Functional Neurologic Disorders
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Outcomes Following Unilateral Selective Dorsal Rhizotomy In
Outcomes and Perioperative Considerations for Unilateral Selective Dorsal Rhizotomy in Children with Spastic Hemiplegia with Pre- and Postoperative Quantitative Gait Analysis Christine Hunt, D.O.1, Nicholas Wetjen, M.D.2, Kenton Kaufman, Ph.D.3, Krista Coleman Wood, P.T., Ph.D.3, Joline Brandenburg, M.D.1, Bradford Landry, D.O.1 1Department of Physical Medicine & Rehabilitation, 2Department of Neurologic Surgery, 3Department of Orthopedic Surgery Mayo Clinic, Rochester, MN Abstract Background & Objectives Methods Results: Postoperative Gait Analysis Discussion Background: Selective dorsal rhizotomy (SDR) is a Background Preoperative Baseline Characteristics Patient 1: Right SDR December 2013 • Pre-SDR, patients undergo an in-depth review of their medical procedure used to improve function, decrease pain and • Several human trials examining outcomes in SDR in children • Patient 1: 6 year old male, spastic right hemiplegia • 62.5% of sensory dorsal rootlets sectioned ( L2 to S1) history and imaging studies, consultation with a physiatrist, reduce spasticity in children and adults with cerebral palsy or neurosurgeon, and orthopedic surgeon, and evaluation with PT with spastic diplegia have been conducted, but there is a • GMFCS Level II • Normalized velocity and stride length stroke. Positive outcomes have been reported by numerous and OT. Testing includes QGA, MRI lumbar spine and brain, paucity of data describing outcomes following SDR for • 12 series of botulinum toxin • Improved hip and knee kinematics and kinetics authors but pediatric -
Peripheral Obliterating Arteritis As a Cause of Triplegia Following Hemiplegia, and of Paraplegia
§60 ■ burr, Camp: PeeipherAIi obliterating arTeritis. of ice, bloodletting, not as a routine, but for distinct indications, and serum-therapy, all appear to have been attended with the same general result—a mortality between 50 and 60 per cent. PERIPHERAL OBLITERATING ARTERITIS AS A CAUSE OF TRIPLEGIA FOLLOWING HEMIPLEGIA, AND OF PARAPLEGIA. By Charles W. Burr, M.D., PROFESSOR OF MENTAL DISEASES, UNIVERSITY OF PENNSYLVANIA, AND C. D. Camp, M.D., ASSISTANT IN NEUROPATHOLOGY, UNIVERSITY OP PENNSYLVANIA. (From the Laboratory of Neuropathology of the University of Pennsylvania.) We purpose to describe a not very infrequent but much neglected form of palsy caused by obliterating arteritis in the extremities affected. When it affects the arteries of the legs in a hemiplegic the result is a triplegia which may be thought to have been caused by cerebrospinal disease if the possibility of local vascular disease and the disability resulting therefrom are not thought of. During the acute stage of a sudden hemiplegia caused by cerebral hemorrhage or thrombosis, but never in the slowly oncoming palsy from cerebral tumor, there is, on account of the bilateral control of movements in the cerebral cortex, a temporary lessening of power of the arm and leg on the same side as the lesion. It is also well known that in the chronic stage of hemiplegia the deep reflexes on the non-paralyzed side are often permanently increased and that even true ankle clonus may be present. This temporary partial palsy and permanent exaggeration of the deep reflexes arise without any disease of the brain and cord except that which caused the primary palsy. -
Adherence to Supervised and Unsupervised Home Exercise Program on Motor Milestones in Spastic Cerebral Palsy
Review Article J Yoga & Physio Volume 4 Issue 2 - March 2018 Copyright © All rights are reserved by Namrata Patil DOI: 10.19080/JYP.2018.04.555634 Adherence to Supervised and Unsupervised Home Exercise Program on Motor Milestones in Spastic Cerebral Palsy Namrata Patil*, G Varadhrajulu and Mandar Malawade Department of Pediatric Physiotherapy, Krishna College of Physiotherpay, India Submission: February 09, 2018; Published: March 19, 2018 *Corresponding author: Namrata Patil, Department of Pediatric Physiotherapy, Krishna College of Physiotherpay, KIMS, Karad 415110, India, Email: Abstract Background: Cerebral palsy (CP) describes a group of developmental disorders of movement and posture, causing activity restriction or disability that is attributed to disturbances occurring in the fetal or infant brain. The motor impairments may be accompanied by a seizure motordisorder abnormality and by impairment (spasticity, of athetosis, sensation, ataxia), cognition, area communication of the body that and is affectedbehavior. (monoplegia, The hallmark diplegia, sign of hemiplegia,group of disorders triplegia, identified tetraplegia) as CP and is locationan impairment of lesion of involuntary the brain motor (pyramidal, control. extra CP frequently pyramidal, involves mixed).Many one or studies more limbs have andbeen the conducted trunk musculature on rehab for and CP is children. classified But by no the study type soof far conducted has compared the effectiveness of supervised and non supervised home exercise program. Hence, the study was undertaken. On adherence to supervised and unsupervised home exercise program on motor milestones for spastic cerebral palsy. Methods: 30 subjects diagnosed with spastic CP (3 months) were selected months .They were divided into two groups and treated with exercises for 2 months. -
Cerebral Palsy a Review for Dental Professionals
CEREBRAL PALSY A REVIEW FOR DENTAL PROFESSIONALS Purpose of this Module The information presented in this module is intended to provide dental providers with the appropriate knowledge needed to modify treatment and preventive procedures to best meet the needs of patients with cerebral palsy. Learning Objectives After reviewing the materials, the participant will be able to: 1. Define cerebral palsy and state the prevalence of this condition. 2. Describe the association of cerebral palsy with premature birth and low birth weight. 3. List additional etiological causes of cerebral palsy in each of the following three categories: prenatal, neonatal and postnatal periods. 4. List and describe common classification/descriptive systems of cerebral palsy. 5. Describe the association of intellectual disability and cerebral palsy. 6. Describe medical problems associated with cerebral palsy and their impact on dental care. 7. Describe the implications of cerebral palsy on issues of dental caries, periodontal disease and malocclusion. 8. Describe procedures for and explain the advantages and disadvantages of treatment of drooling in individuals with cerebral palsy. 9. Describe possible modifications of personal oral hygiene procedures for persons with cerebral palsy. 10. Discuss possible modifications in prosthetic design appropriate for some persons with cerebral palsy. 11. Discuss the advantages and limitations of periodontal surgery for gingival hyperplasia in patients with cerebral palsy. Special Care Advocates in Dentistry Module 4 Cerebral Palsy - 10/26/2013 CEREBRAL PALSY A REVIEW FOR DENTAL PROFESSIONALS INTRODUCTION per 1000 live births for those born between 28 and 31 weeks, 7 per 1000 live births for those The following information is not an extensive born between 32 and 36 weeks, and 1.3 per review of cerebral palsy and the general 1000 live births for those born 37 weeks and management of this condition, but rather a later. -
Effectiveness of Treatment in Children with Cerebral Palsy
Open Access Original Article DOI: 10.7759/cureus.13754 Effectiveness of Treatment in Children With Cerebral Palsy Syed Faraz Ul Hassan Shah Gillani 1 , Akkad Rafique 2 , Muhammad Taqi 3 , Muhammad Ayaz ul Haq Chatta 4 , Faisal Masood 5 , Tauseef Ahmad Blouch 3 , Syed Muhammad Awais 3 1. Orthopedic Surgery, King Edward Medical University/Mayo Hospital Lahore, Lahore, PAK 2. Orthopedics and Traumatology, Mohterma Benazir Bhutto Medical Shaheed College, Mirpur Azad Jammu Kashmir, PAK 3. Orthopedics and Traumatology, King Edward Medical University/Mayo Hospital Lahore, Lahore, PAK 4. Surgery, King Edward Medical University/Mayo Hospital Lahore, Lahore, PAK 5. Orthopaedic Surgery, King Edward Medical University/Mayo Hospital Lahore, Lahore, PAK Corresponding author: Muhammad Taqi, [email protected] Abstract Objective: The objective of this study was to assess the effectiveness of conservative and surgical treatment in cerebral palsy children by evaluating the Medical Research Council (MRC) grading system, modified Ashworth scale, and Barthel Activities of Daily Life (ADL) scale. Method: This prospective case series was performed using a non-probability consecutive sampling technique at the Department of Orthopedic Surgery and Traumatology, King Edward Medical University/Mayo Hospital, Lahore from October 2011 to November 2013. Two hundred children of all ages, having cerebral palsy diagnosed on history and clinical examination were enrolled in the study. Children were treated with conservative and surgical treatment. Pre- and post-treatment, all children were classified based on movement disorder (spastic, athetoid, ataxic, and mixed), parts of the body involved (paraplegic, tetraplegic, diplegic, hemiplegic, monoplegic, double hemiplegic, and triplegic), and gross motor function (GMFCS level I-IV). -
ABSTRACTS MDS-0817-467 Phenomenology
3rd International Conference on Functional (Psychogenic) Neurological Disorders September 6–8, 2017 Edinburgh, Scotland ABSTRACTS MDS-0817-467 Phenomenology 100 Baseline characteristics and outcome of pediatric onset psychogenic non-epileptic seizures Anne Sofie Hansen, Charlotte Rask, Jakob Christensen, René Nielsen (Aalborg, Denmark) Objective: This present study is the first study conducted on a nationwide cohort of children and adolescents with incident PNES. The aim is to investigate baseline characteristics and outcomes of pediatric PNES, i. e. psychiatric and somatic comorbidity and all-cause mortality, by utilizing the Danish healthcare registries and medical records. Background: Five to fifteen percent of children and adolescents referred to epilepsy centers are diagnosed with psychogenic non- epileptic seizures (PNES). PNES are mainly understood as manifestations of psychological distress. PNES resemble epileptic seizures, and the diagnosis is based on an exclusion of epilepsy. A misdiagnosis of epilepsy can result in potentially harmful treatment, whereas a misdiagnosis of PNES can result in lack of treatment and risk of multiple epileptic seizures. In spite of the potential consequences of a misdiagnosis, little is known about baseline characteristics and outcomes of pediatric-onset PNES as existing research primarily focuses on PNES in adults(1). Methods: Firstly, we will identify which ICD-10 diagnoses cover pediatric PNES in the Danish healthcare registers. We will examine a nationwide sample of medical records from patients (age 5-17 years, both included) registered with one of four most commonly used ICD-10 diagnoses combined with a procedure code for electroencephalography(2). Data describing demographic and clinical characteristics at onset will be retrieved from the medical records. -
A CLASSIFICATION of CEREBRAL PALSY by W
SPECIAL ARTICLE A CLASSIFICATION OF CEREBRAL PALSY By W. L. Minear, M.D., Ph.D. A REvuw of the literature reveals con- which the olden term, cerebral spastic paral- fusion in nomenclature and classifica- ysis, is only one of the group. It is fre- tion in the field of cerebral palsy. Using as quently a combination of both motor and a basis the majority opinion from question- sensory involvement. It was formerly con- names sent to the members of the American sidered as involving only a motor handicap, Academy for Cerebral Palsy during 1953 and on this basis confusion arose among (all members were polled; 64 per cent re- those treating such cases, since the other plied) by the Nomenclature and Classifica- associated handicaps were not recognized tion Committee, the following classification and difficulties arising from treating these for cerebral palsy is presented. children were attributed to their being A complete diagnosis should include one mentally defective. However, it is very diffi- on more titles from each of the main head- cult to explain how mental deficiency can ings of this nomenclature. The motor classi- be associated with pure athetosis on ataxia. fication is given precedence. Next, there The brain is a very complicated organ and should be a statement as to topography of any injury or lack of development in it gives the disease (body pants involved). There rise to unusual disturbances of function, also should be a statement as to the etiology both along the line of motor control and of the disease. A statement of the capabili- sensation. -
Challenges in Treating Functional Symptom Syndromes
Todd Ivan MD Clinical Associate Professor of Psychiatry NEOMED November 5, 2016 Arose in the late 1920’s out of the needs of acute-care hospitals for psychiatric services. Served as Liaison between these facilities and Asylums Focus of care rendered is more on the emotional and behavioral manifestations of illness. Training and research in Psychosomatic medicine encompasses the interaction between emotional and physical health. Care delivered in acute care hospital and clinic settings Freud-trained in neurology, inspired to office practice and the care of “nervous conditions.” Initial efforts at “moral treatment” included efforts at conversation. Charcot-untilized techniques of Mesmerism at the Salpietre. This media file is in the public domain in the United States. This applies to U.S. works where the copyright has expired, often because its first publication occurred prior to January 1, 1923. See this page for further explanation. “Cures” of somatic syndromes by means of the talking cure propagated anecdotally throughout the next half century Led to the seminal work of Engel and Romano culminating in the Biopsychosocial model Applied to the range of illnesses treated in all clinical settings Encouraged a holistic approach to the patient, beyond mere pathophysiology In its most dramatic application promised to lessen the disease burden of many “somatic” ills (e.g. psoriasis, asthma, peptic ulcer disease) Encompasses : Somatic Symptom Disorders Conversion Disorders Specified and Unspecified Somatic Symptom Disorders DSM-5 acknowledges that these syndromes are most frequently encountered in acute care medical settings (p 309, 2013) DSM 5 emphasizes the presence of “somatic symptoms associated with significant distress and impairment.” Diagnosis does not require “absence of a medical explanation for somatic symptoms.” (ibid.) Somatic Symptom Disorder Illness Anxiety Disorder Conversion Disorder Psychological Factors Affecting Other Medical Conditions Factitious Disorder Other Specified Somatic Symptom and Related Disorder (e.g. -
Introduction to Cerebral Palsy Written and Reviewed by the My Child Without Limits Advisory Committee
Introduction to Cerebral Palsy Written and reviewed by the My Child Without Limits Advisory Committee Cerebral palsy (CP) is a term used to describe a problem with movement and posture that makes certain activities difficult. Even though someone who has cerebral palsy has problems moving his or her muscles, this is not because there is something wrong with the muscles or nerves. These difficulties are caused because of problems in the brain. The patient might have had an injury to the brain, or had a brain that didn’t develop properly. These problems can affect the way the brain controls movement and posture. Simply stated, "Cerebral" refers to the brain, and "Palsy" refers to muscle weakness/poor control. Although the brain itself will not get worse, people who have cerebral palsy will usually change over time. Sometimes they will get better, and some patients will stay the same. Occasionally they will get worse, usually because of contracture of the joints or changes in the muscle tone; There is currently no cure for cerebral palsy. but, there are different treatment options for people who have cerebral palsy. These options include therapy, medications, surgery, education and support. By taking advantage of one or more of these options, people with cerebral palsy can learn to improve their function and the quality of their lives. Who Does Cerebral Palsy Affect? It is estimated that two out of every 1,000 newborn children will develop cerebral palsy. And approximately 40% of those born with cerebral palsy will have a severe case. Right now, about 10,000 babies and infants are diagnosed with the condition each year. -
Selective Dorsal Rhizotomy for Spasticity Not Associated with Cerebral Palsy: Reconsideration of Surgical Inclusion Criteria
Neurosurg Focus 35 (5):E6, 2013 ©AANS, 2013 Selective dorsal rhizotomy for spasticity not associated with cerebral palsy: reconsideration of surgical inclusion criteria WILLIAM C. GUMP, M.D.,1 IAN S. MUTCHNICK, M.D., M.S.,1 AND THOMAS M. MORIARTY, M.D., PH.D.1,2 1Division of Pediatric Neurosurgery, Norton Neuroscience Institute and Kosair Children’s Hospital; and 2Department of Neurological Surgery, University of Kentucky College of Medicine, Lexington, Kentucky Children with spastic diplegia from cerebral palsy (CP) experience measurable improvement in their spasticity and motor function following selective dorsal rhizotomy (SDR). The role of this operation in the treatment of other spasticity causes is less well defined. A literature review was undertaken to survey outcomes from SDRs performed outside the CP population. Multiple sclerosis was the most common diagnosis found, accounting for 74 of 145 pa- tients described. Selective dorsal rhizotomies have also been reported in patients with traumatic brain and spinal cord injuries, ischemic and hemorrhagic stroke, neurodegenerative disease, hypoxic encephalopathy, and other causes of spasticity. Outcomes from surgery are generally described as favorable, although postoperative assessments and follow-up times are not standardized across reports. Long-term outcomes are sparsely reported. Larger numbers of patients and more detailed outcomes data have the potential to form a basis for expanding the inclusion criteria for SDR. (http://thejns.org/doi/abs/10.3171/2013.8.FOCUS13294) KEY WORDS • selective dorsal rhizotomy • spasticity • cerebral palsy • hypertonia ELECTIVE dorsal rhizotomy (SDR) is a standard treat- nificant sensory loss and ataxia.11 The technique of isolat- ment option for spastic paraparesis associated with ing dorsal lumbar nerve fascicles and dividing only those cerebral palsy (CP) in selected patients. -
Cerebral Palsy Road Map: What to Expect As Your Child Grows
a Cerebral Palsy Road Map: What to Expect as Your Child Grows 1 To help you understand what having cerebral palsy means for your child, Gillette Children’s Specialty Healthcare created the Cerebral Palsy Road Map. This publication will show you how Gillette’s providers can help meet your child’s needs. Every child with cerebral palsy possesses a unique combination of strengths and challenges. This guide will enable you to navigate through your child’s experience with cerebral palsy. We hope it will encourage conversations among patients, families and health care providers. What Is Gillette? Gillette offers comprehensive, coordinated care that can reduce the effect of cerebral palsy on people’s lives. Our medical and rehabilitation specialists provide a broad range of services to meet the needs of children, teens and adults. We work closely with patients and families to develop comprehensive treatment plans. Because cerebral palsy requires lifelong management and care, we offer assistance when it is time for teens to move to adult care. We provide services for adults at Gillette’s adult clinic. What Is Cerebral Palsy? Cerebral palsy is a condition caused by an injury to the brain before, during, or shortly after birth. The brain injury often alters bone and muscle growth. It can restrict movement and affect posture. Associated problems can include difficulties with sensation, perception, cognition, communication, and behavior. Epilepsy and secondary musculoskeletal problems also might occur. Although cerebral palsy can’t be cured, treatments can help ease symptoms and improve your child’s abilities. 1 How to Use This Guide You can use the information in the Cerebral Palsy Road Map to understand how recommended evaluations and interventions might help your child. -
Functional Disorders and Medically Unexplained Symptoms
Functional This book is based on extensive research in assessment and treatment of patients with functional disorders and provides a Functional Disorders thorough background to functional disorders as well as the etiology, classi fication and treatment of the disorders. The book primarily and Medically Disorders targets clinicians in primary care, non-psychiatric specialties and other health care professionals. The chapters combine research Unexplained Symptoms and clinical experience and also provide techniques that can be applied in daily clinical practice, both in terms of identifying the Assessment and treatment and patients as well as helping the patients to better cope with their disorder. Medically The highly structured hands-on treatment programme described in the book is now a compulsory part of the specialist training of Danish primary care physicians and has won the Academy of Psychosomatic Medicine’s Alan Stoudemire Award for Innovation Unexplained and Excellence in Psychosomatic Medicine Education. Symptoms Aarhus University Press a Edited by Per Fink and Marianne Rosendal 1.0_Omslag_FunctionalDisorders.indd 1 18/06/15 16.13 100366_cover_functional disorders_.indd 1 25/06/15 09:39 Functional Disorders and Medically Unexplained Symptoms Functional Disorders and Medically Unexplained Symptoms Assessment and treatment Edited by Per Fink and Marianne Rosendal The Research Clinic for Functional Disorders and Psychosomatics Aarhus University Hospital 2015 This page is protected by copyright and may not be redistributed Functional Disorders and Medically Unexplained Symptoms Edited by Per Fink and Marianne Rosendal English translation by Morten Pilegaard © The authors and Aarhus University Press Layout and typesetting: Narayana Press Cover design: Sparre Grafisk E-book production: Narayana Press ISBN 978-87-7124-936-1 Aarhus University Press www.unipress.dk In collaboration with The Research Clinic for Functional Disorders and Psychosomatics Aarhus University Hospital DK-8000 Aarhus C Denmark International distribution UK & Eire: Gazelle Book Services Ltd.