当前位置： SCI文献检索 > EUROPEAN JOURNAL OF PEDIATRICS期刊下所有文献 > New hospital-based policy for children whose parents present at the ER due to domestic violence, substance abuse and/or a suicide attempt.

New hospital-based policy for children whose parents present at the ER due to domestic violence, substance abuse and/or a suicide attempt.

Abstract：

:Child maltreatment is a major social problem with many adverse consequences, and a substantial number of maltreated children are not identified by health care professionals. In 2010, in order to improve the identification of maltreated children in hospitals, a new hospital-based policy was developed in Amsterdam, The Netherlands. This policy was adapted from another policy that was developed in The Hague, the Netherlands, in 2007. In the new Amsterdam policy, all adults presenting at the emergency department due to domestic violence, substance abuse, and/or a suicide attempt are asked whether they have any children in their care. If this is the case, parents are urged to visit the outpatient pediatric department together with all of their children. During this visit, problems are evaluated and voluntary referrals can be arranged to different care organizations. If parents refuse to cooperate, their children are reported to the Dutch Child Abuse Counseling and Reporting Centre. The two aims of this study are to describe (1) characteristics of the identified families and (2) the referrals made to different voluntary and involuntary care organizations during the first 2 years after implementation of the policy. Data were collected from medical records. One hundred and six children from 60 households were included, of which 68 children because their mother was a victim of domestic violence. Referrals to care organizations were arranged for 99 children, of which 67 on a voluntary basis. The Amsterdam policy seems successful in arranging voluntary support for the majority of identified children.

journal_name

Eur J Pediatr

journal_title

European journal of pediatrics

authors

Hoytema van Konijnenburg EM,Sieswerda-Hoogendoorn T,Brilleslijper-Kater SN,van der Lee JH,Teeuw AH

doi

10.1007/s00431-012-1869-3

subject

Has Abstract

pub_date

2013-02-01 00:00:00

pages

207-14

issue

2

eissn

0340-6199

issn

1432-1076

journal_volume

172

pub_type

杂志文章

相关文献

EUROPEAN JOURNAL OF PEDIATRICS文献大全
  • Breastfeeding, previous Epstein-Barr virus infection, Enterovirus 71 infection, and rural residence are associated with the severity of hand, foot, and mouth disease.

    abstract：:Severe hand, foot, and mouth disease (HFMD) is likely to develop critical complications such as brainstem encephalitis, acute pulmonary edema, and circulatory failure, which cause child mortality during outbreaks. This study aims to investigate factors that predict the severity of HFMD. One hundred sixteen in-patient ...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/s00431-013-1939-1

    authors： Li Y,Dang S,Deng H,Wang W,Jia X,Gao N,Li M,Wang J

    更新日期：2013-05-01 00:00:00

  • Copper and liver disease.

    abstract：:There has been some limited progress in the understanding of the basic defect in Wilson disease and the gene concerned has been located to the chromosome region 13q14. Treatment with zinc has emerged as a definite alternative to penicillamine administration and some shortcomings and/or hazards of both forms of therapy...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章,评审

    doi：10.1007/BF01963553

    authors： Danks DM

    更新日期：1991-01-01 00:00:00

  • Sagittal craniostenosis, congenital heart disease, mental deficiency and various dysmorphies in two sibs--a "new" syndrome?

    abstract：:This is a report on two mentally retarded sibs with similar anomalies (sagittal craniosynostosis, complex cardiovascular malformations, mandibular ankylosis) and various dysmorphic features. They could represent a "new" probably monogenic syndrome. ...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00647293

    authors： Pfeiffer RA,Singer H,Zschiesche S

    更新日期：1987-01-01 00:00:00

  • Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counselling.

    abstract：UNLABELLED:Congenital hydrocephalus is a serious condition that can arise from multiple causes. It comprises a diverse group of conditions which result in impaired circulation and absorption of cerebrospinal fluid. Congenital malformations of the central nervous system, infections, haemorrhage, trauma, teratogens and, ...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章,评审

    doi：10.1007/s004310050830

    authors： Schrander-Stumpel C,Fryns JP

    更新日期：1998-05-01 00:00:00

  • Epinephrine versus dopamine in neonatal septic shock: a double-blind randomized controlled trial.

    abstract：:We compared epinephrine and dopamine as a first-line vasoactive drug in 40 neonates (enrolled in two gestational age strata ≤ 306/7 and ≥ 310/7 weeks) with fluid-refractory septic shock. Epinephrine or dopamine was initiated at 0.2 or 10 μg/kg/min, respectively. If shock persisted after 15 min, epinephrine or dopamine...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章,随机对照试验

    doi：10.1007/s00431-018-3195-x

    authors： Baske K,Saini SS,Dutta S,Sundaram V

    更新日期：2018-09-01 00:00:00

  • Treatment of status epilepticus with thiopentone sodium anaesthesia in a child.

    abstract：:A 4-month-old infant was admitted to the Pediatric Intensive Care Unit with Pneumococcal meningitis. A few hours after admission he developed intractable convulsions that could not be stopped with phenytoin, phenobarbitone and a continuous drip of diazepam. Thiopentone sodium anaesthesia was induced for 24 h terminati...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00441663

    authors： Goitein KJ,Mussaffi H,Melamed E

    更新日期：1983-04-01 00:00:00

  • Concanavalin A capping in polymorphonuclear leukocytes.

    abstract：:Various polymorphonuclear leukocyte (PMN) functions are dependent on an intact intracellular cytoskeleton consisting of the microtubules and the microfilaments. To investigate the microtublule system in PMNs we observed the spontaneous, Colchicine and Diamide induced cap-formation by fluorescence microscopy ion PMNs o...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00441634

    authors： Rister M,Brucke G,Wegener F,Gladtke E

    更新日期：1980-12-01 00:00:00

  • Pre-eruptive varicella encephalitis: case report and review of the literature.

    abstract：UNLABELLED:Varicella-related neurological complications usually appear after the rash. Pre-eruptive neurological complications of primary varicella zoster virus infections have been rarely described. We report on a 5.5-year-old boy who developed encephalitis 4 days before the onset of a mild vesicular skin rash and 5 d...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/s004310050942

    authors： Wagner HJ,Seidel A,Grande-Nagel I,Kruse K,Sperner J

    更新日期：1998-10-01 00:00:00

  • Fear effects by the media.

    abstract：UNLABELLED:Both news media and entertainment fiction may lead to short-term and enduring fright reactions. Even TV programs, movies and news made for children may trigger fear. Preoperational children (3 to 7 years of age) are most afraid of fantasy characters, transformations and interpersonal violence. Operational ch...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/s00431-011-1632-1

    authors： Custers K,Van den Bulck J

    更新日期：2012-04-01 00:00:00

  • Quality control for selective screening of inborn errors of metabolism.

    abstract：:A comprehensive program for proficiency testing of biochemical genetics laboratories is described. Inborn errors of metabolism of amino acids, organic acids, glycosaminoglycans and oligosaccharides are covered, as well as the assay of galactose-1-phosphate. Participants are not only required to report the analytical r...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF02138772

    authors： Hommes FA

    更新日期：1994-01-01 00:00:00

  • Fibrodysplasia ossificans progressiva (FOP): watch the great toes!

    abstract：:Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder and the most disabling condition of heterotopic (extraskeletal) ossification in humans. Extraskeletal bone formation associated with inflammation preceding the osseous conversion usually begins in the first decade, predominantly in the head, neck, ...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/s00431-010-1232-5

    authors： Kartal-Kaess M,Shore EM,Xu M,Schwering L,Uhl M,Korinthenberg R,Niemeyer C,Kaplan FS,Lauten M

    更新日期：2010-11-01 00:00:00

  • Neurological complications of pandemic influenza A H1N1 2009 infection: European case series and review.

    abstract：:Neurological manifestations and outcomes of children with the 2009 H1N1 virus infection have been reported in three American series and from smaller cohorts and case reports worldwide. Of the 83 children admitted between April 2009 and March 2010 with H1N1 virus infection to a tertiary children's hospital in a Europea...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章,评审

    doi：10.1007/s00431-010-1392-3

    authors： Surana P,Tang S,McDougall M,Tong CY,Menson E,Lim M

    更新日期：2011-08-01 00:00:00

  • N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication.

    abstract：:We report the 9-year follow-up of a patient suffering from N-acetylglutamate synthetase deficiency, an urea cycle disorder leading to severe neonatal hyperammonaemia. Hitherto two patients from two families with this inborn error of metabolism had been observed. Our management consisted mainly of a protein-restricted ...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF01955939

    authors： Schubiger G,Bachmann C,Barben P,Colombo JP,Tönz O,Schüpbach D

    更新日期：1991-03-01 00:00:00

  • Chromosome deletion and multiple cartilaginous exostoses.

    abstract：:We report a 13 year-old girl with manifestations strikingly reminiscent of the tricho-rhino-phalangeal (TRP) II or Langer-Giedion syndrome. A terminal deletion of 8q must be assumed to be the cause of her condition till proven otherwise. A similar chromosome abnormality should be searched for (blindly) in other cases ...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00441586

    authors： Bühler EM,Bühler UK,Stalder GR,Jani L,Jurik LP

    更新日期：1980-03-01 00:00:00

  • Increased cerebral blood flow velocities in newborn infants of smoking mothers.

    abstract：:Cerebral blood flow velocities (CBFV) were measured by the pulsed Doppler method in 41 infants of smoking mothers and in 59 apparently healthy control infants. Although gestational age, birth weight, and systolic blood pressure were lower in infants exposed to tobacco smoke prenatally, systolic (65 +/- 11 vs. 47 +/- 1...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF01956151

    authors： Abdul-Khaliq H,Segerer H,Luck W,Obladen M

    更新日期：1993-03-01 00:00:00

  • Exchange transfusion in newborns via a peripheral artery and vein.

    abstract：:Exchange transfusion using a peripheral artery and vein was carried out 18 times in 17 newborn infants. The arteries use to withdraw blood were the radial [13], the ulnar [3] an the posterior tibial [2]. Infusion of blood was carried out simultaneously through a peripheral vein. There was no mortality or morbidity dir...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00443258

    authors： Sagi E,Eyal F,Armon Y,Arad I,Robinson M

    更新日期：1981-11-01 00:00:00

  • Stress response and procedural pain in the preterm newborn: the role of pharmacological and non-pharmacological treatments.

    abstract：UNLABELLED:Repeated invasive procedures occur routinely in neonates who require intensive care, causing pain at a time when it is developmentally unexpected. Multiple lines of evidence suggest that repeated and prolonged pain exposure alters their subsequent pain processing, long-term development, and behaviour. Primar...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章,随机对照试验

    doi：10.1007/s00431-011-1655-7

    authors： Gitto E,Pellegrino S,Manfrida M,Aversa S,Trimarchi G,Barberi I,Reiter RJ

    更新日期：2012-06-01 00:00:00

  • Rheumatoid arthritis and growth retardation in children: treatment with human growth hormone.

    abstract：:Twenty patients with rheumatoid arthritis or Still's disease associated with growth failure were treated with human growth hormone, 7.5 to 17 U/m2 body surface per week. Five patients did not respond with better growth. In the remainder the mean growth rate increased from 1.9 cm/year (range: 0 to 3.3) to 6.2 cm/year (...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00441894

    authors： Butenandt O

    更新日期：1979-01-18 00:00:00

  • Plasma fibronectin levels in meningococcal disease.

    abstract：UNLABELLED:Fibronectin (a glycoprotein which modulates inflammation) may decrease mortality in systemic infection. Children with meningococcal disease (MCD) may have low fibronectin levels. We aimed to compare plasma fibronectin levels in children with MCD and controls, correlate fibronectin levels with interleukin-6 (...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章,多中心研究

    doi：10.1007/s004310050636

    authors： Riordan FA,Bestwick K,Thomson AP,Sills JA,Hart CA

    更新日期：1997-06-01 00:00:00

  • 3-Methylglutaconic and 3-methylglutaric aciduria in a patient with suspected 3-methylglutaconyl-CoA hydratase deficiency.

    abstract：:A girl suffering from marked muscular hypotonia, severe statomotor and mental retardation, bilateral optic atrophy with chorioretinal degeneration, convulsions and a moderate compensated metabolic acidosis is described. Screening for metabolic disorders revealed massive 3-methylglutaconic with 3-methylglutaric aciduri...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00442306

    authors： Lehnert W,Scharf J,Wendel U

    更新日期：1985-03-01 00:00:00

  • Oral vitamin A supplementation in very low birth weight neonates: a randomized controlled trial.

    abstract：:This randomized double-blind placebo-controlled trial evaluated the effects of early postnatal oral vitamin A supplementation (VAS) in 196 inborn very-low birth weight (VLBW) infants requiring respiratory support at 24 h of age. Eligible infants were randomized to receive aqueous syrup of vitamin A (10,000 IU of retin...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章,随机对照试验

    doi：10.1007/s00431-019-03412-w

    authors： Basu S,Khanna P,Srivastava R,Kumar A

    更新日期：2019-08-01 00:00:00

  • Acute idiopathic scrotal oedema: four cases and a short review.

    abstract：:We report four cases of acute idiopathic scrotal oedema, an underreported cause of acute painless or moderately painfull swelling and erythema of the scrotum in young boys. It is a self-limiting disease and to prevent unnecessary surgical exploration or antibiotic therapy, it is very important to distinguish acute idi...

    journal_title：European journal of pediatrics

    pub_type： 信件

    doi：10.1007/s004310100771

    authors： van Langen AM,Gal S,Hulsmann AR,De Nef JJ

    更新日期：2001-07-01 00:00:00

  • Thyroid function testing in neonates born to women with hypothyroidism.

    abstract：:Our aim was to assess the utility of serum thyroxine and thyroid stimulating hormone performed at 10-14 days of life in diagnosing congenital hypothyroidism (CH) in babies born to mothers with hypothyroidism. This was a retrospective study of all babies born in a tertiary referral centre for neonatology over a 12-mont...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/s00431-016-2793-8

    authors： McGovern M,Reyani Z,O'Connor P,White M,Miletin J

    更新日期：2016-12-01 00:00:00

  • Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrum.

    abstract：:Clinically visible corneal opacities were observed in a patient with an extremely severe form of mucopolysaccharidosis II. In a second patient with an unusually mild form of mucopolysaccharidosis II, discrete corneal opacities were detected by slit-lamp examination. Thus clear corneae can no longer be regarded as a ha...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00441369

    authors： Spranger J,Cantz M,Gehler J,Liebaers I,Theiss W

    更新日期：1978-08-17 00:00:00

  • Day case paediatric tonsillectomy: a quality improvement project.

    abstract：:Tonsillectomy is one of the commonest ENT paediatric procedures. Recovery is best achieved at home, and cost-effectiveness of the day case pathway is significant in tonsillectomy. This project scrutinised the local practice regarding the effectiveness of day case pathway in paediatric tonsillectomy in a large regional...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/s00431-018-3220-0

    authors： Atfeh MS,Richardson-May J,Rainsbury J

    更新日期：2018-11-01 00:00:00

  • Growth failure due to protein loss in dermatitis.

    abstract：:A 10-month-old infant is described who suffered from extensive atopic dermatitis, failure to thrive, hypoalbuminaemia and oedema. Large amounts of sticky exudate were lost through the skin and were shown to be rich in albumin. As renal and intestinal loss of protein was excluded, the patient's condition was ascribed t...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00446072

    authors： Abrahamov A,Schifmann R,Goldstein R,Tal Y,Freier S

    更新日期：1986-08-01 00:00:00

  • Obstructive endocarditis in an immunodeficient infant.

    abstract：:We report the case of 5-week-old male infant who presented as a 'near miss cot death'. He had the immunodeficient syndrome of defective neutrophil mobility and delayed umbilical cord separation. He was shown to have staphylococcal endocarditis with a large vegetation on the mitral valve, and acute obstruction of the m...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF02429063

    authors： Walters MD,Deanfield JE,Robinson PJ,Matthew DJ

    更新日期：1986-12-01 00:00:00

  • Mitral valve prolapse in Turner syndrome.

    abstract：:We have evaluated 46 patients with Turner syndrome by clinical examination, M-mode and two-dimensional echocardiography, dynamic exercise testing and 24 h Holter monitoring. Twelve patients (26.1%) had mitral valve prolapse and 7 patients (15.2%) had isolated non stenotic bicuspid aortic valve. Aortic root dilation wa...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00441551

    authors： Bastianon V,Pasquino AM,Giglioni E,Bosco G,Tebaldi L,Cives C,Colloridi V

    更新日期：1989-04-01 00:00:00

  • Achondrogenesis type I: light and electron-microscopic studies.

    abstract：:The light- and electron-microscopic structure of articular and costal cartilage in a case of achondrogenesis type I has been described. The most characteristic ultrastructural change in the chondrocytes was conspicuous dilatation of the rough endoplasmatic reticulum (RER) which contained amorphous electronopaque mater...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章

    doi：10.1007/BF00442406

    authors： Molz G,Spycher MA

    更新日期：1980-06-01 00:00:00

  • Everything the pediatrician ever wanted to know about HLA but was afraid to ask.

    abstract：:Following a description of the genetic aspects of the human histocompatibility antigens system HLA and its principle typing methods, this paper reviews the relationship between HLA antigens, transplantation immunology and certain diseases. In particular, the role of the lymphocyte-defined antigens of the HLA-D system ...

    journal_title：European journal of pediatrics

    pub_type： 杂志文章,评审

    doi：10.1007/BF00441576

    authors： Passarge E,Valentine-Thon E

    更新日期：1980-03-01 00:00:00