Suicide Screening in Sturge-Weber Syndrome: An Important Issue in Need of Further Study.

Abstract:

BACKGROUND:Sturge-Weber syndrome is a neurocutaneous disorder associated with epilepsy, glaucoma, cognitive impairments, and a port-wine birthmark. Although individuals with Sturge-Weber syndrome are vulnerable to known risk factors for suicide, including chronic illness and physical differences (port-wine birthmark), frequency of suicidal ideation and attempts, and the clinical factors associated with suicide risk, in patients with Sturge-Weber syndrome is unknown. METHODS:As a part of routine hospital practice, all outpatients aged eight years and older underwent suicide risk screening during nursing triage using a standardized suicide screening tool. Suicide risk screening results, demographic variables, and medical history (as available) for patients with Sturge-Weber syndrome (N = 34; median age = 15.5; range = 8 to 47 years, 44% male) and other neurological conditions seen at the same institution (N = 369; median age = 14; range = 8 to 78 years, 66% male) were used for retrospective within- and between-group analysis. RESULTS:In the combined sample of Sturge-Weber syndrome and neurologically involved patients, a positive suicide risk screen was related to Sturge-Weber syndrome diagnosis (P = 0.043); analysis by sex showed increased risk of Sturge-Weber syndrome diagnosis in males (P = 0.008), but not in females. Within the Sturge-Weber syndrome group, use of a selective serotonin reuptake inhibitor (P = 0.019) was related to a positive risk screen. CONCLUSION:People with Sturge-Weber syndrome may be at greater risk of suicidal thoughts or behaviors than those with other neurological conditions. Further study of suicide risk in patients with Sturge-Weber syndrome is needed.

journal_name

Pediatr Neurol

journal_title

Pediatric neurology

authors

Sebold AJ,Ahmed AS,Ryan TC,Cohen BA,Jampel HD,Suskauer SJ,Zabel TA,Comi AM,Rybczynski S

doi

10.1016/j.pediatrneurol.2020.03.013

subject

Has Abstract

pub_date

2020-09-01 00:00:00

pages

80-86

eissn

0887-8994

issn

1873-5150

pii

S0887-8994(20)30092-8

journal_volume

110

pub_type

杂志文章
  • Ratio of Alpha 2-Macroglobulin Levels in Cerebrospinal Fluid and Serum: An Expression of Neuroinflammation in Acute Disseminated Encephalomyelitis.

    abstract:BACKGROUND:Acute encephalitis and encephalopathy are life-threatening diseases in children. However, no laboratory examinations are performed for their early diagnosis and treatment. Alpha 2-macroglobulin (α2M) is a blood glycoprotein that increases during the early stages of inflammation. In the present study, we inve...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2019.04.020

    authors: Suzuki Y,Hashimoto K,Hoshi K,Ito H,Kariya Y,Miyazaki K,Sato M,Kawasaki Y,Yoshida M,Honda T,Hashimoto Y,Hosoya M

    更新日期:2019-09-01 00:00:00

  • Adherence of adolescents to multiple sclerosis disease-modifying therapy.

    abstract::In this mixed-methods study, utilization data for disease-modifying therapies were reviewed to determine the adherence rate among our pediatric multiple sclerosis cohort. Adolescents were interviewed to explore their experiences with multiple sclerosis and the impact of peer relationships on adherence to treatment. Se...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2009.03.004

    authors: Thannhauser JE,Mah JK,Metz LM

    更新日期:2009-08-01 00:00:00

  • Efficacy of felbamate in the treatment of intractable pediatric epilepsy.

    abstract::The antiepileptic drug felbamate has demonstrated efficacy against a variety of seizure types in the pediatric population, particularly seizures associated with Lennox-Gastaut syndrome. Postmarketing experience, however, revealed serious idiosyncratic adverse effects not observed during clinical trials, including apla...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2010.02.013

    authors: Zupanc ML,Roell Werner R,Schwabe MS,O'Connor SE,Marcuccilli CJ,Hecox KE,Chico MS,Eggener KA

    更新日期:2010-06-01 00:00:00

  • Severe adolescent head injury: implications for transition into adult life.

    abstract::This report describes the outcomes of 28 children who had severe head injuries between 13-18 years of age. All were unconscious at least 24 hours and have been followed at least 2 years after injury. At present, their ages range from 18 to 27 years. Their educational achievements, social activities, marital status, fu...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(88)90079-3

    authors: Kriel RL,Krach LE,Bergland MM,Panser LA

    更新日期:1988-11-01 00:00:00

  • Cerebral vascular events associated with ulcerative colitis in children.

    abstract::Although peripheral vascular thrombic events are recognized as a serious extra-intestinal complication of inflammatory bowel disease, the occurrence of cerebral vascular events in association with acute exacerbations of this group of diseases is rare. In this article, relevant literature is reviewed and three children...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(00)00264-2

    authors: Keene DL,Matzinger MA,Jacob PJ,Humphreys P

    更新日期:2001-03-01 00:00:00

  • Recurrent intracranial ependymoma in children: salvage therapy with oral etoposide.

    abstract::Chronic oral VP-16 (etoposide) is a chemotherapy regimen with a wide application in oncology and documented efficacy against germ cell tumors, lymphomas, Kaposi's sarcoma, and primary brain tumors. This study was performed to assess the toxicity and activity of chronic oral etoposide in the management of children with...

    journal_title:Pediatric neurology

    pub_type: 临床试验,杂志文章

    doi:10.1016/s0887-8994(00)00249-6

    authors: Chamberlain MC

    更新日期:2001-02-01 00:00:00

  • Phase I trial of pirfenidone in children with neurofibromatosis 1 and plexiform neurofibromas.

    abstract::We aimed to define the dose of pirfenidone in children and adolescents with neurofibromatosis 1 and plexiform neurofibromas that is pharmacokinetically comparable to the active adult dose. Pirfenidone was administered orally on a continuous dosing schedule. The starting dose level was 250 mg/m2/dose. The second dose l...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2007.01.009

    authors: Babovic-Vuksanovic D,Widemann BC,Dombi E,Gillespie A,Wolters PL,Toledo-Tamula MA,O'Neill BP,Fox E,MacDonald T,Beck H,Packer RJ

    更新日期:2007-05-01 00:00:00

  • Childhood chronic inflammatory demyelinating polyneuropathy with nonuniform pathologic features.

    abstract::Nonuniform pathologic changes in chronic inflammatory demyelinating polyneuropathy were previously reported only in adult humans. We analyzed the pathologic features of 12 children, aged 2-17 years, with chronic inflammatory demyelinating polyneuropathy. Six patients manifested a preceding illness. Five patients prese...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2010.04.001

    authors: Luan X,Zheng R,Chen B,Yuan Y

    更新日期:2010-08-01 00:00:00

  • Myotoxicity of lipid-lowering agents in a teenager with MELAS mutation.

    abstract::The use of lipid-lowering statins has been associated with raised serum muscle enzymes and, occasionally, with rhabdomyolysis, especially in patients with pre-existing metabolic myopathies. The A3243G mutation is one of the most common mutations associated with mitochondrial disorders. A teenager harboring the A3243G ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2008.09.002

    authors: Tay SK,Dimauro S,Pang AY,Lai PS,Yap HK

    更新日期:2008-12-01 00:00:00

  • Acute necrotizing encephalopathy associated with hemophagocytic syndrome.

    abstract::A 7-year-old female suddenly exhibited high fever and convulsions, and entered a semi-coma. She also had thrombocytopenia, elevated aminotransferase, prolonged prothrombin time and activated partial thromboplastin time, and hemophagocytes in the bone marrow. The brain magnetic resonance imaging revealed multiple low-i...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2005.08.030

    authors: Akiyoshi K,Hamada Y,Yamada H,Kojo M,Izumi T

    更新日期:2006-04-01 00:00:00

  • Benign hereditary chorea improved on stimulant therapy.

    abstract::Stimulant therapy is usually contraindicated in patients with movement disorders such as tics or chorea. A young boy is reported who had benign hereditary chorea and attention deficit disorder, whose chorea, handwriting, and independent ambulation paradoxically improved with methylphenidate treatment. ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(96)00056-2

    authors: Friederich RL

    更新日期:1996-05-01 00:00:00

  • Modeling developmental plasticity after perinatal stroke: defining central therapeutic targets in cerebral palsy.

    abstract::Perinatal stroke is presented as the ideal human model of developmental neuroplasticity. The precise timing, mechanisms, and locations of specific perinatal stroke diseases provide common examples of well defined, focal, perinatal brain injuries. Motor disability (hemiparetic cerebral palsy) constitutes the primary ad...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/j.pediatrneurol.2012.08.001

    authors: Kirton A

    更新日期:2013-02-01 00:00:00

  • Vagus nerve stimulation for refractory epilepsy in tuberous sclerosis.

    abstract::The goal of the study was to assess the long-term seizure and neuropsychologic outcomes of patients with tuberous sclerosis and refractory epilepsy who received vagus nerve stimulator implantation. Eleven patients with a follow-up period of at least 12 months were studied retrospectively. The mean age at the time of i...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2010.03.003

    authors: Zamponi N,Petrelli C,Passamonti C,Moavero R,Curatolo P

    更新日期:2010-07-01 00:00:00

  • Prognostic correlative values of the late-infancy MRI pattern in term infants with perinatal asphyxia.

    abstract::The aim of this study was to define the risk ratios of the late-infancy magnetic resonance imaging pattern for long-term outcome in term infants with perinatal asphyxia. We evaluated 65 term infants with perinatal asphyxia and performed magnetic resonance imaging examinations between 4-12 months of age. Magnetic reson...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2003.11.012

    authors: Tekgul H,Serdaroglu G,Yalman O,Tutuncuoglu S

    更新日期:2004-07-01 00:00:00

  • Tyrosine hydroxylase deficiency in Taiwanese infants.

    abstract::We analyzed the clinical manifestations, genetic mutations, treatment responses to L-dopa, and long-term neurologic outcomes in Taiwanese infants with tyrosine hydroxylase deficiency. From 1999 to May 2011, we enrolled six infants who had been diagnosed with tyrosine hydroxylase deficiency by identifying point mutatio...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2011.11.012

    authors: Chi CS,Lee HF,Tsai CR

    更新日期:2012-02-01 00:00:00

  • Computed tomography and magnetic resonance imaging in late-onset globoid cell leukodystrophy (Krabbe disease).

    abstract::A five-year-old white male presented with a history of progressive loss of vision that was subsequently followed by progressive corticospinal dysfunction. Evaluation revealed the presence of leukodystrophy which was confirmed by a deficiency of the enzyme, galactosylceramide beta-galactosidase. We present the clinical...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(85)80009-6

    authors: Brownsworth RD,Bodensteiner JB,Schaefer GB,Barnes P

    更新日期:1985-07-01 00:00:00

  • Outcomes of Diagnostic Exome Sequencing in Patients With Diagnosed or Suspected Autism Spectrum Disorders.

    abstract:BACKGROUND:Exome sequencing has recently been proved to be a successful diagnostic method for complex neurodevelopmental disorders. However, the diagnostic yield of exome sequencing for autism spectrum disorders has not been extensively evaluated in large cohorts to date. MATERIALS AND METHODS:We performed diagnostic ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2017.01.033

    authors: Rossi M,El-Khechen D,Black MH,Farwell Hagman KD,Tang S,Powis Z

    更新日期:2017-05-01 00:00:00

  • Calf muscle volume estimates: implications for botulinum toxin treatment?

    abstract::An optimal botulinum toxin dose may be related to the volume of the targeted muscle. We investigated the suitability of using ultrasound and anthropometry to estimate gastrocnemius and soleus muscle volume. Gastrocnemius and soleus muscle thickness was measured in 11 cadaveric human legs, using ultrasound. Lower leg l...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2007.05.019

    authors: Bandholm T,Sonne-Holm S,Thomsen C,Bencke J,Pedersen SA,Jensen BR

    更新日期:2007-10-01 00:00:00

  • Availability of frequency-selective fat-saturation pulse (Fat-Sat) MRI in childhood optic neuritis.

    abstract::A 2-year-old boy with acute optic neuritis, confirmed by gadolinium-DTPA enhancement of the optic nerve using frequency-selective fat-saturation pulse magnetic resonance imaging (Fat-Sat MRI), is reported. Because it is difficult in very young children to sufficiently evaluate visual acuity, visual field, and retroocu...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00254-5

    authors: Takanashi J,Sugita K,Matsubayashi J,Sato K,Niimi H

    更新日期:1996-01-01 00:00:00

  • Wide cavum septum pellucidum: a marker of disturbed brain development.

    abstract::A wide cavum septum pellucidum defined as a separation of greater than 1 cm of the leaves occurs uncommonly. Nine children with wide cavum septum pellucidum were studied; 8 were abnormal. Observed abnormalities included cognitive impairment (8), seizures (4), hypoplasia of the corpus callosum (4), optic nerve hypoplas...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(90)90007-n

    authors: Bodensteiner JB,Schaefer GB

    更新日期:1990-11-01 00:00:00

  • Clinical spectrum of reversible posterior leukoencephalopathy syndrome.

    abstract::Reversible posterior leukoencephalopathy syndrome is a recently recognized disorder with characteristic radiologic findings that mainly involve the white/gray matter of the parieto-occipital lobes. This complex syndrome is associated with cyclosporine A therapy or a variety of other conditions in which blood pressure ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(01)00265-x

    authors: Kwon S,Koo J,Lee S

    更新日期:2001-05-01 00:00:00

  • Myopathy with abnormal distribution of dystrophin, growth retardation, mental retardation, and hypospadia.

    abstract::A 9-year-old boy with severe growth retardation, mild mental retardation, and hypospadia had a high serum CK level without muscle weakness and atrophy. Muscle biopsy revealed a moderate variation in fiber size with a few necrotic and scattered regenerating fibers. Although muscle membranes were clearly stained by immu...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(93)90094-s

    authors: Nagai T,Tuchiya Y,Maruyama A,Sakuta R,Nonaka I

    更新日期:1993-05-01 00:00:00

  • Clinically Mild Encephalopathy With a Reversible Splenial Lesion Type 2 Caused by Human Herpesvirus 6 Infection.

    abstract:BACKGROUND:Clinically mild encephalopathy with a reversible splenial lesion (MERS) is the second commonest cause of encephalopathy. Several pathogens have been detected in patients with MERS type 2, such as influenza A and B, but little is known about the proportion of cases of MERS type 2 with this pathogenesis. Human...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2020.08.021

    authors: Sano F,Fukao T,Tamaru K,Kanemura H,Inukai T,Aihara M

    更新日期:2020-12-01 00:00:00

  • Bacterial meningitis as an etiology of perinatal cerebral infarction.

    abstract::Despite significant improvement in mortality rate, survivors of neonatal bacterial meningitis experience a significant incidence of neurodevelopmental sequelae. Neuropathologic studies have demonstrated vasculitis, arachnoiditis, and ventriculitis with secondary edema and encephalomalacia. Areas of cerebral infarction...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(86)90019-6

    authors: Ment LR,Ehrenkranz RA,Duncan CC

    更新日期:1986-09-01 00:00:00

  • Epidemiology of bacterial meningitis in children: Aichi Prefecture, Japan, 1984-1993.

    abstract::The details of 328 patients with bacterial meningitis, admitted from 1984 through 1993, were obtained from 46 departments of pediatrics of large hospitals through questionnaires. The incidence rate per 100,000 child-years was 2.32, being higher in children aged 0-4 years (rate, 7.22) than 5-15 years (rate, 0.49). The ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(96)00024-0

    authors: Ishikawa T,Asano Y,Morishima T,Nagashima M,Sobue G,Watanabe K,Yamaguchi H

    更新日期:1996-04-01 00:00:00

  • Value of gadolinium in brain MRI examinations for developmental delay.

    abstract::The aim of this study was to evaluate the added utility of gadolinium administration in the magnetic resonance imaging evaluation of developmental delay in children less than 2 years of age. A computerized retrospective study identified all brain magnetic resonance imaging examinations using gadolinium performed at ou...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2006.02.014

    authors: Foerster BR,Ksar J,Petrou M,Eldevik PO,Maly PV,Carlson MD,Sundgren PC

    更新日期:2006-08-01 00:00:00

  • Laterality of brain and ocular lesions in Aicardi syndrome.

    abstract::This study reports a large case series of children with Aicardi syndrome. A new severity scoring system is established to assess sidedness of ocular and brain lesions. Thirty-five children were recruited from Aicardi syndrome family conferences. All children received dilated ophthalmologic examinations, and brain magn...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2011.04.007

    authors: Cabrera MT,Winn BJ,Porco T,Strominger Z,Barkovich AJ,Hoyt CS,Wakahiro M,Sherr EH

    更新日期:2011-09-01 00:00:00

  • Rapid cycling in severely multidisabled children: a form of bipolar affective disorder?

    abstract::A debilitating, regularly recurring, biphasic disorder is described in 6 severely multidisabled children. It was characterized by several days of lethargy, withdrawal, loss of abilities, irritability, and hypersomnolence followed or preceded by a high-energy state for several days during which the children slept very ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)90064-7

    authors: Jan JE,Abroms IF,Freeman RD,Brown GM,Espezel H,Connolly MB

    更新日期:1994-02-01 00:00:00

  • West syndrome following deep hypothermic infant cardiac surgery.

    abstract::Postoperative seizures are among the more common complications of cardiac surgery in children. These seizures have traditionally been considered benign, transient phenomena with little, if any, prognostic significance. We report 4 infants with early postoperative seizures following cardiac surgery who later developed ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(94)90111-2

    authors: du Plessis AJ,Kramer U,Jonas RA,Wessel DL,Riviello JJ

    更新日期:1994-10-01 00:00:00

  • Narcolepsy with cataplexy as presenting symptom of occult neuroblastoma.

    abstract::Neuroblastoma associated with the paraneoplastic syndrome of opsoclonus-myoclonus is well-described. However, presentation with narcolepsy-cataplexy is not well-documented in the literature. Narcolepsy with cataplexy is also rare in children younger than 5 years of age. Here we describe three patients, each presenting...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2012.12.038

    authors: Sinsioco C,Silver K,Forrest KM,Gray J,Nechay A,Sheldon S,Chelmicka Schorr E

    更新日期:2013-07-01 00:00:00