog and Cat
CEREBELLAR DISEASE IN THE DOG AND CAT: A LITERATURE REVIEW AND CLINICAL CASE STUDY (1996-1998) b y Diane Dali-An Lu BVetMed A thesis submitted for the degree of Master of Veterinary Medicine (M.V.M.) In the Faculty of Veterinary Medicine University of Glasgow Department of Veterinary Clinical Studies Division of Small Animal Clinical Studies University of Glasgow Veterinary School A p ril 1 9 9 9 © Diane Dali-An Lu 1999 ProQuest Number: 13815577 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a com plete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 13815577 Published by ProQuest LLC(2018). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States C ode Microform Edition © ProQuest LLC. ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106- 1346 GLASGOW UNIVERSITY lib ra ry ll5X C C ^ Summary SUMMARY________________________________ The aim of this thesis is to detail the history, clinical findings, ancillary investigations and, in some cases, pathological findings in 25 cases of cerebellar disease in dogs and cats which were presented to Glasgow University Veterinary School and Hospital during the period October 1996 to June 1998. Clinical findings were usually characteristic, although the signs could range from mild tremor and ataxia to severe generalised ataxia causing frequent falling over and difficulty in locomotion. -
Hemiballismus: /Etiology and Surgical Treatment by Russell Meyers, Donald B
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.13.2.115 on 1 May 1950. Downloaded from J. Neurol. Neurosurg. Psychiat., 1950, 13, 115. HEMIBALLISMUS: /ETIOLOGY AND SURGICAL TREATMENT BY RUSSELL MEYERS, DONALD B. SWEENEY, and JESS T. SCHWIDDE From the Division of Neurosurgery, State University of Iowa, College ofMedicine, Iowa City, Iowa Hemiballismus is a relatively uncommon hyper- 1949; Whittier). A few instances are on record in kinesia characterized by vigorous, extensive, and which the disorder has run an extended chronic rapidly executed, non-patterned, seemingly pur- course (Touche, 1901 ; Marcus and Sjogren, 1938), poseless movements involving one side of the body. while in one case reported by Lea-Plaza and Uiberall The movements are almost unceasing during the (1945) the abnormal movements are said to have waking state and, as with other hyperkinesias con- ceased spontaneously after seven weeks. Hemi- sidered to be of extrapyramidal origin, they cease ballismus has also been known to cease following during sleep. the supervention of a haemorrhagic ictus. Clinical Aspects Terminology.-There appears to be among writers on this subject no agreement regarding the precise Cases are on record (Whittier, 1947) in which the Protected by copyright. abnormal movements have been confined to a single features of the clinical phenomena to which the limb (" monoballismus ") or to both limbs of both term hemiballismus may properly be applied. sides (" biballismus ") (Martin and Alcock, 1934; Various authors have credited Kussmaul and Fischer von Santha, 1932). In a majority of recorded (1911) with introducing the term hemiballismus to instances, however, the face, neck, and trunk as well signify the flinging or flipping character of the limb as the limbs appear to have been involved. -
PREVENTING SECONDARY MEDICAL COMPLICATIONS: a Guide for Personal Assistants to People with Spinal Cord Injury
PREVENTING SECONDARY MEDICAL COMPLICATIONS: A Guide for Personal Assistants to People with Spinal Cord Injury Medical Rehabilitation Research and Training Center in Secondary Complications in Spinal Cord Injury SPAIN REHABILITATION CENTER University of Alabama at Birmingham Preventing Secondary Medical Complications: A Guide For Personal Assistants to People With Spinal Cord Injury Developed by: Medical Rehabilitation Research and Training Center in Secondary Complications in Spinal Cord Injury Training Office Department of Physical Medicine and Rehabilitation Spain Rehabilitation Center University of Alabama at Birmingham Acknowledgment Our thanks to the following individuals who helped us in the development of this booklet: Lorraine Arrington Judy Matthews Brenda Bass Margaret A. Nosek, PhD Betty Bass Scott and Donna Sartain Cathy Crawford, RD Drenda Scroggin Charles Cowan Anna Smith Allan Drake Brenda Smith David Felton Susan Smith, RN,BSN Peg Hale, RN,BSN Nita Straiton Bobbie Kent Donna Thornton Phillip Klebine Frank Wilkinson C.J. and Cindy Luster Larrie Waters c 1992, Revised 1996, The Board of Trustees of the University of Alabama This publication is supported in part by a grant (#H133B30025) from the National Institute on Disability and Rehabilitation Research, Department of Education, Washington, D.C. 20202. Opinions expressed in this document are not necessarily those of the granting agency. The University of Alabama at Birmingham administers its educational programs and activities, including admissions, without regard to race, color, religion, sex, national origin, handicap or Vietnam era or disabled veteran status. (Title IX of the Education Amendments of 1972 specifically prohibits discrimination on the basis of sex.) Direct inquires to Academic Affirmative Action Officer, The University of Alabama at Birmingham, UAB Station, Birmingham, Alabama, 35294. -
When Normal Multi-Joint Movement Synergies Become Pathologic Marco Santello Arizona State University at the Tempe Campus
Washington University School of Medicine Digital Commons@Becker Open Access Publications 2015 Are movement disorders and sensorimotor injuries pathologic synergies? When normal multi-joint movement synergies become pathologic Marco Santello Arizona State University at the Tempe Campus Catherine E. Lang Washington University School of Medicine in St. Louis Follow this and additional works at: https://digitalcommons.wustl.edu/open_access_pubs Recommended Citation Santello, Marco and Lang, Catherine E., ,"Are movement disorders and sensorimotor injuries pathologic synergies? When normal multi-joint movement synergies become pathologic." Frontiers in Human Neuroscience.8,. 1050. (2015). https://digitalcommons.wustl.edu/open_access_pubs/3648 This Open Access Publication is brought to you for free and open access by Digital Commons@Becker. It has been accepted for inclusion in Open Access Publications by an authorized administrator of Digital Commons@Becker. For more information, please contact [email protected]. REVIEW ARTICLE published: 06 January 2015 HUMAN NEUROSCIENCE doi: 10.3389/fnhum.2014.01050 Are movement disorders and sensorimotor injuries pathologic synergies? When normal multi-joint movement synergies become pathologic Marco Santello1* and Catherine E. Lang 2 1 Neural Control of Movement Laboratory, School of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, USA 2 Program in Physical Therapy, Program in Occupational Therapy, Department of Neurology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA Edited by: The intact nervous system has an exquisite ability to modulate the activity of multiple mus- Ana Bengoetxea, Universidad del País cles acting at one or more joints to produce an enormous range of actions. Seemingly Vasco-Euskal Herriko Unibertsitatea, Spain simple tasks, such as reaching for an object or walking, in fact rely on very complex spatial Reviewed by: and temporal patterns of muscle activations. -
Rapidly Progressive Tetraplegia and Cognitive Deterioration During Rehabilitation: a Case of Neurodegenerative Disease
J Surg Med. 2019;3(1):100-102. Case report DOI: 10.28982/josam.454181 Olgu sunumu Rapidly progressive tetraplegia and cognitive deterioration during rehabilitation: A case of neurodegenerative disease Rehabilitasyon sırasında hızlı ilerleyen tetrapleji ve bilişsel bozulma: Bir nörodejeneratif hastalık olgusu Sevgi İkbali Afşar 1, Oya Ümit Yemişçi 1 1 Department of Physical Medicine and Abstract Rehabilitation, Baskent University, Human prion diseases are fatal, progressive neurodegenerative disorders caused by neurolytic pathogen proteins, called Faculty of Medicine, Ankara, Turkey prions. The most common human prion disease is sporadic Creutzfeldt-Jakob disease, with an approximate annual prevalence of 0.5-1 per million. The symptoms and signs include rapidly progressive dementia, ataxia, myoclonic ORCID ID of the authors SİA: 0000-0002-4003-3646 seizures, akinetic mutism and other neurological and neurobehavioral disorders. The clinical spectrum of Creutzfeldt- OÜY: 0000-0002-0501-5127 Jakob disease is highly variable; therefore it can be difficult to diagnose premortem. This article describes a 78-year- old woman who initially presented with difficulty walking and balance disorder. As a result of the evaluation, the patient was transferred to rehabilitation clinic, with a diagnosis of cervical spinal stenosis. During hospitalization, she showed progressive decline in gait and balance and deteriorated rapidly. The patient was considered to be probable sporadic Creutzfeldt-Jakob disease after further investigations. Keywords: Neurodegenerative disease, Creutzfeldt-Jakob disease, Rehabilitation Öz Corresponding author / Sorumlu yazar: İnsan prion hastalıkları, prionlar olarak adlandırılan nörolitik patojen proteinlerin neden olduğu ilerleyici Sevgi İkbali Afşar Address / Adres: Fevzi Cakmak Cad. 5. Sokak nörodejeneratif hastalıklardır. En yaygın insan prion hastalığı sporadik Creutzfeldt-Jakob hastalığı olup, yıllık No: 48, 06490, Ankara, Türkiye prevalansı yaklaşık milyonda 0.5-1'dir. -
Mechanisms of Injury in Dyskinetic Cerebral Palsy
Mechanisms of Injury in Dyskinetic Cerebral Palsy Alec Hoon, MD Associate Professor of Pediatrics Johns Hopkins University School of Medicine Director, Phelps Center for Cerebral Palsy Kennedy Krieger Institute Neurodevelopmental Evaluation Structure‐Function Genetic, Epigenetic, Clinical Phenotype Abnormalities Environmental Risk Factors CP Diagnosis Etiologic Diagnosis Child‐Family Rehabilitative Characteristics Management Medical Surgical Measurement CAM Cell‐Based therapy Techniques Outcome Key Concepts in Cerebral Palsy • Motor control‐ tone, posture, movement • 2‐3/1000 children • Risk factors include infection, inflammation, low birth weight, prematurity, genetic • Secondary to brain dysgenesis or injury • “Non‐progressive”‐ manifestations can change • Unilateral and bilateral phenotypes • A range of associated disorders • Etiology links to phenotype links to treatment 1 Cerebral Palsy‐ Clinical Phenotypes CEREBRAL PALSY Spastic Dyskinetic Ataxic Hypotonia Bilateral Unilateral Hypertonic Hyperkinetic Spastic Diplegia Hemiplegia Dystonic Rigid Dystonic Tetraplegia Quadriplegia Athetosis Chorea Hemiballismus Cascade of events in brain injury 1. Prenatal antecedents may be suspected‐(Freud) 2. Final common pathways often involve hypoxia‐ ischemia and infection‐inflammation 3. Injury may have a protracted time course 4. Injury may lead to myelin abnormalities, reduced plasticity and decreased cell number 5. Injury changes both developmental trajectory and may sensitive brain to later injury The Evolving Nature of Injury TIME -
HCC Risk Adjustment Terminology: • HCC • CCV • AHA • RAF Score / Risk Score What Is Risk Adjustment?
HCC Risk Adjustment Terminology: • HCC • CCV • AHA • RAF Score / Risk Score What is Risk Adjustment? Who? What? Why? How? Redistributes Actuarial risk funds from plans Medicare To protect against based on with lower-risk Advantage Plans, adverse selection enrollees’ enrollees to plans Health Insurance and risk selection individual risk with higher-risk Exchanges, scores others enrollees RAF Calculation Demographic Health RAF Information StatusHealth Status Score Risk Score Higher risk scores represent members with a higher disease burden resulting in appropriately higher reimbursement. Lower risk scores represent a healthier population, but may also be due to: • Poor chart documentation • Poor diagnosis coding Why is this important? • Results in appropriate reimbursement • Augments the overall patient evaluation process • Allows us to stratify patients by risk • Metric for considering panel size, productivity, access, and coding education efforts Current Scope: Attributed Downside Plan Gain Share Lives Risk NGACO 24,876 80%/6.5 80%/6.5 91.5%- MCW 3,785 100% 100.65% Healthy 91.5%- 4,163 100% Saver 100.65% MA 16,561 50% TBD Current State: HCP-LAN APM Framework Category 3A: 83% Category 3B: 17% FFS APM HCC Risk Model • Diagnosis codes with RAF values are grouped into Condition Categories. • Diseases within a Condition Category are clinically related and are similar in respect to cost patterns. HCC Description Applicable Diagnoses to HCC Category RAF 111 Chronic Obstructive COPD Emphysema 0.346 Pulmonary Disease Chronic Bronchitis 108 Vascular Disease Atherosclerosis (of native or PVD 0.299 bypass grafts with or without Phlebitis and Thrombophlebitis complications [rest pain, (acute or chronic) claudication, etc]) Embolism of Veins (acute or Aortic Aneurysm chronic) (nonruptured) Diabetic Peripheral Angiopathy Arterial Aneurysm • There are 79 identified Condition Categories in 2018.