The Impact of Sleep on Disability and School Functioning: Results From a Tertiary Pediatric Headache Center.

Abstract:

:Pediatric headache patients often experience significant sleep disturbance, which may be a risk factor for poor physical, academic, and emotional functioning, including increased anxiety/fear. The current retrospective cohort study of a clinical sample of youth with persistent headache aimed to examine the impact of sleep on functional outcomes and to explore pain-related fear as a mediator of the association between sleep problems and functioning. A total of 109 youth (aged 7-17 years) with persistent headache presenting to a tertiary pediatric headache center (and their parents) completed measures of sleep problems, fear of pain, functional disability, and school functioning at the time of an initial evaluation and 6 months later. After controlling for age and headache frequency and severity, linear regression analyses indicated that increased sleep problems at baseline were associated with increased functional disability and poorer school functioning at baseline (β = 0.28, P = .01; β = -0.42, P < .001, respectively). Poor sleep at baseline was associated with poorer school functioning (but not functional disability) at follow-up (β = -0.25, P = .02). Mediation models demonstrated an indirect mediating effect of pain-related fear on the association between baseline sleep problems and follow-up functional disability (β = 0.06, 95% confidence interval 0.01, 0.15) and between baseline sleep problems and follow-up school functioning (β = -0.06, 95% confidence interval -0.13, -0.004). Sleep disturbance in youth with headache may be a risk factor for poor functional outcomes, both concurrently and over time, and may be explained partially through pain-related fear. Given the frequency with which pediatric headache patients experience co-occurring sleep problems, sleep should be thoroughly assessed and considered as a potential early treatment target.

journal_name

J Child Neurol

authors

Clementi MA,Chang YH,Gambhir R,Lebel A,Logan DE

doi

10.1177/0883073819887597

subject

Has Abstract

pub_date

2020-03-01 00:00:00

pages

221-227

issue

3

eissn

0883-0738

issn

1708-8283

journal_volume

35

pub_type

杂志文章
  • Diagnostic difficulty in infants and children.

    abstract::Making an accurate diagnosis is the first and most critical step in the treatment of pediatric epilepsy, but it can be a daunting challenge for clinicians. Seizure types and syndromes in infants and very young children do not present with the same clarity and consistency as in adults. Work is currently being done to r...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738020170010401

    authors: Nordli DR Jr

    更新日期:2002-01-01 00:00:00

  • Organizing logopedic therapy for babies with unilateral and bilateral brain lesion in the prespeech period.

    abstract::The goal of the research was to point out the importance of early prespeech therapy for babies suffering from at-birth-acquired unilateral or bilateral lesion in the prespeech period of development. On the basis of existing studies and experience in the field, a protocol and methodology for the observation of the phon...

    journal_title:Journal of child neurology

    pub_type: 临床试验,杂志文章

    doi:10.1177/0883073807299970

    authors: Gec V

    更新日期:2007-01-01 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

  • Speed-Accuracy Trade-Off in a Trajectory-Constrained Self-Feeding Task: A Quantitative Index of Unsuppressed Motor Noise in Children With Dystonia.

    abstract::Motor speed and accuracy are both affected in childhood dystonia. Thus, deriving a speed-accuracy function is an important metric for assessing motor impairments in dystonia. Previous work in dystonia studied the speed-accuracy trade-off during point-to-point tasks. To achieve a more relevant measurement of functional...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073815578526

    authors: Lunardini F,Bertucco M,Casellato C,Bhanpuri N,Pedrocchi A,Sanger TD

    更新日期:2015-10-01 00:00:00

  • Rett syndrome: a mitochondrial disease?

    abstract::Six girls between 2 years 9 months and 15 years of age with Rett syndrome were thoroughly investigated. Blood ammonia levels varied between 42 and 123 mumol/L, and serum lactate concentration was slightly elevated in two girls. Electroencephalograms showed a dysrhythmic pattern during wakefulness; during drowsiness an...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389000500311

    authors: Eeg-Olofsson O,al-Zuhair AG,Teebi AS,Daoud AS,Zaki M,Besisso MS,Al-Essa MM

    更新日期:1990-07-01 00:00:00

  • Blindness from late presenting undiagnosed pancraniosynostosis mimicking pseudotumor cerebri.

    abstract::We report the unique case of late-onset pancraniosynostosis presenting with rapid visual deterioration, without other symptoms of increased intracranial pressure. A 10-year-old girl had episodes of blurry vision for 1 month. Magnetic resonance imaging (MRI) demonstrated a borderline Chiari I malformation. Ophthalmolog...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813495307

    authors: Bonfield CM,Tamber MS,Losee JE

    更新日期:2014-08-01 00:00:00

  • Neurobiology of Rett syndrome.

    abstract::Girls with Rett syndrome display signs of neuronal dysfunction including mental retardation, seizures, stereotyped movements, and abnormal breathing and autonomic control. Decelerating head growth during infancy might reflect a disorder in production or pruning of neuronal synapses or both. Recent immunocytochemical s...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738030180100501

    authors: Johnston MV,Mullaney B,Blue ME

    更新日期:2003-10-01 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

  • Cognitive and psychological profile of males with Becker muscular dystrophy.

    abstract::Duchenne and Becker muscular dystrophy are allelic X-linked disorders causing progressive muscle weakness in males. Duchenne muscular dystrophy is caused by absence of dystrophin in muscle and brain; boys with Duchenne muscular dystrophy have a static cognitive impairment with mean Full Scale IQ approximately 1 standa...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0883073807307975

    authors: Young HK,Barton BA,Waisbren S,Portales Dale L,Ryan MM,Webster RI,North KN

    更新日期:2008-02-01 00:00:00

  • Neonate with spinal hypoplasia on T12 and a localized vertebral malformation on L4.

    abstract::We report a case of a neonate with sectional narrowing of the spinal cord on the level of T12 to L2 and a deformed vertebral body on a different level, L4. In previously described cases of sectional spinal dysgenesis, the vertebral and spinal cord malformations are usually found on the same level. Our case may represe...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380101600819

    authors: Weber A,Maier RF,Felderhoff-Mueser U,Lehmann R,Stöver B,Obladen M

    更新日期:2001-08-01 00:00:00

  • Congenital intramedullary tumor with neonatal manifestations.

    abstract::The authors report on a 45-day-old boy with a congenital intramedullary tumor with clinical manifestations since birth. Neurologic examination disclosed severe bilateral lower-limb hypotonia and diplegia, with exacerbated deep tendon reflexes and clonus associated with severe pain at manipulation. Further evaluation o...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400711

    authors: Nunes ML,Coutinho LM,Janisch C,Ehlers JA

    更新日期:1999-07-01 00:00:00

  • Acquired toxoplasmosis accompanied by facial nerve palsy in an immunocompetent 5-year-old child.

    abstract::Acquired toxoplasmosis, although relatively common in children, is usually asymptomatic but can also be clinically manifested by a benign and self-limited infectious mononucleosis-like syndrome. Neurological complications are very rare in immunocompetent children. The authors report a 5-year-old boy who presented with...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810370480

    authors: Galli-Tsinopoulou A,Kyrgios I,Giannopoulou EZ,Gourgoulia S,Maggana I,Katechaki E,Chatzidimitriou D,Evangeliou AE

    更新日期:2010-12-01 00:00:00

  • Longitudinal electroencephalographic (EEG) findings in pediatric anti-N-methyl-D-aspartate (anti-NMDA) receptor encephalitis: the Padua experience.

    abstract::To contribute to characterize electroencephalographic (EEG) activity in pediatric anti-N-methyl-d-aspartate (anti-NMDA) receptor encephalitis, we reviewed electroclinical data of 5 children with anti-NMDA receptor encephalitis diagnosed in our department. We identified 4 longitudinal electroencephalographic phases: in...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813515947

    authors: Nosadini M,Boniver C,Zuliani L,de Palma L,Cainelli E,Battistella PA,Toldo I,Suppiej A,Sartori S

    更新日期:2015-02-01 00:00:00

  • Venlafaxine in children, adolescents, and young adults with autism spectrum disorders: an open retrospective clinical report.

    abstract::Autism is characterized by social deficits, communication and language impairments, narrow restricted interests, repetitive behaviors, inattention, and hyperactivity. While selective serotonin reuptake inhibitors have demonstrated efficacy in treating core symptoms of autism, norepinephrine reuptake inhibitors have de...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500214

    authors: Hollander E,Kaplan A,Cartwright C,Reichman D

    更新日期:2000-02-01 00:00:00

  • Large Artery Stroke in a Child With Hypoparathyroidism.

    abstract::The association of hypoparathyroidism and ischemic stroke is rare in childhood. We report an interesting case of an 11-year-old girl diagnosed to have hypoparathyroidism and presented with an acute-onset right hemiparesis. Investigations revealed large artery ischemic stroke and uncontrolled hypoparathyroidism. Pediat...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814544366

    authors: Dhawan SR,Jondhale SN,Sahu JK,Vyas S,Singhi PD

    更新日期:2015-07-01 00:00:00

  • Meralgia paresthetica in the pediatric population: a propos of 2 cases.

    abstract::Meralgia paresthetica is a mononeuropathy affecting the lateral femoral cutaneous nerve that is extremely rare in children. Two adolescent females, aged 11 and 13 years, presented due to tingling and pain on the side of the thigh of 2 to 3 weeks duration. The general examination revealed mild obesity; the neurological...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809336130

    authors: Fernández-Mayoralas DM,Fernández-Jaén A,Jareño NM,Pérez BC,Fernández PM,Sola AG

    更新日期:2010-01-01 00:00:00

  • Validation of the Expanded Hammersmith Functional Motor Scale in spinal muscular atrophy type II and III.

    abstract::The relationships between the Expanded Hammersmith Functional Motor Scale (HFMSE) and genotype and motor and respiratory outcomes were examined in patients with spinal muscular atrophy types II and III (n = 70). The correlation between the HFMSE and Gross Motor Function Measure was r = 0.98. Correlations between HFMSE...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811420294

    authors: Glanzman AM,O'Hagen JM,McDermott MP,Martens WB,Flickinger J,Riley S,Quigley J,Montes J,Dunaway S,Deng L,Chung WK,Tawil R,Darras BT,De Vivo DC,Kaufmann P,Finkel RS,Pediatric Neuromuscular Clinical Research Network for Spin

    更新日期:2011-12-01 00:00:00

  • Morvan syndrome following B-cell lymphoma.

    abstract::Morvan syndrome is a rare autoimmune disease named after the French physician Augustin Marie Morvan. It is characterized by multiple, irregular contractions of the long muscles, weakness, pruritus, hyperhidrosis, insomnia, and delirium. Here, we describe a 17-year-old young man, previously diagnosed with B-cell lympho...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809356108

    authors: El-Bitar MK,Muwakkit SA,Abboud MR,Sawaya RA,Boustany RM

    更新日期:2010-08-01 00:00:00

  • Endocrine disorders in two sisters affected by MELAS syndrome.

    abstract::A variety of endocrine and metabolic defects, including hypothalamopituitary hypofunction and diabetes mellitus, has been reported in association with mitochondrial disorders. We describe two sisters affected by mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome in whom DNA anal...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001501108

    authors: Balestri P,Grosso S

    更新日期:2000-11-01 00:00:00

  • Periodic Eye Movements and Epileptic Spasms in West Syndrome.

    abstract::In addition to the typical infantile spasm symptoms, several other symptoms, such as eye movements, have been reported to be associated with infantile spasms, although the relationship between the typical spasms and these other events is not fully understood. Here we present a case with West syndrome. We observed the ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813489169

    authors: Kakisaka Y,Kobayashi T,Hino-Fukuyo N,Uematsu M,Numata Y,Mori M,Kure S

    更新日期:2013-11-01 00:00:00

  • Infant-onset progressive myoclonus epilepsy.

    abstract::We report the clinical, electroencephalographic, neurophysiologic, and neuroimaging findings in eight children with infant-onset progressive myoclonus epilepsy, all of whom had muscle biopsies performed as as part of the diagnostic evaluation. Each child had myoclonic seizures, generalized tonic-clonic seizures, and n...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389100600207

    authors: Harbord MG,Hwang PA,Robinson BH,Becker LE,Hunjan A,Murphy EG

    更新日期:1991-04-01 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

  • A 5-year-old male child with late infantile metachromatic leukodystrophy: a case report.

    abstract::Metachromatic leukodystrophy is a rare disorder of myelin metabolism. This degenerative disorder results from the accumulation of cerebroside sulfatide within the myelin sheath of central and peripheral nervous system, due to deficiency of aryl sulfatase A enzyme. We report a 5-year-old male child, who presented with ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814542948

    authors: Mahmood A,Chacham S,Reddy UN,Rao JN,Rao SP

    更新日期:2015-03-01 00:00:00

  • Pseudoseizures caused by hyperventilation resembling absence epilepsy.

    abstract::During the 4-year period, 1982-1986, 18 patients presented to the Children's Hospital, Camperdown, Sydney, with the following features: (1) Recurrent "absences" clinically indistinguishable from childhood absence epilepsy, (2) Normal clinical examination, (3) Electroencephalogram (EEG) demonstrating normal waking back...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389000500403

    authors: North KN,Ouvrier RA,Nugent M

    更新日期:1990-10-01 00:00:00

  • Myalgia and cramps: dystrophinopathy with wide-ranging laboratory findings.

    abstract::We present 12 cases of males with myalgia and cramps and a normal muscle strength examination. All the patients had muscle dystrophin values consistent with Becker muscular dystrophy. Five of the patients had a normal electromyogram, and five had normal light microscopic muscle biopsy results. Of particular note, four...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389601100105

    authors: Samaha FJ,Quinlan JG

    更新日期:1996-01-01 00:00:00

  • Diffusion-weighted imaging in neonatal cerebral infarction: clinical utility and follow-up.

    abstract::We describe the clinical utility of echo-planar diffusion-weighted imaging in neonatal cerebral infarction. Eight full-term neonates aged 1 to 8 days referred for neonatal seizures were studied. Patients were followed for a mean of 17 months with detailed neurologic examinations at regular intervals. Head computed tom...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500905

    authors: Krishnamoorthy KS,Soman TB,Takeoka M,Schaefer PW

    更新日期:2000-09-01 00:00:00

  • Growth patterns in children with intrauterine growth retardation and their correlation to neurocognitive development.

    abstract::The relationship between somatic growth and neurocognitive outcome was studied in a cohort of 136 children with intrauterine growth retardation. The children were followed up from birth to 9 to 10 years of age by annual measurements of growth parameters, neurodevelopmental evaluations, and IQ. The rate of catch-up for...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808331082

    authors: Fattal-Valevski A,Toledano-Alhadef H,Leitner Y,Geva R,Eshel R,Harel S

    更新日期:2009-07-01 00:00:00

  • Use of corticosteroids in a population-based cohort of boys with duchenne and becker muscular dystrophy.

    abstract::The use of corticosteroids for treatment of Duchenne and Becker muscular dystrophy in clinical practice from 1991 through 2005 was reviewed in a large population-based cohort (MD STARnet) of boys in 4 regional sites and 6 clinics of the United States. Corticosteroid use increased from 20% (11 of 56 individuals) in 199...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810362762

    authors: Matthews DJ,James KA,Miller LA,Pandya S,Campbell KA,Ciafaloni E,Mathews KD,Miller TM,Cunniff C,Meaney FJ,Druschel CM,Romitti PA,Fox DJ,MD STARnet.

    更新日期:2010-11-01 00:00:00

  • Body mass index of children with attention-deficit/hyperactivity disorder.

    abstract::An association between overweight and attention-deficit/hyperactivity disorder (ADHD) in children was previously suggested. We examined the prevalence of overweight, anthropometric changes, and the effect of methylphenidate treatment in 275 children with ADHD without neurological comorbidities and in controls. Data we...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810380051

    authors: Dubnov-Raz G,Perry A,Berger I

    更新日期:2011-03-01 00:00:00

  • Depressed left ventricular contractile reserve diagnosed by dobutamine stress echocardiography in a patient with Duchenne muscular dystrophy.

    abstract::Cardiomyopathy is a leading cause of death in patients with Duchenne muscular dystrophy. Congestive heart failure is often sub-clinical and unrecognized as a result of the severe physical limitations of this patient population. We report the case of a 16-year-old boy with Duchenne muscular dystrophy who demonstrated n...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200031401

    authors: Wong BL,Mukkada VA,Markham LW,Cripe LH

    更新日期:2005-03-01 00:00:00