Management of Children with Cerebral Palsy
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Brain Death and the Cervical Spinal Cord: a Confounding Factor for the Clinical Examination
Spinal Cord (2010) 48, 2–9 & 2010 International Spinal Cord Society All rights reserved 1362-4393/10 $32.00 www.nature.com/sc REVIEW Brain death and the cervical spinal cord: a confounding factor for the clinical examination AR Joffe, N Anton and J Blackwood Department of Pediatrics, Stollery Children’s Hospital, University of Alberta, Edmonton, Alberta, Canada Study design: This study is a systematic review. Objectives: Brain death (BD) is a clinical diagnosis, made by documenting absent brainstem functions, including unresponsive coma and apnea. Cervical spinal cord dysfunction would confound clinical diagnosis of BD. Our objective was to determine whether cervical spinal cord dysfunction is common in BD. Methods: A case of BD showing cervical cord compression on magnetic resonance imaging prompted a literature review from 1965 to 2008 for any reports of cervical spinal cord injury associated with brain herniation or BD. Results: A total of 12 cases of brain herniation in meningitis occurred shortly after a lumbar puncture with acute respiratory arrest and quadriplegia. In total, nine cases of acute brain herniation from various non-meningitis causes resulted in acute quadriplegia. The cases suggest that direct compression of the cervical spinal cord, or the anterior spinal arteries during cerebellar tonsillar herniation cause ischemic injury to the cord. No case series of brain herniation specifically mentioned spinal cord injury, but many survivors had severe disability including spastic limbs. Only two pathological series of BD examined the spinal cord; 56–100% of cases had upper cervical spinal cord damage, suggesting infarction from direct compression of the cord or its arterial blood supply. -
Lower Extremity Orthoses in Children with Spastic Quadriplegic Cerebral Palsy Implications for Nurses, Parents, and Caregivers
NOR200210.qxd 5/5/11 5:53 PM Page 155 Lower Extremity Orthoses in Children With Spastic Quadriplegic Cerebral Palsy Implications for Nurses, Parents, and Caregivers Kathleen Cervasio Understanding trends in the prevalence of children with cerebral prevalence for cerebral palsy in the United States is palsy is vital to evaluating and estimating supportive services for 2.4 per 1,000 children, an increase over previously re- children, families, and caregivers. The majority of children with ported data (Hirtz, Thurman, Gwinn-Hardy, Mohammad, cerebral palsy require lower extremity orthoses to stabilize their Chaudhuri, & Zalusky, 2007). Cerebral palsy is primar- muscles. The pediatric nurse needs a special body of knowledge ily a disorder of movement and posture originating in to accurately assess, apply, manage, teach, and evaluate the use the central nervous system with an incidence of 2.5 per 1,000 live births with spastic quadriplegia being the of lower extremity orthoses typically prescribed for this vulnera- common type of cerebral palsy (Blair & Watson, 2006). ble population. Inherent in caring for these children is the need This nonprogressive neurological disorder is defined as to teach the child, the family, and significant others the proper a variation in movement, coordination, posture, and application and care of the orthoses used in hospital and com- gait resulting from brain injury around birth (Blair & munity settings. Nursing literature review does not provide a Watson, 2006). Numerous associated comorbidities are basis for evidence in designing and teaching orthopaedic care usually present with cerebral palsy requiring various for children with orthoses. A protocol for orthoses management interventions. -
Cerebral Palsy the ABC's of CP
Cerebral Palsy The ABC’s of CP Toni Benton, M.D. Continuum of Care Project UNM HSC School of Medicine April 20, 2006 Cerebral Palsy Outline I. Definition II. Incidence, Epidemiology and Distribution III. Etiology IV. Types V. Medical Management VI. Psychosocial Issues VII. Aging Cerebral Palsy-Definition Cerebral palsy is a symptom complex, (not a disease) that has multiple etiologies. CP is a disorder of tone, posture or movement due to a lesion in the developing brain. Lesion results in paralysis, weakness, incoordination or abnormal movement Not contagious, no cure. It is static, but it symptoms may change with maturation Cerebral Palsy Brain damage Occurs during developmental period Motor dysfunction Not Curable Non-progressive (static) Any regression or deterioration of motor or intellectual skills should prompt a search for a degenerative disease Therapy can help improve function Cerebral Palsy There are 2 major types of CP, depending on location of lesions: Pyramidal (Spastic) Extrapyramidal There is overlap of both symptoms and anatomic lesions. The pyramidal system carries the signal for muscle contraction. The extrapyramidal system provides regulatory influences on that contraction. Cerebral Palsy Types of brain damage Bleeding Brain malformation Trauma to brain Lack of oxygen Infection Toxins Unknown Epidemiology The overall prevalence of cerebral palsy ranges from 1.5 to 2.5 per 1000 live births. The overall prevalence of CP has remained stable since the 1960’s. Speculations that the increased survival of the VLBW preemies would cause a rise in the prevalence of CP have proven wrong. Likewise the expected decrease in CP as a result of C-section and fetal monitoring has not happened. -
Cerebral Palsy and Epilepsy in Children: Clinical Perspectives on a Common Comorbidity
children Article Cerebral Palsy and Epilepsy in Children: Clinical Perspectives on a Common Comorbidity Piero Pavone 1 , Carmela Gulizia 2, Alice Le Pira 1, Filippo Greco 1, Pasquale Parisi 3 , Giuseppe Di Cara 4, Raffaele Falsaperla 5, Riccardo Lubrano 6, Carmelo Minardi 7 , Alberto Spalice 8 and Martino Ruggieri 9,* 1 Unit of Clinical Pediatrics, Department of Clinical and Experimental Medicine, AOU “Policlinico”, PO “G. Rodolico”, University of Catania, 95123 Catania, Italy; [email protected] (P.P.); [email protected] (A.L.P.); [email protected] (F.G.) 2 Postgraduate Training Program in Pediatrics, Department of Clinical and Experimental Medicine, University of Catania, 95123 Catania, Italy; [email protected] 3 NESMOS Department of Pediatrics, Sapienza University of Rome, Sant’Andrea University Hospital, 00161 Rome, Italy; [email protected] 4 Department of Pediatrics, University of Perugia, 06132 Perugia, Italy; [email protected] 5 Neonatal Intensive Care Unit (NICU), Neonatal COVID-19 Center, AOU “Policlinico”, PO San Marco, University of Catania, 95123 Catania, Italy; [email protected] 6 Dipartimento Materno Infantile e di Scienze Urologiche, Sapienza Università di Roma, UOC di Pediatria, Neonatologia, Ospedale Santa Maria Goretti, Polo di Latina, 04010 Latina, Italy; [email protected] 7 Department of Anaesthesia and Intensive Care, University Hospital “G. Rodolico” of Catania, 95123 Catania, Italy; [email protected] 8 Child Neurology Division, Department of Pediatrics, -
Cerebral Palsy
Cerebral Palsy Cerebral palsy encompasses a group of non-progressive and non-contagious motor conditions that cause physical disability in various facets of body movement. Cerebral palsy is one of the most common crippling conditions of childhood, dating to events and brain injury before, during or soon after birth. Cerebral palsy is a debilitating condition in which the developing brain is irreversibly damaged, resulting in loss of motor function and sometimes also cognitive function. Despite the large increase in medical intervention during pregnancy and childbirth, the incidence of cerebral palsy has remained relatively stable for the last 60 years. In Australia, a baby is born with cerebral palsy about every 15 hours, equivalent to 1 in 400 births. Presently, there is no cure for cerebral palsy. Classification Cerebral palsy is divided into four major classifications to describe different movement impairments. Movements can be uncontrolled or unpredictable, muscles can be stiff or tight and in some cases people have shaky movements or tremors. These classifications also reflect the areas of the brain that are damaged. The four major classifications are: spastic, ataxic, athetoid/dyskinetic and mixed. In most cases of cerebral palsy, the exact cause is unknown. Suggested possible causes include developmental abnormalities of the brain, brain injury to the fetus caused by low oxygen levels (asphyxia) or poor circulation, preterm birth, infection, and trauma. Spastic cerebral palsy leads to increased muscle tone and inability for muscles to relax (hypertonic). The brain injury usually stems from upper motor neuron in the brain. Spastic cerebral palsy is classified depending on the region of the body affected; these include: spastic hemiplegia; one side being affected, spastic monoplegia; a single limb being affected, spastic triplegia; three limbs being affected, spastic quadriplegia; all four limbs more or less equally affected. -
Potentially Asphyxiating Conditions and Spastic Cerebral Palsy in Infants of Normal Birth Weight
Fetus-Placenta-N ewborn Potentially asphyxiating conditions and spastic cerebral palsy in infants of normal birth weight Karin B. Nelson, MD, and Judith K. Grether, PhD Bethesda, Maryland, and Emeryville, California OBJECTIVE: Our purpose was to examine the association of cerebral palsy with conditions that can inter rupt oxygen supply to the fetus as a primary pathogenetic event. STUDY DESIGN: A population-based case-control study was performed in four California counties, 1983 through 1985, comparing birth records of 46 children with disabling spastic cerebral palsy without recognized prenatal brain lesions and 378 randomly selected control children weighing 2:2500 g at birth and surviving to age 3 years. RESULTS: Eight of 46 children with otherwise unexplained spastic cerebral palsy, all eight with quadriplegic cerebral palsy, and 15 of 378 controls had births complicated by tight nuchal cord (odds ratio for quadriplegia 18, 95% confidence interval 6.2 to 48). Other potentially asphyxiating conditions were uncommon and none was associated with spastic diplegia or hemiplegia. Level of care, oxytocin for augmentation of labor, and surgical delivery did not alter the association of potentially asphyxiating conditions with spastic quadriplegia. Intrapartum indicators of fetal stress, including meconium in amniotic fluid and fetal monitoring abnormalities, were common and did not distinguish children with quadriplegia who had potentially asphyxiating conditions from controls with such conditions. CONCLUSION: Potentially asphyxiating conditions, chiefly tight nuchal cord, were associated with an appre ciable proportion of unexplained spastic quadriplegia but not with diplegia or hemi-plegia. Intrapartum abnor malities were common both in children with cerebral palsy and controls and did not distinguish between them. -
Cerebral Palsy
Cerebral Palsy What is Cerebral Palsy? Doctors use the term cerebral palsy to refer to any one of a number of neurological disorders that appear in infancy or early childhood and permanently affect body movement and muscle coordination but are not progressive, in other words, they do not get worse over time. • Cerebral refers to the motor area of the brain’s outer layer (called the cerebral cortex), the part of the brain that directs muscle movement. • Palsy refers to the loss or impairment of motor function. Even though cerebral palsy affects muscle movement, it is not caused by problems in the muscles or nerves. It is caused by abnormalities inside the brain that disrupt the brain’s ability to control movement and posture. In some cases of cerebral palsy, the cerebral motor cortex has not developed normally during fetal growth. In others, the damage is a result of injury to the brain either before, during, or after birth. In either case, the damage is not repairable and the disabilities that result are permanent. Patients with cerebral palsy exhibit a wide variety of symptoms, including: • Lack of muscle coordination when performing voluntary movements (ataxia); • Stiff or tight muscles and exaggerated reflexes (spasticity); • Walking with one foot or leg dragging; • Walking on the toes, a crouched gait, or a “scissored” gait; • Variations in muscle tone, either too stiff or too floppy; • Excessive drooling or difficulties swallowing or speaking; • Shaking (tremor) or random involuntary movements; and • Difficulty with precise motions, such as writing or buttoning a shirt. The symptoms of cerebral palsy differ in type and severity from one person to the next, and may even change in an individual over time. -
Treatable Inborn Errors of Metabolism Presenting As Cerebral Palsy Mimics
Leach et al. Orphanet Journal of Rare Diseases 2014, 9:197 http://www.ojrd.com/content/9/1/197 RESEARCH Open Access Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review Emma L Leach1,2, Michael Shevell3,4,KristinBowden2, Sylvia Stockler-Ipsiroglu2,5,6 and Clara DM van Karnebeek2,5,6,7,8* Abstract Background: Inborn errors of metabolism (IEMs) have been anecdotally reported in the literature as presenting with features of cerebral palsy (CP) or misdiagnosed as ‘atypical CP’. A significant proportion is amenable to treatment either directly targeting the underlying pathophysiology (often with improvement of symptoms) or with the potential to halt disease progression and prevent/minimize further damage. Methods: We performed a systematic literature review to identify all reports of IEMs presenting with CP-like symptoms before 5 years of age, and selected those for which evidence for effective treatment exists. Results: We identified 54 treatable IEMs reported to mimic CP, belonging to 13 different biochemical categories. A further 13 treatable IEMs were included, which can present with CP-like symptoms according to expert opinion, but for which no reports in the literature were identified. For 26 of these IEMs, a treatment is available that targets the primary underlying pathophysiology (e.g. neurotransmitter supplements), and for the remainder (n = 41) treatment exerts stabilizing/preventative effects (e.g. emergency regimen). The total number of treatments is 50, and evidence varies for the various treatments from Level 1b, c (n = 2); Level 2a, b, c (n = 16); Level 4 (n = 35); to Level 4–5 (n = 6); Level 5 (n = 8). -
Cerebral Palsy
Health and Safety Guidelines 1 Cerebral Palsy Cerebral Palsy Cerebral palsy is a group of clinical syndromes characterized by abnormal muscle tone, posture, and movement. They are due to abnormalities of the developing brain and range in severity. The syndromes themselves are not progressive but as the person ages and the brain matures, symptoms may change. Cerebral palsy can be divided into spastic syndromes, dyskinetic syndromes (involuntary repetitive movements), and ataxic cerebral palsy. Spastic syndromes are characterized by increased tone and contractures of the affected muscles. These are the most commonly seen and will be presented here. Spastic hemiplegia Sensory problems are often seen in children with spastic hemiplegia and correlate with poor growth on the affected side. Typically, by age 5 or older, someone with spastic hemiplegia would show that: one side of the body is affected the arm is more affected than the leg the elbow is bent inward and the wrist and hand are flexed or bent at the joints and the fingers closed the hip, knee and ankle are flexed the arm or leg may be shorter on the affected side scoliosis may be present intellectual impairment, seizures, and vision problems are common Spastic quadriplegia Persons with spastic quadriplegia are typically severely handicapped. They are more likely to have other impairments such as severe intellectual disability, visual and communication problems, feeding difficulties, lung problems and seizures. The usual causes of spastic quadriplegia include congenital infection, cerebral (brain) development problems, and injuries during or right after birth. Typically, by age 5 or older, someone with spastic quadriplegia would show that: all limbs are affected the upper limbs may be the same or more involved than the lower limbs feeding and respiratory problems are common Disorders related to cerebral palsy: Cerebral palsy is often accompanied by other disorders of brain function. -
Selective Dorsal Rhizotomy (Sdr) St
SELECTIVE DORSAL RHIZOTOMY (SDR) ST. LOUIS CHILDREN’S HOSPITAL • 280 beds, expanding to 473 in 2017 • 3,000 employees • 800 medical staff members • 1,300 auxiliary members and volunteers • More than 30 pediatric subspecialty departments and divisions • Level I Pediatric Trauma Center, the highest level of emergency care available • Serving patients from 50 states and 70 countries • Recognized as one of the Founded in 1879, St. Louis best children’s hospitals in Children’s Hospital is one of the nation by U.S. News the premier children’s hospitals & World Report in the nation. It serves not just the children of St. Louis, but • Has received the nation’s children across the world. The highest honor for nursing hospital provides a full range of excellence, the Magnet pediatric services to the St. Louis designation, from metropolitan area and a primary the American Nurses service region covering six states. Credentialing Center. As the pediatric teaching hospital for Washington University School of Medicine, St. Louis Children’s Hospital offers nationally recognized programs for physician training and research. | 1 | Table of Contents A Life-Changing Procedure ........................................................ 3 Hope for the Future .................................................................... 3 Understanding Muscle Stiffness .................................................. 6 Benefits of Dorsal Rhizotomy ...................................................... 7 Could Your Child Benefit? ......................................................... -
Cerebral Palsy Presentation
Cerebral Palsy Eileen Donovan, MD Pediatric Physical Medicine and Rehabilitation Definition Disorder of the development of posture and movement, causing activity limitations that are attributed to non- progressive disturbances that occurred in the developing fetal or infant brain It is the most common motor disability of childhood Definition 3 major criteria A neuromotor control deficit that alters movement or posture A non-progressive brain lesion Brain injury either before birth or in the first year(s) of life What it is NOT Progressive Genetic/Hereditary Traumatic Cerebral Palsy Although the brain lesion in not progressive, the musculoskeletal pathology is certainly progressive Musculoskeletal progression in CP Static (Brain lesion) Spasticity and weakness Spastic muscles don’t grow as fast as bones Fixed contracture Bony torsion (twist) Progressive Joint instability (Musculoskeletal Dislocation or deformity) degenerative changes Graham HK, Eur J Neurol, 2001 Progressive musculoskeletal deformities Incidence 2-3 per 1000 live births 700,000 children and adults with CP in USA Relatively constant despite medical advancements in maternal, perinatal and NICU care Possibly due to improving survival rates in very premature infants Risk factors for CP In the majority of cases in full term infants, the etiology is unknown Risk factors for CP Prematurity – <37 wks Risk increases with increasing prematurity 34 weeks – 3 important developments for survival Lungs are developed Suck reflex has developed Germinal matrix of the -
Treating Spasticity with Selective Dorsal Rhizotomy (SDR) 2 Nationwide Children’S Hospital Contents
Treating Spasticity with Selective Dorsal Rhizotomy (SDR) 2 Nationwide Children’s Hospital Contents Spasticity and Spastic Cerebral Palsy ............................................................4 What Causes Spasticity? ..............................................................................4 Spasticity Symptoms ...................................................................................4 Spasticity Treatment Options ......................................................................5 What is Selective Dorsal Rhizotomy (SDR)? ...............................................6 Who is a Good Candidate for SDR? ...........................................................6 Undergoing SDR: The Patient Journey ........................................................6 Step by Step: The SDR Procedure ...............................................................7 What to Expect: From the Hospital to Home ..............................................8 Inpatient Rehabilitation ..............................................................................8 Outpatient Physical Therapy .......................................................................8 What are the Benefits of SDR? ....................................................................9 What are the Risks of SDR? ........................................................................9 The SDR Approach and Experience at Nationwide Children’s .........................................................10 Our Surgical Approach ..............................................................................10