Computerized Cognitive Testing in the Management of Youth Sports-Related Concussion.

Abstract:

:Computerized neurocognitive testing has become a growing practice across medical populations, but particularly within sports medicine and the management of sports-related concussion. Although traditional neuropsychological measures are solely administered and interpreted by neuropsychologists, computerized cognitive tests are marketed to and utilized by a wide range of professionals involved in the management of sports-related concussions, many of whom lack specialized psychometric training. Although the benefits of computerized testing allow for many youth athletes to be evaluated quickly, professionals implementing their use should be aware of the potential pitfalls and the high potential for misuse. After briefly reviewing the recommended guidelines set forth by the American Academy of Clinical Neuropsychology and the National Academy of Neuropsychology, we review the benefits/limitations of computerized testing in the management of sports-related concussion and the basic psychometric properties of some of the more widely used computerized measures. Lastly, we discuss the practical application of these devices.

journal_name

J Child Neurol

authors

De Marco AP,Broshek DK

doi

10.1177/0883073814559645

subject

Has Abstract

pub_date

2016-01-01 00:00:00

pages

68-75

issue

1

eissn

0883-0738

issn

1708-8283

pii

0883073814559645

journal_volume

31

pub_type

杂志文章,评审
  • Histocompatibility determinants in childhood postinfectious encephalomyelitis.

    abstract::Postinfectious encephalomyelitis and multiple sclerosis have clinical, immunologic, and neuroradiographic similarities. We studied HLA determinants in six white children consecutively diagnosed with postinfectious encephalomyelitis. Each of the children had HLA determinants which have been associated with multiple scl...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388900400311

    authors: Woody RC,Steele RW,Charlton RK,Smith V

    更新日期:1989-07-01 00:00:00

  • Treatment of subacute sclerosing panencephalitis with interferon-alpha, ribavirin, and inosiplex.

    abstract::Subacute sclerosing panencephalitis is an almost universally fatal late complication of measles infection for which there is no established treatment. We report a patient with subacute sclerosing panencephalitis who was bed-bound and ataxic and had a left hemiparesis and frequent myoclonus. He was started on a new reg...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700911

    authors: Solomon T,Hart CA,Vinjamuri S,Beeching NJ,Malucci C,Humphrey P

    更新日期:2002-09-01 00:00:00

  • Anencephaly in the United States, 1968-1987: the declining incidence among white infants.

    abstract::The ethical issues concerning the use of fetal tissue as a source for organ transplantation has focused interest on anencephaly. For reasons that are not entirely clear, the incidence of anencephaly has been declining. As anencephaly is easily recognized and invariably fatal, mortality figures provide an excellent ref...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389100600403

    authors: Snyder RD,Fakadej AF,Riggs JE

    更新日期:1991-10-01 00:00:00

  • Botulinum toxin type B improves the speed of reaching in children with cerebral palsy and arm dystonia: an open-label, dose-escalation pilot study.

    abstract::Seven children between 2 and 15 years of age with cerebral palsy and upper extremity dystonia were enrolled in an open-label, dose-escalation pilot clinical trial of botulinum toxin type B (Myobloc), injected into the biceps and brachioradialis muscles of I or both arms. The primary outcome measure was the change in m...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/0883073807299975

    authors: Sanger TD,Kukke SN,Sherman-Levine S

    更新日期:2007-01-01 00:00:00

  • Should autistic children be evaluated for mitochondrial disorders?

    abstract::Autism is etiologically heterogeneous; medical conditions are implicated in only a minority of cases, whereas metabolic disorders are even less common. Recently, there have been articles describing the association of autism with mitochondrial abnormalities. We critically review the current literature and conclude that...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307380401900510

    authors: Lerman-Sagie T,Leshinsky-Silver E,Watemberg N,Lev D

    更新日期:2004-05-01 00:00:00

  • Ischemic stroke in the young: evaluation and age comparison of patients six months to thirty-nine years.

    abstract::Ischemic stroke in the young is uncommon, but we currently evaluate at least one young stroke patient at our institutions each week. We undertook this chart review of strokes in patients between the ages of 6 months and 39 years to review all conditions associated with, and thus possibly contributory to, the stroke. W...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389300800311

    authors: Kerr LM,Anderson DM,Thompson JA,Lyver SM,Call GK

    更新日期:1993-07-01 00:00:00

  • Auditory brainstem evoked potentials in early-treated congenital hypothyroidism.

    abstract::To evaluate the effect of early treatment of congenital hypothyroidism on central nervous system development, auditory brainstem evoked potentials were determined in 32 patients with hyperthyrotropinemia diagnosed during neonatal screening. The patients included 27 with congenital hypothyroidism and 5 with transient h...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700707

    authors: Chou YH,Wang PJ

    更新日期:2002-07-01 00:00:00

  • Cognitive profile of Rett syndrome.

    abstract::We report preliminary studies in 18 girls with Rett syndrome (15 typical, three atypical cases) who were studied using a number of neuropsychologic measures. Results indicate a relative preservation of gross motor and daily living skills at the developmental level of the age of onset of the condition. Other adaptive f...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073888003001s05

    authors: Fontanesi J,Haas RH

    更新日期:1988-01-01 00:00:00

  • Cerebrospinal Fluid Analysis for Viruses by Metagenomic Next-Generation Sequencing in Pediatric Encephalitis: Not Yet Ready for Prime Time?

    abstract:BACKGROUND:Metagenomic next-generation sequencing offers an unbiased approach to identifying viral pathogens in cerebrospinal fluid of patients with meningoencephalitis of unknown etiology. METHODS:In an 11-month case series, we investigated the use of cerebrospinal fluid metagenomic next-generation sequencing to diag...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820972232

    authors: Erdem G,Kaptsan I,Sharma H,Kumar A,Aylward SC,Kapoor A,Shimamura M

    更新日期:2020-11-18 00:00:00

  • A neurologic presentation of familial hemophagocytic lymphohistiocytosis which mimicked septic emboli to the brain.

    abstract::Familial hemophagocytic lymphohistiocytosis is an inherited deficiency of natural killer cell function and excessive cytokine activity, which predominantly presents in early childhood. The initial symptoms of familial hemophagocytic lymphohistiocytosis are often nonspecific but may be predominantly neurologic. The cas...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073807304203

    authors: Turtzo LC,Lin DD,Hartung H,Barker PB,Arceci R,Yohay K

    更新日期:2007-07-01 00:00:00

  • Alterations of urinary acetylcarnitine in valproate-treated rats: the effect of L-carnitine supplementation.

    abstract::Urinary excretion of acetylcarnitine was measured by high-performance liquid chromatography in two experimental groups of valproate-treated rats. In the urine of mature rats weighing 180 to 200 g treated with valproate (500 mg/kg/day), acetylcarnitine levels were higher than those in controls on days 4 and 7, while L-...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389200700414

    authors: Murakami K,Sugimoto T,Nishida N,Woo M,Araki A,Kobayashi Y

    更新日期:1992-10-01 00:00:00

  • Primary and secondary carnitine deficiency syndromes.

    abstract::The objective of this article is to review primary and secondary causes of carnitine deficiency, emphasizing recent advances in our knowledge of fatty acid oxidation. It is now understood that the cellular metabolism of fatty acids requires the cytosolic carnitine cycle and the mitochondrial beta-oxidation cycle. Carn...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:

    authors: Pons R,De Vivo DC

    更新日期:1995-11-01 00:00:00

  • Neuropsychological findings in childhood narcolepsy.

    abstract::Narcolepsy with cataplexy is a severely disabling disorder very often arising in childhood. Data on neuropsychological impairment in children are scant. We administered standardized neuropsychological tests to 13 children with narcolepsy with cataplexy. Overall, our patients displayed multiple patterns of cognitive an...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813508315

    authors: Posar A,Pizza F,Parmeggiani A,Plazzi G

    更新日期:2014-10-01 00:00:00

  • Cerebellar Volume in Children With Attention-Deficit Hyperactivity Disorder (ADHD).

    abstract::Attention Deficit Hyperactivity Disorder (ADHD) is associated with altered cerebellar volume and cerebellum is associated with cognitive performance. However there are mixed results regarding the cerebellar volume in young patients with ADHD. To clarify the size and direction of this effect, we conducted the analysis ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0883073816678550

    authors: Wyciszkiewicz A,Pawlak MA,Krawiec K

    更新日期:2017-02-01 00:00:00

  • The multiple causes of multiple sclerosis: the importance of age of infections in childhood.

    abstract::The geographic distribution of multiple sclerosis (MS) may relate to the age of initial exposure and degree of sensitization to common viruses or bacteria which have proteins with epitopes (antigenic determinants) which are homologous with potentially encephalitogenic peptides in central myelin proteins, such as basic...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388700200418

    authors: Alvord EC Jr,Jahnke U,Fischer EH,Kies MW,Driscoll BF,Compston DA

    更新日期:1987-10-01 00:00:00

  • Headache as a sole manifestation in nonconvulsive status epilepticus.

    abstract::Nonconvulsive status epilepticus may present with several manifestations, and many of them may not be obvious. The most important for the diagnosis of nonconvulsive status epilepticus is the electroencephalogram pattern. This is a case report of a 9-year-old boy with severe and continuous headache. He received chemoth...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073807303252

    authors: Ghofrani M,Mahvelati F,Tonekaboni H

    更新日期:2007-05-01 00:00:00

  • Multivoxel magnetic resonance spectroscopy in a rhizomelic chondrodysplasia punctata case.

    abstract::A case of a 5-day-old newborn with rhizomelic chondrodysplasia punctata was investigated with multivoxel magnetic resonance spectroscopy, including chemical shift imaging maps, which disclosed a decrease in the choline peak and the choline signal intensity, respectively, in the right cerebral hemisphere. This is the s...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200081401

    authors: Sigirci A,Alkan A,Kutlu R,Gülcan H

    更新日期:2005-08-01 00:00:00

  • Acute pseudobulbar palsy due to bilateral focal cortical damage: the opercular syndrome of Foix-Chavany-Marie.

    abstract::Two children are described who suddenly developed an encephalitic illness with intractable bilateral facial seizures. The seizures subsided over several days, but the children were left with the signs of pseudobulbar palsy and are unable to speak or swallow effectively. Bilateral destructive lesions in the opercular r...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388900400213

    authors: Grattan-Smith PJ,Hopkins IJ,Shield LK,Boldt DW

    更新日期:1989-04-01 00:00:00

  • Comorbid Medical Conditions in Friedreich Ataxia: Association With Inflammatory Bowel Disease and Growth Hormone Deficiency.

    abstract::Friedreich ataxia is a progressive degenerative disease with neurologic and cardiac involvement. This study characterizes comorbid medical conditions in a large cohort of patients with Friedreich ataxia. Patient diagnoses were collected in a large natural history study of 641 subjects. Prevalence of diagnoses in the c...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0883073816643408

    authors: Shinnick JE,Schadt K,Strawser C,Wilcox N,Perlman SL,Wilmot GR,Gomez CM,Mathews KD,Yoon G,Zesiewicz T,Hoyle C,Subramony SH,Yiu EM,Delatycki MB,Brocht AF,Farmer JM,Lynch DR

    更新日期:2016-08-01 00:00:00

  • Alexander's disease: unique presentation.

    abstract::Subacute necrotizing encephalomyelopathy (Leigh syndrome) refers to a nebulous disease entity characterized by lactic acidosis, a wide variety a clinical manifestations, and a consistent conglomeration of pathologic findings. Several abnormalities in metabolism have been delineated in association with Leigh syndrome, ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400510

    authors: Gingold MK,Bodensteiner JB,Schochet SS,Jaynes M

    更新日期:1999-05-01 00:00:00

  • Relationship of cognitive functioning, whole brain volumes, and T2-weighted hyperintensities in neurofibromatosis-1.

    abstract::Using quantitative magnetic resonance imaging morphometry, we report that the whole brain volumes of patients with neurofibromatosis-1 are significantly larger than normal, confirm the prevalence of macrocephaly as about 50%, and report that macrocephaly in patients with neurofibromatosis-1 does not appear to be relat...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500303

    authors: Cutting LE,Koth CW,Burnette CP,Abrams MT,Kaufmann WE,Denckla MB

    更新日期:2000-03-01 00:00:00

  • Incidental neuroimaging findings in nonacute headache.

    abstract::We studied the frequency and consequences of incidental neuroimaging findings in 400 otherwise healthy, nonacute pediatric headache patients through a retrospective, cross-sectional analysis. We excluded patients with currently recommended clinical criteria to consider diagnostic neuroimaging. We categorized neuroimag...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809353149

    authors: Graf WD,Kayyali HR,Abdelmoity AT,Womelduff GL,Williams AR,Morriss MC

    更新日期:2010-10-01 00:00:00

  • Ependymoma: an update.

    abstract::The authors provide an update on most issues related to biology, diagnosis, and treatment of children with ependymoma based on a literature review. Ependymoma is the third most common brain tumor in children and overall survival ranges from 24% to 75% at 5 years. The extent of surgical resection remains the principal ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073809339212

    authors: Zacharoulis S,Moreno L

    更新日期:2009-11-01 00:00:00

  • Medical Comorbidity of Attention-Deficit/Hyperactivity Disorder in US Adolescents.

    abstract::Understanding patterns of medical comorbidity in attention-deficit/hyperactivity disorder (ADHD) may lead to better treatment of affected individuals as well as aid in etiologic study of disease. This article provides the first systematic evaluation on the medical comorbidity of ADHD in a nationally representative sam...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073816653782

    authors: Jameson ND,Sheppard BK,Lateef TM,Vande Voort JL,He JP,Merikangas KR

    更新日期:2016-10-01 00:00:00

  • Pediatric-Onset Postural Orthostatic Tachycardia Syndrome in a Single Tertiary Care Center.

    abstract:AIM:We characterize the pediatric postural orthostatic tachycardia syndrome (POTS) population seen at a single tertiary care referral center. METHOD:Retrospective chart review of all pediatric POTS patients seen in our center between 2015 and 2017. Pediatric POTS was defined as chronic, at least 3 months, symptoms of ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820916260

    authors: Staples A,Thompson NR,Moodley M

    更新日期:2020-07-01 00:00:00

  • Genetic or Other Causation Should Not Change the Clinical Diagnosis of Cerebral Palsy.

    abstract::High throughput sequencing is discovering many likely causative genetic variants in individuals with cerebral palsy. Some investigators have suggested that this changes the clinical diagnosis of cerebral palsy and that these individuals should be removed from this diagnostic category. Cerebral palsy is a neurodevelopm...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073819840449

    authors: MacLennan AH,Lewis S,Moreno-De-Luca A,Fahey M,Leventer RJ,McIntyre S,Ben-Pazi H,Corbett M,Wang X,Baynam G,Fehlings D,Kurian MA,Zhu C,Himmelmann K,Smithers-Sheedy H,Wilson Y,Ocaña CS,van Eyk C,Badawi N,Wintle RF,Ja

    更新日期:2019-07-01 00:00:00

  • Neurobiology of specific language impairment.

    abstract::This review summarizes what is known about the neurobiology of specific language impairment. Despite its name, specific language impairment is frequently not specific. It is common to find associated impairments in motor skills, cognitive function, attention, and reading in children who meet criteria for specific lang...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738040190070101

    authors: Webster RI,Shevell MI

    更新日期:2004-07-01 00:00:00

  • Papilledema in Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP): A Pediatric Case and Review of the Literature.

    abstract:OBJECTIVE:To analyze the available literature on papilledema in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), report the first detailed pediatric case, and explore the underlying pathophysiology. METHODS:First, we conducted a comprehensive literature review of all cases of papilledema in CIDP. Next...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820925302

    authors: Abrams AW,Sah JP,Pavlakis SG

    更新日期:2020-09-01 00:00:00

  • Neurofibromatosis type 1: magnetic resonance imaging findings.

    abstract::The purpose of this study was to determine the locations and characterize the types of brain abnormalities noted on brain magnetic resonance imaging in patients with probable and definite neurofibromatosis type 1. Patients with definite neurofibromatosis type 1 (n = 17) were studied when clinically indicated, and pati...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389300800105

    authors: DiMario FJ Jr,Ramsby G,Greenstein R,Langshur S,Dunham B

    更新日期:1993-01-01 00:00:00

  • Novel Mutations in CLN5 of Chinese Patients With Neuronal Ceroid Lipofuscinosis.

    abstract::Neuronal ceroid lipofuscinosis is a hereditary disease, and ceroid-lipofuscinosis neuronal protein 5 (CLN5) has been proved to be associated with neuronal ceroid lipofuscinosis. Here we report 3 patients from 2 families diagnosed with CLN5 neuronal ceroid lipofuscinosis. Whole genome sequencing of DNAs from 3 patients...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073818789024

    authors: Ge L,Li HY,Hai Y,Min L,Xing L,Min J,Shu HX,Mei OY,Hua L

    更新日期:2018-11-01 00:00:00