Maternal education and risk factors for sudden death in infants. Working Group of the Groupe Belge de Pédiatres Francophones.

Abstract:

UNLABELLED:To monitor infant care practices associated with risks for sudden infant death, 400 Belgian families with infants less than 6 months old were questioned by 21 paediatricians during routine visits to local paediatric practices and well baby services (11 in urban centres, 10 in rural areas). Because of incomplete information, 35 families were excluded. Of the 365 mothers included in the study, 36.1% had under 7 years of schooling, 38.4% less than 13 years, and 25.5% had a professional school or a university degree. Risk factors for sudden infant death were found in 208 (56.9%) families: a usual non-supine sleep position (31.5% of the infants); sleeping under a duvet (24.1%); mothers smoking during and after gestation (16.4%); a high room temperature (6.6%); use of sedatives (3.8%); necklaces or plastic film in the cot (2.5%); and soft beddings (2.2%). Maternal education, but not the fathers' profession was significantly related to the number of risk factors (mean odds ratio of 4.4; 95% CI: 1.5 to 5.3; P = 0.001). A stepwise logistic regression analysis identified the mother's length of schooling as the single most significant independent factor for the presence of risk (P < 0.005). CONCLUSION:Less educated mothers reported having been informed of risk-reducing recommendations as frequently as better educated mothers. It can be concluded that future reduction in risks for sudden infant death syndrome should include new strategies designed to modify infant care practices.

journal_name

Eur J Pediatr

authors

Kahn A,Bauche P,Groswasser J,Dramaix M,Scaillet S,Working Group, Groupe Belge de Pediatres Francophones.

doi

10.1007/s004310100783

keywords:

subject

Has Abstract

pub_date

2001-08-01 00:00:00

pages

505-8

issue

8

eissn

0340-6199

issn

1432-1076

journal_volume

160

pub_type

杂志文章
  • Schinzel-Giedion syndrome.

    abstract::We describe a female infant with the Schinzel-Giedion syndrome. Features present in 11 patients include coarse face, midface retraction, urogenital anomalies, poor skull vault mineralisation and variable anomalies of the long bones. Outcome is poor and mental retardation is the rule among survivors. Prenatal diagnosis...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF01955902

    authors: Verloes A,Moës D,Palumbo L,Elmer C,François A,Bricteux G

    更新日期:1993-05-01 00:00:00

  • Predictors of intracranial injuries in children after blunt head trauma.

    abstract:UNLABELLED:This study was conducted to determine if clinical features can predict the risk of intracranial injury (ICI) in pediatric closed head trauma. We enrolled 3,806 children under 16 years consecutively referred for acute closed head trauma to the paediatric emergency room of five Italian children's hospitals. Re...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s00431-005-0019-6

    authors: Da Dalt L,Marchi AG,Laudizi L,Crichiutti G,Messi G,Pavanello L,Valent F,Barbone F

    更新日期:2006-03-01 00:00:00

  • Clinical practice. NTBC therapy for tyrosinemia type 1: how much is enough?

    abstract:UNLABELLED:Four patients with tyrosinemia type 1 (ages 6-32 months) were treated with 2-(2-nitro-4-trifluoro-methylbenzoyl)-1,3-cyclohexandion (NTBC) at Cairo University Children's Hospital, Egypt and followed up for 12-27 months. The recommended average dose of NTBC is 1 mg/kg/day. They were started on the following d...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-009-1090-1

    authors: El-Karaksy H,Rashed M,El-Sayed R,El-Raziky M,El-Koofy N,El-Hawary M,Al-Dirbashi O

    更新日期:2010-06-01 00:00:00

  • Longitudinal study on early diagnosis and treatment of phenylketonuria in Poland.

    abstract::Early diagnosis and treatment of phenylketonuria (PKU) in Poland was started in 1965, initially on a voluntary and then on a obligatory basis. Guthrie tests have been used for newborn screening. For confirmation of diagnosis changing with time methods of blood phenylalanine (Phe) and tyrosine estimation were used. In ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/pl00014250

    authors: Cabalska MB,Nowaczewska I,Sendecka E,Zorska K

    更新日期:1996-07-01 00:00:00

  • Two hyperandrogenic adolescent girls with congenital portosystemic shunt.

    abstract:UNLABELLED:We describe two adolescent girls with a congenital portosystemic shunt who exhibited hyperandrogenism in addition to insulin resistant hyperinsulinaemia. Case 1 was referred to our clinic to undergo a routine clinical work-up prior to tonsillectomy at 14 years of age. Mild liver dysfunction was identified an...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310000539

    authors: Satoh M,Yokoya S,Hachiya Y,Hachiya M,Fujisawa T,Hoshino K,Saji T

    更新日期:2001-05-01 00:00:00

  • Spinal tuberculosis in a 14-year-old immigrant in the Netherlands.

    abstract::We present a case of Pott's disease, where the patient presented with neurological impairment due to vertebral granulomatous necrosis, needing immediate decompression and later stabilizing and reconstructive orthopaedic surgery, in order to create awareness for TB in general, especially this forgotten form of spinal t...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-006-0347-1

    authors: van Well GT,van der Mark LB,Vermeulen RJ,van Royen BJ,Wuisman PI,van Furth AM

    更新日期:2007-10-01 00:00:00

  • Unilateral decompressive craniectomy for children with severe brain injury. Report of seven cases and review of the relevant literature.

    abstract:UNLABELLED:Severe head injuries in children (under 15 years of age) have many features that differentiate them from head injuries in adults. In such cases, non-surgical treatment cannot always prevent fatal herniation. We report on seven cases of children with severe head injury, presenting with decorticate posturing a...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,评审

    doi:10.1007/s00431-001-0864-x

    authors: Hejazi N,Witzmann A,Fae P

    更新日期:2002-02-01 00:00:00

  • A 2-month-old infant with vomiting, seizures, and progressive apathy.

    abstract::A 2-month-old infant was admitted to hospital because of recurrent vomiting for 1 week, progressive apathy, and focal seizures. The cranial MRI showed a noticeable result. ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-012-1681-0

    authors: Larsen A,Martin C,Meyer S,Rohrer T,Papanagiotou P,van der Knaap M,Gortner L

    更新日期:2012-06-01 00:00:00

  • The effect of obesity, age, puberty and gender on resting metabolic rate in children and adolescents.

    abstract:UNLABELLED:During puberty fat-free mass (FFM) and fat mass (FM) change quickly and these changes are influenced by sex and obesity. Since it is not completely known how these changes affect resting metabolic rate (RMR), the aim of the present study was to investigate the effect of body composition, age, sex and puberta...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310050618

    authors: Molnár D,Schutz Y

    更新日期:1997-05-01 00:00:00

  • Asymmetry in children with cerebral palsy and oral structure.

    abstract::Twenty-six children with cerebral palsy were examined with respect to structural asymmetry of the mouth. In 19 children there were clear cut correlations between symmetry/asymmetry of voluntary function and the oral findings. Patients with symmetrical patterns of movements had symmetrical dentition, while in those wit...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441639

    authors: Haberfellner H,Richter M

    更新日期:1980-12-01 00:00:00

  • Rett syndrome in a patient with medium chain acyl-CoA dehydrogenase deficiency.

    abstract::A female patient with medium-chain acyl-CoA dehydrogenase (MCAD) deficiency developed normally until 13 months of age after which she showed a gradual developmental delay, followed by progressive dementia, and a decrease in head circumference growth culminating in the diagnosis of Rett syndrome at 3.5 years. ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF01954516

    authors: Beekman RP,Hofstee N,Smeitink JA,Poll-The BT,Duran M

    更新日期:1994-04-01 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

  • Atypical Rothmund-Thomson syndrome in a patient with compound heterozygous mutations in RECQL4 gene and phenotypic features in RECQL4 syndromes.

    abstract::We describe the natural history of the RTSII phenotype in a 7-year-old boy who developed intrauterine and postnatal growth retardation, failure to thrive and persisting diarrhoea. The growth hormone stimulation test identified an isolated growth hormone deficiency. Since infancy, the patient manifested skin lesions ch...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-007-0447-6

    authors: Sznajer Y,Siitonen HA,Roversi G,Dangoisse C,Scaillon M,Ziereisen F,Tenoutasse S,Kestilä M,Larizza L

    更新日期:2008-02-01 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

  • Insulin-like growth factors in lysosomal storage disease.

    abstract::Recent data indicate that insulin-like growth factor II (IGF II) and lysosomal enzymes bind to a common receptor. We measured serum IGF I and II levels in 16 patients with various lysosomal storage disorders. The IGF serum concentrations were normal as long as no marked liver disease was present. Under these condition...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF02073885

    authors: Jaeggi-Groisman SE,Kiess W,Christomanou H,Kessler U,Froesch ER

    更新日期:1992-01-01 00:00:00

  • A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.

    abstract::A five-year-old-girl with a history of recurrent hypoglycemia presented with acidosis, intractable vomiting, and abdominal tenderness; the diagnosis of acute pancreatitis was made by abdominal ultrasonography and supportive biochemical studies. Urinary organic acid analysis revealed metabolites suggestive of HMG-CoA l...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00540255

    authors: Wilson WG,Cass MB,Søvik O,Gibson KM,Sweetman L

    更新日期:1984-09-01 00:00:00

  • Congenital hemihypertrophy and malignant giant pheochromocytoma - a previously undescribed coincidence.

    abstract::This is apparently the first report on connatal hemihypertrophy with malignant pheochromocytoma. The coincidence of hemihypertrophy with other diseases, particularly neuroectodermal dysplasias on the one hand and the frequent association of neuroectodermal dysplasias with pheochromocytoma on the other, are emphasized....

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00481506

    authors: Schnakenburg KV,Müller M,Dörner K,Harms D,Schwarze EW

    更新日期:1976-07-12 00:00:00

  • Introduction of fish and other foods during infancy and risk of asthma in the All Babies In Southeast Sweden cohort study.

    abstract::The etiology of asthma includes lifestyle factors. Breastfeeding and introduction of complementary foods have been suggested to affect asthma risk, but the scientific foundation is not solid. Children from the birth cohort All Babies In Southeast Sweden study were included (n = 9727). Breastfeeding duration and timing...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-018-03312-5

    authors: Klingberg S,Brekke HK,Ludvigsson J

    更新日期:2019-03-01 00:00:00

  • Congenital self-healing non-Langerhans cell histiocytosis.

    abstract::Clinical, morphological, ultrastructural and immunological studies were performed in a case of congenital self-healing non-Langerhans cell histiocytosis. The patient showed several aspects that have not been published before: a large nodule in the vulvar region, vesiculobullous elements and pneumonia (asymptomatic). T...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441808

    authors: Oranje AP,Vuzevski VD,de Groot R,Prins ME

    更新日期:1988-10-01 00:00:00

  • Effects of laryngoscopy and tracheal intubation on cerebral and systemic haemodynamics in children under different protocols of anaesthesia.

    abstract::The effects of laryngoscopy and tracheal intubation on cerebral and systemic haemodynamics were studied in 30 children. The objective was to identify conditions in which the alterations of cerebral and systemic haemodynamics were minimal. The children were intubated after muscular relaxation and following 10 min of me...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF01957527

    authors: Bode H,Ummenhofer W,Frei F

    更新日期:1993-11-01 00:00:00

  • The prevalence of GB virus C/hepatitis G virus RNA among healthy and HCV-infected Catalan children.

    abstract::GB virus C (GBV-C) is a blood-borne flavivirus. The prevalence of GBV-C viremia among healthy adults is 0.5% to 4% and, to date, no disease has been definitely associated with GBV-C infection. We conducted a cross-sectional study to evaluate GBV-C viremia prevalence in a group of 327 healthy children with normal alani...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-007-0624-7

    authors: Claret G,Noguera A,González-Cuevas A,García-García JJ,Fortuny C,Muñoz-Almagro C

    更新日期:2008-09-01 00:00:00

  • Molybdenum cofactor deficiency in two siblings: diagnostic difficulties.

    abstract::Two siblings with molybdenum cofactor deficiency are presented. They showed clinical, biochemical and neuroradiological features very similar to those of the few previously described cases. Difficulties in diagnosis are emphasised. ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF01955243

    authors: Hansen LK,Wulff K,Dorche C,Christensen E

    更新日期:1993-08-01 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

  • Evolution of the proportion of patients with Down's syndrome karyotyped in Belgium since 1960.

    abstract::Estimation of the total number of infants with DS born each year in Belgium allows evaluation of changes in the proportion of children with DS in whom a karyotype has been established. This proportion steadily increased to 95% of the children with DS born in 1978. ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00442300

    authors: Evers-Kiebooms G,Vlietinck R,van den Berghe H

    更新日期:1985-03-01 00:00:00

  • Clinical practice: analgesia in neonates.

    abstract::Effective management of pain remains an important indicator of the quality of care provided to neonates. Since the review of McIntosh in this journal over a decade ago, an extensive number of papers on assessment, prevention, and treatment of pain have been reported. In addition, preclinical insights into neurodevelop...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,评审

    doi:10.1007/s00431-009-0932-1

    authors: Allegaert K,Veyckemans F,Tibboel D

    更新日期:2009-07-01 00:00:00

  • A child with mental retardation and asymmetrical hypertrophy of limbs.

    abstract::A 5-year-old male child presented with progressively increasing asymmetrical overgrowth of limbs, hyperpigmentation on the right half of the body, and mental retardation since 9 months of age. ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-010-1346-9

    authors: Sethi SK,Yadav D,Garg P,Chawla J,Goyal D

    更新日期:2011-06-01 00:00:00

  • Growth hormone treatment in a child with Williams-Beuren syndrome: a case report.

    abstract:UNLABELLED:Growth retardation is a consistent finding in Williams-Beuren syndrome. The cause of short stature in this syndrome is unknown. Endocrine studies have failed to reveal abnormalities in the growth hormone-insulin-like growth factor I axis. We report a boy with confirmed Williams-Beuren syndrome, who was found...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310051118

    authors: Kuijpers GM,De Vroede M,Knol HE,Jansen M

    更新日期:1999-06-01 00:00:00

  • The utility of FDG PET in diagnosis and follow-up of lymphoma in childhood.

    abstract::Hodgkin lymphoma (HL) and non-Hodgkin lymphoma (NHL) are among the most common malignancies of childhood. (18)F-fluorodeoxyglucose (FDG) positron emission tomography (PET) can be employed for accurate staging, treatment planning, and response assessment in pediatric patients with lymphomas, taking advantage of the inc...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,评审

    doi:10.1007/s00431-013-1993-8

    authors: Sioka C

    更新日期:2013-06-01 00:00:00

  • Skin-to-skin contact with an umbilical venous catheter: prospective evaluation in a level 3 unit.

    abstract:UNLABELLED:The aim was to assess the incidence of complications related to skin-to-skin contact (SSC) in newborns with an umbilical venous catheter (UVC). We carried out a prospective follow-up study of all UVCs in a level 3 unit where SSC is systematic. A total of 333 babies were included (mean gestational age of 31.3...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-015-2665-7

    authors: Catherine ZG,Béatrice P,Fabrice L,Claire H,Alain D

    更新日期:2016-04-01 00:00:00

  • Two novel glucose-6-phosphate dehydrogenase variants found in newborn mass-screening for galactosaemia.

    abstract:UNLABELLED:Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked recessive disorder in which haemolytic anaemia is the major symptom. The Beutler spot test employed in mass-screening for galactosaemia in newborns requires several intrinsic erythrocyte enzymes such as G6PD for its reaction and can theoretic...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310000652

    authors: Okano Y,Fujimoto A,Miyagi T,Hirono A,Miwa S,Niihira S,Hirokawa H,Yamano Y

    更新日期:2001-02-01 00:00:00