Total serum bilirubin levels during the first 2 days of life and subsequent neonatal morbidity in very low birth weight infants: a retrospective review.

Abstract:

:To determine the relationship between total serum bilirubin (TSB) during the first 2 days of life and subsequent neonatal morbidity in very low birth weight (VLBW, less than 1500 g) infants. We performed a prospective study of 582 VLBW infants born between July 1, 2005 and December 31, 2009. TSB was measured in umbilical cord blood (UCB), at 24 and 48 h after birth. Demographic and clinical characteristics of infants in hospital were recorded. The interaction between TSB variables during the first 48 h of life and subsequent neonatal morbidity were assessed in logistic regression analyses adjusted for multiple risk factors. It was found that TSB in UCB was in a negative correlation with occurrence of respiratory distress syndrome (RDS) [OR 0.626, 95% confidence interval (95% CI): 0.446-0.879, p = 0.007], and there was also a negative correlation between TSB in UCB and occurrence of intraventricular hemorrhage (IVH) [OR 0.695, 95% CI 0.826-0.981, p = 0.020]. However, TSB in UCB positively correlated with hyperbilirubinemia [OR 2.471, 95% CI 1.326-3.551, p = 0.012], and TSB at 24 h after birth was also in a positive correlation with early onset sepsis (EOS) [OR 1.299, 95% CI 1.067-1.582, p = 0.011]. VLBW infants with low TSB levels in UCB were more likely to develop RDS and IVH, and those with low TSB levels in UCB were less likely to develop hyperbilirubinemia. Infants with high TSB levels at 24 h after birth were more likely to develop EOS. The protective effect of raised TSB in UCB with respect to RDS and IVH warrants further investigation.

journal_name

Eur J Pediatr

authors

Zhu J,Xu Y,Zhang G,Bao Y,Wu M,Du L

doi

10.1007/s00431-011-1634-z

subject

Has Abstract

pub_date

2012-04-01 00:00:00

pages

669-74

issue

4

eissn

0340-6199

issn

1432-1076

journal_volume

171

pub_type

杂志文章
  • Long-term follow-up after stroke in childhood.

    abstract:UNLABELLED:Over the last few years, the importance of paediatric stroke has become more and more evident; however, there is still little known about long-term neurological and especially neuropsychological outcome of these children. By retrospective chart review, questionnaire and clinical examination with structured i...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-003-1357-x

    authors: Steinlin M,Roellin K,Schroth G

    更新日期:2004-04-01 00:00:00

  • Internet use and misuse: a multivariate regression analysis of the predictive factors of internet use among Greek adolescents.

    abstract::The internet is an integral tool for information, communication, and entertainment among adolescents. As adolescents devote increasing amounts of time to utilizing the internet, the risk for adopting excessive and pathological internet use is inherent. The study objectives include assessing the characteristics and pre...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-008-0811-1

    authors: Tsitsika A,Critselis E,Kormas G,Filippopoulou A,Tounissidou D,Freskou A,Spiliopoulou T,Louizou A,Konstantoulaki E,Kafetzis D

    更新日期:2009-06-01 00:00:00

  • Oral zinc sulphate as primary therapeutic intervention in a child with Wilson disease.

    abstract::An 8-year-old boy with an hepatic form of Wilson disease was treated with oral zinc sulphate as the primary and sole therapy. After 4 months, liver function had dramatically improved, and the parameters characterizing copper metabolism had also normalized. ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00441526

    authors: Milanino R,Marrella M,Moretti U,Velo GP,Deganello A,Ribezzo G,Tatò L

    更新日期:1989-06-01 00:00:00

  • Does the severity of congenital heart defects affect disease-specific health-related quality of life in children in Bosnia and Herzegovina?

    abstract:UNLABELLED:The aim of this study was to assess whether the severity of congenital heart defects (CHD) affects disease-specific health-related quality of life (HRQOL) in children after open heart surgery. One hundred and fourteen children with CHD and one of their parents participated in the study. HRQOL was evaluated b...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-009-1060-7

    authors: Tahirović E,Begić H,Nurkić M,Tahirović H,Varni JW

    更新日期:2010-03-01 00:00:00

  • Successful intravenous immunoglobulin therapy for recurrent pneumococcal otitis media in young children.

    abstract::Serum immunoglobulin levels and naturally occurring antibody titres against Streptococcus pneumoniae were measured in seven children aged 1-1.9 years with recurrent pneumococcal acute otitis media (AOM). Three of them had low IgG2 levels. Mean antibody levels of anti-pneumococcal IgG1 and anti-pneumococcal IgG2 were s...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF01958979

    authors: Ishizaka A,Sakiyama Y,Otsu M,Ozutsumi K,Matsumoto S

    更新日期:1994-03-01 00:00:00

  • Treatment of seven cases of chronic granulomatous disease with sulfamethoxazole-trimethoprim (SMX-TMP).

    abstract::Seven male Japanese children with chronic granulomatous disease were given sulfamethoxazole-trimethoprim (SMX-TMP) for recurrent pyogenic infections, most of which had proved difficult to control with other antibiotics. With continous treatment the children remained free of infections severe enough to necessitate hosp...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00493540

    authors: Kobayashi Y,Amano D,Ueda K,Kagosaki Y,Usui T

    更新日期:1978-04-20 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

  • A fatal case of portal hypertension complicating systemic mastocytosis in an adolescent.

    abstract::Portal hypertension was observed in a 17-year-old girl with urticaria pigmentosa since 2 months of age. Liver biopsies showed portal and sinusoidal infiltration with mast cells although spleen biopsies showed only fibrosis. CONCLUSION. Portal hypertension is a complication of systemic mastocytosis that can lead to dea...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF01959789

    authors: Fonga-Djimi HS,Gottrand F,Bonnevalle M,Farriaux JP

    更新日期:1995-10-01 00:00:00

  • Exhaled nitric oxide levels in infants with chronic lung disease.

    abstract:UNLABELLED:Chronic lung disease (CLD) is an inflammatory disorder; in patients with other inflammatory disorders exhaled nitric oxide (NO) levels are elevated. The aim of this study was to test the hypothesis that prematurely born infants with CLD would have elevated exhaled NO levels compared to those without CLD and ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-004-1480-3

    authors: Leipälä JA,Williams O,Sreekumar S,Cheeseman P,Rafferty GF,Hannam S,Milner A,Greenough A

    更新日期:2004-09-01 00:00:00

  • Somatic symptom and related disorders in a tertiary paediatric hospital: prevalence, reach and complexity.

    abstract::Specialist paediatric services manage a variety of presentations of functional somatic symptoms. We aimed to describe the presentation and management of children and adolescents with somatic symptom and related disorders (SSRDs) requiring admission to a tertiary children's hospital with the objective of informing the ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-020-03867-2

    authors: Wiggins A,Court A,Sawyer SM

    更新日期:2020-11-13 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

  • Acute transverse myelitis caused by ECHO virus type 18 infection.

    abstract:UNLABELLED:A 14-year-old boy developed acute quadriplegia, associated with sensory impairment and bowel and urinary dysfunction. MRI of the cervical cord showed diffuse increased signal intensity on T2-weighted images with gadolinium-diethylenetriamine penta-acetic acid enhancement. Based on the clinical presentation a...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF02072107

    authors: Takahashi S,Miyamoto A,Oki J,Azuma H,Okuno A

    更新日期:1995-05-01 00:00:00

  • Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot.

    abstract::When a mother with tetralogy of Fallot has a conotruncal anomaly face, her child might have a 22q11.2 deletion and severe congenital heart disease. ...

    journal_title:European journal of pediatrics

    pub_type: 信件

    doi:10.1007/s00431-001-0890-8

    authors: Ito T,Okubo T,Sato H

    更新日期:2002-03-01 00:00:00

  • Tumour genesis syndrome: severe hypophosphatemia and hypokalemia may be ominous presenting findings in childhood acute myeloid leukaemia.

    abstract::We report a 16-year-old girl who was diagnosed with acute leukaemia and a marked leucocytosis >200 × 109/L. She presented with marked hypophosphatemia, hypokalemia, acute renal failure and acute respiratory failure. These electrolytes disturbances may indicate rapid tumour genesis. These ominous findings required urge...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-017-2899-7

    authors: Chan WK,Chang KO,Lau WH

    更新日期:2017-08-01 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

  • Diet in pregnancy-more than food.

    abstract::High food quality, together with adequate macro- and micronutrient intake in pregnancy, is crucial for the health status of the mother and child. Recent findings suggest that it could also be beneficial or harmful in the context of the well-being of the whole future population. According to the developmental origins o...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,评审

    doi:10.1007/s00431-017-3026-5

    authors: Danielewicz H,Myszczyszyn G,Dębińska A,Myszkal A,Boznański A,Hirnle L

    更新日期:2017-12-01 00:00:00

  • Accuracy of blood volume estimations in critically ill children using 125I-labelled albumin and 51Cr-labelled red cells.

    abstract::Blood volume was estimated using 51chromium labelled red cells and 125iodinated human serum albumin in 5 children with sepsis, in 6 burned children and 7 children with acute lymphoblastic leukaemia. Studies of the equilibration pattern demonstrated that the mixing time of labelled red cells was prolonged to 40 minutes...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF00489987

    authors: Linderkamp O,Holthausen H,Seifert J,Butenandt I,Riegel KP

    更新日期:1977-06-01 00:00:00

  • Fatty acid composition of human milk during the 1st month after term and preterm delivery.

    abstract:UNLABELLED:The fatty acid composition of human breast milk was determined longitudinally after term and preterm delivery by high resolution gas liquid chromatography. Milk samples were obtained at days 5, 10, 20 and 30 after term (n = 38) or preterm (n = 19) delivery. The saturated fatty acids C10:0 and C12:0 and the p...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310050573

    authors: Genzel-Boroviczény O,Wahle J,Koletzko B

    更新日期:1997-02-01 00:00:00

  • Severe hypothyroidism after contrast enema in premature infants.

    abstract::Premature newborns are particularly vulnerable to iatrogenic hypothyroidism due to iodine exposure, usually through skin absorption of iodine-containing disinfectants or intravenous administration of iodinated contrast agents. We report here a case of severe iatrogenic hypothyroidism with goiter and cholestasis, disco...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-008-0782-2

    authors: Lombard F,Dalla-Vale F,Veyrac C,Plan O,Cambonie G,Picaud JC

    更新日期:2009-04-01 00:00:00

  • The influence of growth hormone monotherapy and growth hormone in combination with oxandrolone or testosterone on thyroxid hormone parameters and thyroxine binding globulin in patients with Ullrich-Turner syndrome.

    abstract:UNLABELLED:Administration of human growth hormone (GH) has yielded conflicting results concerning its role on thyroid function in patients with Ullrich-Turner syndrome. Therefore, we investigated the course of thyroid hormone parameters and thyroxin binding globulin in relation to GH therapy, IGF-I and additional oxand...

    journal_title:European journal of pediatrics

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1007/s004310050563

    authors: Schmitt K,Häusler G,Blümel P,Plöchl E,Waldhör T,Frisch H

    更新日期:1997-02-01 00:00:00

  • The effect of systemic corticosteroids on the innate and adaptive immune system in children with steroid responsive nephrotic syndrome.

    abstract:UNLABELLED:The severity and duration of immunosuppression caused by corticosteroids (CSs) usage have not been extensively studied. We aimed to investigate the effects of CSs on the various compartments of immune system in relation to timing of initiation and persistence of therapy. Pediatric patients with idiopathic ne...

    journal_title:European journal of pediatrics

    pub_type: 临床试验,杂志文章

    doi:10.1007/s00431-016-2694-x

    authors: Baris HE,Baris S,Karakoc-Aydiner E,Gokce I,Yildiz N,Cicekkoku D,Ogulur I,Ozen A,Alpay H,Barlan I

    更新日期:2016-05-01 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

  • Adolescents' drug use and drug knowledge.

    abstract:UNLABELLED:Self-medication is a common event. To use drugs correctly, a basic knowledge about drugs is required. Poor data are available about adults' drug knowledge. Furthermore, adolescents' basic drug knowledge has not been investigated. This study was designed in order to explore adolescents' drug use and knowledge...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310000503

    authors: Stoelben S,Krappweis J,Rössler G,Kirch W

    更新日期:2000-08-01 00:00:00

  • Brugada syndrome in childhood: a potential fatal arrhythmia not always recognised by paediatricians. A case report and review of the literature.

    abstract::We report on a youngster followed by his paediatrician from birth until 14 years of age for premature beats, most likely of ventricular origin. The sudden death of his sister provoked a re-assessment of his electrocardiograms (ECG), resulting in the diagnosis of Brugada syndrome and the subsequent implantation of a ca...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,评审

    doi:10.1007/s00431-006-0150-z

    authors: Mivelaz Y,Di Bernardo S,Pruvot E,Meijboom EJ,Sekarski N

    更新日期:2006-08-01 00:00:00

  • Mother-to-child transmission of human immunodeficiency virus type 1: influence of parity and mode of delivery. Paediatric AIDS Group of Switzerland.

    abstract:UNLABELLED:In a national prospective study of risk factors for mother-to-child transmission of human immunodeficiency virus (HIV), 316 children of HIV-positive mothers were followed up for at least 6 months. Infection status was determined in 254 of them and 46 were found to be infected giving a transmission rate of 18...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF02074831

    authors: Kind C

    更新日期:1995-07-01 00:00:00

  • Drug administration errors in paediatric wards: a direct observation approach.

    abstract::Paediatric patients are more vulnerable to drug administration errors due to a lack of appropriate drug dosages and strengths for use in this group of patients. Therefore, the aim of the present study was to determine the extent and types of drug administration errors in two paediatric wards and to identify measures t...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s00431-009-1084-z

    authors: Chua SS,Chua HM,Omar A

    更新日期:2010-05-01 00:00:00

  • Familial hemophagocytic lymphohistiocytosis.

    abstract::Familial hemophagocytic lymphohistiocytosis (FHL) is probably a genetically transmitted disease affecting infants and very young children. Cardinal symptoms are fever, hepatosplenomegaly, and pancytopenia. Frequently meningeal involvement is seen, manifested by neurologic symptoms and a lymphohistiocytic pleocytosis w...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章,评审

    doi:10.1007/BF00443367

    authors: Janka GE

    更新日期:1983-06-01 00:00:00

  • Disseminated Mycobacterium avium infection in a child with decreased tumour necrosis factor production.

    abstract:UNLABELLED:Disseminated atypical mycobacterium infection is essentially reported in cellular immunodeficient children. Cell-mediated immunity including cytokines like tumour necrosis factor alpha (TNF) and gamma interferon (IFN) is the most important factor allowing control of the dissemination of Mycobacterium. We rep...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310050583

    authors: Tuerlinckx D,Vermylen C,Brichard B,Ninane J,Cornu G

    更新日期:1997-03-01 00:00:00

  • Effects of bilirubin on visual evoked potentials in term infants.

    abstract:UNLABELLED:To determine bilirubin-induced neurotoxicity, serial visual evoked potentials (VEPs) of 72 infants with neonatal hyperbilirubinaemia and 22 controls were evaluated and compared in four sessions for 8 weeks after birth. The levels of maximal serum bilirubin were found positively related to the wave latencies ...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/BF02079073

    authors: Chen YJ,Kang WM

    更新日期:1995-08-01 00:00:00

  • Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion.

    abstract:UNLABELLED:The phenotypes of chromosomal 22q11.2 microdeletion are quite variable among individuals and hypoparathyroidism (HP) constitutes a definite portion of the clinical spectrum. For the correct diagnosis and pertinent follow up of the HP children due to del22q11.2, we tried to delineate the clinical characterist...

    journal_title:European journal of pediatrics

    pub_type: 杂志文章

    doi:10.1007/s004310050762

    authors: Adachi M,Tachibana K,Masuno M,Makita Y,Maesaka H,Okada T,Hizukuri K,Imaizumi K,Kuroki Y,Kurahashi H,Suwa S

    更新日期:1998-01-01 00:00:00