The use of enoxaparin in children with acute, nonhemorrhagic ischemic stroke.

Abstract:

:The use of low-molecular-weight heparin offers multiple advantages over unfractionated heparins in pediatric patients with acute ischemic stroke. The safety and efficacy of low-molecular-weight heparin have been demonstrated in adults, but less is known about their use in children. This study reviews retrospectively the use of low-molecular-weight heparin in children with acute, ischemic, nonhemorrhagic strokes. A database search was used to locate all children who experienced an ischemic stroke between July 1991 and January 2001 and who were subsequently treated with low-molecular-weight heparin. Eight children were identified (aged 37 months to 17 years; median age, 133 months) who were treated with the low-molecular-weight heparin enoxaparin. Enoxaparin was used in one case as the sole treatment, in six cases as a bridge to oral anticoagulant therapy with warfarin, and in one case as a replacement treatment after several days of warfarin therapy. The median duration of treatment with enoxaparin was 4 days. During this period, no major bleeding complications were observed, and no new thrombi or extensions of thrombi occurred. One patient did experience mild oozing at an intravenous site, and another experienced an episode of epistaxis. Enoxaparin was discontinued in one patient because of discomfort associated with the subcutaneous injections. Although the number of patients was limited, it appears that enoxaparin is a safe and efficacious alternative to the use of unfractionated heparin in children with acute, nonhemorrhagic ischemic stroke.

journal_name

Pediatr Neurol

journal_title

Pediatric neurology

authors

Burak CR,Bowen MD,Barron TF

doi

10.1016/s0887-8994(03)00270-4

subject

Has Abstract

pub_date

2003-10-01 00:00:00

pages

295-8

issue

4

eissn

0887-8994

issn

1873-5150

pii

S0887899403002704

journal_volume

29

pub_type

杂志文章
  • Stroke patterns in neonatal group B streptococcal meningitis.

    abstract::Neonatal group B streptococcus meningitis causes neurologic morbidity and mortality. Cerebrovascular involvement is a common, poorly studied, and potentially modifiable pathologic process. We hypothesized that imaging patterns of focal brain infarction are recognizable in neonatal group B streptococcal meningitis. A c...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2010.11.002

    authors: Hernández MI,Sandoval CC,Tapia JL,Mesa T,Escobar R,Huete I,Wei XC,Kirton A

    更新日期:2011-04-01 00:00:00

  • Attitudes of medical students toward pediatric neurology.

    abstract::Planning strategies to encourage students to pursue a career in pediatric neurology requires assessment of their attitudes and career choices. A structured 30-item questionnaire was designed to examine students' attitudes toward pediatric neurology. In the study, 161 final-year medical students (1999-2000), 20-26 year...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00386-7

    authors: Jan MM,Fida NM

    更新日期:2002-08-01 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

  • Rasmussen syndrome and long-term response to thalidomide.

    abstract::We report a 13-year-old female who experienced symptoms and signs of Rasmussen encephalitis for the first time at the age of 5 years. Various therapeutic procedures, including conventional and new antiepileptic drugs, steroids, immunoglobulin, plasma exchanges, and partial hemispherectomy, were applied, but their resu...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(03)00216-9

    authors: Marjanovic BD,Stojanov LM,Zdravkovic DS,Kravljanac RM,Djordjevic MS

    更新日期:2003-08-01 00:00:00

  • Effect of treatment of obstructive sleep apnea on seizure outcomes in children with epilepsy.

    abstract::A retrospective review of children with epilepsy and obstructive sleep apnea, treated surgically for their obstructive sleep apnea from January 2008-October 2010, was performed for age, sex, type of epilepsy, antiseizure medications, sleep-study data, and changes in seizure frequency. Twenty-seven subjects (median age...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2012.03.005

    authors: Segal E,Vendrame M,Gregas M,Loddenkemper T,Kothare SV

    更新日期:2012-06-01 00:00:00

  • Angiodysgenetic necrotizing encephalopathy or diffuse meningocerebral angiomatosis.

    abstract::A patient with angiodysgenetic necrotizing encephalopathy or diffuse meningocerebral angiomatosis complicated by intraventricular hemorrhage, posthemorrhagic hydrocephalus, and signs of heart failure is reported. The hydrocephalus and cardiomegaly were diagnosed by fetal ultrasonography. Based on these pathologic find...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(96)00004-5

    authors: Arvanitis DL,Apostolidou IA,Routsis PV,Biskini EI,Kalpoyannis NS

    更新日期:1996-02-01 00:00:00

  • Multiple syndromes of 3-methylglutaconic aciduria.

    abstract::The most common clinical syndromes associated with 3-methylglutaconic aciduria are presented. In some patients these syndromes are multisystemic, progressive disorders of unknown etiology. Tissues deriving significant energy through oxidative metabolism (notably brain and cardiac muscle) are most often affected and in...

    journal_title:Pediatric neurology

    pub_type: 杂志文章,评审

    doi:10.1016/0887-8994(93)90046-f

    authors: Gibson KM,Elpeleg ON,Jakobs C,Costeff H,Kelley RI

    更新日期:1993-03-01 00:00:00

  • Facial dysmorphism in Leigh syndrome with SURF-1 mutation and COX deficiency.

    abstract::Leigh syndrome is an inherited, progressive neurodegenerative disorder of infancy and childhood. Mutations in the nuclear SURF-1 gene are specifically associated with cytochrome C oxidase-deficient Leigh syndrome. This report describes two patients with similar facial features. One of them was a 2(1/2)-year-old male, ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2005.10.020

    authors: Yüksel A,Seven M,Cetincelik U,Yeşil G,Köksal V

    更新日期:2006-06-01 00:00:00

  • Early-onset ataxia with oculomotor apraxia with a novel APTX mutation.

    abstract::Early-onset ataxia with oculomotor apraxia and hypoalbuminemia is an autosomal recessive cerebellar ataxia characterized by oculomotor apraxia, peripheral neuropathy, and hypoalbuminemia. Mutations in aprataxin gene located at chromosome 9q13 have been identified recently in Japanese and European patients. This study ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2005.01.012

    authors: Ito A,Yamagata T,Mori M,Momoi MY

    更新日期:2005-07-01 00:00:00

  • Serum, urine, and saliva levels of ghrelin and obestatin pre- and post-treatment in pediatric epilepsy.

    abstract:INTRODUCTION:In this study, we aimed to determine the serum, urine, and saliva levels of acyl ghrelin, des-acyl ghrelin, and obestatin in the newly diagnosed idiopathic generalized pediatric epilepsy patients in the pretreatment period and in the third month of valproic acid. MATERIAL AND METHODS:Thirty pre- and post-...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2014.05.014

    authors: Taskin E,Atli B,Kiliç M,Sari Y,Aydin S

    更新日期:2014-09-01 00:00:00

  • Neonatal posthemorrhagic hydrocephalus: neuropathologic and immunohistochemical studies.

    abstract::A neuropathologic study was undertaken to examine associated brain damage in patients with fetal and neonatal posthemorrhagic hydrocephalus (PHH). In PHH the association of periventricular leukomalacia and pontosubicular necrosis was not increased, but that of cerebellar subarachnoid hemorrhage and olivo-cerebellar pa...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(95)00183-g

    authors: Fukumizu M,Takashima S,Becker LE

    更新日期:1995-10-01 00:00:00

  • Leukoencephalopathy around a tumor cyst following intracystic methotrexate injection.

    abstract::A 4-year-old female with choroid plexus carcinoma developed progressive disturbance of consciousness 2 years after postoperative treatment with radiotherapy, chemotherapy, and focal methotrexate injection into a residual tumor cyst. Magnetic resonance imaging revealed white matter lesions localized around the expandin...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2004.06.018

    authors: Yano T,Sawaishi Y,Hirayama A,Takaku I,Takada G

    更新日期:2005-01-01 00:00:00

  • Mild encephalopathy with splenial lesion and parainfluenza virus infection.

    abstract::Mild encephalopathy with reversible splenial lesions has mainly been associated with influenza A and B virus infection. Patients present with neurologic symptoms 1 to 3 days after a prodromal illness and recover completely within a few days. Magnetic resonance imaging typically shows reversible lesions with reduced di...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2012.11.007

    authors: Abenhaim Halpern L,Agyeman P,Steinlin M,El-Koussy M,Grunt S

    更新日期:2013-03-01 00:00:00

  • Pediatric Guillain-Barré Syndrome in a 30-Year Nationwide Cohort.

    abstract:BACKGROUND:Guillain-Barré syndrome is the most common cause of acute flaccid paresis in childhood. Few validated large-scale population-based data are available concerning pediatric Guillain-Barré syndrome, including incidence, risk factors, and initial clinical characteristics. METHODS:In the Danish National Patient ...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2020.01.017

    authors: Levison LS,Thomsen RW,Markvardsen LK,Christensen DH,Sindrup SH,Andersen H

    更新日期:2020-06-01 00:00:00

  • Fetal intracerebral hemorrhage in familial thrombophilia.

    abstract::We describe a fetal intracerebral hemorrhage associated with familial thrombophilia. Intraventricular and intraparenchymal hemorrhage of the left cerebral hemisphere was diagnosed at 22 weeks of gestation. Neuropathologic examination demonstrated a large germinal zone hemorrhage and ischemic changes secondary to bleed...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2009.04.027

    authors: Crespin M,Alhenc-Gelas M,Grangé G,Fallet-Bianco C,Fontenay M

    更新日期:2009-10-01 00:00:00

  • Expression of the LIS-1 gene product in brain anomalies with a migration disorder.

    abstract::Miller-Dieker syndrome (MDS) is a prototype of brain malformations characterized by abnormal neuronal migration. To clarify the pathomechanisms underlying these anomalies, we performed immunohistochemical studies using specific antibodies against the protein product of LIS-1, the candidate gene responsible for the MDS...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(96)00260-3

    authors: Isumi H,Takashima S,Kakita A,Yamada M,Ikeda K,Mizuguchi M

    更新日期:1997-01-01 00:00:00

  • MRI and CT findings in Krabbe disease.

    abstract::The progression and characteristics of magnetic resonance imaging (MRI) and computed tomographic (CT) findings in 3 patients with infantile Krabbe disease (i.e., globoid cell leukodystrophy or galactocerebroside beta-galactosidase deficiency) are reported. We obtained initial CT and MRI studies when patients demonstra...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(91)90046-n

    authors: Sasaki M,Sakuragawa N,Takashima S,Hanaoka S,Arima M

    更新日期:1991-07-01 00:00:00

  • MRI in infantile neuroaxonal dystrophy.

    abstract::A 6-year-old boy with the typical clinical features of infantile neuroaxonal dystrophy was examined with magnetic resonance imaging. The findings suggested increased metal deposition in the globus pallidus. Magnetic resonance imaging findings of Hallervorden-Spatz syndrome and infantile neuroaxonal dystrophy are simil...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(89)90083-0

    authors: Ito M,Okuno T,Asato R,Mutoh K,Nakano S,Kataoka K,Fujii T,Mikawa H,Saida K

    更新日期:1989-07-01 00:00:00

  • Choreoathetosis after cardiac surgery with hypothermia and extracorporeal circulation.

    abstract::Eleven children, 4-48 months old, with congenital cyanotic heart defects developed choreoathetoid movements 2-12 days after cardiac surgery with hypothermia and extracorporeal circulation (ECC). The abnormal movements mainly involved the limbs, facial musculature, and tongue, leading to a severe dysphagia. The symptom...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(98)00036-8

    authors: Gherpelli JL,Azeka E,Riso A,Atik E,Ebaid M,Barbero-Marcial M

    更新日期:1998-08-01 00:00:00

  • Comparison of CT and MRI brain tumor imaging using a canine glioma model.

    abstract::A canine gliosarcoma model was used to study the effectiveness of magnetic resonance imaging (MRI) with gadolinium contrast enhancement in defining the histologic margins of brain tumors. The effectiveness of this technique was compared to conventional computed tomography (CT) using iodinated contrast enhancement. Cul...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(88)90066-5

    authors: Whelan HT,Clanton JA,Wilson RE,Tulipan NB

    更新日期:1988-09-01 00:00:00

  • Levetiracetam in continuous spike waves during slow-wave sleep syndrome.

    abstract::We investigated the clinical characteristics of children with continuous spike waves during slow-wave sleep syndrome and their treatment response to levetiracetam. Five boys and one girl, diagnosed with epilepsy with continuous spike waves during slow-wave sleep syndrome, were enrolled. Their clinical characteristics,...

    journal_title:Pediatric neurology

    pub_type: 临床试验,杂志文章

    doi:10.1016/j.pediatrneurol.2008.04.007

    authors: Wang SB,Weng WC,Fan PC,Lee WT

    更新日期:2008-08-01 00:00:00

  • Late Cerebrovascular Complications After Radiotherapy for Childhood Primary Central Nervous System Tumors.

    abstract:BACKGROUND:Brain radiotherapy plays a central role in the treatment of certain types of childhood primary central nervous system tumors. However, damage to surrounding normal brain tissue causes different acute and chronic medical and neurological complications. Despite the expected increase in number of childhood prim...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2015.05.015

    authors: Passos J,Nzwalo H,Marques J,Azevedo A,Netto E,Nunes S,Salgado D

    更新日期:2015-09-01 00:00:00

  • Mutation analysis in Emery-Dreifuss muscular dystrophy.

    abstract::The purpose of this study was to search for STA gene defects in three families with clinically typical Emery-Dreifuss muscular dystrophy. Emery-Dreifuss is an X-linked muscular dystrophy with humeroperoneal weakness and life-threatening, but treatable, cardiac abnormalities in male patients and in female carriers. The...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(99)00023-5

    authors: Nevo Y,Al-Lozi M,Parsadanian AS,Elliott JL,Connolly AM,Pestronk A

    更新日期:1999-07-01 00:00:00

  • Reduction of elevated CSF beta-endorphin by fenfluramine in infantile autism.

    abstract::Fenfluramine therapy has been reported to improve behavior in infantile autism and has been associated with a decrease in abnormally increased blood serotonin content. The primary central effect has not been proved to be serotonergic. Beta-endorphin is involved in the anorexic effect of fenfluramine and may play a rol...

    journal_title:Pediatric neurology

    pub_type: 临床试验,杂志文章

    doi:10.1016/0887-8994(87)90032-4

    authors: Ross DL,Klykylo WM,Hitzemann R

    更新日期:1987-03-01 00:00:00

  • Paramagnetic signals in the globus pallidus as late radiographic sign of juvenile-onset GM1 gangliosidosis.

    abstract:BACKGROUND:The juvenile form of GM1 gangliosidosis lacks specific physical findings and thus is often a diagnostic challenge for clinicians. T2 hypodensity in the globus pallidus is a characteristic radiographic sign of neurodegeneration with iron accumulation in the brain that is observed in GM1 gangliosidosis, but th...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2014.09.022

    authors: Takenouchi T,Kosaki R,Nakabayashi K,Hata K,Takahashi T,Kosaki K

    更新日期:2015-02-01 00:00:00

  • Neurologic consultations in children with systemic cancer.

    abstract::The frequency and severity of neurologic symptoms in children with systemic cancer is unknown. The authors reviewed the records of children with systemic cancer for whom a neurologic consultation was requested between 1993 and 1996. The 157 patients had 161 malignancies and 205 consultations. Leukemia (59) and lymphom...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(98)00114-3

    authors: Antunes NL,De Angelis LM

    更新日期:1999-02-01 00:00:00

  • Outcome and Cost of Inpatient Hospitalization for Intravenous Dihydroergotamine Treatment of Refractory Pediatric Headache.

    abstract:BACKGROUND:To determine the cost and efficacy of admitting patients for intravenous dihydroergotamine treatment and to identify factors associated with a higher likelihood of response to treatment. METHODS:We performed a retrospective review of all pediatric hospitalizations from 2001 to 2010 for intravenous dihydroer...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2016.09.009

    authors: Nelson GR,Bale JF,Kerr LM

    更新日期:2017-01-01 00:00:00

  • Tolosa-Hunt syndrome preceded by facial palsy in a child.

    abstract::We report on a previously healthy 11-year-old boy with unilateral periorbital mild headache and facial nerve palsy, followed during the next 5 months by recurrent unilateral headaches and subsequent extrinsic paresis of the third cranial nerve and paresis of the sixth cranial nerve, each of which improved with steroid...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/j.pediatrneurol.2010.08.018

    authors: Cerisola A,González G,Scavone C

    更新日期:2011-01-01 00:00:00

  • Postinfectious encephalomyelitis with localized basal ganglia involvement.

    abstract::The diagnosis of postinfectious encephalomyelitis with symmetric lesions in the basal ganglia was confirmed by magnetic resonance imaging in 2 patients. A 7-year-old patient experienced severe dystonia and hyperreflexia; magnetic resonance imaging demonstrated bilateral lesions in the putamina and basis pontes. The ot...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/0887-8994(89)90024-6

    authors: Donovan MK,Lenn NJ

    更新日期:1989-09-01 00:00:00

  • Vitamins ameliorate secondary mitochondrial failure in neonatal rat brain.

    abstract::Recirculation after transient intrauterine ischemia has previously been found to be accompanied by secondary mitochondrial dysfunction in the immature rat brain. This study was performed to assess the efficacy of combined treatment with ascorbic acid and alpha-tocopherol in improving secondary brain damage. On the 17t...

    journal_title:Pediatric neurology

    pub_type: 杂志文章

    doi:10.1016/s0887-8994(02)00383-1

    authors: Nakai A,Shibazaki Y,Taniuchi Y,Oya A,Asakura H,Koshino T,Araki T

    更新日期:2002-07-01 00:00:00