Hypothermia as an adjuvant treatment in paediatric refractory or super-refractory status epilepticus.

Abstract:

:Therapeutic hypothermia is among the adjuvant therapies suggested for refractory or super-refractory status epilepticus (R/SR-SE) in paediatric patients. Experimental evidence of neuroprotective and antiseizure effects provides a strong rationale for using therapeutic hypothermia in patients with status epilepticus. Thus, hypothermia between 20°C and 33°C in animals with status epilepticus is associated not only with significantly less neuronal damage, predominantly in the hippocampal CA1, CA2, and CA3 areas, but also with increased seizure latency and decreased seizure frequency and duration. Therapeutic hypothermia has rarely been used in paediatric R/SR-SE. In the few reported cases, seizure control was markedly improved but nearly half the patients experienced recurrences after rewarming. Studies are needed to clarify the modalities and indications of therapeutic hypothermia in paediatric patients with R/SR-SE. WHAT THIS PAPER ADDS: Hypothermia at 20°C to 33°C is neuroprotective and has antiseizure effects in experimental status epilepticus. In children, antiseizure effects are marked but recurrences after rewarming are common.

journal_name

Dev Med Child Neurol

authors

Legriel S

doi

10.1111/dmcn.14562

subject

Has Abstract

pub_date

2020-09-01 00:00:00

pages

1017-1023

issue

9

eissn

0012-1622

issn

1469-8749

journal_volume

62

pub_type

杂志文章,评审
  • Clinically prescribed orthoses demonstrate an increase in velocity of gait in children with cerebral palsy: a retrospective study.

    abstract::The purpose of this study was to determine the effect clinically prescribed ankle-foot orthoses (AFOs) have on the temporal-spatial parameters of gait, as compared with barefoot walking in children with cerebral palsy. A retrospective chart review of data collected between 1995 and 1999 in our motion analysis laborato...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162201001992

    authors: White H,Jenkins J,Neace WP,Tylkowski C,Walker J

    更新日期:2002-04-01 00:00:00

  • Motor imagery training in hemiplegic cerebral palsy: a potentially useful therapeutic tool for rehabilitation.

    abstract::Converging evidence indicates that motor deficits in cerebral palsy (CP) are related not only to problems with execution, but also to impaired motor planning. Current rehabilitation mainly focuses on alleviating compromised motor execution. Motor imagery is a promising method of training the more 'cognitive' aspects o...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1469-8749.2009.03371.x

    authors: Steenbergen B,Crajé C,Nilsen DM,Gordon AM

    更新日期:2009-09-01 00:00:00

  • Motor impairment in very preterm-born children: links with other developmental deficits at 5 years of age.

    abstract:AIM:To elucidate the relation between motor impairment and other developmental deficits in very preterm-born children without disabling cerebral palsy and term-born comparison children at 5 years of (corrected) age. METHOD:In a prospective cohort study, 165 children (81 very preterm-born and 84 term-born)were assessed...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.12295

    authors: Van Hus JW,Potharst ES,Jeukens-Visser M,Kok JH,Van Wassenaer-Leemhuis AG

    更新日期:2014-06-01 00:00:00

  • Tactile extinction in childhood hemiplegia.

    abstract::Tactile extinction was investigated by the Quality Extinction Test (QET) of Schwartz in 39 patients, 34 of whom had congenital hemiplegia and five early-acquired hemiplegia. Extinction values were significantly higher in hemiplegia patients than in controls and usually contralateral to the side of brain damage, except...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1991.tb14962.x

    authors: Lenti C,Radice L,Cerioli M,Musetti L

    更新日期:1991-09-01 00:00:00

  • Assessing the impact of a child with spina bifida on the family.

    abstract::This study examined the characteristics of families which may be more vulnerable than others to the impact of caring for a child with spina bifida. Morbidity and the use of health services were unexpectedly high. The impact on the family was related less to clinical diagnoses than to the characteristics of the child's...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1986.tb03831.x

    authors: McCormick MC,Charney EB,Stemmler MM

    更新日期:1986-02-01 00:00:00

  • Down's syndrome and the family: follow-up of children first seen in infancy.

    abstract::Twenty-three survivors of a prospective study of infants with Down's syndrome were followed up at eight or nine years of age. All but three lived at home, and those three came home for weekends or school holidays. IQs varied from less than 20 to 80 (mean 48). IQ and adaptive behaviour scores were related to birthweigh...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1984.tb04478.x

    authors: Gath A,Gumley D

    更新日期:1984-08-01 00:00:00

  • Dyskinetic cerebral palsy and birth asphyxia.

    abstract::Of 115 children with dyskinetic cerebral palsy (CP) in the Mersey region, 17 were born at term and at an appropriate weight for age, and have preserved cognitive abilities. 10 of these are likely to have sustained intrapartum asphyxial brain-damage as the cause of their CP. In such circumstances, a characteristic patt...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1994.tb11848.x

    authors: Rosenbloom L

    更新日期:1994-04-01 00:00:00

  • White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene.

    abstract:AIM:Mutations in the SLC16A2 gene have been implicated in Allan-Herndon-Dudley syndrome (AHDS), an X-linked learning disability* syndrome associated with thyroid function test (TFT) abnormalities. Delayed myelination is a non-specific finding in individuals with learning disability whose genetic basis is often uncertai...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.2009.03471.x

    authors: Gika AD,Siddiqui A,Hulse AJ,Edward S,Fallon P,McEntagart ME,Jan W,Josifova D,Lerman-Sagie T,Drummond J,Thompson E,Refetoff S,Bönnemann CG,Jungbluth H

    更新日期:2010-05-01 00:00:00

  • Theophylline neurotoxicity resulting in significant unilateral brain-damage.

    abstract::A case of theophylline neurotoxicity in a three-month-old infant is reported. Prolonged focal seizures with secondary generalization resulted in hemiparesis and developmental retardation, and CT demonstrated cerebral hemiatrophy. Later the infant developed recurrent focal and atonic convulsions, which were refractory ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1985.tb03775.x

    authors: Noetzel MJ

    更新日期:1985-04-01 00:00:00

  • Quality of life instruments for children and adolescents with neurodisabilities: how to choose the appropriate instrument.

    abstract:AIM:There are many misconceptions about what constitutes 'quality of life' (QoL). It is often difficult for researchers and clinicians to determine which instruments will be most appropriate to their purpose. The aim of the current paper is to describe QoL instruments for children and adolescents with neurodisabilities...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1469-8749.2009.03324.x

    authors: Waters E,Davis E,Ronen GM,Rosenbaum P,Livingston M,Saigal S

    更新日期:2009-08-01 00:00:00

  • Applying Dutch and US versions of the BSID-II in Dutch children born preterm leads to different outcomes.

    abstract::The aim of the present study was to evaluate whether the application of Dutch versus US test procedures and norms of the Bayley Scales of Infant Development - 2nd edition (BSID-II) leads to different developmental outcomes. The BSID-II was administered to 376 preterm infants (191 males, 185 females; mean gestational a...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.2008.02067.x

    authors: Westera JJ,Houtzager BA,Overdiek B,van Wassenaer AG

    更新日期:2008-06-01 00:00:00

  • Ataxia-telangiectasia: recommendations for multidisciplinary treatment.

    abstract::Ataxia-telangiectasia is a rare, neurodegenerative, and multisystem disease, characterized by cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency, progressive respiratory failure, and an increased risk of malignancies. It demands specialized care tailored to the individual patient's needs. Besides the c...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,实务指引,评审

    doi:10.1111/dmcn.13424

    authors: van Os NJH,Haaxma CA,van der Flier M,Merkus PJFM,van Deuren M,de Groot IJM,Loeffen J,van de Warrenburg BPC,Willemsen MAAP,A-T Study Group.

    更新日期:2017-07-01 00:00:00

  • The development of independent walking in children with cerebral palsy.

    abstract::Electromyographic and kinematic data were collected during treadmill locomotion by normal infants and infants with cerebral palsy. Locomotor patterns of the infants with cerebral palsy were similar to those of normal infants during the stage of supported locomotion, but as they matured, some of the characteristics of ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1991.tb14926.x

    authors: Leonard CT,Hirschfeld H,Forssberg H

    更新日期:1991-07-01 00:00:00

  • Hereditary sensory neuropathy type II without trophic changes.

    abstract::Three cases with sensory peripheral neuropathies are reported. Case 1 presented with scoliosis, and cases 2 and 3 presented with abnormal gait. None had trophic limb changes, evidence of weakness, or a tendency to self-mutilation and each had normal motor studies on neurophysiological testing. Sural nerve biopsies sho...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1990.tb16915.x

    authors: Bye AM,Baker WD,Pollard J,Wise G

    更新日期:1990-02-01 00:00:00

  • Rethinking preventive post-discharge intervention programmes for very preterm infants and their parents.

    abstract::Post-discharge preventive intervention programmes with involvement of the parent may support the resilience and developmental outcomes of infants born very preterm. Randomized controlled trials of home-based family-centred intervention programmes in very preterm infants that aimed to improve cognitive outcome, at leas...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章,评审

    doi:10.1111/dmcn.13049

    authors: van Wassenaer-Leemhuis AG,Jeukens-Visser M,van Hus JW,Meijssen D,Wolf MJ,Kok JH,Nollet F,Koldewijn K

    更新日期:2016-03-01 00:00:00

  • Demographic and modifiable factors associated with knee contracture in children with cerebral palsy.

    abstract:AIM:To identify the prevalence of knee contracture and its association with gross motor function, age, sex, spasticity, and muscle length in children with cerebral palsy (CP). METHOD:Cross-sectional data for passive knee extension were analysed in 3 045 children with CP (1 756 males, 1 289 females; mean age 8y 1mo [SD...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.13659

    authors: Cloodt E,Rosenblad A,Rodby-Bousquet E

    更新日期:2018-04-01 00:00:00

  • Risk of cerebral palsy in relation to pregnancy disorders and preterm birth: a national cohort study.

    abstract:AIM:To assess the risk of developing cerebral palsy in relation to pregnancy disorders and preterm birth. METHOD:By linking the Medical Birth Registry of Norway to other national registries, we identified all live births in Norway from 1967 through to 2001. Risks of cerebral palsy (CP) after preterm delivery and pregn...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.12430

    authors: Trønnes H,Wilcox AJ,Lie RT,Markestad T,Moster D

    更新日期:2014-08-01 00:00:00

  • Gross and fine motor function and accompanying impairments in cerebral palsy.

    abstract::The aim of this study was to describe and analyze gross and fine motor function and accompanying neurological impairments in children with cerebral palsy (CP) born between 1991 and 1998 in western Sweden. A population-based study comprised 411 children with a diagnosis of CP ascertained at 4 to 8 years of age. Gross M...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/S0012162206000922

    authors: Himmelmann K,Beckung E,Hagberg G,Uvebrant P

    更新日期:2006-06-01 00:00:00

  • Respiratory and sleep disorders in female children with atypical Rett syndrome caused by mutations in the CDKL5 gene.

    abstract:AIM:In female children with drug-resistant seizures and developmental delay from birth, atypical Rett syndrome caused by mutations in the CDKL5 gene should be considered. Several clinical features resemble classic Rett syndrome. Respiratory and sleep abnormalities are frequently present in Rett syndrome, whereas little...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.2012.04432.x

    authors: Hagebeuk EE,van den Bossche RA,de Weerd AW

    更新日期:2013-05-01 00:00:00

  • Muscle response to heavy resistance exercise in children with spastic cerebral palsy.

    abstract::Fourteen ambulatory children with spastic diplegia participated in a bilateral quadriceps strengthening program in an attempt to decrease the amount of knee crouch during gait. Each child exercised three times a week for six weeks using free ankle weights at a load of 65 per cent of maximum. A normal comparison group ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1995.tb15019.x

    authors: Damiano DL,Vaughan CL,Abel MF

    更新日期:1995-08-01 00:00:00

  • Physical impairment, disability and handicap in rural Nepal.

    abstract::Observations were made of people with physical impairments, disabilities and handicaps during a two-month journey in remote, mountainous areas of Nepal where traditional forms of village life have been maintained. Descriptions are given of the types and frequency of visible physical impairments and their distribution ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1983.tb13839.x

    authors: Richardson SA

    更新日期:1983-12-01 00:00:00

  • Health care service for families with children at early risk of developmental delay: an All Our Families cohort study.

    abstract:AIM:This study examined children's health care service use, mothers' workforce participation, and mothers' community engagement based on children's risk of developmental delay. METHOD:We used data from the All Our Families study, a prospective pregnancy cohort. Ages and Stages Questionnaire (ASQ) scores at year 2 indi...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.14343

    authors: Russell MJ,Premji S,Mcdonald S,Zwicker JD,Tough S

    更新日期:2020-03-01 00:00:00

  • Neuroimpairments, activity performance, and participation in children with cerebral palsy mainstreamed in elementary schools.

    abstract::Participation and activity performance (motor and cognitive or behavioural) were examined in 148 children with cerebral palsy (CP; 87 males, 61 females; mean age 9y 8mo, SD 1y 11mo; range 6y 1mo to 13y 7mo), mainstreamed in fully inclusive (n=100) and in self-contained classes (n=48) within general schools in Israel, ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/S0012162205001714

    authors: Schenker R,Coster WJ,Parush S

    更新日期:2005-12-01 00:00:00

  • The septum pellucidum and spatial ability of children with optic nerve hypoplasia.

    abstract::Animal studies suggest that spatial skills are dependent on an intact septum pellucidum. This theory was tested by comparing patients who were visually impaired due to bilateral optic nerve hypoplasia: 13 with a septum pellucidum were compared with six children without a septum pellucidum. There was no difference in s...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1994.tb11832.x

    authors: Groenveld M,Pohl KR,Espezel H,Jan JE

    更新日期:1994-03-01 00:00:00

  • Extra-articular subtalar arthrodesis with cancellous bone graft and internal fixation for children with myelomeningocele.

    abstract::Extra-articular subtalar arthrodesis with cancellous bone graft and internal fixation was performed on 20 feet of 12 children with myelomeningocele, whose average age at operation was 7.4 years. Indication for surgery was progressive hindfoot valgus deformity causing difficulty in fitting orthoses. At average follow-u...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1991.tb05112.x

    authors: Aronson DD,Middleton DL

    更新日期:1991-03-01 00:00:00

  • Skin-to-skin contact (Kangaroo Care) accelerates autonomic and neurobehavioural maturation in preterm infants.

    abstract::The effects of mother-infant skin-to-skin contact (Kangaroo Care; KC) on autonomic functioning, state regulation, and neurobehavioural status was examined in 70 preterm infants, half of whom received KC over 24.31 days (SD 7.24) for a total of 29.76 hours (SD 12.86). Infants were matched for sex (19 males and 16 femal...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1017/s0012162203000525

    authors: Feldman R,Eidelman AI

    更新日期:2003-04-01 00:00:00

  • Power mobility for children: a survey study of American and Canadian therapists' perspectives and practices.

    abstract:AIM:To explore the views and practices of paediatric occupational therapists and physical therapists in Canada and the USA regarding the implementation of power mobility for children with mobility limitations. METHOD:This descriptive study utilized a web-based survey that included questions pertaining to therapists' d...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/dmcn.13960

    authors: Kenyon LK,Jones M,Livingstone R,Breaux B,Tsotsoros J,Williams KM

    更新日期:2018-10-01 00:00:00

  • Autism spectrum disorders: sex differences in autistic behaviour domains and coexisting psychopathology.

    abstract::The purpose of the present study was to examine possible differences between high-functioning males and females with autism spectrum disorder (ASD) regarding the core symptoms of autism and coexisting psychopathology. A total of 23 females and 23 males matched for age, IQ, and ASD diagnoses were recruited(mean age 11y...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.2007.00361.x

    authors: Holtmann M,Bölte S,Poustka F

    更新日期:2007-05-01 00:00:00

  • Children with blindness due to retinopathy of prematurity: a population-based study. Perinatal data, neurological and ophthalmological outcome.

    abstract::A population-based group of 27 children with total blindness due to retinopathy of prematurity (ROP), born in Sweden from 1980 to 1990, was examined. They constituted all but two of the total of 29 children with total blindness due to ROP known to the national register of visually impaired children when reviewed from ...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.1998.tb15439.x

    authors: Jacobson L,Fernell E,Broberger U,Ek U,Gillberg C

    更新日期:1998-03-01 00:00:00

  • Unilateral cerebral palsy: a population-based study of gait and motor function.

    abstract:AIM:To investigate the spectrum and relationships between gait patterns and motor function in a population-based cross study of children with unilateral cerebral palsy (CP). METHOD:Children identified with unilateral CP born in Victoria, Australia, from 1990 to 1992 were eligible to participate. Characteristics were r...

    journal_title:Developmental medicine and child neurology

    pub_type: 杂志文章

    doi:10.1111/j.1469-8749.2010.03878.x

    authors: Dobson F,Morris ME,Baker R,Graham HK

    更新日期:2011-05-01 00:00:00